首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 46 毫秒
1.
Spinel-olivine geothermometry in peridotites from ultramafic complexes   总被引：7，自引：0，他引：7  
An empirical calibration of the spinel-olivine geothermometer (Evans and Frost, 1975) is attempted and applied to parageneses of lherzolitic rocks. In ultramafic complexes, most of the derived temperature estimates range between 700 ° and 850 °C, and appear generally lower than those given by other geothermometers, based upon Ca or Al contents of coexisting pyroxenes. A comparison of the different thermometric data in two well studied occurrences, the Ronda ultramafic complex and the San Carlos xenolith field, suggests that differential rates of diffusion and recrystalization may account for the large range of temperatures (between 700 ° and 1200 °C) determined by various mineral geothermometers in peridotites. The equilibrium exchange of Mg and Fe between spinel and olivine would be the fastest one and would continue effectively during the cooling down to relatively low temperatures, while other exchange reactions used as geothermometers in peridotites, like partitioning of Ca and Al in coexisting pyroxenes, are blocked at higher temperatures.  相似文献   

2.
方同辉  马鸿文 《现代地质》1998,12(2):197-203
摘　要　利用穆斯堡尔谱仪对辽宁宽甸地幔岩包体中的矿物进行了三价铁的测定‚测试结果 与国内外已发表的数据接近。Fe 3＋ ／∑Fe 比值分别为：斜方辉石0∙066～0∙196‚单斜辉石 0∙216～0∙344‚尖晶石0∙283～0∙299‚石榴石0∙057～0∙223。依据电价平衡原理计算的 Fe 3＋ 含量受 Si 4＋ 、Al 3＋ 和 Cr 3＋ 的电子探针分析误差影响很大。根据地幔矿物的电子探针分析结果 计算平衡温度、压力和氧逸度时‚二辉石 En、Ca 转移反应温度计和石榴石 斜方辉石 Al 压力 计的计算结果不超过温压计的一般误差范围‚而石榴石 单斜辉石 Fe 2＋ Mg 交换反应温度计 在忽略 Fe 3＋ 时计算的温度值可偏高100℃以上;采用橄榄石／斜方辉石／尖晶石组合氧压力计 计算的氧逸度值‚误差一般约在±0∙7个对数单位。  相似文献   

3.
橄榄岩中尖晶石化学成分分带的机理及其地质意义   总被引：1，自引：1，他引：1  
李建平 Provo  A 《矿物学报》1997,17(2):156-163
橄榄岩中尖晶石的化学成分分带显示，在由温度降低引起的亚固相平衡过程中，与橄榄石及斜方辉石相邻的尖晶石边缘贫Mg和Al、富Fe和Cr，而与单斜辉石相邻的尖晶石边线相反。尖晶石的Fe和Mg分带为其他矿物的粒间Fe－Mg离子扩散所致；尖晶石中的Cr和Al分带则是尖晶石晶体内部Cr－Al离子的交互扩散所致。本文从热力学理论角度说明了尖晶石晶体内部的Cr－Al交互扩散受其Fe－Mg分带的控制；从热力学计算证明了尖晶石内Al必须从富Fe处向富Mg处扩散，解释了尖晶石中Mg和Al及Fe和Cr分带的一致性。  相似文献   

4.
The Red Mountain alpine peridotie forms the basal, dominantlyharzburgitic tectonite portion of an ophiolite suite in SouthIsland, New Zealand. Olivine and pyroxene Mg/Fe compositionsare constant for individual lithologies, but generally increasethrough the series harzburgite, orthopyroxenite, harzburgiticdunite, dunite. An olivine-clinopyroxene dominated transitionalperidotite along the western margin of the mass has more Fe-richsilicates than in the harzburgitic suite. Fe-Mg silicate-spinelrelationships and the distribution of Al between coexistingpyroxene and spinel indicate nearly complete post-layering equilibration.A partial re-equilibration is suggested by narrow compositionalrims on pyroxenes and spinel. Relative to the mineral cores,the rims show enhanced partitioning of Al into spinel relativeto pyroxene. The Fe-Mg relationships between silicates and spinel,and the compositional variations from cores to rims of pyroxenesand spinels indicate that the rims formed at lower temperaturesthan the mineral cores. This conclusion is supported by theapplication of several geothermometers, which give average temperaturesof equilibration and partial re-equilibration of 1000–1070?C and 920–1030 ?C, respectively. Pyroxene overgrowthson olivine probably represent pre-equilibration cooling phenomena.Equilibration pressures cannot be estimated with precision becauseRed Mountain pyroxenes have Al contents that vary as a functionof whole-rock Al2O3, and other compositional variables, as wellas of T and P of equilibration. The lack of plagioclase in theharzburgite tectonites, and the wide range of (Al/Cr)spinelindicate equilibration at fairly high pressures, probably atdepths within the 25–80 km range. The transitional peridotiteprobably formed by re-equilibration of residual crystals withbasaltic melt at shallower (<25 km) depths, and is evidencesupporting the conclusion that the ultramafic and mafic partsof the ophiolite suite at Red Mountain represent complementaryparts of the same melting event.  相似文献   

5.
The thermal history of four spinel lherzolites (Lhz-13. Lhz-28, Lhz-29 and Lhz-53) from tuff breccia of the Ichinomegata crater, northeast Japan, has been studied in detail. Lhz-13 and Lhz-53 showed nearly perfect chemical homogeneity of the constituent minerals, and increase of Ca near the rim of olivine is the only disequilibrium evidence observed. In addition to the Ca zoning in olivine, Lhz-28 and Lhz-29 revealed compositional zoning in the Mg/Mg + Fe ratio and Ca content in ortho- and clinopyroxenes. Lhz-13 and Lhz-53 equilibrated at about 800°C in the upper mantle, based on Fe/Mg partitioning between olivine/spinel and olivine/clinopyroxene, and on the mutual solubility of Ca between olivine and pyroxenes. Lhz-28 and Lhz-29 also equilibrated originally at about 800°C, but were preheated at about 1000°C prior to their entrapment by the ascending host magma. The Fe/Mg partitioning between olivine /spinel and olivine/clinopyroxene reequilibrated during the preheating event: however, the Ca solubility did not reequilibrate. Olivine alone has rehomogenized with a high-Ca content but pyroxenes were compositionally zoned with Ca. The preheating event, indicated by the high-Ca content in the core of olivine, is recognized from about a half of the Ichinomegata Iherzolites (50 xenoliths were studied).The duration of heating during the transport of the xenolith by the magma (estimated from the width of the Ca zoning in the rim of olivine) ranges between several hours to a year depending on the rock specimen. From the requirement to reset olivine core compositions, the duration of the preheating event was estimated as greater than 1000 yr.  相似文献   

6.
The occurrence of rhythmic layering of chromite and host serpentinites in the deformed layered igneous complexes has been noticed in the Nuggihalli schist belt (NSB) in the western Dharwar craton, Karnataka, South India. For this study, the chromitite rock samples were collected from Jambur, Tagadur, Bhakatarhalli, Ranganbetta and Byrapur in the NSB. Petrography and ore microscopic studies on chromite show intense cataclasis and alteration to ferritchromite. The ferritchromite compositions are characterized by higher Cr number (Cr/[Cr+Al]) (0.68–0.98) and lower Mg number (Mg/[Mg+Fe]) (0.33–0.82) ratios in ferritchromite compared to that of parent chromite. The formation process for the ferritchromite is thought to be related to the exchange of Mg, Al, Cr, and Fe between the chromite, surrounding silicates (serpentines, chlorites), and fluid during serpentinization.  相似文献   

7.
The partitioning of divalent (Co, Ni) and trivalent (Sc, Cr) trace elements between olivine, ortho- and clinopyroxene and spinel from spinel peridotite xenoliths has been investigated. These peridotites cover a wide range in modal composition from dunite to primitive lherzolites and have equilibrated in the upper mantle between >900° C and <1,200° C.The distribution of Co and Ni shows only minor variation through the whole sequence. In contrast, Sc partitioning between ortho- and clinopyroxene and olivine and clinopyroxene as well as Cr partitioning between olivine and clinopyroxene or olivine and orthopyroxene display high but systematic variations which can be assigned to dependences upon equilibration temperatues. Empirical temperature calibrations are given for Sc-orthopyroxene/clinopyroxene, Sc-olivine/clinopyroxene and Cr-olivine/clinopyroxene which, in principle, may permit to estimate equilibration temperatures not only for lherzolites or harzburgites but for orthopyroxene-free peridotites, too.Sc and Ni partition coefficients between spinel and mantle silicate minerals are primarily dependent upon the major element composition of spinel (e.g. Cr and Al) although a temperature dependence can still be identified. Probably such compositional effects are not observed for trace element partitioning between pyroxenes and olivine or ortho- and clinopyroxene only for the reason that in normal spinel peridotites these minerals show much less variation in major element composition than their coexisting spinels.  相似文献   

8.
New evidence for ultrahigh‐pressure metamorphism (UHPM) in the Eastern Alps is reported from garnet‐bearing ultramafic rocks from the Pohorje Mountains in Slovenia. The garnet peridotites are closely associated with UHP kyanite eclogites. These rocks belong to the Lower Central Austroalpine basement unit of the Eastern Alps, exposed in the proximity of the Periadriatic fault. Ultramafic rocks have experienced a complex metamorphic history. On the basis of petrochemical data, garnet peridotites could have been derived from depleted mantle rocks that were subsequently metasomatized by melts and/or fluids either in the plagioclase‐peridotite or the spinel‐peridotite field. At least four stages of recrystallization have been identified in the garnet peridotites based on an analysis of reaction textures and mineral compositions. Stage I was most probably a spinel peridotite stage, as inferred from the presence of chromian spinel and aluminous pyroxenes. Stage II is a UHPM stage defined by the assemblage garnet + olivine + low‐Al orthopyroxene + clinopyroxene + Cr‐spinel. Garnet formed as exsolutions from clinopyroxene, coronas around Cr‐spinel, and porphyroblasts. Stage III is a decompression stage, manifested by the formation of kelyphitic rims of high‐Al orthopyroxene, aluminous spinel, diopside and pargasitic hornblende replacing garnet. Stage IV is represented by the formation of tremolitic amphibole, chlorite, serpentine and talc. Geothermobarometric calculations using (i) garnet‐olivine and garnet‐orthopyroxene Fe‐Mg exchange thermometers and (ii) the Al‐in‐orthopyroxene barometer indicate that the peak of metamorphism (stage II) occurred at conditions of around 900 °C and 4 GPa. These results suggest that garnet peridotites in the Pohorje Mountains experienced UHPM during the Cretaceous orogeny. We propose that UHPM resulted from deep subduction of continental crust, which incorporated mantle peridotites from the upper plate, in an intracontinental subduction zone. Sinking of the overlying mantle and lower crustal wedge into the asthenosphere (slab extraction) caused the main stage of unroofing of the UHP rocks during the Upper Cretaceous. Final exhumation was achieved by Miocene extensional core complex formation.  相似文献   

9.
Three methods of geothermometry, currently used for spinel lherzolites, are refined based on new experiments on subsolidus phase equilibria of olivine, pyroxenes and spinel in CaO-MgO-Al2O3-SiO2 and natural rock systems at 16 kb and 1200 °C. Although quasi-thermodynamic modelling is employed, the methods are essentially based on the pyroxene solvus, alumina contents in clinopyroxene and orthopyroxene. Increasing alumina contents in pyroxenes reduce enstatite and diopside components in clinopyroxene and orthopyroxene, respectively. Thus, neglect of alumina in pyroxenes causes underestimates of temperatures by the solvus method.The three geothermometers were tested by applying them to homogeneous spinel lherzolites which were especially selected for this purpose. Coincidence of the three temperatures thus estimated gives confidence in the effectiveness of the geothermometers.They were also applied to spinel lherzolite nodules in basalts and intrusive lherzolites described in the literature. It was found that equilibration temperature of the nodules varies from 1000 °C to 1300 °C, i.e., temperatures somewhat higher than have been generally thought. In contrast to the nodules, the intrusive spinel lherzolites show extensive disequilibrium, which is probably due to retrogressive metamorphism suffered by the intrusives.  相似文献   

10.
Whole-rock, major and trace element analyses and microprobe mineral analyses were conducted on serpentinized peridotites recovered from the walls of a MAR (Mid-Atlantic Ridge) 43° N fracture zone. These peridotites are extensively serpentinized; serpentine usually makes up 30–100 vol. percent of the bulk rocks. The relict minerals observed consist mainly of olivine and orthopyroxene with subordinate amounts of clinopyroxene and brown spinel. The range in olivine composition is very limited (Fo91–92). Orthopyroxene forms large, anhedral crystals with clinopyroxene exsolution lamellae and shows undulose extinction with bent cleavages and lamellae. Broad beam microprobe analyses indicate that the composition range of orthopyroxene is also limited (En89.1–87.6Fs8.2-8.0Wo2.7–4.4; Al2O3=1.82–2.64 wt%; Cr2O3=0.63–0.88 wt%). Clinopyroxene tends to fringe large orthopyroxene crystals or fills the interstices between them. The Mg/Fe ratios of clinopyroxene are practically constant; however, the Ca/(Ca + Mg + Fe) ratios range from 0.48 to 0.45. The Cr/(Cr+Al) and Mg/(Mg+ Fe2+) ratios of brown spinel range from 0.57 to 0.36 and 0.69 to 0.56, respectively. The geothermometers utilizing coexisting spinel lherzolite mineral assemblages suggest that the MAR 43° N peridotites attained equilibrium at temperatures from 1100° to 1250° C.Peridotites recovered from the ocean floor are generally considered to have been subjected to partial melting processes and are regarded as residues left after primary magma was removed. Major element chemistry of the MAR 43° N peridotites are compared with those of the ocean-floor ultramafic tectonites reported previously and used together with those published data to demonstrate that the major element abundances of the oceanfloor peridotites define an average trend which is compatible with removal of primary magma from these peridotites at moderate pressures (10–15 kb). Then, the most primitive abyssal tholeiite glasses could be produced by ca. 10% olivine fractionation of such primary magma. Extensive fractionation of olivine and/or orthopyroxene from picritic liquids which are in equilibrium with the lherzolitic or harzburgitic mantle sources at higher pressures (>20 kb) could not yield the majority of the most primitive abyssal tholeiite glasses.  相似文献   

11.
Data from analyses of three coexisting pairs of pyroxenes with a wide range of Fe content from each of two localities are used to show the large systematic variation and predictable correlation of Fe (or Mg) of a pyroxene with its content of Al, Mn and Na in mafic granulites. Comparisons of pyroxenes can then be made more meaningful by normalizing Al, or other elements, to an appropriate Mg value. As both P and T may affect the element distribution of the two pyroxenes differently (especially Al and Na) the factor used in normalizing is found to vary from region to region.  相似文献   

12.
A detailed crystal chemical study of coexisting olivine, orthopyroxene, clinopyroxene and spinel from selected Victorian (Australia) lherzolite suites was carried out by means of single crystal x-ray diffraction and electron probe microanalysis to obtain actual site occupancies. The aim of this study was primarily to characterise the intracrystalline configurations and related cation ordering on sites in major mantle constituents. The results demonstrate that cation ordering on sites is subject to distinctive crystallographic controls which depend on the petrological evolution of the suite. Mg-Fe2+ ordering in M1–M2 pyroxene sites depends on variations of the smaller cations, mainly Alvi, Ti4+, Fe3+, and related configurations of M 1. Pressuresensitive Alvi is crucial to Fe2+, the more ordered clinopyroxene showing high Alvi configurations which tend to exclude the larger bivalent cations and yield small polyhedral volumes for M 1, M 2, T sites and the unit cell. Conversely, the coexisting orthopyroxene, characterised by lower Alvi configuration and higher M 1 and unit cell volumes, is relatively more disordered. Olivine is consistent with the coexisting clinopyroxene, the more disordered crystals coexisting with more disordered clinopyroxene, while Al-Mg order in the coexisting spinel shows the reverse relationship. Estimated temperatures of apparent equilibration based on current geothermometers are not considered realistic. Assumptions of ideal cation mixing on sites in pyroxene and spinel are not supported.  相似文献   

13.
Composition of chromiferous spinel included in olivines of Mg-rich basalts and gabbros of the Deccan Traps (Gujarat and Western Ghats) are reported here. They vary from Al-rich compositions [Al2O3 = 53wt.%; Cr#, 100Cr/(Cr + Al) = 12] to Cr-rich compositions [Cr2O3 = 51wt.%; Cr# = 84], and from Cr-Al rich compositions towards Cr-rich Ti-magnetite (TiO2 up to 23 wt.%, ulvöspinel up to 67mol.%). The Mg# [100Mg/(Mg + Fe2+)] of spinel decreases from 81 to nearly zero. The highest Cr# has been found in the Bushe Fm., Thakurvadi Fm., and some high-Ti basalts of the Pavagadh section, whereas some of the low-Ti basalts of Saurashtra have Al-rich compositions typical of spinels found in mid-ocean ridge basalts. The chemical composition of the Deccan Trap spinels is completely different compared to that observed in mantle spinel suites, with very few exceptions. The decreasing Al and increasing Fe and Ti of spinel seems to be mainly the result of decrease of Mg in the locally coexisting melts and favourable cationic substitutions in the lattice. There is barely any evidence of general relationships between the composition of the Deccan spinels and inferred mantle sources of the host magmas. Pyroxene inclusions in spinels may witness a high-pressure stage of crystallization, but the possibility of non-equilibrium crystallization, or even magma mixing, cannot be ruled out. Overall, the compositional ranges of chromiferous spinel in the Deccan Traps closely match those observed in the other Large Igneous Provinces having mafic/ultramafic intrusions and mafic magma compositions (e.g., Siberian Traps, Karoo, Emeishan).  相似文献   

14.
Metagabbros from two widely separated areas in the Adirondacks show development of coronas. In the Southern Adirondacks, these are cored by olivine which is enclosed in a shell of orthopyroxene that is partially, or completely, rimmed by symplectites consisting of clinopyroxene and spinel. Compositions of the corona phases have been determined by electron probe and are consistent with a mechanism involving three partial reactions, thus:
  1. Olivine=Orthopyroxene+(Mg, Fe)++.
  2. Plagioclase+(Mg, Fe)+++Ca++=Clinopyroxene+Spinel+Na+.
  3. Plagioclase+(Mg, Fe)+++Na+=Spinel+more sodic plagioclase+Ca++.
Reaction (a) occurs in the inner shell of the corona adjacent to olivine; reaction (b) in the outer shell; and (c) in the surrounding plagioclase, giving rise to the spinel clouding which is characteristic of the plagioclase in these rocks. Alumina and silica remain relatively immobile. These reactions, when balanced, can be generalized to account for the aluminous nature of the pyroxenes and for changing plagioclase composition. Summed together, the partial reactions are equivalent to:
  1. Olivine + Anorthite = Aluminous orthopyroxene + Aluminous Clinopyroxene + Spinel (Kushiro and Yoder, 1966).
In the Adirondack Highlands, coronas between olivine and plagioclase commonly have an outer shell of garnet replacing the clinopyroxene/spinel shell. The origin of the garnet can also be explained in terms of three partial reactions:
  1. Orthopyroxene+Ca++=Clinopyroxene+(Mg, Fe)++.
  2. Clinopyroxene+Spinel+Plagioclase+(Mg, Fe)++=Garnet+Ca+++Na+.
  3. Plagioclase+(Mg, Fe)+++Na+=Spinel + more sodic plagioclase+Ca++.
These occur in the inner and outer corona shell and the surrounding plagioclase, respectively, and involve the products of reactions (a)-(d). Alumina and silica are again relatively immobile. Balanced, and generalized to account for aluminous pyroxenes and variable An content of plagioclase, they are equivalent to:
  1. Orthopyroxene+Anorthite+Spinel=Garnet (Green and Ringwood, 1967).
Amphibole coronas about opaque oxides in rocks of both areas are the result of oxide/plagioclase reactions with addition of magnesium from coexisting olivine. Based on published experimental data, pressure and temperature at the time of corona formation were on the order of 8 kb and 800° C for the garnet bearing coronas, with somewhat lower pressures indicated for the clinopyroxene/spinel coronas.  相似文献   

15.
Spinel-pyroxene-garnet relationships and their dependence on Cr/Al ratio   总被引：2，自引：0，他引：2  
The partitioning of Cr and Al between coexisting spinel and clinopyroxene and the dependence of spinel-cpxgarnet equilibria on Cr/Al ratio have been investigated by a combination of phase equilibrium experiments, high temperature solution calorimetry and thermodynamic calculations.The exchange equilibrium: has a measured enthalpy change for pure phases of –2,100±500 cal at 970 K and 1 atm. Experimental reversals of Cr-Al partitioning between the spinel and clinopyroxene phases yield the following partitioning relationship: where X i j refers to atomic fraction of i in the octahedral sites of phase j. The compositional dependence of partitioning implies that Al-Cr mixing in spinel is nonideal with, on the symmetrical model, a W Cr-Al Sp of 2,700±500 cal/gm. atom. In contrast, aluminum-chromium mixing in clinopyroxene is close to ideal.The measured stability field of knorringite (Mg3Cr2Si2O12) and mixing properties of garnet have been used in conjunction with our experimental data to calculate the influence of Cr/Al ratio on the important reaction: orthopyroxene+clinopyroxene+spinel=olivine+garnetThe stability field of spinel lherzolite increases by about 2.8 Kb for every increase of 0.1 in Cr/(Cr+Al) ratio up to Cr/(Cr+Al) of 0.7. The calculated stabilization is in very good agreement with the experimental results of O'Neill (1981). The partitioning relationships are such that, at the low ratios of Cr/Al (0.07) of primitive lherzolite, clinopyroxene buffers spinel composition and sharpens the spinelgarnet reaction interval from 10 Kb (little or no clinopyroxene) down to about 2 Kb in pyroxene-rich pyrolite.  相似文献   

16.
变质橄榄岩中尖晶石的分形结构因子类型及其成因意义   总被引：4，自引：2，他引：4  
沈步明 《岩石学报》1994,10(2):111-125
利用沈步明（１９９３）提出的分形结构因子的新方法，计算了橄榄岩包体、方辉橄榄岩、纯橄榄岩和铬铁矿等六种尖晶石的分形结构因子。划分了四种尖晶石分形结构因子类型：Ａ１和Ｃｒ强变异型、Ａ１和Ｃｒ变异型、Ｍｇ和Ｆｅ２－变异型、Ｍｇ和Ｆｅ２－强变异型，结合尖晶石的地质产状讨论了这四种类型的成因意义。通过大量分形结构子的计算和图表．有力说明分形结构因子对于表征物质在空间分布的结构性和数据之间的相关性，是一种有效的定量化手段。在推测尖晶石和主岩的成因方面，尖晶石的Ｃｒ（Ａ１）和Ｍｇ（Ｆｅ２＋）的ＦＳＦ值图解更优于尖晶石的Ｃｒ／（Ｃｒ＋Ａ１）－Ｍｇ／（Ｍ＋Ｆｅ２－）图解。  相似文献   

17.
This paper studies the hydrous facies of mantle-derived megacryst clinopyroxenes and pyroxenes of xeno-liths of pyroxenolite and spinel peridotite as well as garnet pyroxenolite in a kimberlitic lamprophyre pipe in Anyuan, Jiangxi, by Fourier Transform Infrared (FTIR). It explores the relationship between the water content of pyroxene on the one hand and its composition and source depths on the other hand. All the samples contain constitution water. Spectra of the clinopyroxene are dominated by two groups of bands: 3607-3630 cm-1 and 3522-3542 cm-1. Spectra of the orthopy-roxene are dominated by three groups of bands: 3410-3424 cm-1,3510-3516 cm-1 and 3560-3595 cm-1. The water content of the clinopyroxenes has a positive correlation with their FeO and Al2O3 contents. The source depths of mantle-derived clinopyroxene megacrysts, pyroxenolite, spinel peritotite and garnet pyroxenelite increase gradually in order. The Al2O3 and water contents of four pyroxenes have similar correlation with the source depth  相似文献   

18.
Chemical interdiffusion of Fe–Mg along the c-axis [001] in natural diopside crystals (X Di = 0.93) was experimentally studied at ambient pressure, at temperatures ranging from 800 to 1,200 °C and oxygen fugacities from 10?11 to 10?17 bar. Diffusion couples were prepared by ablating an olivine (X Fo = 0.3) target to deposit a thin film (20–100 nm) onto a polished surface of a natural, oriented diopside crystal using the pulsed laser deposition technique. After diffusion anneals, compositional depth profiles at the near surface region (~400 nm) were measured using Rutherford backscattering spectroscopy. In the experimental temperature and compositional range, no strong dependence of D Fe–Mg on composition of clinopyroxene (Fe/Mg ratio between Di93–Di65) or oxygen fugacity could be detected within the resolution of the study. The lack of fO2-dependence may be related to the relatively high Al content of the crystals used in this study. Diffusion coefficients, D Fe–Mg, can be described by a single Arrhenius relation with $$D^{{{\text{Fe}} - {\text{Mg}}}} = 2. 7 7\pm 4. 2 7\times 10^{ - 7} {\text{exp(}}-3 20. 7\pm 1 6.0{\text{ kJ}}/{\text{mol}}/{\text{RT)m}}^{ 2} /{\text{s}}.$$ D Fe–Mg in clinopyroxene appears to be faster than diffusion involving Ca-species (e.g., D Ca–Mg) while it is slower than D Fe–Mg in other common mafic minerals (spinel, olivine, garnet, and orthopyroxene). As a consequence, diffusion in clinopyroxene may be the rate-limiting process for the freezing of many geothermometers, and compositional zoning in clinopyroxene may preserve records of a higher (compared to that preserved in other coexisting mafic minerals) temperature segment of the thermal history of a rock. In the absence of pervasive recrystallization, clinopyroxene grains will retain compositions from peak temperatures at their cores in most geological and planetary settings where peak temperatures did not exceed ~1,100 °C (e.g., resetting may be expected in slowly cooled mantle rocks, many plutonic mafic rocks, or ultra-high temperature metamorphic rocks).  相似文献   

19.
Phenocryst and groundmass pyroxenes in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively by electron microprobe. Results and conclusions: i) Tholeiites contain augite, pigeonite, and bronzite; alkalic rocks contain salite, augite, and ferroaugite; and nephelinic rocks have salite, sometimes of Wo>50 mole %. ii) The three suites can be distinguished by Ca contents of pyroxenes: High-Ca pyroxenes of tholeiitic rocks have Wo30–40; those of alkalic rocks have Wo38–48; and those of the nephelinic rocks have Wo47–51; i.e. Wo in clinopyroxene increases from tholeiitic, to alkalic, to nephelinic suites, iii). In the alkalic suite, rock types can be distinguished on the basis of clinopyroxene composition: Alkalic olivine and alkalic basalts have Wo38–45, hawaiites and mugearites have Wo45–48. Trachytes can be distinguished from both groups by higher Fe (Fs22–30) and Ca contents (Wo43–47). iv) Pyroxenes in tholeiitic rocks show higher intrarock variability (e.g. Fs12Wo40-Fs37Wo30) than those of the alkalic and nephelinic suites, v) Na2O bulk-rock content affects Na2O content of the precipitating high-Ca pyroxene; e.g. Na2O in groundmass pyroxene increases from tholeiitic, to alkalic (mafic members only), to nephelinic suites; a similar relationship is present within the differentiated alkalic suite, vi) In tholeiites, changes in groundmass high-Ca pyroxene compositions are related to changes in bulk rock compositions, e.g. FeO/FeO+MgO+CaO in clinopyroxene increases as this ratio increases in the bulk rock; this is not true for alkalic and nephelinic rocks, vii) In groundmass high-Ca pyroxene, Al2O3, Na20, and TiO2 contents increase and MnO content decreases with increasing Wo content from tholeiitic, to alkalic (mafic members only), to nephelinic suites, viii) Groundmass high-Ca pyroxenes are richer in MnO and Na2O and poorer in Cr2O3 compared to coexisting phenocrysts. High-Ca pyroxene phenocrysts in nephelinic rocks and in one mugearite are depleted in SiO2 and enriched in Al2O3 relative to coexisting groundmass clinopyroxene, indicating increased SiO2 activity during crystallization. Some tholeiites show the reverse; this Si—Al relationship is not clear in other samples.  相似文献   

20.
Iron isotope and major- and minor-element compositions of coexisting olivine, clinopyroxene, and orthopyroxene from eight spinel peridotite mantle xenoliths; olivine, magnetite, amphibole, and biotite from four andesitic volcanic rocks; and garnet and clinopyroxene from seven garnet peridotite and eclogites have been measured to evaluate if inter-mineral Fe isotope fractionation occurs in high-temperature igneous and metamorphic minerals and if isotopic fractionation is related to equilibrium Fe isotope partitioning or a result of open-system behavior. There is no measurable fractionation between silicate minerals and magnetite in andesitic volcanic rocks, nor between olivine and orthopyroxene in spinel peridotite mantle xenoliths. There are some inter-mineral differences (up to 0.2‰ in 56Fe/54Fe) in the Fe isotope composition of coexisting olivine and clinopyroxene in spinel peridotites. The Fe isotope fractionation observed between clinopyroxene and olivine appears to be a result of open-system behavior based on a positive correlation between the Δ56Feclinopyroxene-olivine fractionation and the δ56Fe value of clinopyroxene and olivine. There is also a significant difference in the isotopic compositions of garnet and clinopyroxene in garnet peridotites and eclogites, where the average Δ56Feclinopyroxene-garnet fractionation is +0.32 ± 0.07‰ for six of the seven samples. The one sample that has a lower Δ56Feclinopyroxene-garnet fractionation of 0.08‰ has a low Ca content in garnet, which may reflect some crystal chemical control on Fe isotope fractionation. The Fe isotope variability in mantle-derived minerals is interpreted to reflect subduction of isotopically variable oceanic crust, followed by transport through metasomatic fluids. Isotopic variability in the mantle might also occur during crystal fractionation of basaltic magmas within the mantle if garnet is a liquidus phase. The isotopic variations in the mantle are apparently homogenized during melting processes, producing homogenous Fe isotope compositions during crust formation.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号