穆斯堡尔光谱仪在揭示地幔氧逸度研究中的应用

利用地幔橄榄岩包体中平衡矿物对的氧逸度计可以有效限定岩石圈地幔的氧化-还原状态.本文使用中国地质大学(武汉)新购置的WSS-10型常温穆斯堡尔光谱仪对华北地块西北部狼山地区橄榄岩包体的四相矿物开展了铁价态的直接测定.结果显示,斜方辉石Fe³⁺/∑Fe为0.05～0.11,单斜辉石的为0.16～0.25,尖晶石的为0.16～0.22,橄榄石为0.利用橄榄石-斜方辉石-尖晶石氧逸度计,获得狼山地区岩石圈地幔氧逸度为FMQ-0.82至FMQ-0.39(均值为FMQ-0.65).该值略高于依据电子探针测试数据计算获得的氧逸度值(FMQ-1.49至FMQ-0.8,均值为FMQ-1.25),造成这一差异的原因可能是后者忽略了尖晶石晶格中Fe³⁺过剩和阳离子空位导致的非化学计量比.与全球克拉通岩石圈地幔氧逸度值(均值为FMQ-0.35)相比,华北地块西北缘狼山地区岩石圈地幔整体表现为较还原状态,推测与深部地幔低fO₂熔体上升交代有关.     

辽宁宽甸地幔矿物三阶铁的穆斯堡尔谱测定及意义

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阶铁的测定,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     

甘肃金川Ⅱ号岩体辉石化学特征及其地质意义

金川Ⅱ号岩体主要由二辉橄榄岩和硫化物橄榄岩构成,单斜辉石和斜方辉石为岩相中主要造岩矿物,单斜辉石含量一般高于斜方辉石.矿物间的结构关系表明主要造岩矿物的结晶顺序为:橄榄石-斜方辉石-单斜辉石-斜长石.单斜辉石的TiO2,Al2O3,Cr2O3和Na2O质量分数依次为:0.29%～1.26%、3.17%～3.59%、0.86%～1.14%、0.29%～0.57%,斜方辉石的TiO2,Al2O3,Cr2O3和Na2O质量分数普遍低于单斜辉石,依次为:0.16%～0.40%、1.85%～2.38%、0.48%～0.68%、0.03%～0.10%.元素间的相关关系显示辉石的类质同像置换方式为:M1Fe2 2 Si=M1Ti 2IV Al,M1Fe2 Si=M1Fe3 IVAl,Fe3 和Ti进入矿物晶格置换Fe2 来平衡Al置换Si产生的正电价差.两种辉石较低的TiO2,Al2O3和Na2O质量分数显示出母岩浆为拉斑玄武岩浆的特征.二辉石温度计和单辉石温度计算表明斜方辉石的结晶温度下限和单斜辉石结晶温度上限大致在1146℃～1166℃之间,单斜辉石的结晶一直持续到1032℃或者更低.金川Ⅱ号岩体单斜辉石演化明显表现出向透辉石端员偏离,暗示岩浆在结晶分异过程中,可能与富钙质围岩发生了同化混染作用.     

玄武岩中幔源岩石包体内尖晶石特征及其热力学状态

大陆碱性玄武岩中幔源宕石包体是研究大陆上地幔最直接的样品之一。尖晶石是幔源岩石包体中常见的副矿物。对其成分、平衡温度、压力及氧逸度热力学状态研究,不仅可阐明上地幔条件下尖晶石的矿物学特证,揭示它们及其寄主幔源岩石的成因,而且还可获得研究区上地幔热力学状态、物质组分、矿物相变及地幔不均一性等信息。 本文利用我国东部31个地区的新生代玄武岩中的橄榄岩类和辉石岩类包体中的16O个尖晶石探针分析资料、及所分析的共生矿物橄榄石、斜方辉石及单斜辉石的大量数据。采用新的较合理的温度、压力和氧逸度计算方法进行计算和作图,得到如卜结论:1 随着上地幔岩石部分熔融程度的增加。其橄榄岩类残留物中的尖晶石的颜色由浅褐变为深褐色.Cr和Fe含量增加。而Al和Mg含量降院,2 碱性玄武岩中辉石类包体的尖晶石和橄榄岩类包体的尖晶石的颜鬼及成分有很大差异.说明两者成因不同 3 碱性玄武岩中幔源岩石包体内的尖晶石的主要成分是Cr、Al、Fe、Mg。Cr和Al、Fe和Mg之间存在着广泛的类质同象替代,而Fe与Al、Cr之间的替代作用是有限的。4 我国东部新生代时上地幔中,尖晶石形成的平衡温度为1100～1500°K(约827～1227℃)。其形成压力为(1.2～60) 10 Pa.但大部分尖晶石形成的平衡压力<40×10~8Pa(即     

地幔岩矿物压力计评述

适用于地幔岩石的矿物压力计有石榴石-斜方辉石压力计、石榴石-单斜辉石压力计、橄榄石-单斜辉石压力计、铬尖晶石压力计、二辉石压力计等有限几类.本文通过将这些压力计应用于岩石学相平衡实验数据,检验了其精确度.再将它们应用到天然地幔岩石样品,包括石榴石相二辉橄榄岩、尖晶石相二辉橄榄岩、石榴石-尖晶石过渡相二辉橄榄岩、含金刚石和石墨的地幔岩石,检验了其准确度.初步结论是,现有的石榴石-斜方辉石压力计(Nickel and Green,1985;Taylor,1998;Brey et al．,2008)质量相对最优,石榴石-单斜辉石压力计(Nimis and Taylor,2000;Simakov and Taylor,2000)次之.在应用这些压力计时,可配合二辉石温度计(Brey et al．,1990;Taylor,1998)或石榴石-橄榄石温度计(Wu and Zhao,2007),来同时估算平衡压力和温度.其余的压力计精确度和准确度都还很不够,需要更精确深入的实验研究来标定质量优良的压力计.     

矽卡岩矿床共生单科辉石—石榴石氧逸度计及主要金属矿化类型矽岩生成的氧逸度条件

基于我国主要类型矽卡岩矿床的研究，结合Ca-Fe-Si-C-O体系的实验成果，以共 生矿物固溶体热力学分析为手段，建立了共生单斜辉石一石榴石氧逸度计。对我国主要类型矽卡 岩的研究表明:不同金属矿化及不同产出条件的矽卡岩形成于不同的氧逸度环境，具有不同的氧 逸度变化趋势和温度一氧逸度效应。共生单斜辉石一石榴石矿物对是形成介质的良好氧逸度计、酸度计。它有助于判别矽卡岩的金属矿化类型。     

碱性玄武岩中幔源岩石包体内尖晶石成分特征及其岩石学成因意义

通过对我国东部北起黑龙江省南至海南省３１个产地的新生代碱性玄武岩中橄榄岩类 （纯橄岩、方辉橄榄岩及二辉橄榄岩） 包体和辉石岩类包体中的１６０ 多个尖晶石电子探针分析数据, 论述了尖晶石的Ｃｒ－Ａｌ, Ｆｅ－Ｍｇ, Ｎｉ－Ｍｇ 主元素及有关比值和端员组分之间的关系, 分析研究了不同岩类包体中尖晶石的颜色、成分及成因之间的联系。并利用所分析的有关橄榄石、斜方辉石、单斜辉石共生矿物的电子探针分析数据, 采用新的、较合理的Ｂｒｅｙ－Ｋｏｈｌｅｒ温度计及Ｋｏｈｌｅｒ－Ｂｒｅｙ 压力计和Ｂａｌｌｈａｕｓ ｅｔａｌ． 氧逸度计算方法进行了计算, 探讨了尖晶石成分与其形成温度、压力和氧逸度状态的关系, 指出了尖晶石成分所反映的地幔亏损程度及部分熔融程度的变化规律及尖晶石 （相） 稳定的温度、压力和氧逸度范围。     

地幔橄榄岩部分熔融及相转变（尖晶石相→斜长石相）过程中的固相化学成分演化──Ⅱ．在自然岩石中的应用

分析了全球一些有代表性的上地幔尖晶石橄榄岩和斜长石橄榄岩中各矿物的化学成分变化特征。发现在斜长石橄榄岩中，尖晶石和斜方辉石富Ｔｉ，且Ｔｉ含量随Ｃｒ／（Ｃｒ＋Ａｌ）的增大而增大；单斜辉石富Ｔｉ贫Ｎａ，其Ｔｉ含量随Ｎａ含量的增大而减少。据此，结合实验结果，可以肯定世界各地大多数斜长石二辉橄榄岩在斜长石相域内未经受部分熔融。岩体所曾经受的部分熔融只发生在尖晶石或石榴石相。它们的相对熔融度可以用下面两个指标来估计：（１）最贫Ｔｉ尖晶石的Ｃｒ／（Ｃｒ＋Ａｌ）；（２）单斜辉石的最高Ｎａ含量。对于尖晶石橄榄岩，从二辉橄榄岩、方辉橄榄岩到纯橄榄岩，其尖晶石和斜方辉石的Ｃｒ／（Ｃｒ＋Ａｌ）逐渐增大，而含量很低的Ｔｉ或Ｎａ在尖晶石、斜方辉石及单斜辉石中保持不变或趋向逐渐减小。尖晶石橄榄岩的相对熔融度可据尖晶石的Ｃｒ／（Ｃｒ＋Ａｌ）和单斜辉石的Ｎａ含量来判断。     

北淮阳金寨—苏仙石地区中生代花岗岩的成因类型及岩浆演化特征

摘 要　 北淮阳金寨—苏仙石地区中生代侵入岩出露面积约150km 2 ‚按岩石谱系单位的划 分原则‚可分为3个超单元（包括10个单元）和3个独立单元。根据主要造岩矿物及副矿物组 合、岩石化学和地球化学特征判别结果‚岩体成因类型以 I 型为主‚少数为 A 型和 S 型。岩 浆来源约30km 深处‚相当于下地壳或壳幔过渡部位。岩体形成深度约3～4km‚压力约0∙1 ～0∙2GPa。形成温度约866～1150℃‚氧逸度 log f O 2 平均为—10∙97。进一步讨论了岩浆的 水逸度、水压及岩浆密度、岩浆演化和侵入岩与火山岩的成因关系。     

铬尖晶石和石榴石的相变: 大陆科学钻探CCSD-PP3孔超镁铁岩超高压变质作用的证据

PP3超镁铁岩主要岩石类型有纯橄岩和石榴石橄榄岩,两者为渐变,主要矿物为橄榄石、铬尖晶石、石榴石、单斜辉石和斜方辉石.铬尖晶石的Cr#[Cr/(Cr+Mg) ×100]从51~89变化,TiO₂和MnO₂值分别低于0.26%和0.46%.铬尖晶石矿物表现为4期次演化的特点,反映了从岩浆期、榴辉岩相、角闪岩相和绿片岩相演化特征.随着超镁铁岩的演化,铬尖晶石表现为Cr#不断增大,而Mg#[Mg×100/(Mg+Fe2+) ]不断减少、氧逸度不断增加的过程.PP3铬尖晶石反映了地幔来源,为大陆岩石圈超镁铁岩特征,后期随折返而演化.从石榴石与铬尖晶石相互转变过程看出,PP3超镁铁岩经历了深度加大的过程,超镁铁岩曾经到达100km以上的岩石圈地幔深处.在绿片岩相-绿片角闪岩相变质过程中,铬尖晶石中Cr、Mg和Al减少,Fe相对增加,产生富Cr尖晶石变质作用样式.晚期剪切变形等次生变化影响了铬尖晶石矿物成分.      

扬子地块东段大陆岩石圈地幔的氧逸度

由尖晶石相橄榄岩包体中的矿物化学成分，采用新近校准的ＦＦＭ地质氧逸度计和地质温－压计，计算包体的平衡氧逸度，Δｌｏｇ（ｆＯ２）ＦＭＱ＝－３．３２－０．１２，它反映了扬子地块东段大陆岩石圈地幔的氧化还原状态。两种氧逸度计计算结果相差在０．５ｌｏｇｆＯ２单位内。     

Empirical geothermometers and geothermobarometers for spinel peridotite phase assemblages

Experimental synthesis of spinel peridotite phase assemblages for a range of compositions that mimic natural samples is used to derive a set of empirical geothermometers and geothermobarometers represented by multiple linear regression best-fit surfaces that link the variables of temperature, pressure, and composition. The calibrated geothermometers use reactions that govern the solubility of Al and Cr in both pyroxenes and the Mg–Fe exchange between silicates and spinel. Geothermobarometers map the Mg–Fe exchange between coexisting olivine and clinopyroxene and pyroxenes and Ca–Mg exchange between coexisting pyroxenes. Application of the geothermometers and geothermobarometers to suites of naturally occurring samples indicates that while reactions governing the Cr and Al solubility and solvus of orthopyroxene give useful estimates of ‘original’ mantle temperatures and pressures, respectively, comparable reactions for clinopyroxene yield estimates that are variably dependent on the transport phase of the sample suites. Temperature and pressure estimates from reactions governing Mg and Fe exchange between silicates and spinel and coexisting silicates are all sensitive to the later transport stage of the samples.     

藏北可可西里中新世钾质火山岩矿物化学及温压计算

对藏北可可西里中新世钾质火山岩的主要斑晶矿物化学成份进行了电子探针分析,结果表明,火山岩中的辉石为普通辉石、紫苏辉石和古铜辉石,角闪石为钙质角闪石,云母为钛铁黑云母和富铁黑云母,长石为中长石、更长石、钠透长石和透长石,不透明矿物主要为钛铁矿和磁铁矿,可见钛铁矿?磁铁矿固溶体。根据火山岩中单斜辉石?熔体温压计估算的辉石斑晶的形成温度和压力分别为1 065～1 100 ℃和5.3～9.1 kbar。二辉石地质温度计结果表明,辉石的共结温度为976～1 020 ℃。而钛铁矿?磁铁矿固溶体平衡计算结果表明,钛?磁铁矿的平衡温度为841～974 ℃,logfO2为－13.71～－10.87。研究结果显示,可可西里火山岩岩浆房的埋深深度小于30 km,中?酸性系列火山岩是岩浆房在相对低压条件下的中上部地壳部位,经分离结晶后形成。     

青海沱沱河地区赛多浦岗日二长花岗岩中黑云母化学成分特征及地质意义

电子探针分析结果表明,沱沱河地区赛多浦岗日二长花岗岩中黑云母具有富MgO、SiO_2、(Na_2O+K_2O),相对贫Al_2O_3、FeO~t的特征;镁质率(M=0.60~0.65)高,∑Al值(1.30~1.39)偏低,中等Fe/(Mg+Fe)(0.42~0.44)比值,为镁质黑云母;估算其结晶温度为580℃~645℃,且岩浆体系具有较高的氧逸度。黑云母的成分特征显示其寄主岩体为造山背景下形成的钙碱性花岗岩,其源区具有壳-幔混源的特征。     

大兴安岭托河林场毕利亚山碱长花岗岩黑云母地球化学特征及地质意义

根据大兴安岭毕利亚山碱长花岗岩黑云母的电子探针(EPMA)测试结果,对黑云母的化学成分特征、成因类型及结晶时的温度和氧逸度进行了研究,并探讨岩浆源区的性质及成岩背景。毕利亚山碱长花岗岩黑云母具有高Si(SiO_2:39.876%~42.419%)、富Mg(MgO:18.138%~20.02%)、贫Fe(FeO~t:10.549%~11.468%)特征,属镁质黑云母;黑云母的结晶温度为590℃~650℃,且具有较高的氧逸度。其∑Al的值为1.01~1.044,Fe/(Mg+Fe)的值为0.228~0.262。Mg/(Mg+Fe~(2+)+Mn)的值为0.673~0.834,FeO~t/(FeO~t+MgO)的值为0.345~0.387,指示了其岩浆源区为富镁的岩石圈地幔,并且在岩浆演化过程中发生混染作用。     

Mössbauer and ELNES spectroscopy of (Mg,Fe)(Si,Al)O3 perovskite: a highly oxidised component of the lower mantle

(Mg,Fe)(Si,Al)O₃ perovskite samples with varying Fe and Al concentration were synthesised at high pressure and temperature at varying conditions of oxygen fugacity using a multianvil press, and were characterised using ex?situ X-ray diffraction, electron microprobe, Mössbauer spectroscopy and analytical transmission electron microscopy. The Fe³⁺/ΣFe ratio was determined from Mössbauer spectra recorded at 293 and 80?K, and shows a nearly linear dependence of Fe³⁺/ΣFe with Al composition of (Mg,Fe)(Si,Al)O₃ perovskite. The Fe³⁺/ΣFe values were obtained for selected samples of (Mg,Fe)(Si,Al)O₃ perovskite using electron energy-loss near-edge structure (ELNES) spectroscopy, and are in excellent agreement with Mössbauer data, demonstrating that Fe³⁺/ΣFe can be determined with a spatial resolution on the order of nm. Oxygen concentrations were determined by combining bulk chemical data with Fe³⁺/ΣFe data determined by Mössbauer spectroscopy, and show a significant concentration of oxygen vacancies in (Mg,Fe)(Si,Al)O₃ perovskite.     

Mantle metasomatism and magma formation in continental lithosphere: Data on xenoliths in alkali basalts from the Makhtesh Ramon,Negev desert,Israel

Mantle xenoliths (lherzolites, clinopyroxene dunites, wehrlites, and clinopyroxenites) in the Early Cretaceous volcanic rocks of Makhtesh Ramon (alkali olivine basalts, basanites, and nephelinites) represent metasomatized mantle, which served as a source of basaltic melts. The xenoliths bear signs of partial melting and previous metasomatic transformations. The latter include the replacement of orthopyroxene by clinopyroxene in the lherzolites and, respectively, the wide development of wehrlites and olivine clinopyoroxenites. Metasomatic alteration of the peridotites is accompanied by a sharp decrease in Mg, Cr, and Ni, and increase of Ti, Al, Ca contents and ³⁺Fe/²⁺Fe ratio, as well as the growth of trace V, Sc, Zr, Nb, and Y contents. The compositional features of the rocks such as the growth of ³⁺Fe/²⁺Fe and the wide development of Ti-magnetite in combination with the complete absence of sulfides indicate the high oxygen fugacity during metasomatism and the low sulfur concentration, which is a distinctive signature of fluid mode during formation of the Makhtesh Ramon alkali basaltic magma. Partial melting of peridotites and clinopyroxenites is accompanied by the formation of basanite or alkali basaltic melt. Clino- and orthopyroxenes are subjected to melting. The crystallization products of melt preserved in the mantle rock are localized in the interstices and consist mainly of fine-grained clinopyroxene, which together with Ti-magnetite, ilmenite, amphibole, rhenite, feldspar, and nepheline, is cemented by glass corresponding to quartz–orthopyroxene, olivine–orthopyroxene, quartz–feldspar, or nepheline–feldspar mixtures of the corresponding normative minerals. The mineral assemblages of xenoliths correspond to high temperatures. The high-Al and high-Ti clinopyroxene, calcium olivine, feldspar, and feldspathoids, amphibole, Ti-magnetite, and ilmenite are formed at 900–1000°. The study of melt and fluid inclusions in minerals from xenoliths indicate liquidus temperatures of 1200–1250°C, solidus temperatures of 1000–1100°C, and pressure of 5.9–9.5 kbar. Based on the amphibole–plagioclase barometer, amphibole and coexisting plagioclase were crystallized in clinopyroxenites at 6.5–7.0 kbar.     

First report of eclogites from central Tibet,China: evidence for ultradeep continental subduction prior to the Cenozoic India‐Asian collision

Eclogites characterized by a garnet + clinopyroxene + orthopyroxene + sanidine + rutile assemblage are reported for the first time in the eastern Bangong suture, central Tibet (China). Garnet and sanidine are exsolved from clinopyroxene. Al‐exchange barometer for orthopyroxene and garnet and K concentrations in clinopyroxene indicate a peak pressure of ～4 GPa. The occurrence of these ultrahigh‐pressure rocks implies the subduction of continental crust to a depth of >130 km along the eastern Bangong suture zone during the Early Jurassic. The denudation of these ultrahigh‐pressure metamorphic rocks could have provided a significant source for the Jurassic turbidites in the western Bangong ocean basin.     

Stability of the assemblage orthopyroxene-sillimanite-quartz in the system MgO-FeO-Fe2O3-Al2O3-SiO2-H2O

The stability of coexisting orthopyroxene, sillimanite and quartz and the composition of orthopyroxene in this assemblage has been determined in the system MgO-FeO-Fe₂O₃-Al₂O₃-SiO₂-H₂O as a function of pressure, mainly at 1,000° C, and at oxygen fugacities defined mostly by the hematite-magnetite buffer. The upper stability of the assemblage is terminated at 17 kbars, 1,000° C, by the reaction opx+Al-silicate gar+qz, proceeding toward lower pressures with increasing Fe/(Fe+Mg) ratio in the system. The lower stability is controlled by the reaction opx+sill+qz cord, which occurs at 11 kbars in the iron-free system but is lowered to 9 kbars with increasing Fe/(Fe+Mg). Spinel solid solutions are stabilized, besides quartz, up to 14 kbars in favour of garnet in the iron-rich part of the system (Fe/(Fe+Mg)0.30). Ferric-ferrous ratios in orthopyroxene are increasing with increasing ferro-magnesian ratio. At least part of the generally observed increase in Al content with Fe²⁺ in orthopyroxene is not due to an increased solubility of the MgAlAlSiO₆ component but rather of a MgFe³⁺AlSiO₆ component. The data permit an estimate of oxygen fugacity from the composition of orthopyroxene in coexistence with sillimanite and quartz.     

Peridotites from the Mid-Atlantic Ridge at 43° N and their petrogenetic relation to abyssal tholeiites

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 (Fo_91–92). 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 (En_89.1–87.6Fs_8.2-8.0Wo_2.7–4.4; 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.