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1.
南极拉斯曼丘陵高级长英质片麻岩的夕线片麻岩中可有两类结构和变质矿物组合均有所不同的两种域,一种含夕线石部分对应于片理组合,另一种对应无夕线石的非片理化组合.岩石的变形尤其是破裂性裂隙的率先出现对于富夕线石部分的形成是必要的.在非破裂性片麻理岩石域中,中-低压/高温条件下黑云斜长片麻岩进变质发展的结果往往是形成Grt+Qtz±Opx组合.这两种不同的变质域的组合与应变分解造成的强应变带和弱应变域相一致.而且,夕线石的形成不是简单的变质早期矿物固相反应的结果,而是反应链上的一部分.其出现是由开放体系中组分的差异迁移造成的,这种差异迁移实际上是碱土金属迁出(淋滤)的过程,与变形相伴的流体活动使得SiO2发生强烈淋滤,残留组分中SiO2活度大为降低,并使长英质组分和镁铁质组分分凝,主要组分大都可以单独富集(集中)、形成复杂的矿物演化和分布.这种演化还可从MgO等碱(土)金属组分的外迁程度差异来理解.随着碱(土)金属丢失程度的减小,依次出现夕线石、石榴子石、斜方辉石和堇青石,或者说,不同的变质或分异阶段形成不同的矿物(组合):变形-变质起始阶段,碱(土)金属组分迁移初期残留形成夕线石,之后为镁(铁)质组分迁移,初期残留不透明钛铁氧化物,晚期残留组分形成堇青石.石榴子石-长英质组合为体系基本封闭情况下的结晶.此外,夕线石的形成往往标志着深熔作用的开始,一旦深熔作用发展完善,夕线石呈准稳定状态或趋于消失.拉斯曼丘陵与夕线石有关的长英质岩石经历了复杂的变形、变质和流体活动变化.  相似文献   

2.
目前,在大别-苏鲁榴辉岩的磷灰石中已经观察到多种出溶现象,出溶体矿物主要是独居石和铁、铜硫化物,个别有硅钍石[1]、铁氧化物和重晶石[2,3].对于出溶体现象的解释,一般认为是超高压变质条件下形成的磷灰石在退变质减压、降温作用以及氧逸度fO2变化下,其中的LREE与[PO4]3-结合形成独居石,而S、Fe、Cu等元素结合形成硫化物,并沿着一定的晶格方向出溶.  相似文献   

3.
夕线石(Sil)是泥质变质岩的重要特征变质矿物,一直被视作高温变质矿物的典型,并常以其在岩石中的首次出现作为变质作用进入峰期的标志.然而近来发现有些夕线石并非产于高温变质岩之中,而是出现于变质程度较低的黑云片岩或二云片岩之中.因而有必要对夕线石的成因机制作深入分析,以便准确建立变质矿物的生成演化序列. 自然界产出的夕线石按其形态和产状不同主要有如下几种:(1)巨晶板柱状或竹节状夕线石,主要以变班晶形式存在于夕线石榴钾长片麻岩之中,形态规则、产出量大,共生矿物有石榴石(Gt)、钾长石(Kf)和黑云母(Bt)等,无堇青石(Crd).(2)针柱状或乳滴状夕线石集合体,常以包体形式存在于大颗粒的茧青石、钾长石或石英之中.集合体形态多样,有时规则排列,有时则强烈弯曲甚至形成小褶皱.该夕线石主要产于夕线石榴茧青黑云钾长片麻岩之中.(3)纤维毛发状夕线石聚集体,常与黑云母残片交生在一起,彼此呈渐变过渡关系.该种夕线石可产出在两种截然不同的岩石之中,反映其不同的成因特征.一种为夕线石榴(堇青)黑云片麻岩,夕线石沿黑云母解理缝方向呈纤维状分布,由里向外夕线石粒径逐渐变细,表现出一种熔融特征;另一种为含石榴夕线黑云片岩或二云片岩,这种夕线石和黑云母往往遭受了强烈的揉皱,呈不规则的毛团状和扫帚状,夕线石粒径极细以至在光学镜下很难分辨.由于矿物组合中缺少十字石(Stau)、堇青石和钾长石等特征矿物,表明其变质温度较低(相当于绿片岩相-低角闪岩相).  相似文献   

4.
本文通过夕线石的结构、成分及产出状态,系统讨论和总结了其变质形成过程.含夕线石的变质岩原岩未必对应泥质岩,富夕线石岩石成分上更不能与任何的泥质岩成分对应.原岩本身富铝如多数泥质岩是形成夕线石非常有利的成分条件,但是,即使有合适的温压条件,也未必能够形成夕线石,组分的差异性迁移才是夕线石形成的必要条件.夕线石的形成与变形...  相似文献   

5.
主要研究了磷酸铝(Al PO4)的加入量对氧化亚铁硫杆菌HX3培养液中铁矿物形成的影响,并对相应沉淀产物进行了结构表征分析。结果表明,Al PO4的加入对细菌培养过程中Fe2+的氧化无明显影响,但可促进Fe3+的水解和初始铁矿物相的形成,也可加速黄钾铁矾的转化形成。Al/Fe(摩尔比)为0. 04~1的培养液中主要形成产物为施威特曼石和黄钾铁矾; Al/Fe为0. 4和1时另有磷酸铁矿形成。较高的Al/Fe比值和磷酸根含量有利于磷酸铁矿的形成。  相似文献   

6.
通过对聂拉木高喜马拉雅结晶岩系石榴子石带-十字石带-蓝晶石带-夕线石带倒转变质的研究,认为除夕线石带以外的其它变质带主要由固相变质反应形成。夕线石的出现并非蓝晶石或十字石带递增变质所致。"倒转变质"不应包括所谓的夕线石带。实际上,夕线石化与深熔作用之后的溶液(或熔体)活动更为密切。时间顺序上应是递增变质作用及分带→深熔作用→夕线石化,夕线石的出现不是深熔作用的开始,而是深熔作用的结束。夕线石的形成主要与变形作用过程中黑云母和/或钾长石的分解及碱(土)金属组分的迁移有关,关键在于溶液(或熔体)组分沿裂隙迁移过程中发生的组分逐步沉淀,最早沉凝的Al、Si组分形成夕线石和石英,之后陆续有其它的组分的结晶;细夕线石粗粒化即进一步转化形成柱状夕线石的同时形成蠕英结构和斜长石生长边。夕线石化可能与深熔花岗(片麻)岩的上升过程有关。  相似文献   

7.
贺义兴  马瑞等 《地质论评》2001,47(1):82-87,T005,T006
河北省平山县阜平群是一套高角闪岩相岩石。根据宏观现象,某些地段曾经历过深熔作用过程。深熔效应以小觉地区的夕线石钾长浅粒岩最为典型。通过电子显微镜观测确认,所研究的夕线石钾长浅粒岩经受了深熔作用的改造,具有丰富而显著的微区矿物学标志。主要表现为前存矿物,如钾长石、条纹长石、石英、钠长石、黑云母和磁铁矿等,不同程度地被熔蚀,主要组成元素发生迁移和重组,沿矿物的解理、裂隙及粒间形成夕线石、石英、云母、长石、金红石等再结晶相。在深熔过程中,元素的迁移有两种可能形式:①选择性地从前存矿物晶格中移出;②通过前存矿物的熔融。Fe、Ti等元素从黑云母中移出,形成再结晶磁铁矿和金红石;Si、AI等元素则从黑云母和长石中移出,形成夕线石和再结晶石英。  相似文献   

8.
关于东南极拉斯曼丘陵夕线片麻岩类原岩恢复问题的讨论   总被引:2,自引:0,他引:2  
南极拉斯曼丘陵及其邻区的(含)夕线片麻岩类的原岩可以是杂砂岩、亚杂砂岩、石英砂岩、泥质岩或页岩等。粘土岩或页岩之类的富铝沉积岩与富夕线片麻岩并没有直接对应关系。没有一种泥质岩的化学组成可以与富夕线片麻岩相对应。研究区内夕线石片麻岩的形成主要与黑云斜长片麻岩有关,影响夕线石出现的决定性因素是特定温压条件下的变形变质改造过程,而不是原岩成分。夕线石片麻岩在很大程度上是黑云斜长片麻岩经长英质组分迁移之后的滞留-残留体。夕线石化过程中岩石组分发生了改造,相关变质作用已经明显偏离等化学过程,基本上属于开放体系。原岩中Al2O3的含量也不能控制夕线石的出现与否,含夕线石的岩石未必富铝,反之亦然,岩石富铝也可以不出现夕线石;但是夕线石化过程往往是Al2O3相对增加的过程,这些认识对于夕线石片麻岩成岩环境的确定和原岩建造的重建都具有重要意义。  相似文献   

9.
铁细菌胞外多聚物作用下聚集的铁可通过氧化或者沉淀作用使铁稳定或沉积,从而形成铁矿物。本文基于铁细菌胞外多聚物(extracellular polymeric substances,EPS)对铁矿物形成的调控作用,介绍了Cl-/SO_4~(2-)的Fe(Ⅲ)或Fe(Ⅱ)盐作用下,含可溶性EPS的氧化亚铁硫杆菌(Acidithiobacillus ferrooxidans)溶液中铁矿物的形成,观察了溶液pH值变化及形成铁矿物的矿相与结构,并采用XRD、FTIR和FESEM对其进行表征。结果发现反应溶液中OH-离子可与Fe3+形成微米级"针垫"聚集球状或纳米级小球形施威特曼石和微米级"菱形"块状黄钾铁矾铁矿物沉淀。反应溶液中的可溶性EPS可调控和促进铁矿物的形成,但对Fe2+的氧化未产生影响;外源Fe盐可促进施威特曼石向黄钾铁矾转化。随着Cl-/SO_4~(2-)摩尔比例的增加(即Cl-含量的不断增加),两矿相间的转化明显受到抑制,且铁矿物颗粒之间的集聚作用明显减弱;反之,SO_4~(2-)含量升高时,有利于铁矿物间的转化和聚集球状颗粒形貌结构的形成。  相似文献   

10.
铁同位素体系及其在矿床学中的应用   总被引:7,自引:4,他引:3  
王跃  朱祥坤 《岩石学报》2012,28(11):3638-3654
本文报道了世界范围内不同含铁矿物的Fe同位素组成,进一步了解了铁同位素在不同含铁矿物中的基本分布特征;系统总结了铁同位素在不同储库和不同类型矿床中的分布特征,构筑了铁同位素体系的基本框架;结合最新的研究成果,较全面地总结了铁同位素在矿床学领域的应用,得出了铁同位素可以用来示踪流体出溶、流体演化、表生蚀变作用和成矿物质来源的基本认识。在流体出溶过程中,相对于岩体,出溶的流体富集铁的轻同位素;成矿流体体系的演化过程中,矿物的结晶沉淀会导致铁同位素发生分馏,随着Fe(III)矿物的结晶沉淀,流体逐渐富集铁的轻同位素,随着Fe(II)矿物的结晶沉淀,流体逐渐富集铁的重同位素,随着矿物的结晶沉淀,流体的Fe同位素组成随时间发生演化;在成矿后的表生蚀变作用过程,高温蚀变作用形成的产物相对于原矿物富集铁重同位素,低温蚀变作用形成的产物基本保留了原矿物的铁同位素组成;Fe同位素在示踪成矿物质来源具有应用潜力,流体出溶、流体演化等重要成矿作用过程中Fe同位素组成的变化规律是利用Fe同位素示踪Fe来源的关键所在。  相似文献   

11.
巨晶普通辉石的M1位分裂李一良,支霞臣,李玉芝,李铁,张裕恒(中国科学技术大学,合肥230026)关键词巨晶辉石,M1位分裂,面积约束法,近邻边效应,T位铁单斜辉石的穆斯堡尔谱学研究历时已久。但由于其晶体结构和成份的复杂性、化学不均一性及出溶现象等[...  相似文献   

12.
潘群雄  潘晖华 《矿物学报》2002,22(3):275-279
通过组成-自由能关系曲线的分析,提出斜方顽火辉石-正铁辉石(MgSiO3-FeSiO3)固溶体出溶的临界温度约为753K;组成XFe为0.82左右的富铁辉石固溶体处于介稳态,出溶作用有利于系统自由能降低;出溶作用是以Fe^2 、Mg^2 离子逆扩散的方式进行的;出溶作用的推动力是上凸区域介稳相与平衡相之间的化学位差。  相似文献   

13.
In the Boi Massif of Western Timor the Mutis Complex, which is equivalent to the Lolotoi Complex of East Timor, is composed of two lithostratigraphical components: various basement schists and gneisses; and the dismembered remnants of an ophiolite. Cordierite-bearing pelitic schists and gneisses carry an early mineral assemblage of biotite + garnet + plagioclase + Al-silicate, but contain no prograde muscovite; sillimanite occurs in a textural mode which suggests that it replaced and pseudomorphed kyanite at an early stage and some specimens of pelitic schist contain tiny kyanite relics in plagioclase. Textural relations between, and mineral chemistries of, ferro-magnesian phases in these pelitic chists and gneisses suggest that two discontinuous reactions and additional continuous compositional changes have been overstepped, possibly with concomitant anatexis, as a result of decrease in Pload during high temperature metamorphism. The simplified reactions are: garnet and/or biotite + sillimanite + quartz + cordierite + hercynite + ilmenite + excess components. P-T conditions during the development of the early mineral assemblage in the pelitic gneisses are estimated to have been P + 10 kbar and T > 750°C, based upon the plagioclase-garnet-Al-silicate-quartz geobarometer and the garnet-biotite geothermometer. P-T conditions during the subsequent development of cordierite-bearing mineral assemblages in the pelitic gneisses are estimated to have been P + 5 kbar and T + 700°C with XH2O < 0.5, based upon the Fe content of cordierite occurring in the assemblage quartz + plagioclase + sillimanite + biotite + garnet + cordierite coexisting with melt. Final equilibration between some of the phases suggests that conditions dropped to P > 2.3 kbar and T > 600°C. A similar exhumation P-T path is suggested for the pelitic schists with early metamorphic conditions of P > 6.2 kbar and T > 745°C and subsequent development of cordierite under conditions in the range P = 3-4 kbar and T = 600-700°C. The tectonic implications of these P-T estimates are discussed and it is concluded that the P-T path followed by these rocks was caused by decompression during rifting and synmetamorphic ophiolite emplacement resulting from processes during the initiation and development of a convergent plate junction located in Southeast Asia during late Jurassic to Cretaceous time.  相似文献   

14.
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.  相似文献   

15.
Aluminum silicate triple-point occurrences are common in metamorphicrocks of northern New Mexico. The three polymorphs show extensivesolid solution, with Fe and Mn substituting for Al. Mineraltextures, the spatial distribution of phases, and the systematicpartitioning of Fe and Mn indicate that the kyanite-andalusite-sillimaniteassemblages crystallized in equilibrium. The compositions ofminerals in the three-phase assemblage vary across the studyarea, recording regional variations in the pressures and temperaturesof metamorphism. The highest-pressure rocks, exposed at RioMora, contain kyanite at higher elevations and sillimanite atlower elevations. A sub-horizontal isograd separates the twominerals. Kyanite and sillimanite have nearly identical Fe contentwhich varies systematically with XFe2O3 in hematite or ilmenite.Andalusite occurs only along a single manganiferous layer, incrystals rich in MnAlSiO5 and saturated in FeAlSiO5. Triple-pointassemblages can be found wherever the folded manganiferous layercrosses the unfolded kyanite-sillimanite isograd. The TruchasRange, preserving slightly lower pressures of metamorphism,shows kyanite-andalusite-sillimanite in rocks with titaniferoushematite. Andalusite is enriched in Fe relative to kyanite andsillimanite, but no polymorphs contain Mn. Rocks with lowerXFe2O3 in hematite have kyanite and sillimanite without andalusite,whereas rocks with pure hematite contain only andalusite. Theshallowest erosional levels are preserved in the western PicurisRange where the three polymorphs occur as pure minerals in ilmenite-bearingrocks. Hematitic samples contain only andalusite which showsextensive solid solution of both Fe and Mn. The assemblage kyanite-andalusite-sillimanite is not invariant.Iron and manganese both add degrees of freedom. These transitionmetals have stabilized the three-phase assemblage, in apparentchemical equilibrium, across a P-T interval of 500-540 ?C, 3?8-4?6kb in rocks from New Mexico. The saturation level of FeAlSiO5in andalusite does not vary with Mn content but does vary withpressure and temperature. Calculations indicate that a 2-3 kbdecrease in pressure or a 25-50 ?C increase in temperature resultsin a 1 mole per cent increase in XFeAlSiO5 in iron-saturatedandalusite.  相似文献   

16.
黑云母不仅是理想的40Ar-39Ar年代学定年矿物,其化学组成还可用来指示母岩浆物理化学条件、岩浆源区及分异演化程度、成矿潜力和成岩构造环境.本文对辽宁赛马碱性杂岩体中分布最为广泛的霓霞正长岩中的黑云母开展系统电子探针分析和40Ar-39Ar定年,结合pMELTS软件对前人全岩主量元素分析数据开展了平衡结晶计算,探讨了母岩浆物理化学性质、演化过程和成岩构造背景.电子探针分析结果表明赛马霓霞正长岩黑云母具有高铁高钛特征,属铁质黑云母.根据黑云母主量元素含量及比值估算黑云母结晶温度为770~800℃,lgfO2介于-16~-14,而pMELTS平衡结晶计算结果表明整个霓霞正长岩岩浆体系于1 300℃以上便已开始结晶,且随温度降低氧逸度呈现不断降低的趋势,这种较高温度和持续降低的氧逸度环境不利于岩浆热液的分异,使得碱金属(Na)、挥发分及铀钍稀有元素保留在岩浆房内并在后期钠质岩浆(异霞正长岩)结晶分异过程中富集成矿.部分黑云母发育完好的振荡环带,且核部较幔部具有更高的TiO2、Na2O含量和更低的SiO2含量和Fe3+/(Fe3++Fe2+)比值,也进一步证实黑云母结晶后残余岩浆具有更低氧逸度和更高Na含量.赛马碱性岩是华北克拉通北缘近东西向碱性岩带的一部分,本文获得其黑云母40Ar-39Ar年龄为222 Ma左右,形成于古亚洲洋闭合之后的后碰撞伸展构造背景.   相似文献   

17.
(Fe, Mn)S and (Fe, Mg)S solid solutions are examined to study and compare the properties of Fe2+ in two different B1-structured hosts, and also to study the relative stability of the B1 (NaCl) and B8 (NiAs) structures at high pressure. The Mössbauer spectra of (Fe, Mn)S and (Fe, Mg)S B1 solid solutions are quadrupole doublets at 298 K with parameters which vary smoothly with Fe2+ concentration. At 4.2 K the Mössbauer spectra of (Fe, Mn)S and Fe-rich (Fe, Mg)S B1 solid solutions are magnetically split into eight lines, but the spectra of Mg-rich (Fe, Mg)S solid solutions are quadrupole doublets. The line widths of the magnetic spectra are broad, consistent with a multiaxial spin arrangement. Some properties of the hypothetical phase FeS(B1) are calculated from the solid solution data; the phase is inferred to be relatively ionic compared to FeS(B8) and has a molar volume that is 7.2 percent larger than the B8 phase at 298 K. The large inferred volume difference between FeS(B1) and FeS(B8) should cause exsolution of a B8-structured phase from (Fe, Mn)S and (Fe, Mg)S B1 solid solutions at high pressure. This behaviour is confirmed experimentally at high pressure using X-ray diffraction and Mössbauer spectroscopy, and the results are correlated with thermodynamic calculations of the phase boundaries based on estimates of the volume and free energy differences between the B1 and B8 phases of FeS derived from atmospheric pressure data. The absence of an increase in solubility of Mg and Mn in the B8 phase with pressure suggests that any polymorphism in MnS and MgS at high pressure is unlikely to involve the B8 phase. Shock wave data for MgO and Fe0.94O reported in the literature suggest similar behaviour in the system FeO-MgO at high pressure, namely exsolution of essentially pure FeO(hpp) from (Fe, Mg)O B1 solid solutions.  相似文献   

18.
Sapphirine occurs in the orthopyroxene-cordierite and feldspar-sillimanite granulites in the Sipiwesk Lake area of the Pikwitonei granulite terrain, Manitoba (97°40W, 55°05N). The orthopyroxene-cordierite granulites have extremely high Al2O3 (24.5 wt%) and MgO (24.6 wt%) contents and contain sapphirine (up to 69.2 wt% Al2O3), aluminous orthopyroxene (up to 8.93 wt% Al2O3), cordierite, spinel, phlogopite, and corundum. Sapphirine forms coronas mantling spinel and corundum. Corona sapphirine is zoned and its composition varies through the substitution (Mg, Fe, Mn) Si=2 Al as a function of the phases with which it is in contact. Textural and chemical relationships of sapphirine with coexisting phases indicate that spinel + cordierite reacted to form orthopyroxene + sapphirine under conditions of increasing pressure. Moreover, decreasing core to rim variation of Al2O3 in orthopyroxene porphyroblasts suggests decreasing temperature during sapphirine formation. On the basis of experimentally determined P-T stability of the assemblage enstatite + sapphirine + cordierite, and the Al content of hypothetical Fe2+-free orthopyroxene associated with sapphirine and cordierite, metamorphic temperatures and pressures are estimated to be 860–890° C and 3.0–11.2 kbar.In the feldspar-sillimanite granulites, sapphirine occurs as a relict phase mantled by sillimanite and/or by successive coronas of sillimanite and garnet. These textural relations suggest the reaction sapphirine + garnet + quartz = orthopyroxene + sillimanite with decreasing temperature. Compositions of minerals in the assemblage garnet-orthopyroxene-sillimanite-plagioclase-quartz, indicate metamorphic P-T conditions of 780–880° C and 9±1 kb.The metamorphic conditions estimated in this study suggest that the sapphirine bearing granulites in the Sipiwesk Lake area represent Archean lower crustal rocks. Their formation might be related to the crustal thickening processes in this area as suggested by Hubregtse (1980) and Weber (1983).  相似文献   

19.
为了理清白云矿床硅钾蚀变与金沉淀的成因关系,对硅钾蚀变岩石和未蚀变的矽线石云母片岩进行主微量元素测试分析,同时选取蚀变岩型和石英脉型矿石中黄铁矿进行电子探针分析.以Al2O3作为不活动组分,通过质量平衡计算,发现明显带入的组分为CaO、K2O、Na2O、SiO2、Ag、As、Co、Cu、Ni,迁出组分为FeO、Cr、Zn.蚀变岩型和石英脉型矿石中黄铁矿均表现出亏S和富Fe的特征,二者的Au/Ag值都大于0.5,Fe/(S+As)值变化范围为0.857~0.896.两种矿石中黄铁矿均为热液型,形成于中浅成的中温环境.在硅钾蚀变过程中,热液中的含硫组分损失,还原硫活度降低破坏了金-硫络合物的稳定性,导致Au的沉淀.   相似文献   

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