共查询到20条相似文献，搜索用时 31 毫秒
1.
在滇西鲁甸地区金沙江结合带新发现退变榴辉岩,其在野外呈透镜体状产于石榴子石白云母石英片岩中.利用电子探针及激光拉曼分析发现石榴子石和锆石中残留绿辉石包体.石榴子石及基质中的白云母为多硅白云母(Si(p.f.u)=3.27~3.53),指示岩石经历了高压变质作用过程.石榴子石发育进变质生长成分环带.岩相学及矿物化学特征显示,退变榴辉岩大致经历了进变质角闪岩相、峰期榴辉岩相、早期退变质以及晚期强退变这4个世代矿物组合,各阶段典型的矿物组合依次为Grt+AmpI+Qtz、Grt+Omp+Rt+Qtz+Phe、Pl+Di+AmpⅡ+Ilm+Spn+Qtz、AmpⅢ+Pl+Czo+Ilm+Qtz.该新发现对金沙江结合带复杂的变质演化P-T-t轨迹样式及年代格架、以金沙江洋为代表的整个西南三江地区古特提斯洋-陆俯冲-碰撞-造山的复杂构造演化历史以及微陆块的拼贴机制等关键科学问题的解决提供了极为重要的素材和更多的约束,具有重要的科学意义. 相似文献
2.
The Menderes Massif comprises an inner crystalline core with gneissic rocks and an outer surrounding schist belt with predominantly metasedimentary rocks. Both units have a complex metamorphic history including a late Alpine overprint. Temperatures inferred from oxygen isotope compositions of coexisting minerals increase from 420 to 600°C from the rim to the center. More positive '18O values in all minerals from the schist belt may reflect a higher abundance of sedimentary precursor material, whereas biotites and muscovites in core and rim are indistinguishable in hydrogen isotope composition. 'D values of muscovites range from -35 to -60, whereas 'D values of biotites range from -65 to -125, indicating normal values for muscovite but anomalously negative values for some biotites. For muscovite the trend can be interpreted in terms of increasing loss of water with rising metamorphic temperature. For biotite the 'D values decrease with increasing H2O content and decreasing Na2O+K2O content, which provides evidence for alteration processes or exchange of K and Na with water from interlayers of biotite forming hydro-biotite. The data suggest isotopic resetting of pre-Alpine characteristics during Alpine metamorphism. The hydrogen isotope composition of biotite was later disturbed, probably during extensional neotectonic movements in this region, as this allowed infiltration of and exchange with D-depleted meteoric water; however, the muscovites retained its Alpine characteristics. 相似文献
3.
Philippa M. Black 《Contributions to Mineralogy and Petrology》1975,49(4):269-284
Variations in chemistry and related physical properties of sheet silicates in the Ouégoa district with metamorphic grade are investigated. Weakly metamorphosed rocks prior to the crystallization of lawsonite contain phengite (d 006=3.317–3.323 Å), chlorite and occasionally paragonite while interstratified basaltic sills contain chlorite, minor phengite and stilpnomelane. Pyrophyllite crystallizes before lawsonite in some metamorphosed acid tuffs and is also stable in the lawsonite zone. Paragonite, phengite and chlorite appear to be stable through the sequence from weakly metamorphosed rocks into high-grade “eclogitic” schists and gneisses. Optical, chemical and some X-ray diffraction data is given for representative sheet silicates. Electron probe analyses of 55 phengites, 21 paragonites, 57 chlorites, 12 vermiculites, 2 stilpnomelanes, and 2 chloritoids are presented in graphical form. All K-micas analysed are consistently phengitic (3.29–3.55 Siiv ions per formula unit) and show limited solid solution with paragonite (4 to 13% Pa). The K∶Na ratio of the phengite is strongly dependant on the assemblage in which it occurs; the amount of phengite component and its Fe∶Mg ratio depends on bulk-rock composition. Phengites from acid volcanics have the highest Fe∶Mg ratio, highest phengite component and β refractive indices. Phengites from basic volcanics and metasediments of the epidote zone have the lowest Fe∶Mg ratio. Phengites from lawsonite-zone metasediments have intermediate Fe∶Mg ratios. The phengites show a small decrease in phengite component with increasing metamorphic grade. d 006 for phengites varied from 3.302 to 3.323 Å but at least in the lawsonite and epidote zones appears to reflect composition and had little systematic variation with metamorphic grade; phengites from very low-grade rocks showed the longest values of d 006. Paragonite shows almost no phengite-type substitution and only limited solid solution (4–12%) with muscovite. All paragonites (6) and most phengites (20) which have been examined are 2M1 polymorphs; one Fe2+-phengite appears to be a 1M polymorph. The chemistry of chlorites closely reflects parent-rock chemistry. Chlorites from metasediments have distinctly higher Fe/(Fe+Mg) ratios than chlorites from basic igneous rocks; chlorites from the lawsonite and lawsonite-epidote transitional zone metasediments have the highest Fe/(Fe+Mg) ratios. In metabasalts Fe/(Fe+Mg) ratios appear to reflect individual variations in bulk-rock chemistry and show no direct correlation with metamorphic grade. There is little difference in Al/(Si+Al) ratio between chlorites from sediments and basic igneous rocks although in both lithologies the chlorites from the epidote zone appear to be slightly more aluminous. Fe-rich chlorites of the lawsonite zone metasediments have been altered by a process involving leaching of Fe and Mg and introduction of alkalies to a brown pleochroic Fe-vermiculite. Chemical and physical data for this vermiculite are given. The decrease in Fe/(Fe+Mg) ratio in chlorites and phengites on passing from the lawsonite to the epidote zone can be correlated with the crystallization of Fe-rich epidote and almandine in the epidote zone. Elemental partitioning between coexisting minerals has shown Ti to be partitioned into phengite, while Fe and Mn are strongly partitioned into chlorite. When either stilpnomelane or chloritoid coexists with phengite or chlorite, Fe and Mn are slightly enriched in the stilpnomelane or chloritoid relative to the chlorite. 相似文献
4.
Jrg Hermann 《Lithos》2003,70(3-4):163-182
The peak metamorphic conditions of subducted continental crust in the Dora-Maira massif (Western Alps) have been revised by combining experimental results in the KCMASH system with petrologic information from whiteschists. Textural observations in whiteschists suggest that the peak metamorphic assemblage garnet+phengite+kyanite+coesite±talc originates from the reaction kyanite+talc↔garnet+coesite+liquid. In the experimentally determined petrogenetic grid, this reaction occurs above 45 kbar at 730 °C. At lower pressures, talc reacts either to orthopyroxene and coesite or, together with phengite, to biotite, coesite and kyanite. The liberated liquid contains probably similar amounts of H2O and dissolved granitic components. The composition of the liquid in the whiteschists at peak metamorphic conditions, a major unknown in earlier studies, was probably very similar to the liquid composition produced in the experiments. Therefore, the experimentally determined petrogenetic grid represents a good model for the estimation of the peak metamorphic conditions in whiteschists. Experimentally determined Si-isopleths for phengite further constrain peak pressures to 43 kbar for the measured Si=3.60 of phengite in the natural whiteschists. All these data provide evidence that the whiteschists reached diamond-facies conditions.
The fluid-absent equilibrium 4 kyanite+3 CELADONITE=4 coesite+3 muscovite+pyrope has been calibrated on the basis of garnet and phengite compositions in the experiments and serves as a geothermobarometer for ultra-high-pressure (UHP) metapelites. For graphite-bearing metapelites and kyanite–phengite eclogites, forming the country rocks of the whiteschists, peak metamorphic pressures of about 44±3 kbar were calculated from this barometer for temperatures of 750 °C estimated from garnet–phengite thermometry. Therefore, the whole ultra-high-pressure unit of the Dora-Maira massif most likely experienced peak metamorphic conditions in the diamond stability field. While graphite is common in the metapelites, diamond has not been found so far. The absence of metamorphic microdiamonds might be explained by the low temperature of metamorphism, the absence of a free fluid phase in the metapelites and a short residence time in diamond-facies conditions resulting in kinetic problems in the conversion of graphite to diamond. 相似文献
5.
五台山早前寒武纪变质岩中的白云母属二八面体的2M型多型变体,其中五台群中的白云母为富含绿鳞石分子的普通白云母,滹沱群为多硅白云母。通过对这些白云母化学成分和b_0值测定,确定五台群变质条件属中低压相系,滹沱群属中高压相系。五台群绿片岩相的变质压力为0.3—0.5 GPa,滹沱群为0.5—0.6 GPa。基于白云母成分和b_0值的研究,对划分变质级别、变质类型;确定变质作用期次;进行地层对比和构造分析等方面是可行的。 相似文献
6.
Fine grained rodingite‐like rocks containing epidote, clinozoisite, garnet, chlorite, phengite and titanite occur within antigorite serpentinite boudins from the high‐pressure metamorphic Maksyutovo Complex in the Southern Urals. Pseudomorphs after lawsonite, resorption of garnet by chlorite and phengite and stoichiometry suggest the reaction lawsonite + garnet + K‐bearing fluid → clinozoisite + chlorite + phengite, and define a relic assemblage of lawsonite + garnet + chlorite + titanite ± epidote as well as a later post‐lawsonite assemblage of clinozoisite + phengite + chlorite + titanite. The reaction lawsonite + titanite → clinozoisite + rutile + pyrophyllite + H2O delimits the maximum stability of former lawsonite + titanite to pressures >13 kbar. P–T conditions of 18–21 kbar/520–540 °C result, if the average chlorite, Mg‐rich garnet rim and average epidote compositions are used as equilibrium compositions of the former lawsonite assemblage. These estimates indicate a similar depth of formation but lower temperatures to those recorded in nearby eclogites. The metamorphic conditions of the lawsonite assemblage are considerably higher than previously suggested and, together with published structural data, support a model in which a normal fault within the Maksyutovo complex acted as the major transport plane of eclogite exhumation. The maximum Si content of phengite and minimum Fe content in clinozoisite constrain the metamorphic conditions of the later pseudomorph assemblage to be >4.5 kbar and <440 °C. Rb–Sr isotopic dating of the pseudomorph assemblage results in a formation age of 339 ± 6 and 338 ± 5 Ma, respectively. These results support the recent exhumation models for this complex. 相似文献
7.
Archaean meta-sediments near Yellowknife, Canada, exhibit alow-pressure facies series and broad metamorphic zonation rounda central pluton. Meta-pelites and meta-greywackes from thebiotite zone have been studied using analyses of 59 mineralsand 14 rocks. Mineral compositions were controlled by both host-rockcomposition and metamorphic grade. Increased grade commonly imposed on the minerals a progressivecompositional maturation. This involved progressive compositionalchange (especially in meta-greywacke biotites) and/or narrowingof compositional range (particularly in muscovites). Specificeffects of increased grade are as follows. Biotites in meta-greywackesexhibit increased Mg/Fe and Na/K but decreased (Na+K) content.Biotites in meta-pelites change little except for increasedAlIV/Si. The muscovites display decreasing maximum Si contents,increased AlVI at the expense of Fe and Mg, and increased Na/K.The chlorites show only a slight general increase in Mg/Fe. Bulk compositional control is manifested in various ways. Insome instances minerals from subtly different rock types areperceptibly distinct; in others the pro-grade maturation trendsof minerals in these rock types are different. Thus Si is moreabundant in meta-greywacke biotites than in meta-pelite biotitesand (Na+Ba+K) content of muscovites is greater in meta-greywackes. The observed features are used to deduce mechanisms of controlby grade and bulk composition and to discuss general circumstancesunder which they operate. 相似文献
8.
The stability and phase relations of phengitic muscovite in a metapelitic bulk composition containing a mixed H2O+CO2 fluid were investigated at 6.5–11 GPa, 750–1050°C in synthesis experiments performed in a multianvil apparatus. Starting material consisted of a natural calcareous metapelite from the coesite zone of the Dabie Mountains, China, ultrahigh-pressure metamorphic complex that had experienced peak metamorphic pressures greater than 3 GPa. The sample contains a total of 2.1 wt.% H2O and 6.3 wt.% CO2 bound in hydrous and carbonate minerals. No additional fluid was added to the starting material. Phengite is stable in this bulk composition from 6.5 to 9 GPa at 900°C and coexists with an eclogitic phase assemblage consisting of garnet, omphacite, coesite, rutile, and fluid. Phengite dehydrates to produce K-hollandite between 8 and 11 GPa, 750–900°C. Phengite melting/dissolution occurs between 900°C and 975°C at 6.5–8 GPa and is associated with the appearance of kyanite in the phase assemblage. The formation of K-hollandite is accompanied by the appearance of magnesite and topaz-OH in the phase assemblage as well as by significant increases in the grossular content of garnet (average Xgrs=0.52, Xpy=0.19) and the jadeite content of omphacite (Xjd=0.92). Mass balance indicates that the volatile content of the fluid phase changes markedly at the phengite/K-hollandite phase boundary. At P≤8 GPa, fluid coexisting with phengite appears to be relatively CO2-rich (XCO2/XH2O=2.2), whereas fluid coexisting with K-hollandite and magnesite at 11 GPa is rich in H2O (XCO2/XH2O=0.2). Analysis of quench material and mass balance calculations indicate that fluids at all pressures and temperatures examined contain an abundance of dissolved solutes (approximately 40 mol% at 8 GPa, 60 mol% at 11 GPa) that act to dilute the volatile content of the fluid phase. The average phengite content of muscovite is positively correlated with pressure and ranges from 3.62 Si per formula unit (pfu) at 6.5 GPa to 3.80 Si pfu at 9 GPa. The extent of the phengite substitution in muscovite in this bulk composition appears to be limited to a maximum of 3.80–3.85 Si pfu at P=9 GPa. These experiments show that phengite should be stable in metasediments in mature subduction zones to depths of up to 300 km even under conditions in which aH2O1. Other high-pressure hydrous phases such as lawsonite, MgMgAl-pumpellyite, and topaz-OH that may form in subducted sediments do not occur within the phengite stability field in this system, and may require more H2O-rich fluid compositions in order to form. The wide range of conditions under which phengite occurs and its participation in mixed volatile reactions that may buffer the composition of the fluid phase suggest that phengite may significantly influence the nature of metasomatic fluids released from deeply subducted sediments at depths of up to 300 km at convergent plate boundaries. 相似文献
9.
多硅白云母压力计在退变质作用中的稳定性探讨 总被引：1，自引：0，他引：1
探讨多硅白云母地质压力计在低温退变质过程中的稳定性，在对大别山东缘和苏鲁造山带西缘郯庐左旋走滑韧性剪切带糜棱岩中的多硅白云母残斑由中心向两侧边缘进行电子探针分析后发现：由中心向两侧边缘Si减少,Al增加,Fe，Mg略有降低，部分样品中K，Na有不同程度的增加．而Ti则显示不活动富集。这是由于退变质过程中流体的活动常会改变残斑白云母的成分．并且在流体活动过程相对短暂的情况下，使残斑白云母的成分不能发生充分变化．最终会导致白云母不同部位具有不同的成分。因而,经历了富流体活动的退变质作用后,岩石中的多硅白云母残斑已不能完全保存其形成时的压力信息。 相似文献
10.
Two types of biotite isograd are defined in the low-grade metamorphism of the Wazuka area, a Ryoke metamorphic terrain in the Kii Peninsula, Japan. The first, BI1, is defined by the reaction of chlorite+K-feldspar= biotite+muscovite+quartz+H2O that took place in psammitic rocks, and the second, BI2, by the continuous reaction between muscovite, chlorite, biotite and quartz in pelitic rocks. The Fe/Mg ratios of the host rocks do not significantly affect the reactions. From the paragenesis of pelitic and psammitic metamorphic rocks, the following mineral zones were established for this low-pressure regional metamorphic terrain: chlorite, transitional, chlorite-biotite, biotite, and sillimanite. The celadonite content of muscovite solid solution in pelitic rocks decreases systematically with the grade of metamorphism from 38% in the chlorite zone to 11% in the biotite zone. Low pressure does not prohibit muscovite from showing the progressive change of composition, if only rocks with appropriate paragenesis are chosen. A qualitative phase diagram of the AKF system relevant to biotite formation suggests that the higher the pressure of metamorphism, the higher the celadonite content of muscovite at BI1, which is confirmed by comparing the muscovites from the Barrovian and Ryoke metamorphism. 相似文献
11.
M. Frey J. C. Hunziker E. Jäger W. B. Stern 《Contributions to Mineralogy and Petrology》1983,83(1-2):185-197
Some 150 white K-micas from the Central Alps were analysed for their polymorph and phengite content. Pre-Alpine white K-micas and those belonging to the Meso-Alpine Lepontine Metamorphic “High” show exclusively the 2M1 polymorph. The 3T structural form, on the other hand, has been found in one third of the white K-micas formed during the Alpine regional metamorphism. In most cases this trigonal structure coexists with varying amounts of the 2M1 form. The 3T distribution pattern suggests that this polymorph originated during the Eo-Alpine high-pressure/“low temperature” metamorphism. Provided this interpretation is correct, the sporadic occurrence of this polymorph within the Meso-Alpine staurolite zone may be used as a tracer for the Eo-Alpine metamorphism. The following improved correlation between the (060, 331) reflections of 2M1 white K-micas and the RM-content (= 2Fe2O3+FeO+MgO in molar proportions), based on 24 micas from granitoid rocks, is presented: d(060, 331)= 1.498+0.082 RM. The phengite content of Alpine white K-micas belonging to the assemblage muscovite-biotite-K-feldspar-quartz was estimated from RM values or derived from chemical analyses and was found to be clearly related to metamorphic grade. Phengite-rich micas were formed during the Eo-Alpine high-P/“ low-T” metamorphism while aluminous muscovite was found within the Meso-Alpine thermal high of the Lepontine gneiss area. White K-micas from areas which underwent both the Eo-Alpine and the Meso-Alpine metamorphism display variable phengite contents. Although these micas show Tertiary Rb-Sr and K-Ar ages, the variable phengite content presumably reflects conditions during the Eo-Alpine high-P/“low-T” metamorphism. This interpretation implies that the cations occupying the interlayer positions are more easily equilibrated than those in octahedral and tetrahedral structural sites. A compilation of 3T white K-mica occurrences described in the literature is given in the appendix. 相似文献
12.
Lancang Group within the Changning-Menglian complex belt in the Sanjiang area, Yunnan Province involves many kinds of meta-sediments, including staurolite-kyanite-bearing garnet-mica schist, garnet-mica schist, chloritoid-white mica schist and chlorite-glaucophane-albite schist. Detailed petrographic observation, mineral chemistry analysis and phase equilibrium modelling have shown that these meta-sediments preserve distinctly metamorphic evolutions. The staurolite-kyanite-bearing garnet-mica schist records the decompression and cooling histories related to retrograded metamorphic processes from middle-temperature eclogite facies to amphibolite facies with a peak mineral assemblage of garnet + kyanite + phengite + jadeite formed at the P-T condition of about 19 similar to 30kbar and 600 similar to 750 degrees C. For the garnet-mica schist, the peak metamorphic mineral association constrained by X-Prp and X-Grs in garnet, and Si content in phengite includes garnet + phengite + omphacite + lawsonite + paragonite and the related P-T condition is around 17 similar to 19. 5kbar and 430 similar to 475 degrees C . The chloritoid-white mica schist is characterized by the mineral assemblage of chloritoid + phengite + paragonite + chlorite whereas the peak mineral assemblage includes phengite + paragonite + carpholite. The peak P-T condition defined by Si content in phengite is limited in the range of 17 similar to 19kbar and 300 similar to 330 degrees C. Both garnet-mica schist and chloritoid-white mica schist consistently record heating and decompression processes from lawsonite-blueschist facies to epidote-blueschist facies. Metamorphic reactions and mineralogy of chlorite-glaucophane-albite schist roughly give the P-T condition of 9 similar to 11kbar and 430 similar to 520 degrees C. Studies on the geochemistry of Lancang Group reveal that these meta-sediments show the geochemistry affinity to the continental arc, active continental margin and upper crust sediments. The protoliths are mainly mud rock and sandstone with low maturity and a little of mafic-intermediate volcanic rock. The sediment sources are predominantly intermediate-acid magmatic rocks with old sedimentary contamination to different degree. Tectonic discrimination diagrams show that meta-sediments in the Lancang Group are mainly derived from the continental island arc or active continental margin tectonic setting. Combined with the metamorphism and geochemistry characteristics of these rocks in the Changning-Menglian complex belt, it is therefore inferred that the meta-sediments of Lancang Group display various metamorphic evolutions. Lancang Group are considered to have experienced multi-phase/stage and complex tectonic evolution histories. 相似文献
13.
攀西中元古结晶片岩系遭受了前进区域变质作用。盐边和米易的砂屑岩和泥质岩分别可划出:绿泥石、黑云母、铁铝榴石、十字石和夕线石带以及绿泥石、黑云母-石榴子石、红柱石和夕线石带。在中、低级泥砂质岩石中,白云母的Na/(Na+K)比值随变质级增高。白云母、绿泥石和黑云母中的契尔马克替换范围大体上随变质级增高而降低。白云母和绿泥石之间契尔马克替换交换反应的分配系数,大致是白云母的绿鳞石含量的函数,并随变质温度升高而降低,在夕线石带,该分配系数变得很小。黑云母和白云母契尔马克替换交换反应的分配系数有类似的趋势。 相似文献
14.
柴北缘锡铁山一带榴辉岩的岩石学特征及其退变PT轨迹 总被引：1，自引：1，他引：0
柴北缘锡铁山地区榴辉岩以透镜体的形式存在于花岗质片麻岩和副变质片麻岩中.根据矿物组合的不同,可以分为多硅白云母榴辉岩和角闪石榴辉岩.在多硅白云母榴辉岩中首次发现了柯石英假象.利用榴辉岩中Grt-Cpx-Phn矿物温压计.结合绿辉石中存在柯石英假象包体的现象,得到锡铁山榴辉岩的峰期温压条件为751～791℃,2.71～3.17GPa,证明了锡铁山地区与柴北缘其他地块一样,也经历了超高压变质作用.通过PT视剖面图计算了榴辉岩退变的PT轨迹具有2个阶段演化特征：即先等温降压,然后再降温降压的PT轨迹.详细的岩石学研究探讨了榴辉岩在退变过程中,各矿物的成分和结构的改变过程.石榴石在等温降压过程中成分变化不大,而在角闪石出现后,其边部镁铝榴石含量明显降低,进而形成了韭闪石+斜长石的冠状体.绿辉石在水饱和状态下经过贫硬玉化改造,而后形成了Di+Ab+Amp的后生合晶.多硅白云母分解形成白云母+黑云母及少量石英及钾长石的组合.角闪石随着温压条件的降低由钠钙质闪石逐渐向钙质闪石转化. 相似文献
15.
深熔过程中熔体成分与锆石行为模拟计算 总被引：3，自引：2，他引：1
发生深熔作用是高级变质作用的一个重要特征。深熔过程中产生的熔体可为淡色花岗岩提供潜在的源区;深熔过程中锆石的行为直接影响对变质锆石记年地质意义的理解。在含Zr体系下的相平衡模拟显示泥质成分深熔过程中产生熔体的成分在P-T空间中规律变化。温度升高时熔体Zr/Si值、Zr、FeO、MgO以及CaO等含量明显增加,压力较高时K2O含量也随温度升高而明显增加。Na2O含量随温度升高而降低,但随压力升高而增加。压力升高时Al/Si值显著升高。温度较高时Na/(Na+K)等值线较陡,减压熔融过程不会显著改变熔体Na/(Na+K)值,而升温减压过程以及近等压升温过程都会明显降低熔体Na/(Na+K)值。中压时随温度升高熔体Fe/(Fe+Mg)值缓慢升高,而石榴石的生长发育会迅速降低熔体Fe/(Fe+Mg)值。不同温压条件下对应的固相线熔融、白云母脱水熔融以及黑云母脱水熔融形成的熔体成分具有明显差异。对比模拟熔体成分在P-T空间的演化,喜马拉雅地区电气石淡色花岗岩对应熔体的形成温压条件应低于二云母淡色花岗岩,同类型淡色花岗岩之间在形成条件上也可能存在一定差异,并经历了差异性演化过程。含Zr体系下的相平衡关系显示进变过程是消耗锆石的过程,因而在进变过程中变质锆石难以生长,发生深熔作用的岩石中的变质锆石主要在退变过程中形成并记录退变质年龄。熔体丢失相关模拟显示不同温度阶段发生熔体丢失对锆石稳定性的影响不同。温度较低时Zr含量较少的熔体丢失会扩大持续进变过程中锆石的稳定范围,而温度较高时富Zr熔体的丢失会降低持续进变过程中锆石的稳定温度。类似于分离熔融作用的过程最利于残留相中剩余锆石在持续进变过程中的保存。 相似文献
16.
Phengite geobarometry based on the limiting assemblage with K-feldspar,phlogopite, and quartz 总被引：37，自引：0，他引：37
Hans -Joachim Massonne Werner Schreyer 《Contributions to Mineralogy and Petrology》1987,96(2):212-224
Following and extending the early work of Velde (1965) the pressure-temperature dependence of the compositions of potassic white micas coexisting with K-feldspar, quartz, and phlogopite in the model system K2O-MgO-Al2O3-SiO2-H2O was investigated up to fluid pressures of 24 kbar by synthesis experiments. There is a strong, almost linear increase of the Si content per formula unit (p.f.u.) of phengite, ideally KAl2–xMgx[Al1–xSi3+xO10] (OH)2 with pressure, as well as a moderate decrease of Si (or x) with temperature. The most siliceous phengite with Si near 3.8 p.f.u. becomes stable near 20 kbar depending on temperature. However, contrary to Velde's assumption, these phengites coexisting with the limiting assemblage are invariably not of an ideal dioctahedral composition (as given by the above formula) but have total octahedral occupancies as high as about 2.1 p.f.u.The stability field of the critical assemblage phengite — K-feldspar — phlogopite — quartz ranges, in the presence of excess H2O, from at least 350° C to about 700° C but has an upper pressure limit in the range 16–22 kbar, when K-feldspar and phlogopite react to form phengite and a K, Mg-rich siliceous fluid.For the purpose of using these phase relationships as a new geobarometer for natural rocks, the influence of other components in the phengite (F, Fe, Na) is evaluated on the basis of literature data. Water activities below unity shift the Si isopleths of phengite towards higher pressures and lower temperatures, but the effects are relatively small. Tests of the new geobarometer with published analytical and PT data on natural phengite-bearing rocks are handicapped by the paucity of reliable values, but also by the obvious lack of equilibration of phengite compositions in many rocks that show zonation of their phengites or even more than one generation of potassic white micas with different compositions. From natural phengites that do not coexist with the limiting assemblage studied here but still with a Mg, Fe-silicate, at least minimum pressures can be derived with the use of the data presented. 相似文献
17.
Microprobe analyses are performed on micas (biotite, muscovite and phlogopite) and chlorite from 1.9–1.8 Ga acid K- or Na-rich metavolcanics, cordierit-emica schists and manganiferous rocks from the Hästefält area in central Sweden. The results indicate that Fe-rich biotites and muscovites containing 10 to 25% celadonite and/or pyrophyllite are common in the K- and Na-rich metavolcanics. In the cordierite-mica schists the biotites are Mg-rich and the muscovites contain less than 10% celadonite and/or pyrophyllite. The predominant mica in the manganiferous rocks are phlogopite and less frequent rather pure muscovite. The chlorites show a wide range in composition, but principally those occurring in the K- and Na-rich metavolcanics are brunsvigite and diabantite and those in the cordierite-mica schists and the manganiferous rocks are mainly sheridanite and clinochlore. The chlorites of the manganiferous rocks show enrichment in Mn compared to those in other rock types. In general the compositional variations in the micas and less commonly chlorites are strongly controlled by rock type and fluid chemistry, particularly with respect to the ratio of FeO/(FeO+MgO). Estimates of maximum prograde metamorphic temperature, based on phyllosilicates and co-existing cordierite and garnets, indicate a value of up to 500° C. 相似文献
18.
《Journal of Structural Geology》2002,24(6-7):1139-1156
In metapelitic rocks of western Maine, a pluton-related M3 metamorphic gradient ranging in grade from garnet to upper sillimanite zone was superposed on a fairly uniform M2 regional metamorphic terrain characterized by the assemblage andalusite+staurolite+biotite+/−garnet. As a result, M2 assemblages re-equilibrated to the P, T, and aH2O conditions of M3, and both prograde and retrograde pseudomorphism of M2 porphyroblasts occurred. The type of pseudomorph and degree of development is directly related to the rock's position within the M3 metamorphic gradient, a function of its proximity to the Mooselookmeguntic pluton. Several ‘hinge’ zones occur in which the M3 minerals that pseudomorphed a particular M2 phase change. For example, M2 garnet was replaced by M3 chlorite or biotite, depending on its position within the M3 gradient. Similarly, in a transition zone between M3 upper staurolite and lower sillimanite zones, M2 staurolite was stable and shows M3 growth rims. Downgrade from this transition zone, staurolite was pseudomorphed by chlorite and muscovite, whereas upgrade, the pseudomorphs contain muscovite and some biotite. M3 pseudomorphs commonly retain crystal shapes of the original M2 porphyroblasts, reflecting relatively low regional deviatoric stress during and after M3. Although evidence for textural disequilibrium is common, chemical equilibrium was closely approached during M3. This study demonstrates for M3 that: (1) the pseudomorphic replacement was a constant volume process, and (2) fabrics produced by tectonic events can be erased by subsequent deformation and/or sufficiently intense subsequent recrystallization. 相似文献
19.
内蒙古头道桥地区出露了一套经高压变质形成的岩石组合。本次研究通过岩相学和矿物化学分析,根据矿物组合的不同,识别出蓝片岩、绿片岩两种不同类型的岩石类型。其中,蓝片岩的矿物组合为角闪石（蓝闪石、蓝透闪石）+绿帘石+钠长石+绿泥石+石英+赤铁矿±多硅白云母±方解石±榍石;绿片岩的矿物组合为绿泥石+钠长石+石英±绿帘石±角闪石（阳起石、镁角闪石、蓝透闪石、冻蓝闪石等）±多硅白云母±赤铁矿。确定了蓝片岩的峰期变质级别为绿帘-蓝闪片岩相,峰期变质温度为400~600℃,压力为1.2~1.4 GPa。绿片岩的峰期变质级别为绿帘-角闪岩相。结合前人研究成果,认为蓝片岩和绿片岩的形成与额尔古纳地块和兴安地块的碰撞拼合有关。 相似文献
20.
C. V. GUIDOTTI F. P. SASSI R. SASSI J. G. BLENCOE 《Journal of Metamorphic Geology》1994,12(6):779-788
Chemical data for 139 natural paragonite-muscovite (Pg-Ms) pairs illustrate the effects of ferromagnesian components on the P-T-X topology of the Pg-Ms solvus. The pairs were selected on the basis of: reasonably accurate knowledge of the P-T conditions of formation; evidence for close approach to equilibrium at peak metamorphic conditions; exclusion of pairs in which paragonite contains more than 5 mol% margarite; and exclusion of pairs from polymetamorphic rocks that contain more than one set of cogenetic Pg-Ms pairs. Graphical analysis reveals considerable scatter in the data; nevertheless, it is evident that the muscovite limb of the solvus shifts markedly toward end-member muscovite with increasing pressure from approximately 7 kbar to 21 kbar. This shift is attributed to a pressure-induced increase of the ferromagnesian content of muscovite, which increases the size of the XII alkali site - to the effect that K is more readily accommodated than Na. The data also suggest that the paragonite limb of the solvus migrates slightly toward end-member paragonite with increasing pressure. Broadening of the Pg-Ms solvus with increasing pressure reflects increasingly nonideal Na-K mixing as the phengite content of muscovite increases. Due to the wide scatter of data for Pg-phengitic-Ms pairs, it is concluded that, at the present time, Pg-Ms solvus thermometry is only viable for quasibinary Pg-Ms pairs. 相似文献