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1.
集安岩群石榴石以富铁为特征，均属铁铝榴石。形成于高角闪岩相的石榴石成分比较稳定，＜ＦｅＯ＞平均含量３２．２０％，ＭｇＯ５．１７％，Ｘ＿（Ｍｇ）平均值０．２３；结晶于低角闪岩相的石榴石（ＦｅＯ＋ＭｇＯ）含量３３．５０％，（ＭｎＯ＋ＣａＯ）６．９１％。石榴石微区成分不均匀，晶体内具有一些微区成分环带，这种环带不是各进变质作用阶段ｐ－Ｔ条件平衡或近平衡的产物。石榴石边缘存在着明显的扩散环带，表现为晶体边缘相对晶体核部，Ｃａ含量和＜ＦｃＯ＞含量增高，ＭｇＯ含量降低，Ｘ＿（Ｍｇ）值变小，反映本区变质峰期后经历的是一个近等压冷却的地质动力学过程。  相似文献   

2.
石榴子石为东疆哈尔里克变质带中的常见矿物。从外形上可分为两种 类型,一种是晶形发育较好的石榴子石,为断裂区域变质作用形成;另一种是破碎状、裂纹 发育的石榴子石,为早期热变质作用形成,呈残留状出现。二者在空间上共存。对于晶形较 好的石榴子石的化学成分研究表明,石榴子石发育生长环带,在晶体粒径与核部MnO的含量 之间存在着相关关系。其峰期MnO的含量反映了递增变质带变质温度变化的趋势。  相似文献   

3.
在中国东部皖北地区分布着新元古代镁铁质岩,其中一些碱性基性岩为金刚石的赋矿岩石。为了确定安徽栏杆金刚石矿区的石榴子石种类,对矿区内不同类型的石榴子石进行系统采样,测定了62件石榴子石微区化学成分。结果显示,安徽栏杆石榴子石矿物化学式A_3~(2+)B_2~(3+)(SiO_4)_3中的A组阳离子由Mg~(2+)、Fe~(2+)和Ca~(2+)离子占位,B主要由Al~(3+)、Fe~(3+)、Mn~(3+)和Cr~(3+)离子占位,三价阳离子主要为Al~(3+),二价阳离子主要为Ca~(2+),表明研究区石榴子石主要为钙铝-钙铁-镁铝石榴子石系列。在62个样品中,发现了超硅石榴子石。经过计算其形成的压力范围为12.1～12.8GPa,深度可达300km。  相似文献   

4.
滇西红牛矽卡岩型铜矿床石榴子石特征   总被引：13，自引：7，他引：6  
高雪  邓军  孟健寅  闫寒  李建新  杨春海  孙诺  魏超 《岩石学报》2014,30(9):2695-2708
红牛矽卡岩型铜矿床是义敦岛弧南段格咱火山-岩浆弧新探明的铜矿床之一,目前探明铜金属资源量已达大型规模。与由侵入岩和大理岩直接接触形成的典型矽卡岩矿床不同,红牛铜矿床是隐伏岩体远程矽卡岩化的产物,其矽卡岩矿体与地层产状基本一致,通常相间排列,且距离岩体较远,大理岩中可见粗粒石榴子石和硅灰石,矽卡岩中常见大理岩捕掳体。根据矽卡岩矿物组合可将该矿床矽卡岩类型划分为石榴子石矽卡岩、石榴子石透辉石(或透辉石石榴子石)矽卡岩、透辉石矽卡岩、符山石-石榴子石矽卡岩、硅灰石-石榴子石矽卡岩、绿帘石-石榴子石矽卡岩、阳起石-绿帘石矽卡岩、硅灰石矽卡岩和绿帘石矽卡岩,其中以石榴子石矽卡岩、透辉石矽卡岩和硅灰石矽卡岩为主。石榴子石是最重要的矽卡岩矿物,分布广泛、颜色变化大,且石榴子石矽卡岩中黄铜矿、黄铁矿、磁黄铁矿化最好。本文通过对0ZK10、3ZK11和7ZK16钻孔岩芯的地质编录,查明石榴子石在红牛铜矿床的空间分布和矿化特征,采集该矿区新鲜的石榴子石矽卡岩、矽卡岩化大理岩和角岩磨制成光薄片,开展详细的显微镜下鉴定工作,观察石榴子石的颜色、粒度、结构、光性等岩相学特征,并通过电子探针分析其化学成分。红牛铜矿床石榴子石集中产出于矽卡岩中,少量产出于矽卡岩化大理岩和角岩中,具有明显的两期。早期石榴子石分布广泛,多呈褐色-红褐色,非均质性,异常干涉色,粒径一般在0.2~4mm之间,半自形-自形中细粒结构,韵律环带发育。SiO2含量变化范围为35.18%~37.69%、CaO为33.34%~36.35%、Al2O3为3.64%~13.69%、FeO为11.90%~24.18%、MgO为0.00%~0.08%,FeO和Al2O3含量变化呈负相关,SiO2和CaO含量变化整体呈正相关。石榴子石端员组分总体以钙铁榴石(36.88%~82.36%)为主,其次为钙铝榴石(16.59%~60.75%),还有少量的镁铝榴石、铁铝榴石和锰铝榴石,属于钙铁榴石-钙铝榴石系列(And37-82Gro17-61Spe+Pyr+Alm0.33-3.71)。晚期石榴子石呈浅褐色-浅红色,多发育于矽卡岩化角岩和大理岩中,少量发育于矽卡岩中,半自形-他形粒状结构,均质性,全消光,常具有溶蚀结构。SiO2含量变化范围为35.06%~36.27%、CaO为33.07%~33.77%、Al2O3为0.04%~1.05%、FeO为27.38%~28.18%、MgO为0.00%~0.04%,属于钙铁榴石(94.42%~98.46%)。早期石榴子石韵律环带发育,其主量元素含量变化显示出一定的规律性,由核部向边缘,SiO2和CaO基本保持不变,FeO含量增加,Al2O3含量减少,钙铁榴石含量增加,钙铝榴石含量减少,反映在石榴子石形成早期,成岩环境为低氧逸度、酸性还原环境;形成过程中氧逸度增加,成矿溶液由酸性向弱碱性演化。黄铜矿、磁黄铁矿、辉钼矿等金属硫化物多呈他形充填于石榴子石颗粒之间,或在石榴子石的裂隙中形成细脉,或沿石榴子石生长环带面交代,表明石榴子石形成于矽卡岩早期、早于铜矿化,并为金属硫化物的沉淀富集提供了空间。  相似文献   

5.
Mineral textures, coupled with thermodynamic modelling in the MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (MnNCKFMASH) model system, of mid‐amphibolite facies metapelites from the Georgetown Inlier, northeast Australia, point to the recording of two separate and unrelated metamorphic events. The first occurred contemporaneously with Palaeo‐ to Mesoproterozoic orogenesis and involved heating and burial to temperatures and pressures of approximately 600–650 °C and 6.0–7.0 kbar. Textural evidence for the up‐temperature (and pressure) prograde part of this path is inferred from the inclusion of garnet in biotite and staurolite. The second metamorphic event resulted in a low‐pressure thermal overprint that is equated with the advective addition of heat to the terrane via the emplacement of the Forsayth Batholith (c. 1550 Ma). This event is inferred from subsequent growth of andalusite and randomly orientated fibrolitic sillimanite after garnet, biotite and staurolite. This two stage metamorphic evolution, when coupled with a number of other distinct geological characteristics, suggests that the Georgetown Inlier is dissimilar to the other Australian Palaeoproterozoic terranes with which it is commonly correlated.  相似文献   

6.
High‐pressure granulites are generally characterized by the absence of orthopyroxene. However, orthopyroxene is reported in a few high‐pressure, felsic–metapelitic granulites, such as the Huangtuling felsic high‐pressure granulite in the North Dabie metamorphic core complex in east‐central China, which rarely preserves the high‐pressure granulite facies assemblage of garnet + orthopyroxene + biotite + plagioclase + K‐feldspar + quartz. To investigate the effects of bulk‐rock composition on the stability of orthopyroxene‐bearing, high‐pressure granulite facies assemblages in the NCKFMASHTO (Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3) system, a series of P–T–X pseudosections based on the melt‐reintegrated composition of the Huangtuling felsic high‐pressure granulite were constructed. Calculations demonstrate that the orthopyroxene‐bearing, high‐pressure granulite facies assemblages are restricted to low XAl [Al2O3/(Na2O + CaO + K2O + FeO + MgO + Al2O3) < 0.35, mole proportion] or high XMg [MgO/(MgO + FeO) > 0.85] felsic–metapelitic rock types. This study also reveals that the XAl values in the residual felsic–metapelitic, high‐pressure granulites could be significantly reduced by a high proportion of melt loss. We suggest that orthopyroxene‐bearing, high‐pressure granulites occur in residual overthickened crustal basement under continental subduction–collision zones and arc–continent collision belts.  相似文献   

7.
Stromatic metatexites occurring structurally below the contact with the Ronda peridotite (Ojén nappe, Betic Cordillera, S Spain) are characterized by the mineral assemblage Qtz+Pl+Kfs+Bt+Sil+Grt+Ap+Gr+Ilm. Garnet occurs in low modal amount (2–5 vol.%). Very rare muscovite is present as armoured inclusions, indicating prograde exhaustion. Microstructural evidence of melting in the migmatites includes pseudomorphs after melt films and nanogranite and glassy inclusions hosted in garnet cores. The latter microstructure demonstrates that garnet crystallized in the presence of melt. Re‐melted nanogranites and preserved glassy inclusions show leucogranitic compositions. Phase equilibria modelling of the stromatic migmatite in the MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2–O2–C (MnNCaKFMASHOC) system with graphite‐saturated fluid shows P–T conditions of equilibration of 4.5–5 kbar, 660–700 °C. These results are consistent with the complete experimental re‐melting of nanogranites at 700 °C and indicate that nanogranites represent the anatectic melt generated immediately after entering supersolidus conditions. The P–T estimate for garnet and melt development does not, however, overlap with the low‐temperature tip of the pure melt field in the phase diagram calculated for the composition of preserved glassy inclusions in garnet in the Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) system. A comparison of measured melt compositions formed immediately beyond the solidus with results of phase equilibria modelling points to the systematic underestimation of FeO, MgO and CaO in the calculated melt. These discrepancies are present also when calculated melts are compared with low‐T natural and experimental melts from the literature. Under such conditions, the available melt model does not perform well. Given the presence of melt inclusions in garnet cores and the P–T estimates for their formation, we argue that small amounts (<5 vol.%) of peritectic garnet may grow at low temperatures (≤700 °C), as a result of continuous melting reactions consuming biotite.  相似文献   

8.
Spinel-anthophyllite rocks that may be classified as ultrabasic low-Ca spinel amphibolites have been first discovered in the Kokchetav collision zone (northern Kazakhstan). They outcrop 2 km west of Enbek-Berlyk Village among schists and quartzites and are closely associated with spinel harzburgites and garnet pyroxenites. The main hosted minerals are spinel (hercynite) and anthophyllite. The rocks bear magnetite-hornblende-spinel-anthophyllite pseudomorphs with rounded and polygonal sections, which might have been resulted from the replacement of garnet grains. The prismatic anthophyllite crystals and scarce olivine relics contain elongate parallel spinel inclusions resembling spinel-olivine syntactic intergrowths in the Enbek-Berlyk spinel harzburgites. The spinel-anthophyllite rocks are similar to the associated spinel harzburgites in CaO, MnO, SiO2, and Al2O3 contents but are richer in FeO and poorer in MgO (F = FeO/(FeO + MgO) = 57% against 35% in the harzburgites). Geological, mineralogical, and geochemical data suggest that the spinel-anthophyllite rocks formed during the isochemical contact metamorphism of garnet-bearing spinel harzburgites, which contained more FeO and less MgO than garnet-free harzburgites of the same area. Variations in FeO and MgO contents in both types of harzburgites seem to be due to different chemical compositions of the chlorite protoliths of these rocks.  相似文献   

9.
Garnet-bearing mineral assemblages are commonly observed in pelitic schists regionally metamorphosed to upper greenschist and amphibolite facies conditions. Modelling of thermodynamic data for minerals in the system Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O, however, predicts that garnet should be observed only in rocks of a narrow range of very high Fe/Mg bulk compositions. Traditionally, the nearly ubiquitous presence of garnet in medium- to high-grade pelitic schists is attributed qualitatively to the stabilizing effect of MnO, based on the observed strong partitioning of MnO into garnet relative to other minerals. In order to quantify the dependence of garnet stability on whole-rock MnO content, we have calculated mineral stabilities for pelitic rocks in the system MnO–Na2O–K2O–FeO–MgO–Al2O3–SiO2–H2O for a moderate range of MnO contents from a set of non-linear equations that specify mass balance and chemical equilibrium among minerals and fluid. The model pelitic system includes quartz, muscovite. albite, pyrophyllite, chlorite, chloritoid, biotite, garnet, staurolite, cordierite, andalusite, kyanite. sillimanite, K-feldspar and H2O fluid. In the MnO-free system, garnet is restricted to high Fe/Mg bulk compositions, and commonly observed mineral assemblages such as garnet–chlorite and garnet–kyanite are not predicted at any pressure and temperature. In bulk compositions with XMn= Mn/(Fe + Mg + Mn) > 0.01, however, the predicted garnet-bearing mineral assemblages are the same as the sequence of prograde mineral assemblages typically observed in regional metamorphic terranes. Temperatures predicted for the first appearance of garnet in model pelitic schist are also strongly dependent on whole-rock MnO content. The small MnO contents of normal pelitic schists (XMn= 0.01–0.04) are both sufficient and necessary to account for the observed stability of garnet.  相似文献   

10.
Chemically zoned porphyroblasts in metamorphic rocks indicate that diffusional processes could not maintain equilibrium conditions on a grain scale during porphyroblast growth or establish it afterwards. An effect of this inability to maintain equilibrium is the progressive removal of elements forming garnet cores from any metamorphic reaction that occurs at the porphyroblast boundaries or in the matrix of the rock. To examine this effect on mineral assemblages, the Bence–Albee matrix correction was applied to X‐ray intensity maps collected using eclogite samples from northern New Caledonia in order to determine the chemical composition of all parts of the sample. The manipulation of these element maps allows a quantitative analysis of the fractionation of the bulk rock composition between garnet cores and the matrix. A series of calculated equilibrium‐volume compositions represents the change in matrix chemistry with progressive elemental fractionation as a consequence of prograde garnet growth under high‐P conditions. Pressure–temperature pseudosections are calculated for these compositions, in the CaO–Na2O–FeO–MgO–Al2O3–SiO2–H2O system. Assemblages, modal proportions and mineral textures observed in the New Caledonian eclogites can be closely modelled by progressively ‘removing’ elements forming garnet cores from the bulk rock composition. The pseudosections demonstrate how chemical fractionation effects the peak metamorphic assemblage, prograde textures and the development of retrograde assemblages.  相似文献   

11.
Micas from coarse granular Iherzolites in S. African kimberlites may be separated into two groups; those showing primary textural relationships with coexisting silicates and those with secondary, alteration relationships with other silicates. Primary-textured micas form a tight cluster with a mean composition from 10 coarse garnet lherzolites of: SiO2 41.0, TiO2 0.18, Al2O3 13.5, Cr2O3 0.82, total Fe as FeO 2.60, MnO 0.02, MgO 26.0, NiO 0.22, CaO 0.01, BaO 0.29, Na2O 0.31, K2O 10.0, Rb2O 0.028, Cl 0.08, F 0.43 wt%. Primary-textured micas in aggregates with clinopyroxene have higher TiO2 and four specimens which look similar to the primary group but have textural ambiguities have still higher TiO2Micas with secondary textures have wide ranges of composition which may be correlated with details of the textural parageneses. Micas from kelyphitic rims around garnets tend to be Cr-rich while those from veinlets are Cr-poor. Both groups tend to have higher FeO and TiO2 than the primary group. Micas produced by alteration of, or filling veinlets through, orthopyroxene have a wide compositional range which overlaps that of the primary-textured micas, especially for harzburgite specimens.The primary-textured micas show a positive correlation with coexisting pyroxenes for MgO/(MgO + FeO) and TiO2, but not for Cr2O3. Secondary-textured micas do not show correlations with coexisting pyroxenes for any elements.The ‘primary-metasomatic’ micas described by Harte and Gurney (1975) and metasomatic and other micas described by Boettcher et al. (1979) and Boettcher and O'neil (1979) are richer in FeO and TiO2 than the present primary-textured micas, and are attributed to crystallization from fractionated fluids.  相似文献   

12.
Cordierite–orthoamphibole gneisses and rocks of similar composition commonly contain low‐variance mineral assemblages that can provide useful information about the metamorphic evolution of a terrane. New calculated petrogenetic grids and pseudosections are presented in the FeO–MgO–Al2O3–SiO2–H2O (FMASH), Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O (NCKFMASH) and Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 (NCKFMASHTO) chemical systems to investigate quantitatively the phase relations in these rocks. Although the bulk compositions of cordierite–orthoamphibole gneisses are close to FMASH, calculations in this system do not adequately account for the observed range of mineral assemblages. Calculations in NCKFMASH and NCKFMASHTO highlight the role of minor constituents such as Ca, Na and Fe3+ in the mineral assemblage evolution of such rocks and these systems are more appropriate for interpreting the evolution of natural examples.  相似文献   

13.
Fe‐rich metapelitic granulites of the Musgrave Block, central Australia, contain several symplectic and coronal reaction textures that post‐date a peak S2 metamorphic assemblage involving garnet, sillimanite, spinel, ilmenite, K‐feldspar and quartz. The earliest reaction textures involve spinel‐ and quartz‐bearing symplectites that enclose garnet and to a lesser extent sillimanite. The symplectic spinel and quartz are in places separated by later garnet and/or sillimanite coronas. The metamorphic effects of a later, D3, event are restricted to zones of moderate to high strain where a metamorphic assemblage of garnet, sillimanite, K‐feldspar, magnetite, ilmenite, quartz and biotite is preserved. Quantitative mineral equilibria calculations in the system K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3 (KFMASHTO) using Thermocalc 3.0 and the accompanying internally consistent dataset provide important constraints on the influence of TiO2 and Fe2O3 on biotite‐bearing and spinel‐bearing equilibria, respectively. Biotite‐bearing equilibria are shifted to higher temperatures and spinel‐bearing equilibria to higher pressures and lower temperatures in comparison to the equivalent equilibria in K2O–FeO–MgO–Al2O3–SiO2–H2O (KFMASH). The sequence of reaction textures involving spinel is consistent with a D2 P–T path that involved a small amount of decompression followed predominantly by cooling within a single mineral assemblage stability field. Thus, the reaction textures reflect changes in modal proportions within an equilibrium assemblage rather than the crossing of a univariant reaction. The D3 metamorphic assemblage is consistent with lower temperatures than those inferred for D2.  相似文献   

14.
The mineralogy and petrochemistry of the garnet-amphibolites from the highgrade part of the Abukuma metamorphic belt have been studied, using five analyses of rocks, five of hornblendes, three of garnets and one analysis of cummingtonite, Garnetiferous amphibolites are rich in Fe, whereas non-garnetiferous ones are rich in Mg, especially in cummingtonite-amphibolite. The chemical composition of hornblendes associated with garnet is pargasitic and rich in FeO and poor in CaO, but that of non-garnetiferous rocks is rich in MgO. The garnets are rich in almandine molecule. Mg/Mg + Fe2+ ratios of both hornblendes and garnets correspond with those of the host rocks. The development of garnet in the Adirondack metabasites belonging to the upper almandine-amphibolite and granulite facies is observed in Mg-rich rocks as well as in Fe-rich rocks, in which both garnet and hornblende are rich in Mg respectively. However, under the conditions of the andalusite-sillimanite type metamorphism as shown in the Abukuma Plateau, Fe-rich garnet occurs in Fe-rich basic rocks, but cummingtonite occurs in Mg-rich ones instead of Mg-rich garnet. Finally, the problem of polymetamorphism is discussed. The cummingtonite-amphibolite may be the product of polymetamorphism, and Mg-rich garnet which had been present previously was decomposed to cummingtonite and plagioclase by the subsequent regional metamorphism of andalusite-sillimanite type.  相似文献   

15.
The a–x relations recently presented in White et al. ( 2014 , Journal of Metamorphic Geology, 32, 261–286) are extended to include MnO. This provides a set of internally consistent a–x relations for metapelitic rocks in the MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–O2 (MnNCKFMASHTO) system. The mixing parameters for the Mn‐bearing minerals were estimated using the micro‐? approach of Powell et al. ( 2014 , Journal of Metamorphic Geology, 32, 245–260). Then the Mn‐end‐member thermodynamic properties were calibrated using a database of co‐existing minerals involving literature data from rocks and from experiments on natural materials. Mn‐end‐members were calibrated for orthopyroxene, cordierite, staurolite, chloritoid, chlorite, biotite, ilmenite and hematite, assuming known properties for the garnet end‐member spessartine. The addition of MnO to phase diagram calculations results in a marked expansion of the stability of garnet‐bearing assemblages. At greenschist facies conditions garnet stability is extended down temperature. At amphibolite facies conditions, the garnet‐in boundary shifts to lower pressure. While the addition of MnO greatly influences the stability of garnet, it has relatively little effect on the stability of other common metapelitic minerals, with the resultant diagrams being topologically very similar to those calculated without MnO. Furthermore, the addition of MnO in the amounts measured in most metapelites has only a small effect on the mode of garnet, with calculated garnet modes remaining smaller than 1% in the P–T range outside its predicted Mn‐free P–T range.  相似文献   

16.
A highly-fractionated garnet-bearing muscovite granite represents the marginal granitic facies of the Abu-Diab multiphase pluton in the Central Eastern Desert of Egypt. New electron microprobe analyses(EMPA) and laser ablation inductively coupled plasma mass spectrometry(LA-ICP-MS) data from garnets are reported, in order to constrain their origin and genesis. Garnet in the Abu-Diab host granite is euhedral to subhedral, generally homogeneous and, in rare cases, it shows weak zonation. The garnet contains appreciable amounts of MnO and FeO, with lesser amounts of MgO and CaO, yielding an end-member formula of Sps_(61–72)Alm_(25–35)Prp_(1–4)Adr_(0–1). Moreover, it is depleted in large ion lithophile elements(LILE) with lower values of Ba, Nb and Sr relative to the primitive mantle. Additionally, it contains high concentrations of HREE and Y and their REE pattern shows strong negative Eu anomalies. The garnet was crystallized under relatively low temperature(646°C–591°C) and pressure( 3 kbar) conditions. The textural and chemical features indicate that the garnet is magmatic in origin and is chemically similar to that from highly-fractionated A-type granite. It was probably formed at the expense of biotite in a highly-evolved MnO-rich magma and/or by hydroxyl complexing of Mn during the ascending fluid phases.  相似文献   

17.
Iron-magnesium distribution coefficients for coexisting ortho- and clinopyroxene in 22 amphibolites from the New Jersey Precambrian Highlands range from 1.40 to 1.90. No systematic areal variation of the distribution coefficient is discernable within a 700 mi2 area. The distribution coefficient is, however, systematically related to pyroxene composition. The distribution coefficient tends to increase with increasing pyroxene weight % FeO (Fe as FeO) and decrease with increasing MgO and Al2O3. Data from other workers indicates that the distribution coefficient versus pyroxene composition trends found in the Highlands amphibolites are also present in both igneous and metamorphic rock suites from several other areas. Possible influence of pyroxene CaO on the distribution coefficient is also indicated. The Highlands amphibolite type trends are, however, directly opposite to those previously reported for Australian granulites. Both types of trends are apparently valid since both are present in at least one instance in metamorphic rocks from a relatively small area. The causes for the development of the two types of trends are imperfectly understood. Data presented indicates, however, that the New Jersey amphibolite type trends are apparently more characteristic of Fe-poor pyroxenes, whereas, the Australian granulite type trends are more characteristic of Fe-rich pyroxenes.The distribution coefficient in the Highlands amphibolites is also systematically related to bulk-rock composition due to the sympathetic variation of pyroxene Fe-Mg content with total rock MgO/FeO(Fe as FeO). The observed range of the distribution coefficient in the Highlands amphibolites may, consequently, mostly reflect variation in bulk-rock composition and not variation in crystallization temperature.  相似文献   

18.
The CCSD‐PP1 drillhole penetrated a 110‐m‐thick sequence of the Zhimafang ultramafic body in the Sulu ultrahigh‐pressure (UHP) metamorphic belt, east China. The sequence consists of interlayered garnet‐bearing (Grt) and garnet‐free (GF) peridotite. Eleven layers of Grt‐peridotite, ranging from 1.2 to 9.5 m in thickness, have an aggregate thickness of 54.49 m, whereas eight layers of GF‐peridotite, ranging from 2.2 to 14.2 m in thickness, have a total thickness of 57.53 m. The boundaries between the two rock types are gradational. The Grt‐peridotites have slightly higher contents of Al2O3, CaO and SiO2, and lower Mg#s (0.90–0.92) than the GF‐peridotites (Mg#s 0.91–0.93). Both contain low TiO2 (<0.05 wt%) and have higher modal abundances of enstatite (average 10 vol.%) than diopside (1–5 vol.%), typical of depleted‐type upper mantle. The diopside in these rocks has high and relatively uniform Mg# members (0.93–0.95), but highly variable Al2O3 (0.2–2.3 wt%), Na2O (0.5–2.5 wt%) and Cr2O3 (0.38–2.09 wt%). Enstatite (En92?93) contains very low Al2O3 (0–0.3 wt%). Both porphyroblastic and equigranular garnet are present. The equigranular varieties are zoned, from core to rim in Cr2O3 (3.4–4.2 wt%), MgO (18.4–17.5 wt%) and Al2O3 (21.1–20.1 wt%). Titania is very low in all the garnet, mostly <0.05 wt%. Chromite or chromium (Cr)‐spinel occur both in the Grt‐ and GF‐peridotite, and are characterized by high contents of Cr2O3 (49–58 wt%) and FeO (24–43 wt%), similar to that in iron‐rich Alpine‐type peridotites. Based on the bulk‐rock MgO–FeO compositions, the Zhimafang Grt‐peridotite probably underwent 20–30% partial melting, whereas the GF‐peridotite may have undergone as much as 35–40% partial melting, suggesting that the two rock types owe their differences to different degrees of partial melting rather than to pressure differences during metamorphism.  相似文献   

19.
In the Champawat area, Kumaun Himalaya, greenschist facies regionally metamorphosed rocksviz chlorite-phyllite and schist have been subjected to thermal metamorphism due to emplacement of batholithic granite/granodiorite body. As a consequence, biotite, garnet, andalusite, fibrolite, sillimanite and perthite minerals have formed in the contact rocks. The conspicuous absence of cordierite and staurolite reported from such aureole rocks is due to higher FeO/MgO ratio of the bulk rock composition in the former while the absence of staurolite is due to low Al2O3/FeO+MgO ratio in the schists. AFM diagram demonstrates that in muscovite-bearing schist, the bulk composition of chlorite- and cordierite-bearing rocks are restricted to low FeO/MgO side and thus the restricted occurrence of former and the absence of latter in the contact rocks of the area. This is further evident from the common occurrence of almandine-rich garnet in the rocks.  相似文献   

20.
Sixteen gabbro (hyperite)/amphibolite pairs were collected from geological situations where it seems clear that the amphibolite formed from material similar in composition to that of the adjacent hyperite.Major element analyses show that the hyperite to amphibolite transition was not an isochemical one. K2O, H2O, P2O5 and Fe2O3 were increased strongly. CaO and FeO were diminished; SiO2 may have been also. TiO2, total iron, MgO, MnO and Na2O were static; so probably was Al1O3.  相似文献   

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