共查询到19条相似文献，搜索用时 250 毫秒
1.
本文根据垄青石晶体结构特点和有关热力学资料,建立了堇青石热膨胀系数的理论计算模式:半定量计算方法,α=αMgO × 1/3 × 2/3;定量计算方法,α=ΔS/ΔT/2/(a × b).分别计算了堇青石、印度石的线热膨胀系数,半定量计算结果:α=3.31 × 10-6℃-1(堇青石、印度石);定量计算结果,a=1.54 × 10-6℃-1(堇青石),α=0.85 × 10-6℃-1(印度石),与实验测定结果(堇青石:α=2.3 × 10-6℃-1,印度石:α=1.0 × 10-6℃-1)吻合。 相似文献
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我們在前一篇文章里曾討論了Ca2+-HPO42--F1--H2O体系中氟对磷酸盐矿物形成影响的若干方面。为了使該項模拟試驗工作更符合于表生作用条件,我們在叶連俊教授的指导下,在上述实驗体系中增加了一个組分--HCO31-,进行了Ca2+-HPO42--HCO31-F1--H2O体系的試驗研究。其目的为进一步探索在合有HCO31-組分的体系中氟对磷酸盐矿物形成的影响,以及CO32-能否进入磷灰石晶格和磷酸盐矿物与碳酸盐矿物的沉积分异順序等問題。 相似文献
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近些年来,人们广泛地利用火山岩的主元素或微量元素的特征对火山岩进行地球化学、成因岩石学和构造岩石学的研究。Mullen(1983)利用玄武岩的 MnO、TiO2和P2O5建立大洋型玄武岩的 MnO×10-TiO2-P2O5×10的构造背景判别图(以下简称MTP图)和圈出了大陆拉斑玄武岩在 MTP 图中的分布范围。他选择了能反映玄武岩形成过程中的重要地球化学特征和成因机制的元素组作为该图的端元组分。 相似文献
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地球大气圈中40Ar/36Ar的现代比值被公认为295.5,在利用K-Ar法测定地球物质年龄时,它是校正大气氩混染量的重要参数。陨石中原始捕获(trapped)的(40Ar/36Ar)t比值是否和地球大气圈中氩同位素丰度相一致,这个问题不但在地质年龄测定中具有现实意义,而且对探索太阳系的形成和演化也有重要理论价值。近十几年,随着质谱分析技术的提高以及登月计划的实施,国外出现了一批有关月岩中氩同位素原始组分的资料,但至今对陨石中原始氩同位素丰度的报道很少。笔者采用40Ar/39Ar快中子活化技术和约克方程[3,4],对吉林陨石雨2号标本进行了原始捕获的(40Ar/36Ar)t比值进行了测定,并探讨了它的地质意义。 相似文献
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大容山花岗岩带中石榴子石,堇青石的成因研究 总被引：7，自引：0，他引：7
该花岗岩带中石榴子石富MgO而贫MnO,并且具正成分环带构造,证明是原岩残留晶;堇青石与残留包体中堇青石成分相似,均属镁堇青石,Na_2O<0.33％,表明不是岩浆晶出矿物,而是岩浆源区残留晶。矿物谱学工作表明,堇青石中赋存原生CO_2和H_2O,某组成是矿物形成温度的灵敏指示剂;另一方面,由于挥发分的存在,“湿”堇青石畸变系数△不能反映硅铝有序度,而红外分裂指数能够及“干”堇青石△可能能够反映硅铝有序度。石榴子石-堇青石组合是理想的地质温压逸度计,它给出了大容山岩体及旧州岩体源区的T、P、f_(H_2O)和P_(H_2O)。 相似文献
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用Rb-Sr法测定地质年龄,对地质样品中的锶往往要进行两种同位素分析:非稀释分析以测定87Sr/86Sr比值;稀释分析以测定样品中86Sr的含量。随着稀释剂84Sr丰度的提高,Wasserburg et al.(1964),Van schmus(1965),Wetherill与Bickford(1965)采用了以一代二的办法——用稀释分析既测定含量又测87Sr/86Sr比值。由于稀释剂中84Sr高度富集,87Sr/86Sr受到的影响小,在当时的技术条件下,这些作者没有对一些数据处理进行讨论。但随着计算技术的应用,大大提高了测量精度,稀释剂对87Sr/87Sr的影响则必须加以考虑。 相似文献
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K. K. Podlesskii 《Petrology》2010,18(4):350-368
Consistent thermodynamic data on the properties of pure mineral end members and the mixing properties of solid solutions in
the system FeO-MgO-Al2O3-SiO2 were employed to simulate phase relations of sapphirine, garnet, spinel, orthopyroxene, cordierite, quartz, Al silicates,
and corundum. Compositional variations of the solid solutions with temperature notably modify the topology of the P-T diagrams, which differ from the petrogenetic grids widely used in the literature. It is worth noting that the evaluation
of P-T metamorphic conditions based on reaction relations in sapphirine-bearing assemblages cannot be so far considered reliable
enough. The lower stability limit of the sapphirine + quartz assemblage in the system in question is possibly located at much
lower P-T parameters: at least 835°C and ∼6 kbar. The sapphirine + kyanite assemblage can be stable at temperatures below 860°C and
a pressure of ∼11 kbar, and the stability field of the sapphirine + olivine assemblage is narrow and constrained to temperatures
no higher than ∼800°C. 相似文献
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Stability of the assemblage sapphirine + quartz in Mg–Al-rich granulites implies ultrahigh temperature (UHT) condition of metamorphism but their direct contact is rarely preserved in natural rocks. The present study shows contrasting textural relations between sapphirine and quartz in different parts of the same occurrence of a Mg–Al-rich granulite, Eastern Ghats Belt, India. Textural data suggest stabilization of the assemblage sapphirine + quartz with orthopyroxene and cordierite during the metamorphic peak. Thermometric estimates yield temperature exceeding 950 °C for the stability of this assemblage. Most of such sapphirine grains (Spr1) are texturally separated from quartz and cordierite grains by double corona of sillimanite + orthopyroxene that results due to isobaric cooling during the post-peak stage. Sapphirine (Spr2) also forms a symplectic intergrowth with quartz and orthopyroxene at the fringe of coarse orthopyroxene. This textural feature can be explained by the breakdown of (Fe, Mg)-Tschermak components of orthopyroxene during the same isobaric cooling episode from UHT peak condition. The preservation of grain contact of this intergrown sapphirine and quartz can be attributed to a problem in reaction kinetics. In the other mode, sapphirine (Spr3) occurs with quartz with a thin skin of cordierite near a quartz vein. Such texture could result from isothermal decompression of the cooled crust. Alternatively and more possibly, cordierite could form from ingress of CO2–H2O rich fluid during terminal stage of cooling. Finally, sapphirine (Spr4) and quartz show direct contact close to the quartz vein. Direct contact of such sapphirine and quartz represents textural disequilibrium as this particular quartz is introduced as a vein much later than the peak metamorphism but prior to the major foliation-forming deformation. Coarse sapphirine and vein quartz, therefore, accidentally came in contact with each other and persisted metastably. Therefore, though coexistence of sapphirine and quartz is considered to be a strong evidence for ultrahigh temperature condition, care should be taken to decipher their stable coexistence. Different types of textural relations involving this mineral pair could originate in a single rock, probably in different stages of its metamorphic history. 相似文献
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Abstract Sapphirine-bearing rocks occur in three conformable, metre-size lenses in intrusive quartzo-feldspathic orthogneisses in the Curaçà valley of the Archaean Caraiba complex of Brazil. In the lenses there are six different sapphirine-bearing rock types, which have the following phases (each containing phlogopite in addition): A: Sapphirine, orthopyroxene; B: Sapphirine, cordierite, orthopyroxene, spinel; C: Sapphirine, cordierite; D: Sapphirine, cordierite, orthopyroxene, quartz; E: Sapphirine, cordierite, orthopyroxene, sillimanite, quartz; F: Sapphirine, cordierite, K-feldspar, quartz. Neither sapphirine and quartz nor orthopyroxene and sillimanite have been found in contact, however. During mylonitization, introduction of silica into the three quartz-free rocks (which represent relict protolith material) gave rise to the three cordierite and quartz-bearing rocks. Stable parageneses in the more magnesian rocks were sapphirine–orthopyroxene and sapphirine–cordierite. In more iron-rich rocks, sapphirine–cordierite, sapphirine-cordierite–sillimanite, cordierite–sillimanite, sapphirine–cordierite–spinel–magnetite and quartz–cordierite–orthopyroxene were stable. The iron oxide content in sapphirine of the six rocks increases from an average of 2.0 to 10.5 wt % (total Fe as FeO) in the order: C,F–A,D–B,E. With increase in Fe there is an increase in recalculated Fe2O3 in sapphirine. The four rock types associated with the sapphirine-bearing lenses are: I: Orthopyroxene, cordierite, biotite, quartz, feldspar tonalitic to grandioritic gneiss; II: Biotite, quartz, feldspar gneiss; III: Orthopyroxene, clinopyroxene, hornblende, plagioclase meta-norite; IV: Biotite, orthopyroxene, quartz, feldspar, garnet, cordierite, sillimanite granulite gneiss. The stable parageneses in type IV are orthopyroxene–cordierite–quartz, garnet–sillimanite–quartz and garnet–cordierite–sillimanite. Geothermobarometry suggests that the associated host rocks equilibrated at 720–750°C and 5.5–6.5 kbar. Petrogenetic grids for the FMASH and FMAFSH (FeO–MgO–Al2O3–Fe2O3–SiO2–H2O) model systems indicate that sapphirine-bearing assemblages without garnet were stabilized by a high Fe3+ content and a high XMg= (Mg/ (Mg+Fe2+)) under these P–T conditions. 相似文献
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Abstract Phase relations and mineral chemistry for garnet (Grt), orthopyroxene (Opx), sapphirine (Spr), water-undersaturated cordierite (Crd), osumilite (Osu), sillimanite (Sil), K-feldspar (Kfs), quartz (Qtz) and a water-undersaturated liquid (Liq) have been determined experimentally in the system KFMASH (K2O-FeO-MgO-Al2O3-SiO2-H2O) under low PH2O and fO2 conditions. Four compositions have been studied with 100 [Mg/(Mg + Fe)] ranging from 65.6 to 89.7. Based on our experimental data, a P-T grid is derived for the KFMASH system in the presence of quartz, orthopyroxene and liquid. Osumilite has been found in various mineral assemblages from 950 to 1100°C and 7.5 to 11 kbar. In the temperature range 1000-1100°C, the pair Os-Grt is stable over a pressure range of about 3kbar. The divariant reaction Os + Opx = Grt + Kfs + Qtz runs to the right with increasing pressure. Because osumilite is the most magnesian phase it is restricted to Mg-rich compositions at high pressure. The reaction defining the upper pressure stability limit of Os-Grt is located around 11 kbar with a nearly flat dP/dT slope over the temperature range 950–100°C. Over the entire temperature range investigated osumilite is not stable beyond 12 kbar. The data imply a restricted pressure range between 11 and 12 kbar for the stability of the assemblage Os-Opx-Sil-Kfs-Qtz. At 1050°C and above, osumilite occurs in various mineral assemblages together with the high-T pair Spr-Qtz. When coexisting with garnet, orthopyroxene or sapphirine, osumilite is always the most magnesian phase. At 1050 and 1100°C, liquid is invariably the most Fe-rich phase in the run product. Our data support a theoretical P-T grid for the KFMAS system in which osumilite is stable outside the field of the high-T assemblage Spr-Qtz. Moreover, our grid indicates that Os-Opx-Sil-Kfs-Qtz has a more restricted pressure and compositional stability domain than Os-Grt, in agreement with natural occurrences. Osumilite is stable over a large pressure range, such that in Mg-rich rocks, and at high temperature, it can occur at any depth in normal thickness continental crust. 相似文献
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D. E. Kelsey R. W. White T. J. B. Holland R. Powell 《Journal of Metamorphic Geology》2004,22(6):559-578
Sapphirine, coexisting with quartz, is an indicator mineral for ultrahigh‐temperature metamorphism in aluminous rock compositions. Here a new activity‐composition model for sapphirine is combined with the internally consistent thermodynamic dataset used by THERMOCALC, for calculations primarily in K2O‐FeO‐MgO‐Al2O3‐SiO2‐H2O (KFMASH). A discrepancy between published experimentally derived FMAS grids and our calculations is understood with reference to H2O. Published FMAS grids effectively represent constant aH2O sections, thereby limiting their detailed use for the interpretation of mineral reaction textures in compositions with differing H2O. For the calculated KFMASH univariant reaction grid, sapphirine + quartz assemblages occur at P–T in excess of 6–7 kbar and 1005 °C. Sapphirine compositions and composition ranges are consistent with natural examples. However, as many univariant equilibria are typically not ‘seen’ by a specific bulk composition, the univariant reaction grid may reveal little about the detailed topology of multi‐variant equilibria, and therefore is of limited use for interpreting the P–T evolution of mineral assemblages and reaction sequences. Calculated pseudosections, which quantify bulk composition and multi‐variant equilibria, predict experimentally determined KFMASH mineral assemblages with consistent topology, and also indicate that sapphirine stabilizes at increasingly higher pressure and temperature as XMg increases. Although coexisting sapphirine and quartz can occur in relatively iron‐rich rocks if the bulk chemistry is sufficiently aluminous, the P–T window of stability shrinks with decreasing XMg. An array of mineral assemblages and mineral reaction sequences from natural sapphirine + quartz and other rocks from Enderby Land, Antarctica, are reproducible with calculated pseudosections. That consistent phase diagram calculations involving sapphirine can be performed allows for a more thorough assessment of the metamorphic evolution of high‐temperature granulite facies terranes than was previously possible. The establishment of a a‐x model for sapphirine provides the basis for expansion to larger, more geologically realistic chemical systems (e.g. involving Fe3+). 相似文献
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Exsolution textures in orthopyroxene in aluminous granulites as indicators of UHT metamorphism: New evidence from the Eastern Ghats Belt, India 总被引：1，自引：0，他引：1
Highly aluminous orthopyroxene, coexisting with sapphirine, cordierite, sillimanite, quartz and garnet in various combinations, constitute granoblastic mosaic peak metamorphic assemblages in aluminous granulites from three localities in the Eastern Ghats Belt, India. Orthopyroxene contains four types of intergrowths: (a) involving sapphirine with or without cordierite, (b) involving spinel, but without sapphirine, (c) involving cordierite, but without sapphirine and spinel, and (d) involving garnet, without sapphirine, spinel or cordierite. On the basis of textural and compositional data, origin of the intergrowths is ascribed to breakdown of Mg-Tschermak component, locally also involving Fe- and Ti-Tschermak. An attempt is made to compute the “pre-breakdown” compositions of orthopyroxene by image analysis, which shows maximum Al2O3 content of 13.4 wt.% in the pristine orthopyroxene. Geothermometry, phase equilibria consideration and application of existing experimental data on alumina solubility in orthopyroxene coexisting with sapphirine and quartz, collectively indicate extreme thermal conditions of metamorphism (> 1000 °C) for the studied assemblages. This re-affirms the notion that Al2O3 solubility in orthopyroxene is the most powerful indicator of UHT metamorphism (Harley, S.L., 2004. Extending our understanding of ultrahigh temperature crustal metamorphism. J. Mineral. Petrol. Sci. 99, 140–158). The intergrowths are considered to have formed due to cooling from the thermal peak spanning a temperature range of approximately 150 °C. Appearance of diverse types of intergrowths is probably related to subtle differences in bulk composition, particularly Fe:Mg ratios. 相似文献
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世界上很多海域中的现代碳酸盐沉积正在形成,如巴哈马滩、美国的佛罗里达湾、古巴的巴塔诺湾、中东的波斯湾等地,以及丹麦的某些近海地区。产于这些海域中的现代碳酸盐沉积物,其矿物组成主要是文石,其次为镁方解石,纯方解石较少,现代白云石沉积更为少见。我国的现代碳酸盐沉积见于南海诸岛及海南岛的沿海地带。作者曾利用粉晶照相鉴定了采自我国南海二十余种珊瑚、瓣鳃类、腹足类、有孔虫等现代海相生物壳体的物相,发现除有孔虫和海胆壳是由镁方解石构成外,其余生物壳体皆由文石构成。 相似文献
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一、引言铸石是利用天然岩石,如玄武岩、辉绿岩或某些工业废渣为原料,经配料或直接熔化、浇铸成型、结晶、退火而成的一种工艺岩石。它的矿物组分主要为单斜辉石,磁铁矿的量很少,在个别情况下可有少量橄榄石。从生产技术来看,铸石就是把天然玄武岩类所含的复杂矿物相用人工转变为单一矿物相,也就是将原料中大量的斜长石和相当量的橄榄石 相似文献