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1.
Pyroxenoids on the join MnSiO3-CaSiO3 were synthesized from (Mn, Ca)-carbonate solid solutions and SiO2 in CO2-H2O mixtures at a total pressure of 2 kb. The type of structure found (pyroxmangite, rhodonite, bustamite or wollastonite) is mainly dependent on the Mn/Ca ratio, but also to a lesser extent on temperature. Johannsenite-type structures were encountered at low temperatures over a wide compositional range. It has been possible to convert the pyroxenoids pyroxmangite → rhodonite, rhodonite → bustamite, bustamite → wollastonite, and johannsenite → bustamite or wollastonite with increase of temperature, but not the reverse. The compositional ranges of the synthetic pyroxenoids are very similar to those found in natural pyroxenoids. 相似文献
2.
Philip E. Brown Eric J. Essene Donald R. Peacor 《Contributions to Mineralogy and Petrology》1980,74(4):417-425
Electron microprobe analysis of manganese silicates from Balmat, N.Y., has helped elucidate phase relations for Mn-bearing pyroxenes and pyroxenoids. A compilation of these data along with published and unpublished analyses for phases plotting on the CaSiO3-MgSiO3-MnSiO3 and CaSiO3-FeSiO3-MnSiO3 faces of the RSiO3 tetrahedron has constrained the subsolidus phase relations. For the system CaSiO3-FeSiO3-MnSiO3, the compositional gaps between bustamite/hedenbergite, bustamite/ rhodonite and rhodonite/pyroxmangite are constrained for middle-upper amphibolite facies conditions and extensive solid solutions limit possible three phase fields. For the CaSiO3-MgSiO3-MnSiO3 system much less data are available but it is clear that the solid solutions are much more limited for the pyroxenoid structures and a continuum of compositions is inferred for clinopyroxenes from diopside to kanoite (MnMgSi2O6) for amphibolite facies conditions (T=650° C). At lower temperatures, Balmat kanoites are unstable and exsolve into C2/c calciumrich (Ca0.68Mn0.44Mg0.88Si2O6) and C2/c calciumpoor (Ca0.12Mn1.02Mg0.86Si2O6) phases. At temperatures of 300–400° C the calcium-poor phase subsequently has undergone a transformation to a P21/c structure; this exsolution-inversion relationship is analogous to that relating augites and pigeonites in the traditional pyroxene quadrilateral. Rhodonite coexisting with Mn-clinopyroxenes is compositionally restricted to Mn0.75–0.95Mg0.0–0.15Ca0.05–0.13SiO3. For the original pyroxene+rhodonite assemblage, the Mg and Ca contents of the rhodonite are fixed for a specific P (6kbars)-T (650° C)-X(H2O)-X(CO2) by the coexistence of talc+quartz and calcite+quartz respectively.Contribution No. 363, from the Mineralogical Laboratory, Department of Geological Sciences, The University of Michigan, Ann Arbor MI 48109, USA 相似文献
3.
福建马坑铁（钼）矿床矽卡岩矿物学特征及分带研究 总被引：3，自引：0，他引：3
马坑大型铁(钼)矿赋存于莒舟-大洋花岗岩体外接触带黄龙组(C2h)灰岩和林地组(C1l)碎屑岩层间构造破碎带中,铁矿与矽卡岩密切共生,但矿床成因尚存在争议。本文就马坑铁矿矽卡岩进行了矿物学特征研究。电子探针分析结果表明:该矿矽卡岩矿物组合主要为辉石、石榴子石和钙蔷薇辉石,退化蚀变岩矿物组合为角闪石、绿帘石、绿泥石、石英等。单斜辉石以透辉石和钙铁辉石为主,仅存在少量锰钙辉石;似辉石为钙蔷薇辉石和蔷薇辉石;石榴子石端元成分以钙铁榴石为主,钙铝榴石少量;角闪石属于钙角闪石,矿物学特征表明它们形成于相对较氧化的条件下。马坑铁矿的矽卡岩是由热流体沿灰岩与碎屑岩之间层间构造破碎带交代形成的,铁矿石大部分产于矽卡岩内,磁铁矿多稍晚于矽卡岩,不仅广泛交代矽卡岩,而且还直接交代灰岩、砂岩等围岩,呈交代结构;主矿体下盘常出现厚层石英岩,碎屑岩也出现了明显的交代,矽卡岩分带现象普遍,与典型矽卡岩矿床特征一致。结合矿床地质特征,马坑铁矿矿床类型应为层控矽卡岩型矿床。 相似文献
4.
5.
The miscibility gap between rhodonite and bustamite has been experimentally determined at temperatures between 600° and 1,100° C. For temperatures below 700° C the resulting limbs have been extrapolated on T-X-diagram as at such low temperatures equilibrium could not be attained. According to microprobe analyses for the natural assemblages of Ravinella di Sotto (Ivrea zone, Italy) and Broken Hill (N.S.W., Australia) equilibrium temperatures are estimated to be at 500° to 550° C. However these assemblages are thought to have re-equilibrated during cooling and the compositions of equilibrium assemblages are also pressure dependent. According to experiments and to molar volume data the rhodonite structure is stabilized by high pressures whereas bustamite by high temperatures. Based on available experimental results and natural data an isobaric T-X
Ca diagram and two isotherm
-X
Ca diagrams (for T=400° C and T=600° C) are given. 相似文献
6.
R. J. Angel 《Contributions to Mineralogy and Petrology》1984,85(3):272-278
The CaMnSi2O6 clinopyroxene, johannsenite, inverts to bustamite at elevated temperatures. The inversion boundary has been reversibly determined at five pressures up to 22 kbar, using synthetic phases, and shown to have the equation; P(kbar)=0.0411T(°C)–10.7The determination allows the calculation of the enthalpies and free energies of formation for both clinopyroxene and bustamite of CaMnSi2O6 composition, and these are compared with data available for the CaFeSi2O6 composition which shows analagous inversion behaviour. Johannsenite appears to be of comparable stability to hedenbergite at STP, but at elevated temperatures hedenbergite may be stabilised by crystal field effects associated with the Fe2+ ion. Together with the stabilisation of the bustamite structure by manganese, this accounts for the low inversion temperature of johannsenite compared to that for hedenbergite. 相似文献
7.
Jürgen Abrecht 《Contributions to Mineralogy and Petrology》1980,74(3):253-260
In the system CaSiO3-CaMnSi2O6-CaFeSi2O6 extensive miscibility gaps between pyroxenoids and clinopyroxenes are observed. The miscibility gap between Mn-bustamite and Mn-wollastonite has been determined experimentally by a hydrothermal technique between 400° and 1200° C at P
f= 2 kbar. Further experiments have been performed at P
f=9 kbar, which revealed a shifting of the miscibility gap towards more Ca-rich compositions. The bustamite phase is stabilized by high pressures and the wollastonite structure is the stable phase at high temperatures.Similar phase relations as along the join CaSiO3-CaMnSi2O6 exist along the join CaSiO3-CaFeSi2O6 but with a more extensive two-phase field of bustamite-clinopyroxene.Possible phase relations along the joins CaSiO3-CaMnSi2O6, CaSiO3-CaFeSi2O6 and CaFeSi2O6-CaMnSi2O6 are given in temperature-composition diagrams for low pressures, based on natural and experimental data. 相似文献
8.
The existence of errors in the periodicity of the tetrahedral chains in pyroxenes and pyroxenoids is predicted. With high resolution electron microscopy of rhodonite, (Mn, Ca)5[Si5O15], and pyroxmangite, (Mn,Fe,Ca)7 [Si7O21], it is demonstrated that these errors are arranged into planar periodicity faults. The chain periodicity faults are compared with other planar faults described for chain silicates: chain multiplicity faults and chain arrangement faults. 相似文献
9.
Abstract Textural evolution and compositional variation of clinopyroxenes in Ward Creek metabasites are described. Pyroxenes change, with increasing grade, from finegrained aggregates through fan-shaped medium-grained prisms to blocky coarse crystals. Characteristic features of metamorphic pyroxenes include: (1) the occurrence of coexisting pyroxene pairs, the compositions of which are used to delineate compositional gaps; (2) the existence of large compositional variations of pyroxenes, within a single specimen, which record a considerable span of P and/or T for crystallization; and, (3) the development of compositional trends in single specimens and in three metamorphic zones which are progressive in nature. The first formed clinopyroxene (Jd20Aug65Ac15) in the lower lawsonite zone mimics the composition of relict igneous augite. It changes continuously, with increasing grade, at nearly constant low XJd content towards acmite. At a composition around Jd20Aug30Ac50, the trend turns towards jadeite and intersects a solvus to form two coexisting clinopyroxenes in the middle lawsonite zone. At higher grade, the compositional gap becomes restricted towards the jadeite-omphacite join and clinopyroxene increases in XJd toward jadeite. A reversed compositional trend occurs at higher grade; clinopyroxenes decrease in jadeite component at nearly constant Aug/Ac ratio of 50/50 and finally become omphacite in the uppermost pumpellyite and epidote zones. The Na–Ca pyroxenes, close to the binary join Jd–Ac, occur in the lawsonite- and pumpellyite-zones, ranging from XJd= 1.0–0.30 together with Ab and Qz. The ubiquitous occurrence of aragonite at temperature estimates of 170–240° C by Taylor & Coleman (1968) for these zones does not support the low-temperature extrapolation of the Jd–Ab–Qz curve by Holland (1980). The estimated metamorphic field gradient indicates an inflection point at 7 kbar, 200° C. Below this, blueschist facies metamorphism proceeded under dominant pressure-increase from 4 to 7 kbar at nearly constant temperature, about 150–200° C, whereas at higher grade recrystallization, above the inflection point, the metamorphic temperature increased from 200 to 350° C at nearly constant pressure, about 7–8 kbar. Such an inflection point suggests the depth of underplating of either seamounts or accretionary packages in a subduction zone. 相似文献
10.
YOSUKE KAWACHI RODNEY H. GRAPES DOUGLAS S. COOMBS MARTIN DOWSE 《Journal of Metamorphic Geology》1983,1(4):353-372
Abstract. Pink piemontite-spessartine-bearing and grey-green spessartine-bearing manganiferous quartzose schists derived from siliceous pelagites, and green quartzofeldspathic schists, are described from the greenschist facies of the Haast Schist terrane, near Arrow Junction, western Otago. Electron microprobe data are reported for sphene, spessartine-rich garnet, manganoan epidote, piemontite, tourmaline, phengitic muscovite, chlorite, albite, haematite, rutile, manganoan calcite and chalcopyrite. Metamorphism occurred at about 6.4kbar, 400°C. Xco2 was above the quartz-rutile-calcite-sphene buffer (Xco2± 0.02) throughout the recorded metamorphic history of the piemontite schists. It dropped from above to below this critical buffering value in a spessartine-rich schist and it was close to or below the buffering value in the quartzofeldspathic schists. Production of piemontite required high fO2, believed to be inherited from MnOx in the parent pelagite. Substantial loss of O2 (e.g. minimum of 0.19% by weight in one rock) during diagenesis and/or metamorphism is inferred. In the grey-green schists this inhibited piemontite formation. Slight loss of O2 and Ca2+ accompanied minor late-stage replacement of piemontite by second generation spessartine. Observed zoning and mineral replacements indicate rise of temperature, drop in pressure, or invasion by solutions of lower fO2 and XCO2 equilibrated with surrounding schists. The detailed chemistry of the minerals studied correlates with available Mn and with bulk-rock (Fe3+ x 100)/(Fe2++ Fe3+). The oxidation ratio ranges from 24 in average green quartzofeldspathic schist, through 78 in average grey-green manganiferous quartzose schist, to almost 100 in some piemontite-bearing schists. As Fe2+ gives way to Fe3+, Mg/Fe ratios tend to rise in chlorite, phengite, tourmaline, spessartine, and calcite, Mn increases and Ti decreases in haematite, Mn increases in spessartine and calcite, and Fe increases in rutile. Available divalent cations are depleted relative to Al; chlorite is more aluminous, and phengite more paragonitic than in typical Haast schists. 相似文献
11.
Brian Mason 《Australian Journal of Earth Sciences》2013,60(4):397-404
Sixteen unpublished analyses of Broken Hill manganese silicates (two pyrox‐mangite, one rhodonite, four hedenbergite, and nine bustamite) from the papers of the late Dr W. T. Schaller are presented. They have been complemented with additional analyses by the electron microprobe to define the compositional fields of these minerals. Data are provided on the relationship of these minerals with tephroite and garnet. The occurrence of roepperite (zincian tephroite) at Broken Hill is discredited, and its validity is doubtful. Dannemorite from Broken Hill has a composition close to Mn2(Fe,Mg)5Si8O22(OH)2, and can be considered a valid amphibole subspecies. 相似文献
12.
Orogenic gold mineralization at the Damang deposit, Ghana, is associated with hydrothermal alteration haloes around gold‐bearing quartz veins, produced by the infiltration of a H2O–CO2–K2O–H2S fluid following regional metamorphism. Alteration assemblages are controlled by the protoliths with sedimentary rocks developing a typical assemblage of muscovite, ankerite and pyrite, while intrusive dolerite bodies contain biotite, ankerite and pyrrhotite, accompanied by the destruction of hornblende. Mineral equilibria modelling was undertaken with the computer program thermocalc , in subsets of the model system MnO–Na2O–CaO–K2O–FeO–MgO–Al2O3–SiO2–CO2–H2O–TiO2–Fe2O3, to constrain conditions of regional metamorphism and the subsequent gold mineralization event. Metapelites with well‐developed amphibolite facies assemblages reliably constrain peak regional metamorphism at ~595 °C and 5.5 kbar. Observed hydrothermal alteration assemblages associated with gold mineralization in a wide compositional range of lithologies are typically calculated to be stable within P–T–X(CO2) arrays that trend towards lower temperatures and pressures with increasing equilibrium fluid X(CO2). These independent P–T–X(CO2) arrays converge and the region of overlap at ~375–425 °C and 1–2 kbar is taken to represent the conditions of alteration approaching equilibrium with a common infiltrating fluid with an X(CO2) of ~0.7. Fluid‐rock interaction calculations with M–X(CO2) diagrams indicate that the observed alteration assemblages are consistent with the addition of a single fluid phase requiring minimum fluid/rock ratios on the order of 1. 相似文献
13.
Holger Ried 《Physics and Chemistry of Minerals》1984,10(5):230-235
Intergrowth of clinopyroxenes (augite, A) and pyroxenoids (Fe-rhodonite and pyroxferroite, Pxo) was observed by transmission electron microscopy. The following orientation relationship was found: (001)Pxo is parallel to \((1\mathop {\bar 1}\limits^ + \bar 1)_{\text{A}}\) and \([1\bar 10]_{Pxo}\) is parallel to [011]A. This relationship can be explained by similarities of the structures of clinopyroxenes and pyroxenoids. It contradicts a suggestion based on structural arguments of Koto et al. (1976). Chain periodicity faults parallel to \((1\mathop {\bar 1}\limits^ + \bar 1)\) are also observed in pure clinopyroxenes. 相似文献
14.
A new type of fault, called a chain periodicity fault, has been observed in Fünferketten and Siebenerketten pyroxenoids. The faults are mainly parallel to (001) and are due to irregularities in the periodicity along c, the direction of the silicate chains. For example, pyroxmangite (Siebenerketten) contains slabs of rhodonite (Fünferketten) one unit cell thick in the c direction. A periodic arrangement of chain periodictiy faults in synthetic iron rhodonite gives rise to a superstructure, where eight Fünferketten units along a chain are followed by one Siebenerketten unit. When different pyroxenoids are intergrown, they have a sublattice exactly or nearly in common. Synthesis of pyroxferroite and iron rhodonite (all Mn replaced by Fe) was carried out at low pressure. 相似文献
15.
The model for the thermodynamic properties of multicomponent pyroxenes (Part I) is calibrated for ortho- and clinopyroxenes in the quadrilateral subsystem defined by the end-member components Mg2Si2O6, CaMgSi2O6, CaFeSi2O6, and Fe2Si2O6. This calibration accounts for: (1) Fe-Mg partitioning relations between orthopyroxenes and augites, and between pigeonites and augites, (2) miscibility gap features along the constituent binary joins CaMgSi2O6-Mg2Si2O6 and CaFeSi2O6-Fe2Si2O6, (3) calorimetric data for CaMgSi2O6-Mg2Si2O6 pyroxenes, and (4) the P-T-X systematics of both the reaction pigeonite=orthopyroxene+augite, and miscibility gap featurs, over the temperature and pressure ranges 800–1500°C and 0–30 kbar. The calibration is achieved with the simplifying assumption that all regular-solution-type parameters are constants independent of temperature. It is predicated on the assumptions that: (1) the Ca-Mg substitution is more nonideal in Pbca pyroxenes than in C2/c pyroxenes, and (2) entropies of about 3 and 6.5 J/K-mol are associated with the change of Ca from 6- to 8-fold coordination in the M2 site in magnesian and iron C2/c pyroxenes, respectively. The model predicts that Fe2+-Mg2+ M1-M2 site preferences in C2/c pyroxenes are highly dependent on Ca and Mg contents, with Fe2+ more strongly preferring M2 sites both in Ca-rich C2/c pyroxenes with a given Fe/(Fe+Mg) ratio, and in magnesian C2/c pyroxenes with intermediate Ca/(Ca+Fe+Mg) ratios.The proposed model is internally consistent with our previous analyses of the solution properties of spinels, rhombohedral oxides, and Fe-Mg olivines and orthpyroxenes. Results of our calibration extend an existing database to include estimates for the thermodynamic properties of the C2/c and Pbca pyroxene end-members clinoenstatite, clinoferrosilite, hedenbergite, orthodiopside, and orthohedenbergite. Phase relations within the quadrilateral and its constitutent subsystems are calculated for temperatures and pressures over the range 800–1700°C and 0–50 kbar and compare favorably with experimental constraints. 相似文献
16.
羊场磷矿是近年来在云南评价确认的沉积大型磷矿床,磷矿体赋存于下寒武统梅树村组碳酸盐岩-泥质碎屑岩沉积中部的一套含磷岩系中,呈层状、似层状展布于羊场背斜两翼,其产状与地层产状基本一致,含矿岩性为含磷白云岩、磷质岩、磷块岩、硅质岩建造。通过分析该矿床矿体特征和梅树村组磷块岩的主微量元素组成,研究了羊场磷矿的地球化学特征及其沉积环境。结果表明,羊场磷矿磷块岩具有富钙（w（CaO）=42.07%~45.01%）、磷（w（P2O5）=27.66%~39.25%）和贫硅（w（SiO2）=8.27%~15.40%）的特征;w（P2O5）与w（CaO）呈较好的正相关关系,与w（MgO）呈负相关关系,与w（Al2O3）呈较明显的负相关关系。矿石的w（Th）/w（U）值小于1、Pb （亲硫元素）和Sr富集（Pb平均富集系数16.66,Sr平均富集系数1.17）特征表明,羊场磷矿可能是热水沉积成矿与生物成矿双重作用的结果;微量元素特征值反映,羊场磷矿形成于深海到浅海的变化环境,为海相沉积型磷块岩,沉积时水体呈还原环境。 相似文献
17.
Summary At the northeastern flank of Gebel Yelleq, northern Sinai, pure limestones of Upper Cretaceous age were subjected to a thermal overprint, caused by a c. 80m thick Tertiary olivine dolerite sill. Metasomatic supply of Si, Al, Fe, Mg and Ti was greater to the c. 7m wide upper than to the c. 25m wide lower thermal aureole. The greater width of the lower aureole is possibly due to a longer duration of the thermal overprint at this contact. Mineral assemblages in both aureoles are (from the contact outward):(i) clinopyroxene + garnet ± wollastonite + calcite(ii) garnet ± wollastonite + calcite;(iii) wollastonite + calcite.In places, late stage xenoblasts of apophyllite and witherite overgrow these assemblages. Garnets are grandites to melanites with Grs56–86Adr14–42Sch0–2Sps0–0.2Prp0 in the lower, and Grs29–94Adr5–64Sch0–12Sps0–0.2Prp0–1.7 in the upper aureole. Close to the upper contact, clinopyroxene is virtually pure diopside with X
Mg = Mg/(Mg + Fe2+) = 0.97–1.0, whereas clinopyroxenes farther away from the upper contact and in the lower aureole have X
Mg-values of 0.49 and 0.53, respectively.The minimum temperatures reached during contact metamorphism in the upper and lower aureole are defined by the lower stability limit of wollastonite. The temperatures are inferred with a calculated T-X(CO2) projection in the system CMASCH and are estimated at c. 290 °C and 380 °C for X(CO2) values of 0.05 and 0.25, respectively. A pressure of roughly 100 bar is estimated for the lower dolerite-limestone contact. As indicated by one-dimensional thermal modelling, a maximum temperature of 695 °C was attained at this contact, assuming a magma temperature of 1150 °C. Further modelling results indicate (i) wollastonite, which occurs first 13 m away from the lower contact, formed at a maximum temperature of c. 575 °C, (ii) there, wollastonite formation lasted for approximately 170 years and, (iii) at the outer rim of the lower aureole, the maximum temperature reached was 480 °C, and temperatures sufficient for wollastonite formation lasted for about 140 years. 相似文献
18.
狼娃山铁矿为矽卡岩型铁矿,位于甘肃省肃北县狼娃山地区,中亚造山带以南,该区地质特征的认识仍不够全面,找矿方向尚未明确。本文基于野外调查及室内测试研究,归纳总结狼娃山铁矿床地质特征,探讨该地区铁矿找矿方向。研究表明:下石炭统白山组下亚组上、下段的流纹质凝灰熔岩为狼娃山铁矿主要含矿层;铁矿石全岩主要化学成分为w(TFe)=38.18%、w(SiO2)=21.96%、w(CaO)=7.05%、w(MgO)=6.80%、w(Al2O3)=6.14%,约占总量的80%,表明铁、石英、绢云母及碳酸盐岩为其主要构成,属酸性铁矿石;铁矿石物相w(TFe)平均为34.95%,w(mFe)平均为27.18%,mFe占TFe的77.78%,铁矿石主要矿物为磁铁矿(磁铁矿矿石);单矿物磁铁矿、赤铁矿电子探针测试分别属于普通磁铁矿、赤铁矿。铁矿成矿多发育在红石山南华力西期岛弧带,下石炭统白山组安山质熔凝灰岩及英安质凝灰岩控制铁矿产出,矽卡岩化可指示找矿;分析认为,狼娃山矿床深度在400~800m空间范围内仍存在很大的找矿潜力,可发展为以铁为主的多金属矿床。 相似文献
19.
A. I. Brusnitsyn 《Geology of Ore Deposits》2006,48(3):193-214
The mineralogy of slightly metamorphosed manganese ore at the South Faizulino hydrothermalsedimentary deposit in the southern Urals has been studied; 32 minerals were identified. Quartz, hausmannite, rhodochrosite, tephroite, ribbeite, pyroxmangite, and caryopilite are major minerals; calcite, kutnahorite, alleghanyite, spessartine, rhodonite, clinochlore, and parsettensite are second in abundance. This mineralic composition was formed in the process of gradual burial of ore beneath the sequence of Middle Devonian-Lower Carboniferous rocks. The highest parameters of metamorphism are T ≈ 250°C and P ≈ 2.5 kbar. The relationships between minerals and their assemblages made it possible to reconstruct the succession of ore transformation with gradually increasing temperature and pressure. Manganese accumulated in the initial sediments as oxides and a gel-like Mn-Si phase. Rhodochrosite and neotocite were formed at the diagenetic stage. In the course of a further increase in temperature and pressure, neotocite was replaced with caryopilite; ribbeite, tephroite, pyroxmangite, and other silicates crystallized afterwards. In addition to the PT parameters, the formation of various metamorphic mineral assemblages was controlled by the Mn/(Mn + Si) ratio in ore and X CO2 in pore solution. The latter parameter was determined by the occurrence of organic matter in the ore-bearing rocks. Ore veinlets as products of local hydrothermal redistribution of Mn, Si, and CO2 were formed during tectonic deformations in the Middle Carboniferous and Permian. 相似文献
20.
Dr. Niranjan D. Chatterjee 《Contributions to Mineralogy and Petrology》1967,14(2):114-122
The reaction 2 epidote+2 calcite+3 wollastonite3 grossular-andraditess+ 2 CO2+1 H2O has been explored by hydrothermal experiments at a total fluid pressure of 1000 bars. For a grossular-andraditess of andradite
25
composition, the isobaric univariant curve passes through the points 458°C: XCO2=0.00; 521°C: XCO2=0.026; 523°C: XCO2=0.052; 526°C: 0.088; 528°C: XCO2=0.104. This curve intersects the isobaric univariant curve of the reaction calcite+quartz+[H2O] wollastonite+CO2+[H2O] at the isobaric invariant point around 528°C and XCO2=0.12. At higher values of XCO2, this reaction is replaced by another one, namely: 2 epidote+5 calcite+3 quartz3 grossular-andraditess+5 CO2+ 1 H2O. It is demonstrated that both the reactions do actually take place during the metamorphism of calcareous rocks. The petrologic significance of contrasted sequence of reactions within this system observed by various workers is also discussed. 相似文献