Contributions to mineral chemistry of Hawaiian rocks

Small gabbroic dikes of high TiO₂ content transect massive hawaiite in the Kaena Quarry, Waianae Range, Oahu. One dike studied consists of two rock types: (a) border zone alkali gabbro of high titanomagnetite and titanaugite content and, (b) interior mugearite that contains iron-rich pyroxenes and K-feldspar. The dike probably formed as an in situ latestage segregation enriched in TiO₂, SiO₂, and alkalis.     

Contributions to the mineral chemistry of Hawaiian rocks

Phenocryst and groundmass pyroxenes in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively by electron microprobe. Results and conclusions: i) Tholeiites contain augite, pigeonite, and bronzite; alkalic rocks contain salite, augite, and ferroaugite; and nephelinic rocks have salite, sometimes of Wo>50 mole %. ii) The three suites can be distinguished by Ca contents of pyroxenes: High-Ca pyroxenes of tholeiitic rocks have Wo_30–40; those of alkalic rocks have Wo_38–48; and those of the nephelinic rocks have Wo_47–51; i.e. Wo in clinopyroxene increases from tholeiitic, to alkalic, to nephelinic suites, iii). In the alkalic suite, rock types can be distinguished on the basis of clinopyroxene composition: Alkalic olivine and alkalic basalts have Wo_38–45, hawaiites and mugearites have Wo_45–48. Trachytes can be distinguished from both groups by higher Fe (Fs_22–30) and Ca contents (Wo_43–47). iv) Pyroxenes in tholeiitic rocks show higher intrarock variability (e.g. Fs₁₂Wo₄₀-Fs₃₇Wo₃₀) than those of the alkalic and nephelinic suites, v) Na₂O bulk-rock content affects Na₂O content of the precipitating high-Ca pyroxene; e.g. Na₂O in groundmass pyroxene increases from tholeiitic, to alkalic (mafic members only), to nephelinic suites; a similar relationship is present within the differentiated alkalic suite, vi) In tholeiites, changes in groundmass high-Ca pyroxene compositions are related to changes in bulk rock compositions, e.g. FeO/FeO+MgO+CaO in clinopyroxene increases as this ratio increases in the bulk rock; this is not true for alkalic and nephelinic rocks, vii) In groundmass high-Ca pyroxene, Al₂O₃, Na₂0, and TiO₂ contents increase and MnO content decreases with increasing Wo content from tholeiitic, to alkalic (mafic members only), to nephelinic suites, viii) Groundmass high-Ca pyroxenes are richer in MnO and Na₂O and poorer in Cr₂O₃ compared to coexisting phenocrysts. High-Ca pyroxene phenocrysts in nephelinic rocks and in one mugearite are depleted in SiO₂ and enriched in Al₂O₃ relative to coexisting groundmass clinopyroxene, indicating increased SiO₂ activity during crystallization. Some tholeiites show the reverse; this Si—Al relationship is not clear in other samples.     

Contributions to the mineral chemistry of Hawaiian rocks

Feldspar phenocrysts, microphenocrysts, groundmass feldspar, interstitial material of feldspar composition, and residual SiO₂-K₂O-rich glass in 24 rocks of the tholeiitic, alkalic, and nephelinic suites from Haleakala and West Maui volcanoes, Maui, Hawaii, were analyzed quantitatively with the electron microprobe. Rocks studied include tholeiite, olivine tholeiite, oceanite, alkalic olivine basalt, alkalic basalt, hawaiite, mugearite, trachyte, basanite, and basanitoid. Results and conclusions: i) In all rocks studied, An decreases and Or increases from phenocrysts to microphenocrysts to groundmass feldspar to interstitial material of feldspar composition. ii) Phenocrysts occur in rocks of the tholeiitic and alkalic suites and, in spite of differences in bulk rock compositions, overlap in composition. iii) Groundmass feldspar in rocks of the tholeiitic suite are nearly identical in composition; the same is true for rocks of the nephelinic suite. However, in the highly differentiated alkalic suite, groundmass feldspar composition ranges from labradorite to sanidine; i.e. the higher the bulk rock CaO, the higher is the An content, and the higher the bulk K₂O, the higher is the Or content. iv) In general, rocks with phenocrysts have groundmass feldspar less An-rich than those without phenocrysts. v) In rocks of the tholeiitic suite, normative feldspar approaches modal feldspar. However, in rocks of the alkalic and nephelinic suites, normative feldspar, because of the presence of highly alkalic interstitial material and the absence of nepheline in the mode but its presence in the norm, is drastically different from modal feldspar. vi) Hawaiites contain labradorite and not andesine, as per definition, and mugearite contains andesine and not oligoclase, as groundmass feldspar. In fact, when considering phenocrysts and interstitial material of feldspar composition, hawaiites range from bytownite to sanidine and mugearite from andesine to sodic sanidine, but normative feldspar plots in the andesine field for hawaiites and the oligoclase field for mugearite. vii) Rocks of the three suites can be distinguished on the basis of Or and An in groundmass feldspar, the presence of thin rims of groundmass composition of phenocrysts of rocks of the alkalic suite, and the presence of interstitial material of anorthoclase to sanidine composition in rocks of the alkalic and nephelinic suites. iix) Rocks transitional between the tholeiitic and alkalic suites are observed and are characterized by transitional mineral compositions.This paper was first presented as a talk before the 68. Annual Meeting of the Cordilleran Section of the Geological Society of America, Honolulu, Hawaii, March 29–April 1, 1972.     

Significance of mineral chemistry of syenites and associated rocks of Elagiri complex,Southern Granulite Terrane of the Indian shield

The Elagiri complex (12°31′ N: 78°35′ E) represents one of the important silica — oversaturated syenite plutons of the Southern Granulite Terrane of the Indian shield. This article for the first time reports the mineral chemistry of the Elagiri complex and brings out important petrogenetic significance. The litho-members of Elagiri complex are intrusive into high grade country rocks viz. granite gneiss, amphibolite and pyroxene granulite. The country rocks are foliated bearing evidences of multiple folding and deformation. On the other hand, the constituent litho members of the Elagiri complex (syenites, gabbro and later intrusives marked by lamprophyre and carbonatite) show preservation of igneous layering in terms of discernible parallelism of the constituent minerals. The Elagiri complex shows presence of sharp contacts among litho members and marked absence of chilled facies peripheral to the margin. Electron microprobe data have been critically used to systematize the constituent mineral-phases of the different lithomembers of the complex. Geothermobarometric data indicate a temperature of equilibration in the range of ∼700° to 500°C at ∼2.0 to 5.2 kb which corresponds to shallow level (cf. 18.2 km) equilibration-depth of the complex. Field observations and mineral chemistry data suggest that liquid immiscibility plays an important role during the evolution of the Elagiri complex.     

Petrochemistry and mineral chemistry studies on metamorphic ultramafic rocks in Yanghou area, Northern Fujian, China

Petrochemical studies indicate that the Yanghou metamorphie ultramafic rocks are composed of metamorphosed harzburgite and ultramafic cumulate.Trace element geochemistry and mineral chemistry of the metamorphic harzburgite indicate that they are relicts of depleted mantle.Systematic petrochemical,mineral chemical and geochronological studies led to such a conclusion that the Yanghou metamorphic ultramafic rocks may be the components of Late Sinian-Early Paleozoic ophiolite in South China.     

The pyrope-coesite rocks and their country rocks at Parigi,Dora Maira Massif,Western Alps: detailed petrography,mineral chemistry and PT-path

Both the coarse- and fine-grained varieties of the partly coesite-bearing pyrope-quartzites, their interlayered jadeite-kyanite rocks, and the biotite-phengite gneiss country rock common to all of them were subjected to detailed petrographic and textural studies in order to determine the sequence of crystallisation of their mineral constituents, which were also studied analytically by microprobe. Prior to pyrope and coesite growth, the Mg-rich metapelites were talc-kyanite-chlorite-rutile-ellenbergerite schists which — upon continued prograde metamorphism — developed first pyrope megacrysts in silica-deficient local environments at the expense of chlorite + talc + kyanite, and subsequently the smaller pyrope crystals with coesite inclusions from reacting talc + kyanite. Based on geobarometrically useful mineral inclusions as well as on experimentally determined phase relations, a prograde PT-path — simplified for water activity = 1 — is constructed which passes through the approximate PT-conditions 16 kbar and 560° C, 29 kbar and 720° C, and finally up to 37 kbar at about 800° C, where the Mg-rich metapelite was a pyrope-coesite rock with phengite, kyanite, and talc still present. During the retrograde path, pyrope was altered metasomatically either into phlogopite + kyanite + quartz or, at a later stage, to chlorite + muscovite + quartz. Both assemblages yield PT-constraints, the latter about 7–9 kbar, 500–600° C. The country rock gneisses have also endured high-pressures of at least 15 kbar, but they provide mostly constraints on the lowest portion of the uplift conditions within the greenschist facies (about 5 kbar, 450° C). Microprobe data are presented for the following minerals: pyrope, ellenbergerite, dumortierite (unusually MgTi-rich), jadeite, vermiculite (formed after Na-phlogopite?), paragonite, and for several generations of phengite, chlorite, talc, phlogopite, dravite, and glaucophane in the high-pressure rocks, as well as for biotite, chlorite, phengites, epidote, garnet, albite, and K-feldspar in the country rock gneisses. An outstanding open problem identified in this study is the preservation of minerals as inclusions within kyanite and pyrope beyond their PT-stability limits.     

Scheme of mineral facies of metamorphic rocks

The proposed PT grid of mineral facies of metamorphic rocks, which retains the commonly adopted nomenclature (greenschist, epidote-amphibolite, amphibolite, granulite, glaucophane-schist, and eclogite facies), is based on original calculations and the published calculated and experimental data on mineral equilibria. To validate the facies and subfacies PT boundaries, the mineral equilibria in metapelitic and metabasic rocks have been used.     

基性岩流变的复杂性与成分对岩石流变影响的实验研究

在采用天然基性岩样品进行的流变实验中,存在因实验温度低而样品处于半脆性变形域与因实验温度高而样品颗粒边界出现熔体的矛盾。文献中给出的流变参数中,应力指数n的可靠性高,具有良好的重复性,激活能Q在一定范围内具有重复性,而系数A重复性差。采用6种样品进行流变实验。结果表明,矿物成分对岩石流变的影响比根据端员组分确定的双组分和多组分岩石流变物理模型要复杂得多。由斜长石、单斜辉石和角闪石组成的样品中,当斜长石和单斜辉石含量接近,而角闪石含量低于10%,斜长石和单斜辉石控制了岩石的流变;如果样品中有超过10%的角闪石参与流变,角闪石在变形中所起作用非常显著。由斜长石、石英和角闪石组成的样品,当石英含量小于10%而斜长石和角闪石含量接近时,斜长石和角闪石控制了岩石的流变;当斜长石含量达到70%时,样品变形更接近长石特性;如果石英含量超过20%时,石英在变形中起到主要作用。选择与基性麻粒岩中主要矿物成分接近的天然辉长岩(辉绿岩),或者从天然基性麻粒岩中挑选出主要矿物,通过热压合成人工样品,进行高温流变实验是研究基性麻粒岩流变的最有效途径。     

Pyroxene mineral chemistry of the Jinchuan intrusion,China

Summary Chemical compositions of orthopyroxene and clinopyroxene from the Jinchuan ultramafic intrusion have been obtained by electron microprobe analysis. The Mg number (MgO/(MgO + FeO)) for both pyroxenes falls within narrow ranges, 82–87 for clinopyroxene and 81–85.5 for orthopyroxene, suggesting limited magma differentiation in regard to the present igneous body. The Al₂O₃ content ranges from 2.44 wt.% to 4.43 wt.% and increases with decreasing Mg of the pyroxenes, i.e., with the more evolved magma. This is attributed to the relatively greater effects of Al₂O₃, TiO₂, Cr₂O₃ and Fe₂O₃ than that of SiO₂ on pyroxene crystallization.Negative linear relationships between Ti⁴⁺ and Si⁴⁺, and Al³⁺ and Si⁴⁺ characterize the pyroxenes. In clinopyroxene, regression of Si⁴⁺ versus Al³⁺ results in a straight line with a slope of –1.012, indicating that the decrease of Si⁴⁺ in the crystal structure is matched by an increase only in tetrahedral Al³⁺; octahedral Al³⁺ has remained relatively constant. The negative linear relationship between Ti⁴⁺ and Si⁴⁺ in clinopyroxene reflects either a greater tendency of Ti⁴⁺ to occupy octahedral sites than Al³⁺, or that replacement of Al³⁺ for Si⁴⁺ demands a more efficient charge balance. The scatter in plots of Ti⁴⁺ versus Si⁴⁺ for orthopyroxene indicates that charge balance is not as critical as structure symmetry.The crystallization temperature of pyroxene is calculated to be 1108–1229°C usingWood andBanno's (1973) two pyroxene thermometer, and is within 40°C of that calculated fromWells's (1977) thermometer. The distribution coefficient (Kd) for Mg²⁺ and Fe²⁺ between clinopyroxene and orthopyroxene is estimated to be 0.86, which is higher than that of the other intrusions and lower than that of mantle nodules, but still falls within their Kd-1/T trend. This suggests that the Kd value of pyroxene is controlled mainly by temperature.

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Mineralchemie der Pyroxene der Jinchuan-Intrusion, China

Zusammenfassung Die chemische Zusammensetzung von Orthopyroxenen und Klinopyroxenen aus der ultramafischen Jinchuan Intrusion wurden mit der Mikrosonde bestimmt. Die Mg-Zahl (MgO/(MgO + FeO)) beider Pyroxene liegt innerhalb enger Grenzen, 82–87 für Klinopyroxen und 81–85.5 für Orthopyroxen. Dies weist auf beschränkte magmatische Differentiation der Intrusion hin. Der Al₂O₃-Gehalt liegt zwischen 2.44 Gew.%. und 4.43 Gew.%. und nimmt mit der abnehmenden Mg-Zahl der Pyroxene ab, d.h. mit dem mehr entwickelten Magma. Dies wird damit erklärt, daß Al₂O₃, TiO₂, Cr₂O₃ und Fe₂O₃ einen größeren Einfluß auf die Kristallisation der Pyroxene ausüben als SiO₂.Die Pyroxene werden durch negative lineare Beziehungen zwischen Ti⁴⁺ und Si⁴⁺, sowie Al³⁺ und Si⁴⁺ charakterisiert. In Klinopyroxenen resultiert die Regression von Si⁴⁺ gegen Al³⁺ in einer geraden Linie mit einer Neigung von –1.012. Dies weist darauf hin, daß die Abnahme der Si⁴⁺ Gehalte in die Kristallstruktur durch Zunahme von ausschliesslich tetraedrischem Al³⁺ kompensiert wird; oktaedrisches Al³⁺ ist relativ konstant geblieben. Die negative lineare Beziehung zwischen Ti⁴⁺ und Si⁴⁺ in Klinopyroxenen geht entweder auf eine stärkere Tendenz des Ti₄O₂, oktaedrische Plätze zu besetzen zurück, oder darauf daß ein Ersatz von Al³⁺ für Si⁴⁺ einen effizienteren Ladungsausgleich verlangt. Die unregelmäßige Verteilung der Plots von Ti⁴⁺ gegen Si⁴⁺ in Orthopyroxenen läßt erkennen, daß Ladungsausgleich hier nicht so kritisch ist wie die Symmetrie der Struktur.Die Kristallisationstemperatur der Pyroxene wurde mit dem Zwei Pyroxenthermometer nachWood undBanno (1973) mit 1108–1229°C bestimmt. Diese Werte liegen innerhalb von 40°C des vonWells (1977) berechneten. Der Verteilungskoeffizient (Kd) für Mg²⁺ und Fe²⁺ zwischen Klinopyroxen und Orthopyroxen wird auf 0.86 berechnet; das ist höher als der aus anderen Intrusionen und niedriger als der von Mantelxenolithen, fällt aber immer noch innerhalb des Kd-1/T Trends derselben. Dies legt den Gedanken nahe, daß der Kd Wert der Pyroxene hauptsächlich durch Temperatur bestimmt wird.

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With 6 Figures     

Geochemistry and mineral chemistry of pyroxenite xenoliths and host volcanic alkaline rocks from north west of Marand (NW Iran)

Mineralogy and Petrology - The Plio-Quaternary alkaline volcanic rocks from the northwest of Marand (NW Iran) consist of trachy-andesites, trachy-basaltic andesites, leucite-tephrites and...     

福建平潭岛花岗质岩石成因:来自锆石U-Pb定年、O-Hf同位素及黑云母矿物化学的约束

东南沿海地区发育具有"等同位素组成"特征的晚中生代双峰式火成岩,其成因备受争论。本文选择了福建省平潭岛双峰式杂岩体中的花岗闪长岩、英云闪长岩与花岗岩开展了高精度锆石U-Pb定年、原位O-Hf同位素和黑云母矿物化学方面的研究,以探讨这些花岗质岩石的成因。分析结果显示,花岗闪长岩、英云闪长岩与花岗岩的锆石U-Pb年龄分别为116.8±1.0Ma、116.3±1.0Ma与117.4±1.0Ma,表明它们均侵位于早白垩世。这三类岩石也有较为相似的锆石O-Hf同位素组成。其中,锆石的δ18O分别变化为4.6%~5.3‰、4.8%~5.3‰及5.0%~5.6‰,与地幔的O同位素值基本一致。锆石的εHf(t)变化范围分别为+2.0^+7.1、+2.8^+6.5及+1.8^+5.6,相应的两阶段模式年龄tDM2分别为741~1046Ma、754~995Ma及815~1058Ma。锆石O-Hf同位素数据反映其熔融源区主要为相对较年轻的地壳物质,来自华夏地块古老基底的贡献较少。另外,黑云母矿物化学暗示这三类岩石具有Ⅰ型花岗岩的特征。但是,黑云母种属在不同岩性间存在差异,其中花岗闪长岩与英云闪长岩中的黑云母为镁质类型,花岗岩中的黑云母为铁质类型。从花岗闪长岩、英云闪长岩到花岗岩,黑云母的结晶温度和岩浆体系的氧逸度均逐渐降低,这与钙碱性岩浆分异演化的趋势基本一致。结合前人研究资料及区域地质演化历程,我们认为平潭岛杂岩体中的花岗质岩石形成于古太平洋俯冲背景,其熔融源区主要为新增生地壳物质。花岗质岩石内部岩性的差别主要是母岩浆经历不同程度分异演化的结果。我们的研究结果暗示壳幔岩浆混合在东南沿海早白垩世长英质岩石形成过程中所具有的作用可能较为有限。     

走滑断裂对超高压变质岩石折返的贡献及青藏高原北部白垩纪隆升之新思考

青藏高原已识别出柴北缘、南阿尔金和高喜马拉雅三条超高压变质带。这些超高压变质带提供了一个不可多得的研究超高压变质岩石形成和折返的机会。柴北缘超高压变质带位于阿尔金断裂的东边,是柴达木—东昆仑地体与祁连—阿尔金微地体和阿拉善—敦煌地体碰撞的产物,由榴辉岩、石榴石橄榄岩和含柯石英片麻岩组成,榴辉岩形成时代500~440Ma,峰期超高压变质年龄440Ma。南阿尔金超高压变质带位于阿尔金断裂带的西边,以产出榴辉岩和石榴石橄榄岩为特征,榴辉岩形成时代为500Ma。南阿尔金超高压变质带被认为是柴北缘超高压变质带的西延,两者被阿尔金断裂左旋位移约400km。阿尔金断裂是巨大的深度>200km的岩石圈走滑断裂,断裂的活动时代至少早到240~220Ma,认为走滑过程中伴随的隆升作用有可能为柴北缘和南阿尔金超高压变质岩石的折返和出露地表做出了贡献,其中阿尔金断裂起到了类似剪刀型断裂的作用。高喜马拉雅超高压变质带在巴基斯坦和印度被发现,以榴辉岩中含柯石英或金刚石为特征,榴辉岩的超高压变质年龄为46Ma,表明超高压变质岩石发生在雅鲁藏布江缝合线关闭后并快速折返。喀喇昆仑断裂走滑过程中伴随的抬升作用则可能对高喜马拉雅地区超高压变质岩石的折返和出露地表做出贡献。在中国东部出露的大别—苏鲁超高压变质带被巨大郯庐断裂左旋走滑位移约500km,可以看作是走滑作用伴随的抬升运动对超高压变质岩石的最后折返和出露地表做出重要贡献的又一例证。青藏高原的隆升通常被认为是印度板块和欧亚大陆新生代以来的碰撞结果。根据高原北部断裂的时代、火山活动和沉积盆地的形成,我们提出高原的隆升是两次俯冲碰撞的结果。第一次发生在中特提斯班公湖-怒江洋盆在白垩纪时期的关闭,其时由于北部来自塔里木盆地和北中国板块及东部来自太平洋板块俯冲产生的抵柱效应,高原北部开始隆升;第二次发生在印度板块的新生代俯冲碰撞作用,造成高原的整体抬升,由此可以解释高原北部平均海拔(5000m)要高于高原南部(平均海拔4000m)。     

Agpaicity revisited: pattern recognition in the chemistry of nepheline syenite rocks

An attempt is made to describe global variations in the geochemistry of major and minor elements within a population of nepheline syenite samples defined by mineralogical criteria.Using correspondence analysis, a new pattern recognition procedure, it is possible to define a few trends of common behaviour which reflect most of the initial dispersion.As Al and Na participate in the scattering along the two main trends, agpaicity is recorded by them. However, the traditional form of the coefficient which measures it is proved to be unsatisfactory as variations of K are not significant.     

Relationship between sediments and their igneous source rocks using clay mineral multi-element chemistry: the Cenozoic lacustrine Anloua basin (Adamaoua, Cameroon)

The Cenozoic lacustrine basin of Anloua (Adamaoua, Cameroon), is filled with the weathering products of the surrounding rocks. In order to determine the origin of these sediments, multi-element, especially trace element, analysis of their < 2 μm fraction was undertaken. The chemical compositions of these fractions were compared with those of the rocks surrounding the basin by multivariate statistical analysis and also graphically. A principal component analysis allowed the most discriminant elements to be selected, and a hierarchical ascending classification (HAC) made with these elements divided the samples into groups. Some of these groups contain < 2 μm fractions of both the lake sediments and surrounding rocks. These sediments are determined as deriving by weathering from the surrounding rocks. Some of the other groups contain no samples from the surrounding rocks and their petrographic origin cannot be given. A graphic comparison of the relative amounts of the elements (determined by HAC) from the < 2 μm fractions of the various groups and the rocks surrounding the basin allowed attribution of a petrographic origin for the various sediments analysed by using the fit between the curves.

The clay mineralogy, the amounts of Ti, Zr, and heavy minerals in the < 2 μm fractions and their distribution in the area studied, as well as the presence of angular quartzite pebbles in some sediments gives an indication of the paleogeography of the Anloua basin. There was deltaic input towards the north and a high energy input, possibly torrential, to the west.     

Petrography and mineral chemistry of Ca-rich inclusions in the Allende meteorite

There are two types of white, coarse-grained, Ca-Al-rich inclusions in Allende. Type A inclusions contain 80–85 per cent melilite, 15–20 per cent spinel, 1–2 per cent perovskite and rare plagioclase, hibonite, wollastonite and grossularite. Clinopyroxene, if present, is restricted to thin rims around inclusions or cavities in their interiors. Type B inclusions contain 35–60 per cent pyroxene, 15–30 per cent spinel, 5–25 per cent plagioclase and 5–20 per cent melilite. The coarse pyroxene crystals in Type B's contain >15 per cent Al₂O₃ and >1.8 per cent Ti, some of which is trivalent. Type A pyroxenes contain <9 per cent Al₂O₃ and <0.7 per cent Ti.Electron microprobe analyses of 600 melilite, 39 pyroxene, 35 plagioelase, 33 spinel and 20 perovskite grains were performed in 16 Type A, 1 intermediate and 9 Type B inclusions in Allende and 1 Type A in Grosnaja. Melilite composition histograms from individual Type A inclusions are usually peaked between Ak10 and Ak30 and are 15–20 mole % wide while those from Type B inclusions are broader, unpeaked and displaced to higher åkermanite contents. Most pyroxenes contain < 1 per cent FeO. All plagioclase is An 98 to An 100. Spinel is almost pure MgAl₂O₄. Perovskite contains small (< 1 per cent) but significant amounts of Mg, Al, Fe, Y, Zr and Nb.Inferred bulk chemical compositions of Type A inclusions are rather close to those expected for high-temperature condensates. Those of Type B inclusions suggest slightly lower temperatures but their Ca/Al ratio seems less than the Type A's, indicating that the Type B's may not be their direct descendants. Some textural features suggest that the inclusions are primordial solid condensetes while others indicate that they may have been melted after condensation. Fragmentation and metamorphism may have also occurred after condensation.     

Application of mineral thermometers and barometers to granitoid igneous rocks: the Etive Complex, W Scotland

Summary The Etive complex, one of the Caledonian Newer Granites of Scotland, is a ring complex of Devonian age, ranging in composition from pyroxene-diorite to leucogranite. Six samples, representing the major rock units in the southern parts of the Etive complex were chosen for mineral chemical studies and for estimation of the pressure and temperature conditions of magmatic crystallisation. Application of Al- in-hornblende barometry and crossite contents of amphiboles indicates a pressure <3kbar for the intrusion, in good agreement with published independent pressure estimates of 2kbar from mineral equilibria in metasedimentary hornfelses in the Etive thermal aureole. Thermometry, using ternary and binary feldspar systems, yields low temperatures, which probably reflect late-stage, post-magmatic re-equilibration of these minerals. Several geothermometers have been applied to the Quarry Diorite, the outermost intrusion of the complex. The highest temperature for the rocks comes from orthopyroxene–clinopyroxene solvus thermometry, and is 1000°C; this is interpreted to reflect the initial crystallisation of the diorite magma immediately after its emplacement. The maximum temperature from hornblende-plagioclase thermometer is 816°C, which probably reflects late-stage crystallisation of the magma.     

流体晶、流体晶矿物组合、流体岩及其研究意义

流体是地球各圈层之间相互作用的纽带,在成岩、成矿过程中起着十分重要的作用。目前,流体的研究主要集中在流体对先存矿物岩石进行的交代作用方面,而对流体直接结晶形成的矿物领域研究较少。文中根据作者近几年的研究成果对从流体直接结晶而成的矿物——流体晶以及流体晶矿物组合、流体岩等的定义、特征进行了归纳总结。最新的研究结果显示：岩浆中可以含有大量的流体,这些流体来源既可以是岩浆演化富集、岩浆与围岩相互作用产生,亦可以是外部来源。因此,流体晶矿物、流体岩在自然界应该是普遍存在的。流体晶矿物的提出将深化人们对地质过程的理解,发展岩石学及矿床学的研究新领域,有利于矿床勘探和成矿预测。