Greenschist amphiboles from Haast river,New Zealand

A section across the Haast Schist Group in the Southern Alps of New Zealand shows a sequence of metamorphosed eugeosynclinal sediments. Meta-basic rocks (greenschists) have been studied to determine the nature of the actinolite-hornblende transition and to investigate the change in amphibole composition through the Metamorphic Facies Series.Electron microprobe analyses of 21 representative amphiboles, including 3 amphibole pairs can be shown to support theories of a miscibility break in the calciferous amphibole solid solution series. The existence of a miscibility break is further supported by the widespread appearance, even at low metamorphic grades, of exsolution lamellae in actinolite and hornblende amphiboles.Amphibolite facies amphiboles differ from greenschist facies amphiboles in that (a) there are increased amounts of Ti entering the lattice and (b) that there is an increased occupancy of the A site at higher metamorphic grades.     

A petrochemical study of calcic amphiboles from the East Bull Lake anorthosite-gabbro layered complex,District of Algoma,Ontario

Calcic amphiboles are ubiquitous in the East Bull Lake anorthosite-gabbro complex, northeastern Ontario. The mode of occurrence suggests the amphiboles replaced clinopyroxene throughout the stratigraphic levels of the pluton, but they are also prolific in the top younger units. Three types of amphiboles, namely (1) tremolite-actinolite, (2) actinolitic hornblende and (3) hornblende, were identified. The composition of the amphiboles shows that they define a continuous series without any obvious compositional-miscibility gap. The analyses further indicated that the amphiboles evolved from actinolite to hornblende through coupled substitution involving edenite and tschermakite end members. Among the three coexisting amphiboles, chlorine is concentrated in hornblende. This is due to preferential location of hornblende along grain boundaries and/or its favourable structure.The compositional variability of amphiboles is controlled by (1) bulk rock composition and (2) faulting and fracturing. The most Fe- and Al-rich hornblendes are confined generally to top units in the gabbro. These units are rich in Si and Fe, but relatively poor in Mg. The Mg-rich tremolite is restricted to a Si-poor, Mg-rich troctolite unit. Amphiboles in gabbro samples from fault zones also contain relatively Mg-rich calcic amphibole. The fault gabbro is highly oxidized.     

青藏高原北羌塘新生代高钾钙碱岩系火山岩角闪石类型有痕量元素地球化学

利用电子探针和激光探针剥蚀系统（LA－ICP－MS）对北羌塘新第三纪高钾钙碱岩系英安岩中角闪石的主元素和微量、角闪石强烈富集Sc、Ti、V、Cr、Co、Ni等不相容亲铁元素，而相对亏损Th、U、Pb、Rb等强不相容的大离子亲石元素。稀土元素丰度高，且无Eu异常，批示北羌塘这套高钾钙碱岩系火山岩可能是青藏高原加厚的相当于榴辉岩相物质组成的下部陆壳脱水熔融的产物。     

Chemical types of amphiboles from the Tyrnyauz deposit

Based on the results of microprobe analyses, six groups of calcium amphiboles were distinguished for the Tyrnyauz deposit. Group I (mainly edenite) includes amphiboles of hornfels and periskarn rocks. Groups II-VI (actinolite-hastingsite series) are related to post-skarn metasomatic rocks of the productive stage after hornfels (II), the tonalite and plagiogranite complex (III), ultrabasic rocks (IV), pyroxene-plagioclase periskarn rocks (V), and skarn (VI). Group IV is represented by actinolite; group VI, by hastingsite; groups II, III, and V, by hornblende varieties.     

Geochemistry of actinolitic hornblendes from tonalitic rocks,Northern Portugal

Chemical analyses are given for actinolitic hornblendes of tonalitic rocks from the Hercynian belt of Northern Portugal. The distribution of elements between amphibole and co-existing biotite is studied. The composition of the amphiboles is analysed in the light of experimental data on amphiboles and the physical conditions of crystallization inferred from the study of the biotite and rock series. The data on the biotites lead to the definition of a temperature of 800°C for the crystallization of actinolitic hornblendes with Mg/(Mg + Fe) ratios of 0·72-0·61 at pressures of about 3 Kb and fO₂ defined by FMQ.     

The Serra da Graciosa A-type Granites and Syenites, southern Brazil. Part 3: Magmatic evolution and post-magmatic breakdown of amphiboles of the alkaline association

Amphiboles are the main mafic minerals in most metaluminous to peralkaline alkali-feldspar granites and syenites, and they usually preserve an important record of the compositional evolution of the melts from which they crystallize. In the alkaline association of the Serra da Graciosa A-type Granites and Syenites (southern Brazil), amphibole compositions span a large range, including calcic, sodic–calcic, and sodic amphiboles. Calcic amphiboles are typically observed in the metaluminous rocks, while sodic amphiboles are characteristic of the more strongly peralkaline rocks; sodic–calcic amphiboles are found in intermediate varieties. Compositional variations record the differentiation trends within two petrographic series of the alkaline association. The overall evolution of amphibole compositions is similar in both: they reveal a progressive increase in Na and Fe³⁺ with differentiation (increase in alkalinity of the magmas), a characteristic shared by undersaturated peralkaline (or agpaitic) differentiation trends. In detail, however, the evolutions of the amphibole compositions in the two series are distinct. In Alkaline series 1, the cores of the crystals form a continuum from calcic to sodic compositions, with the exception of a small compositional gap within the sodic–calcic amphiboles. The rims, however, show compositions that diverge from this main trend; this divergence results from increasing amounts of the oxy-amphibole component, and reflects more oxidizing conditions at the final stages of magmatic crystallization. In Alkaline series 2, these oxidation trends are much more subtle and a reverse trend is observed in the sodic amphiboles. Sodic–calcic amphiboles are in several cases replaced by intergrowths of post-magmatic sodic amphibole and Al-poor (“tetrasilicic”) biotite.     

Alkali Amphiboles from the Blueschists of Cazadero, California

Alkali amphiboles from Type III and Type IV metamorphic zonesin blueschist facies rocks of Cazadero, California, and fromcomparable New Caledonian rocks have been characterized by X-raycrystallographic, optical, and chemical methods. The compositionof any particular alkali amphibole is strongly controlled bythe bulk composition of the host rock. Within the blueschistfacies, metamorphic zones are not characterized by changes inamphibole composition. All the alkali amphiboles studied hereinbelong to the C2/m space group and complete miscibility betweenglaucophane and riebeckite has been demonstrated for the conditionsprevailing during metamorphism in the Cazadero and New Caledonianblueschists. Linear relationships are found between unit-celldimensions and variations in composition between glaucophaneand riebeckite. The alkali amphiboles of glaucophane compositionsbelong to the high pressure-low temperature series, glaucophaneII-riebeckite. Limited miscibility of actinolite in glaucophanemay be characteristic of blueschist facies metamorphism.     

华北克拉通中生代拆沉陆壳物质对岩石圈地幔的改造:来自橄榄岩捕虏体中角闪石的成分制约

对鲁西和太行山南段早白垩世高镁闪长岩中橄榄岩捕虏体中的角闪石进行了主量元素和痕量元素分析,并讨论了角闪石成分与改造岩石圈地幔熔体的性质与来源之间的关系。研究结果表明,橄榄岩类捕虏体中的角闪石主要为交代成因。在化学上,它们属于钙质角闪石。太行山南段符山橄榄岩捕虏体中的角闪石属于镁质普通角闪石和浅闪石或浅闪石质普通角闪石;鲁西铁铜沟橄榄岩捕虏体中的角闪石为韭闪石质普通角闪石、浅闪石质普通角闪石和镁绿钙闪石质普通角闪石。与板内橄榄岩捕虏体中的角闪石相比,鲁西和太行山南段早白垩世高镁闪长岩橄榄岩捕虏体中的角闪石具有相对高的Mg#(鲁西:86.0~90.8;太行山:90.7~94.2)和SiO2(鲁西:44.04%~46.98%;太行山:47.09%~49.79%)以及相对低的Na2O(1.92%~2.51%)、TiO2(0.01%~1.46%)、Nb(0.29×10-6~1.98×10-6)和Zr(1.61×10-6~5.34×10-6),这与来自俯冲带之上地幔楔橄榄岩捕虏体中的角闪石相类似。综合橄榄岩捕虏体的地球化学特征,可以判定华北克拉通早白垩世岩石圈地幔遭受了起源于拆沉陆壳物质熔融熔体的改造。     

Mineralogy of New Caledonian metamorphic rocks

The chemistry and phase relations of calcic and sodic amphiboles in the Ouégoa blueschists are investigated. The first appearance of sodic amphiboles is controlled by bulkrock chemistry. Sodic amphibole appears first in weakly-metamorphosed pumpellyite metabasalts prior to the crystallization of lawsonite but does not crystallize in pelitic schists until the middle of the lawsonite zone; sodic amphibole continues as an apparently stable phase in rocks of all bulk compositions into, and throughout, the highest-grade rocks in the district. Calcic amphibole is widespread in metabasalts of the lawsonite and epidote zones and also occurs in metasediments of appropriate composition. Coexisting pairs of calcic and sodic amphiboles are common in metabasalts but they have also been found in some metasediments. A grunerite-riebeckite pair is described.Electron-probe analyses of 120 amphiboles from representative rock-types are presented in graphical form. Sodic amphiboles show an increased Mg/(Mg+Fe) ratio with increasing metamorphic grade. Sodic amphiboles in pelitic schists are ferroglaucophane in the lawsonite zone and crossite and glaucophane in the epidote zone. Sodic amphiboles in metabasalts are iron-rich crossites in weakly-metamorphosed rocks and more-magnesian crossites and glaucophanes in the lawsonite and epidote zones. The abrupt increase in Mg/(Mg+Fe) ratio in sodic amphiboles at the epidote isograd is attributed to the crystallization of epidote and almandine which take the place of lawsonite and spessartine of the lawsonite zone. Calcic amphiboles are fibrous actinolites in the lawsonite zone and grade with increasing Al and Na/Ca ratio into prismatic blue-green hornblendes (barroisites) in the upper epidote zone. In calcic amphiboles, increasing metamorphic grade effects the coupled substitution of (Na+Al) for (Ca+Mg) and a small increases in Fe/Mg ratio; octahedrally and tetrahedrally coordinated Al increases in an approximately 11 ratio. Both the calcic and the sodic amphiboles show an increase in A-site occupancy with increasing metamorphic grade. In two-amphibole assemblages Ti, Mn and K are concentrated in the calcic amphibole.The textural and chemical relations between coexisting calcic and sodic amphiboles are discussed. If the calcic and sodic amphiboles are an equilibrium pair then the data collected from the Ouégoa amphiboles gives a picture of a very asymmetric solvus in the system glaucophane-actinolite-hornblende, i.e. steep-sided to glaucophane and with a gentle slope to the calcic amphibole field; there is no indication of any termination of the solvus under the pressure-temperature conditions of crystallization of the Ouégoa schists.     

Parageneses and compositions of amphiboles from Franciscan jadeite–glaucophane type facies series metabasites at Cazadero, California

Abstract Sodic amphiboles are common in Franciscan type II and type III metabasites from Cazadero, California. They occur as (1) vein-fillings, (2) overgrowths on relict augites, (3) discrete tiny crystals in the groundmass, and (4) composite crystals with metamorphic Ca–Na pyroxenes in low-grade rocks. They become coarse-grained and show strong preferred orientation in schistose high-grade rocks. In the lowest grade, only riebeckite to crossite appears; with increasing grade, sodic amphibole becomes, first, enriched in glaucophane component, later coexists with actinolite, and finally, at even higher grade, becomes winchite. Actinolite first appears in foliated blueschists of the upper pumpellyite zone. It occurs (1) interlayered on a millimetre scale with glaucophane prisms and (2) as segments of composite amphibole crystals. Actinolite is considered to be in equilibrium with other high-pressure phases on the basis of its restricted occurrence in higher grade rocks, textural and compositional characteristics, and Fe/Mg distribution coefficient between actinolite and chlorite. Detailed analyses delineate a compositional gap for coexisting sodic and calcic amphiboles. At the highest grade, winchite appears at the expense of the actinolite–glaucophane pair. Compositional characteristics of Franciscan amphiboles from Ward Creek are compared with those of other high P/T facies series. The amphibole trend in terms of major components is very sensitive to the metamorphic field gradient. Na-amphibole appears at lower grade than actinolite along the higher P/T facies series (e.g. Franciscan and New Caledonia), whereas reverse relations occur in the lower P/T facies series (e.g. Sanbagawa and New Zealand). Available data also indicate that at low-temperature conditions, such as those of the blueschist and pumpellyite–actinolite facies, large compositional gaps exist between Ca- and Na-amphiboles, and between actinolite and hornblende, whereas at higher temperatures such as in the epidote–amphibolite, greenschist and eclogite facies, the gaps become very restricted. Common occurrence of both sodic and calcic amphiboles and Ca–Na pyroxene together with albite + quartz in the Ward Creek metabasites and their compositional trends are characteristic of the jadeite–glaucophane type facies series. In New Caledonia blueschists, Ca–Na pyroxenes are also common; Na-amphiboles do not appear alone at low grade in metabasites, instead, Na-amphiboles coexist with Ca-amphiboles throughout the progressive sequence. However, for metabasites of the intermediate pressure facies series, such as those of the Sanbagawa belt, Japan and South Island, New Zealand, Ca–Na pyroxene and glaucophane are not common; sodic amphiboles are restricted to crossite and riebeckite in composition and clinopyroxenes to acmite and sodic augite, and occur only in Fe₂O₃-rich metabasites. The glaucophane component of Na-amphibole systematically decreases from Ward Creek, New Caledonia, through Sanbagawa to New Zealand. This relation is consistent with estimated pressure decrease employing the geobarometer of Maruyama et al. (1986). Similarly, the decrease in tschermakite content and increase in NaM₄ of Ca-amphiboles from New Zealand, through Sanbagawa to New Caledonia is consistent with the geobarometry of Brown (1977b). Therefore, the difference in compositional trends of amphiboles can be used as a guide for P–T detail within the metamorphic facies series.     

Determination of Lithium, Beryllium and Boron at Trace Levels by Laser Ablation-Inductively Coupled Plasma-Sector Field Mass Spectrometry

The analytical capabilities of laser ablation (LA)-ICP-MS in determining Li, Be and B at trace levels in geological samples have been tested on a series of glass reference materials and natural samples. The LA-ICP-MS instrument used consisted of a sector-field ICP-MS coupled with a laser ablation microprobe operating at either 266 or 213 nm wavelength. Reference glasses from NIST (SRM 612, 614 and 616) and MPI-DING (KL2-G, ML3B-G, StHs6/80-G, GOR128-G, GOR132-G, T1-G and ATHO-G) were selected to develop the analytical method and to assess the best instrumental configuration. A series of calcic amphiboles with different Li, Be and B concentrations were also analysed using both LA-ICP-MS and SIMS to test the applicability of the method to natural minerals. Results indicated that with a spot size of 40 μm the agreement between measured and reference values of Li, Be and B is generally better than 10% for NIST SRM 612 and 20% for NIST SRM 614. Average reproducibility at the 2s level was 10% for Li, 20% for Be and 15% for B. Limits of detection were approximately 100 ng g^-1 for Be and B and 200 ng g^-1 for Li. These results were confirmed by analyses carried out on natural amphiboles and compared well in terms of precision and accuracy with those commonly achieved by SIMS.     

KAERSUTITE, A POSSIBLE INTERNATIONAL MICROPROBE STANDARD

Two kaersutite amphiboles from the Kakanui mineral breccia, South Island, New Zealand, have been prepared for electron microprobe analysis. Chemical analyses of bulk samples by XRF techniques are tabulated. These samples may be suitable as international standards.     

超高压闪石的发现及其成因矿物学意义

在缅甸硬玉岩区发现了 6种相对罕见的钠质、钠钙质角闪石 (蓝闪石、灰闪石、铝钠闪石、镁红闪石、镁钠钙闪石和蓝透闪石 ) ,其中蓝透闪石、灰闪石和镁红闪石的发现属首次。灰闪石和镁红闪石只产于挪威、中国大别和阿尔卑斯超高压带 ,或在超高压实验岩石学的实验中被合成。同时还研究了这些闪石的化学组成、种属间的关系及形成条件 ,这些闪石形成时压力不低于 2 .2× 1 0 6 k Pa,因此缅甸硬玉岩区可能是世界上又一个超高压区。     

Evolution cristallochimique des amphiboles dans la série granitique de Fort-Trinquet (Mauritanie)

The precambrian postorogenic pluton of the Fort-Trinquet area (Northern Mauretania) is composed by a series of granitic rocks in which amphiboles are the characteristic mafic minerals. Twenty six amphiboles have been separated and chemically analysed; the optical properties and the unit-cell data are also given.The crystallographic and chemical differences between these minerals reflect the variations in bulk composition of the host-rocks. In the plutonic suite, two igneous trends have been recognized: 1) a granitic trend (quartz monzonite-adamellite-granite) and 2) a syenitic trend (syenite-quartz bearing syenite-alkali granite). The amphiboles of the first trend belong to the tremolite-hastingsite series; they become richer in hastingsite mole with increasing proportion of quartz and decreasing Mg/(Mg+Fe) ratio in the rocks. The granitoids of the second trend are characterized by the occurrence of two amphiboles: a primary prismatic green-coloured actinolitic hornblende generally surrounded by a dark blue rim of riebeckite composition; the riebeckite may also form some acicular crystals associated to needles of stilpnomelane. These coexisting amphiboles would result from autometasomatic reactions which affected the rocks of the syenitic trend and which gave rise to the late alkali pegmatites where the constituent is a low arfvedsonitic riebeckite. The major substitutions involved in that amphibole transformation are Na^x R³⁺Ca^x R²⁺ and Na^xSiCa^xAl^IV.Comparison with experimental data allows to estimate the physical conditions during the emplacement and the tardimagmatic evolution of this granitoid series.     

Chemistry of calcic amphiboles from the area around Terakanambi,southern Karnataka

Chemial analyses of twelve amphiboles from the area around Terakanambi are presented. Results indicate that they are ferro-hornblende and ferro-pargasitic hornblende types in banded iron formations; magnesio hornblende in ultramafic rocks and edenite; and ferroan pargasite and ferroan pargasitic hornblende types in calcamphibolites. Titanium content in the amphiboles of the present study is relatively low compared to results from similar zones elsewhere. The lower titanium content of the amphiboles may be attributed to either bulk chemical composition or to low oxygen fugacity. Mg/Fe ratios vary considerably and it is mainly controlled by host rock composition. The plots of calcic amphiboles on (lOONa/Ca + Na)/(100 Al/Si + Al) and Al^iv/Al^vi diagrams indicate that they are of medium to low pressure type.     

青海纳日贡玛斑岩钼(铜)矿含矿斑岩矿物学特征及成岩成矿意义

本文侧重于矿物学特征分析对纳日贡玛赋矿斑岩进行了研究,结果表明:斑岩中黑云母斑晶种属为含铁金云母和富镁黑云母,角闪石种属为镁角闪石、透闪石与阳起石。纳日贡玛含矿斑岩属于I型花岗岩类,由幔源岩浆同熔壳源物质而形成;斑岩结晶压力值为1.18×108～1.39×108Pa;闪长玢岩和黑云母花岗斑岩的结晶温度为550℃～650℃,而浅色花岗斑岩则下降为500℃～550℃。斑岩中黑云母的Mg/Fe、Ti、Al、K、Na、Ca及F、Cl等元素含量及比值可以显示纳日贡玛具有良好的含矿性。纳日贡玛结晶压力、温度都较玉龙矿带低,反映纳日贡玛结晶岩浆房更靠近地表。纳日贡玛岩浆源区向壳源区靠近,而玉龙矿带则更靠近幔源区,表明成岩源区中壳幔物质混合比例的不同。     

中国夕卡岩矿床中的角闪石

文章综合分析研究了中国21个夕卡岩矿床中的130个角闪石的成分分析数据。根据夕卡岩类型及其伴生金属矿化的不同，把角闪石分为4大类：钙夕卡岩中的角闪石多属钙角闪石，包括绿钙闪石、铁角闪石、镁绿钙闪石、铁浅闪石、阳起石、铁阳起石、铁镁钙闪石和铁韭闪石等；镁夕卡岩中的角闪石以透闪石为主，局部有浅闪石或韭闪石；锰质夕卡岩中的角闪石有锰质阳起石、锰质透闪石、锰直闪石和锰镁闪石；碱质夕卡岩中的角闪石属钠-钙角闪石或钠角闪石类，包括钠透闪石、镁亚铁钠闪石、亚铁钠闪石、镁铝钠闪石和镁钠闪石。碳酸盐围岩和有关侵入岩的成分对角闪石的类型、成分及其伴生金属矿化起重要的作用。     

Coexisting amphiboles in an eclogite from the Western Alps: new constraints on the miscibility gap between sodic and calcic amphiboles

Abstract Crystal-chemical relationships between coexisting sodic and calcic amphiboles have been studied in eclogitic metagabbros from the Aosta Valley, Western Alps. Textural analysis gives evidence of three successive high-pressure parageneses:
1. Pre-kinematic high-grade blueschist assemblages, preserved as polymineralic inclusions in garnet cores and made of glaucophane and actinolite (stage A).
2. Synkinematic eclogite assemblages, composed of garnet + omphacite + glaucophane ± actinolite ± white mica ° Clinozoisite + quartz + rutile (stage B).
3. Post-kinematic epitactic overgrowths of barroisitic amphibole on glaucophane and actinolite (stage C).
P–T conditions of the eclogitic metamorphism have been estimated at around 500–550°C, 16 kbar.
Glaucophane and actinolite coexist as discrete grains in stage A and B assemblages. This texture and the chemistry of the amphiboles unambiguously denotes the existence of a miscibility gap between sodic and calcic amphiboles (from Na^M4= 0.80 in actinolite to Na^M4= 1.70 in glaucophane at T = 500–550°C). A comparison with published analyses allows a new solvus along the glaucophane–actinolite join to be drawn.
The later barroisitic amphibole (stage C) exhibits strong chemical zonation indicating disequilibrium growth. This amphibole cannot either be used to define a miscibility gap with glaucophane or actinolite or be considered as an intermediate stage between these two end-members.     

The Serra da Graciosa A-type Granites and Syenites, southern Brazil: Part 2: Petrographic and mineralogical evolution of the alkaline and aluminous associations

The Serra da Graciosa Granites and Syenites comprise five distinct plutons in the Brasiliano/Pan-African Graciosa A-type Province, southern Brazil. Six petrographic series can be identified in these plutons: (1) Alkaline series 1, composed of amphibole-bearing alkali feldspar syenites with varied mafic mineralogy and quartz contents, from alkali feldspar syenites with calcic amphibole, clinopyroxene, olivine and allanite to alkali feldspar quartz syenites with sodic–calcic amphibole and chevkinite–perrierite and to alkali feldspar granites with sodic amphibole; (2) Alkaline series 2, characterized by amphibole-bearing alkali feldspar granites, with limited modal variations but amphibole compositions also varying from calcic to sodic; (3) Alkaline series 3, of limited occurrence, which includes alkali feldspar syenites with olivine and clinopyroxene and no amphibole; (4) Aluminous series 1, of widespread occurrence, with various petrographic facies of biotite granites with amphibole; (5) Aluminous series 2, characterized by alkali feldspar granites with biotite and only minor amphibole; (6) Monzodiorites, typically with biotite, calcic amphibole and augitic clinopyroxene, partially mingled with granitic magmas. The mafic minerals present are, in general, Fe-rich with correspondingly low Mg and Al contents. In Alkaline series 1, amphiboles crystallized in progressively more oxidizing and alkaline conditions, while in Alkaline series 2, the initial conditions were somewhat more oxidizing and shifted to reducing in the final stages. In Aluminous series 1 and Aluminous series 2, amphiboles are calcic and comparatively homogeneous. The amphiboles in the monzodioritic rocks, while also homogeneous, are more Mg-rich and show compositions quite distinct from the calcic varieties in the other associations, and this is also the case for clinopyroxene. Mg# in biotite decreases from the monzodioritic rocks to Aluminous series 1 and further to Aluminous series 2. Contrasting evolution of the various associations suggests that several coeval magmatic series are present in the Serra da Graciosa granites.     

Amphiboles of a Metagabbro--Amphibolite Sequence, Hidaka Metamorphic Belt, Hokkaido

The western part of the Hidaka Metamorphic Belt, Hokkaido, consistsof primary pyroxene gabbro and lesser amounts of olivine gabbrothat have been dynamically metamorphosed to metagabbro—gabbroicamphibolite-amphibolite-epidote amphibolite during uplift andshearing about 23 m.y. ago. Textures and the presence of relic and recrystallized amphiboleand plagioclase in the same rock indicate incomplete reactionand non attainment of equilibrium during recrystallization. EPMA and bulk analyses of 165 amphiboles indicate a continuousoverall compositional range from actinolite to dark green hornblende(with 100 mg/(Mg+Fe²⁺+Fe³⁺Mn) ratios varying from 89.5 to 32.0)marked by increasing Al, Fe, Ti, and Na. A compositional gapis usually present between relic and recrystallized amphibolesin any one rock which becomes more prominent with increasingshearing. In addition to host rock chemical control, amphibole compositionis largely dependent on the An content of coexisting plagioclase.Locally epidote and sphene exert a strong influence on bothamphibole and plagioclase compositions. Amphibole Ti and Mncontents decrease with shearing and Fe enrichment of the hostrocks largely as a result of the incoming of rutile, sphene,and Fe-Ti oxides. Analysis of host rock oxidation ratio andamphibole compositions indicates that the rocks essentiallybehaved as closed systems to oxygen during metamorphism. Al^1V-Al^IV, Al^IV-Fe³⁺, and Al^IV-(Na, K)^A are the main substitutionsin the amphiboles. Within any one rock the recrystallized amphibolesare enriched in Al, Fe, Ti, and Na relative to the relice amphiboles.Increasing metamorphism results in a progressive change of amphiboles(recrystallized) to more Fe and Si (rather than Al) rich compositionsreflecting the trend towards greenschist where Fe-actinolite(+Mg chlorite) would be stable. Differentiation of the amphiboles is within the limits of SiAlreplacement and the compositional limits of the early stagereaction rim and replacement amphiboles in the host olivineand pyroxene metagabbros.