酸性岩的变质相

在沸石相变质条件下,花岗岩里浊沸石交代了斜长石和石英,在酸性火山岩里产生明矾石、埃洛石或高岭石。经受绿纤石-葡萄石相变质的花岗岩,其中黑云母变为钙铝榴石、帘石、绿纤石和葡萄石集合体,同时斜长石发生绢云母化。绿片岩相内酸性岩的浅色矿物有石英、微斜长石、钠长石和绿帘石,暗色矿物有绿泥石和黑云母。在角闪岩相变质的酸性岩中,开始出现中、基性斜长石,其中暗色矿物黑云母的镁铁比值要大于角闪石的镁铁比值。经受麻粒岩相变质后,紫苏花岗岩的矿物组成没有变化,但有铀、钍和钾的迁出。     

Secondary Ca-Al silicates as low-grade alteration products of granitoid biotite

Secondary Ca-Al silicates, including andradite-grossular garnet, epidote, pumpellyite, and prehnite are shown to be extremely widespread as low-grade alteration products of granitoid biotite. All may occur within metadomains on the scale of a single biotite pseudomorph. They all generally have a lensoid habit parallel to the host biotite cleavage, which may, or may not be deformed. A cleavage or parting inherited from the host biotite cleavage is usually present.Prehnite, pumpellyite and epidote are unusually Fe-rich: 100 Fe/Fe + Al for prehnite and pumpellyite reaching 19.1 and 49.1 respectively and epidote Ps₃₆-Ps₄₈. Garnet compositions are relatively uniform averaging approximately andradite₅₆ grossular₃₅ hydrogrossular₇.Correlation of prehnite Fe³⁺ with host biotite Fe³⁺ and oxidation state support the textural evidence that prehnite in this paragenesis often replaces the host biotite. Sericitization of plagioclase and commonly a complete lack of hornblende indicate that plagioclase (An₅₀-An₁₅) is the chief source of Ca. Chlorite and muscovite (whose compositions are both directly related to the host biotite composition), aluminian sphene (Al₂O₃ reaching 7.72%), and K-feldspar (Or₉₉₊) are complimentary to the biotite breakdown reaction.Host rock composition to some extent controls the development of the Ca-Al silicates which do not occur in granitoids whose whole-rock CaO is less than 1%. An aqueous pore fluid with locally varying activities of ions enabled concentration of Ca in micro-metadomains, allowing development of Ca-Al silicates in relatively low-Ca granitoids. Individual phases generally appear to have developed independently due to fluctuation in chemical environment in micro-space and/or T, P fluctuation with time. Textures suggest that grandite may have locally replaced epidote in response to increasing temperature.In granitoids of the Victoria Range, South Island, New Zealand the alteration has probably occurred with P<2kb and T< 300 °–350 °C. Here alteration can be ascribed to strictly deuteric activity in only one of the two groups of granitoids so affected.     

Progressive sequence of reactions of the Ryoke metamorphism in the Yanai district, southwest Japan: the formation of cordierite

The compositions of biotite and muscovite were examined in terms of the paragenesis and the metamorphic grade in low- to medium-grade pelitic rocks of the Ryoke metamorphism in the Yanai district, southwest Japan. The biotite and muscovite that coexist with K-feldspar have a higher K component in an A'KF diagram than those in rocks lacking K-feldspar. This fact reflects an increase in the K₂O content in muscovite, but in biotite it reflects an increase of not only the K₂O content but also of the octahedral vacancy.
At higher metamorphic grade beyond the cordierite isograd, where cordierite coexists with neither chlorite nor K-feldspar, the biotite shows an increase in illite, K Aliv □xii−1 Si−1, and Tschermak components, Alvi Aliv R+−1 Si−1, where □xii and R+ denote the interlayer vacancy and (Fe+Mg+Mn), respectively. A reaction to define the cordierite isograd is proposed by treating this chemical change as being responsible for the first appearance of cordierite, i.e. K,Al-poor biotite+phengitic muscovite=K,Al-rich biotite+cordierite+quartz+water .By treating this as a key reaction in medium-grade metamorphism, a set of reaction in a progressive metamorphism is established for the Ryoke metamorphism, a typical low-pressure type metamorphism. Some textures in one of the high-grade areas, the K-feldspar-cordierite zone, suggest that a further two prograde reactions have taken place, i.e. andalusite+biotite+quartz=cordierite+K-feldspar+water
and   andalusite=sillimanite.quartz=cordierite+K-feldspar+water
This implies that this zone probably has a P–T  path involving isobaric heating.     

Gas pressures and redox reactions in geothermal fluids in Iceland

The gas and redox chemistry of 100–300 °C geothermal fluids in Iceland has been studied as a function of fluid temperature and fluid composition. The partial pressures of CO₂ in dilute (mCl<500 ppm) and saline (mCl>500 ppm) geothermal fluids above 200 °C are controlled by the mineral buffer clinozoisite+prehnite+calcite+quartz. Two buffers are considered to control the H₂S and H₂ partial pressures above 200 °C depending on fluid salinity, epidote+prehnite+pyrite+pyrrhotite for dilute fluids and pyrite+prehnite+quartz+magnetite+anhydrite+clinozoisite+quartz for saline fluids. Below 200 °C, the partial pressures of CO₂, H₂S and H₂ also seem to be buffered but other minerals must be involved. Zeolites are expected to replace prehnite and epidote. Redox potential calculated on the assumption of equilibrium for the H⁺/H₂ redox couple decreases in dilute geothermal fluids with increasing temperature from about −0.5 V at 100 °C to −0.8 V at 300 °C, whereas saline geothermal fluids at 250 °C display a redox potential of about −0.45 V. A systematic discrepancy between redox couples of about 0.05–0.09 V is observed in the redox potential for the dilute geothermal fluids, whereas redox potentials agree within 0.02–0.04 V for saline geothermal waters. The discrepancies in the calculated redox potential for dilute geothermal fluids are thought to be due to a general lack of equilibrium between CH₄, CO₂ and H₂ and between H₂S, SO₄ and H₂. It is, accordingly, concluded that an overall equilibrium among redox species has not been reached for dilute geothermal fluids whereas it appears to be more closely approached for the saline geothermal fluids. The latter conclusion is based on limited database and should be treated with care. Since the various redox components are not in an overall equilibrium in geothermal fluids in Iceland these fluids cannot be characterised by a unique hydrogen fugacity, oxygen fugacity or redox potential at a given temperature and pressure.     

Zones of Progressive Regional Burial Metamorphism in Part of the Tasman Geosyncline, Eastern Australia

A succession of metamorphic zones can be recognized along theMolong Geanticline, an ancient rise within the Tasman Geosynclineof Eastern Australia. In order of increasing grade, the zonesin the volcanogenic rocks are: (1) an albite-quartz zone, containingneither prehnite, pumpellyite, actinolite, nor biotite; (2)a prehnite zone; (3) a prehnite-pumpellyite zone; (4) an actinolitezone; and (5) a biotite zone. Zeolite associations are not developed.Zones 4 and 5 lie within the greenschist facies. The rocks alongthis geanticline are generally only slightly deformed, lackingcleavage. The grade of this metamorphism within the Molong Geanticlineincreases partly in accordance with increasing stratigraphicdepth and partly increases eastwards towards the adjacent HillEnd Trough. Within the Trough, rocks show metamorphic assemblagesakin to those of Zones 4 and 5 as defined within the MolongGeanticline, but deformation is more extreme and a regionalcleavage is characteristic. In the region about the Hill EndTrough and the adjacent geanticlines there is an apparent variationfrom essentially static burial metamorphism of the geanticlinesthrough transitional types to tectonic dynamothermal metamorphismof the trough. Both metamorphisms are envisaged as having arisenduring the same general period of metamorphism, but deformationof the geanticlines was much less than deformation in the interveningHill End Trough.     

Chemistry, reaction mechanisms and micro-structures during retrograde metamorphism of gedrite-biotite-plagioclase bearing rocks from Bergslagen, south-central Sweden

The Proterozoic rhyolitic volcanics constituting the foot-wall rocks in the Stollberg ore-field, Bergslagen, south-central Sweden, locally contain gedrite altered to chlorite and serpentine, biotite altered to chlorite and plagioclase altered to epidote.

The intergrowths between the host gedrite and the chlorite/serpentine inclusions are oriented with the a^* of gedrite parallel to the c^* of serpentine and chlorite. The biotite has been altered to chlorite by brucitization of both the K-interlayer and talc-like layer. In both cases the net change in volume during chloritization is small.

The assumption that Al is conserved during alteration of gedrite and biotite agrees very well with the micro-structures and orientation relations observed by transmission electron microscopy. Normalizing the chlorite to 1.00 mole, the overall chemical change that took place during the retrograde metamorphism of the Stollberg rocks can be written as: 0.84Ged+0.14Bio+0.65Mg+4.76H₂O+0.42H=1.00Chl+0.57Alb+0.72Fe+0.01Na+0.12K+0.01Ti+0.05Mn+0.95H₄SiO₄ The reaction results in ca 9% increase in volume for the solid phases. Thus, a slightly acidic Mg-rich fluid started the reaction and, upon leaving the system, the metasomatic fluid was enriched in Na, Fe, K, and Si.     

西藏墨竹工卡地区早侏罗世花岗岩地球化学、岩石成因及其地质意义

为了研究南冈底斯晚三叠世-早侏罗世时期岩浆岩的成因类型和构造背景，针对墨竹工卡地区的松多黑云母二长花岗岩体进行岩相学、年代学、全岩地球化学研究.LA-ICP-MS锆石U-Pb定年结果显示，松多黑云母二长花岗岩结晶年龄为190.2±2.9 Ma，形成于早侏罗世.在地球化学组成上，黑云母二长花岗岩具有低TiO₂（0.68%~0.75%），富SiO₂（65.22%~66.13%）、Al₂O₃（16.26%~16.73%）、Na₂O（4.05%~4.29%）、K₂O（3.96%~4.24%）的特点，显示钾玄岩系列和弱过铝质（A/CNK=1.04~1.11）的主量元素地球化学特征；在微量元素蛛网图上，具有富集Rb、Th、K、Zr、Hf元素和亏损Ba、Nb、Ta、Sr、Ti、P元素的特征；锆石饱和温度介于805~835℃，FeOT/MgO比值高，样品显示出具有部分A型花岗岩特征.结合前人研究表明，晚三叠世-早侏罗世时期南冈底斯岩浆岩构造背景与新特提斯洋北向俯冲有关，松多黑云母二长花岗岩形成于新特提斯洋板片北向俯冲引起的弧后伸展环境；其成因与软流圈上涌导致幔源岩浆底侵引起下地壳的部分熔融有关.      

A new petrogenetic grid for low-grade metabasites

Abstract We have used internally-consistent thermodynamic data to present calculated phase equilibria for the system Na₂O-CaO-MgO-Al₂O₃-SiO₂-H₂O (NCMASH), in the range 0–500° C and 0.1–10 kbar, involving the phases anorthite, glaucophane, grossular, heulandite, jadeite, laumontite, lawsonite, paragonite, prehnite, pumpellyite, stilbite, tremolite, wairakite, zoisite with excess albite, clinochlore, quartz and pure water. Average activity terms derived from published mineral chemical data were included for clinochlore, glaucophane, prehnite, pumpellyite, tremolite, and zoisite. The new petrogenetic grid delineates stability fields and parageneses of common index minerals in zeolite, prehniteactinolite, prehnite-pumpellyite, pumpellyite-actinolite, blueschist and greenschist facies metabasites. The stability fields of mineral assemblages containing prehnite, pumpellyite, epidote, actinolite (+ albite + chlorite + quartz) were analysed in some detail, using activity data calculated from five specific samples. For example, the prehnite-actinolite facies covers a P-T field ranging from about 220 to 320° C at pressures below 4.5 kbar. The transition from the prehnite-actinolite and pumpellyite-actinolite to greenschist facies occurs at about 250–300° C at 1–3 kbar and at about 250–350° C at 3–8 kbar. P-T fields of individual facies overlap considerably due to variations in chemical composition.     

Determining mineral weathering rates based on solid and solute weathering gradients and velocities: application to biotite weathering in saprolites

Chemical weathering gradients are defined by the changes in the measured elemental concentrations in solids and pore waters with depth in soils and regoliths. An increase in the mineral weathering rate increases the change in these concentrations with depth while increases in the weathering velocity decrease the change. The solid-state weathering velocity is the rate at which the weathering front propagates through the regolith and the solute weathering velocity is equivalent to the rate of pore water infiltration. These relationships provide a unifying approach to calculating both solid and solute weathering rates from the respective ratios of the weathering velocities and gradients. Contemporary weathering rates based on solute residence times can be directly compared to long-term past weathering based on changes in regolith composition. Both rates incorporate identical parameters describing mineral abundance, stoichiometry, and surface area.

Weathering gradients were used to calculate biotite weathering rates in saprolitic regoliths in the Piedmont of Northern Georgia, USA and in Luquillo Mountains of Puerto Rico. Solid-state weathering gradients for Mg and K at Panola produced reaction rates of 3 to 6×10⁻¹⁷ mol m⁻² s⁻¹ for biotite. Faster weathering rates of 1.8 to 3.6×10⁻¹⁶ mol m⁻² s⁻¹ are calculated based on Mg and K pore water gradients in the Rio Icacos regolith. The relative rates are in agreement with a warmer and wetter tropical climate in Puerto Rico. Both natural rates are three to six orders of magnitude slower than reported experimental rates of biotite weathering.     

Prehnite--Epidote Phase Relations in the Nordre Aputit?q and Kruuse Fjord Layered Gabbros, East Greenland

Layered gabbros at Nordre Aputit?q and Kruuse Fjord were emplacedduring extensional tectonism that led to the formation of theNorth Atlantic basin in the Early Tertiary. Sub-solidus reactionsbetween the gabbros and hydrothermal fluids formed superimposedalteration assemblages in fractures, cavities, and the adjacentgabbros. The earliest secondary minerals are Ca-Al amphibole+ clinopyroxene + biotite ? plagioclase that form thin veinsor porous pegmatitic masses. These minerals are crosscut, overgrownor partially replaced by one or more generations of prehniteand epidote bearing assemblages associated with filling of thefractures and cavities, and with extensive wall rock albitization. Wide variations in the partitioning of Fe³⁺ and Al between coexistingprehnite and epidote solid solutions occur in these alteredgabbros. The partitioning data define distinct clusters in termsof associated mineralogy and paragenetic relations. This, togetherwith prehnite and epidote compositions from active geothermalsystems, are used to evaluate the thermodynamic properties ofthe intercrystalline exchange reaction:When compared to thecompositions of prehnite and epidote in the Nordre Aputit?qand Kruuse Fjord intrusions, it is concluded that the latestand lowest temperature generations of prehnite and epidote displaydisequilibrium partitioning of Fe³⁺ and Al, manifested by theoccurrence of prehnite that is relatively enriched in Fe³⁺ Thermodynamic analysis of phase relations in the system Na₂O-CaO-Al₂O₃-Fe₂O₃-FeO-SiO₂-H₂O-HClis used to determine local equilibrium constraints on Fe³⁺-Alsubstitution in prehnite and epidote. It appears that parageneticand compositional relations of prehnite and epidote are sensitiveindicators of local fluctuations in fluid composition and temperature.The complex magmatic and structural history of the gabbros atNordre Aputit?q relative to Kruuse Fjord is considered to beresponsible for the differences in mineral paragenesis and compositionsof prehnite and epidote within these intrusions.     

浙西南遂昌—大柘地区八都岩群印支期变质变形序列

浙西南遂昌-大柘地区八都岩群在印支期变质事件影响下发生变质变形,通过详细野外调查和岩相学研究,可将其划分为3期变质变形序列：S₁变形期,NW向片麻理记录的残留紧闭褶皱,共生矿物组合为石榴子石变斑晶及其内部定向分布的包裹体矿物,石榴子石+黑云母+石英（泥质）和石榴子石+角闪石+斜长石+石英（长英质）;S₂变形期,区域性宽缓褶皱及NE向缓倾透入性片麻理,共生矿物组合为石榴子石变斑晶及定向分布的基质矿物,矽线石+石榴子石+黑云母+石英+斜长石±钾长石（泥质）和石榴子石+钾长石+斜长石+黑云母+石英（长英质）;S₃变形期,NE向陡倾透入性片麻理及韧脆性断裂大部分被花岗斑岩脉填充,共生矿物组合为石榴子石变斑晶及其周围退变矿物,石榴子石+矽线石+堇青石+斜长石+黑云母+石英±钾长石（泥质）和角闪石+斜长石+黑云母+钛铁矿（长英质）。结合前人研究成果,八都岩群印支期变质事件峰期变质程度达到麻粒岩相,显示顺时针近等温降压（ITD）型的p-T演化轨迹,S₁-S₃变质变形反映出从俯冲碰撞到快速折返冷却的演化过程,伴随S₃同期侵位的花岗斑岩锆石U-Pb定年结果,将该演化过程完成时间约束在229.7 Ma,可能是浙西南地区对印支期古特提斯洋域内印支-华南-华北板块之间俯冲-碰撞过程的响应。     

Decompressional coronas and symplectites in granulites of the Musgrave Complex, central Australia

Abstract In granulite facies metapelitic rocks in the Musgrave Complex, central Australia, reaction between S1 garnet and sillimanite involves the development in S2 of both garnet + cordierite + hercynitic spinel + biotite and hercynitic spinel + cordierite + sillimanite + biotite. The S2 assemblages occur either in coronas and symplectites, mainly around garnet, or, in rocks in which S2 is more strongly developed, as recrystallized assemblages. Ignoring the presence of biotite and ilmenite, the mineral textures can be accounted for qualitatively by a consideration of the model system FeO-MgO-Al₂O₃-SiO₂ (FMAS); the textural relationships accord with decompression accompanying the change from S1 to S2. However, since biotite and ilmenite are involved in the assemblages, the parageneses are better accounted for in terms of equilibria in the expanded model system K₂O-FeO-MgO-Al₂O₃-SiO₂-H₂-TiO₂-Fe₂O₃ (KFMASHTO), i.e. AFM + TiO₂+ Fe₂O₃. The coronas reflect the tectonic unroofing of at least part of the Musgrave Complex from peak S1 conditions of about 8 kbar to S2 conditions of about 4 kbar.     

Hydrothermal alteration of plagioclase in granitic rocks from Proterozoic basement of SE Sweden

Petrographic examinations and electron microprobe analyses of Proterozoic granitic rocks, SE Sweden aimed to characterize and unravel the mechanisms and conditions of plagioclase alterations. These alterations include saussuritization, albitization and replacement of plagioclase by K‐feldspar. The hydrothermal alterations, which are inferred to have occurred at ca. 250–400°C, resulted in concomitant formation of Al‐rich titanite, epidote, calcite, pumpellyite, prehnite and iron oxides. Replacement of plagioclase by K‐feldspar occurs in red‐stained zones, which have developed close to thin fractures owing to the precipitation of tiny Fe‐oxide pigment particles within the altered plagioclase, whereas saussuritized plagioclase has less systematic spatial relationships to these fractures. Albitization of plagioclase occurred in rocks that are poor in biotite compared to rocks that suffered extensive saussuritization. The chemical and textural characterization of various types of plagioclase alterations allows elucidation of the granitic hydrothermal systems. Features of feldspar alteration in the granitic rocks are similar to those encountered in feldspathic sandstones and should hence be considered in studies on diagenetic changes of siliciclastic successions during basin evolution. Copyright © 2009 John Wiley & Sons, Ltd.     

华北克拉通东缘金岭杂岩体岩浆源区及构造背景:来自岩相学、岩石地球化学及年代学的证据

金岭杂岩体由细粒黑云角闪闪长岩、中细粒黑云角闪闪长岩、中细粒黑云角闪二长闪长岩和细粒角闪二长闪长岩组成,是鲁西地区典型矽卡岩型富铁矿(金岭铁矿)控矿岩体。本次研究对细粒黑云角闪闪长岩和细粒角闪二长闪长岩进行了锆石LA‐ICP‐MS U‐Pb定年,其结果分别为129.2±3.2 Ma和132.8±1.2 Ma,表明该杂岩体的侵位时代为早白垩世。样品SiO2、K2O和Na2O含量分别介于54.17%~63.73%、1.92%~4.76%和3.10%~5.41%之间,K2O/Na2O为0.58~0.94,A/CNK为0.60~0.93,具有轻稀土富集,重稀土亏损的右倾型稀土配分模式,轻、重稀土分馏程度中等((La/Yb)N=9.94~23.49),Eu异常不明显(δEu=0.84~1.10),具中—弱负Ce异常(δCe=0.56~0.92)。样品以富集大离子亲石元素(Ba、K、U、Pb等)、亏损高场强元素(Nb、Ta、Ti)以及高Sr/Y为特征。金岭杂岩体为燕山晚期岩浆活动产物,属准铝质高钾钙碱性系列,岩浆主要来源于富集岩石圈地幔的部分熔融,并在岩浆上升侵位的过程中有地壳物质的同化混染。燕山晚期华北克拉通在古太平洋板块俯冲后后撤引起的板内伸展环境下,增厚陆壳减薄阶段,岩浆上侵就位形成金岭杂岩体。     

Geothermobarometry in albite-garnet orthogneisses: A case study from the Gran Paradiso nappe (Western Alps)

The aim of this paper is to estimate syntectonic P-T conditions within albite- and garnet-bearing orthogneisses. These rocks are generally characterized by the assemblage quartz + albite + biotite + phengite + CaFe-garnet + epidote + titanite. Garnet contains up to 55 mole per cent of grossular. K-feldspar is a relict magmatic phase.

P-T conditions are estimated using several independent methods. First, it is shown that exchange reactions based on the Fe---Mg partitioning between garnet and biotite or garnet and phengite cannot be used to estimate temperatures in these rocks, due to the high grossular content of garnet. Second, maximum and minimum pressures are constrained, respectively, by the occurrence of albite instead of jadeite + quartz and by the assemblage phengite + biotite + quartz. Third, phase equilibria in albite- and garnet-bearing metagranites are modelled in the system K₂O---CaO---FeO---Al₂O₃---SiO₂---H₂O. Equilibrium curves are calculated for the observed phase compositions. Uncertainties in P-T estimates mainly result from the choice of appropriate non-ideal solution models for the garnet.

An application is developed for granites from the Gran Paradiso nappe (Western Alps). These granites show an heterogeneous deformation of Alpine age expressed by mylonitic shear zones cutting across weakly deformed domains. Estimated P-T conditions for the synkinematic assemblages are 10–16 kbar at 550±50°C.     

The age of orogenesis in the Nambucca Slate Belt: A K‐Ar study of low‐grade regional metamorphic rocks

K‐Ar ages of biotite and hornblende from undeformed granodiorite plutons and of slaty and phyllitic rocks, ranging from prehnite‐pumpellyite metagreywacke to greenschist fades, have been determined in an attempt to define the age of orogenesis in the eastern part of the Nambucca Slate Belt. The plutons have K‐Ar ages of 226–227 m.y. (biotite) and 228–231 m.y. (hornblende) that provide a younger age limit for deformation. The lower grade metamorphic rocks yield a range of ages including some comparable with the depositional age of the rocks as indicated by fossils. Rocks of pumpellyite‐actinolite and greenschist facies give a more coherent group of ages which suggest orogenesis at about 250–255 m.y. Specimens of these latter rocks that have been affected by a later structural episode than that during which slaty cleavage formed, yield slightly older ages, which may result from the inclusion of minor amounts of environmental excess ⁴⁰Ar.

Support for the 250–255 m.y. age comes from previously determined radiometric ages from the western part of the Slate Belt, although the presence of granitic bodies perhaps as old as 289 m.y., some closely associated with high‐grade regional metamorphic rocks, may indicate the presence of additional earlier orogenic movements in this region.     

Geochemical aspects of the evolution and mineralization of the Amo Younger Granite Complex (northern Nigeria)

The Amo Complex forms one of the prominent ring intrusions in the Jos Plateau and it is lithologically composed of granite porphyry, riebeckite biotite granite, hornblende biotite granite and later intrusives of biotite granite. There are also small intrusions of albite riebeckite granite and albite biotite granite.

Major-element compositions of the principal rock units do not show significant differences. Comparison of the variations found in the granites with results of laboratory studies suggest either that water vapor and volatile transfer were important in the local magma series or at least they accompanied other systematic variations.

Trace-element associations vary; anomalous enrichments of Rb, Li, F, U, Th, Zr, Nb and HREE occur over mildly peralkaline riebeckite biotite granite, peralkaline albite riebeckite granite and albite biotite granite with peralkaline tendency, in contrast to their peraluminous equivalents. These cannot be explained by crystal-liquid fractionation processes and require the evolution of a Na-enriched fluid.

It is suggested that in the albite riebeckite granite and the albite biotite granite the combined effect of F, Li and Rb along with other volatiles may have led to a lower crystallization temperature such that two separate alkali feldspars (albite and microcline) crystallized individually.

Cassiterite and columbite mineralization occur mainly as magmatic disseminations within the terminal phases of the biotite granites and albite biotite granite. Diffused greisenization in association with quartz veins also carry cassiterite mineralization in the Tega and Timber Creek biotite granite phases. Although the magma may have supplied the ore elements and F for complexing, actual mineralization appears to be a product of postmagmatic processes.     

A thermodynamic model for titanium and ferric iron solution in biotite

Recent crystallographic data indicate that in biotite Ti orders preferentially onto the M2 octahedral site rather than onto the M1 site as assumed in previous solution models for K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–O₂ (KFMASHTO) biotite. In view of these data, we reformulate and reparameterize former biotite solution models. Our reparameterization takes into account Fe–Mg order–disorder and ferric iron contents of natural biotite as well as both natural and experimental observations on biotite Ti-content over a wide range of physicochemical conditions. In comparison with previous biotite models, the new model reproduces the Ti-content and stability field of biotite as constrained by experiments with significantly better accuracy. The predictive power of the model is tested by comparison with petrologically well-characterized natural samples of SiO₂-saturated and SiO₂-undersaturated rocks that were not used in the parameterization. In all these tests, the reformulated model performs well.     

Prehnite–pumpellyite to greenschist facies transition, Smartville Complex, near Auburn, California

The Smartville Complex is a late Jurassic, rifted volcanic arc in the northern Sierra Nevada, California. Near Auburn, California, it consists of a lower volcanic unit, dominated by basaltic flows, and an upper volcanic unit of andesitic volcaniclastic rocks, both of which have been intruded by dykes and irregular bodies of diabase. These rocks contain relict igneous minerals, and the metamorphic minerals albite, chlorite, quartz, pumpellyite, prehnite, epidote, amphibole, titanite, garnet, biotite, K-feldspar, white mica, calcite, and sulphide and oxide minerals.
Prehnite–pumpellyite (PrP), prehnite–actinolite (PrA), and greenschist (GS) zones have been identified. The pumpellyite-out isograd separates the PrP and PrA zones, and the prehnite-out isograd separates the PrA and GS zones. The minerals Ab + Qtz + Mt + Tn are common to most assemblages in all three zones. The MgO/(MgO + FeO) ratio of the effective bulk composition has an important and systematic effect on the observed mineral assemblages in the PrP zone. Prehnite-bearing assemblages contain the additional minerals, Pmp + Amp + Ep + Chl in MgO-rich rocks, and either Pmp + Ep + Chl or Amp + Ep + Chl in less magnesian rocks. Subcalcic to calcic amphibole is common in the PrP zone. The mineral assemblage Prh + Act + Ep + Chl, without Pmp, characterizes the PrA zone, and the mineral assemblage Act + Ep + Chl, without Prh or Pmp, characterizes the GS zone. The disappearance of pumpellyite and prehnite occurred by continuous reactions.
The sequence of mineral assemblages was produced by burial metamorphism at P–T conditions of 300° 50°C at approximately 2.5 ± 0.5 kbar. During metamorphism, the composition of the fluid phase was nearly 100% H₂O and the oxygen fugacity was between the hematite–magnetite and quartz–fayalite–magnetite buffers.     

西藏双湖地区南措铜金矿区花岗闪长岩锆石U-Pb年代学、岩石地球化学及成因

对南措铜金矿区与成矿相关的黑云母花岗闪长岩体进行了岩相学、锆石U-Pb年代学、岩石地球化学等方面的研究。结果表明:该岩体年龄为153.40±0.67 Ma,属晚侏罗世。岩石为准铝质-过铝质岩石,属钙碱性系列。LaN/YbN=9.31~12.65,轻重稀土元素分馏明显,δEu=1.21~1.66,Eu表现为正异常;样品微量元素表现为相对富集大离子亲石元素(LILE)K、与高场强元素(HFSE)Sr、Zr,而亏损高场强元素(HFSE)U、Nb、Ce、Nd、P的特征。岩体具有I型花岗岩特征。样品Zr/Hf值为42.23~45.82,平均值为44.2;Rb/Sr比值为0.07~0.19,平均值为0.13;Nd/Th值为1.65~2.18,平均为1.99,具壳源岩浆的特征,并有地幔物质混入。样品的Mg#值为49.80~57.22,Sr值为443.3~874.9,Yb值为0.80~1.39,Y值为8.96~16.60,Na2O/K2O2(2.18~2.97),为洋壳型埃达克岩,并在上升过程中可能有少量地幔楔物质混入。结合前人研究成果认为,该花岗闪长岩形成于晚侏罗世班公湖—怒江洋盆向北俯冲的火山弧环境。