南岭地区高度演化花岗岩类的稀土元素模型

本文应用现有的理论模型和矿物／熔体分配系数讨论南岭地区高度演化花岗岩类的ＲＥＥ模型，包括重稀土富集型和稀土亏损型。在花岗岗岩浆分异演化过程中，副矿物（尤其是稀土矿物）的晶出种类，顺序和物理化学条件是控制ＲＥＥ强烈分馏的关键因素。ＲＥＥ分布型式不能简单地作为鉴别岩石成因的标志。     

ASPECTS OF THE EVOLUTION OF MAGMATIC MELTS IN THE CRYSTALLIZATION OF HYBRID MAGMAS,AS ILLUSTRATED BY TERTIARY GRANITIC ROCKS OF KAMCHATKA

Melting of basic to intermediate composition effusives enclosed in granitic magma forms a hybrid magma which subsequently can crystallize into granodiorite, quartz-diorite, and diorite. Crystallization of this hybrid magmatic melt proceeds along lines different from a normal differentiation of granitic magmas. Plagioclase in hybrid rocks is strongly zoned and dominantly andesine approaching, in places, the composition of labradorite. Outer zones of these crystals are andesine and oligoclase. In granitic rocks plagioclase is acid andesine to oligoclase. Outer zones get up to albite in composition. Pyriboles and biotite also show diagnostic optical features for crystallization of hybrid vs primary granitic magmas. Plagioclase composition that is coprecipitating with the crystallization of ferromagnesians, potassic feldspar, and quartz is of critical importance. Granitic and alaskitic magmas, in contrast to hybrid magmas, undergo anchieutectic crystallization. Changes in the alkali regimen of each of the two magma types affects the composition and crystallization order of the rock-forming minerals. Assimilation phenomena associated with the formation of hybrid rocks is aided by diffusion flow and infiltration flow of particles. --R. M. Hutchinson.     

The release of Pb and REE from granitoids by the dissolution of accessory phases

The release of Pb and rare earth elements (REE) during granitoid weathering was investigated through dissolution experiments of fresh granite and soil samples. Two aliquots of a granite sample from the El-Capitan Granite, Sierra Nevada, California, were leached several times using a dilute acid at pH = 1. The results of the experiment were compared with Pb and REE data from soils developed on the same rock. During the early stages of granitoid dissolution, Pb and REE were preferentially released from some of the accessory phases (i.e., allanite, sphene, and apatite). This caused higher ²⁰⁶Pb/²⁰⁷Pb and ²⁰⁸Pb/²⁰⁷Pb values and different REE patterns in solution compared with the rock values. Based on Pb isotopes and REE patterns, three stages of rock dissolution can be identified. In the first stage the dissolution of allanite dominates the release of Pb and REE from accessory phases, as ²⁰⁸Pb/²⁰⁷Pb, Ce/Pb, and chondrite-normalized Ce/Yb ratios in solution increase and approach the values of allanite. In the second stage, the dissolution of apatite and sphene become more significant. In the third stage, the isotopic ratios of Pb and the normalized-REE patterns reflect the depletion of accessory phases and the increase in the rate of feldspar dissolution. According to our estimate (based on Si release from the rock) all three stages account for the first 500 kyr of granitoid weathering.Using the isotopic ratios of Pb, major elemental compositions, and REE concentrations both in the experimental solutions and in the soil we were able to establish the following order of the weathering rates of accessory phases: allanite > apatite > sphene. In addition, we have demonstrated that biotite is significantly less resistant to weathering than hornblende under acidic conditions, and is probably dissolved completely after approximately 500 kyr of rock weathering. We also suggest that within 500 kyr of granitoid weathering K-feldspar accounts for 15% of the released K.     

Rare Earth Element Behaviour During Evolution and Alteration of the Dartmoor Granite, SW England

The distribution of rare earth elements (REE) within the compositionallyzoned Dartmoor pluton is used to constrain models of graniteevolution and to assess the effects of pervasive hydrothermalalteration on REE mobility. The main process of magma evolutionwas crystal fractionation of early plagioclase, biotite, andaccessory minerals (apatite, monazite, zircon, and xenotime).Concentrations of REE (particularly LREE and Eu) and other elements(Fe₂O₃t, MgO, CaO, TiO₂, Zr, Ba, and Sr) decrease strongly withevolution of the pluton from 71 to 74% SiO2. These trends, andthe inward zoning of the pluton, are compatible with differentiationby crystal fractionation at the level of emplacement, a processthat gave rise to a marginal cumulate granite (CGM) modifiedby country rock assimilation, a body of inner granite (PM),and a late-stage evolved granite (FG) that intruded the earliertypes. REE modelling of the Dartmoor granite types by fractionalcrystallization of REE-enriched accessory minerals from a parentPM-granite shows that the FG-granite cannot have formed froma residual liquid left by crystallization of the CGM-granite.Two discrete stages of crystallization occurred; side-wall cumulateCGM-granite crystallization dominated by LREE-en-riched monazitefractionation followed by a late-stage mobile residual FG-granitein which fractionation was dominated by HREE-enriched apatiteand zircon. Modelling supports the idea that large-scale assimilationof country rock was not the dominant process during Dartmoorgranite evolution. Pervasive hydrothermal alteration locally affected all Dartmoorgranite types, altering primary plagioclase, biotite, apatite,monazite, and, to a lesser extent, zircon and xenotime. Duringpervasive sericitization, chloritization, and tourmalinization,REE were mobilized over distances of centimetres only and redistributedinto the secondary alteration products seridte, chlorite, tourmaline,allanite, and sphene. Whole-rock REE abundances were not affected     

Petrogenetic modelling of in situ fractional crystallization in the zoned Loch Doon pluton,Scotland

The late Caledonian Loch Doon granitic intrusion ranges in composition from hypersthene diorite at the margin, through quartz diorite, granodiorite and granite to cordierite microgranite at its core. Petrogenetic modelling of trace element variations and least squares analysis of major elements indicate that two distinct magmas are involved, each magma controlled by crystallization of plag-opx-cpx-bio. Late stage rocks related to the second magma include the cordierite microgranites and aplites, which are interpreted as the final residue which crystallized rapidly after a build up and loss of volatiles.Analyses of whole rocks and minerals for REE's and other elements of moderate-high ionic potential indicate that these elements are strongly controlled by minor phase crystallization; apatite, zircon, sphene and allanite are dominant at intermediate compositions but other accessory minerals such as monazite and xenotime may also become important at acid compositions.It is probable that within each magma the mechanisms of crystal settling and filter pressing operated, the former being initially dominant, and the latter becoming more important with increasing degree of fractional crystallization.     

Differential Fractionation of Rare Earth Elements in Oxidized and Reduced Granitic Rocks: Implication for Heavy Rare Earth Enriched Ion Adsorption Mineralization

Ion adsorption rare earth element (REE) deposits in southern China are the exclusive source of heavy REEs (HREEs) in the world, and this HREE‐enriched character of the deposits is inherited from the REE compositions of the underlying granitic rocks. Such HREE‐enriched rocks form from heavy fractionation of reduced granitic magmas. We explore why reduced granitic magmas are enriched in HREEs during the fractionation, based on the REE geochemistry of granitic rocks and abundance of REEs in their constituent minerals in the southwestern Japan arc of Cretaceous to Paleogene age. The compilation of the whole rock geochemistry and REE compositions of the granitic rocks of the Sanin (oxidized), Sanyo (reduced) and Ryoke (reduced) belts in the southwestern Japan arc indicates that: (i) light REEs (LREEs) decease with fractionation of the granitoids in the Sanin belt but this trend is not clear in the granitoids in the Sanyo belt and LREEs rather increase in the Ryoke granitoids; (ii) Eu decreases with fractionation in all the belts; and (iii) HREEs slightly, but steadily decrease in the Sanin belt but enrich significantly in the Sanyo and Ryoke belts with fractionation. Analytical results of REE concentrations by scanning electron microscope with energy dispersive X‐ray spectroscope and laser ablation‐inductively coupled plasma mass spectrometer in the constituent minerals in a granodiorite sample from the Sanin belt show a moderate concentration of REEs in hornblende (577 ppm) in addition to high concentrations in allanite (~20 %), britholite (~30 %), primary titanite (8922 ppm), apatite (4062 ppm), and zircon (1693 ppm). Because primary titanite and allanite are commonly present in the oxidized granitoids but not in the reduced ones, the REE depletion in the fractionated, oxidized granites is attributed to the crystallization of these minerals. In contrast, scarcity of these minerals in the reduced granitoids enriches REEs, in particular HREEs in the fractionated magmas, which finally precipitate REEs in the granites and pegmatites. Both positive, but different correlation ratios between the Nb and Dy concentrations in the granitoids of the Sanin and Sanyo‐Ryoke belts suggest that columbite–pyrochlore‐group and fergusonite‐group minerals are the major HREE host in the oxidized and reduced granites, respectively.     

陕西省华阳川铀铌铅矿床碳酸岩岩石学及地球化学特征

陕西省华阳川铀铌铅矿床是小秦岭成矿带中成矿特征最为独特的矿床,碳酸岩脉的破碎带是重要的成矿空间。未矿化的碳酸岩中矿物以方解石为主,其他矿物很少;发育铀矿化的碳酸岩脉中矿物种类繁多,大部分为方解石,其次为角闪石、金云母、榍石、褐帘石、铌钛铀矿、重晶石、磷灰石、石英、磁铁矿、碱性长石等矿物。碳酸岩的LREE含量异常高,δ13CV-PDB和δ18OV-SMOW值显示典型的火成碳酸岩特征。基于碳酸岩脉的Sr、Nd、Pb同位素比值(87Sr/86Sr-206Pb/204Pb、207Pb/204Pb-206Pb/204Pb-143Nd/144Nd-87Sr/86Sr)的关系图,初步判断华阳川铀铌铅碳酸岩脉是源于EMI的碱性硅酸盐-碳酸盐熔体-溶液结晶分异的产物。     

Alkaline gabbroids of the Chirii outcrop (North Minusa depression): mineralogy and melt evolution

We studied the chemical composition of rock-forming minerals in gabbroids from the Chirii outcrop and the evolutionary features of parental basic melt during the crystallization of these rocks. Results were compared with data for basanites from pipes of the North Minusa depression. The mineralogical composition and thermobarogeochemical data of the gabbroids were examined in detail, and chemical analyses of rock-forming minerals (clinopyroxene, plagioclase, amphibole, biotite, titanomagnetite, and apatite) were carried out. Based on the homogenization temperatures of primary melt inclusions, we established the minimum temperatures and sequence of mineral crystallization in the gabbroids: clinopyroxene (>1160 °C), plagioclase, magnetite → amphibole (>950 °C) → biotite. The rock crystallization proceeded at shallow depths. Thermometric data are confirmed by results of modeling of equilibrium gabbroid crystallization. The crystallization of parental basic melt was accompanied by the accumulation of SiO₂, Al₂O₃, alkalies, and Cl and depletion in femic components. The melt evolved to granodiorite and alkali-syenite compositions. Compared with basanites from pipes, the parental melt had a longer evolution. The geochemical features of the gabbroids indicate that they, like basanites, crystallized from intraplate alkali-basaltoid magmas. But in petrochemistry and mineralogy the Chirii gabbroids differ considerably from the pipe basanites.     

Minor-element and Sr-isotope geochemistry of tertiary stocks,Colorado mineral belt

Rocks of the northeast portion of the Colorado mineral belt form two petrographically, chemically and geographically distinct rock suites: (1) a silica oversaturated granodiorite suite; and (2) a silica saturated, high alkali monzonite suite. Rocks of the granodiorite suite generally have Sr contents less than 1000 ppm, subparallel REE patterns and initial ⁸⁷Sr/ ⁸⁶Sr ratios greater than 0.707. Rocks of the monzonite suite are restricted to the northeast part of the mineral belt, where few rocks of the granodiorite suite occur, and generally have Sr contents greater than 1000 ppm, highly variable REE patterns and ⁸⁷Sr/⁸⁶Sr initial ratios less than 0.706.Despite forming simple, smooth trends on major element variation diagrams, trace element data for rocks of the granodiorite suite indicate that they were not derived from a single magma. These rocks were derived from magmas having similar REE patterns, but variable Rb and Sr contents, and Rb/Sr ratios. The preferred explanation for these rocks is that they were derived by partial melting of a mixed source, which yielded pyroxene granulite or pyroxenite residues.The monzonite suite is chemically and petrographically more complex than the granodiorite suite. It is subdivided here into alkalic and mafic monzonites, and quartz syenites, based on the textural relations of their ferromagnesian phases and quartz. The geochemistry of these three rock types require derivation from separate and chemically distinct magma types. The preferred explanation for the alkalic monzonites is derivation from a heterogeneous mafic source, leaving a residue dominated by garnet and clinopyroxene. Early crystallization of sphene from these magmas was responsible for the severe depletion of the REE observed in the residual magmas. The lower Sr content and higher Rb/Sr ratios of the mafic monzonites requires a plagioclase-bearing source.The Sr-isotope systematics of the majority of these rocks are interpreted to be largely primary, and not the result of crustal contamination. The positive correlation of Rb/Sr and ⁸⁷Sr/⁸⁶Sr ratios for the least fractionated samples indicate that the sources from which parent magmas of both the granodiorite and monzonite suites were derived are Precambrian in age.     

Residence of REE, Y, Th and U in Granites and Crustal Protoliths; Implications for the Chemistry of Crustal Melts

A systematic study with laser ablation—ICP-MS, scanningelectron microscopy and electron microprobe revealed that 70–95wt% of REE (except Eu), Y, Th and U in granite rocks and crustalprotoliths reside within REEYThU-rich accessories whose nature,composition and associations change with the rock aluminosity.The accessory assemblage of peraluminous granites, migmatitesand high-grade rocks is composed of monazite, xenotime (in low-Cavarieties), apatite, zircon, Thorthosilicate, uraninite andbetafite-pyrochlore. Metaluminous granites have allanite, sphene,apatite, zircon, monazite and Thorthosilicaie. Peralkaline graniteshave aeschinite, fergusonite, samarskite, bastnaesite, fluocerite,allanite, sphene, zircon, monazite, xenotime and Th-orthosilicate.Granulite-grade garnets are enriched in Nd and Sm by no lessthan one order of magnitude with respect to amphibolite-gradegarnets. Granulitegrade feldspars are also enriched in LREEwith respect to amphibolite-grade feldspars. Accessories causenon-Henrian behaviour of REE, Y, Th and U during melt—solidpartitioning. Because elevated fractions of monazite, xenotimeand zircon in common migmatites are included within major minerals,their behaviour during anatexis is controlled by that of theirhost. Settling curves calculated for a convecting magma showthat accessories are too small to settle appreciably, beingseparated from the melt as inclusions within larger minerals.Biotite has the greatest tendency to include accessories, therebyindirectly controlling the geochemistry of REE, Y, Th and U.We conclude that REE, Y, Th and U are unsuitable for petrogeneticalmodelling of granitoids through equilibrium-based trace-elementfractionation equations. KEY WORDS: accessory minerals; geochemical modelling; granitoids; REE, Y, Th, U     

REE distribution in some layered migmatites: constraints on their petrogenesis

The REE distributions in mesosomes, neosomes, leucosomes and melanosomes of four layered migmatites have been investigated. In one example (Arvika migmatites) the REE patterns in adjacent paragneisses, the presumed parent rock of the migmatites, were also determined. REE patterns of neosomes and mesosomes of Arvika migmatites are similar to the finegrained layers and coarse-grained layers, respectively, observed in the adjacent paragneiss. This is in agreement with the layer-by-layer paragneiss-migmatite transformation model.

The REE patterns of mesosomes and neosomes indicate that these lithologies may have been closed systems (for REE) during the formation of the migmatites. No indication of metasomatic reactions, melt segregation or injection could be detected. Within the neosomes, leucosomes are depleted and melanosomes enriched in REE contents. This is interpreted to be due to separation and concentration of accessory minerals (monazite, epidote, allanite, zircon, sphene, apatite, garnet) into the melanosomes. The behaviour of accessory minerals during migmatite formation is closely allied to that of biotite, which is also concentrated in the melanosomes.     

Rare earth element partition between sphene,apatite and other coexisting minerals of the Kangerdlugssuaq intrusion,E. Greenland

Cumulus apatite, sphene, feldspar, amphibole and biotite from the pulaskite of the Kangerdlugssuaq alkaline intrusion have been analysed for rare earth elements (REE) by instrumental neutron activation analysis. The apatite is particularly rich in REE, contains 3.6% Ce and shows a steep, light REE-enriched, chondrite-normalised pattern. The other minerals have light REE enrichment but with sphene showing a peak at Ce on a chondrite-normalised plot. REE partition coefficient values show that the light REE are preferentially accommodated by apatite relative to sphene. The differences in these coefficients result from differences in the co-ordination of the REE in the two minerals.     

The description of the primary textures of “Cordilleran” granitic rocks

Variation in the primary textures of “Cordilleran” granitic rocks is described relative to three identifiable stages of the crystallisation interval; namely: (1) crystallisation in suspension; (2) growth of a touching crystal framework; (3) interstitial crystallisation. Crystals that initially grow in isolation will start to impinge and form small clusters as crystallisation proceeds and the volume of solid material increases, eventually forming a continuous interconnected crystal framework. Subsequent crystallisation involves solidification of the melt occupying the interstices of the framework, and therefore shows similarities to the way in which the porosity occludes in sedimentary systems. A case study of textural development in Cordilleran granitic rocks from the zoned Linga superunit of the Peruvian Coastal Batholith, reveals that compositional zonation from granodiorite through to syenogranite is accompanied by a systematic variation in the textures, specifically those of the three felsic phases (plagioclase, quartz and alkali feldspar). Plagioclase was the first phase to appear on the liquidus, and was joined by the other two phases as crystallisation proceeded and the melt evolved. The melt fraction at which quartz and alkali feldspar started to crystallise influenced the early growth of plagioclase, and the way in which the texture developed through each stage of the crystallisation interval. The geometry of plagioclase progressively changes from a touching framework of crystals in the granodiorite, to small aggregates or isolated crystals suspended in an equant mosaic of the other felsic phases in the syenogranite. This variation can be explained by an earlier evolution of the melt to the cotectic (i.e. at higher melt fractions) as the rocks become more acidic, and hence a greater contribution of alkali feldspar and quartz to the growth of the framework at the expense of plagioclase and the mafic phases. Textural observations are comparable to the crystallisation pathways of the felsic phases modelled in the quaternary An-Ab-Or-Qz system from the bulk compositions. All compositions lie in the plagioclase volume, and evolved to three-phase saturation on the cotectic via either the quartz/plagioclase divariant surface (granodiorites) or the alkali feldspar/plagioclase divariant surface (monzogranite and syenogranite).     

Geochemistry of intrusive rocks associated with the Latir volcanic field,New Mexico,and contrasts between evolution of plutonic and volcanic rocks

Plutonic rocks associated with the Latir volcanic field comprise three groups: 1) 25 Ma high-level resurgent plutons composed of monzogranite and silicic metaluminous and peralkaline granite, 2) 23–25 Ma syenogranite, and alkali-feldspar granite intrusions emplaced along the southern caldera margin, and 3) 19–23 Ma granodiorite and granite plutons emplaced south of the caldera. Major-element compositions of both extrusive and intrusive suites in the Latir field are broadly similar; both suites include high-SiO₂ rocks with low Ba and Sr, and high Rb, Nb, Th, and U contents. Moreover, both intermediateto siliciccomposition volcanic and plutonic rocks contain abundant accessory sphene and apatite, rich in rare-earth elements (REE), as well as phases in which REE's are essential components. Strong depletion in Y and REE contents, with increasing SiO₂ content, in the plutonic rocks indicate a major role for accessory mineral fractionation that is not observed in volcanic rocks of equivalent composition. Considerations of the rheology of granitic magma suggest that accessory-mineral fractionation may occur primarily by filter-pressing evolved magmas from crystal-rich melts. More limited accessory-mineral crystallization and fractionation during evolution of the volcanic magmas may have resulted from markedly lower diffusivities of essential trace elements than major elements. Accessory-mineral fractionation probably becomes most significant at high crystallinities. The contrast in crystallization environments postulated for the extrusive and intrusive rocks may be common to other magmatic systems; the effects are particularly pronounced in highly evolved rocks of the Latir field. High-SiO₂ peralkaline porphyry emplaced during resurgence of the Questa caldera represents non-erupted portions of the magma that produced the Amalia Tuff during caldera-forming eruption. The peralkaline porphyry continues compositional and mineralogical trends found in the tuff. Amphibole, mica, and sphene compositions suggest that the peralkaline magma evolved from metaluminous magma. Extensive feldspar fractionation occurred during evolution of the peralkaline magmas, but additional alkali and iron enrichment was likely a result of high halogen fluxes from crystallizing plutons and basaltic magmas at depth.     

Highly fractionated I-type granites in NE China (I): geochronology and petrogenesis

Northeastern (NE) China is the easternmost part of the Central Asian Orogenic Belt (CAOB), which is celebrated for its accretionary tectonics and the world's most important juvenile crust production in the Phanerozoic era. Abundant granitoids occur in the Great Xing'an, Lesser Xing'an and Zhangguangcai Ranges in NE China. This paper presents partial results of a series of studies on the granitoids from this region, aiming to understand their role in the building of new continental crust in eastern Asia. Three composite granite plutons (Xinhuatun, Lamashan and Yiershi) were chosen for geochemical and isotopic study in order to determine their emplacement ages and petrogenesis. Petrographically, they range from granodiorite (minor), monzogranite, syenogranite to alkali-feldspar granite. Quartz and perthitic feldspar are principal phases, accompanied by minor amounts of plagioclase, biotite (<5%) and other accessory minerals. In addition, many contain abundant miarolitic cavities which suggest that they were emplaced at shallow levels with extensive fractional crystallization. Geochemically, the granites are silica-rich, peraluminous and have high contents of alkalis. They invariably show enrichment in light rare earth elements (LREE) and significant negative Eu anomalies. All the granitic rocks demonstrate the characteristic negative anomalies in Ba, Nb, Sr, P, Eu, and Ti, and a positive anomaly in Pb in the spidergram.

The emplacement of the Xinhuatun pluton took place at 184±4 Ma as revealed by zircon SHRIMP U–Pb data. This is also supported by the slightly younger Rb–Sr whole-rock (WR) isochron age of 173±3 Ma. A whole-rock (WR) Rb–Sr isochron age of 154±3 Ma was obtained for the Lamashan pluton, which is interpreted as close to the time of emplacement. The Yiershi pluton was intruded at about 140 Ma as evidenced by a zircon U–Pb age of 137±2 Ma and WR Rb–Sr isochron age of 143±5 Ma. Biotite-WR Rb–Sr isochrons and ⁴⁰Ar/³⁹Ar ages of feldspars allow us to estimate the cooling rate of each pluton.

Geochemical data suggest that the rocks are highly fractionated I-type granites. Fractionation of biotite and feldspars was the principal process of magmatic differentiation and responsible for major element variation. Rb, Sr and Ba concentrations were controlled by feldspar separation, whereas REE elements were fractionated by accessory minerals, such as apatite, allanite and monazite.     

The Cretaceous Ofuku Pluton and Its Relation to Mineralization in the Western Akiyoshi Plateau,Yamaguchi Prefecture,Japan

The relationship between the magmatism of the Cretaceous Ofuku pluton and mineralization in and around the Akiyoshi Plateau, Yamaguchi Prefecture, Japan was investigated using a combination of field observation, petrographic and geochemical analyses, K–Ar geochronology, and fluid inclusion data. The Ofuku pluton has a surface area of 1.5 × 1.0 km, and was intruded into the Paleozoic accretionary complexes of the Akiyoshi Limestone, Ota Group and Tsunemori Formation in the western part of the Akiyoshi Plateau. The pluton belongs to the ilmenite‐series and is zoned, consisting mainly of early tonalite and granodiorite that share a gradational contact, and later granite and aplite that intruded the tonalite and granodiorite. Harker diagrams show that the Ofuku pluton has intermediate to silicic compositions ranging from 60.4 to 77.9 wt.% SiO₂, but a compositional gap exists between 70.5 to 73.4 wt.% SiO₂ (anhydrous basis). Modal and chemical variations indicate that the assumed parental magma is tonalitic. Quantitative models of fractional crystallization based on mass balance calculations and the Rayleigh fractionation model using major and trace element data for all crystalline phases indicate that magmatic fractionation was controlled mainly by crystal fractionation of plagioclase, hornblende, clinopyroxene and orthopyroxene at the early stage, and quartz, plagioclase, biotite, hornblende, apatite, ilmenite and zircon at the later stage. The residual melt extracted from the granodiorite mush was subsequently intruded into the northern and western parts of the Ofuku pluton as melt lens to form the granite and aplite. The age of the pluton was estimated at 99–97 Ma and 101–98 Ma based on K–Ar dating of hornblende and biotite, respectively. Both ages are consistent within analytical error, indicating that the Ofuku pluton and the associated Yamato mine belong to the Tungsten Province of the San‐yo Belt, which is genetically related to the ilmenite‐series granitoids of the Kanmon to Shunan stages. The aplite contains Cl‐rich apatite and REE‐rich monazite‐(Ce), allanite‐(Ce), xenotime and bastnäsite‐(Ce), indicating that the residual melt was rich in halogens and REEs. The tonalite–granodiorite of the Ofuku pluton contains many three‐phase fluid inclusions, along with daughter minerals such as NaCl and KCl, and vapor/liquid (V/L) volume ratios range from 0.2 to 0.9, suggesting that the fluid was boiling. In contrast, the granite and aplite contain low salinity two‐phase inclusions with low V/L ratios. The granodiorite occupies a large part of the pluton, and the inclusions with various V/L ratios with chloride daughter minerals suggest the boiling fluids might be related to the mineralization. This fluid could have carried base metals such as Cu and Zn, forming Cu ore deposits in and around the Ofuku pluton. The occurrence and composition of fluid inclusions in the igneous rocks from the Akiyoshi Plateau are directly linked to Cu mineralization in the area, demonstrating that fluid inclusions are useful indicators of mineralization.     

Monazite as a monitor for melt‐rock interaction during cooling and exhumation

Granulite facies cordierite–garnet–biotite gneisses from the southeastern Reynolds Range, central Australia, contain both orthopyroxene‐bearing and orthopyroxene‐free quartzofeldspathic leucosomes. Mineral reaction microstructures at the interface of gneiss and leucosome observed in outcrop and petrographically, reflect melt‐rock interaction during crystallization. Accessory monazite, susceptible to fluid alteration, dissolution and recrystallization at high temperature, is tested for its applicability to constrain the chemical and P–T–time evolution of melt‐rock reactions during crystallization upon cooling. Bulk rock geochemistry and phase equilibria modelling constrain peak pressure and temperature conditions to 6.5–7.5 kbar and ~850°C, and U–Pb geochronology constrains the timing of monazite crystallization to 1.55 Ga, coeval with the Chewings Orogeny. Modelling predicts the presence of up to 15 vol.% melt at peak metamorphic conditions. Upon cooling below 800°C, melt extraction and in situ crystallization of melt decrease the melt volume to less than 7%, at which time it becomes entrapped and melt pockets induce replacement reactions in the adjacent host rock. Replacement reactions of garnet, orthopyroxene and K‐feldspar liberate Y, REE, Eu and U in addition to Mg, Fe, Al, Si and K. We demonstrate that distinguishing between monazite varieties solely on the basis of U–Pb ages cannot solve the chronological order of events in this study, nor does it tie monazite to the evolution of melt or stability of rock‐forming minerals. Rather, we argue that analyses of various internal monazite textures, their composition and overprinting relations allow us to identify the chronology of events following the metamorphic peak. We infer that retrograde reactions involving garnet, orthopyroxene and K‐feldspar can be attributed to melt‐rock interaction subsequent to partial melting, which is reflected in the development of compositionally distinct monazite textural domains. Internal monazite textures and their composition are consistent with dissolution and precipitation reactions induced by a high‐T melt. Monazite rims enriched in Y, HREE, Eu and U indicate an increased availability of these elements, consistent with the breakdown of orthopyroxene, garnet and K‐feldspar observed petrographically. Our study indicates that compositional and textural analysis of monazite in relation to major rock‐forming minerals can be used to infer the post‐peak chemical evolution of partial melts during high‐ to ultrahigh‐temperature metamorphism.     

Petrogenesis of angrites

The recent discovery of two new angrites, Sahara 99555 and D'Orbigny, has revived interest in this small group of achondrites. We measured trace element abundances in the individual minerals of these two angrites and compared them with the three Antarctic angrites, LEW 86010, LEW 87051 and Asuka 881371. Trace element variations in four of these meteorites (LEW 87051, Asuka 881371, Sahara 99555 and D'Orbigny) indicate rapid crystallization under near closed system conditions, consistent with their mineralogical and textural features. All four appear to be closely related and crystallized from very similar magmas. Discrepancies between their bulk REE compositions and melts calculated to be in equilibrium with the major phases may be due in part to kinetic effects of rapid crystallization. Prior crystallization of olivine and/or plagioclase may also account for the elevated parent melt composition of clinopyroxene in some of the angrites such as Asuka 881371.LEW 86010 also crystallized from a melt and represents a liquid composition, but trace element trends in clinopyroxene and olivine differ from those of the other angrites. This meteorite seems to have crystallized from a different source magma.     

硅酸盐-盐（硫酸盐）流体不混溶：蒙古南部Mushugai-Khuduk含火成碳酸岩杂岩体矿物中的熔体包裹体研究

Crystalline and melt inclusions were studied in garnet,diopside,potassium feldspar,and sphene from the garnet syenite porphyry of the carbonatite-bearing complex Mushugai-Khuduk,southern Mongolia.Phlogopite,clinopyroxene,albite,potassium feldspar,spheric,wollastonite,magnetite,Ca and Sr sulfates,fluorite,and apatite were identified among the crystalline inclusions. The melt inclusions were homogenized at 1010～1080℃and analyzed on an electron microprobe.Silicate,salt,and combined silicate- salt melt inclusions were found.Silicate melts show considerable variations in SiO_2 concentration(56 to 66wt% ),high Na_2O K_2O (up to 17wt% ),and elevated Zr,F,and C1 contents.In terms of bulk rock chemistry,the silicate melts are alkali syenites.During thermometric experiments,salt melt inclusions quenched into homogeneous glasses of predominantly sulfate compositions containing no more than 1.3wt% SiO_2.These melts are enriched in alkalis,Ba,Sr,P,F,and C1.The investigation of the silicate and salt melt inclusions in minerals of the garnet syenite porphyries indicate that these rocks were formed under influence of the processes of crystallization differentiation and magma separation into immiscible silicate and salt(sulfate)liquids.     

Geochemical and Sm–Nd isotopic study of titanite from granitoid rocks of the eastern Dharwar craton,southern India

Titanite occurs as an accessory phase in a variety of igneous rocks, and is known to concentrate geologically important elements such as U, Th, rare earth element (REE), Y and Nb. The differences in the abundances of the REEs contained in titanite from granitoid rocks could reflect its response to changes in petrogenetic variables such as temperature of crystallization, pressure, composition, etc. Widespread migmatization in the granodiorite gneisses occurring to the east of Kolar and Ramagiri schist belts of the eastern Dharwar craton resulted in the enrichment of the REEs in titanite relative to their respective host rocks. A compositional influence on the partitioning of REEs between titanite and the host rock/magma is also noticed. The relative enrichment of REEs in titanite from quartz monzodiorite is lower than that found in the granodioritic gneiss. Depletion of REE and HFSE (high field-strength elements) abundances in granitic magmas that have equilibrated with titanite during fractional crystallization or partial melting has been modelled. As little as 1% of titanite present in residual phases during partial melting or in residual melts during fractional crystallization can significantly lower the abundances of trace elements such as Nb, Y, Zr and REE which implies the significance of this accessory mineral as a controlling factor in trace element distribution in granitoid rocks. Sm–Nd isotope studies on titanite, hornblende and whole rock yield isochron ages comparable to the precise U–Pb titanite ages, invoking the usefulness of Sm–Nd isochron ages involving minerals like titanite.