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1.
The Zargat Na’ am ring complex crops out 90 km NW of Shalatin City in the Southeastern Desert of Egypt. The ring complex forms a prominent ridge standing high above the surrounding mafic-ultramafic hills. It is cut by two sets of joints and faults which strike predominantly NNW-SSE and E-W, and is injected by dikes, porphyritic alkaline syenites, and felsite porphyries. It consists of alkali syenites, alkali quartz syenites, and peralkaline arfvedsonite-bearing granitic and pegmatitic dikes and sills. The complex is characterized locally by extreme enrichments in REEs, wolframite and rare, high field strength metals (HFSM), such as Zr and Nb. The highest concentrations (1.5 wt% Zr, 0.25 wt% Nb, 0.6 wt% Σ REEs) occur in aegirine-albite aplites that formed around arfvedsonite pegmatites. Quartzhosted melt inclusions in arfvedsonite granite and pegmatite provide unequivocal evidence that the peralkaline compositions and rare metal enrichments are primary magmatic features. Glass inclusions in quartz crystals also have high concentrations of incompatible trace elements including Nb (750 ￠ 10−6), Zr (2500 × 10−6) and REEs (1450 × 10−6). The REEs, Nb and Zr compositions of the aegirine-albite aplites plot along the same linear enrichment trends as the melt inclusions, and Y/Ho ratios mostly display unfractionated, near-chondritic values. The chemical and textural features of the aegirine-albite aplites are apparently resultant from rapid crystallization after volatile loss from a residual peralkaline granitic melt similar in composition to the melt inclusions.  相似文献   

2.
The Abu Dom complex is one of a cluster of Younger Granite ring-complexes piercing the Proterozoic gneisses of the Bayuda Desert of Sudan. Intrusive rocks predominate and range from early metaluminous syenites to later peralkaline syenites and granites. They are disposed as ring-dykes, nested intrusions, and cone-sheet swarms. Field evidence and geochemical variation indicate that the peralkaline rocks evolved from a metaluminous syenitic parent magma as a result of high-level fractionation. The suite carries a clear within-plate signature exemplified by marked enrichments in HFS elements such as Zr and Nb.  相似文献   

3.
塔里木巴楚小海子正长岩杂岩体的岩石成因探讨   总被引：6，自引：4，他引：2  
位荀  徐义刚 《岩石学报》2011,27(10):2984-3004
巴楚小海子正长岩杂岩体是二叠纪塔里木大火成岩省的重要组成部分.SIMS锆石U-Pb定年显示其形成于279.7±2.0Ma,与本区辉绿岩脉和石英正长斑岩岩脉近于同时侵位.根据矿物学特征,小海子正长岩体可分为铁橄榄石正长岩和角闪正长岩两类.前者主要由碱性长石、铁橄榄石、单斜辉石、角闪石和少量石英、斜长石组成,后者主要由碱性长石、角闪石、黑云母和少量的石英、斜长石组成.小海子正长岩体为铁质、碱性系列,轻稀土相对富集,重稀土亏损,具有明显的Eu正异常,无Nb、Ta负异常,相对低的(87Sr/86Sr);(0.7033 ～0.7038)和正的εNd(t)值(+3.1～+3.8),暗示它们来自亏损的地幔源区,没有地壳物质的加入.主微量和同位素地球化学分析,暗示巴楚小海子正长岩的母岩浆为碱性的幔源玄武质岩浆经橄榄石、单斜辉石分离结晶后的残余熔体,并且含有堆晶的碱性长石.这种含有碱性长石堆晶的熔体,在相对还原的条件下结晶,形成铁橄榄石正长岩;在相对氧化的条件下结晶,并经过不同程度斜长石的分离结晶形成角闪正长岩.  相似文献   

4.
We remelted and analyzed crystallized silicate melt inclusions in quartz from a porphyritic albite-zinnwaldite microgranite dike to determine the composition of highly evolved, shallowly intruded, Li- and F-rich granitic magma and to investigate the role of crystal fractionation and aqueous fluid exsolution in causing the extreme extent of magma differentiation. This dike is intimately associated with tin- and tungsten-mineralized granites of Zinnwald, Erzgebirge, Germany. Prior research on Zinnwald granite geochemistry was limited by the effects of strong and pervasive greisenization and alkali-feldspar metasomatism of the rocks. These melt inclusions, however, provide important new constraints on magmatic and mineralizing processes in Zinnwald magmas.The mildly peraluminous granitic melt inclusions are strongly depleted in CAFEMIC constituents (e.g., CaO, FeO, MgO, TiO2), highly enriched in lithophile trace elements, and highly but variably enriched in F and Cl. The melt inclusions contain up to several thousand ppm Cl and nearly 3 wt% F, on average; several inclusions contain more than 5 wt% F. The melt inclusions are geochemically similar to the corresponding whole-rock sample, except that the former contain much more F and less CaO, FeO, Zr, Nb, Sr, and Ba. The Sr and Ba abundances are very low implying the melt inclusions represent magma that was more evolved than that represented by the bulk rock. Relationships involving melt constituents reflect increasing lithophile-element and halogen abundances in residual melt with progressive magma differentiation. Modeling demonstrates that differentiation was dominated by crystal fractionation involving quartz and feldspar and significant quantities of topaz and F-rich zinnwaldite. The computed abundances of the latter phases greatly exceed their abundances in the rocks, suggesting that the residual melt was separated physically from phenocrysts during magma movement and evolution.Interactions of aqueous fluids with silicate melt were also critical to magma evolution. To better understand the role of halogen-charged, aqueous fluids in magmatic differentiation and in subsequent mineralization and metasomatism of the Zinnwald granites, Cl-partitioning experiments were conducted with a F-enriched silicate melt and aqueous fluids at 2,000 bar (200 MPa). The results of the experimentally determined partition coefficients for Cl and F, the compositions of fluid inclusions in quartz and other phenocrysts, and associated geochemical modeling point to an important role of magmatic-hydrothermal fluids in influencing magma geochemistry and evolution. The exsolution of halogen-charged fluids from the Li- and F-enriched Zinnwald granitic magma modified the Cl, alkali, and F contents of the residual melt, and may have also sequestered Li, Sn, and W from the melt. Many of these fluids contained strongly elevated F concentrations that were equivalent to or greater than their Cl abundances. The exsolution of F-, Cl-, Li-, ± W- and Sn-bearing hydrothermal fluids from Zinnwald granite magmas was important in effecting the greisenizing and alkali-feldspathizing metasomatism of the granites and the concomitant mineralization.Editorial Handling: B. Lehmann  相似文献   

5.
Baerzhe Be–Nb–Zr–REE deposit is hosted in alkaline granite (125 Ma) which intrudes in the late Jurassic Baiyingaolao Formation in the middle of the Great Hinggan Metallogenic Belt in China. The ore‐forming granite consists of three lithological facies: arfvedsonite‐bearing alkaline granite at the bottom, aegirine‐bearing albite aplite in the middle and pegmatite crust on the top. The albite aplite is the main orebody. We recognized three magmatic‐hydrothermal stages: orthomagmatic stage, late‐magmatic stage and hydrothermal stage, with the late‐magmatic stage being divided into two substages, the pegmatite substage and the aplite substage. Petrographic study on the granite, the microthermometric study on fluid inclusions and in situ laser‐ablation inductively coupled plasma mass spectrometry analysis for quartz‐hosted melt inclusions reveal the process of magmatic‐hydrothermal evolution. The finding indicates that primary magma evolved to more peralkaline by fractional crystallization, with synchronously increasing high field strength elements. An extremely high content of Zr and Nb are in the melt inclusions from last stage albite aplite (Zr, min 52 548 ppm, and Nb, min 4104 ppm). This implies that the residual magma directly formed the orebody of rare metal elements. Meanwhile, volatility was increasing during the magma evolution process and F‐bearing aqueous fluid was oversaturated at temperatures higher than 800°C. The separation of fluid from magma caused Li‐REE enrichment in F‐bearing fluid and depletion in residual melt, and led to the difference of the Y/Ho ratio between whole rock compositions and melt inclusion data. Fluid separated into a high‐salinity liquid and a low density vapor phase above 697°C, and enriched REE in the high‐salinity liquid. The oxygen isotope data shows mixing between primary magmatic‐hydrothermal fluid and meteoric water. The ubiquitous pseudo‐secondary fluid inclusions have a wide range of salinity below 462°C, which is similar to the melting temperatures of REE‐bearing daughter minerals. A model involving the mixing by meteoric water could be a mechanism for precipitation of REE minerals.  相似文献   

6.
The Neoproterozoic pluton of Gabal Gharib granite Eastern Desert of Egypt is intruded in subduction-related calc-alkaline granitic rocks of granodiorite to adamellite composition. A zone of metasomatized granite was developed along the contacts at the expense of the calc-alkaline granite. The granite of Gabal Gharib is hypersolvus, composed mainly of orthoclase-microperthite, quartz, and interstitial arfvedsonite. Fluorite, zircon, ilmenite, allanite, and astrophyllite are the main accessories. Pegmatite pods as well as miarolitic cavities (mineral-lined cavities) are common and ranging in size from a few millimeters to 50?cm. Rare-metal minerals such as columbite, cassiterite, and fluorite have been identified from the miarolitic cavities. Geochemical studies revealed that Gabal Gharib granite is a highly fractionated granite, homogeneous in composition, with high contents of SiO2, and alkalis, high Ga/Al, and Fe/Mg ratios, and low concentrations of Al, Mg, and CaO relative to granodiorite?Cadamellite country rocks. Gabal Gharib granite is metaluminous to peralkaline with ASI (0.94?C1.07). Trace element characteristics of Gabal Gharib granite include abundances of Rb, Nb, Ta, Sn, Th, U, Y, Ga, Zn, rare earth elements (REEs, except Eu), and F, and depletion in Sr, and Ba relative to granodiorite?Cadamellite country rocks. It has the geochemical characteristic of anorogenic A-type granite. The uniform trends of differentiation, normal REE distribution patterns, and low calculated tetrad effects of REE (<0.2) indicate that the effect of post-magmatic subsolidus processes were minimal in the studied granite. Fluid inclusions were studied in quartz crystals from Gabal Gharib granite, quartz pods, and metasomatized granite. The study revealed the presence of high-temperature (480?C550°C), high-salinity (19.45?C39.13?wt.% NaCl eq.) primary inclusions in both metasomatized and rare-metal granites coexisting with melt inclusions and medium-temperature (350?C450°C), medium-salinity (10?C16?wt.% NaCl esq.) aqueous inclusions coexisting hydrocarbon-bearing inclusions. Hydrocarbon is represented by magmatic CH4 in Gabal Gharib granite, while heavier aliphatic compounds may be present in quartz pods. Melt inclusions with temperatures of homogenization >600°C were also reported. Petrographic, geochemical, and fluid inclusion studies constrain that the peralkaline anorogenic granite of Gabal Gharib was derived from highly evolved magma probably originated by fractional crystallization of mantle source.  相似文献   

7.
I. A. Andreeva 《Petrology》2016,24(5):462-476
Melt inclusions were studied by various methods, including electron and ion microprobe analysis, to determine the compositions of melts and mechanisms of formation of rare-metal peralkaline granites of the Khaldzan Buregtey massif in Mongolia. Primary crystalline and coexisting melt inclusions were found in quartz from the rare-metal granites of intrusive phase V. Among the crystalline inclusions, we identified potassium feldspar, albite, tuhualite, titanite, fluorite, and diverse rare-metal phases, including minerals of zirconium (zircon and gittinsite), niobium (pyrochlore), and rare earth elements (parisite). The observed crystalline inclusions reproduce almost the whole suite of major and accessory minerals of the rare-metal granites, which supports the possibility of their crystallization from a magmatic melt. Melt inclusions in quartz from these rocks are completely crystallized. Their daughter mineral assemblage includes quartz, microcline, aegirine, arfvedsonite, polylithionite, a zirconosilicate, pyrochlore, and a rare-earth fluorocarbonate. The melt inclusions were homogenized in an internally heated gas vessel at a temperature of 850°C and a pressure of 3 kbar. After the experiments, many inclusions were homogeneous and consisted of silicate glass. In addition to silicate glass, some inclusions contained tiny quench zircon crystals confined to the boundary of inclusions, which indicates that the melts were saturated in zircon. In a few inclusions, glass coexisted with a CO2 phase. This allowed us to estimate the content of CO2 in the inclusion as 1.5 wt %. The composition of glasses from the homogeneous melt inclusions is similar to the composition of the rare-metal granites, in particular, with respect to SiO2 (68–74 wt %), TiO2 (0.5–0.9 wt %), FeO (2.2–4.6 wt %), MgO (0.02 wt %), and Na2O + K2O (up to 8.5 wt %). On the other hand, the glasses of melt inclusions appeared to be strongly depleted compared with the rocks in CaO (0.22 and 4 wt %, respectively) and Al2O3 (5.5–7.0 and 9.6 wt %, respectively). The agpaitic index is 1.1–1.7. The melts contain up to 3 wt % H2O and 2–4 wt % F. The trace element analysis of glasses from homogenized melt inclusions in quartz showed that the rare-metal granites were formed from extensively evolved rare-metal alkaline melts with high contents of Zr, Nb, Th, U, Ta, Hf, Rb, Pb, Y, and REE, which reflects the metallogenic signature of the Khaldzan Buregtey deposit. The development of unique rare metal Zr–Nb–REE mineralization in these rocks is related to the prolonged crystallization differentiation of melts and assimilation of enclosing carbonate rocks.  相似文献   

8.
To determine the pre-eruptive composition of peralkaline magma at Frantale volcano, Ethiopia, we have studied glass inclusions in phenocrysts from a lateceupting, glassy pantelleritic lava flow. Matrix glass and crystal-free glass inclusions in quartz were analyzed for all major and most minor elements by electron microprobe and for H2O and 15 lithophile trace elements by ion microprobe (SIMS). Compositions of inclusions may have been slightly modified by post-trapping quartz crystallization, the average concentrations of all constituents but silica may be artificially high by 10% relative. Glass inclusions contain extreme enrichments in H2O (mean of 4.6 to 4.9 wt%) and several lithophile trace elements, which suggest that the lava erupted from a highly evolved, water-rich fraction of magma. The pre-eruptive concentration of water was much higher than that generally considered to occur in pantellerite magmas. Trends observed for lithophile elements in whole-rock samples from pre-,syn-and post-caldera eruptive units are mimicked in glass inclusions from the studied pantellerite lava; concentrations of Rb, Y, Zr, Nb, and Ce±Cl increase with progressive differentiation. With the exception of Cl and H2O contents, the composition of matrix glass is similar to that of glass inclusions suggesting: that few constituents exsolved from magma or cooling glass; eruption and quench of the lava occurred rapidly; and the matrix glass is, largely, compositionally representative of melt. Higher average abundances of Cl and H2O in glass inclusions suggest that these volatiles exsolved after melt entrapment; degassing could have occurred as either an equilibrium or disequilibrium process.  相似文献   

9.
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.  相似文献   

10.
We report new geological, mineralogical, geochemical and geochronological data about the Katugin Ta-Nb-Y-Zr (REE) deposit, which is located in the Kalar Ridge of Eastern Siberia (the southern part of the Siberian Craton). All these data support a magmatic origin of the Katugin rare-metal deposit rather than the previously proposed metasomatic fault-related origin. Our research has proved the genetic relation between ores of the Katugin deposit and granites of the Katugin complex. We have studied granites of the eastern segment of the Eastern Katugin massif, including arfvedsonite, aegirine-arfvedsonite and aegirine granites. These granites belong to the peralkaline type. They are characterized by high alkali content (up to 11.8 wt% Na2O + K2O), extremely high iron content (FeO1/(FeO1 + MgO) = 0.96–1.00), very high content of most incompatible elements – Rb, Y, Zr, Hf, Ta, Nb, Th, U, REEs (except for Eu) and F, and low concentrations of CaO, MgO, P2O5, Ba, and Sr. They demonstrate negative and CHUR-close εNd(t) values of 0.0…−1.9. We suggest that basaltic magmas of OIB type (possibly with some the crustal contamination) represent a dominant part of the granitic source. Moreover, the fluorine-enriched fluid phases could provide an additional source of the fluorine. We conclude that most of the mineralization of the Katugin ore deposit occurred during the magmatic stage of the alkaline granitic source melt. The results of detailed mineralogical studies suggest three major types of ores in the Katugin deposit: Zr mineralization, Ta-Nb-REE mineralization and aluminum fluoride mineralization. Most of the ore minerals crystallized from the silicate melt during the magmatic stage. The accessory cryolites in granites crystallized from the magmatic silicate melt enriched in fluorine. However, cryolites in large veins and lens-like bodies crystallized in the latest stage from the fluorine enriched melt. The zircons from the ores in the aegirine-arfvedsonite granite have been dated at 2055 ± 7 Ma. This age is close to the previously published 2066 ± 6 Ma zircon age of the aegirine-arfvedsonite granites, suggesting that the formation of the Katugin rare-metal deposit is genetically related to the formation of peralkaline granites. We conclude that Katugin rare-metal granites are anorogenic. They can be related to a Paleoproterozoic (∼2.05 Ga) mantle plume. As there is no evidence of the 2.05 Ga mantle plume in other areas of southern Siberia, we suggest that the Katugin mineralization occurred on the distant allochtonous terrane, which has been accreted to Siberian Craton later.  相似文献   

11.
新疆拜城县波孜果尔A型花岗岩类为富含铌、钽、锆等有用元素的含矿岩体。通过偏光显微镜、电子探针(EPMA)化学成分分析、电子探针背散射(BSE)对波孜果尔A型花岗岩类的矿物学特征进行了研究,并对岩浆形成的温度条件与构造背景进行了讨论。结果表明,波孜果尔A型花岗岩类包括霓石钠闪石英碱性长石正长岩、霓石钠闪碱性长石花岗岩、黑云母碱性长石正长岩3种岩石类型。主要造岩矿物包括石英、钠长石、钾长石、霓石、钠铁闪石和铁叶云母。副矿物包括锆石、烧绿石、钍石、萤石、独居石、氟碳铈镧矿、磷钇矿等。岩浆平均温度832~839℃,形成于非造山的板内构造环境,且具高温、无水、低氧逸度的成岩特点。  相似文献   

12.
峨眉山大火成岩省太和花岗岩的成因及构造意义   总被引：5，自引：0，他引：5  
攀西地区的太和花岗质岩体和赋存超大型钒钛磁铁矿矿床的辉长岩体在空间上共生,成因上均与峨眉山地幔柱头的上升密切相关.太和花岗质岩体主要由超碱质花岗岩和石英正长岩及少量正长岩组成;富含高场强元素并具高Ga/Al值(3.74～5.63),显示典型A型花岗岩的特征.花岗岩、正长岩和辉长岩的Nb/Ta和Zr/Hf值与洋岛玄武岩(OIB)的相应比值近似.花岗质岩石具较低的87Sr/86Sr初始值(0.7025～0.7049)和正的εNd(t)值(1.9～3.5),与辉长岩的值相近[(87Sr/86Sr)i =0.7049～0.7052; εNd(t) =2.4～3.3].太和花岗质岩体的εNd(t)为正值,显示地幔柱来源的底侵玄武质岩浆对其形成起主要作用.辉长质和花岗质岩石具相似的钕同位素组成,表明其母岩浆来自于同一源区.我们认为太和花岗质侵入体主要由底侵于下地壳的玄武质岩浆分异出的花岗质熔体侵位及随后经结晶分异而形成.因此,晚古生代时幔源岩浆底侵造成的地壳增生在峨眉山大火成岩省中表现极为显著.  相似文献   

13.
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.  相似文献   


14.
New fieldwork, mineralogical and geochemical data and interpretations are presented for the rare-metal bearing A-type granites of the Aja intrusive complex(AIC) in the northern segment of the Arabian Shield. This complex is characterized by discontinuous ring-shaped outcrops cut by later faulting. The A-type rocks of the AIC are late Neoproterozoic post-collisional granites, including alkali feldspar granite, alkaline granite and peralkaline granite. They represent the outer zones of the AIC, surrounding a core of older rocks including monzogranite, syenogranite and granophyre granite. The sharp contacts between A-type granites of the outer zone and the different granitic rocks of the inner zone suggest that the AIC was emplaced as different phases over a time interval, following complete crystallization of earlier batches. The A-type granites represent the late intrusive phases of the AIC, which were emplaced during tectonic extension, as shown by the emplacement of dykes synchronous with the granite emplacement and the presence of cataclastic features. The A-type granites consist of K-feldspars, quartz, albite, amphiboles and sodic pyroxene with a wide variety of accessory minerals, including Fe-Ti oxides, zircon, allanite, fluorite, monazite, titanite, apatite, columbite, xenotime and epidote. They are highly evolved(71.3–75.8 wt% SiO_2) and display the typical geochemical characteristics of post-collisional, within-plate granites. They are rare-metal granites enriched in total alkalis, Nb, Zr, Y, Ga, Ta, REE with low CaO, MgO, Ba, and Sr. Eu-negative anomalies(Eu/Eu* = 0.17–0.37) of the A-type granites reflect extreme magmatic fractionation and perhaps the effects of late fluid-rock interactions. The chemical characteristics indicate that the A-type granites of the AIC represent products of extreme fractional crystallization involving alkali feldspar, quartz and, to a lesser extent, ferromagnesian minerals. The parent magma was derived from the partial melting of a juvenile crustal protolith with a mantle contribution. Accumulation of residual volatile-rich melt and exsolved fluids in the late stage of the magma evolution produced pegmatite and quartz veins that cut the peripheries of the AIC. Post-magmatic alteration related to the final stages of the evolution of the A-type granitic magma, indicated by alterations of sodic amphibole and sodic pyroxene, hematitization and partial albitization.  相似文献   

15.
Abstract. The REE-mineralized alkaline granites in Egypt are divided into the following three classes: (1) Mesozoic, anorogenic nepheline syenite ring complexes with REE amounting up to 1.3 %, particularly in their fenitized parts (e.g. Abu Khruq), (2) an orogenic peralkaline syenite-granite, composed of i) Zr, Nb, - REE, and Th-enriched peralkaline granite-syenite complexes with REE amounting up to 0.5 % (e.g. Um Hibal, Tarbite North and South, Gharib, and Zarget Naam) and ii) Y, Th, HREE, and P-enriched post-Cretaceous peralkaline complexes that intrude the Phanerozoic rocks of the Southwestern Desert with REE amounting up to 2 % (e.g. Gara El Hamra), and (3) upper Proterozoic, post-orogenic siderophyllite alkali feldspar granite with REE amounting up to 0.8 %, particularly in their apical miarolitic pegmatites and albitized zones (e.g. Kadabora-Abu Dob and Um Naggat). Special attention is given to the Abu Khruq and Gara El Hamra granitic bodies.  相似文献   

16.
The Boziguoer A-type granitoids in Baicheng County,Xinjiang,belong to the northern margin of the Tarim platform as well as the neighboring EW-oriented alkaline intrusive rocks.The rocks comprise an aegirine or arfvedsonite quartz alkali feldspar syenite,an aegirine or arfvedsonite alkali feldspar granite,and a biotite alkali feldspar syenite.The major rock-forming minerals are albite,K-feldspar,quartz,arfvedsonite,aegirine,and siderophyllite.The accessory minerals are mainly zircon,pyrochlore,thorite,fluorite,monazite,bastnaesite,xenotime,and astrophyllite.The chemical composition of the alkaline granitoids show that SiO2 varies from 64.55％ to 72.29％ with a mean value of 67.32％,Na2O＋K2O is high （9.85％-11.87％） with a mean of 11.14％,K2O is 2.39％-5.47％ （mean =4.73％）,the K2O/Na2O ratios are 0.31-0.96,Al2O3 ranges from 12.58％ to 15.44％,and total FeOT is between 2.35％ and 5.65％.CaO,MgO,MnO,and TiO2 are low.The REE content is high and the total SREE is （263-1219） ppm （mean =776 ppm）,showing LREE enrichment and HREE depletion with strong negative Eu anomalies.In addition,the chondrite-normalized REE patterns of the alkaline granitoids belong to the ＂seagull＂ pattern of the right-type.The Zr content is （113-1246） ppm （mean =594 ppm）,Zr＋Nb＋Ce＋Y is between （478-2203） ppm with a mean of 1362 ppm.Furthermore,the alkaline granitoids have high HFSE （Ga,Nb,Ta,Zr,and Hf） content and low LILE （Ba,K,and Sr） content.The Nb/Ta ratio varies from 7.23 to 32.59 （mean =16.59） and the Zr/Hf ratio is 16.69-58.04 （mean =36.80）.The zircons are depleted in LREE and enriched in HREE.The chondrite-normalized REE patterns of the zircons are of the ＂seagull＂ pattern of the left-inclined type with strong negative Eu anomaly and without a Ce anomaly.The Boziguoer A-type granitoids share similar features with A1-type granites.The average temperature of the granitic magma was estimated at 832-839℃.The Boziguoer A-type granitoids show crust-mantle mixing and may have formed in an anorogenic intraplate tectonic setting under high-temperature,anhydrous,and low oxygen fugacity conditions.  相似文献   

17.
Based on the analysis of data on the composition of melt inclusions in minerals and quenched glasses of igneous rocks, we considered the problems of the formation of peralkaline silicic magmas (i.e., whose agpaitic index, the molar ratio AI = (Na2O + K2O)/Al2O3, is higher than one). The mean compositions of peralkaline silicic melts are reported for island arcs and active continental margins and compared with the compositions of melts from other settings, primarily, intraplate continental areas. Peralkaline silicic rocks are rather common in the latter. Such rocks are rare in island arcs and active continental margins, but agpaitic melts were observed in inclusions in phenocrysts of plagioclase, quartz, pyroxene, and other minerals. Plagioclase fractionation from an alkali-rich melt with AI < 1 is considered as a possible mechanism for the formation of peralkaline silicic melts (Bowen’s plagioclase effect). However, the analysis of available experimental data on plagioclase-melt equilibria showed that natural peralkaline melts are almost never in equilibrium with plagioclase. For the same reason, the melting of the majority of crustal rocks, which usually contain plagioclase, does not produce peralkaline melts. The existence of peralkaline silicic melt inclusions in plagioclase phenocrysts suggests that plagioclase can crystallize from peralkaline melts, and the plagioclase effect may play a certain role. Another mechanism for the formation of peralkaline silicic magmas is the melting of alkali-rich basic and intermediate rocks, including the spilitized varieties of subalkali basalts.  相似文献   

18.
Kerimasi calciocarbonatite consists principally of calcite together with lesser apatite, magnetite, and monticellite. Calcite hosts fluid and S-bearing Na–K–Ca-carbonate inclusions. Carbonatite melt and fluid inclusions occur in apatite and magnetite, and silicate melt inclusions in magnetite. This study presents statistically significant compositional data for quenched S- and P-bearing, Ca-alkali-rich carbonatite melt inclusions in magnetite and apatite. Magnetite-hosted silicate melts are peralkaline with normative sodium-metasilicate. On the basis of our microthermometric results on apatite-hosted melt inclusions and forsterite–monticellite phase relationships, temperatures of the early stage of magma evolution are estimated to be 900–1,000°C. At this time three immiscible liquid phases coexisted: (1) a Ca-rich, P-, S- and alkali-bearing carbonatite melt, (2) a Mg- and Fe-rich, peralkaline silicate melt, and (3) a C–O–H–S-alkali fluid. During the development of coexisting carbonatite and silicate melts, the Si/Al and Mg/Fe ratio of the silicate melt decreased with contemporaneous increase in alkalis due to olivine fractionation, whereas the alkali content of the carbonatite melt increased with concomitant decrease in CaO resulting from calcite fractionation. Overall the peralkalinity of the bulk composition of the immiscible melts increased, resulting in a decrease in the size of the miscibility gap in the pseudoquaternary system studied. Inclusion data indicate the formation of a carbonatite magma that is extremely enriched in alkalis with a composition similar to that of Oldoinyo Lengai natrocarbonatite. In contrast to the bulk compositions of calciocarbonatite rocks, the melt inclusions investigated contain significant amount of alkalis (Na2O + K2O) that is at least 5–10 wt%. The compositions of carbonatite melt inclusions are considered as being better representatives of parental magma composition than those of any bulk rock.  相似文献   

19.
Melt composition control of Zr/Hf fractionation in magmatic processes   总被引：9，自引：0，他引：9  
Zircon (ZrSiO4) and hafnon (HfSiO4) solubilities in water-saturated granitic melts have been determined as a function of melt composition at 800° and 1035°C at 200 MPa. The solubilities of zircon and hafnon in metaluminous or peraluminous melts are orders of magnitude lower than in strongly peralkaline melt. Moreover, the molar ratio of zircon and hafnon solubility is a function of melt composition. Although the solubilities are nearly identical in peralkaline melts, zircon on a molar basis is up to five times more soluble than hafnon in peraluminous melts. Accordingly, calculated partition coefficients of Zr and Hf between zircon and melt are nearly equal for the peralkaline melts, whereas for metaluminous and peraluminous melts DHf/DZr for zircon is 0.5 to 0.2. Consequently, zircon fractionation will strongly decrease Zr/Hf in some granites, whereas it has little effect on the Zr/Hf ratio in alkaline melts or similar depolymerized melt compositions.The ratio of the molar solubilities of zircon and hafnon for a given melt composition, temperature, and pressure is proportional to the Hf/Zr activity coefficient ratio in the melt. The data imply that this ratio is nearly constant and probably close to unity for a wide range of peralkaline and similar depolymerized melts. However, it changes by a factor of two to five over a relatively small interval of melt compositions when a nearly fully polymerized melt structure is approached. For most ferromagnesian minerals in equilibrium with a depolymerized melt, DHf > DZr. Typical values of DHf/DZr range from 1.5 to 2.5 for clinopyroxene, amphibole, and titanite. Because of the change in the Hf/Zr activity ratio in the melt, the relative fractionation of Zr and Hf by these minerals will disappear or even be reversed when the melt composition approaches that of a metaluminous or peraluminous granite. It is thus not surprising that fractional crystallization of such granitic magmas leads to a decrease in Zr/Hf, whereas fractional crystallization of depolymerized melts tends to increase Zr/Hf. There is no need to invoke fluid metasomatism to explain these effects. Results demonstrate that for ions with identical charge and nearly identical radius, crystal chemistry does not alone determine relative compatibilities. Rather, the effect of changing activity coefficients in the melt may be comparable to or even larger than elastic strain effects in the crystal lattice.  相似文献   

20.
The South Dehgolan pluton, in NW Iran was emplaced into the Sanandaj–Sirjan magmatic–metamorphic zone. This composite intrusion comprises three main groups: (1) monzogabbro–monzodiorite rocks, (2) quartz monzonite–syenite rocks, and (3) a granite suite which crops out in most of the area. The granites generally show high SiO2 content from 72.1%–77.6 wt.% with diagnostic mineralogy consisting of biotite and amphibole along the boundaries of feldspar–quartz crystals which implies anhydrous primary magma compositions. The granite suite is metaluminous and distinguished by high FeOt/MgO ratios (av. 9.6 wt.%), typical of ferroan compositions with a pronounced A‐type affinity with high Na2O + K2O contents, high Ga/Al ratios, enrichment in Zr, Nb, REE, and depletion in Eu. The quartz monzonite–syenites show intermediate SiO2 levels (59.8%–64.5 wt.%) with metaluminous, magnesian to ferroan characteristics, intermediate Na2O + K2O contents, enrichment in Zr, Nb, REE, Ga/Al, and depletion in Eu. The monzogabbro–monzodiorites show overall lower SiO2 content (48.5%–55.9 wt.%) with metaluminous and calc‐alkaline compositions, relatively lower Na2O + K2O contents, low Ga/Al ratios, and FeOt/MgO (av. 1.6 wt.%) ratios, low abundances of Zr, Nb, and lower REE element concentrations relative to the granites and quartz monzonite–syenites. These geochemical differences among the three different rocks suites are likely to indicate different melt origins. We suggest that the South Dehgolan pluton resulted from a change in the geodynamic regime, from compression to extension in the Sanandaj–Sirjan zone during Mesozoic subduction of the Neo‐Tethys oceanic crust beneath the Central Iranian microcontinent. Copyright © 2015 John Wiley & Sons, Ltd.  相似文献   

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