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1.
The profound geochemical conseqences of accessory phase behaviour during partial melting of highgrade metapelites are demonstrated with reference to two geochemically distinct crustal melts produced by biotite dehydration melting reactions under granulite facies (kbar, 860°CC) conditions. These two leucogneiss suites, from the Brattstrand Bluffs coastline, eastern Antarctica, have similar field relations, transport distances (10–100 s of metres) and major element chemistry. Type 1 leucogneisses have low Zr, Th and LREE, positive Eu anomalies and Zr/Zr* and LREEt/LREEt * values less than 1.0 (i.e. less than required to saturate the melt). Mass balance constraints suggest that these melts have been extracted before equilibration with host melanosomes. The dry, peraluminous nature of vapour-undersaturated melts inhibits monazite and zircon solubility and results in concentration of these phases in the residue. Melts are consequently depleted in LREE and HREE. Melanosomes show complementary enrichment in LREE, while HREE patterns are dominated by residual garnet. Type 2 leucogneisses, in contrast, have strongly enriched Zr, Th and LREE abundances, negative Eu anomalies and Zr/Zr* and LREEt/LREEt *>1 resulting from accessory phase entrainment. Vapour-absent partial melting under moderate (6–8 kbar) pressure granulite-facies conditions of a pelitic source containing monazite is likely to give disequilibrium melts depleted in LREE and HREE as monazite and garnet are concentrated in the residue. If temperatures are high enough (850–870° C) to permit relatively large degrees of partial melting then the feldspar component of the source will be removed almost completely, giving melts with large positive Eu anomalies. Melts formed under vapour-present conditions are unlikely to show such extreme LREE and HREE depletion or positive Eu anomalies, even at high degrees of partial melting. Disequilibrium melting coupled with source entrainment could fortuitously produce REE and trace element signatures similar to those typical of S-type granites and usually ascribed to equilibrium melting conditions.  相似文献   

2.
The distribution of REE minerals in metasedimentary rocks was investigated to gain insight into the stability of allanite, monazite and xenotime in metapelites. Samples were collected in the central Swiss Alps, along a well‐established metamorphic field gradient that record conditions from very low grade metamorphism (250 °C) to the lower amphibolite facies (～600 °C). In the Alpine metapelites investigated, mass balance calculations show that LREE are mainly transferred between monazite and allanite during the course of prograde metamorphism. At very low grade metamorphism, detrital monazite grains (mostly Variscan in age) have two distinct populations in terms of LREE and MREE compositions. Newly formed monazite crystallized during low‐grade metamorphism (<440 °C); these are enriched in La, but depleted in Th and Y, compared with inherited grains. Upon the appearance of chloritoid (～440–450 °C, thermometry based on chlorite–choritoid and carbonaceous material), monazite is consumed, and MREE and LREE are taken up preferentially in two distinct zones of allanite distinguishable by EMPA and X‐ray mapping. Prior to garnet growth, allanite acquires two growth zones of clinozoisite: a first one rich in HREE + Y and a second one containing low REE contents. Following garnet growth, close to the chloritoid–out zone boundary (～556–580 °C, based on phase equilibrium calculations), allanite and its rims are partially to totally replaced by monazite and xenotime, both associated with plagioclase (± biotite ± staurolite ± kyanite ± quartz). In these samples, epidote relics are located in the matrix or as inclusions in garnet, and these preserve their characteristic chemical and textural growth zoning, indicating that they did not experience re‐equilibration following their prograde formation. Hence, the partial breakdown of allanite to monazite offers the attractive possibility to obtain in situ ages, representing two distinct crystallization stages. In addition, the complex REE + Y and Th zoning pattern of allanite and monazite are essential monitors of crystallization conditions at relatively low metamorphic grade.  相似文献   

3.
BEA  F. 《Journal of Petrology》1996,37(3):521-552
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  相似文献   

4.
1INTRODUCTION THELATEPRECAMBRIANGRANITOIDSOFTHEARABONU BIANSHIELDINEGYPTWEREEXPOSEDBYEARLYTOMIDDLE TERTIARYUPLIFTANDENSUINGEROSIONDURINGTHEREDSEA RIFTINGEVENT(GREENBERG,1981).THEREAREANUMBER OFEFFECTIVEANDRELATIVELYSUCCESSFULSCHEMESFORTHE CLASSIFICATIONOF…  相似文献   

5.
Paleoproterozoic metapelites of the Vorontsovskaya structure contain accessory REE phosphates (monazite, xenotime, and REE-apatite), fluorine-carbonates (bastnaesite and synchysite), and silicate (allanite). Analysis of phase equilibria involving REE-bearing minerals indicates that bastnaesite is stable only in the greenschist facies and decomposes with the synthesis of monazite at temperatures below the staurolite isograde (490–500°C) at a pressure of 3 kbar. Monazite first appears in the greenschist facies, and its stability expands with increasing temperature, including the granulite facies. A diversity of reaction textures suggests that the mineral is formed in the garnet zone by a reaction of bastnaesite with apatite and by the partial decomposition of REE-bearing chlorite. Monazite is produced in the garnet and staurolite zones by a reaction of allanite with apatite and by a decomposition reaction of REE-bearing apatite.  相似文献   

6.
Rare earth element (REE) and yttrium concentrations of coexisting monazite and xenotime were determined from a suite of seven metapelites from the Variscan fold belt in NE Bavaria, Germany. The metapelites include a continuous prograde, mainly low-P (3–5 kbar) metamorphic profile from greenschist (c. 400 °C) to lower granulite facies conditions (c. 700 °C). The LREE (La–Sm) are incorporated preferentially in monoclinic monazite (REO9 polyhedron), whereas the HREE plus Y are concentrated in tetragonal xenotime (REO8 polyhedron). The major element concentrations of both phases in all rocks are very similar and do not depend on metamorphic grade. Monazite consists mainly of La, Ce and Nd (La0.20–0.23, Ce0.41–0.45, Nd0.15–0.18)PO4, all other elements are below 6 mol%. Likewise, xenotime consists mainly of YPO4 with some Dy and Gd solid solutions (Y0.76–0.80, Dy0.05–0.07, Gd0.04–0.06). In contrast, the minor HREE concentrations in monazite increase strongly with increasing metamorphic grade: Y, Dy and Gd increase by a factor of 3–5 from greenschist to granulite facies rocks. Monazite crystals often show zonation with cores low in HREE and rims high in HREE that is interpreted as growth zonation attained during prograde metamorphism. Similarly, Sm and Nd in xenotimes increase by a factor of 3–4 with increasing metamorphic grade. Prograde zonation in single crystals of xenotime was not observed. The XHREE+Y in monazite and XLREE in xenotime of the seven rocks define two limbs along the strongly asymmetric miscibility gap from c. 400 °C to 700 °C. The empirical calibration of the monazite miscibility gap limb coexisting with xenotime is appropriate for geothermometry. Due to its contents of U and Th, monazite has often been used for U–Pb age determination. The combination of our empirical thermometer on prograde zoned monazite along with possible age determination of zoned single crystals may provide information about prograde branches of temperature–time paths.  相似文献   

7.
邹家山铀矿床伴生重稀土元素的赋存特征   总被引：1，自引：0，他引：1  
初步研究发现,相山矿田邹家山矿床中伴生有较高的重稀土元素,回收这些珍稀的资源和探索其成因具有重要的意义,而查明这些伴生稀土在铀矿床中的赋存特征是前期基础性工作。为此本文采用电子探针和激光剥蚀电感耦合等离子体质谱分析了邹家山铀矿床中稀土元素的赋存状态。结果显示：该矿床稀土矿物主要为独居石、氟碳钙铈矿和磷钇矿;独居石、氟碳钙铈矿的LREE/HREE>1,为轻稀土富集型;而磷钇矿的LREE/HREE<1,为重稀土富集型。沥青铀矿、钛铀矿、铀钍石、铀石、钍石、锆石等铀钍矿物的稀土特征为重稀土富集型;铀钍矿物稀土总量（∑REE+Y）较高,为（3 805.78~65 307.00）×10-6,LREE/HREE<1,为0.01~0.80,平均为0.29。其他伴生矿物磷灰石、钾长石为轻稀土富集型,萤石为轻、重稀土富集型两类都有,而伊利石、黄铁矿的轻重稀土无明显相对富集。重稀土在磷钇矿和铀钍矿物中以类质同象形式存在,少量赋存于伴生矿物。  相似文献   

8.
The REE (Ln), Y, Sc, and Th distribution in the unique complex rare-metal ores of the Tomtor deposit is considered. Significant variability of these components and REE composition is revealed. Ore blocks with elevated Y and HREE contents are identified among prevailing LREE-enriched ores. It is established that the REE variations in the ores are correlated with evolution of REE carriers during epigenetic transformations of the carbonatite weathering products, in particular, with a replacement of Ce-bearing minerals (monazite and florencite) by Y-bearing mineral, xenotime. It is found that LREE and HREE exhibit different behavior during formation of the Tomtor ores, which is expressed in the inert behavior and residual accumulation of Ce-group REE at essential introduction of Y, HREE, Sc, and Th during epigenetic transformation of weathering products of carbonatites, which represent one of the main factors of the formation of the unique rare-metal ores of the Tomtor deposit.  相似文献   

9.
Zircon from a lower crustal metapelitic granulite (Val Malenco, N‐Italy) display inherited cores, and three metamorphic overgrowths with ages of 281 ± 2, 269 ± 3 and 258 ± 4 Ma. Using mineral inclusions in zircon and garnet and their rare earth element characteristics it is possible to relate the ages to distinct stages of granulite facies metamorphism. The first zircon overgrowth formed during prograde fluid‐absent partial melting of muscovite and biotite apparently caused by the intrusion of a Permian gabbro complex. The second metamorphic zircon grew after formation of peak garnet, during cooling from 850 °C to c. 700 °C. It crystallized from partial melts that were depleted in heavy rare earth elements because of previous, extensive garnet crystallization. A second stage of partial melting is documented in new growth of garnet and produced the third metamorphic zircon. The ages obtained indicate that the granulite facies metamorphism lasted for about 20 Myr and was related to two phases of partial melting producing strongly restitic metapelites. Monazite records three metamorphic stages at 279 ± 5, 270 ± 5 and 257 ± 4 Ma, indicating that formation ages can be obtained in monazite that underwent even granulite facies conditions. However, monazite displays less clear relationships between growth zones and mineral inclusions than zircon, hampering the correlation of age to metamorphism. To overcome this problem garnet–monazite trace element partitioning was determined for the first time, which can be used in future studies to relate monazite formation to garnet growth.  相似文献   

10.
This study explores the origin and geochemical evolution ofapatite, monazite, and xenotime along two metamorphic traverses.The first, from the Kigluaik Mountains, Seward Peninsula, Alaska,consists of a localized (85 cm) orthopyroxene–clinopyroxene-bearingdehydration zone. The second consists of orthopyroxene ±clinopyroxene-bearing granulite facies metabasite layers interlayeredwith metapelites over a 3–4 km traverse, along the ValStrona, Ivrea–Verbano Zone, Northern Italy (IVZ). In bothdehydration zones small Th- and U-poor inclusions of monaziteand/or xenotime occur in the apatite. These inclusions are metasomaticallyinduced and nucleated within the apatite via the coupled substitutionsNa+ + (Y + REE)3+ = 2 Ca2+ and Si4+ + (Y + REE)3+ = P5+ + Ca2+.These are not present in apatite from the original amphibolitefacies gneiss. Apatite, in both dehydration zones, also showsa relative increase in both F and Cl compared with apatite fromthe amphibolite facies zone. Granulite facies metabasites inthe IVZ also contain isolated monazite grains, which range fromuniform to complexly zoned in Th the (13–30·1 mol% ThSiO4). These are the product of breakdown and subsequentmobilization of the lanthanides and actinides from monazite-(Ce)in the metapelite layers into the metabasite layers at the startof granulite facies metamorphism. KEY WORDS: apatite; monazite; xenotime; KCl–NaCl brines; metasomatism; phosphate minerals; charnockite–enderbite; granulite facies metamorphism  相似文献   

11.
Zircon populations of Neoproterozoic and early Paleozoic age occur in metabasites of a high-pressure amphibolite-facies unit of the Austroalpine basement south of the Tauern Window. The host rocks for these zircons are eclogitic amphibolites of N-MORB-type character, hornblende gneisses with volcanic-arc basalt signature, and alkaline within-plate-basalt amphibolites. Bulk rock magmatic trace element patterns were preserved during amphibolite-facies high-pressure and subsequent high-temperature events, as well as a greenschist-facies overprint. Positive Ce and negative Eu anomalies and enrichment of HREE in normalized zircon REE patterns, as analysed by LA-ICP-MS, are typical for an igneous origin of these zircon suites. Zircon Y is well correlated to HREE, Ce, Th, U, Nb, and Ta and allows discrimination of compositional fields for each host rock type. Low Th/U ratios are correlated to low Y and HREE abundances in zircon from low bulk Th/U host rocks. This is likely a primary igneous characteristic that cannot be attributed to metamorphic recrystallization. Variations of zircon/host rock element ratios confirm that ionic radii and charges control abundances of many trace elements in zircon. The trace element ratios—presented as mineral/melt distribution coefficients—indicate a selectively inhibited substitution of Zr and Si by HREE and Y in zircon which crystallized from a N-MORB melt. Correlated host rock and zircon trace element concentrations indicate that the metabasite zircons are not xenocrysts but crystallized from mafic melts, represented by the actual host rocks.  相似文献   

12.
Field study of granitic rocks in the Gebel Abu Brush-Dahis (ABD) area, Southeastern Desert, Egypt, shows that they comprise two granitic groups, namely A- and I-type suites. The A type is distinguished mineralogically by abundant orthoclase and sodic plagioclase, ferrohornblende, monazite, and allanite. In contrast, the I type has more hornblende and biotite, which are more magnesian in composition, and less feldspar. The parental magmas of both suites have many similar geochemical characteristics, although the A type has slightly higher alkalis, Zr, Hf, Zn, and LREE, and lower CaO, MgO, Sr, Ni, and Fe+2. The geochemical properties characteristic of leucocratic A-type granites-such as high Ga/Al ratios, Nb, Y, HREE, and F contents-are only manifest in the more felsic members of the A-type suite. These features were produced by 70% fractional crystallization of feldspar, hornblende, quartz, and biotite. Geotectonically, the study revealed that the A-and I-type granites are typical of an arc setting, but the more felsic members of the A-type suite plot in a within-plate regime. Geochemically, the granites are subalkaline and peraluminous to metaluminous. The granodiorites/adamellites (I-type suite) have fractionated LREE and slightly fractionated or nearly flat HREE, with small or no Eu anomalies. The alkali-feldspar granites (A-type suite) have flat REE with large Eu anomalies, except for one sample, which shows increasing LREE and decreasing HREE with large Eu anomalies; the quartz-monzonites have fractionated LREE and nearly flat HREE with no Eu anomaly. The flat HREE and/or HREE enrichment is attributed to involvement of garnet and/or zircon in melt generation at the source.

The uranium and thorium contents in the granitic rocks are present in the accessory minerals—particulary in monazite, titanite, zircon, allanite, fluorite, apatite, and opaques. Anomalous high radioactivity in the bostonite (alkaline) dike as well as uranium mineralization are largely confined to contacts and fracture zones. Uranophane is the characteristic uranium mineral in the oxidation zone. An XRD study of the high anomalies in pegmatite and bostonite reveals that the uranium mineralizations produced uranophane (Usilicate), thorianite, soddyite, zippeite, and becquerelite.  相似文献   

13.
在野外地质调查的基础上,结合室内显微镜观察及电子探针分析测试,对新疆拜城波孜果尔碱性岩中的副矿物的矿物学特征和化学成分进行了研究.发现这些副矿物常以共生组合的形式产在碱性岩中,主要分布在石英二长闪长岩和石英二长岩中.烧绿石中U、Th和REE替代Ca、Na.独居石富含LREE,Th和LREE相互替代;根据独居石中w(La+ Ce) ＞40％和La/Nd比值在1.6～4.5,推断独居石为热液成因.磷钇矿中富含REE,且以HREE为主;w(Th)＞w(U).锆石中Zr/Hf比值在60％以上,符合碱性岩特征;其Th/U比值为0.6,属于岩浆锆石.星叶石中w(Rb2O)、w(Cs2O)较高.萤石中Y、Ce替代Ca.锆石中的钍石w(U)明显高于磁铁矿中钍石w(U).在石英二长岩中,烧绿石的w(CaO)、w(TiO2)、w(ZrO2)、w(U3O8),磷钇矿的w(Y2O3),星叶石的w(TiO2),萤石的w(Ca),氟碳铈镧矿的w(CaO)较丰富;而在石英二长闪长岩中,烧绿石的w(Ce2O3),磷钇矿的REE含量,星叶石的w(Nb2O5)、w(Rb2O),萤石w(Ce)、w(Y)和氟碳铈镧矿的w(La2O3)较高.  相似文献   

14.
Simultaneously in-situ analyses of U–Pb isotopes and trace elements were carried out for zircons, in combination with the in-situ analyses of trace elements in coexisting minerals, from low-T/UHP metagranite in the Dabie orogen. The results provide geochemical evidence for the existence of supercritical fluid during continental subduction-zone metamorphism. The zircons are categorized into three types based on their patterns of REE distribution. Type I zircons show increasing enrichment from La to Lu, with prominent positive Ce anomalies and negative Eu anomalies, which are typical of magmatic zircon. Some of them display regular or blurred oscillatory-zoned texture and apparent 206Pb/238U ages of 341 to 780 Ma, suggesting metamorphic modification by solid-state recrystallization with no significant involvement of metamorphic fluid. Type II zircons share similar Th, U and HFSE contents and REE patterns to Type I zircons. However, they exhibit blurred oscillatory-zoned texture or are unzoned, have apparent 206Pb/238U ages of 348 to 709 Ma, and are LREE-enriched relative to Type I zircons. This suggests that they underwent metamorphic reworking by replacement recrystallization in the presence of metamorphic fluid. The LREE enrichment is due to the presence of microscale LREE-bearing mineral inclusions (such as apatite, monazite or epidote) in the zircons. Type III zircons, representing the majority of the present analyses, are characterized by spongy texture and consistent enrichment of LREE, HREE, Th, U and HFSE relative to Type I zircons. They yield nearly concordant U–Pb ages close to the discordia lower-intercept. The consistent enrichment of trace elements relative to the magmatic zircon indicates involvement of a special UHP metamorphic fluid that has a strong capacity to extract significant amounts of LREE, HREE, Th, U and HFSE from such accessory minerals as allanite, garnet, rutile and zircon. Because these minerals are stable in the field of hydrous melt in granite–water systems, they are not able to be decomposed during the exhumation of deeply subducted continental crust. Thus, a supercritical fluid is suggested to transport the LREE, HREE, Th, U and HFSE in the accessory minerals to recrystallized zircons. The mechanism of dissolution recrystallization is responsible for the spongy texture and the very high concentration of trace elements in this type of metamorphic zircons. Therefore, the action of supercritical fluid is evident under the low-T/UHP metamorphic conditions.  相似文献   

15.
Rare‐earth element and Y partitioning between garnet and monazite was measured in metamorphic rocks from western Norway to provide more confidence in tying monazite U/Th–Pb dates to P–T conditions recorded in garnet. A subset of samples has low‐Y garnet mantles and low‐Y monazite cores that gave Y‐partitioning temperatures similar to independently determined metamorphic temperatures. In combination with previously published data, these monazite–garnet pairs have temperature‐dependent partitioning of the HREE from Dy to Lu, and nonsystematic partitioning of the LREE from La–Gd. The temperature‐dependent partitioning must be considered when using HREE to assess which portions of garnet and monazite might have coexisted, but experiments are needed to place the dependence on a firm footing.  相似文献   

16.
The strongly peraluminous, perphosphorous (<0.85 wt% P2O5) and low-Ca granites from the Belvís de Monroy pluton contain the most U-rich monazite-(Ce) and xenotime known in igneous rocks. Along with these accessory minerals, P-rich zircon occurs, reaching uncommon compositions particularly in the more fractionated units of this zoned pluton. Monazite displays a wide compositional variation of UO2 (<23.13 wt%) and ThO2 (<19.58 wt%), positively correlated with Ca, Si, P, Y and REE. Xenotime shows a high UO2 content (2.37–13.34 wt%) with parallel increases of LREE, Ca and Si. Zircon contains comparatively much lower UO2 (<1.53 wt%) but high P2O5 (<14.91 wt%), Al2O3 (<6.96 wt%), FeO (<2.93 wt%) and CaO (<2.24 wt%) contents. The main mechanism of incorporating large U and Th amounts in studied monazite and U in xenotime is the cheralite-type [(Th,U)4+ + Ca2+ = 2(Y,REE)3+] substitution. Zircon requires several coupled mechanisms to charge balance the P substitution, resulting in non-stoichiometric compositions with low analytical totals. Compositional variations in the studied accessory phases indicate that the substitution mechanisms during crystal growth depend on the availability of non-formula elements. The strong P-rich character of the studied granites increases monazite crystallization, triggering a progressive impoverishment in Th and LREE in the residual melts, and consequently increasing extraordinarily the U content in monazite and xenotime. This is in marked contrast to other peraluminous (I-type or P-poor S-type) granite series. The P-rich and low-Ca peraluminous melt inhibits uraninite crystallization, so contributing to the U availability for monazite and xenotime.  相似文献   

17.
Composite multiphase solid (MS) inclusions composed of carbonate and silicate minerals have been found for the first time in metamorphic garnet from ultrahigh‐P eclogite from the Dabie orogen. These inclusions are morphologically euhedral to subhedral, and some show relatively regular shapes approaching the negative crystal shape of the host garnet. Radial fractures often occur in garnet hosting the inclusions. The inclusions are primarily composed of variable proportions of carbonate and silicate minerals such as calcite, quartz, K‐feldspar and plagioclase, with occasional occurrences of magnetite, zircon and barite. They are categorized into two groups based on the proportions of carbonate and silicate phases. Group I is carbonate‐dominated with variable proportions of silicate minerals, whereas Group II is silicate‐dominated with small proportions of carbonates. Trace element analysis by LA‐ICPMS for the two groups of MS inclusions yields remarkable differences. Group I inclusions exhibit remarkably lower REE contents than Group II inclusions, with significant LREE enrichment and large fractionation between LREE and HREE in the chondrite‐normalized REE diagram. In contrast, Group II inclusions show rather flat REE patterns with insignificant fractionation between LREE and HREE. In the primitive mantle‐normalized spidergram, Group I inclusions exhibit positive anomalies of Zr and Hf, whereas Group II inclusions show negative anomalies of Zr and Hf. Nevertheless, both groups exhibit positive anomalies of Ba, U, Pb and Sr, but negative anomalies of Nb and Ta, resembling the composition of common continental crust. Group I inclusions have higher Ba and U contents than Group II inclusions. Combined with petrological observations, the two groups of MS inclusions are interpreted as having crystallized from composite silicate and carbonate melts during continental subduction‐zone metamorphism. The differences in trace element composition between the two groups are primarily attributed to the proportions of carbonate and silicate phases in the MS inclusions. The silicate melts were derived from the breakdown of hydrous minerals such as paragonite and phengite, whereas the occurrence of carbonate melts indicates involvement of carbonate minerals in the partial melting and thus has great bearing on recycling of supracrustal carbon into the mantle. The coexistence of silicate and carbonate melts in the eclogitic garnet provides insights into the nature of hydrous melts in the subduction factory.  相似文献   

18.
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  相似文献   

19.
An eclogite–mafic granulite occurs as a rare boudin within a felsic kyanite–K‐feldspar granulite in a low‐strain zone. Its boundary is marked by significant metasomatism–diffusional gain of potassium at the centimetre‐scale, and probable infiltration of felsic melt on a larger scale. This converted the eclogite–mafic granulite into an intermediate‐composition, ternary‐feldspar‐bearing granulite. Based on inclusions in garnet, the peak P–T conditions of the original eclogite are 18 kbar at 850–950 °C, with later matrix re‐equilibration at 12 kbar and 950 °C. Four samples from the transition of the eclogite–mafic granulite through to the intermediate granulite were studied. In the eclogite, REE patterns in the garnet core show no Eu anomaly, compatible with crystallization in the absence of plagioclase and consistent with eclogite facies conditions. Towards the rim of garnet, LREE decrease, and a weak negative Eu anomaly appears, reflecting passage into HP granulite facies conditions with plagioclase present. The rims of garnet next to ternary feldspar in the intermediate granulite show the lowest LREE and deepest Eu anomalies. Zircon from the four samples was analysed by LASS (laser ablation–split‐stream inductively coupled plasma–mass spectrometry). It shows U–Pb ages from 404 ± 4.0 to 331 ± 3.3 Ma, with a peak at 340 ± 4.0 Ma corresponding to the likely exhumation of the rocks to 12 kbar. Older ages from zircon with steep HREE patterns indicate the minimum age of the protolith, and ages <360 ± 4.0 Ma are interpreted to correspond to the eclogite facies metamorphism. Only some zircon grains ≤350 ± 4.0 Ma have flat HREE patterns, suggesting that these are primarily modified protolith grains, rather than new zircon crystallized in the eclogite‐ or granulite facies. The metasomatic processes that converted the eclogite–mafic granulite to an intermediate granulite may have facilitated zircon modification as zircon in the intermediate granulite has flat HREE and ages of 340 ± 4.0 Ma. The difference between the oldest and youngest ages with flat REE patterns indicates a 16 ± 5.6 Ma period of zircon modification in the presence of garnet.  相似文献   

20.
Collision‐related granitoid batholiths, like those of the Hercynian and Himalayan orogens, are mostly fed by magma derived from metasedimentary sources. However, in the late Neoproterozoic calcalkaline (CA) batholiths of the Arabian–Nubian Shield (ANS), which constitutes the northern half of the East African orogen, any sedimentary contribution is obscured by the juvenile character of the crust and the scarcity of migmatites. Here, we use paired in situ LASS‐ICP‐MS measurements of U–Th–Pb isotope ratios and REE contents of monazite and xenotime and SHRIMP‐RG analyses of separated zircon to demonstrate direct linkage between migmatites and granites in the northernmost ANS. Our results indicate a single prolonged period of monazite growth at 640–600 Ma, in metapelites, migmatites and peraluminous granites of three metamorphic suites: Abu‐Barqa (SW Jordan), Roded (S Israel) and Taba–Nuweiba (Sinai, Egypt). The distribution of monazite dates and age zoning in single monazite grains in migmatites suggest that peak thermal conditions, involving partial melting, prevailed for c. 10 Ma, from 620 to 610 Ma. REE abundances in monazite are well correlated with age, recording garnet growth and garnet breakdown in association with the prograde and retrograde stages of the melting reactions, respectively. Xenotime dates cluster at 600–580 Ma, recording retrogression to greenschist facies conditions as garnet continued to destabilize. Phase equilibrium modelling and mineral thermobarometry yield P–T conditions of ~650–680°C and 5–7 kbar, consistent with either water‐fluxed or muscovite‐breakdown melting. The expected melt production is 8–10 vol.%, allowing a melt connectivity network to form leading to melt segregation and extraction. U–Pb ages of zircon rims from leucosomes indicate crystallization of melt at 610 ± 10 Ma, coinciding with the emplacement of a vast volume of CA granites throughout the northern ANS, which were previously considered post‐collisional. Similar monazite ages (c. 620 Ma) retrieved from the amphibolite facies Elat schist indicate that migmatites are the result of widespread regional rather than local contact metamorphism, representing the climax of the East African orogenesis.  相似文献   

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