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1.
贾望鲁  高山等 《地球科学》2003,28(2):121-128
俯冲玄武质洋壳的部分熔融作用是一种重要的大陆生长作用，但是陆壳物质在俯冲过程中能否发生部分熔融缺少直接的证据。笔者利用已有的微量元素分配系数，讨论了岛弧玄武岩在脱水和部分熔融2种过程中微量元素行为和铅同位素演化的差异。Pb在2种过程中都属于不相容元素，但在脱水过程中其不相容性明显高于Rb、Ba、Th、U，而在熔融过程中则低于上述元素，在ω(Rb)/ω(Pb)-ω(Rb)、ω（Ba)/ω(Pb)-ω(Ba)、ω（Th)/ω(Pb)-ω(Th)、ω（U）／ω(Pb)-ω(U)相关图上2种过程的演化方向差别明显。此外，Pb和Th、U的相容性的差异也使得石榴石和绿辉石的单矿物铅同位素在2种过程中明显不同。在此基础上，结合大别－苏鲁榴辉岩的实测数据，认为大别－苏鲁榴辉岩可能部分是岛弧玄武岩部分熔融后的残余体，部分为单纯脱水的产物。大陆玄武质岩石在俯冲过程中也可能发生部分熔融作用。  相似文献   

2.
Mineral stable isotopic and trace element studies in 2 GPa banded eclogites of the Tauern Window, eastern Alps, record mm- to cm-scale heterogeneities that reflect compositional variations in the accompanying metamorphic fluids. A close correlation between dolomite mode and dolomite δ18O is consistent with equilibrium partitioning among coexisting minerals and fluids. Small variations in dolomite δ13C values correspond with δ18O variations, but an overall decrease in dolomite δ13C by c. 1%o across a 12-cm sample is a relict feature that pre-dates eclogite equilibration. Garnet, omphacite, and clinozoisite rims show little systematic mineral-mineral partitioning behaviour for Ti, V, Cr, Y, Sr, or Zr; major elements, however, are well equilibrated among these same minerals. Despite the apparent lack of mineral-mineral trace element equilibration, most of the trace elements vary systematically with water activity calculated in each layer. Trace element behaviour during the eclogite metamorphism thus appears to have been controlled largely by mineral-fluid interactions along grain boundaries. Shallow structural levels in other subduction complexes (c. 10-45 km) typically exhibit fracture-controlled permeability and extensive metasomatism, but there is no field or geochemical evidence for extensive fluid advection during high-pressure metamorphism in the Tauern eclogites. Because most dewatering and devolatilization during tectonic burial occurs prior to eclogite conditions, the volumetric fluid/rock ratio in eclogites should generally be low. Low fluid/rock ratios, coupled with the possible non-wetting nature of the fluids, permits the production and preservation of fine-scale chemical heterogeneities in deeply subducted eclogites and associated fluids. However, the eventual breakdown at greater depth of volatile-bearing dolomite, phengite, clinozoisite, zoisite, or amphibole could lead to renewed fracture-controlled fluid release from the subducted rocks to regions appropriate for arc magma generation.  相似文献   

3.
ZACK  T.; FOLEY  S. F.; RIVERS  T. 《Journal of Petrology》2002,43(10):1947-1974
Despite the widespread presence of hydrous phases in subduction-related systems, experimental DMin/Fluid trace element valuesfor many hydrous phases are lacking. To fill this gap, we presenta set of DMin/Clinopyroxene values (where Min indicates amphibole,zoisite, phengite, paragonite or apatite) derived from equilibriumparageneses of eclogites from Trescolmen (Central Alps, Switzerland).These data can be combined with experimental data for DClinopyroxene/Fluid,to estimate DMin/Fluid values for the hydrous phases, thus circumventingexperimental problems with the direct determination of suchvalues. We analysed Li, Be, B, Sr, Y, Zr, Nb, Ba, Ce, Nd, Sm,Pb, Th and U in coexisting phases by laser ablation microprobeinductively coupled plasma mass spectrometry. Many of the valuesare extremely low; for example, Nb, Ba, Ce, Th and U are inthe lower ppb range in clinopyroxene. Attainment of equilibriumwas evaluated by textural, and major and trace element characteristics.Non-equilibrated assemblages are common in most eclogite localities,including Trescolmen, and using such samples would lead to thederivation of erroneous values for equilibrium partitioning.However, four of the 10 studied eclogites from Trescolmen havinghomogeneous clinopyroxene compositions and preferred orientationof high-pressure phases yielded consistent DMin/Clinopyroxenevalues in all four samples (where Min indicates amphibole, phengite,paragonite, apatite), and hence were studied in detail. Thelow abundances in some phases result from strong preferentialincorporation of trace elements into other minor phases. Fromthe investigated hydrous phases (amphibole, zoisite, clinozoisite,phengite, paragonite, apatite and talc), zoisite was found tobe the most important carrier of Sr, light rare earth elements,Pb, Th and U, whereas phengite hosts Ba and is, along with clinopyroxeneand paragonite, an important phase for B. However, because oftheir low modal abundance in eclogite-facies rocks, phengiteand paragonite do not control the B whole-rock budget. We inferthat estimated DMin/Clinopyroxene values from equilibrium assemblagescan be used as a good approximation for partition coefficientsunder the given PT conditions (  相似文献   

4.
In order to better understand the role of fluids during subduction and subsequent exhumation, we have investigated whole-rock and mineral chemistry (major and trace elements) and Li, B as well as O, Sr, Nd, Pb isotopes on selected continuous drill-core profiles through contrasting lithological boundaries from the Chinese Continental Scientific Drilling Program (CCSD) in Sulu, China. Four carefully selected sample sets have been chosen to investigate geochemical changes as a result of fluid mobilization during dehydration, peak metamorphism, and exhumation of deeply subducted continental crust. Our data reveal that while O and Sr-Nd-Pb isotopic compositions remain more or less unchanged, significant Li and/or B isotope fractionations occur between different lithologies that are in close contact during various metamorphic stages. Samples that are supposed to represent prograde dehydration as indicated by veins formed at high pressures (HP) are characterized by element patterns of highly fluid-mobile elements in the veins that are complementary to those of the host eclogite. A second sample set represents a UHP metamorphic crustal eclogite that is separated from a garnet peridotite by a thin transitional interface. Garnet peridotite and eclogite are characterized by a >10% difference in MgO, which, together with the presence of abundant hydroxyl-bearing minerals and compositionally different clinopyroxene grains demonstrate that both rocks have been derived from different sources that have been tectonically juxtaposed during subduction, and that hydrous silicate-rich fluids have been added from the subducting slab to the mantle. Two additional sample sets, comprising retrograde amphibolite and relatively fresh eclogite, demonstrate that besides external fluids, internal fluids can be responsible for the formation of amphibolite. Li and B concentrations and isotopic compositions point to losses and isotopic fractionation during progressive dehydration. On the other hand, fluids with isotopically heavier Li and B are added during retrogression. On a small scale, mantle-derived rocks may be significantly metasomatized by fluids derived from the subducted slab. Our study indicates that during high-grade metamorphism, Li and B may show different patterns of enrichment and of isotopic fractionation.  相似文献   

5.
本文通过对CCSD主孔100～1100m范围内榴辉岩中单矿物的LA-ICP-MS分析，探讨了榴辉岩中单矿物之间的微量元素分配，发现超高压变质作用中石榴石和绿辉石之间Ti和C0的分配显著受Mg控制（如DCo^Grt/Omp=3．43DMg^Grt/Omp-0．34），而REE、Sr和Y的分配则受Ca分配所控制。绿辉石中REE、Pb和Th的含量则明显受超高压副矿物磷灰石的出现与否所控制。结合岩石学特征，对角闪石和绿辉石中微量元素的研究表明角闪石主要是绿辉石退变质的产物。但退变质矿物的微量元素组成不仅受原矿物控制，而且受退变质矿物组合类型影响。绿帘石的出现会显著降低共生角闪石中LREE和Sr的含量，而多硅白云母的分解则会增加角闪石中的Rb、Ba含量。另外，退变质过程中的流体活动也会影响退变质矿物中的LREE、Sr和Pb等。结合REE在榴辉岩各主要矿物间分配系数随温度、压力的变化，我们推测部分石榴石边部MREE的富集特征可能反映榴辉岩在折返过程中经历了短时增温作用，这可能是引起苏鲁地区榴辉岩相向麻粒岩相转变叠加现象以及超高压岩石经历部分熔融作用的重要原因。此外，榴辉岩中金红石Nb和Ta组成的高度不均一性为金红石形成于超高压变质阶段富Ti磁铁矿相变作用的成因机制提供了佐证。  相似文献   

6.
High-pressure(HP)or ultrahigh-pressure(UHP)rutile-quartz veins that form at mantle depths due to fluid-rock interaction can be used to trace the properties and behavior of natural fluids in subduction zones.To explore the fluid flow and the associated element mobility during deep subduction and exhumation of the continental crust,we investigated the major and trace elements of Ti-rich minerals.Additionally,U–Pb dating,trace element contents,and Lu–Hf isotopic composition of zircon grains in the UHP eclogite and associated rutile-quartz veins were examined in the North Qaidam UHP metamorphic belt,Yuka terrane.The zircon grains in the rutile-quartz veins have unzoned or weak oscillatory zonings,and show low Th/U ratios,steep chondrite-normalized patterns of heavy rare earth elements(HREEs),and insignificant negative Eu anomalies,indicating their growth in metamorphic fluids.These zircon grains formed in 4313 Ma,which is consistent with the 4322 Ma age of the host eclogite.As for the zircons in the rutile-quartz veins,they showed steep HREE patterns on one hand,and were different from the zircons present in the host eclogite on the other.This demonstrates that their formation might have been related to the breakdown of the early stage of garnet,which corresponds to the abundance of fluids during the early exhumation stage.The core-rim profile analyses of rutile recorded a two-stage rutile growth across a large rutile grain;the rutile core has higher Nb,Ta,W,and Zr contents and lower Nb/Ta ratios than the rim,indicating that the rutile domains grew in different metamorphic fluids from the core towards the rim.The significant enrichment of high field strength elements(HFSEs)in the rutile core suggests that the peak fluids have high solubility and transportation capacity of these HFSEs.Furthermore,variations in the Nb vs.Cr trends in rutile indicate a connection of rutile to mafic protolith.The zircon grains from both the rutile-quartz veins and the host eclogite have similar Hf isotopic compositions,indicating that the vein-forming fluids are internally derived from the host eclogite.These fluids accumulated in the subduction channel and were triggered by local dehydration of the deeply subducted eclogite during the early exhumation conditions.  相似文献   

7.
《International Geology Review》2012,54(13):1443-1463
Fluid inclusions hosted by quartz veins in high-pressure to ultrahigh-pressure (HP-UHP) metamorphic rocks from the Chinese Continental Scientific Drilling (CCSD) Project main drillhole have low, varied hydrogen isotopic compositions (δD?=??97‰ to??69‰). Quartz δ18O values range from??2.5‰ to 9.6‰; fluid inclusions hosted in quartz have correspondingly low δ18O values of??11.66‰ to 0.93‰ (T h?=?171.2～318.8°C). The low δD and δ18O isotopic data indicate that protoliths of some CCSD HP-UHP metamorphic rocks reacted with meteoric water at high latitude near the surface before being subducted to great depth. In addition, the δ18O of the quartz veins and fluid inclusions vary greatly with the drillhole depth. Lower δ18O values occur at depths of ～900–1000 m and ～2700 m, whereas higher values characterize rocks at depths of about 1770 m and 4000 m, correlating roughly with those of wall-rock minerals. Given that the peak metamorphic temperature of the Dabie-Sulu UHP metamorphic rocks was about 800°C or higher, much higher than the closure temperature of oxygen isotopes in quartz under wet conditions, such synchronous variations can be explained by re-equilibration. In contrast, δD values of fluid inclusions show a different relationship with depth. This is probably because oxygen is a major element of both fluids and silicates and is much more abundant in the quartz veins and silicate minerals than is hydrogen. The oxygen isotope composition of fluid inclusions is evidently more susceptible to late-stage re-equilibration with silicate minerals than is the hydrogen isotope composition. Therefore, different δD and δ18O patterns imply that dramatic fluid migration occurred, whereas the co-variation of oxygen isotopes in fluid inclusions, quartz veins, and wall-rock minerals can be better interpreted by re-equilibration during exhumation.

Quartz veins in the Dabie-Sulu UHP metamorphic terrane are the product of high-Si fluids. Given that channelized fluid migration is much faster than pervasive flow, and that the veins formed through precipitation of quartz from high-Si fluids, the abundant veins indicate significant fluid mobilization and migration within this subducted continental slab. Many mineral reactions can produce high-Si fluids. For UHP metamorphic rocks, major dehydration during subduction occurred when pressure–temperature conditions exceeded the stability of lawsonite. In contrast, for low-temperature eclogites and other HP metamorphic rocks with peak metamorphic P–T conditions within the stability field of lawsonite, dehydration and associated high-Si fluid release may have occurred as hydrous minerals were destabilized at lower pressure during exhumation. Because subduction is a continuous process whereas only a minor fraction of the subducted slabs returns to the surface, dehydration during underflow is more prevalent than exhumation even in subducted continental crust, which is considerably drier than altered oceanic crust.  相似文献   

8.
The transfer of fluid and elements from subducting crust to the overlying mantle wedge is a fundamental process affecting arc magmatism and the chemical differentiation of the Earth. While the production of fluid by breakdown of hydrous minerals is well understood, the liberation of trace elements remains generally unconstrained. In this paper, we evaluate the behaviour of trace elements during prograde metamorphism and dehydration using samples of high-pressure, low-temperature metamorphic rocks from New Caledonia. Samples examined include mafic and pelitic rock-types that range in grade from lawsonite blueschist to eclogite facies, and represent typical lithologies of subducting crust. Under lawsonite blueschist facies conditions, the low temperatures of metamorphism inhibit equilibrium partitioning between metamorphic minerals and allow for the persistence of igneous and detrital minerals. Despite this, the most important hosts for trace-elements include lawsonite, (REE, Pb, Sr), titanite (REE, Nb, Ta), allanite (LREE, U, Th), phengite (LILE) and zircon (Zr, Hf). At epidote blueschist to eclogite facies conditions, trace-element equilibrium may be attained and epidote (REE, Sr, Th, U, Pb), garnet (HREE), rutile (Nb, Ta), phengite (LILE) and zircon (Zr, Hf) are the major trace-element hosts. Chlorite, albite, amphibole and omphacite contain very low concentrations of the investigated trace elements. The comparison of mineral trace-element data and bulk-rock data at different metamorphic grades indicates that trace elements are not liberated in significant quantities by prograde metamorphism up to eclogite facies. Combining our mineral trace-element data with established phase equilibria, we show that the trace elements considered are retained by newly-formed major and accessory minerals during mineral breakdown reactions to depths of up to 150 km. In contrast, significant volumes of fluid are released by dehydration reactions. Therefore, there is a decoupling of fluid release and trace element release in subducting slabs. We suggest that the flux of trace elements from the slab is not simply linked to mineral breakdown, but results from complex fluid-rock interactions and fluid-assisted partial melting in the slab.Electronic Supplementary Material Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s00410-003-0495-5.Editorial responsibility: J. Hoefs  相似文献   

9.
The complex vein associations hosted in southern Sulu ultrahigh-pressure (UHP) eclogites contain quartz ± omphacite (or jadeite) ± kyanite ± allanite ± zoisite ± rutile ± garnet. These minerals have chemical compositions similar to those of host eclogites. Inclusions of polycrystalline quartz pseudomorphs after coesite were identified in vein allanite and garnet, and coesite inclusions were found in vein zircon. These facts suggest that the veins together with host eclogites have been subjected to synchronous UHP metamorphism. The vein minerals contain relatively high concentrations of rare earth elements (REE), high-field-strength elements (HFSE) and transition metal elements (TME). A kyanite-quartz vein has a whole-rock composition similar to adjacent UHP metamorphic granitic gneisses. Abundant primary multi-solid fluid inclusions trapped within UHP vein minerals contain complex daughter minerals of muscovite, calcite, anhydrite, magnetite, pyrite, apatite, celestite and liquid and gas phase of H2O with solids up to 30-70% of the inclusion volume. The presence of daughter minerals anhydrite and magnetite indicates the subduction fluids were oxidizing, and provides a possible interpretation for the high oxygen fugacity of subduction zone magmas. These characteristics imply that the UHP vein minerals were crystallized from supercritical silicate-rich aqueous fluids that were in equilibrium with peak-UHP minerals, and that the fluids in deeply subducted continental crust may contain very high concentrations of silicate as well as HREE, HFSE and TME. Such fluids might have resulted in major fractionation between Nb and Ta, i.e. the UHP fluids have subchondritic Nb/Ta values, whereas the host eclogites after extraction of the fluids have suprachondritic Nb/Ta values. Therefore, voluminous residual eclogites with high Nb/Ta ratios may be the complementary suprachondritic reservoir capable of balancing the subchondritic depleted mantle and continental crust reservoirs.  相似文献   

10.
Volatile element, major and trace element compositions were measured in glass inclusions in olivine from samples across the Kamchatka arc. Glasses were analyzed in reheated melt inclusions by electron microprobe for major elements, S and Cl, trace elements and F were determined by SIMS. Volatile element–trace element ratios correlated with fluid-mobile elements (B, Li) suggesting successive changes and three distinct fluid compositions with increasing slab depth. The Eastern Volcanic arc Front (EVF) was dominated by fluid highly enriched in B, Cl and chalcophile elements and also LILE (U, Th, Ba, Pb), F, S and LREE (La, Ce). This arc-front fluid contributed less to magmas from the central volcanic zone and was not involved in back arc magmatism. The Central Kamchatka Depression (CKD) was dominated by a second fluid enriched in S and U, showing the highest S/K2O and U/Th ratios. Additionally this fluid was unusually enriched in 87Sr and 18O. In the back arc Sredinny Ridge (SR) a third fluid was observed, highly enriched in F, Li, and Be as well as LILE and LREE. We argue from the decoupling of B and Li that dehydration of different water-rich minerals at different depths explains the presence of different fluids across the Kamchatka arc. In the arc front, fluids were derived from amphibole and serpentine dehydration and probably were water-rich, low in silica and high in B, LILE, sulfur and chlorine. Large amounts of water produced high degrees of melting below the EVF and CKD. Fluids below the CKD were released at a depth between 100 and 200 km due to dehydration of lawsonite and phengite and probably were poorer in water and richer in silica. Fluids released at high pressure conditions below the back arc (SR) probably were much denser and dissolved significant amounts of silicate minerals, and potentially carried high amounts of LILE and HFSE. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.  相似文献   

11.
We studied the elemental and isotopic (Pb, B and Li isotopes) composition of melt inclusions hosted in highly forsteritic (Fo83–91) olivines that were collected from San Bartolo lava and pumice (ST79p, ST82p and ST531p) samples erupted by Stromboli in historical times. The studied melt inclusions have primitive calcalkaline to shoshonitic basaltic compositions. They cover a compositional range far wider than that exhibited by the whole-rocks and differ in key trace element ratios. San Bartolo melt inclusions are characterized by lower incompatible trace element abundances, higher ratios between fluid-mobile (B, Pb, U and LILE) and less fluid-mobile (REE, Th, HFSE) elements and lower La/Yb ratios relative to the pumice-hosted melt inclusions and pumiceous melts erupted during paroxysmal events. Trace elements, along with different Pb, B and Li isotopic signatures, attest to source heterogeneity on the small scale and provide new insights into subducted components beneath Stromboli. Results of a mixing model suggest that metasomatism of the mantle source of pumice-hosted melt inclusions was driven by solute-rich high-pressure fluids (<20%) expelled from the deep portion of the slab. Heterogeneous Pb isotopic composition together with light δ11B (−8.6 to −13.7‰) and δ7Li (+2.3 to −1.7‰) indicates that high-pressure liquids were released in variable proportions from highly dehydrated metabasalts and metasediments. On the other hand, the elemental and isotopic (δ11B ~ −1.9 to −5.9‰) composition of San Bartolo melt inclusions is better explained by the addition of a prevalent aqueous component (~2 to 4%) escaped at shallower depths from sediments and altered basaltic crust in almost equivalent proportions, with a smaller contribution by high-pressure fluids. Owing to the high-angle dip of the subducted cold Ionian slab, aqueous fluids and high-pressure fluids would rise through the mantle wedge and locally superimpose on each other, thus giving origin to variously metasomatized mantle domains.  相似文献   

12.
Zhang Zeming  Xu Zhiqin  Xu Huifen 《Lithos》2000,52(1-4):35-50
The 558-m-deep ZK703 drillhole located near Donghai in the southern part of the Sulu ultrahigh-pressure metamorphic belt, eastern China, penetrates alternating layers of eclogites, gneisses, jadeite quartzites, garnet peridotites, phengite–quartz schists, and kyanite quartzites. The preservation of ultrahigh-pressure metamorphic minerals and their relics, together with the contact relationship and protolith types of the various rocks indicates that these are metamorphic supracrustal rocks and mafic-ultramafic rock assemblages that have experienced in-situ ultrahigh-pressure metamorphism. The eclogites can be divided into five types based on accessory minerals: rutile eclogite, phengite eclogite, kyanite–phengite eclogite, quartz eclogite, and common eclogite with rare minor minerals. Rutile eclogite forms a thick layer in the drillhole that contains sufficient rutile for potential mining. Two retrograde assemblages are observed in the eclogites: the first stage is characterized by the formation of sodic plagioclase+amphibole symplectite or symplectitic coronas after omphacite and garnet, plagioclase+biotite after garnet or phengite, and plagioclase coronas after kyanite; the second stage involved total replacement of omphacite and garnet by amphibole+albite+epidote+quartz. Peak metamorphic P–T conditions of the eclogites were around 32 to 40 kbar and 720°C to 880°C. The retrograde P–T path of the eclogites is characterized by rapidly decreasing pressure with slightly decreasing temperature. Micro-textures and compositional variations in symplectitic minerals suggest that the decompression breakdown of ultrahigh-pressure minerals is a domainal equilibrium reaction or disequilibrium reaction. The composition of the original minerals and the diffusion rate of elements involved in these reactions controlled the symplectitic mineral compositions.  相似文献   

13.
对中国大陆科学钻探工程主孔榴辉岩退变质过程中的微量元素地球化学行为进行了研究。对退变质程度连续变化样品的不同部分的对比研究表明，流体作用下的退变质过程中大离子亲石元素（Cs、Rb、Ba、Sr、K、Th、U）和轻稀土元素表现出较大的活动性，重稀土元素和高场强元素变化相对较小。退变质后大离子亲石元素的显著增加和高场强元素、重稀土元素的轻微变化（甚至相对降低），表明与退变质作用有关的流体中的络阴离子含量很少，并不富集高场强元素和重稀土元素。退变质后总体上表现出的Si、大离子亲石元素和轻稀土元素的明显变化，表明外来流体参与了榴辉岩的退变质过程，带入和带出了一些元素。结合榴辉岩中单矿物微量元素组成以及前人对D^Mineral/Fluid的研究成果，对流体-榴辉岩作用形成的退变质分带（富石英条带→角闪岩→退变质榴辉岩→新鲜榴辉岩）的微量元素组成变化进行了详细研究。结果表明在流体作用下的榴辉岩退变质过程中，大离子亲石元素、轻稀土元素和高场强元素含量的变化除了受退变质流体性质的影响外，更大程度上取决于退变质过程中的矿物相（尤其是副矿物）的变化。  相似文献   

14.
Metamorphic dehydration and partial melting are two important processes during continental collision. They have significant bearing on element transport at the slab interface under subduction‐zone P–T conditions. Petrological and geochemical insights into the two processes are provided by a comprehensive study of leucocratic veins in ultrahigh‐pressure (UHP) metamorphic rocks. This is exemplified by this study of a polymineralic vein within phengite‐bearing UHP eclogite in the Dabie orogen. The vein is primarily composed of quartz, kyanite, epidote and phengite, with minor accessory minerals such as garnet, rutile and zircon. Primary multiphase solid inclusions occur in garnet and epidote from the both vein and host eclogite. They are composed of quartz ± K‐feldspar ± plagioclase ± K‐bearing glass and exhibit irregular to negative crystal shapes that are surrounded by weak radial cracks. This suggests their precipitation from solute‐rich metamorphic fluid/melt that involved the reaction of phengite breakdown. Zircon U–Pb dating for the vein gave two groups of concordant ages at 217 ± 2 and 210 ± 2 Ma, indicating two episodes of zircon growth in the Late Triassic. The same minerals from the two rocks give consistent δ18O and δD values, suggesting that the vein‐forming fluid was directly derived from the host UHP eclogite. The vein is much richer in phengite and epidote than the host eclogite, suggesting that the fluid is associated with remarkable concentration of such water‐soluble elements as LILE and LREE migration. Garnet and rutile in the vein exhibit much higher contents of HREE (2.2–5.7 times) and Nb–Ta (1.8–2.0 times) than those in the eclogite, indicating that these normally water‐insoluble elements became mobile and then were sunken in the vein minerals. Thus, the vein‐forming agent would be primarily composed of the UHP aqueous fluid with minor amounts of the hydrous melt, which may even become a supercritical fluid to have a capacity to transport not only LILE and LREE but also HREE and HFSE at subduction‐zone metamorphic conditions. Taken together, significant amounts of trace elements were transported by the vein‐forming fluid due to the phengite breakdown inside the UHP eclogite during exhumation of the deeply subducted continental crust.  相似文献   

15.
The stability and phase relations of phengitic muscovite in a metapelitic bulk composition containing a mixed H2O+CO2 fluid were investigated at 6.5–11 GPa, 750–1050°C in synthesis experiments performed in a multianvil apparatus. Starting material consisted of a natural calcareous metapelite from the coesite zone of the Dabie Mountains, China, ultrahigh-pressure metamorphic complex that had experienced peak metamorphic pressures greater than 3 GPa. The sample contains a total of 2.1 wt.% H2O and 6.3 wt.% CO2 bound in hydrous and carbonate minerals. No additional fluid was added to the starting material. Phengite is stable in this bulk composition from 6.5 to 9 GPa at 900°C and coexists with an eclogitic phase assemblage consisting of garnet, omphacite, coesite, rutile, and fluid. Phengite dehydrates to produce K-hollandite between 8 and 11 GPa, 750–900°C. Phengite melting/dissolution occurs between 900°C and 975°C at 6.5–8 GPa and is associated with the appearance of kyanite in the phase assemblage. The formation of K-hollandite is accompanied by the appearance of magnesite and topaz-OH in the phase assemblage as well as by significant increases in the grossular content of garnet (average Xgrs=0.52, Xpy=0.19) and the jadeite content of omphacite (Xjd=0.92). Mass balance indicates that the volatile content of the fluid phase changes markedly at the phengite/K-hollandite phase boundary. At P≤8 GPa, fluid coexisting with phengite appears to be relatively CO2-rich (XCO2/XH2O=2.2), whereas fluid coexisting with K-hollandite and magnesite at 11 GPa is rich in H2O (XCO2/XH2O=0.2). Analysis of quench material and mass balance calculations indicate that fluids at all pressures and temperatures examined contain an abundance of dissolved solutes (approximately 40 mol% at 8 GPa, 60 mol% at 11 GPa) that act to dilute the volatile content of the fluid phase. The average phengite content of muscovite is positively correlated with pressure and ranges from 3.62 Si per formula unit (pfu) at 6.5 GPa to 3.80 Si pfu at 9 GPa. The extent of the phengite substitution in muscovite in this bulk composition appears to be limited to a maximum of 3.80–3.85 Si pfu at P=9 GPa. These experiments show that phengite should be stable in metasediments in mature subduction zones to depths of up to 300 km even under conditions in which aH2O1. Other high-pressure hydrous phases such as lawsonite, MgMgAl-pumpellyite, and topaz-OH that may form in subducted sediments do not occur within the phengite stability field in this system, and may require more H2O-rich fluid compositions in order to form. The wide range of conditions under which phengite occurs and its participation in mixed volatile reactions that may buffer the composition of the fluid phase suggest that phengite may significantly influence the nature of metasomatic fluids released from deeply subducted sediments at depths of up to 300 km at convergent plate boundaries.  相似文献   

16.
Andreas Stracke  Ernst Hegner 《Lithos》1998,45(1-4):545-560
The Tabar–Lihir–Tanga–Feni (TLTF) volcanic island chain occurs in a zone of lithospheric extension superimposed on a post-collisonal tectonic setting along the Pacific and Indo-Australian plates northeast of Papua New Guinea. We present geochemical and Sr, Nd, and Pb isotope data for volcanic rocks from these islands and three recently discovered seamounts located at Lihir island. Major element data document an alkalic affinity of the sample suite and trachybasalts as the predominant rock type. Negative Nb-anomalies in extended trace element patterns, enrichment of the light rare earth elements, and Ce/Pb ratios of about 4 are typical of the values in calc alkaline island arc volcanics and support an origin from subduction-modified mantle. 87Sr/86Sr ratios of 0.7037 to 0.7044 and Nd values of +5.6 to +6.8 indicate that the upper mantle evolved with a time-integrated depletion in LREE, however, not as severe as that recorded in basalts from the East Pacific Rise. Variable 87Sr/86Sr ratios at less variable 143Nd/144Nd ratios suggest that 87Sr/86Sr ratios of the melts were modified by secondary processes, such as assimilation of seawater Sr from crustal rocks. The Pb isotope ratios are uniform, moderately radiogenic (206Pb/204Pb ca. 18.7 to 18.8), and similar to those reported for the active Mariana arc. Elevated 207Pb/204Pb ratios relative to Pacific MORB suggest melting of small amounts of subducted sediments (ca. 1–2 wt.%). An important control of subducted sediment on the chemistry of the melts can also be inferred from the ratios of highly incompatible trace elements (e.g., Th, U, Pb, La, and Nb). Additional mantle enrichment by subduction derived fluids is reflected in high values of highly incompatible trace element ratios between fluid mobile (e.g., Ba) and fluid immobile elements (e.g., Th, Nb). The results of this study document that the chemical composition of igneous rocks from post-collisional tectonic settings are strongly influenced by previous plate tectonics. This conclusion implies that the information conveyed by tectonic discrimination diagrams for these rocks must be interpreted with care.  相似文献   

17.
大陆俯冲过程中的流体   总被引：5，自引：1，他引：5  
李曙光  侯振辉 《地学前缘》2001,8(3):123-129
含水矿物矿物稳定性的实验研究和超高压岩石的同位素地球化学研究表明 ,大陆地壳在俯冲过程中 ,随着变质程度的升高和部分含水矿物的相继分解 ,会有流体释放出来。当俯冲深度接近5 0km ,俯冲陆壳岩石中大量低级变质含水矿物 (如绿泥石、绿帘石、阳起石 )会脱水并从俯冲陆壳逸出形成流体流。这一流体流可溶解带走俯冲陆壳内已从云母类矿物逸出的放射成因Ar及部分U、Pb ,并导致w(U) /w(Pb)升高。这一阶段逸出的流体有可能交代、水化仰冲壳楔 ,为其发生部分熔融形成同碰撞花岗岩或加速山根下地壳的榴辉岩化创造条件。在俯冲深度为 5 0～ 10 0km ,变镁铁质岩石中的角闪石相继分解并释放出H2 O。由于变镁铁质岩石在陆壳中所占比例较少 ,因此 ,这一阶段释放的水不能形成大规模的流体流 ,因而不能使体系内的过剩Ar大量散失 ,但足以形成局部循环 ,加速变镁铁质岩石及其互层或邻近围岩的榴辉岩化变质反应。在俯冲深度 >10 0km的超高压变质阶段 ,仅有少量的含水矿物分解 ,而多硅白云母仍保持稳定。这时俯冲陆壳内只可能有少量粒间水存在 ,从而导致俯冲陆壳与周围软流圈地幔不能发生充分的相互作用。  相似文献   

18.
Ion microprobe data for minerals from the eclogites of the Atbashi Range (South Tianshan) constrain the distribution of trace (Rb, Sr, Ba, Cr, V, Zr, Hf, Nb, Ta, U, Th, and Y) and rare-earth elements (REE) in zoned garnets and mineral inclusions in them. This study showed that garnets from the Atbashi eclogites are the main hosts for heavy REE; epidotes are important hosts for REE, Y, Sr, Th, and U; and omphacites are depleted in almost all trace elements compared with the bulk-rock compositions. Garnet, as well as epidote and omphacite inclusions exhibit systematic rimward depletion in a number of trace elements, which is related to the depletion of the rock matrix in these elements during crystallization. Deviations from this trend, including the enrichment of garnet rims in HREE and strong variations in the REE contents of garnets and mineral inclusions, can be explained by metamorphic reactions involving the destabilization of REE-bearing minerals. Our data suggest that the mobility of trace elements under eclogites-facies conditions is mainly controlled by the stability of certain minerals.  相似文献   

19.
An integrated study of U–Pb ages and trace elements was carried out for titanite and zircon from ultrahigh‐pressure (UHP) metagranites in the Sulu orogen, east‐central China. The results provide constraints on the composition of metamorphic fluids during the exhumation of deeply subducted continental crust. Titanite has two domain types based on REE patterns and trace element variations, Ttn‐I and Ttn‐II respectively. These two domains show indistinguishable U–Pb ages of 232 ± 14 to 220 ± 8 Ma, in general agreement with anatectic zircon U–Pb ages of 223 ± 4 to 219 ± 2 Ma for the partial melting event during early exhumation. The Ttn‐I domains have significantly higher REE, Th, Ta and Sr, and higher Th/U ratios than the Ttn‐II domains, indicating that the two domains have grown from metamorphic fluids with different compositions. For the Ttn‐I domains, Zr‐in‐titanite thermometry yields high temperatures of 773–851 °C at 2.5 GPa, and petrographic observations reveal the presence of melt pseudomorphs. Thus, they are interpreted to have grown from hydrous melts in the early exhumation stage. In contrast, the Ttn‐II domains were texturally equilibrated with amphibolite facies minerals such as biotite and plagioclase and contain inclusions of plagioclase and quartz. The Zr‐in‐titanite thermometry yields lower temperatures of 627–685 °C at 1.0 GPa. In combination with their REE patterns, they are interpreted to have grown from aqueous solutions at amphibolite facies metamorphic conditions during further exhumation. The differences in Th and Sr contents are prominent between the Ttn‐I and Ttn‐II domains, signifying the compositional difference between the hydrous melts and aqueous solutions. Therefore, the polygenetic titanite in the UHP metamorphic rocks provides insights into the geochemical property of metamorphic fluids during the continental subduction‐zone processes.  相似文献   

20.
The Shuanghe garnet-bearing paragneiss from the Dabie ultra-high–pressure (UHP) orogen occurs as an interlayer within partially retrogressed eclogite. A first UHP metamorphic stage at 680°C, 3.8–4.1 GPa is documented by Zr-in-rutile temperatures coupled with phengite inclusions (Si = 3.55) in clinozoisite and grossular-rich garnet. Relic matrix phengite and phengite inclusions in zircon rims display lower Si of 3.42. Combined with garnet compositions and Ti-in-zircon temperatures, they provide evidence for a second UHP metamorphic stage at 800–850°C, ~3.8 GPa. Such isobaric heating at UHP conditions has not been documented so far from the adjacent eclogites and other rock types in the Dabie orogen and indicates proximity to the hot, convecting mantle wedge. The dominant mineral assemblage consisting of plagioclase, epidote, biotite, and amphibole provides evidence for widespread retrogression during the exhumation of the UHP paragneiss. Several types of polyphase mineral inclusions were identified. Phengite inclusions hosted by clinozoisite are partially replaced by kyanite and K-feldspar, whereas inclusions in host garnet consist of relic phengite, K-feldspar, and garnet, indicating limited sub-solidus dehydration of phengite by the reaction Ph→Kfs+Ky±Grt+fluid. Tightly intergrown K-feldspar and quartz are preserved as inclusions with sharp boundaries and radial cracks in garnet. Analyses of whole inclusions also show small enrichments in light rare earth elements. These inclusions are interpreted to be derived from melting of an inclusion assemblage consisting of Ph+Coe±Czo. A third type of polyphase inclusion consists of typical nanogranite (Ab+Kfs+Qz±Ep) inclusions in recrystallized metamorphic zircon. Ti-in-zircon thermometry and the Si content of phengite included in these zircon domains indicate that melting occurred at 800–850°C and 3.8–4.0 GPa during isobaric heating at UHP conditions. The partial melting event led to an equilibration of trace elements in garnet, phengite, and apatite. Using published partition coefficients between these minerals and hydrous granitic melt, the trace element composition of the UHP anatectic melt can be constrained. The melts are characterized by high LILE contents and pronounced relative enrichments of U over Th and Ta over Nb. The REE are below primitive mantle values, likely due to the presence of residual clinozoisite and garnet during partial melting. So far, no major granitic bodies have been found that share the same trace element pattern as the partial melts from the UHP anatexis of the Shuanghe paragneiss.  相似文献   

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