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1.
大别山北部饶拔寨超镁铁岩体微量元素地球化学   总被引：3，自引：4，他引：3  
本文报道了饶拔寨超镁铁岩体的5个钻孔15个岩心样品的主量元素和微量元素成分。该岩体由上、下两部分构成。岩性以方辉橄榄岩为主，纯橄榄岩和二辉橄榄岩次之。主量元素成分表明岩体由饱满地幔经过不同程度部分熔融，形成了亏损程度不同的大陆岩石圈地幔。总体上下部岩体较上部亏损程度大。原始地幔标准化REE等不相容微量元素丰度模式表明岩体在熔融作用后又经过了地幔交代作用，形成不同程度LREE和LILE的富集。样品中有角闪石和金云母等含水矿物，表明有实性地幔交代作用。对比LREE与LILE的富集特征，表明可能有两类地幔交代作用，有两种不同性质的交代介质，LREE和Sr等的富集可能与硅酸盐熔体有关，而Rb、Ba、K等的富集可能与俯冲带流体活动有关。总体上下部岩体的交代作用较上部岩体的强。  相似文献   

2.
The peridotite bodies of the Ulten Zone (Upper Austroalpine, Italian Eastern Alps) are enclosed in Variscan migmatites and derive from a mantle wedge environment. They display the progressive transformation of porphyroclastic spinel peridotites (T=1,200°C; P=1.5 GPa) into fine-grained garnet–amphibole peridotites (T=850°C; P=3 GPa). Detailed bulk-rock and mineral trace element analyses of a sample suite documenting the entire metamorphic evolution of the peridotites revealed several stages of metasomatism. The spinel peridotites derive from a depleted mantle that became enriched in some large ion lithophile element (LILE) and light rare earth elements (LREE). The same signature pertains to clinopyroxene and orthopyroxene, indicating that this metasomatic signature was acquired at the recorded temperature of 1,200°C. Such a temperature is considerably above the wet peridotite solidus and hence the metasomatic agent must have been a hydrous melt. Moreover, the Li-enrichment of the spinel-facies pyroxenes (up to 24 ppm Li) reflects disequilibrium distribution after exchange with a presumably mafic melt. cpx/opx D Li=3–7 and cpx/ol D Li=2.7–8 indicate that the spinel-facies clinopyroxene hosts higher Li amounts than the coexisting minerals. LREE fractionation, variable LREE enrichment, LILE enrichment with respect to HFSE (average clinopyroxene Pb N /Nb N =16–90) in spinel lherzolites can be related to chromatographic effects of porous melt flow. The significant enrichment of pyroxenes from the spinel lherzolites in Pb, U and Li indicates that the metasomatic melt was subduction-related. All these features suggest that the spinel lherzolites formed a mantle wedge layer percolated by melts carrying recycled crustal components and rising from a deeper source of subduction magmas. The garnet + amphibole peridotites equilibrated at temperatures well below the wet solidus in the presence of an aqueous fluid. Bulk-rock trace element patterns display pronounced positive anomalies in Cs, Ba, Pb and U and moderate enrichment in Li, indicating addition of a crustal component to the mantle rocks. Amphibole hosts most of these trace elements. Clinopyroxene displays high LILE/HFSE (Pb N /Nb N =300–600), low Ce/Pb (1.4–2.7 in garnet-facies clinopyroxene compared with 2.6–24.5 in the spinel-facies one) and variable LILE and LREE enrichments. The coupled increase of modal amphibole, Sr and Pb, together with positive Pb–Sr and Pb–U correlations, further indicate that incompatible element influx in these samples was fluid-mediated. In the garnet-facies samples, amphibole and, interestingly, olivine have similarly high Li concentrations as clinopyroxene, leading to cpx/amph D Li=0.7 and cpx/ol D Li=0.7–0.8, the latter being up to ten times lower than in the spinel-facies rocks. Due to its high modal abundance, olivine is the main host of Li in the garnet–amphibole peridotites. The observed metasomatic features provide evidence for the infiltration of an aqueous fluid in the mantle wedge above a subducting slab. This fluid most likely derived from subducted crustal rocks that underwent partial melting. Successive retrograde re-equilibration during exhumation of the garnet peridotite is accompanied by garnet and clinopyroxene breakdown and amphibole formation. This process produced minor changes, such as an increase of HREE and Li in amphibole, and an increase of Li in olivine. The general trace element signature remains essentially unchanged during retrogression and further hydration, indicating that fluids with a similar composition to the one present at the garnet–amphibole peridotite formation, were responsible for increased amphibole formation. The combined evidence from the metamorphic and metasomatic evolution indicates that the peridotites experienced first corner flow in a mantle wedge, followed by subduction and finally entrapment and exhumation within a crustal slab. During their entire history the Ulten peridotites were percolated first by melts and then by aqueous fluids, which added recycled crustal components to the mantle wedge.  相似文献   

3.
Glaucophane-lawsonite facies blueschists representing a metamorphosed sequence of basic igneous rocks, cherts and shales have been investigated northeast of the district of Tav?anli in Northwest Turkey. Sodic amphiboles are rich in magnesium reflecting the generally high oxidation states of the blueschists. Lawsonite has a very uniform composition with up to 2.5 wt.% Fe2O3. Sodic pyroxenes show an extensive range of compositions with all the end-members represented. Chlorites are uniform in their Al/(Al+Fe+Mg) ratio but show variable Fe/ (Fe+Mg) ratios. Garnets from metacherts are rich in spessartine (>50%) whereas those from metabasites are largely almandine. Pistacite rich epidote is found in metacherts coexisting with lawsonite. Phengites are distinctly higher in their Fe, Mg and Si contents than those from greenschist facies. Hematites with low TiO2 are ubiquitous in metacherts. Fe2+/Mg partitioning between chlorite and sodic amphibole is strongly controlled by the calcium content of the sodic amphibole and ranges from 1.1 for low calcium substitution to 0.8 for higher calcium substitution. The Al/Fe3+ partition coefficient between sodic amphibole and sodic pyroxene is 2.1. A model system has been constructed involving projections from lawsonite, iron-oxide and quartz onto a tetrahedron with Na, Al, Fe2+ and Mg at its apices. Calcite is treated as an indifferent phase. The model system illustrates the incompatibility of the sodic pyroxene with chlorite in the glaucophanelawsonite facies; this assemblage is represented by sodic amphibole. Sodic amphibole compositions are plotted in terms of coexisting ferromagnesian minerals. Five major areas on the sodic amphibole compositional field are delineated, each associated with one of the following minerals: chlorite, stilpnomelane, talc, almandine, deerite.  相似文献   

4.
Geochemical differences between island arc basalts (IAB) andocean-floor basalts (mid-ocean ridge basalts; MORB) suggestthat the large-ion lithophile elements (LILE) K, Ba, Rb andCs are probably mobilized in subduction zone fluids and melts.This study documents LILE enrichment of eclogite, amphibolite,and epidote ± garnet blueschist tectonic blocks and relatedrocks from melanges of two subduction complexes. The samplesare from six localities of the Franciscan Complex, California,and related terranes of Oregon and Baja California, and fromthe Samana Metamorphic Complex, Samana Peninsula, DominicanRepublic. Most Franciscan blocks are MORB-like in their contentsof rare earth elements (REE) and high field strength elements(HFSE); in contrast, most Samana blocks show an IAB signatureof these elements. The whole-rock K2O contents of both groupsrange from 1 to 3 wt %; K, Ba, Rb, and Cs are all strongly intercorrelated.Many blocks display K/Ba similar to metasomatized transitionzones and rinds at their outer margins. Some transition zonesand rinds are enriched in LILE compared with host blocks; othersare relatively depleted in these elements. Some LILE-rich blockscontain ‘early’ coarse-grained muscovite that isaligned in the foliation defined by coarse-grained omphaciteor amphibole grains. Others display ‘late’ muscovitein veins and as a partial replacement of garnet; many containboth textural types. The muscovite is phengite that contains3.25–3.55 Si per 11 oxygens, and 0.25–0.50 Mg per11 oxygens. Lower-Si phengite has a significant paragonite component:Na per 11 oxygens ranges to 0.12. Ba contents of phengite rangeto over 1 wt % (0.027 per 11 oxygens). Ba in phengite does notcovary strongly with either Na or K. Ba contents of phengiteincrease from some blocks to their transition zones or rinds,or from blocks to their veins. Averaged K/Ba ratios for phengiteand host samples define an array which describes other subsamplesof the block and other analyzed blocks. Phengite carries essentiallyall of the LILE in otherwise mafic eclogite, amphibolite, andgarnet blueschist blocks that are enriched in these elementscompared with MORB. It evidently tracks a distinctive type ofLILE metasomatism that attends both high-T and retrograde subductionzone metamorphism. An obvious source for the LILE is a fluidin equilibrium with metasedimentary rocks. High-grade semipeliticschists from subduction complexes and subductable sediment displayLILE values that resemble those seen in the most LILE-rich blocks.Modeling of Ba and Ti suggests that 1–40 wt % of phengiteadded to MORB can produce their observed LILE enrichment. Thus,the release of LILE from such rocks to fluids or melts in veryhigh-T and -P parts of subduction zones probably depends criticallyon the stability and solubility relations of phengite, whichis thought to be stable at pressures as high as 95–110kbar at T=750–1050°C. KEY WORDS: geochemistry; LT eclogite; mineral chemistry; metasomatism; phengite  相似文献   

5.
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   

6.
The Chinese western Tianshan high-pressure/low-temperature (HP–LT) metamorphic belt, which extends for about 200 km along the South Central Tianshan suture zone, is composed of mainly metabasic blueschists, eclogites and greenschist facies rocks. The metabasic blueschists occur as small discrete blocks, lenses, bands, laminae or thick beds in meta-sedimentary greenschist facies country rocks. Eclogites are intercalated within blueschist layers as lenses, laminae, thick beds or large massive blocks (up to 2 km2 in plan view). Metabasic blueschists consist of mainly garnet, sodic amphibole, phengite, paragonite, clinozoisite, epidote, chlorite, albite, accessory titanite and ilmenite. Eclogites are predominantly composed of garnet, omphacite, sodic–calcic amphibole, clinozoisite, phengite, paragonite, quartz with accessory minerals such as rutile, titanite, ilmenite, calcite and apatite. Garnet in eclogite has a composition of 53–79 mol% almandine, 8.5–30 mol% grossular, 5–24 mol% pyrope and 0.6–13 mol% spessartine. Garnet in blueschists shows similar composition. Sodic amphiboles include glaucophane, ferro-glaucophane and crossite, whereas the sodic–calcic amphiboles mainly comprise barroisite and winchite. The jadeite content of omphacite varies from 35–54 mol%. Peak eclogite facies temperatures are estimated as 480–580 °C for a pressure range of 14–21 kbar. The conditions of pre-peak, epidote–blueschist facies metamorphism are estimated to be 350–450 °C and 8–12 kbar. All rock types have experienced a clockwise P–T path through pre-peak lawsonite/epidote-blueschist to eclogite facies conditions. The retrograde part of the P–T path is represented by the transition of epidote-blueschist to greenschist facies conditions. The P–T path indicates that the high-pressure rocks formed in a B-type subduction zone along the northern margin of the Palaeozoic South Tianshan ocean between the Tarim and Yili-central Tianshan plates.  相似文献   

7.
A stratigraphically coherent blueschist terrane near Aksu in northwestern China is unconformably overlain by unmetamorphosed sedimentary rocks of Sinian age (～600 to 800 Ma). The pre-Sinian metamorphic rocks, termed the Aksu Group, were derived from shales, sandstones, basaltic volcanic rocks, and minor cherty sediments. They have undergone multi-stage deformation and transitional blueschist/greenschist-facies metamorphism, and consist of strongly foliated chlorite-stilpnomelane-graphite schist, stilpnomelane-phengite psammitic schist, greenschist, blueschist, and minor quartzite, metachert, and meta-ironstone. Metamorphic minerals of basaltic blueschists include crossitic amphibole, epidote, chlorite, albite, quartz, and actinolite. Mineral parageneses and compositions of sodic amphibole suggest blueschist facies recrystallization at about 4 to 6 kbar and 300 to 400° C. Many thin diabasic dikes cut the Aksu Group; they are characterized by high alkali, TiO2, and P2O5 contents and possess geochemical characteristics of within-plate basalts; some of these diabasic rocks contain sodic clinopyroxene and amphibole as primary phases and have minor pumpellyite, albite, epidote, chlorite, and calcite as the prehnite/pumpellyite-facies metamorphic assemblage. This prehnite/pumpellyite-facies overprint did not affect the host rocks of the blueschist-facies lithologies.

K-Ar and Rb-Sr ages of phengite and whole rocks from pelitic schists are ～690 to 728 Ma, and a 40Ar/39Ar age of crossite from the blueschist is 754 Ma. The basal conglomerate of the overlying Sinian to Eocambrian sedimentary succession contains clasts of both the blueschist and cross-cutting dike rocks, clearly demonstrating that conditions required for blueschist-facies metamorphism were attained and ceased at least 700 Ma. The northward-increasing metamorphic grade of the small blueschist terrane may reflect northward subduction of an accretionary complex beyond the northern edge of the Tarim craton. Abundant subparallel diabasic dikes indicate a subsequent period of Pre-Sinian rifting and diabasic intrusion along the northern margin of Tarim; a Sinian siliciclastic and carbonate sequence was deposited unconformably atop the Aksu Group and associated diabase dikes.  相似文献   

8.
An Early Palaeozoic (Ordovician ?) metamudstone sequence near Wojcieszow, Kaczawa Mts, Western Sudetes, Poland, contains numerous metabasite sills, up to 50 m thick. These subvolcanic rocks are of within-plate alkali basalt type. Primary igneous phases in the metabasites, clinopyroxene (salite) and kaersutite, are veined and partly replaced by complex metamorphic mineral assemblages. Particularly, the kaersutite is corroded and rimmed by zoned sodic, sodic–calcic and calcic amphiboles. The matrix is composed of actinolite, pycnochlorite, albite (An ≤ 0.5%), epidote (Ps 27–33), titanite, calcite, opaques and, occasionally, biotite, phengite and stilpnomelane. The sodic amphiboles are glaucophane to crossite in composition with NaB from 1.9 to 1.6. They are rimmed successively by sodic–calcic and calcic amphiboles with compositions ranging from magnesioferri-winchite to actinolite. No compositions between NaB= 0.92 and NaB= 1.56 have been ascertained. The textures may be interpreted as representing a greenschist facies overprint on an earlier blueschist (or blueschist–greenschist transitional) assemblage. The presence of glaucophane and no traces of a jadeitic pyroxene + quartz association indicate pressures between 6 and 12 kbar during the high-pressure episode. Temperature is difficult to assess in this metamorphic event. The replacement of glaucophane by actinolite + chlorite + albite, with associated epidote, allows restriction of the upper pressure limit of the greenschist recrystallization to <8 kbar, between 350 and 450°C. The mineral assemblage representing the greenschist episode suggests the P–T conditions of the high-pressure part of the chlorite or lower biotite zone. The latest metamorphic recrystallization, under the greenschist facies, may have taken place in the Viséan.  相似文献   

9.
Metabasaltic rocks in the Klamath Mountains of California with ‘komatiitic’ major element concentrations were investigated in order to elucidate the origin of the magnesian signature. Trace-element concentrations preserve relict igneous trends and suggest that the rocks are not komatitic basalts, but immature arc rocks and within-plate alkalic lavas. Correlation of ‘excess’ MgO with the volume per cent hornblende (±clinopyroxene) suggests that the presence of cumulus phases contributes to the MgO-rich compositions. Early submarine alteration produced regional δ18O values of +10±1.5%° and shifts in Al2O3, Na2O, and K2O concentrations. Regional metamorphic grade in the study area varies from biotite-zone greenschist facies (350–550°C, c. 3 kbar) southward to prehnite–actinolite facies (200–400°C, ≤3 kbar), but little isotopic or elemental change occurred during the regional recrystallization. The greenschist facies assemblage is actinolitic hornblende + phengite + epidote + sodic plagioclase + microcline + chlorite + titanite + hematite + quartz in Ti-poor metabasaltic rocks; in addition to these phases biotite is present in Ti-rich analogues. Lower grade greenstones contain prehnite and more nearly stoichiometric actinolite. The moderate to low pressures of regional metamorphism are compatible with P–T conditions in a magmatic arc. Later contact metamorphism at 2–2.9±0.5 kbar and at peak temperatures approaching 600° C around the English Peak and Russian Peak granodiorites produced 3–4–km-wide aureoles typified by gradual, systematic increases in the pargasite content of amphibole, muscovite content of potassic white mica, and anorthite content of plagioclase compositions. Metasomatism during contact metamorphism produced further increases in bulk-rock δ18OSMOW of as much as +6%°. Thus, the unusually MgO-rich nature of the Sawyers Bar rocks may be attributed at least partly to metasomatism and the presence of magnesian cumulus phases.  相似文献   

10.
In this paper, we present data on major and trace elements in highly metamorphosed mafic rocks from the granulite-gneiss complex of the Angara-Kan block (southwestern Siberian craton), identify igneous protoliths of the metabasites, and assess the mobility of elements during metamorphism. Two types of rocks with different geologic relations and compositions were recognized. Garnet-bearing two-pyroxene granulites (Cpx + Pl + Grt + Opx) occur as sheet- and boudin-like bodies, which were folded and deformed with their host paragneisses. Dikes, which in most cases underwent only brittle deformation, are composed of metabasites characterized by the assemblage Cpx + Hbl + Pl + Grt. The major element compositions of igneous protoliths for the mafic granulites and metabasite dykes correspond to variously differentiated basaltic magmas. The protoliths of the metabasites are depleted in K2O, LILE, Zr, Nb, and LREE and were derived from a depleted mantle source. The major and trace element compositions of the dike metabasites are similar to those of low-K tholeiitic basalts of oceanic island arcs. Continental intraplate basalts derived from an enriched mantle source are possible igneous protoliths for the mafic granulites enriched in Ba, LREE, Nb, Ta, Zr, and Hf. It is assumed that lower Rb, Th, and U contents in the mafic granulites compared with continental flood basalts, high K/Rb and La/Th, and moderate Th/U ratios reflect the loss of Rb, Th and U during granulite-facies metamorphism.  相似文献   

11.
The whole-rock chemistry of eclogites, partially amphibolitized eclogites, and dyke amphibolites from the metamorphic Kechros complex in the eastern Rhodope Mountains preserves evidence of the geodynamic framework for the origin of their protoliths. Major and trace-element concentrations define two distinct protolith groups for the eclogites. The low-Fe–Ti (LFT) eclogites have low-TiO2 content (<0.67 wt%), negative high field strength element anomalies, and variable enrichments in large ion lithophile elements (LILE). The rare earth element (REE) patterns are characterized by strong light-REE (LREE) enrichment and heavy-REE (HREE) depletion. The high-Fe–Ti (HFT) eclogites have small to moderate LILE enrichment and lack Nb anomalies. The REE patterns of the HFT eclogites are characterized by LREE depletion and relatively flat MREE–HREE patterns. The rock compositions and petrographic features of the LFT eclogites resemble gabbros formed in a continental rift environment with minor to moderate contamination of a mantle-derived mafic magma by continental crust, whereas the HFT eclogites resemble mafic rocks formed in extensional oceanic environments. We interpret the HFT suite to represent a later stage in an evolution from continental rift to open ocean, following the origin of the LFT suite. Dyke amphibolite compositions, except for probable SiO2 loss associated with metamorphic dehydration reactions, appear to represent liquid compositions quenched in conduits through the lower crust. MELTS modeling shows that dyke amphibolite compositions can be related to each other by fractional crystallization under strongly oxidizing conditions at ~0.5 GPa pressure, and all can be derived from a low-degree melt of modified fertile peridotite from around 1.7 GPa. Cumulates crystallized from the parental liquids of the amphibolites under oxidizing conditions may have yielded the protoliths of the HFT suite.  相似文献   

12.
Basic and ultrabasic blocks within ophiolitic mélanges of the Cycladic Blueschist Unit in southern Evia provide a detailed insight into its ocean floor igneous and hydrothermal evolution, as well as the regional poly‐metamorphism occurring during Alpine orogenesis. The upper structural levels (Mt. Ochi exposures) are dominated by metamorphosed wehrlites, gabbros and highly light rare earth element (LREE)‐enriched pillow basalts, whereas the underlying Tsaki mélange consists of basic protoliths with much less fractionated REE patterns as well as mantle harzburgites. Most of the metabasites show Nb anomalies, indicative of derivation from a subduction‐affected mantle. The igneous bodies were juxtaposed and incorporated into the enclosing sedimentary sequences prior to high‐pressure/low‐temperature (HP/LT) metamorphism (M1). Glaucophane, epidote, sodic clinopyroxene and high‐Si phengite constitute the Eocene M1 assemblage, which is estimated to have formed at >11 kbar and 400–450 °C. High δ18O values of M1 minerals in Ochi metagabbros indicate that the formation of the high‐pressure assemblage was controlled by infiltration of fluids from the dehydrating host sediments. Cooling during decompression is indicated by an overprinting (M2, Early Miocene) pumpellyite–actinolite facies assemblage in metabasic rocks, calculated to have developed at P<8 kbar and T <350 °C. Possible mechanisms for such cooling include: exhumation from shallower burial levels relative to the eclogites of the NW Cyclades, accretion of colder rocks from below and extensional unroofing by low‐angle normal faults and detachments. The occurrence of sodic augite in the M2 assemblage of Tsaki metagabbros indicates that rocks at the base of the Blueschist Unit cooled faster or longer than their higher level Ochi counterparts. This suggests that differential cooling of the blueschists was enhanced by the underthrusting of colder rock units.  相似文献   

13.
The end of an orogenic Wilson cycle corresponds to amalgamation of terranes into a Pangaea and is marked by widespread magmatism dominated by granitoids. The post-collision event starts with magmatic processes still influenced by subducted crustal materials. The dominantly calc-alkaline suites show a shift from normal to high-K to very high-K associations. Source regions are composed of depleted and later enriched orogenic subcontinental lithospheric mantle, affected by dehydration melting and generating more and more K- and LILE-rich magmas. In the vicinity of intra-crustal magma chambers, anatexis by incongruent melting of hydrous minerals may generate peraluminous granitoids bearing mafic enclaves. The post-collision event ends with emplacement of bimodal post-orogenic (PO) suites along transcurrent fault zones. Two suites are defined, (i) the alkali-calcic monzonite–monzogranite–syenogranite–alkali feldspar granite association characterised by [biotite+plagioclase] fractionation and moderate [LILE+HFSE] enrichments and (ii) the alkaline monzonite–syenite–alkali feldspar granite association characterised by [amphibole+alkali feldspar] fractionation and displaying two evolutionary trends, one peralkaline with sodic mafic mineralogy and higher enrichments in HFSE than in LILE, and the other aluminous biotite-bearing marked by HFSE depletion relative to LILE due to accessory mineral precipitation. Alkali-calcic and alkaline suites differ essentially in the amounts of water present within intra-crustal magma chambers, promoting crystallisation of various mineral assemblages. The ultimate enriched and not depleted mantle source is identical for the two PO suites. The more primitive LILE and HFSE-rich source rapidly replaces the older orogenic mantle source during lithosphere delamination and becomes progressively the thermal boundary layer of the new lithosphere. Present rock compositions are a mixture of major mantle contribution and various crustal components carried by F-rich aqueous fluids circulating within convective cells created around magma chambers. In favourable areas, PO suites pre-date a new orogenic Wilson cycle.  相似文献   

14.
Primary multiphase brine fluid inclusions in omphacite and garnet from low‐ to medium‐temperature eclogites have been analysed for Cl, Br, I, F, Li and SO4. Halogen contents and ratios provide information about trapped lower crustal fluids, even though the major element (Na, K, Ca) contents of inclusion fluids have been modified by fluid–mineral interactions and (step‐) daughter‐crystal formation after trapping. Halogens in the inclusion fluids were analysed with crush–leach techniques. Cl/Br and Cl/I mass ratios of eclogite fluids are in the range 31–395 and 5000–33 000, respectively. Most fluids have a Cl/Br ratio lower than modern seawater and a Cl/I ratio one order of magnitude lower than modern seawater. Fluids with the lowest Cl/Br and highest Cl/I ratios come from an eclogite that formed by hydration of granulite facies rocks, and may indicate that Br and I are fractionated into hydrous minerals. Reconstructions indicate that the inclusion fluids originally contained 500–4000 ppm Br, 1–14 ppm I and 33–438 ppm Li. Electron microprobe analyses of eclogite facies amphibole, biotite, phengite and apatite indicate that F and Cl fractionate most strongly between phengite (F/Cl mass ratio of 1469 ± 1048) and fluid (F/Cl mass ratio of 0.008), and the least between amphibole and fluid. The chemical evolution of Cl and Br in pore fluids during hydration reactions is in many ways analogous to Cl and Br in seawater during evaporation: the Cl/Br ratio remains constant until the aH2O value is sufficiently lowered for Cl to be removed from solution by incorporation into hydrous minerals.  相似文献   

15.
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   

16.
High-pressure metamorphic (HPM) rocks (derived from igneous protoliths) and their metasomatised rinds from the island of Syros (Greece) were analysed for their B and Cl whole-rock abundances and their H2O content by prompt-gamma neutron-activation analysis (PGNAA) and for their Li and Be whole-rock abundances by ICP-OES. In the HPM rocks, B?/Be and Cl?/Be ratios correlate with H2O contents and appear to be controlled by extraction of B and Cl during dehydration and prograde metamorphism. In contrast, samples of the metasomatised rinds show no such correlation. B?/Be ratios in the rinds are solely governed by the presence or absence of tourmaline, and Cl?/Be ratios vary significantly, possibly related to fluid inclusions. Li/Be ratios do not correlate with H2O contents in the HPM rocks, which may in part be explained by a conservative behaviour of Li during dehydration. However, Li abundances exceed the vast majority of published values for Li abundances in fresh, altered, or differentiated oceanic igneous rocks and presumably result from metasomatic enrichment of Li. High Li concentrations and highly elevated Li/Be ratios in most metasomatised samples demonstrate an enrichment of Li in the Syros HP mélange during fluid infiltration. This study suggests that B and Cl abundances of HPM meta-igneous rocks can be used to trace prograde dehydration, while Li concentrations seem to be more sensitive for retrograde metasomatic processes in such lithologies.  相似文献   

17.
Mineralisation of uraninite and brannerite occurs in the albitised metasedimentary and intrusive igneous rocks of Kerpura-Tiwari-ka-bas area in Sikar district, Rajasthan. Samples collected from well dumps contain 0.016 to 1.52% U3O8 with very low ThO2. The host rocks show wide variation in chemical composition due to varying degree of alkali metasomatism, associated alteration and composition of protoliths. The spatial distribution of uranium in groundwater as well as rock samples from well dumps indicates localisation of the uranium mineralisation along NNE-SSW and NWSE directions in Kerpura block. Petrographic and lithogeochemical studies point towards close genetic relationship between alkali metasomatism and uranium mineralisation. The mineralisation seems to be due to mobilisation of uranium and other LILEs by metasomatising fluids and their deposition along shear zones at a later stage, which may not be spatially related to zones of intense albitisation.  相似文献   

18.
Calcsilicate xenoliths occur in large numbers in some lavas and pyroclastic flows of Lascar Volcano. Their whole-rock major element and REE compositions indicate that the protolith was the Upper Cretaceous Yacoraite Formation, which crops out extensively in NW Argentina. The whole-rock major element compositions of the xenoliths fall into specific groups suggesting a strong geochemical zonation in the skarn zone. Three geochemical zones have been identified; (1) an outer metamorphic zone rich in wollastonite; (2) a middle zone rich in pyroxene and garnet; (3) an inner zone rich in pyroxene and magnetite. The two innermost zones have developed from the wollastonite zone by infiltration of metasomatic fluids rich in Fe, Mn, Mg, Ti and Al. Whole-rock REE patterns have not changed significantly during prograde metamorphism and metasomatism, indicating REE immobility in the altering fluids. Retrograde alteration by acid-sulphate fluids produced anhydrite skarns and secondary calcite and wilkeite veins in the wollastonite zone. The carbon and oxygen isotopic compositions of this calcite indicate that it formed by Rayleigh crystallization from a low-temperature (<200 °C) fluid containing dissolved H2CO3. The calculated δ18O of the water in this fluid suggests a magmatic origin whereas the calculated δ13C of the dissolved carbonate is consistent with derivation from rocks of the Yacoraite Formation at 350 °C. It is suggested that the magmatic acid-sulphate fluid was responsible for leaching carbonate from the surrounding carbonate rocks and redepositing it in the skarn zone. REEs were mobilized during the retrograde acid-sulphate and acid-carbonate alteration. A negative Ce anomaly associated with this carbonate and sulphate indicates high oxygen fugacities in the mineralizing fluids.  相似文献   

19.
A wide range of trace elements have been analysed in mantle xenoliths (whole rocks, clinopyroxene and amphibole separates) from alkaline lavas in the Eastern Carpathians (Romania), in order to understand the process of metasomatism in the subcontinental mantle of the Carpatho-Pannonian region. The xenoliths include spinel lherzolites, harzburgites and websterites, clinopyroxenites, amphibole veins and amphibole clinopyroxenites. Textures vary from porphyroclastic to granoblastic, or equigranular. Grain size increases with increasing equilibrium temperature of mineralogical assemblages and results from grain boundary migration. In peridotites, interstitial clinopyroxenes (cpx) and amphiboles resulted from impregnation and metasomatism of harzburgites or cpx-poor lherzolites by small quantities of a melt I with a melilitite composition. Clinopyroxenites, amphibole veins and amphibole clinopyroxenites are also formed by metasomatism as a result of percolation through fracture systems of large quantities of a melt II with a melanephelinite composition. These metasomatic events are marked by whole-rock enrichments, relative to the primitive mantle (PM), in Rb, Th and U associated in some granoblastic lherzolites and in clinopyroxene and amphibole veins with enrichments in LREE, Ta and Nb. Correlations between major element whole-rock contents in peridotites demonstrate that the formation of interstitial amphibole and clinopyroxene induced only a slight but variable increase of the Ca/Al ratio without apparent modifications of the initial mantle composition. Metasomatism is also traced by enrichments in the most incompatible elements and the LREE. The Ta, Nb, MREE and HREE contents remained unchanged and confirm the depleted state of the initial but heterogeneous mantle. Major and trace element signature of clinopyroxene suggests that amphibole clinopyroxenites and some granoblastic lherzolites have been metasomatized successively by melts I and II. Both melts I and II were Ca-rich and Si-poor, somewhat alkaline (Na > K). Melt I differed from melt II in having higher Mg and Cr contents offset by lower Ti, Al, Fe and K contents. Both were highly enriched in all incompatible trace elements relative to primitive mantle, showing positive anomalies in Rb, Ba, Th, Sr and Zr. They contrasted by their Ta, Nb and LREE contents, lower in melt I than in melt II. Melts I and II originate during a two-stage melting event from the same source at high pressure and under increasing temperature. The source assemblage could be that of a metasomatized carbonated mantle but was more likely that of an eclogite of crustal affinity. Genetic relationships between calc-alkaline and alkaline lavas from Eastern Carpathians and these melts are thought to be only indirect, the former originating from partial melting of mantle sources respectively metasomatized by the melts I and II. Received: 17 March 1997 / Accepted: 14 July 1997  相似文献   

20.
The paper presents results of a detailed petrologic study of metasomatites and their host metagabbroids in the northwestern part of Kiy Island, Onega Bay, White Sea. The first evidence is acquired that coronitization and amphibolization of the host rocks took place at the peak of Svecofennian metamorphism at Т = 700–640°C, Р = 9–10 kbar, and \({a_{{H_2}O}}\) = 0.2–0.3. Accompanying metasomatism has formed a number of long (up to several meters long) melanocratic hornblendite and garnet–amphibole veins 0.3–2 m thick. In this area, metasomatites of another type make up single relatively thin amphibole–zoisite lenses that sometimes host ruby-like corundum. The fluid phase that induced metasomatism was poor in salts (Na,K)Cl, and hence, the rocks do not contain sodic plagioclase, and their amphibole is tschermakite but not pargasite. The compositions of the metasomatites of the two types are proved to be complementary, and this indicates that they were most likely produced by high-temperature metasomatism but not via the removal of components by fluid from migmatization zones.  相似文献   

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