Geochemistry of granitization and magmatic replacement of basic volcanic rocks in the contact aureole of the Yurchik gabbronorite intrusion, Ganal Range, Kamchatka

Geological and geochemical data indicate that the formation of the granulite-like rocks in the contact aureole of the Yurchik gabbronorite intrusion of the Ganal Range, Kamchatka, was caused by the contact metamorphism, metasomatism, and local melting of the initial volcanosedimentary rocks of the Vakhtalka Sequence of the Ganal Group. The temperature in the inner part of the aureole reached 700–800°C and caused the transformation of the basic volcanic rocks of the sequence into two pyroxene-plagioclase, clinopyroxene-amphibole-plagioclase, and amphibole-plagioclase hornfelses, while sedimentary rocks were converted into garnet-biotite ± cordierite hornfelses. The hornfelsed basic volcanic rocks were locally subjected to metasomatic alteration and magmatic replacement with formation of biotite-orthopyroxene-plagioclase metasomatic bodies containing biotite-orthopyroxene-plagioclase ± garnet veinlets and aggregates. During these processes, sedimentary interlayers were converted into garnet enderbites at 700–800°C and 3.2–4.8 kbar. The comparison of the chemical composition of basic volcanic rocks of the Vakhtalka Sequence and their transformation products indicates that the metasomatic alteration and magmatic replacement correspond to siliceous-alkaline metasomatism (granitization) and cause subsequent and uneven influx of SiO₂, Al₂O₃, Na₂O, K₂O, Rb, Ba, Zr, Nb, and Cl and removal of Fe, Mg, Mn, Ca, Cr, Co, Ti, Y, and S. REE data on basic metavolcanic rocks, hornfelses, and metasomatites suggest that the processes of hornfelsation, metasomatism, and magmatic replacement of the initial volcanic rocks were accompanied by significant increase in LREE and slight decrease in HREE. The Sr and Nd isotope study of the rocks in the aureole showed that the initial basic volcanic rocks of the Vakhtalka Sequence are isotopically close to both mature island arc tholeiites and mid-ocean ridge basalts. The metasomatic alteration and magmatic replacement of volcanic rocks in the aureole lead to the decrease of ¹⁴³Nd/¹⁴⁴Nd and increase of ⁸⁷Sr/⁸⁶Sr approximately parallel to mantle array. Pb isotopic ratios in the studied rocks become more radiogenic from initial metavolcanic rocks to metasomatites. It is suggested that the processes of metamorphism, metasomatism, and magmatic replacement were caused by highly mineralized mantle fluids, which percolated along magmatic channels serving as pathways for gabbroid magma.     

Barium and strontium in the upper mantle of the Pamirs and Tien Shan

The distribution of Ba and Sr in deep-seated xenoliths, mantle alkaline melts, and their minerals from the Pamirs and Tien Shan and some other regions was considered. In contrast to ordinary magmatic series, the mantle rocks show a correlation of Sr with both Ca and alkalis. The most extensive accumulation of Ba and Sr in the upper mantle occurs during the processes of mantle metasomatism and melting of metasomatized materials. The influx of these elements is probably related to ultradeep plume-type sources. Ba and Sr were transported from the mantle into the crust by both high-temperature alkaline melts and low-temperature hydrothermal solutions. It is supposed that the late Alpine celestite deposits of the huge Sr province of the Mediter-ranean belt are of mantle origin. Geochemical provinces show distinctive concentrations and proportions of Ba and Sr in mantle-derived alkaline basic rocks, metasomatic rocks, and their minerals. The type of Ba-Sr relations is inherited by crustal rocks.     

Petrological, geochemical and isotopic characteristics of the lithospheric mantle beneath Sardinia (Italy) as indicated by ultramafic xenoliths enclosed in alkaline lavas

Mantle xenoliths hosted in Miocene-Quaternary mafic alkaline volcanic rocks from Sardinia have been investigated with electron microprobe, laser ablation microprobe-inductively coupled plasma-mass spectrometry and thermal ionization mass spectrometry techniques. The xenoliths are anhydrous clinopyroxene-poor lherzolites and harzburgites, plus very rare websterites and olivine-websterites. Glassy pods having thin subhedral to euhedral microlites of olivine, clinopyroxene and spinel have been found in harzburgites and websterites. Clinopyroxene shows trace element variability, with values of (La/Yb)_N ranging from sub-chondritic (0.01) to supra-chondritic (8.6). The Sr–Nd isotopic ratios of the clinopyroxenes fall mostly in the field of the European lithospheric mantle xenoliths (⁸⁷Sr/⁸⁶Sr from 0.70385 to 0.70568 and ¹⁴³Nd/¹⁴⁴Nd ranging from 0.512557 to 0.512953). The geochemical characteristics of the Sardinian xenoliths testify to the variable degrees of earlier partial melt extraction, followed by metasomatic modification by alkaline melts or fluids. Websterites are considered to represent small lenses or veins of cumulitic (i.e. magmatic) origin within the mantle peridotite.     

The Gumeshevo skarn-porphyry copper deposits in the Central Urals,Russia: Evolution of the ore-magmatic system as deduced from isotope geochemistry (Sr,Nd, C,O, H)

The Early Devonian Gumeshevo deposit is one of the largest ore objects pertaining to the dioritic model of the porphyry copper system paragenetically related to the low-K quartz diorite island-arc complex. The (⁸⁷Sr/⁸⁶Sr)_t and (ɛ_Nd)_t of quartz diorite calculated for t = 390 Ma are 0.7038–0.7045 and 5.0–5.1, respectively, testifying to a large contribution of the mantle component to the composition of this rock. The contents of typomorphic trace elements (ppm) are as follows: 30–48 REE sum, 5–10 Rb, 9–15 Y, and 1–2 Nb. The REE pattern is devoid of Eu anomaly. Endoskarn of low-temperature and highly oxidized amphibole-epidote-garnet facies is surrounded by the outer epidosite zone. Widespread retrograde metasomatism is expressed in replacement of exoskarn and marble with silicate (chlorite, talc, tremolite)-magnetite-quartz-carbonate mineral assemblage. The ⁸⁷Sr/⁸⁶Sr ratios of epidote in endoskarn and carbonate in retrograde metasomatic rocks (0.7054–0.7058 and 0.7053–0.7065, respectively) are intermediate between the Sr isotope ratios of quartz dioritic rocks and marble (⁸⁷Sr/⁸⁶Sr = 0.70784 ± 2). Isotopic parameters of the fluid equilibrated with silicates of skarn and retrograde metasomatic rocks replacing exoskarn at 400°C are δ¹⁸O = +7.4 to +8.5‰ and δD = −49 to −61‰ (relative to SMOW). The δ¹³C and δ¹⁸O of carbonates in retrograde metasomatic rocks after marble are −5.3 to +0.6 (relative to PDB) and +13.0 to +20.2% (relative to SMOW), respectively. Sulfidation completes metasomatism, nonuniformly superimposed on all metasomatic rocks and marbles with formation of orebodies, including massive sulfide ore. The δ³⁴S of sulfides is 0 to 2‰ (relative to CDT);⁸⁷Sr/⁸⁶Sr of calcite from the late calcite-pyrite assemblage replacing marble is 0.704134 ± 6. The δ¹³C and ⁸⁷Sr/⁸⁶Sr of postore veined carbonates correlate positively (r = 0.98; n = 6). The regression line extends to the marble field. Its opposite end corresponds to magmatic (in terms of Bowman, 1998b) calcite with minimal δ¹³C, δ¹⁸O, and ⁸⁷Sr/⁸⁶Sr values (−6.9 ‰, +6.7‰, and 0.70378 ± 4, respectively). The aforementioned isotopic data show that magmatic fluid was supplied during all stages of mineral formation and interacted with marble and other rocks, changing its Sr, C, and O isotopic compositions. This confirms the earlier established redistribution of major elements and REE in the process of metasomatism. A contribution of meteoric and metamorphic water is often established in quartz from postore veins.     

Sr isotopic heterogeneity in primitive basaltic rocks,southeastern Australia: correlation with mantle metasomatism

Rb/Sr data for seven basaltic provinces (K-Ar ages 50-0 Ma) in southeastern Australia imply isotopic heterogeneities in the mantle sources. The total range of ⁸⁷Sr/ ⁸⁶Sr is 0.7031–0.7054. Effects of crustal contamination are negligible, since the rocks analyzed represent primary or primitive magma compositions. The inferred scales of heterogeneity range from <1 km for small intraprovince variations, to in the order of 100 km for the larger differences between provinces.Correlation of regional high ⁸⁷Sr/⁸⁶Sr in basaltic rocks with the presence of amphibole-bearing upper mantle xenoliths suggests that the degree of metasomatic activity in the underlying mantle is a major control on the Rb/Sr and ⁸⁷Sr/⁸⁶Sr values of mantle source volumes and partial melts derived from these. Xenolith data also indicate that both pervasive metasomatism and the presence of crystallized melts or cumulates as veins and dykes in mantle wall rock are possible mechanisms for metasomatic additions.Mantle isochrons can be constructed both within some provinces and between provinces. However, episodic metasomatism in the mantle source regions, with correlated enrichment in Rb/Sr and ⁸⁷Sr/⁸⁶Sr, can produce artificial isochrons which may have no relevance to mantle differentiation events.     

Proterozoic Gremyakha-Vyrmes Polyphase Massif, Kola Peninsula: An example of mixing basic and alkaline mantle melts

The paper presents newly obtained data on the geological structure, age, and composition of the Gremyakha-Vyrmes Massif, which consists of rocks of the ultrabasic, granitoid, and foidolite series. According to the results of the Rb-Sr and Sm-Nd geochronologic research and the U-Pb dating of single zircon grains, the three rock series composing the massif were emplaced within a fairly narrow age interval of 1885 ± 20 Ma, a fact testifying to the spatiotemporal closeness of the normal ultrabasic and alkaline melts. The interaction of these magmas within the crust resulted in the complicated series of derivatives of the Gremyakha-Vyrmes Massif, whose rocks show evidence of the mixing of compositionally diverse mantle melts. Model simulations based on precise geochemical data indicate that the probable parental magmas of the ultrabasic series of this massif were ferropicritic melts, which were formed by endogenic activity in the Pechenga-Varzuga rift zone. According to the simulation data, the granitoids of the massif were produced by the fractional crystallization of melts genetically related to the gabbro-peridotites and by the accompanying assimilation of Archean crustal material with the addition of small portions of alkaline-ultrabasic melts. The isotopic geochemical characteristics of the foidolites notably differ from those of the other rocks of the massif: together with carbonatites, these rocks define a trend implying the predominance of a more depleted mantle source in their genesis. The similarities between the Sm-Nd isotopic characteristics of foidolites from the Gremyakha-Vyrmes Massif and the rocks of the Tiksheozero Massif suggest that the parental alkaline-ultrabasic melts of these rocks were derived from an autonomous mantle source and were only very weakly affected by the crust. The occurrence of ultrabasic foidolites and carbonatites in the Gremyakha-Vyrmes Massif indicates that domains of metasomatized mantle material were produced in the sublithospheric mantle beneath the northeastern part of the Fennoscandian Shield already at 1.88 Ga, and these domains were enriched in incompatible elements and able to produce alkaline and carbonatite melts. The involvement of these domains in plume-lithospheric processes at 0.4–0.36 Ga gave rise to the peralkaline melts that formed the Paleozoic Kola alkaline province.     

Multi-proxy isotopic tracing of magmatic sources and crustal recycling in the Palaeozoic to Early Jurassic active margin of North-Western Gondwana

We trace source variations of active margin granitoids which crystallised intermittently over ~300 Ma in varying kinematic regimes, by combining zircon Lu-Hf isotopic data from Early Palaeozoic to Early Jurassic igneous and metaigneous rocks in the Mérida Andes, Venezuela and the Santander Massif, Colombia, with new whole rock Rb/Sr and Sm-Nd isotopic data, and quartz O isotopic data. These new data are unique in South America because they were obtained from discrete magmatic and metamorphic zircon populations, providing a high temporal resolution dataset, and compare several isotopic systems on the same samples. Collectively, these data provide valuable insight into the evolution of the isotopic structure of the continental crust in long-lived active margins.Phanerozoic active margin-related granitoids in the Mérida Andes and the Santander Massif yield zircon Lu-Hf model ages ranging between 0.77 Ga and 1.57 Ga which clearly define temporal trends that can be correlated with changes in tectonic regimes. The oldest Lu-Hf model ages of >1.3 Ga are restricted to granitoids which formed during Barrovian metamorphism and crustal thickening between ~499 Ma and ~473 Ma. These granitoids yield high initial ⁸⁷Sr/⁸⁶Sr ratios, suggesting that evolved, Rb-rich middle to upper crust was the major source of melt. Granitoids and rhyolites which crystallised during subsequent extension between ~472 Ma and ~452 Ma yield younger Lu-Hf model ages of 0.80 Ga–1.3 Ga and low initial ⁸⁷Sr/⁸⁶Sr ratios, suggesting that they were derived from much more juvenile, Rb-poor sources such as mafic lower crust and mantle-derived melts. The rapid change in magmatic sources at ~472 Ma can be attributed either to reduced crustal assimilation during extension, or a short pulse of crustal growth by addition of juvenile material to the continental crust. Between ~472 Ma and ~196 Ma Lu-Hf model ages remain mostly constant between ~1.0 and ~1.2 Ga. The large scatter and the absence of definite trends in initial ⁸⁷Sr/⁸⁶Sr ratios suggest that both mafic, Rb-poor, and evolved Rb-rich sources were important precursors of active margin magmas in Colombia and Venezuela throughout the Palaeozoic to the Early Jurassic.Previous studies have shown that the genesis of arc magmas may be stimulated by heat advection to the crust during the underplating of mantle derived melt, but the absence of permanent younging trends in Lu-Hf model ages from ~472 Ma to ~196 Ma suggests that very little new crust was generated during this period in the studied region. An overwhelming majority of the analysed igneous rocks yield zircon Lu-Hf model ages of >1 Ga which may be accounted for by documented local crustal end members of 1 Ga–1.6 Ga, and do not require contributions from the depleted mantle. Therefore, recycling of ~1 Ga and older crust was a dominant process in the north-western corner of Gondwana between ~472 Ma and ~196 Ma.This study shows that whole rock Sm-Nd and zircon Lu-Hf data can be interpreted similarly regarding the age of the source regions, whereas Rb-Sr and O isotope data from the same rocks yield valuable information regarding the geochemical nature of the source.     

Quartz-albite-microcline metasomatic rocks in the Main Sayan Fault Zone: Evolution of metasomatism and composition of accessory minerals

Quartz-albite-microcline metasomatic rocks (qualmites) localized in the Main Sayan Fault Zone at the boundary of Irkutsk oblast and Buryatia (Eastern Sayan, middle reaches of the Kitoi River) were formed after dynamometamorphic biotite and biotite-amphibole granite gneisses. The zone of alkaline metasomatism up to 250–300 m thick extends for about 12 km along the Main Sayan Fault. Riebeckite-aegirine and hornblende-clinopyroxene qualmites were formed during the early alkaline stage of metasomatism. Biotite-magnetite qualmites, which are occasionally superimposed on riebeckite-aegirine rocks, are products of the following stage of increasing acidity. The ⁴⁰Ar/³⁹Ar age of amphibole from metasomatic rocks is 321 ± 5 Ma. The metasomatic rocks are enriched by 2–4 times in Zr, Nb, Y, REE, Be, Th, and U relative to unaltered granite gneisses and contain rare-metal mineralization (fergusonite-(Y), betafite, Nb- and Y- bearing titanites, gadolinite-(Y), zircon, thorite, allanite-(Ce), chevkinite-(Ce), etc.). The composition of accessory minerals was studied on a LEO-1430VP SEM. Their composition and mineral assemblages show that meta-somatic alteration and Ti-Nb-Zr-REE mineralization were formed synchronously. The stage of acid solution neutralization was characterized by crystallization of epidote and andradite and by replacement of chevkinite with allanite and titanite in metasomatic rocks. Hydro- and fluorcarbonates of LREE, phosphates (monazite-(Ce)), and fluorides (F-bearing thorianite?) were formed during the final low-temperature stage.     

Petrogenesis of plio-quaternary intra-plate continental alkaline lavas from the İskenderun Gulf (Southern Turkey): Evidence for metasomatized lithospheric mantle

The Quaternary alkaline volcanic field of Southern Turkey is characterized by intra-continental plate-type magmatic products, exposed to the north of the ?skenderun Gulf along a NE-SW trending East Anatolian Fault, to the west of its intersection with the N–S trending Dead Sea Fault zone. The ?skenderun Gulf alkaline rocks are mostly silica-undersaturated with normative nepheline and olivine and are mostly classified as basanites and alkaline basalts with their low-silica contents ranging between 43 and 48?wt.% SiO₂. They display Ocean Island Basalt (OIB)–type trace element patterns characterized by enrichments in large-ion-lithophile elements (LILE) and light rare earth element (LREE), and have (La/Yb)_N?=?8.8–17.7 and (Hf/Sm)_N?=?0.9–1.6 similar to those of basaltic rocks found in intraplate suites. The basanitic rocks have limited variations Sr-Nd isotopic ratios (⁸⁷Sr/⁸⁶Sr?=?0.70307–0.70324, ¹⁴³Nd/¹⁴⁴Nd?=?0.512918–0.521947), whereas the alkali basalts display more evolved Sr-Nd isotopic ratios (⁸⁷Sr/⁸⁶Sr?=?0.70346-0.70365, ¹⁴³Nd/¹⁴⁴Nd?=?0.512887–0.521896). The ?skenderun Gulf alkaline rocks also display limited Pb isotopic variations with ²⁰⁶Pb/²⁰⁴Pb?=?18.75–19.09 ²⁰⁷Pb/²⁰⁴Pb?=?15.61–15.66 and²⁰⁸Pb/²⁰⁴Pb?=?38.65–39.02, indicating that they originated from an enriched lithospheric mantle source. Calculated fractionation vectors indicate that clinopyroxene and olivine are the main fractionating mineral phases. Similarly, based on Sr-Nd isotopic ratios, the assimilation and fractional crystallization (AFC) modeling shows that the alkali basalts were affected by AFC processes (r?=?0.2) and were slightly contaminated by the upper crustal material.The high TiO₂ contents, enrichments in Ba and Nb, and depletions in Rb can likely be explained by the existence of amphibole in the mantle source, which might, in turn, indicate that the source mantle has been affected by metasomatic processes. The modeling based on relative abundances of trace elements suggests involvement of amphibole-bearing peridotite as the source material. ?skenderun Gulf alkaline rocks can thus be interpreted as the products of variable extent of mixing between melts from both amphibole-bearing peridotite and dry peridotite.     

Amphibole-rich xenoliths and host alkali basalts: petrogenetic constraints and implications on the recent evolution of the upper mantle beneath Ahaggar (Central Sahara,Southern Algeria)

Quaternary basanitic to nephelinitic volcanoes from Tahalra (western Ahaggar, southern Algeria) contain numerous Mg-ilmenite and amphibole-rich inclusions (±olivine, ±salite) and spinel lherzolite (±pargasite) inclusions associated with kaersutite megacrysts. On the basis of petrological, geochemical and Sr isotopic study of representative xenoliths (including a composite nodule defined as a vein cross-cutting peridotite) and lavas, we attribute the series of amphibole-rich xenoliths and megacrysts to segregation under upper mantle conditions from a hydrous high Ti and LREE melt geochemically similar to the Quaternary basanite but isotopically different. Amphibole-rich rocks and megacrysts are the results of magmatic events (less than 40 Ma) probably contemporaneous with the various pre-Quaternary volcanic phases recognized in Ahaggar. The amphibole-rich veins and the Quaternary lavas have a garnet lherzolitic source enriched in REE (7 to 9 times chondritic in LREE, 2 times in HREE). This enrichment probably results from former metasomatic events unrelated to the recent magmatic history. Melts from which these veins precipitated within upper mantle peridotite also account for mantle enrichment processes; they induced a local partial melting and contact metasomatism (pargasitization). The upper mantle beneath the volcanic areas of Ahaggar is veined and hydrous, and consequently lightened: thus, the uplift of basement may be the isostatic response to magmatism and related metasomatism and therefore the result of the Cenozoïc igneous activity.     

Late Archean magmatic complexes of the Azov terrane,Ukrainian Shield: Geological setting,isotopic age,and sources of material

Geochemical, isotopic-geochemical, and geochronological information was obtained on magmatic rocks from the Saltychan anticlinorium in the Azov domain of the Ukrainian Shield. The rocks affiliate with the calc-alkaline series and a high-Mg series. The rocks of these series notably differ in concentrations of trace elements and REE and range from gabbro to granodiorite-quartz diorite in composition. The NORDSIM ionprobe U-Pb zircons ages of rocks belonging to the Obitochnen Complex and having both elevated and normal mg# correspond to 2908–2940 Ma. The Osipenkovskaya intrusion has an age of 2855 ± 19 Ma. The most alkaline North Obitochnen intrusion was emplaced in the Proterozoic, at 2074 ± 11 Ma. The age of the amphibolite metamorphism of the host gneisses is reliably dated at 3120–3000 Ma. The model Sm-Nd ages of the intrusive rocks do not exceed 3150 Ma. According to geochemical evidence, the parental melts of the magmatic rocks were derived from mantle domains variably enriched in lithophile elements. The results obtained by studying the Sm-Nd isotopic system corroborate the conclusion drawn from geochemical evidence that most of the melts were derived from the mildly enriched mantle, practically without involvement of ancient crustal material. The mantle became enriched in LREE at approximately 3000 Ma, which corresponds to the age of metamorphism of the supracrustal rocks. This process was separated from the derivation of the melts by a time span of 70–80 Ma. The relative age of the intrusive rocks and their variable composition can be most adequately explained by a contribution of heat and material from a plume to the derivation of the parental melts of these rocks.     

Hot-fluid Driven Metasomatism of Samalpatti Carbonatites, South India: Evidence from Petrology, Mineral Chemistry, Trace Elements and Stable Isotope Compositions

The magmatic heritage of carbonatites can be identified on the basis of a combination of geological criteria such as, their mode of occurrence, the nature of associated igneous rocks, the presence of minerals of igneous origin, fenitization, characteristic trace element contents and isotopic composition. Late Proterozoic Samalpatti carbonatites were studied in view of these criteria, and were found to contain metamorphic minerals that normally form under thermal metamorphic conditions and which have unusual chemical compositions. A combination of criteria points clearly to a magmatic origin for these carbonatites. Field relations indicate that the dominant modes of intrusion of carbonatite into the encompassing pyroxenites and syenites include small dykes, veins, or lenses. The igneous nature of these carbonatites has been described elsewhere and chemically they are classified as calico-carbonatites. Currently, very little is known about the metamorphic textures and mineralogy observed in the Samalpatti carbonatites. In this study, several metamorphic minerals are reported including diopside, grossularite, vesuvianite, K-feldspar and wollastonite, and a hornfelsic texture is described. These mineral phases and texture characterize thermal metamorphism under low pressure and high temperature (LP-HT) metamorphic conditions (650°_750°C) or metasomatism aided by hot-fluid advection. The metamorphic nature of minerals reported is also confirmed by electron microprobe study. The Samalpatti carbonatite samples show much lower values of characteristic trace elements (P, Sr, Ba, Zr, Nb, Th, Y and REEs) than average concentrations for magmatic carbonatite. Stable isotopic (d¹³C and d¹⁸O) compositions of Samalpatti carbonatites do not fall in the primary igneous carbonatite (PIC) domain. The petrological and chemical signatures of these carbonatites suggest metasomatism in conjunction with fluid advection. Such a metasomatic process may drastically change the chemistry of the rocks in addition to enrichment of heavier stable isotopes. During this metasomatic process, characteristic elements would be dissolved in the high d¹⁸O fluid, and together with Rayleigh fractionation would contribute to enhanced concentrations of ¹³C and ¹⁸O in Samalpatti carbonatites.     

Metasomatism and the crystallization of zircon megacrysts in Archaean peridotites from the Lewisian complex,NW Scotland

Zircon megacrysts are locally abundant in 1–40 cm-thick orthopyroxenite veins within peridotite host rocks in the Archaean Lewisian gneiss complex from NW Scotland. The veins formed by metasomatic interaction between the ultramafic host and Si-rich melts are derived from partial melting of the adjacent granulite-facies orthogneisses. The interaction produced abundant orthopyroxene and, within the thicker veins, phlogopite, pargasite and feldspathic bearing assemblages. Two generations of zircon are present with up to 1 cm megacrystic zircon and a later smaller equant population located around the megacryst margins. Patterns of zoning, rare earth element abundance and oxygen isotopic compositions indicate that the megacrysts crystallized from crustal melts, whereas the equant zircon represents new neocryst growth and partial replacement of the megacryst zircon within the ultramafic host. Both zircon types have U–Pb ages of ca. 2464 Ma, broadly contemporaneous with granulite-facies events in the adjacent gneisses. Zircon megacrysts locally form?>?10% of the assemblage and may be associated to zones of localized nucleation or physically concentrated during movement of the siliceous melts. Their unusual size is linked to the suppression of zircon nucleation and increased Zr solubility in the Si-undersaturated melts. The metasomatism between crustal melts and peridotite may represent an analog for processes in the mantle wedge above subducting slabs. As such, the crystallization of abundant zircon in ultramafic host rocks has implications for geochemistry of melts generated in the mantle and the widely reported depletion of high field strength elements in arc magmas.     

Unravelling the effects of melt depletion and secondary infiltration on mantle Re-Os isotopes beneath the French Massif Central

Spinel lherzolite xenoliths from Mont Briançon, French Massif Central, retain evidence for multiple episodes of melt depletion and melt/fluid infiltration (metasomatism). Evidence for primary melt depletion is still preserved in the co-variation of bulk-rock major elements (MgO 38.7-46.1 wt.%; CaO 0.9-3.6 wt.%), and many samples yield unradiogenic bulk-rock Os isotope ratios (¹⁸⁷Os/¹⁸⁸Os = 0.11541-0.12626). However, many individual xenoliths contain interstitial glasses and melt inclusions that are not in equilibrium with the major primary minerals. Incompatible trace element mass balance calculations demonstrate that metasomatic components comprise a significant proportion of the bulk-rock budget for these elements in some rocks, ranging to as much as 25% of Nd and 40% of Sr Critically, for Re-Os geochronology, melt/fluid infiltration is accompanied by the mobilisation of sulfide. Consequently, bulk-rock isotope measurements, whether using lithophile (e.g. Rb-Sr, Sm-Nd) or siderophile (Re-Os) based isotope systems, may only yield a perturbed and/or homogenised average of these multiple events.Osmium mass balance calculations demonstrate that bulk-rock Os in peridotite is dominated by contributions from two populations of sulfide grain: (i) interstitial, metasomatic sulfide with low [Os] and radiogenic ¹⁸⁷Os/¹⁸⁸Os, and (ii) primary sulfides with high [Os] and unradiogenic ¹⁸⁷Os/¹⁸⁸Os, which have been preserved within host silicate grains and shielded from interaction with transient melts and fluid. The latter can account for >97% of bulk-rock Os and preserve geochronological information of the melt from which they originally precipitated as an immiscible liquid. The Re-depletion model ages of individual primary sulfide grains preserve evidence for melt depletion beneath the Massif Central from at least 1.8 Gyr ago despite the more recent metasomatic event(s).     

锦州-迁安太古宙赞岐岩类片麻岩成因及其动力学意义

详细的野外地质调查和综合研究表明冀东-辽西南部地区太古宙变质基底主要由富钾花岗质岩石组成,由锦州至迁安构成一条NEE向延伸200余千米的富钾花岗质岩石带。这些富钾花岗质岩石主要由似斑状/中粒石英二长闪长质-花岗闪长质-二长花岗质片麻岩和中粒二长花岗岩-正长花岗岩构成。全岩地球化学分析表明这些石英二长闪长质-花岗闪长质-二长花岗质片麻岩具有高FeO~T、MgO、K_2O和Mg~#值的地球化学特征,与全球范围内中-新太古宙赞歧岩类相似。LA-ICP-MS锆石U-Pb同位素定年结果表明这些岩石形成于2546~2543Ma。岩石成因研究表明这些赞歧岩类片麻岩形成于俯冲板片及其拖曳的洋壳沉积物、增生楔物质的熔体和受俯冲流体、熔体交代的地幔楔之间相互作用引发的一系列的岩浆作用。这一多样化的赞岐岩类岩浆作用形成了一条新太古代赞岐岩类带,该赞岐岩类带反映了冀东-辽西南部地区新太古代从NNW向SSE向板片热俯冲的动力学体制。     

Late Paleozoic volcanic rocks of the Intra-Sudetic Basin, Bohemian Massif: petrological and geochemical characteristics

Late Paleozoic volcanic rocks in the Intra-Sudetic Basin of the Bohemian Massif in the Czech Republic can be subdivided into two series: (I) a minor bimodal trachyandesite-rhyolite series of Upper Carboniferous age with initial ⁸⁷Sr/⁸⁶Sr of ca. 0.710 and ε_Nd values of −6.1 also characteristic of volcanics of the near Krkonoše Piedmont Basin (0.707 and −6.0, Ulrych et al., 2003) and (II) a major differentiated basaltic trachyandesite-trachyandesite-trachyte-rhyolite series of Lower Permian age with lower initial ⁸⁷Sr/⁸⁶Sr of ca. 0.705-0.708 and ε_Nd values ranging from −2.7 to −3.4/−4.1/. The newly recognized volcanic rocks of trachytic composition indicate that the rocks were formed by magmatic differentiation of similar parental melts rather than constituting a bimodal mafic-felsic sequence from different sources. Both series are generally of subalkaline affinity and calc-alkaline character with some tholeiitic tint (FeO/MgO vs. SiO₂, presence of orthopyroxene). The magmatic activity occurred in cycles in a layered chamber, each starting primarily with felsic volcanics and ending with mafic ones. The mafic rocks represent mantle-melt(s) overprinted by crust during assimilation-fractional crystallization. The Sr-Nd isotopic data confirm a significant crustal component in the volcanic rocks that may have been inherited from the upper mantle source and/or from assimilation of older crust during magmatic underplating and shallow-level melt fractionation.     

Partial melting of deeply subducted continental crust during exhumation: insights from felsic veins and host UHP metamorphic rocks in North Qaidam,northern Tibet

A combined petrological, geochronological and geochemical study was carried out on felsic veins and their host rocks from the North Qaidam ultrahigh‐pressure (UHP) metamorphic terrane in northern Tibet. The results provide insights into partial melting of deeply subducted continental crust during exhumation. Partial melting is petrograpically recognized in metagranite, metapelite and metabasite. Migmatized gneisses, including metagranite and metapelite, contain microstructures such as granitic aggregates with varying outlines, small dihedral angles at mineral junctions and feldspar with magmatic habits, indicating the former presence of felsic melts. Partial melts were also present in metabasite that occurs as retrograde eclogite. Felsic veins in both the eclogites and gneisses exhibit typical melt crystalline textures such as large euhedral feldspar grains with straight crystal faces, indicating vein crystallization from anatectic melts. The Sr–Nd isotope compositions of felsic veins inside gneisses suggest melt derivation from anatexis of host gneisses themselves, but those inside metabasites suggest melt derivation from hybrid sources. Felsic veins inside gneisses exhibit lithochemical compositions similar to experimental melts on the An–Ab–Or diagram. In trace element distribution diagrams, they exhibit parallel patterns to their host rocks, but with lower element contents and slightly positive Eu and Sr anomalies. The geochemistry of these felsic veins is controlled by minerals that would decompose and survive, respectively, during anatexis. Felsic veins inside metabasites are rich either in quartz or in plagioclase with low normative orthoclase. In either case, they have low trace element contents, with significantly positive Eu and Sr anomalies in plagioclase‐rich veins. Combined with cumulate structures in some veins, these felsic veins are interpreted to crystallize from anatectic melts of different origins with the effect of crystal fractionation. Nevertheless, felsic veins in different lithologies exhibit roughly consistent patterns of trace element distribution, with variable enrichment of LILE and LREE but depletion of HFSE and HREE. There are also higher contents of trace elements in veins hosted by gneisses than veins hosted by metabasites. Anatectic zircon domains from felsic veins and migmatized gneisses exhibit consistent U–Pb ages of c. 420 Ma, significantly younger than the peak UHP eclogite facies metamorphic event at c. 450–435 Ma. Combining the petrological observations with local P–T paths and experimentally constrained melting curves, it is inferred that anatexis of UHP gneisses was caused by muscovite breakdown while anatexis of UHP metabasites was caused by fluid influx. These UHP metagranite, metapelite and metabasite underwent simultaneous anatexis during the exhumation, giving rise to anatectic melts with different compositions in various elements but similar patterns in trace element distribution.     

Phase equilibrium and stable isotope constraints on the formation of metasomatic garnet-vesuvianite veins (SW Adamello,N Italy)

 Metasomatic garnet-vesuvianite veins occur within the contact metamorphic marble sequence of the Lower Triassic Prezzo formation in a narrow, 1–5 m wide zone along an intrusive marble-granodiorite contact at the southwestern border of the Tertiary Adamello batholith. The metasomatic mineral assemblage is comprised of garnet, vesuvianite, clinopyroxene, wollastonite, and pyrrhotite, which were precipitated from the vein-forming fluid in a preexisting calcite matrix at conditions of about 2800 bars and 630° C. The veins are enriched in silicon, aluminum, iron, magnesium, titanium and depleted in calcium with respect to the unaltered contact metamorphic marble. Graphite, which is present in the unaltered Prezzo Marble is absent in the veins. Irregularly shaped mineralogically distinct zones with different degrees of silicification can be distinguished within the veins. The isotopic compositions of calcite (cc) in the unaltered marble are about δ¹⁸O (SMOW; Standard mean Ocean Water)=21.0‰ and δ¹³C(PDB; Peedee belemnite)=0.0‰. They are reset to significantly lower values within the veins, where δ¹⁸O_cc is 15.0 to 16.0‰ and δ¹³C_cc is −4.5 to −3.5‰. The isotopic front coincides with an abrupt change in the microscopic texture of matrix carbonate which occurs at the sharp boundary between graphite-bearing and graphite-free material. Within the veins the oxygen isotope fractionation between calcite and garnet (gar) varies systematically with distance from highly silicified zones. The variations in Δ¹⁸O_cc-gar are as large as 2‰, on a millimeter scale, indicating garnet-calcite isotopic disequilibrium. Vein formation was due to the infiltration of a water rich fluid of magmatic provenance into the carbonate country rock along fractures. Removal of graphite from the wall rock by dissolution through the metasomatic fluid induced recrystallization of matrix calcite. Permeability was enhanced during calcite recrystallization facilitating material transport into the wall rock and metasomatic alteration. Vein garnet was precipitated in isotopic equilibrium with the metasomatic fluid. The isotopic composition of preexisting calcite was initially out of equilibrium with the vein-forming fluid and it was shifted towards equilibrium by surface-reaction controlled calcite-fluid isotopic exchange during calcite recrystallization. Due to the short lifetime of the metasomatic system, calcite-fluid isotopic equilibrium was generally not attained. Within the veins, oxygen and carbon transport was fast relative to mineral-fluid exchange of their isotopes and the geometry of the isotopic pattern is largely controlled by the kinetics of mineral-fluid exchange. Received: 16 June 1994/Accepted: 20 May 1995     

Evolution in accessory mineral paragenesis,during metasomatic alteration of granites in eastern Transbaykalia massifs

This study is concerned with formation of minerals containing Li, Be, Cb, Ta, W, Bi, and other elements. The distribution of 35 accessory minerals was examined in biotite granite massifs occupying an area of 10 km² . These minerals formed during the late magmatic stage and mainly during the subsequent metasomatic processes, such as rnuscovitization, early albitization, greisenization, late albitization, and microclinization. Tantalum and columbium mineralization is associated with rocks intensely altered by the processes of alkaline metasomatism and reflects differentiation of rare earth's mineralization in marginal granite massifs. Minerals containing Be, W, Bi, Sn, and Mo were deposited during the acidic stage of metasomatism. The subsequent alkaline stage of metasomatism resulted in leaching of these elements and their redeposition outside the massif. The paper is of interest as a guide in prospecting for tantalum and columbium in granitic intrusions.--E. A. Alexandrov.     

New geochronometer for the direct isotopic dating of native platinum minerals (190Pt-4He method)

A new method of isotope geochronology was proposed for dating native platinum minerals on the basis of the ??-decay of the natural isotope ¹⁹⁰Pt. The analysis of the thermal desorption of helium in the crystal lattice of native metals, including platinum, allowed us to predict a very high thermal stability (retentivity) of radiogenic ⁴He in native platinum minerals up to their melting temperatures. In order to validate the proposed ¹⁹⁰Pt-⁴He method, direct isotopic dating was performed for isoferroplatinum from the Galmoenan dunite-clinopyroxenite and Kondyor alkaline ultramafic massifs. The results of dating obtained by this method for primary ore platinum from the Galmoenan Massif (70 ± 5 Ma) are consistent with geological observations and mean Sm-Nd and Rb-Sr isotopic age estimates. The ¹⁹⁰Pt-⁴He age obtained for placer isoferroplatinum from the Kondyor Massif (112 ± 7 Ma) also agrees with geological observations and is close to the K-Ar and Rb-Sr ages of koswites (phlogopite-magnetite pyroxenites, gabbros, nepheline syenites, and metasomatic rocks after dunites). Our experimental data demonstrated that the ¹⁹⁰Pt-⁴He method is a promising tool for dating native platinum minerals.