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1.
Mineralogical-geochemical data obtained on a large xenolith of spinel lherzolite from basanites of Shavaryn Tsaram volcano (Middle Pleistocene) provide evidence that the xenolith was affected by heat and fluid that came from the basalt melt and induced geochemical heterogeneity of the xenolith. Olivine crystals from the central portion of the xenolith contain much more CaO than this mineral from the peripheral zones of the xenolith as well as in xenocrystals of the host basalts. The large xenolith was unevenly annealed by the host basalt melt, and this predetermined the heterogeneous diffusion-controlled “purification” of olivine crystals from their CaO admixture. The xenolith is heterogeneously enriched in LREE and some trace elements (Zr, Hf, Nb, Th, and U), and their distribution demonstrates unclearly pronounced concentric zoning: these elements enriched the outer portions of the xenolith. The enrichment of the xenolith in LREE and other mobile trace elements is explained by their occurrence not only as structurally bound (isomorphic) components in minerals but also in the form of nonstructural admixtures (contaminant), as minute grains of compounds hosted in the interstitial space and tiny cracks cutting mineral grains. The enrichment of the xenolith in these admixtures proceeded via their infiltration-controlled introduction with fluid from the basalt along minute cracks.  相似文献   

2.
Leander Franz  Rolf L. Romer 《Lithos》2010,114(1-2):30-53
Petrologic, geochemical and isotopic investigations on two ultramafic xenoliths with metasomatic veins from the TUBAF Seamount in the Bismarck Archipelago NE of Papua New Guinea reveal different styles of metasomatic overprinting. The first xenolith, a clinopyroxene–poor spinel lherzolite, was part of the depleted upper mantle. It contains an orthopyroxene-rich vein that formed by hydrous metasomatism at ~ 980 °C and ~ 1.5 GPa. The second xenolith is a clinopyroxene-dominated spinel olivine websterite that formed as a magmatic cumulate at the transition of the upper mantle to the oceanic crust. The websterite contains a vein with orthopyroxenes and clinopyroxenes, which give evidence for high-temperature crystallization at ~ 1300 °C and < 0.36 GPa. Both xenoliths were transported to the seafloor by a Quaternary trachybasalt in a fore-arc position. The vein minerals show a strong affinity to a supra-subduction zone or island arc setting. The REE pattern of the vein in the clinopyroxene–poor lherzolite strongly resembles the one from the host trachybasalt, with a high enrichment of the LREE and a strong to moderate enrichment of the MREE and HREE. Although broadly similar in shape, the REE pattern of the vein in the websterite shows a much weaker enrichment. The same applies to the trace-element patterns, although there are significant differences in the Eu, Zr, Hf and Nb concentrations. The isotope signatures of both veins suggest a derivation from a subducted slab that had been hydrothermally altered by seawater (high 87Sr/86Sr values).The contrasting crystallization temperatures of the vein minerals as well as their overall geochemical differences indicate that the metasomatic agents responsible for the vein in the websterite were mobilized from a previously depleted source at a much deeper mantle level than those forming the vein of the clinopyroxene–poor lherzolite. The metasomatic agents may also have been mobilized at different times and from different plates, i.e., the deeply subducted Solomon Sea Microplate (for the veins in the websterite) and the shallow dehydrating Pacific Plate (for the veins in the clinopyroxene–poor lherzolite).Metasomatic agents responsible for similar petrologic phenomena, i.e., modal or cryptic metasomatism, may have distinctly different origins and show contrasting histories. A strongly depleted lherzolite may totally lose its initial geochemical signature by the influence of an enriched metasomatic agent, whereas a primarily enriched ultramafic rock, e.g., a websterite, may strongly obscure the trace-element pattern of a less enriched metasomatic vein. Furthermore, the geochemistry of the ultramafic xenoliths may reflect polyphase cryptic and modal metasomatism related to veining and later transport by the hosting melt to the seafloor.  相似文献   

3.
Mineralization with ion adsorption rare earth elements (REEs) in the weathering profile of granitoid rocks from Nanling region of Southeast China is an important REE resource, especially for heavy REE (HREE) and Y. However, the Jurassic granites in Zhaibei which host the ion adsorption light REE (LREE) ores are rare. It is of peraluminous and high K calc-alkaline composition, which has similar geochemical features of high K2O + Na2O and Zr + Nb + Ce + Y contents and Ga/Al ratio to A-type granite. Based on the chemical discrimination criteria of Eby [Geology 20 (1992) 641], the Zhaibei granite belongs to A1-type and has similar source to ocean island basalts. The rock is enriched in LREE and contains abundant REE minerals including LREE-phosphates and halides. Minor LREE was also determined in the feldspar and biotite, which shows negligible and negative Eu anomalies, respectively. This indicates that the Zhaibei granite was generated by extreme differentiation of basaltic parent magmas. In contrast, granites associated with ion adsorption HREE ores contain amounts of HREE minerals, and show similar geochemical characteristics with fractionated felsic granites. Note that most Jurassic granitoids in the Nanling region contain no REE minerals and cannot produce REE mineralization. They belong to unfractionated M-, I- and S-type granites. Therefore, accumulation of REE in the weathering profile is controlled by primary REE mineral compositions in the granitoids. Intense fractional crystallization plays a role on REE enrichment in the Nanling granitoid rocks.  相似文献   

4.
In this paper we report zircon U–Pb age, chemical compositions of rock-forming minerals, and whole-rock elemental and Sr–Nd isotopic data for the No. II mafic-ultramafic intrusive complex (N2MC) in the Quruqtagh area at the northeastern margin of the Tarim Block, northwestern China to evaluate its petrogenesis and tectonic significance. The N2MC with an exposure area of ca. 12 km2 has a funnel-shaped cross-section and intruded the Paleoproterozoic basement. U–Pb zircon dating gives a crystallization age of 760 ± 6 Ma. Rock types of the N2MC include lherzolite, pyroxenite, gabbro and minor diorite. Major elements geochemistry of these rocks exhibits a tholeiitic trend with a wide range of SiO2 contents (38.8–60 wt.%). On the other hand, they are systematically enriched in LILE, LREE and depleted in HFSE and HREE, thus leading to low HFSE/LREE ratios (e.g., Nb/La ≈ 0.3). Isotopically, the studied rocks are characterized by negative whole-rock εNd(t) values (? 7.6 to ? 2.8) and variable high (87Sr/86Sr)i (0.7095–0.7059). These features, together with chemical compositions of the rock-forming minerals and the presence of the primary phlogopite and hornblende, suggest that N2MC was likely formed via crystal fractionation/cumulation (with negligible crustal contamination) of a tholeiitic magma derived from a metasomatized subcontinental lithosphere mantle (SCLM) in an extensional environment. The enrichment of the mantle source could be ascribed to the metasomatism by subducted-slab-released fluids before partial melting. Overall, reported Neoproterozoic igneous rocks throughout the Tarim Block constitute two major phases of Neoproterozoic igneous activities, i.e., ca. 825–800 Ma and ca. 780–745 Ma, respectively. Similar to that of many other Rodinian continents, this feature is interpreted to be related to the two phases of Neoproterozoic mantle plume activity under the Rodinia. Furthermore, there exist two types of mafic-ultramafic complex at Quruqtagh, i.e., the ca. 820 Ma carbonatite-bearing and the ca. 760 Ma tholeiitic, which could reflect the presence of two different mantle sources.  相似文献   

5.
We studied clastics of high-alumina garnet-kyanite-mica schists and garnet-kyanite-quartz granofelses, including diamond-bearing ones, found in the eluvial sediments near Lake Barchi. In contents of major elements the studied rocks correspond to argillaceous shales. The garnet-kyanite-quartz granofelses are poorer in K (0.49-1.35 wt.% K2O) than the garnet-kyanite-mica schists (4.9-2.2 wt.% K2O) but have the same contents of other major components. The REE patterns of most of the garnet-kyanite-phengite schists are similar to those of the Post-Archean Australian Shale (PAAS) (xLa/Yb = 13). All garnet-kyanite-quartz rocks are much stronger depleted in LREE (xLa/Yb = 1.4) and other incompatible elements. Our studies show that allanite and monazite are the main concentrators of LREE and Th in the garnet-kyanite-phengite rocks of the Barchi site. Monazite, occurring as inclusions in garnet, contains not only LREE but also Th, U, and Pb. Rutile of the nondepleted rocks is enriched in Fe and Nb impurities only. The garnet-kyanite-quartz granofelses bear rutile, apatite, and xenotime as accessory phases. Rutile of the depleted rocks shows wide variations in contents of Nb, Ta, and V impurities. In places, the contents of Nb and Ta reach 10.5 and 2.3 wt.%, respectively. The rutile decomposes into rutile with Nb (1.4 wt.%) and Fe (0.87 wt.%) impurities and titanium oxide rich in Fe (6.61 wt.%), Nb (up to 20.8 wt.%), and Ta (up to 2.81%) impurities. Based on the measured contents of incompatible elements in differently depleted high-alumina rocks, the following series of element mobility during UHP metamorphism has been established: Th > Ce > La > Pr > Nd > K > Ba > Rb > Cs > Sm > Eu. The contents of U, P, and Zr in the depleted rocks are similar to those in the nondepleted rocks. The studies have shown that metapelites subducted to the depths with diamond stability conditions can be depleted to different degrees. This might be either due to their exhumation from different depths of the subduction zone or to the presence of an external source of water controlling the temperature of dissolution of phengite and the formation of supercritical fluid/melt.  相似文献   

6.
Geochemical characteristics of spinel lherzolite xenoliths, enclosed in Miocene alkali basalt from Boeun, Korea, provide important clues for understanding the lithosphere composition, equilibrium temperature and pressure conditions, and depletion and enrichment processes of subcontinental lithospheric mantle beneath Boeun. The spinel lherzolite xenoliths with protogranular to porpyroclastic textures were accidentally trapped by the ascending alkali basalt magma. The spinel lherzolite xenoliths originated at depths between 50 and 63 km with equilibrium temperatures ranging from 847 to 1030 °C. These xenoliths may have undergone small degrees (1–2%) of partial melting and cryptic metasomatism by an alkali basaltic melt. Based on Sr and Nd isotope compositions, the subcontinental lithospheric mantle beneath Boeun was heterogeneous and similar to that beneath East China and Central Mongolia rather than the Japanese Island Arc.  相似文献   

7.
Oxygen isotope signatures of ruby and sapphire megacrysts, combined with trace-element analysis, from the Mbuji-Mayi kimberlite, Democratic Republic of Congo, and the Changle alkali basalt, China, provide clues to specify their origin in the deep Earth. At Mbuji-Mayi, pink sapphires have δ18O values in the range 4.3 to 5.4‰ (N = 10) with a mean of 4.9 ± 0.4‰, and rubies from 5.5 to 5.6‰ (N = 3). The Ga/Mg ratio of pink sapphires is between 1.9 and 3.9, and in rubies, between 0.6 and 2.6. The blue or yellow sapphires from Changle have δ18O values from 4.6 to 5.2 ‰, with a mean of 4.9 ± 0.2‰ (N = 9). The Ga/Mg ratio is between 5.7 and 11.3. The homogenous isotopic composition of ruby suggests a derivation from upper mantle xenoliths (garnet lherzolite, pyroxenite) or metagabbros and/or lower crustal garnet clinopyroxenite eclogite-type xenoliths included in kimberlites. Data from the pink sapphires from Mbuji-Mayi suggest a mantle origin, but different probable protoliths: either subducted oceanic protolith transformed into eclogite with δ18O values buffered to the mantle value, or clinopyroxenite protoliths in peridotite. The Changle sapphires have a mantle O-isotope signature. They probably formed in syenitic magmas produced by low degree partial melting of a spinel lherzolite source. The kimberlite and the alkali basalt acted as gem conveyors from the upper mantle up to the surface.  相似文献   

8.
A diagnostic leaching showed that partial oxidation of the sulphide minerals in a gold ore was beneficial for thiosulphate leaching of gold. A pre-treatment process with oxidative ammoniacal solution enhanced the thiosulphate leaching of the sulphide ore, while the thiosulphate consumption was substantially reduced. The sulphide minerals partially decomposed in the pre-treatment process, exposing gold to the leach solution. Oxygen input by air bubbling and a longer contact time enhanced the oxidative ammonia pre-treatment process and hence accelerated subsequent thiosulphate leaching of the sulphide ore. Gold extraction in 0.8 M ammonia and 0.1 M thiosulphate solution after 24 h increased from 69% without pre-treatment to 81%, 84%, 90% and 94% respectively after 1, 3, 7 and 22 h pre-treatment. The consumption of sodium thiosulphate was 2.37 kg/t after 24 h leaching without pre-treatment, but was negligible after over 1 h oxidative ammonia pre-treatment. A counter-current leaching process was conducted in the leaching of the sulphide ore. The fresh leachant still gave higher leaching rates in contact with the pre-leached ore, while the pre-used leachant had significantly lower leaching kinetics and overall gold extraction in contact with the fresh ore. This 2-step counter-current leaching process proved that the leachant, other than the passivation, was the determinant factor causing the gold leaching rates to decrease after a certain time of leaching. The findings enable the thiosulphate leaching of high sulphide containing gold ores to be more efficient at lower thiosulphate consumption following the oxidative ammoniacal pre-treatment.  相似文献   

9.
The tectonic history of the Kyrgyz South Tianshan in the western Central Asian Orogenic Belt (CAOB) remains controversial, first of all, due to the limited amount of geochemical and isotope data. Our paper presents the first results of a detailed geochemical study (major and trace elements, Sr, Nd and Pb isotopes) of Middle Paleozoic mafic volcanic and subvolcanic rocks of the Ferghana and Atbashi–Kokshaal accretionary belts of the South Tianshan orogen in Kyrgyzstan, which formed during the evolution of the Turkestan Ocean. A special focus is given to the relation between magmatic rocks and sedimentary units of marine origin, chert, siliceous shale/mudstone, volcanogenic–carbonate clastics, seamount carbonates, and turbidites, which we consider as elements of Ocean Plate Stratigraphy (OPS). The age range of marine sediments is Late Silurian to Early Carboniferous, but the age of the most volcanic rocks associated with fossil-bearing OPS sediments is Devonian. The magmatic rocks have geochemical affinity to oceanic island basalts (OIB-type) and, to a lesser extent, mid-oceanic ridge (MORB-type) basalts associated with hemipelagic siliceous mudstone and pelagic chert. The rocks with OIB-type affinity are associated with chert, siliceous shale and carbonaceous clastics and carbonates. They are enriched in TiO2, LREE (La/Smn = 1.9), and Nb (Zr/Nbav. = 10), have differentiated HREE (Gd/Ybn = 2.0), medium to low εNd (~ 5.7) and are characterized by clear Nb positive anomalies in normalized multi-element plots (Nb/Thpm = 1.3, Nb/Lapm = 1.1). The OIBs formed by relatively low degrees of melting (< 5%) of mantle sources in the garnet stability field and erupted in an oceanic island setting. The MORB-type samples associated with siliceous mudstone and chert are less enriched in incompatible elements, possess flat REE and multi-element pattern, and show higher εNd values (~ 9.1); they were probably produced by high-degree melting of spinel lherzolite and/or harzburgite and erupted in a mid-oceanic ridge setting. The geological, lithological and geochronological data suggest that the OPS units with dominantly OIB-type basalts formed at one or several seamount chains of the Turkestan Ocean, which were accreted to the Kazakhstan continent, and thus contribute to our understanding of the Paleozoic tectonic evolution of the western CAOB during the Serpukhovian–Bashkirian.  相似文献   

10.
Whole-rock geochemical and Sr, Nd and Pb isotope data are presented for the Harrat Al-Madinah volcanic field, in the north western part of the Arabian plate, aiming to understand their origin and the composition of their mantle source. This area is an active volcanic field characterized by the occurrence of two historic eruptions approximately in 641 and 1256 A.D. Field investigation of the main volcanic landforms indicates dominantly monogenetic strombolian eruptions, in addition to local phreatomagmatic eruption style. The lavas consist mainly of alkali olivine basalt, olivine transitional basalt, and hawaiite with ocean island basalt (OIB)-like characteristics. Evolved rocks, represented by mugearites, benmoreites, and trachytes, occur mainly as domes, tuff cones and occasionally as lava flows. Chemical variations in the evolved rocks indicated their evolution by low pressure crystal fractionation of olivine, plagioclase, clinopyroxene, and Fe–Ti oxides from the relatively primitive basalts. The isotopic compositions of 143Nd/144Nd (0.512954–0.512995), 87Sr/86Sr (0.702899 to–0.702977) and Pb (206Pb/204Pb = 18.5515–18.7446, 207Pb/204Pb = 15.5120–15.5222, 208Pb/204Pb = 38.1347–38.4468), show restricted variations suggesting only minor crustal contamination. They defined an array consistent with mixing of two geochemically distinct components of depleted MORB-mantle (DMM) and high 238U/204Pb ratio (HIMU). The variations in Tb/Yb, La/Yb and Sm/Yb ratios in the relatively primitive basalts (MgO > 6 wt.%) indicated garnet peridotite source. However, the positive Nb, Sr, Ba and Ti anomalies in the primitive mantle-normalized incompatible element patterns and the significant variation between Zr/Nb vs. Ce/Y and La/Yb vs. Yb suggest contribution of an amphibole-bearing spinel lherzolite source. Moreover, the negative correlations between SiO2 vs. 87Sr/86Sr and Th vs. 143Nd/144Nd are interpreted as an indication of mixing melts derived from two end-members; one is garnet bearing asthenospheric source with OIB characteristic and the other is amphibole-bearing spinel lherzolite. The Harrat Al-Madinah volcanic field occurs near the Red Sea Rift System and its origin reflects a strong lithospheric control on the loci of partial melting. The dominantly NNW alignment patterns of the volcanoes, which is similar to the regional Red Sea trend, may suggest that the magmas were produced by decompression partial melting triggered by lithospheric extension related to the Red Rift.  相似文献   

11.
Numerous small dismembered ophiolite fragments occur in South Mongolia, but they are very poorly studied. The lack of age data and geochemical analysis hampers our understanding of the Paleozoic tectonic evolution of the region. We conducted detailed studies on the Manlay ophiolitic complex and Huree volcanic rocks south of the Main Mongolian Lineament (MML) to provide some constraints on these rocks. The Manlay ophiolite consists of dunite, harzburgite, pyroxenite, gabbro, plagiogranite, basalt and chert, locally with chromite mineralization in dunite. The gabbro and plagiogranite yielded SHRIMP zircon weighted mean 206Pb/238U ages of 509 ± 5 Ma and 482 ± 4 Ma, respectively. The basalt and dolerite samples of this complex show enrichment in LREE and LILE and negative Nb, Ta and Ti anomalies, and the chrome spinel from the chromitite lens in the dunite is characterized by high Cr# and low TiO2 contents. These features suggest a supra-subduction zone (SSZ) origin for the ophiolitic complex. The Huree volcanic rocks, ranging from basalt to dacite, display enrichment in LREE and LILE, weak Eu anomalies and distinctly negative Nb, Ta and Ti anomalies, consistent with those of typical magmas in a subduction environment. An andesite sample from this arc yielded a SHRIMP 206Pb/238U zircon age of 487 ± 5 Ma, which is the oldest reliable age for an island arc in South Mongolia. Recognition of an Early Paleozoic ophiolitic complex and a coeval island arc indicates that South Mongolia underwent a period of active volcanism during Late Cambrian to Ordovician. Additionally, the tuff overlying the ophiolitic complex and a granite intruding the ophiolite have SHRIMP zircon U–Pb ages of 391 ± 5 Ma and 304 ± 4 Ma, respectively. Combining the available data, we propose that the Early Paleozoic subduction–accretionary complexes likely constitute the basement of the Late-Paleozoic arc formations and correlate with the Lake Zone in western Mongolia.  相似文献   

12.
Trace element geochemistry was studied in geothermal fluids in Iceland. The major and trace element compositions of hot springs, sub-boiling, and two-phase (liquid and vapor) wells from 10 geothermal areas were used to reconstruct the fluid composition in the aquifers at depth. Aquifer fluid temperatures ranged from 4 to 300 °C, pH values between 4.5 and 9.3, and fluids typically contained total dissolved solids <1000 ppm, except in geothermal areas that have seawater and seawater-meteoric water mixtures. Trace alkali elements Li, Rb and Cs are among the most mobile elements in aquifer fluids, with concentrations in the range of <1 ppb to 3.49 ppm Li, <0.01 to 57 ppb Cs, and <1 ppb to 3.77 ppm Rb. Their chemistry is thought to be dominated by rock leaching and partitioning into Na- and K-containing major alteration minerals. Arsenic, Sb, Mo and W are typically present in concentrations in the range of 1–100 ppb. They are relatively mobile, yet Mo may be limited by molybdenite solubility. The alkaline earth elements Ba and Sr are quite immobile with concentrations in the range of <0.1–10 ppb Ba and <1–100 ppb Sr in the dilute fluids, but up to 5.9 ppm Ba and 8.2 ppm Sr in saline fluids. These elements show a systematic relationship with Ca, possibly due to substitution for Ca in Ca-containing major alteration minerals like calcite, epidote and anhydrite. Incorporation into major Ca-minerals may also be important for Mn. Many metals including Fe, Cr, Ni, Zn, Cu, Co, Pb and Ag have low mobility and concentrations, typically <1 ppb for Ag, Cd, Co, Cr, Cu, Ni, and Pb, <10 ppb for Zn and < 100 ppb for Fe, although for some metals higher concentrations are associated with saline fluids. Based on the metals assessed, saturation is approached with respect to many sulfide minerals and in some cases oxide minerals but Cu, Ni and Pb minerals are slightly but systematically undersaturated, and Ag phases significantly undersaturated. Evaluation of mineral-fluid equilibria for these metals is problematic due to their low concentrations, problems associated with assessing the aqueous species distribution by thermodynamic calculations, and uncertainties concerning the exact minerals possibly involved in such reactions. Reaction path calculations, poor comparison of concentrations measured in the samples collected at the wellhead and published downhole data as well as boiling, cooling and mass precipitation calculations suggest removal of many metals due to changes upon depressurization boiling and conductive cooling of the aquifer fluids as they ascend in wells. These results imply that processes such as mass precipitation upon fluid ascent may be highly important and emphasize the importance of considering mass movement in geothermal systems.  相似文献   

13.
The Jinping–Fan Si Pan (JFP) Cenozoic magmatic and Cu–Mo–Au metallogenic belt in the southeastern part of the Ailao Shan shear zone host the Tongchang, Chang′an, Habo, and Chinh Sang Cu–Mo–Au deposits. These deposits form an integrated epithermal-porphyry regional mineralization system associated with 40–32 Ma high-K alkaline magmatism. The magmatic rocks in the belt have relatively low TiO2 (<0.73 wt%), P2O5 (<0.29 wt%), and FeO* (<4.99 wt%), and high Na2O (2.86–4.75 wt%) and K2O (4.01–7.98 wt%). They also have high contents of incompatible trace elements, and are enriched in LILE (Rb, Ba, K, Sr) and LREE. They have marked Nb, Ta, Ti and P depletion in primitive mantle-normalized spidergrams, and plot close to the EMII mantle field in the Sr–Nd isotopic diagram. These characteristics are similar to those of the Eocene high-K alkaline rocks along the northern Ailao Shan belt, eastern Tibet plateau. The sulfur and lead isotope analyses of sulfide minerals from both the ores and related magmatic rocks confirm the involvement of a magmatic ore fluid. The Cenozoic alkaline intrusions and Cu–Mo–Au mineralization in the JFP were formed prior to the initiation of left-lateral shearing along the Ailao Shan shear zone. The magmas appear to have been derived from enriched mantle, possibly with mixing of materials from the buried Tethyan oceanic lithosphere, and/or crust.  相似文献   

14.
South Korea separates two mantle source domains for Late Cenozoic intraplate volcanism in East Asia: depleted mid-ocean-ridge basalt (MORB) mantle-enriched mantle type 1 (DMM-EM1) in the north and DMM-EM2 in the south. We determined geochemical compositions, including Sr, Nd, Pb, and Hf isotopes for the Jeongok trachybasalts (∼0.51 to 0.15 Ma K–Ar ages) from northernmost South Korea, to better constrain the origin and distribution of the enriched mantle components. The Jeongok basalts exhibit light rare earth element (LREE)-enriched patterns ([La/Yb]N = 9.2–11.6). The (La/Yb)N ratios are lower than that of typical oceanic island basalt (OIB). On a primitive mantle-normalized incompatible element plot, the Jeongok samples show OIB-like enrichment in highly incompatible elements. However, they are depleted in moderately incompatible elements (e.g., La, Nd, Zr, Hf, etc.) compared with the OIB and exhibit positive anomalies in K and Pb. These anomalies are also prime characteristics of the Wudalianchi basalts, extreme EM1 end-member volcanics in northeast China. We have compared the geochemistry of the Jeongok basalts with those of available Late Cenozoic intraplate volcanic rocks from East Asia (from north to south, Wudalianchi, Mt. Baekdu and Baengnyeong for DMM-EM1, and Jeju for DMM-EM2). The mantle source for the Jeongok volcanics contains an EM1 component. The contribution of the EM1 component to East Asian volcanism increases toward the north, from Baengnyeong through Jeongok to Mt. Baekdu and finally to Wudalianchi. Modeling of trace element data suggests that the Jeongok basalts may have been generated by mixing of a Wudalianchi-like melt (EM1 end-member) and a melt that originated from a depleted mantle source, with some addition of the lithospheric mantle beneath the Jeongok area. In Nd–Hf isotope space, the most enriched EM1-component-bearing Jeongok sample shows elevation of 176Hf/177Hf at a given 143Nd/144Nd compared with OIB. Recycled pelagic sediments may explain the EM1-end-member component of northeastern Asian volcanism, possibly from the mantle transition zone.  相似文献   

15.
Late Mesozoic volcanism is widespread throughout NE China. On the basis of lithological associations and spatial relationships, the volcanic rocks in the Lesser Hinggan Range can be divided into two formations, i.e., felsic-dominant Fuminghe Formation and overlying mafic-dominant Ganhe Formation. The Dong'an gold deposit, a typical adularia–sericite epithermal system, is spatially closely associated with rhyolitic porphyry, which is a subvolcanic intrusion of the Fuminghe Formation. Total measured, indicated, and inferred resources for the Dong'an deposit are 70 tonnes (2.25 Moz) of gold with the grade of 5.04 g/t Au, making it one of the largest epithermal gold deposits in China.SHRIMP U–Pb zircon and 40Ar/39Ar geochronology applied to one rhyolitic porphyry sample and sericite separated from auriferous quartz veins of the main mineralization stage were carried out to constrain magmatic and hydrothermal events. The results suggest that the mineralization age of 107.2 ± 0.6 Ma overlaps with the age of the rhyolitic porphyry 108.1 ± 2.4 Ma. Our new age data indicate that there was a previously unrecognized mineralization event in NE China at 107–108 Ma.Systematic geochemical investigations on the volcanic rocks in the Lesser Hinggan Range show that both Fuminghe and Ganhe Formations are characterized by significant large ion lithophile elements (LILE) and light rare earth elements (LREE) enrichment coupled with high field strength elements (HFSE) depletion, but they have distinct Sr and Nd isotopic compositions. The Fuminghe Formation has relative high 87Sr/86Sr ratios of 0.707253 to 0.707373, and negative εNd(t) values of ?2.78 to ?3.05 (t = 108 Ma), whereas the Ganhe Formation displays slightly lower 87Sr/86Sr range of 0.705434–0.705763 and positive εNd(t) values of + 0.76 to +1.83. These geochemical data suggest that the rhyolitic magmas of the Fuminghe Formation probably represent the final differentiates of parental andesitic magmas, resulted from the partial melting of mafic lower crust, whereas the volcanic rocks of the Ganhe Formation were produced by fractionation of basaltic magmas generated from partial melting of a mixture of an incompatible element depleted anhydrous lherzolite asthenospheric mantle source and a hydrous enriched lithospheric mantle source in an extensional tectonic setting, in response to upwelling of asthenospheric mantle. The rhyolite porphyries of the Fuminghe Formation are inferred to have supplied heat that drove the convective hydrothermal system at Dong'an deposit, but also provided some of the fluid sources responsible for the development of the Dong'an epithermal system.  相似文献   

16.
The last stage in the formation of the Arabian Nubian Shield in Jordan was dominated by post-orogenic igneous activity of the ∼610–542 Ma Araba Suite, including a monzogabbroic stock intruding the Saramuj Conglomerate, near the southeastern corner of the Dead Sea. The geological setting, petrography, geochemistry and geothermometry of the monzogabbro and other cogenetic varieties are used to shed light on the petrogenesis of this stock and reveal its magma source. The monzogabbro, megaporphyry dikes, and scattered syenite pockets are co-magmatic and alkaline, potassic and shoshonitic in nature. REE and trace elements patterns indicate that these magmas were produced from a mantle that had been modified by subduction-related metasomatism. The parental mafic magma could have been derived by 10% partial melting of LILE-enriched phlogopite-bearing spinel lherzolite, probably lithospheric mantle, in association with post-collisional extension. Fractional crystallization of this parental magma by olivine and pyroxene gave rise to the monzogabbroic magma.The megaporphyry dikes with their giant labradorite plagioclase megacrysts represent feeders of a voluminous volcanic activity that could have lasted for about 105 years.Thermodynamic modeling applying the MELTS software indicates crystallization of this suite in the temperature range of 1184–760 °C at a pressure of 2 kbars, agreeing with olivine-pyroxene, pyroxene, and two-feldspar thermometry. The modeled mineralogy and sequence of crystallization of constituent minerals using MELTS is in remarkable agreement with the observed modal mineralogy of the monzogabbro. Furthermore, a great degree of congruity exists between the modeled and observed chemistry of the major minerals with only minor discrepancies between modeled composition of biotite and olivine.  相似文献   

17.
The Paleoarchean (ca. 3.5–3.3 Ga) Onverwacht Suite (OS) of the Barberton Greenstone Belt consists of a 15‐km thick imbricate tectonic stack of seven complexes consisting predominantly of volcanic rocks and intrusions. Tectonostratigraphically from base to top they are the Sandspruit, Theespruit, Komati, Hooggenoeg, Noisy, Kromberg and Mendon Complexes. The Hooggenoeg and Noisy Complexes in the middle of the OS are separated by a significant unconformity resulting from the uplift of the submarine lavas and deep erosion, demonstrating the onset of tectonic accretion prior to 3455 Ma. The basic lavas of the tectonostratigraphic lower (Theespruit, Sandspruit and Komati) and upper (Mendon) complexes are composed of komatiite, komatiitic basalt and high-MgO basalt, whereas those in the middle part (Hooggenoeg and Kromberg) are predominantly high- to low-MgO tholeiitic basalts. Felsic volcanic rocks and intrusions are important in two of the complexes (Theespruit and Noisy). The ultramafic to basaltic lavas show REE patterns that are almost flat and resemble those of modern MORB, whereas those of the felsic rocks are flat from Lu to Gd and moderately to strongly enriched in LREE, similar to modern arcs. Average εNd (T) values are close to depleted mantle growth curves. In MORB-normalised multi-element diagrams, the komatiitic to basaltic rocks exhibit flat patterns from Lu through La and consistent relative enrichment in the elements Pb, U, Th, Ba and Cs. Apart from the Komati Complex, the majority of the lavas show significant negative Nb and Ta anomalies. Enrichment in non-conservative incompatible elements (Cs, Ba, Th, LREE) relative to conservative elements (Ta, Nb, Zr, Hf, Ti, Y, HREE) shows that the komatiitic to basaltic magmas were generated from metasomatised mantle above subducting altered oceanic crust. The geochemistry of the felsic rocks indicates an origin by melting of subducted amphibolite and eclogite. The tectonostratigraphy and the geochemical characteristics of the lavas and intrusions are consistent with successive obduction and accretion of segments of oceanic crust formed in back-arc basins and volcanic arcs.  相似文献   

18.
Olivine, clinopyroxene and orthopyroxene in variably metasomatised peridotite xenoliths from three lithospheric mantle sections beneath the East African Rift in Tanzania (Lashaine, Olmani, Labait) show systematic differences in their average Li concentrations (2.4 ppm, 2.0 ppm and 1.5 ppm, respectively) and intermineral isotopic fractionations, with olivine being heaviest (δ7Li = + 2.3 to + 13.9‰, average + 5.0‰), followed by orthopyroxene (? 4.1 to + 6.5‰, average + 0.8‰) and clinopyroxene (? 6.7 to + 4.1‰, average ? 1.6‰). These features are ascribed to the effects of kinetic Li isotope fractionation combined with different Li diffusivities in mantle minerals.Two main mechanisms likely generate diffusion-driven kinetic Li isotope fractionation in mantle xenoliths (1) Li diffusion from grain boundary melt into minerals during recent metasomatism or entrainment in the host magma and (2) subsolidus intermineral Li-redistribution. The latter can produce both isotopically light (Li-addition) and heavy (Li-loss) minerals and may occur in response to changes in pressure and/or temperature.Modelling shows that non-mantle-like δ7Li in clinopyroxene (< + 2‰), combined with apparent equilibrium olivine-clinopyroxene elemental partitioning in most peridotite xenoliths from all three Tanzanian localities probably reflects incipient Li addition during interaction with the host magma. Low δ7Li (< ? 3‰), combined with high Li concentrations (> 3 ppm) in some clinopyroxene may require very recent (minutes) Li ingress from a Li-rich melt (100s of ppm) having mantle-like δ7Li. This might happen during late fragmentation of some mantle xenoliths caused by a volatile- (and Li-) rich component exsolved from the host basalt. In contrast, high Li concentrations (> 2 ppm) and δ7Li (> 4‰) in olivine from many Labait and Olmani samples are attributed to an older, pre-entrainment enrichment event during which isotopic equilibrium was attained and whose signature was not corrupted during xenolith entrainment. Low Li concentrations and mantle-like isotopic composition of olivine from most Lashaine xenoliths indicate limited metasomatic Li addition.Thus, Li concentrations and isotope compositions of mantle peridotites worldwide may reflect two processes, with olivine mainly preserving a signature of depletion in refractory samples (low Li contents and δ7Li) or of older (precursory) melt addition in metasomatised samples (high Li contents and δ7Li), while non mantle-like, low δ7Li in almost all clinopyroxene can be due to Li ingress during transport in the host magma and/or slow cooling, if the samples were erupted in lavas. In Tanzania, the peridotites experienced rift-related heating prior to entrainment and were quenched upon eruption, so Li ingress is the most likely process responsible for the isotopically light clinopyroxene here.  相似文献   

19.
The present work is a first comprehensive study of the trace-element composition and zoning in clinopyroxene- and amphibole-group minerals from carbonatites, incorporating samples from 14 localities worldwide (Afrikanda, Aley, Alnö, Blue River, Eden Lake, Huayangchuan, Murun, Oka, Ozernaya Varaka, Ozernyi, Paint Lake, Pinghe, Prairie Lake, Turiy Mys). The new electron-microprobe data presented here significantly extend the known compositional range of clinopyroxenes and amphiboles from carbonatites. These data confirm that calcic and sodic clinopyroxenes from carbonatites are not separated by a compositional gap, instead forming an arcuate trend from nearly pure diopside through intermediate aegirine–augite compositions confined to a limited range of CaFeSi2O6 contents (15–45 mol%) to aegirine with < 25 mol% of CaMgSi2O6 and a negligible proportion of CaFeSi2O6. A large set of LA-ICPMS data shows that the clinopyroxenes of different composition are characterized by relatively low levels of Cr, Co and Ni (≤ 40 ppm) and manifold variations in the concentration of trivalent lithophile and some incompatible elements (1–150 ppm Sc, 26–6870 ppm V, 5–550 ppm Sr, 90–2360 ppm Zr, and nil to 150 ppm REE), recorded in some cases within a single crystal. The relative contribution of clinopyroxenes to the whole-rock Rb, Nb, Ta, Th and U budget is negligible. The major-element compositional range of amphiboles spans from alkali- and Al-poor members (tremolite) to Na–Al-rich Mg- or, less commonly, Fe-dominant members (magnesiohastingsite, hastingsite and pargasite), to calcic–sodic, sodic and potassic–sodic compositions intermediate between magnesio-ferrikatophorite, richterite, magnesioriebeckite, ferri-nyböite and (potassic-)magnesio-arfvedsonite. In comparison with the clinopyroxenes, the amphiboles contain similar levels of tetravalent high-field-strength elements (Ti, Zr and Hf) and compatible transition elements (Cr, Co and Ni), but are capable of incorporating much higher concentrations of Sc and incompatible elements (up to 500 ppm Sc, 43 ppm Rb, 1470 ppm Sr, 1230 ppm Ba, 80 ppm Pb, 1070 ppm REE, 140 ppm Y, and 180 ppm Nb). In some carbonatites, amphiboles contribute as much as 25% of the Zr + Hf, 15% of the Sr and 35% of the Rb + Ba whole-rock budget. Both clinopyroxenes and amphiboles may also host a significant share (~ 10%) of the bulk heavy-REE content. Our trace-element data show that the partitioning of REE between clinopyroxene (and, in some samples, amphibole) and the melt is clearly bimodal and requires a revision of the existing models assuming single-site REE partitioning. Clinopyroxenes and amphiboles from carbonatites exhibit a diversity of zoning patterns that cannot be explained exclusively on the basis of crystal chemistry and relative compatibility of different trace-element in these minerals. Paragenetic analysis indicates that in most cases, the observed zoning patterns develop in response to removal of selected trace elements by phases co-precipitating with clinopyroxene and amphibole (especially magnetite, fluorapatite, phlogopite and pyrochlore). With the exception of magnesiohastingsite–richterite sample from Afrikanda, the invariability of trace-element ratios in the majority of zoned clinopyroxene and amphibole crystals implies that fluids are not involved in the development of zoning in these minerals. The implications of the new trace-element data for mineral exploration targeting REE, Nb and other types of carbonatite-hosted rare-metal mineralization are discussed.  相似文献   

20.
The Dongguashan skarn-porphyry Cu-Au deposit, located in the Tongling district of the Middle-Lower Yangtze River Valley metallogenic belt (MLYB), consists of skarn ore bodies in the upper part and porphyry ore bodies in the lower part, both of which are hosted in quartz diorite and quartz monzodiorite. Zircon U-Pb age and geochemical studies show that the quartz diorite of the Dongguashan intrusion formed at 140.3 ± 2.0 Ma (MSWD = 0.19) and belongs to the high potassium calc-alkaline series. It is enriched in large ion lithophile elements (LILE) and light rare earth elements (LREE), depleted in high field-strength elements (HFSE) and heavy rare earth elements (HREE), and has a slightly negative Eu anomaly. 176Hf/177Hf values of the rims of zircons show a variable range (0.282087–0.282391), corresponding with calculated εHf(t) values of − 10.72 to − 21.46. Plagioclases in the quartz diorite have unbalanced structure characterized by bright andesine and labradorite (An = 37.0–65.5) cores with higher contents of Fe and Sr and are corroded by dark oligoclase (An = 13.8–27.6) rim. Major elements, trace elements, Hf isotope, and the composition of plagioclases indicate that the parental magma of the Dongguashan intrusion was produced by the mixing of underplating mafic magma and felsic magma formed by remelting of Paleoproterozoic and Neoarchean crustal rocks, Neoproterozoic crust may also provide some material to the felsic magma. Mafic magma played a key role and made the parental magma rich in water, sulfur, metals (Cu, Au) and gave it a high oxygen fugacity. During its magmatic evolution, the parental magma underwent fractional crystallization of hornblende, apatite, sphene and other mafic minerals. Some quartz diorite and quartz monzodiorite samples that show adakitic signatures, may result from injection of mafic magma. Some inherited zircons of the quartz diorite in the Dongguashan intrusion gave ages of 2.40–2.50 Ga, 1.95–2.05 Ga and 0.74–0.81 Ga, coming from ultramafic, mafic and andesitic igneous rocks, and this indicates that there may have been three periods (2.4, 2.0, and 0.8 Ga) of magmatic activity in the Tongling district.  相似文献   

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