Showing papers by "Yong-Fei Zheng published in 2014"

Geochemistry of continental subduction-zone fluids

Abstract: The composition of continental subduction-zone fluids varies dramatically from dilute aqueous solutions at subsolidus conditions to hydrous silicate melts at supersolidus conditions, with variable concentrations of fluid-mobile incompatible trace elements. At ultrahigh-pressure (UHP) metamorphic conditions, supercritical fluids may occur with variable compositions. The water component of these fluids primarily derives from structural hydroxyl and molecular water in hydrous and nominally anhydrous minerals at UHP conditions. While the breakdown of hydrous minerals is the predominant water source for fluid activity in the subduction factory, water released from nominally anhydrous minerals provides an additional water source. These different sources of water may accumulate to induce partial melting of UHP metamorphic rocks on and above their wet solidii. Silica is the dominant solute in the deep fluids, followed by aluminum and alkalis. Trace element abundances are low in metamorphic fluids at subsolidus conditions, but become significantly elevated in anatectic melts at supersolidus conditions. The compositions of dissolved and residual minerals are a function of pressure-temperature and whole-rock composition, which exert a strong control on the trace element signature of liberated fluids. The trace element patterns of migmatic leucosomes in UHP rocks and multiphase solid inclusions in UHP minerals exhibit strong enrichment of large ion lithophile elements (LILE) and moderate enrichment of light rare earth elements (LREE) but depletion of high field strength elements (HFSE) and heavy rare earth elements (HREE), demonstrating their crystallization from anatectic melts of crustal protoliths. Interaction of the anatectic melts with the mantle wedge peridotite leads to modal metasomatism with the generation of new mineral phases as well as cryptic metasomatism that is only manifested by the enrichment of fluid-mobile incompatible trace elements in orogenic peridotites. Partial melting of the metasomatic mantle domains gives rise to a variety of mafic igneous rocks in collisional orogens and their adjacent active continental margins. The study of such metasomatic processes and products is of great importance to understanding of the mass transfer at the slab-mantle interface in subduction channels. Therefore, the property and behavior of subduction-zone fluids are a key for understanding of the crust-mantle interaction at convergent plate margins.

Geochemical insights into the role of metasomatic hornblendite in generating alkali basalts

Abstract: Experimental petrology suggested the role of hornblendite in generating alkali basalt. This mechanism is confirmed by an integrated study of major-trace elements and radiogenic isotopes for Mesozoic alkali basalts from the Qinling orogen in China. The alkali basalts have high contents of MgO (4.8–11.1 wt %, Mg# = 47–69), Na2O + K2O (2.9–5.4 wt %), TiO2 (2.0–3.1 wt %) but low content of SiO2 (41.4–49.6 wt %), which are generally silica-undersaturated with normative minerals of nepheline and olivine. They exhibit OIB-like trace element distribution patterns, with enrichment of LILE and LREE but no depletion of HFSE relative to the primitive mantle. They also show relatively depleted Sr-Nd-Hf isotope compositions, with low initial 87Sr/86Sr ratios of 0.7028–0.7058, positive eNd(t) values of 4.0–9.8 and eHf(t) values of 8.8–13.5 for whole-rock, and positive eHf(t) values of 5.2–16.4 for zircon. Such element and isotope features indicate their origination from the juvenile subcontinental lithospheric mantle (SCLM) source with involvement of crustal components. The alkali basalts generally have high K2O/Na2O ratios, and high K2O and TiO2 contents, suggesting their derivation from partial melting of hornblendite-rich mantle lithology. They also exhibit variable K/La and Ti/La ratios that are correlated with (La/Yb)N ratios, indicating a geochemical heterogeneity of the SCLM source. Taken together, all the above geochemical features can be accounted for by partial melting of a hornblendite-rich SCLM source. The hornblendite would be generated by reaction of the juvenile SCLM wedge peridotite with hydrous felsic melts derived from subducted Palaeotethyan oceanic crust at the slab-mantle interface in the subduction channel. Therefore, orogenic alkali basalts record recycling of the subducted fossil oceanic crust, and the metasomatic hornblendite is an important lithology in local SCLM domains above fossil subduction channels.

Dehydration and anatexis of UHP metagranite during continental collision in the Sulu orogen

Abstract: Dehydration and anatexis of ultrahigh-pressure (UHP) metamorphic rocks during continental collision are two key processes that have great bearing on the physicochemical properties of deeply subducted continental crust at mantle depths. Determining the time and P–T conditions at which such events take place is needed to understand subduction-zone tectonism. A combined petrological and zirconological study of UHP metagranite from the Sulu orogen reveals differential behaviours of dehydration and anatexis between two samples from the same UHP slice. The zircon mantle domains in one sample record eclogite facies dehydration metamorphism at 236 ± 5 Ma during subduction, exhibiting low REE contents, steep MREE–HREE patterns without negative Eu anomalies, low Th, Nb and Ta contents, low temperatures of 651–750 °C and inclusions of quartz, apatite and jadeite. A second mantle domain records high-T anatexis at 223 ± 3 Ma during exhumation, showing high REE contents, steeper MREE–HREE patterns with marked negative Eu anomalies, high Hf, Nb, Ta, Th and U contents, high temperatures of 698–879 °C and multiphase solid inclusions of albite + muscovite + quartz. In contrast, in a second sample, one zircon mantle domain records limited hydration anatexis at 237 ± 3 Ma during subduction, exhibiting high REE contents, steep MREE–HREE patterns with marked negative Eu anomalies, high Hf, Nb, Ta, Th and U contents, medium temperatures of 601–717 °C and multiphase solid inclusions of albite + muscovite + hydrohalite. A second mantle domain in this sample records a low-T dehydration metamorphism throughout the whole continental collision in the Triassic, showing low REE contents, steep MREE–HREE patterns with weakly negative Eu anomalies, low Th, Nb and Ta contents, low temperatures of 524–669 °C and anhydrite + gas inclusions. Garnet, phengite and allanite/epidote in these two samples also exhibit different variations in texture and major-trace element compositions, in accordance with the zircon records. The distinct P–T–t paths for these two samples suggest separate processes of dehydration and anatexis, which are ascribed to the different geothermal gradients at different positions inside the same crustal slice during continental subduction-zone metamorphism. Therefore, the subducting continental crust underwent variable extents of dehydration and anatexis in response to the change in subduction-zone P–T conditions.

Composite carbonate and silicate multiphase solid inclusions in metamorphic garnet from ultrahigh‐P eclogite in the Dabie orogen

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

Fluid-rock interaction and geochemical transport during protolith emplacement and continental collision: A tale from Qinglongshan ultrahigh-pressure metamorphic rocks in the Sulu orogen

Abstract: Ultrahigh-pressure (UHP) metamorphic rocks from the Qinglongshan region of the Sulu orogen are comprehensively studied for their whole-rock geochemistry, mineral O isotopes and zirconology. The metamorphic minerals, which experienced eclogite- to amphibolite-facies metamorphism, exhibit low to negative δ18O values, suggesting that the 18O-depletion of UHP rocks was acquired from their igneous protolith due to high-T meteoric-hydrothermal alteration during the Neoproterozoic. The O isotope heterogeneity in the protolith was not homogenized during the Triassic UHP metamorphism, indicating very limited fluid flow during orogenesis. However, the fluid flow is locally significant during exhumation of the UHP rocks, resulting in the formation of quartz veins, symplectites and coronas. Geochemical transport due to fluid action is evident in whole-rock geochemistry and mineralogical composition. The UHP rocks exhibit unreasonably low 87Sr/86Sr ratios at t1 = 750 Ma but much radiogenic Sr isotopes at t2 = 230 Ma, suggesting the mobility of water-soluble elements due to hydrothermal alteration during protolith emplacement and metamorphic dehydration during continental collision. Fluid-rock interaction during exhumation would also have mobilized Al, Si, Ca and LREE, resulting in the formation of high-pressure veins in the UHP eclogites. The protolith zircon of magmatic origin underwent different types of metamorphic recrystallization in response to fluid-mineral interaction, leading to differential redistribution of trace elements and O-Hf isotopes. Newly grown zircons of metamorphic origin exhibit negative δ18O values, indicating precipitation from negative δ18O fluids that were likely generated by metamorphic dehydration of the hydrothermally altered negative δ18O rock-forming minerals during the Triassic. The metamorphic zircons exhibit relatively homogeneous Hf isotope compositions, suggesting that fluid Hf isotopes originated from the same Hf isotope composition of the protolith. Relict zircon domains of magmatic origin exhibit both positive eHf(t) and negative eHf(t) values, indicating that the protolith of UHP rocks formed by reworking of both juvenile and ancient crustal rocks.