Meteoric water-rock interaction in the lower plate of the Whipple Mountain metamorphic core complex, California

Oxygen isotope ratios, whole rock major and trace element compositions, and petrological characteristics of 52 samples from nine distinct igneous lithologies in the lower plate of the Whipple Mountain metamorphic core complex of south-eastern California indicate that both mylonitic and non-mylonitic lithologies underwent exchange with surface-derived meteoric waters. Broadly granodioritic lithologies are characterized by whole rock δ¹⁸O values that range from 10.6 to 2.6‰. Isotopic compositions of quartz and feldspar mineral separates indicate that quartz has largely retained original igneous compositions but that feldspar has undergone variable and often large ¹⁸O-depletions (up to 6.5‰). Over 4 km of structural relief is exposed in lower plate gneisses below the Whipple detachment fault including non-mylonitic lithologies at shallow structural levels above the mylonite front, and mylonitic gneisses at intermediate to deep levels below the mylonite front. Coupled δ¹⁸O_qtz - δ¹⁸O_Fsp systematics of non-mylonitic and mylonitic andesite to rhyolite dykes from shallow and intermediate structural levels of the lower plate document two episodes of hydrothermal alteration: a high-temperature (>c.600d?C) episode involving a metamorphic or magmatic fluid with δ¹⁸O values ～ 7‰ and a low-temperature (c.350d?C) episode involving low-δ¹⁸O meteoric fluids. All the dykes that document exchange with meteoric fluids are non-mylonitic. Coupled δ¹⁸O_Fsp systematics of non-mylonitic and mylonitic granodioritic gneisses from above and below the mylonite front also document low-temperature (c. 350d? C) exchange with meteoric fluids. The data indicate that infiltration of meteoric fluids occurred as lower plate lithologies were juxtaposed against the base of the faulted upper plate. High-angle normal faults in the upper plate served as the conduits for the downward circulation of surface-derived fluids. Meteoric fluids were able to penetrate across the detachment fault into the lower plate. Uplift rates coupled with independent cooling rates indicate that surface-derived fluids penetrated to a depth of c.4km and possibly as deep as c.8km. Penetration of surface-derived fluid into the ductile deformation regime is not required to explain the low δ¹⁸O values observed in lower plate lithologies of the Whipple Mountain metamorphic core complex.     

A stable isotope study of the migmatitic rocks in the Ballachulish contact aureole, Scotland

The highest grade pelitic and semipelitic rocks of the Ballachulish aureole are dominantly potash feldspar + cordierite + biotite hornfelses with widely variable amounts of quartz, plagioclase, andalusite, sillimanite and corundum (together with accessory phases). On a microscopic scale these hornfelses show textural evidence of the presence of melt, whilst on a mesoscopic scale they contain a variety of leucosomes. Oxygen isotope studies have been carried out on both whole rocks and mineral separates in order to: (1) assess the sources of molten and volatile constituents and (2) determine the extents of isotopic homogenization and equilibration. Data from localities with both restricted and extensive evidence of leucosomes and melt development are compared, as well as one locality with petrographic evidence of melt incursion from the igneous complex. The whole-rock δ¹⁸O values of the leucosomes (10.5–14.9%.) are in general similar to the immediately adjacent mesosomes (9.9–14.5%.) which are typically cordierite- and feldspar-rich hornfelses. Isotopic evidence is thus consistent with an in-situ partial melt origin for the leucosomes, without the substantial addition of externally derived components. In the area of extensive melt development, the ‘chaotic zone’, it is possible there was addition of an H₂O-rich fluid phase (6-13 wt%) from the igneous complex which resulted in a slight lowering of δ¹⁸O values by 0.5–1.0%. Quartz mineral separates were used to assess the degree of local isotopic homogenization. In the extensively molten area (chaotic zone) there is extensive homogenization between rock layers (quartz δ¹⁸O usually within 1.0%), whilst in less molten areas δ¹⁸O quartz has a range of c. 3.0%. The greater homogenization in the chaotic zone is attributed to the increased degree of melting and infiltration of H₂O-rich fluid from the igneous complex.     

Petrology of an intrusion-related high-grade migmatite: implications for partial melting of metasedimentary rocks and leucosome-forming processes

Intrusion-related migmatites comprise a substantial part of the high-grade part of the southern Damara orogen, Namibia which is dominated by Al-rich metasedimentary rocks and various granites. Migmatites consist of melanosomes with biotite+sillimanite+garnet+cordierite+hercynite and leucosomes are garnet- and cordierite-bearing. Metamorphic grade throughout the area is in the upper amphibolite to lower granulite facies (5–6 kbar at 730–750 °C). Field evidence, petrographic observations, chemical data and mass balance calculations suggest that intrusion of granitic magmas and concomitant partial melting of metasedimentary units were the main processes for the generation of the migmatites. The intruding melts were significantly modified by magma mixing with in situ partial melts, accumulation of mainly feldspar and contamination with garnet from the wall rocks. However, it is suggested that these melts originally represented disequilibrium melts from a metasedimentary protolith. The occurrence of LILE-, HFSE- and LREE-enriched and -depleted residues within the leucosomes implies that both quartzo-feldspathic and pelitic rocks were subjected to partial melting. Isotope ratios of the leucosomes are rather constant (¹⁴³Nd/¹⁴⁴Nd (500 Ma): 0.511718–0.511754, ε Nd (500 Ma): ?3.54 to ?5.11) and Sr (⁸⁷Sr/⁸⁶Sr (500 Ma): 0.714119–0.714686), the metasedimentary units have rather constant Nd isotope ratios (¹⁴³Nd/¹⁴⁴Nd (500 Ma): 0.511622–0.511789, ε Nd (500 Ma): ?3.70 to ?6.93) but variable Sr isotope ratios Sr (⁸⁷Sr/⁸⁶Sr (500 Ma): 0.713527–0.722268). The most restitic melanosome MEL 4 has a Sr isotopic composition of ⁸⁷Sr/⁸⁶Sr (500 Ma): 0.729380. Oxygen isotopes do not mirror the proposed contamination process, due to the equally high δ¹⁸O contents of metasediments and crustal melts. However, the most LILE-depleted residue MEL 4 shows the lowest δ¹⁸O value (<10). Mass balance calculations suggest high degrees of partial melting (20–40%). It is concluded that partial melting was promoted by heat transfer and release of a fluid phase from the intruding granites. High degrees of partial melting can be reached as long as the available H₂O, derived from the crystallization of the intruding granites, is efficiently recycled within the rock volume. Due to the limited amounts of in situ melting, it seems likely that such regional migmatite terranes are not the sources for large intrusive granite bodies. The high geothermal gradient inferred from the metamorphic conditions was probably caused by exhumation of deep crustal rocks and contemporaneous intrusion of huge masses of granitoid magmas. The Davetsaub area represents an example of migmatites formed at moderate pressures and high temperatures, and illustrates some of the reactions that may modify leucosome compositions. The area provides constraints on melting processes operating in high-grade metasedimentary rocks.     

Geology and D-O-C Isotope Systematics of the Tieluping Silver Deposit,Henan, China: Implications for Ore Genesis

The Tieluping silver deposit, which is sited along NE-trending faults within the high-grade metamorphic basement of the Xiong‘er terrane, is part of an important Mesozoic orogenic-type Ag-Pb and Au belt recently discovered. Ore formation includes three stages: Early (E), Middle (M) and Late (L), which include quartz-pyrite (E),polymetallic sulfides (M) and carbonates (L), respectively. The E-stage fluids are characterized by δD=-90%c,δ^13CCO2=2.0‰ and δ^18O=9‰ at 373℃, and are deeply sourced; the L-stage fluids, with δD=-70‰, δ^13C CO2=-1.3%c and δ^18O=-2‰, are shallow-sourced meteoric water; whereas the M-stage fluids, with δD=-109‰, δ^13C CO2=0.1%c and δ^18O2‰, are a mix of deep-sourced and shallow-sourced fluids. Comparisons of the D-O-C isotopic systematics of the Estage ore-forming fluids with the fluids derived from Mesozoic granites, Archean-Paleoproterozoic metamorphic basement and Paleo-Mesoproterozoic Xiong‘er Group, show that these units cannot generate fluids with the measured isotopic composition (high δ^180 and δ^13C ratios and low δD ratios) characteristic of the ore-forming fluids. This suggests that the E-stage ore-forming fluids originated from metamorphic devolatilization of a carbonate-shale-chert lithological association, locally rich in organic matter, which could correspond to the Meso-Neoproterozoic Guandaokou and Luanchuan Groups, rather than to geologic units in the Xiong‘er terrane, the lower crust and the mantle. This supports the view that the rocks of the Guandaokou and Luanchuan Groups south of the Machaoying fault might be the favorable sources. A tectonic model that combines collisional orogeny, metallogeny and hydrothermal fluid flow is proposed to explain the formation of the Tieluping silver deposit. During the Mesozoic collision between the South and North China paleocontinents, a crustal slab containing a lithological association consisting of carbonate-shale-chert, locally rich in organic matter (carbonaceous shale) was thrust northwards beneath the Xiong‘er terrane along the Machaoying fault.Metamorphic devolatilization of this underthrust slab provided the ore-forming fluids to develop the Au-Ag-(Pb-Zn) ore belt, which includes the Tieluping silver deposit.     

Oxygen isotopic study of Late Mesozoic cooling of the Mount Barcroft area,central White Mountains,eastern California

The Middle Jurassic Barcroft mafic granodiorite and Late Cretaceous, ternary-minimum McAfee Creek Granite are important components of the igneous arc sited along the SW North American margin. Bulk-rock analyses of 11 samples of the metaluminous, I-type Barcroft comagmatic suite have an average δ¹⁸O value of 7.4±0.6‰ (all values±1σ). Four Barcroft specimens average ε_Nd=?3.6±1.8, ⁸⁷Sr/⁸⁶Sr=0.707±0.001. The pluton consists of petrochemically gradational, Ca-amphibole-rich gabbro/diorite, granodiorite, metadiorite, and rare alaskite–aplite; for most of the pluton, oxygen isotope exchange of quartz, feldspar(s), biotite, and Ca-amphibole accompanied local deuteric alteration. Eight specimens of slightly peraluminous granitic rocks of the muscovite-bearing McAfee Creek series have an average δ¹⁸O of 8.6±0.5‰. Four McAfee-type samples average ε_Nd=?7.8±1.7, ⁸⁷Sr/⁸⁶Sr=0.711±0.004. For both plutons, bulk-rock evidence of exchange with near-surface water is lacking, suggesting ~5–10 km cooling depths. Barcroft minerals exhibit regular oxygen isotopic partitioning from high to low δ¹⁸O in the sequence quartz>plagioclase>K-feldspar>>amphibole≥biotite. Along the SE margin of the pluton, quartz and biotite in Lower Cambrian quartzites are higher in δ¹⁸O, and show slightly larger fractionations than igneous analogues. Exchange with fluids derived from these heated, contact-metamorphosed country rocks increased bulk ¹⁸O/¹⁶O ratios of Barcroft border rocks (and constituent plagioclase+subsolidus tremolite–actinolite), especially of granitic dikes transecting the wall rocks. Oxygen isotope thermometry for seven Barcroft pluton quartz–amphibole and six quartz–biotite pairs indicate apparent subsolidus temperatures averaging 519±49 °C. Quartz–plagioclase pairs from two Barcroft granodiorites yield values of 519 and 515 °C. A quartz–biotite pair from a quartzite adjacent to the Barcroft pluton yields an apparent temperature of 511 °C, in agreement with estimates based on contact metamorphic parageneses. Except for its SE margin, Barcroft pluton silicates evidently exchanged oxygen isotopes under local deuteric conditions. Compatible with Ca-amphibole thermobarometric analyses, areal distributions for quartz–plagioclase, quartz–amphibole, and quartz–biotite pairs reveal that putative annealing temperatures are lowest in NE-trending axial portions of the Barcroft body, so it simply cooled inwards. Intrusion ~70 million years later by the McAfee Creek Granite had no discernable effect on δ¹⁸O values of Barcroft minerals and bulk rocks.     

Discussion: Stratigraphy and structural summary of the Cooma metamorphic complex

Field and petrographic studies on granitic, hematitic and chloritic breccias in the central portion of the Mount Painter Inlier, South Australia, indicate that: (i) breccias and brecciated basement extend to depths exceeding 400 m and have gradational contacts; (ii) clasts are mainly autochthonous and contain fine‐scale hematite, chlorite or quartz veinlets and fractures; (iii) K‐metasomatism preceded hematitisation and chloritisation; (iv) hematitic breccia intrudes a pegmatite dyke correlated with the Ordovician Arkaroola Pegmatite; and (v) U, F and REE‐containing minerals are present in the Proterozoic basement rocks, and concentrated in the breccias.

With a single exception, δ³⁴S values for pyrite from the breccias and brecciated granites fall in the narrow range —2.9% to +3.5%, implying formation from magmatic emanations or reducing fluids that leached sulphide minerals of magmatic derivation. δ³⁴S values for three barite samples are all close to +16%o, and firm conclusions cannot be drawn from these data. Calcites from the same rock‐types as the pyrite have δ¹³C values of — 22.3%o to —4.2%o and δ¹⁸O values of —4.0%o to +23.1%., with an inverse δ¹³C/δ¹⁸O relationship. The more ¹³C‐depleted calcites probably incorporated CO₂ from organic C, and their δ¹⁸O values are compatible with precipitation from magmatic or metamorphic fluids; mixing of such fluids with meteoric waters is implied by the calcites with variably lower δ¹⁸O values.

The above features indicate that the major processes leading to brecciation and associated metasomatism were hydraulic fracturing and hydrothermal activity resulting from ascent of granitic magmas to shallow crustal levels during late stages (late Ordovician‐?Silurian) of the Delamerian Orogeny. Tectonic and sedimentary processes appear to have played relatively minor roles in breccia formation.     

A reconnaissance study of stable isotope ratios in archaean rocks from the yilgarn block,Western Australia

Isotopic compositions of sulphur, carbon, and oxygen have been determined for constituents from a total of 103 samples of sedimentary rocks, mafic and ultramafic igneous rocks, nickel ores, and gold ores from the Archaean Yilgarn Block.

Sulphides in the bulk of the sedimentary rocks have δ³⁴S values close to 0‰ and appear to have precipitated from solutions which incorporated magmatic sulphur (either juvenile or derived from older rocks). There is no evidence for widespread sulphate reduction.

δ³⁴S values of sulphides in the nickel deposits and associated mafic/ultramafic igneous rocks are within the magmatic range. The small, high‐grade deposits of the Kambalda‐Nepean‐Scotia type have small positive δ³⁴S values, and the large, low‐to‐medium grade dunite‐associated deposits of the Mount Keith‐Perseverance type have small negative δ³⁴S values.

Sulphides in the Kalgoorlie gold ores are enriched in ³²S relative to those in their host dolerite, supporting an epigenetic origin for the gold, under moderately high fO₂ conditions.

The δ¹³C values do not provide unequivocal evidence for the source(s) of the reduced carbon (kerogen) in the sedimentary rocks. Whilst they are compatible with biogenic derivation, it is not possible to rule out contributions from pre‐biotic organic ‘soup’ or from hydrothermal solutions of deep‐seated origin.

Carbonate in the sedimentary rocks are predominantly in epigenetic, sulphide‐bearing veinlets. In many cases, their δ¹³C values suggest precipitation from hydro‐thermal solutions containing magmatically derived CO₂. In only two samples are the petrographic features and δ¹³C values compatible with marine carbonates. Talc‐carbonate altered ultramafic igneous rocks have δ¹³C values consistent with their incorporation of magmatically derived CO₂.

The ?δ¹³C (carbonate‐kerogen) values for most of the sedimentary rock studied fall in a narrow range around +10‰, suggesting isotopic exchange between oxidized and reduced carbon species at moderately high temperatures (>250°C).

δ¹⁸O values of carbonate from both sedimentary rocks and igneous rocks are mainly within the range +7.2‰ to +18.0‰. If the values are primary they are consistent with the formation of carbonate from hydrothermal solutions of magmatic and/or metamorphic origin. However, it is also possible the δ¹⁸O values are the result of post‐depositional equilibration with meteoric waters.     

A novel model for silicon recycling in the lithosphere: Evidence from the Central Asian Orogenic Belt

Global-scale cycling of silicon through the biosphere, atmosphere, and hydrosphere has received much attention although, silicon cycling in the Earth’s lithosphere remains poorly understood. As the products of internal heat and material exchange, igneous rocks preserve significant information of silicon migration through the lithosphere. Here we report silicon isotopic compositions of nine peraluminous granites from the Chinese Altai, which forms part of the Central Asian Orogenic Belt. These rocks are characterized by the heaviest δ³⁰Si values (−0.13 ± 0.03‰ to +0.78 ± 0.05‰) compared to global granites, with a linear variation in the silicon isotopic values against silica content, with high silica-rich granites displaying more depleted isotopic compositions. In conjunction with the whole rock weakly negative ɛ_Nd(t) and uniform δ²⁶Mg values, as well as high δ¹⁸O values, we suggest that the δ³⁰Si values of these granites were mainly inherited from the magma source, rather than produced by magmatic fractionation. In addition, the wide range of initial ⁸⁷Sr/⁸⁶Sr ratios and high Ba content of the samples suggest the role of aqueous fluids. The Chinese Altai is considered to have formed through accretion of volcanic arcs associated with subduction of the Paleo-Asian oceanic lithosphere. The magma derived through partial melting of metasomatic mantle scavenges the heavy ³⁰Si isotopes derived through fluids released from oceanic sediments and transfers to the upper crust where partial melting of crustal sedimentary rocks occur. Mixing of these two melts generated the peraluminous granites. Our study offers a novel insight into a potentially important mechanism of silicon cycling in the lithosphere.     

Carbon,hydrogen, and oxygen isotope studies of the regional metamorphic complex at Naxos,Greece

At Naxos, Greece, a migmatite dome is surrounded by schists and marbles of decreasing metamorphic grade. Sillimanite, kyanite, biotite, chlorite, and glaucophane zones are recognized at successively greater distances from the migmatite dome. Quartz-muscovite and quartz-biotite oxygen isotope and mineralogie temperatures range from 350 to 700°C.The metamorphic complex can be divided into multiple schist-rich (including migmatites) and marblerich zones. The δ¹⁸O values of silicate minerals in migmatite and schist units and quartz segregations in the schist-rich zones decrease with increase in metamorphic grades. The calculated δ¹⁸O_H2O values of the metamorphic fluids in the schist-rich zones decrease from about 15‰ in the lower grades to an average of about 8.5‰ in the migmatite.The δD values of OH-minerals (muscovite, biotite, chlorite, and glaucophane) in the schist-rich zones also decrease with increase in grade. The calculated δD_H2O values for the metamorphic fluid decrease from ?5‰ in the glaucophane zone to an average of about ?70‰ in the migmatite. The δD values of water in fluid inclusions in quartz segregations in the higher grade rocks are consistent with this trend.Theδ¹⁸O values of silicate minerals and quartz segregations in marble-rich zones are usually very large and were controlled by exchange with the adjacent marbles. The δD values of the OH minerals in some marble-rich zones may reflect the value of water contained in the rocks prior to metamorphism.Detailed data on 20 marble units show systematic variations of δ¹⁸O values which depend upon metamorphic grade. Below the 540°C isograd very steep δ¹⁸O gradients at the margins and large δ¹⁸O values in the interior of the marbles indicate that oxygen isotope exchange with the adjacent schist units was usually limited to the margins of the marbles with more exchange occurring in the stratigraphic bottom than in the top margins. Above the 540°C isograd lower δ¹⁸O values occur in the interior of the marble units reflecting a greater degree of recrystallization and the occurrence of Ca-Mg-silicates.Almost all the δ¹³C values of the marbles are in the range of unaltered marine limestones. Nevertheless, the δ¹³C values of most marble units show a general correlation with δ¹⁸O values.The $\text{CO}{}_2\text{H}{}_2\text{O}$ mole ratio of fluid inclusions in quartz segregations range from 0.01 to 2. Theδ¹³C values of the CO₂ range from ?8.0 to 3.6‰ and indicate that at some localities CO₂ in the metamorphic fluid was not in carbon isotopic equilibrium with the marbles.     

Geology, Fluid Inclusion and Isotopic Study of the Neoproterozoic Suoi Thau Copper Deposit, Northwest Vietnam

The Sin Quyen-Lung Po district is an important Cu metallogenic province in Vietnam, but there are few temporal and genetic constraints on deposits from this belt. Suoi Thau is one of the representative Cu deposits associated with granitic intrusion. The deposit consists of ore bodies in altered granite or along the contact zone between granite and Proterozoic meta-sedimentary rocks. The Cu-bearing intrusion is sub-alkaline I-type granite. It has a zircon U-Pb age of ~776 Ma, and has subduction-related geochemical signatures. Geochemical analysis reveals that the intrusion may be formed by melting of mafic lower crust in a subduction regime. Three stages of alteration and mineralization are identified in the Suoi Thau deposit, i.e., potassic alteration; silicification and Cu mineralization; and phyllic alteration. Two-phase aqueous fluid inclusions in quartz from silicification stage show wide ranges of homogenization temperatures(140–383℃) and salinities(4.18wt%–19.13wt%). The high temperature and high salinity natures of some inclusions are consistent with a magmatic derivation of the fluids, which is also supported by the H-O-S isotopes. Fluids in quartz have δD values of –41.9‰ to –68.8‰. The fluids in isotopic equilibrium with quartz have δ~(18)O values ranging from 7.9‰ to 9.2‰. These values are just plotted in the compositional field of magmatichydrothermal fluids in the δD_(water) versus δ~(18)O_(water) diagram. Sulfide minerals have relatively uniform δ~(34)S values from 1.84‰ to 3.57‰, which is supportive of a magmatic derivation of sulfur. The fluid inclusions with relatively low temperatures and salinities most probably represent variably cooled magmatic-hydrothermal fluids. The magmatic derivation of fluids and the close spatial relationship between Cu ore bodies and intrusion suggest that the Cu mineralization most likely had a genetic association with granite. The Suoi Thau deposit, together with other deposits in the region, may define a Neoproterozoic subduction-related ore-forming belt.     

Oxygen and Carbon Isotope Study of Calcite and Dolomite in the Disseminated Au-Ag Telluride Bulawan Deposit, Negros Island, Philippines

Abstract: The disseminated Au‐Ag telluride Bulawan deposit, Negros island, Philippines, is hosted by dacite porphyry breccia pipes which formed in a Middle Miocene dacite porphyry stock. Electrum and Au‐Ag tellurides occur mostly as grains intergrown with or filling voids between sphalerite, pyrite, chalcopyrite, galena and tennantite. Calcite, quartz and rare dolomite are the principal gangue minerals. Four types of alteration were recognized in the deposit, namely; propylitic, K‐feldspar‐sericitic, sericitic and carbonate alteration. Carbonate alteration is correlatable to the gold deposition stage and occurs mostly along fault zones. The δ¹⁸O and δ¹³C compositions of calcite and dolomite in propylite zone and ore‐stage dacite porphyry breccia were determined. The δ¹⁸O values of calcite in propylitized andesite range from +12.2 to +14.7%, and their δ¹³C values range from ‐6.1 to ‐1.0%. The δ¹⁸O values of calcite and dolomite in sericite‐ and carbonate‐altered, mineralized dacite porphyry breccia and dacite porphyry rocks range from +15.1 to +23.1%, and the δ¹³C values of calcite and dolomite range from ‐3.9 to +0.9%. The δ¹⁸O and δ¹³C values of the hydrothermal fluids were estimated from inferred temperatures of formation on the basis of fluid inclusion microthermometry. The δ¹⁸O values of hydrothermal fluid for the propylitic alteration were calculated to be +8.5 ‐ +9.5%, assuming 375°C. On the other hand, the δ¹⁸O values of ore solutions for base metal and Au mineralization were computed to be +13.6 ‐ +14.6%, assuming 270°C. The hydrothermal fluids that formed the Bulawan deposit are dilute and ¹⁸O‐enriched fluids which reacted with ¹⁸O‐ and ¹³C‐rich wallrocks such as limestone.     

Petrogenesis of the Xihuashan Granite in Southern Jiangxi Province,South China: Constraints from Zircon U-Pb Geochronology,Geochemistry and Nd Isotopes

Mesozoic granitic intrusions are widely distributed in the Nanling region,South China.Yanshanian granites are closely connected with the formation of tungsten deposits.The Xihuashan granite is a typica...     

High‐temperature,low‐pressure metamorphism and development of prograde symplectites,Marble Hall Fragment,Bushveld Complex (South Africa)

Metapelitic rocks from the Marble Hall Fragment, enclosed in the granites of the magmatic Bushveld Complex, record a two‐stage, low‐pressure, high‐temperature metamorphism. An early paragenesis containing chiastolitic andalusite, cordierite, biotite and quartz ± garnet crystallized in most rocks and equilibrated at 550–600 °C, 0.2 GPa. It was transformed during the second, peak event into various parageneses that commonly coexist within a single thin section. These include garnet–cordierite–biotite–K‐feldspar–quartz, sillimanite–cordierite–K‐feldspar–quartz and spectacular quartz‐undersaturated cordierite–spinel symplectites replacing the chiastolite porphyroblasts. Based on a detailed phase diagram analysis, we argue that these parageneses result from rapid heating at an approximately constant pressure to temperatures of more than about 720 °C. At these temperatures, the internally buffered activity of water was reduced by incipient water‐saturated partial melting, while only minor quantities of melt were produced. Subsequent dry conditions inhibited large‐scale equilibration and, together with local inhomogeneities in mineral distribution, led to the development of contrasting parageneses and symplectite textures. No signs of widespread fluid‐absent melting of biotite were found, and so the temperature probably did not exceed 760 °C. The peak metamorphic event is attributed to the emplacement of the hot Nebo granite, whereas the early metamorphism was probably caused by the intrusion of one of the phases of the Rustenburg Layered Suite. We infer the conditions of development of the cordierite–spinel intergrowths and we show that, although symplectites are commonly associated with retrograde processes (cooling and/or decompression), they can record a prograde metamorphic evolution. Furthermore, our contribution emphasizes the importance of the concept of reduced equilibration volume for the understanding and interpretation of some particular textures and parageneses in common rocks.     

A two-stage fluid history for the Orocopia Schist and associated rocks related to flat subduction and exhumation,southeastern California

ABSTRACT

Stable isotopes combined with pre-existing ⁴⁰Ar/³⁹Ar thermochronology at the Gavilan Hills and Orocopia Mountains in southeastern California record two stages of fluid–rock interaction: (1) Stage 1 is related to prograde metamorphism as Orocopia Schist was accreted to the base of the crust during late Cretaceous–early Cenozoic Laramide flat subduction. (2) Stage 2 affected the Orocopia Schist and is related to middle Cenozoic exhumation along detachment faults. There is no local evidence that schist-derived fluids infiltrated structurally overlying continental rocks. Mineral δ¹⁸O values from Orocopia Schist in the lower plate of the Chocolate Mountains fault and Gatuna normal fault in the Gavilan Hills are in equilibrium at 490–580°C with metamorphic water (δ¹⁸O = 7–11‰). Phengite and biotite δD values from the Orocopia Schist and upper plate suggest metamorphic fluids (δD ~ –40‰). In contrast, final exhumation of the schist along the Orocopia Mountains detachment fault (OMDF) in the Orocopia Mountains was associated with alteration of prograde biotite and amphibole to chlorite (T ~ 350–400°C) and the influx of meteoric-hydrothermal fluids at 24–20 Ma. Phengites from a thin mylonite zone at the top of the Orocopia Schist and alteration chlorites have the lowest fluid δD values, suggesting that these faults were an enhanced zone of meteoric fluid (δD < –70‰) circulation. Variable δD values in Orocopia Schist from structurally lower chlorite and biotite zones indicate a lesser degree of interaction with meteoric-hydrothermal fluids. High fluid δ¹⁸O values (6–12‰) indicate low water–rock ratios for the OMDF. A steep thermal gradient developed across the OMDF at the onset of middle Cenozoic slip likely drove a more vigorous hydrothermal system within the Orocopia Mountains relative to the equivalent age Gatuna fault in the Gavilan Hills.     

Geology and Isotope Geochemistry of the Yinchanggou-Qiluogou Pb-Zn Deposit, Sichuan Province, Southwest China

The Yinchanggou-Qiluogou Pb-Zn deposit,located in the western Yangtze Block,southwest China,is hosted by the Upper Sinian Dengying Formation dolostone.Ore bodies occur in the Qiluogou anticline and the NS-and NNW-trending faults.Sulfide ores mainly consist of sphalerite,pyrite,galena and calcite,with subordinate dolomite and quartz.Seventeen ore bodies have been discovered to date and they have a combined 1.0 million tons of sulfide ores with average grades of 2.27wt%Zn and 6.89wt%Pb.The δD_(H2O-SMOW) and δ~(18)O_(H2O-SMOW) values of fluid inclusions in quartz and calcite samples range from-68.9‰ to-48.7‰ and 7.3‰ to 15.9‰,respectively,suggesting that H_2O in the hydrothermal fluids sourced from metamorphic water.Calcite samples have δ~(13)C_(PDB) values ranging from-6.2‰ to-4.1‰ and δ~(18)O_(SMOW) values ranging from 15.1‰ to 17.4‰,indicating C and O in the hydrothermal fluids likely derived from a mixed source of metamorphic fluids and the host carbonates.The δ~(34)S_(CDT) values of sulfide minerals range from 5.5‰ to 20.3‰,suggesting that thermal chemical reduction of sulfate minerals in evaporates were the most probable source of S in the hydrothermal fluids.The ~(206)Pb/~(204)Pb,~(207)Pb/~(204)Pb and ~(208)Pb/~(204)Pb ratios of sulfide minerals fall in the range of 18.11 to 18.40,15.66 to 15.76 and 38.25 to 38.88,respectively.The Pb isotopic data of the studied deposit plot near the upper crust Pb evolution curve and overlap with the age-corrected Proterozoic basement rocks and the Upper Sinian Dengying Formation hosting dolostone.This indicates that the Pb originated from a mixed source of the basement metamorphic rocks and the ore-hosting carbonate rocks.The ore geology and C-H-O-S-Pb isotopic data suggest that the YinchanggouQiluogou deposit is an unusual carbonate-hosted,strata-bound and epigenetic deposit that derived ore-forming materials from a mixed source of the underlying Porterozoic basements and the Sinian hosting carbonates.     

Hydrothermal Alteration and Mineralization of Middle Jurassic Dexing Porphyry Cu-Mo Deposit, Southeast China

The Dexing deposit is located in a NE‐trending magmatic belt along the southeastern margin of the Yangtze Craton. It is the largest porphyry copper deposit in China, consisting of three porphyry copper orebodies of Zhushahong, Tongchang and Fujiawu from northwest to southeast. It contains 1168 Mt of ores with 0.5% Cu and 0.01% Mo. The Dexing deposit is hosted by Middle Jurassic granodiorite porphyries and pelitic schist of Proterozoic age. The Tongchang granodiorite porphyry has a medium K cal‐alkaline series, with medium K₂O content (1.94–2.07 wt%), and low K₂O/(Na₂O + K₂O) (0.33–0.84) ratios. They have high large‐ion lithophile elements, high light rare‐earth elements, and low high‐field‐strength elements. The hydrothermal alteration at Tongchang is divided into four alteration mineral assemblages and related vein systems. They are early K‐feldspar alteration and A vein; transitional (chlorite + illite) alteration and B vein; late phyllic (quartz + muscovite) alteration and D vein; and latest carbonate, sulfate and oxide alteration and hematite veins. Primary fluid inclusions in quartz from phyllic alteration assemblage include liquid‐rich (type 1), vapor‐rich (type 2) and halite‐bearing ones (type 3). These provide trapping pressures of 20–400 ´ 10⁵ Pa of fluids responsible for the formation of D veins. Igneous biotite from least altered granochiorite porphyry and hydrothermal muscovite in mineralized granodiorite porphyry possess δ¹⁸O and δD values of 4.6‰ and ?87‰ for biotite and 7.1–8.9‰, ?71 to ?73‰ for muscovite. Stable isotopic composition of the hydrothermal water suggests a magmatic origin. The carbon and oxygen isotope for hydrothermal calcite are ?4.8 to ?6.2‰ and 6.8–18.8‰, respectively. The δ³⁴S of pyrite in quartz vein ranges from ?0.1 to 3‰, whereas δ³⁴S for chalcopyrite in calcite veins ranges from 4 to 5‰. These are similar to the results of previous studies, and suggest a magmatic origin for sulfur. Results from alteration assemblages and vein system observation, as well as geochemical, fluid inclusion, stable isotope studies indicate that the involvement of hydrothermal fluids exsolved from a crystallizing melt are responsible for the formation of Tongchang porphyry Cu‐Mo orebodies in Dexing porphyry deposit.     

Fluid generation, vein formation and the degree of fluid–rock interaction during decompression of high-pressure terranes: the Schistes Lustrés, Alpine Corsica, France

Centimetre‐ to decimetre‐wide quartz+calcite veins in schistes lustrés from Alpine Corsica were formed during exhumation at 30–40 Ma following blueschist facies metamorphism. The δ¹⁸O and δ¹³C values of the veins overlap those of the host schistes lustrés, and the δ¹⁸O values of the veins are much higher than those of other rocks on Corsica. These data suggest that the vein‐forming fluids were derived from the schistes lustrés. Fluids were probably generated by reactions that broke down carpholite, lawsonite, chlorite and white mica at 300–350 °C during decompression between c. 1400 and 800 MPa. However, the δ¹⁸O values of the veins are locally several per mil higher than expected given those of their host rocks. The magnitude of oxygen isotope disequilibrium between the veins and the host rock is inversely proportional to the δ¹⁸O value of the host rock. Additionally, calcite in some schists is in isotopic equilibrium with calcite in adjacent veins, but not with the silicate fraction of the schists. Locally, the schists are calcite bearing only within 1–20 cm of the veins. The vein‐forming fluids may have been preferentially derived from calcite‐bearing, high‐δ¹⁸O rocks that are common within the schistes lustrés and that locally contain abundant (>15%) veins. If the fluids were unable to completely isotopically equilibrate with the rocks, due to relatively rapid flow at moderate temperatures or being confined to fractures, they could form veins with higher δ¹⁸O values than those of the surrounding rocks. Alteration of the host rocks was probably inhibited by isolation of the fluid in ‘quartz‐armoured’ veins. Overall, the veins represent a metre‐ to hectometre‐scale fluid‐flow system confined to within the schistes lustrés unit, with little input from external sources. This fluid‐flow system is one of several that operated in the western Alps during exhumation following high‐pressure metamorphism.     

Pre‐ to syn‐tectonic emplacement of early Palaeozoic granites in southeastern South Australia

Stratigraphic and structural observations indicate that the Encounter Bay Granites concordantly intruded the youngest formations of the Kanmantoo Group in the Mount Lofty Ranges metamorphic belt prior to the culmination of the first phase of folding and associated schistosity development recorded during the early Palaeozoic Delamerian Orogeny. Metamorphic textures in the metasediments of the Kanmantoo Group suggest that cordierite crystallized locally near the granites prior to and during the F ₁ folding, whereas andalusite crystallized on a regional scale during the F ₁ folding and in the post‐F ₁ and pre‐F ₂ static phase.

Rb‐Sr isotope data for total‐rock, feldspar, and muscovite samples of the meta‐sediment‐contaminated border facies and the uncontaminated inner facies of the Encounter Bay Granites indicate that the granites were emplaced between 515 ± 8 m.y. and 506 ± 6 m.y. ago in the Late Cambrian epoch. Rb‐Sr and K‐Ar data for biotite from the granites record variable radiogenic Sr loss until about 469 m.y. ago and comparatively uniform radiogenic Ar loss until 460–475 m.y. ago. Rb‐Sr data for Kanmantoo Group metasediments and a metamorphic pegmatite indicate crystallization ages between 459–463 m.y. ago. Thus the regional andalusite‐grade temperatures and pressures, which appear responsible for the leakage of radiogenic Sr and Ar from biotite in the granites and the redistribution of Rb and Sr in the metasediments, seem to have persisted for some 50 m.y. after emplacement of the granites until the Early Ordovician epoch. There is evidence for further leakage of Sr and Ar from biotite in deformed granites from the margins of the intrusion more than 50 m.y. afterwards in the Late Silurian or Early Devonian, possibly during the F ₂ folding.

Geological observations and radiometric data for other granitic rocks in southeastern South Australia, including the Palmer Granite, are consistent with this structural and metamorphic history of the Encounter Bay region.     

Mesothermal Gold Vein Mineralization of the Seolhwa Mine,Asan Mining District,Korea

Gold mineralization of the Seolhwa mine occurs in a single stage of massive quartz veins which filled the north‐east‐trending fault shear zones in the Jurassic granitoid of 161 Ma within the Gyeonggi Massif. The vein quartz contains three main types of fluid inclusions at 25°C: (i) aqueous type I inclusions (0–15 wt.% NaCl) containing small amounts of CO₂; (ii) gas‐rich (more than 70 vol. %), vapor‐homogenizing, aqueous type II inclusions; and (iii) low‐salinity (less than 5 wt.% NaCl), liquid CO₂‐bearing, type III inclusions. The H₂O‐CO₂‐CH₄‐N₂‐NaCl inclusions represent immiscible fluids trapped earlier along the solvus curve in the temperature range 250–430°C at pressures of ～1 kb. Detailed fluid inclusion chronologies suggest a progressive decrease in pressure during the mineralization. Aqueous inclusion fluids represent either later fluids evolved through extensive fluid unmixing from a homogeneous H₂O‐CO₂‐CH₄‐N₂‐NaCl fluid due to decreases in temperature and pressure, or the influence of deep circulated meteoric waters. Initial fluids were homogeneous H₂O‐CO₂‐CH₄‐N₂‐NaCl fluids as follows: 250° to 430°C, 16–62 mol% CO₂, 5–14 mol% CH₄, 0.06–0.31 mol% N₂ and salinities of 0.4–4.9 wt.% NaCl. The T‐X data for the Seolhwa mine suggest that the hydrothermal system has been probably located nearer to the granitic melt, which facilitated the CH₄ formation and resulted in a reduced fluid state indicated by the predominance of pyrrhotite. Measured and calculated isotopic compositions of the hydrothermal fluids [δ¹⁸O = 5.3–6.5‰; δD =?69 to ?84‰] provide evidence of the CH₄‐H₂O equilibria and further indicate that the auriferous fluids were magmatically derived. Both the dominance of δ³⁴S values of sulfides close to the meteoric reference (?0.6–1.4‰; δ³⁴S_ΣS values of 0.3–1.1‰) and the available δ¹³C data (?4‰) are consistent with their deep igneous source. The Seolhwa mine was probably formed by extensive fracturing and veining due to the thermal expansion of water derived from the Jurassic granitoid melt.     

The interpretation of reaction textures in Fe‐rich metapelitic granulites of the Musgrave Block,central Australia: constraints from mineral equilibria calculations in the system K2O–FeO–MgO–Al2O3–SiO2–H2O–TiO2–Fe2O3

Fe‐rich metapelitic granulites of the Musgrave Block, central Australia, contain several symplectic and coronal reaction textures that post‐date a peak S2 metamorphic assemblage involving garnet, sillimanite, spinel, ilmenite, K‐feldspar and quartz. The earliest reaction textures involve spinel‐ and quartz‐bearing symplectites that enclose garnet and to a lesser extent sillimanite. The symplectic spinel and quartz are in places separated by later garnet and/or sillimanite coronas. The metamorphic effects of a later, D3, event are restricted to zones of moderate to high strain where a metamorphic assemblage of garnet, sillimanite, K‐feldspar, magnetite, ilmenite, quartz and biotite is preserved. Quantitative mineral equilibria calculations in the system K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O–TiO₂–Fe₂O₃ (KFMASHTO) using Thermocalc 3.0 and the accompanying internally consistent dataset provide important constraints on the influence of TiO₂ and Fe₂O₃ on biotite‐bearing and spinel‐bearing equilibria, respectively. Biotite‐bearing equilibria are shifted to higher temperatures and spinel‐bearing equilibria to higher pressures and lower temperatures in comparison to the equivalent equilibria in K₂O–FeO–MgO–Al₂O₃–SiO₂–H₂O (KFMASH). The sequence of reaction textures involving spinel is consistent with a D2 P–T path that involved a small amount of decompression followed predominantly by cooling within a single mineral assemblage stability field. Thus, the reaction textures reflect changes in modal proportions within an equilibrium assemblage rather than the crossing of a univariant reaction. The D3 metamorphic assemblage is consistent with lower temperatures than those inferred for D2.