Prediction of Hidden Ore Bodies using Integrated Geology, Source of Fluids and Stratagem EH4 Geophysical Survey in Kuoerzhenkuola Gold Deposit in Xinjiang, China

The Kuoerzhenkuola gold deposit is located in the Sawur gold belt in Xinjiang, China. An integrated geological, geochemical and geophysical investigation was carried out in the Kuoerzhenkuola gold deposit, to determine the extension of the principal mineralized system, in the search for new resources. Re‐examination of the rocks and structures in the Kuoerzhenkuola area showed that the study area features an elliptical caldera where the gold deposit lies. A re‐investigation of the mine geology found that the mineralization at the Kuoerzhenkuola gold deposit is not controlled by the EW‐striking regional fault as previously assumed, but by a caldera fracture system locally superimposed by regional faults; the host rocks are andesites and dacites of the Carboniferous Heishantou Group rather than the crypto‐explosive breccia of the Devonian Sawurshan Group. Gas components of fluid inclusions from quartz, trace element chemistry of pyrite and fluid inclusions in pyrite, Pb isotopes of pyrite, and whole‐rock geochemistry and Pb isotopes of the country rocks are used to study the source of fluids at Kuoerzhenkuola gold deposit. The ore‐forming fluids are characterized by low–moderate temperatures and low salinities estimated from fluid inclusion microthermometry. Quadrupole mass spectrometry indicated a CO₂‐bearing fluid. Inductively coupled plasma–mass spectrometry of the fluid inclusions indicated high Cu (average 70 ppm) for the Au mineralization, whereas the host rocks have low Cu (average 33 ppm), indicating that Cu of the ore‐forming fluids originated from magmatic fluid rather than the volcanic rocks. Pb isotopes of ores and host volcanic rocks indicate a similar, mixed source and some Pb could be sourced from the volcanism. This implied that magmatic fluids could play an important role in the Au mineralization process. These new geological findings and the fluids derived mainly from the magmatic fluids suggest that the ore‐forming fluids originate at depth, and are transported and precipitated within the caldera fracture system. Thus, we proposed a conceptual target area at depth. A detailed Stratagem EH4 measurement was carried out to test the validity of the conceptual target. Stratagem EH4 soundings over six parallel traverses perpendicular to the mineralized trend showed that the caldera fracture system could extend for approximately 900 m in the dip direction at the center of the caldera, an indication of the presence of potential deep mineralization under the surveyed area. Detailed modeling of the Stratagem EH4 sounding images provided well‐defined targets for test drilling. Subsequent test drilling on one of these targets, which extends down 850 m at an angle of 87°, returned encouraging results because four core‐intercepts of gold ore bodies at down‐hole depths of 40.5–42.0 m, 70.5–73.5 m, 357.0–358.5 m, and 384.5–385.5 m and a long interval gold mineralized body (0–720 m) were encountered.     

Effects of Deep Fluids on Hydrocarbon Generation and Accumulation in Chinese Petroliferous Basins

Deep fluids in a petroliferous basin generally come from the deep crust or mantle beneath the basin basement, and they transport deep substances(gases and aqueous solutions) as well as heat to sedimentary strata through deep faults. These deep fluids not only lead to large-scale accumulations of CO_2, CH_4, H_2, He and other gases, but also significantly impact hydrocarbon generation and accumulation through organic-inorganic interactions. With the development of deep faults and magmatic-volcanic activities in different periods, most Chinese petroliferous basins have experienced strong impacts associated with deep fluid activity. In the Songliao, Bohai Bay, Northern Jiangsu, Sanshui, Yinggehai and Pearl Mouth Basins in China, a series of CO_2 reservoirs have been discovered. The CO_2 content is up to 99%, with δ~(13)C_(CO2) values ranging from-4.1‰ to-0.37‰ and ~3He/~4He ratios of up to 5.5 Ra. The abiogenic hydrocarbon gas reservoirs with commercial reserves, such as the Changde, Wanjinta, Zhaozhou, and Chaoyanggou reservoirs, are mainly distributed in the Xujiaweizi faulted depression of the Songliao Basin. The δ~(13)CCH4 values of the abiogenic alkane gases are generally -30‰ and exhibit an inverse carbon isotope sequence of δ~(13)C_(CH4)δ~(13)C_(C2H6)δ~(13)C_(C3H8)δ~(13)C_(C4H10). According to laboratory experiments, introducing external H_2 can improve the rate of hydrocarbon generation by up to 147% through the kerogen hydrogenation process. During the migration from deep to shallow depth, CO_2 can significantly alter reservoir rocks. In clastic reservoirs, feldspar is easily altered by CO_2-rich fluids, leading to the formation of dawsonite, a typical mineral in high CO_2 partial pressure environments, as well as the creation of secondary porosity. In carbonate reservoirs, CO_2-rich fluids predominately cause dissolution or precipitation of carbonate minerals. The minerals, e.g., calcite and dolomite, show some typical features, such as higher homogenization temperatures than the burial temperature, relatively high concentrations of Fe and Mn, positive Eu anomalies, depletion of 18 O and enrichment of radiogenic ~(87)Sr. Due to CO_2-rich fluids, the development of high-quality carbonate reservoirs is extended to deep strata. For example, the Well TS1 in the northern Tarim Basin revealed a high-quality Cambrian dolomite reservoir with a porosity of 9.1% at 8408 m, and the Well ZS1 C in the central Tarim Basin revealed a large petroleum reserve in a Cambrian dolomite reservoir at ~6900 m. During the upward migration from deep to shallow basin strata, large volumes of supercritical CO_2 may extract petroleum components from hydrocarbon source rocks or deep reservoirs and facilitate their migration to shallow reservoirs, where the petroleum accumulates with the CO_2. Many reservoirs containing both supercritical CO_2 and petroleum have been discovered in the Songliao, Bohaiwan, Northern Jiangsu, Pearl River Mouth and Yinggehai Basins. The components of the petroleum trapped with CO_2 are dominated by low molecular weight saturated hydrocarbons.     

The isotopic and chemical composition of CO2-rich thermal waters in the Mont-Dore region (Massif-Central,France)

Chemical and isotope compositions of fluid samples, collected between 1974 and 1986 from 52 springs or shallow boreholes located in the Mont-Dore region (Massif Central, France), were examined. Some springs and wells were sampled several times during this period. The fluids emerge from Quaternary volcanic rocks or Paleozoic granite at temperatures between 4 and 62°C, and the origin of the H₂O is meteoric. The waters can be classified into three groups: bicarbonate fluids, mixed bicarbonate-chloride fluids (with a mineralization up to 8 g/l), and acid-sulfate fluids. Only two fluids contain sufficient Cl⁻ to be considered as ‘mature’ waters. Previous work has demonstrated that they all contain partly mantle-derived CO₂ gas, and that the CO₂-rich gas phase and bicarbonate-chloride waters are separated at substantial depth.Mineralized fluids circulate at depth and undergo several processes, such as cooling or dilution with recent freshwater, during their ascent to the surface. Therefore, the CO₂-rich gas phase can be partly dissolved in the freshwater, or in deep fluids after their dilution. This process leads to the dissolution of surrounding rocks; such dissolution is discussed on the basis of major-element concentrations (Na, K, Ca, Mg), as well as the Sr 87/86 isotope ratio. Dissolution of S-bearing minerals has also been demonstrated. The presence of the CO₂-rich gas phase also leads to isotope exchange between CO₂ and H₂O. Some mineralized fluids are less affected by these processes than others, in which case they display the chemical and isotopic characteristics of the original deep fluids.It was shown that the applicability of geothermometer calculations for these waters is hampered by several processes that modify the chemical composition. However, some geothermometers can be used for estimating the temperature of the deep fluids using the chemical composition of the less modified fluids. They indicate that fluids emerging from volcanic rocks in the Dordogne valley reach temperatures of around 100–130°C at depth, while the temperature of the fluid that issues from the granite at Saint-Nectaire is 160–175°C at depth.     

Formation Process of Zircon Associated with REE‐Fluorocarbonate and Niobium Minerals in the Nechalacho REE Deposit,Thor Lake,Canada

The two drill holes, which penetrated sub‐horizontal rare earth element (REE) ore units at the Nechalacho REE in the Proterozoic Thor Lake syenite, Canada, were studied in order to clarify the enrichment mechanism of the high‐field‐strength elements (HFSE: Zr, Nb and REE). The REE ore units occur in the albitized and potassic altered miaskitic syenite. Zircon is the most common REE mineral in the REE ore units, and is divided into five types as follows: Type‐1 zircon occurs as discrete grains in phlogopite, and has a chemical character similar to igneous zircon. Type‐2 zircon consists of a porous HREE‐rich core and LREE–Nb–F‐rich rim. Enrichment of F in the rim of type‐2 zircon suggests that F was related to the enrichment of HFSE. The core of type‐2 zircon is regarded to be magmatic and the rim to be hydrothermal in origin. Type‐3 zircon is characterized by euhedral to anhedral crystals, which occur in a complex intergrowth with REE fluorocarbonates. Type‐3 zircon has high REE, Nb and F contents. Type‐4 zircon consists of porous‐core and ‐rim, but their chemical compositions are similar to each other. This zircon is a subhedral crystal rimmed by fergusonite. Type‐5 zircon is characterized by smaller, porous and subhedral to anhedral crystals. The interstices between small zircon grains are filled by fergusonite. Type‐4 and type‐5 zircon grains have low REE, Nb and F contents. Type‐1 zircon is only included in one unit, which is less hydrothermally altered and mineralized. Type‐2 and type‐3 zircon grains mainly occur in the shallow units, while those of type‐4 and type‐5 are found in the deep units. The deep units have high HFSE contents and strongly altered mineral textures (type‐4 and type‐5) compared to the shallow units. Occurrences of these five types of zircon are different according to the depth and degree of the hydrothermal alteration by solutions rich in F and CO₃, which permit a model for the evolution of the zircon crystallization in the Nechalacho REE deposit as follows: (i) type‐1 (discrete magmatic zircon) is formed in miaskitic syenite. (ii) LREE–Nb–F‐rich hydrothermal zircon formed around HREE‐rich magmatic zircon (type‐2). (iii) type‐3 zircon crystallized through the F and CO₃‐rich hydrothermal alteration of type‐2 zircon which formed the complex intergrowth with REE fluorocarbonates; (iv) the CO₃‐rich hydrothermal fluid corroded type‐3, forming REE–Nb‐poor zircon (type‐4). Niobium and REE were no longer stable in the zircon structure and crystallized as fergusonite around the REE–Nb‐leached zircon (type‐4); (v) type‐5 zircon is formed by the more CO₃‐rich hydrothermal alteration of type‐4 zircon, suggested by the fact that type‐4 and type‐5 zircon grains are often included in ankerite. Type‐3 to type‐5 zircon grains at the Nechalacho REE deposit were continuously formed by leaching and/or dissolution of type‐2 zircon in the presence of F‐ and/or CO₃‐rich hydrothermal fluid. These mineral associations indicate that three representative hydrothermal stages were present and related to HFSE enrichment in the Nechalacho REE deposit: (i) F‐rich hydrothermal stage caused the crystallization of REE–Nb‐rich zircon (type‐2 rim and type‐3), with abundant formation of phlogopite and fluorite; (ii) F‐ and CO₃‐rich hydrothermal stage led to the replacement of a part of REE–Nb–F‐rich zircon by REE fluorocarbonate; and (iii) CO₃‐rich hydrothermal stage resulted in crystallization of the REE–Nb–F‐poor zircon and fergusonite, with ankerite. REE and Nb in hydrothermal fluid at the Nechalacho REE deposit were finally concentrated into fergusonite by way of REE–Nb–F‐rich zircon in the hydrothermally altered units.     

Fluid Inclusions and Metallization of the Kendekeke Polymetallic Deposit in Qinghai Province,China

The Kendekeke polymetallic deposit, located in the middle part of the magmatic arc belt of Qimantag on the southwestern margin of the Qaidam Basin, is a polygenetic compound deposit in the Qimantag metallogenic belt of Qinghai Province. Multi-periodic ore-forming processes occurred in this deposit, including early-stage iron mineralization and lead-zinc-gold-polymetallic mineralization which was controlled by later hydrothermal process. The characteristics of the ore-forming fluids and mineralization were discussed by using the fluid inclusion petrography, Laser Raman Spectrum and micro-thermometry methods. Three stages, namely, S1-stage(copper-iron-sulfide stage), S2-stage(lead-zinc-sulfide stage) and C-stage(carbonate stage) were included in the hydrothermal process as indicated by the results of this study. The fluid inclusions are in three types: aqueous inclusion(type I), CO2-aqueous inclusion(type II) and pure CO2 inclusion(type III). Type I inclusions were observed in the S1-stage, having homogenization temperature at 240–320oC, and salinities ranging from 19.8% to 25.0%(wt % NaCl equiv.). All three types of inclusions, existing as immiscible inclusion assemblages, were presented in the S2-stage, with the lowest homogenization temperature ranging from 175 oC to 295oC, which represents the metallogenic temperature of the S2-stage. The salinities of these inclusions are in the range of 1.5% to 16%. The fluid inclusions in the C-stage belong to types I, II and III, having homogenization temperatures at 120–210oC, and salinities ranging from 0.9% to 14.5%. These observations indicate that the ore-forming fluids evolved from high-temperature to lowtemperature, from high-salinity to low-salinity, from homogenization to immiscible separation. Results of Laser Raman Spectroscopy show that high density of CO2 and CH4 were found as gas compositions in the inclusions. CO2, worked as the pH buffer of ore-forming fluids, together with reduction of organic gases(i.e. CH4, etc), affected the transport and sediment of the minerals. The fluid system alternated between open and close systems, namely, between lithostatic pressure and hydrostatic pressure systems. The calculated metallogenic pressures are in the range of 30 to 87 Mpa corresponding to 3 km mineralization depth. Under the influence of tectonic movements, immiscible separation occurred in the original ore-forming fluids, which were derived from the previous highsalinity, high-temperature magmatic fluids. The separation of CO2 changed the physicochemical properties and composition of the original fluids, and then diluted by mixing with extraneous fluids such as meteoric water and groundwater, and metallogenic materials in the fluids such as lead, zinc and gold were precipitated.     

Compositions of magmatic melts and evolution of mineral-forming fluids in the banska Stiavnica epithermal Au-Ag-Pb-Zn deposit, Slovakia: A study of inclusions in minerals

Melt and fluid inclusions were investigated in minerals from igneous rocks and ore (Au-Ag-Pb-Zn) veins of the Stiavnica ore field in Central Slovakia. High H₂O (7.1–12.0 wt %) and Cl (0.32–0.46 wt %) contents were found in silicate melt inclusions (65–69 wt % SiO₂ and 5.2–5.6 wt % K₂O) in plagioclase phenocrysts (An 68–36) from biotite-homblende andesites of the eastern part of the caldera. Similar high water contents are characteristic of magmatic melts (71–76 wt % SiO₂ and 3.7–5.1 wt % K₂O) forming the sanidine rhyolites of the Vyhne extrusive dome in the northwestern part of the Stiavnica caldera (up to 7.1 wt %) and the rhyolites of the Klotilda dike in the eastern part of the ore field (up to 11.5 wt %). The examination of primary inclusions in quartz and sanidine from the Vyhne rhyolites revealed high concentrations of N₂ and CO₂ in magmatic fluid (8.6 g/kg H₂O and 59 g/kg H₂O, respectively). Fluid pressure was estimated as 5.0 kbar on the basis of primary CO₂ fluid inclusions in plagioclase phenocrysts from the Kalvari basanites. This value corresponds to a depth of 18 km and may be indicative of a deep CO₂ source. Quartz from the granodiorites of the central part of the Stiavnica-Hodrusa complex crystallized from a melt with 4.2–6.1 wt % H₂O and 0.24–0.80 wt % Cl. Magmatic fluid cogenetic with this silicate melt was represented by a chloride brine with a salinity of no less than 77–80 wt % NaCl equiv. Secondary inclusions in quartz of the igneous rocks recorded a continuous trend of temperature, pressure, and solution salinity, from the parameters of magmatic fluids to the conditions of formation of ore veins. The gold mineralization of the Svyatozar vein system was formed from boiling low-salinity fluids (0.3–8.0 wt % NaCl equv.) at temperatures of 365–160°C and pressures of 160–60 bar. The Terezia, Bieber, Viliam, Spitaler, and Rozalia epithermal gold-silver-base metal veins were also formed from heterogeneous low-salinity fluids (0.3–12.1 wt %) at temperatures of 380–58°C and pressures of 240–10 bar. It was found that the salt components of the solutions were dominated by chlorides (high content of fluorine, up to 0.45 mol/kg H₂O, was also detected), and sulfate solutions appeared in the upper levels. The dissolved gas of ore-forming solutions was dominated by CO₂ (0.1–8.4 mol %, averaging 1.3 wt %) and contained minor nitrogen (0.00–0.85 mol %, averaging 0.05 mol %) and negligible methane admixtures (0.00–0.05 mol %, averaging 0.004 mol %). These data allowed us to conclude that the magmatic melts could be sources of H₂O, Cl, CO₂, and N₂. The formation of the epithermal mineralization of the Stiavnica ore field was associated with the mixing of magmatic fluid with low-concentration meteoric waters, and the fluid was in a heterogeneous state.     

Tomographic models and seismotectonics of the Reggio Emilia region, Italy

The aim of this study is to define the Vp and Vp/Vs structure of the fault zone ruptured by the M_L 5.1 earthquake of October 15, 1996 which occurred near Reggio Emilia (central-northern Italy). A 1-month-long seismic sequence followed the mainshock and occurred in a small region along the outer border of the northern Apenninic belt, at depth ranging between 10 and 17 km. P- and S-wave arrival times from 304 aftershocks recorded by two local dense seismic arrays installed in the epicentral region have been inverted to obtain one- and three-dimensional velocity models by using state of the art local earthquake tomographic techniques. Velocity models and aftershock relocation help us to infer the seismotectonic of the region. Earthquakes originated along a NW-dipping backthrust of a NE-trending main thrust, composing the western part of the broad Ferrara Arc. A main high Vp and high Vp/Vs region delineates a pop-up structure in the center of the area. The high Vp/Vs within the pop-up structure supports the presence of a zone with increased pore pressure. The hypocentral depth of both mainshock and aftershocks is greater than those usually found for the main seismogenic regions of the Apenninic belt. P-wave velocity values in the seismogenic area, obtained by tomography, are compatible with rocks of the Mesozoic cover and suggest that seismicity occurred within the Mesozoic units stack at present by compressional tectonics.     

Seismogenesis of the uninterrupted occurrence of the aftershock activity in the 2001 Bhuj earthquake zone, Gujarat, India, during 2001�C2010

Seismogenesis of aftershocks occurring in the Kachchh seismic zone for more than last 10?years is investigated through modeling of fractal dimensions, b-value, seismic velocities, stress inversion, and Coulomb failure stresses, using aftershock data of the 2001 Bhuj earthquake. Three-dimensional mapping of b-values, fractal dimensions, and seismic velocities clearly delineate an area of high b-, D-, and Vp/Vs ratio values at 15?C35?km depth below the main rupture zone (MRZ) of the 2001 mainshock, which is attributed to higher material heterogeneities in the vicinity of the MRZ or deep fluid enrichment due to the release of aqueous fluid/volatile CO₂ from the eclogitisation of the olivine-rich lower crustal rocks. We notice that several aftershocks are occurred near the contacts between high (mafic brittle rocks) and low velocity regions while many of the aftershocks including the 2001 Bhuj mainshock are occurred in the zones of low velocity (low dVp, low dVs and large Vp/Vs) in the 15?C35?km depth range, which are inferred to be the fractured rock matrixes filled with aqueous fluid or volatiles containing CO₂. Further support for this model comes from the presence of hydrous eclogitic layer at sub-lithospheric depths (34?C42?km). The depth-wise stress inversions using the P- and T-axes data of the focal mechanisms reveal an increase in heterogeneity (i.e., misfit) with an almost N?CS ??₁ orientation up to 30?km depth. Then, the misfit decreases to a minimum value in the 30?C40?km depth range, where a 60^o rotation in the ??₁ orientation is also noticed that can be explained in terms of the fluid enrichment in that particular layer. The modeling of Coulomb failure stress changes (??CFS) considering three tectonic faults [i.e., NWF, GF, and Allah bund fault (ABF)] and the slip distribution of the 2001 mainshock on NWF could successfully explain the occurrences of moderate size events (during 2006?C2008) in terms of increase in positive ??CFS on GF and ABF. In a nutshell, we propose that the fluid-filled mafic intrusives are acting as stress accentuators below the Kachchh seismic zone, which generate crustal earthquakes while the uninterrupted occurrence of aftershocks is triggered by stress transfer and aqueous fluid or volatile CO₂ flow mechanisms. Further, our results on the 3-D crustal seismic velocity structure, focal mechanisms, and b-value mapping will form key inputs for understanding wave propagation and earthquake hazard-related risk associated with the Kachchh basin.     

Three dimensional velocity structure of the Koyna-Warna region using local earthquake tomography

A dense seismic network (～100 stations) was operated in the Koyna-Warna region from January 2010 to May 2010, that allow us to collect 400 high-quality local earthquake data of magnitude less than 4. In this region, the fault structure and tectonic setting that accommodate the induced seismicity is not well understood. To investigate the seismotectonics of the region, we have inverted 7826 P- and 7047 S-P arrival times for 3-D Vp and Vp/Vs tomographic models along with hypocenters parameters in the region. Although, Dixit et al. (2014) have performed 3-D local earthquake tomography with double-difference tomography code using catalog differential time data. In this paper, Simulps14 code on the same data set is applied. For better approach P arrival time and S-P travel times are inverted directly for Vp, Vp/Vs variations and earthquake locations. High Vp ～5.9 to 6.5 and low to high Vp/Vs ～1.69-1.74 imaged in the hypocenter region. These features interpreted as a fluid bearing rock mass under high pore pressure. It is also observed that below the trap basement form a local topography depression between the Koyna and Warna Reservoirs. To the South of the Warna reservoir, intense seismic activity defines a major cluster of ～ 5 km width at 3 to7 km deep, located under the trap, where the basement is deepening. Such regions are inferred to be associated with the seismically active faults zones. The obtain velocity anomalies are reliable down to a depth of 10 km. This is also confirmed by the analysis of three resolution parameters viz. Hit count, Derivative Weight sum (DWS) and Resolution Diagonal Elements (RDE).     

Petrological model of the northern Izu–Bonin–Mariana arc crust: constraints from high-pressure measurements of elastic wave velocities of the Tanzawa plutonic rocks, central Japan

Ultrasonic compressional wave velocities (Vp) and shear wave velocities (Vs) were measured with varying pressure up to 1.0 GPa in a temperature range from 25 to 400 °C for a suite of tonalitic–gabbroic rocks of the Miocene Tanzawa plutonic complex, central Japan, which has been interpreted as uplifted and exposed deep crust of the northern Izu–Bonin–Mariana (IBM) arc. The Vp values of the tonalitic–gabbroic rocks increase rapidly at low pressures from 0.1 to 0.4 GPa, and then become nearly constant at higher pressures above 0.4 GPa. The Vp values at 1.0 GPa and 25 °C are 6.3–6.6 km/s for tonalites (56.4–71.1 wt.% SiO₂), 6.8 km/s for a quartz gabbro (53.8 wt.% SiO₂), and 7.1–7.3 km/s for a hornblende gabbro (43.2–47.7 wt.% SiO₂). Combining the present data with the P wave velocity profile of the northern IBM arc, we infer that 6-km-thick tonalitic crust exists at mid-crustal depth (6.1–6.3 km/s Vp) overlying 2-km-thick hornblende gabbroic crust (6.8 km/s Vp). Our model shows large differences in acoustic impedance between the tonalite and hornblende gabbro layers, being consistent with the strong reflector observed at 12-km-depth in the IBM arc. The measured Vp of Tanzawa hornblende-bearing gabbroic rocks (7.1–7.3 km/s) is significantly lower than that Vp modeled for the lowermost crustal layer of the northern IBM arc (7.3–7.7 km/s at 15–22 km depth). We propose that the IBM arc consists of a thick tonalitic middle crust and a mafic lower crust.     

http://www.sciencedirect.com/science/article/pii/S1674987113001369

The 3-D P- and S-wave velocity models of the upper crust beneath Southwest Iberia are determined by inverting arrival time data from local earthquakes using a seismic tomo~raphy method. We used a total of 3085 P- and 2780 S-wave high quality arrival times from 886 local earthquakes recorded by a per- manent seismic network, which is operated by the Institute of Meteorology （IM）, Lisbon, Portugal. The computed P- and S-wave velocities are used to determine the 3-D distributions of Vp/Vs ratio. The 3-D velocity and Vp/Vs ratio images display clear lateral heterogeneities in the study area. Significant veloc- ity variations up to ~6% are revealed in the upper crust beneath Southwest lberia, At 4 km depth, both P- and S-wave velocity take average to high values relative to the initial velocity model, while at 12 km, low P-wave velocities are clearly visible along the coast and in the southern parts. High S-wave velocities at 12 km depth are imaged in the central parts, and average values along the coast; although some scattered patches of low and high S-wave velocities are also revealed. The Vp/Vs rztio is generally high at depths of 4 and 12 km along the coastal parts with some regions of high Vp/Vs ratio in the north at 4 km depth, and low Vp/Vs ratio in the central southern parts at a depth of 12 km, The imaged low velocity and high Vp/Vs ratios are related to the thick saturated and unconsolidated sediments covering the region; whereas the high velocity regions are generally associated with the Mesozoic basement rocks.     

Biodegradation of CO2, CH4 and volatile organic compounds (VOCs) in soil gas from the Vicano–Cimino hydrothermal system (central Italy)

We investigated the effect of microbial activity on the chemistry of hydrothermal fluids related to the Vicano–Cimino system, central Italy. The database included the composition and δ¹³C CO₂ and δ¹³C CH₄ values for soil gas from an area characterized by intense degassing of fluids having a deep origin. The δ¹³C CH₄ values along vertical profiles in the soil indicated that CH₄ was controlled by microbial oxidation occurring at shallow (< 50 cm) depth, where free O₂ was available. This was consistent with the vertical gradients of CH₄, H₂S and O₂ concentrations. The δ¹³C CO₂ values in soil gas, characterized by a composition similar to that of the hydrothermal fluids, were not significantly influenced by biodegradation. On the contrary, gas strongly affected by air contamination showed a significant δ¹³C CO₂ fractionation. Microbial activity caused strong consumption of hydrothermal alkanes, alkenes, cyclics and hydrogenated halocarbons, whereas benzene was recalcitrant. Oxygenated compounds from hydrocarbon degradation consisted of alcohols, with minor aldehydes, ketones and carboxylic acids. A predominance of alcohols at a high rate of degassing flux, corresponding to a short residence time of hydrothermal gas within the soil, indicated incomplete oxidation. N-bearing compounds were likely produced by humic substances in the soil and/or related to contamination by pesticides, whereas α-pinene traced air entering the soil. The study demonstrates that microbial communities in the soil play an important role for mitigating the release to the atmosphere of C-bearing gases, especially CH₄, through diffuse soil degassing, a mechanism that in central Italy significantly contributes to the discharge of CO₂-rich gas from deep sources.     

河北太行山南段符山杂岩体岩浆作用深部过程及其大地构造意义

华北克拉通中生代岩石圈减薄过程中,其深部复杂的壳-幔岩浆过程及深部岩浆房系统研究薄弱,岩石圈减薄过程的浅部响应也存在较大争议。本文以华北克拉通中部的邯邢地区符山杂岩体为研究对象,通过详细的野外地质调查、岩相学观察、岩石地球化学分析、锆石年代学和矿物电子探针分析等研究多重岩浆房系统、岩浆深部作用过程和浅部响应。锆石U-Pb测年结果显示,符山早期岩套中细粒二长岩的年龄为129 Ma,晚期似斑状岩套的斑状角闪二长岩的年龄为122 Ma。岩相学观察及背散射电子(back scatter electron,BSE)图像显示,符山杂岩体的角闪石和斜长石均具有复杂的环带结构,并通过对它们的晶体生长过程分析和环带成因讨论,表明其具有复杂的生长环境和过程。符山杂岩体的高镁、高钾、高Sr 等地球化学特征和角闪石、斜长石的环带成因证明了深部岩浆在幔源流体的活化作用下发生了强烈的岩浆混合作用和多重岩浆房过程。符山杂岩体早期岩套侵入岩定位深度为7 km,晚期岩套侵入岩定位深度为1.5 km,表明在7 Ma内地壳隆升了5.5 km。符山杂岩体中大部分侵入岩具高Sr、低Y及δEu正异常等地球化学特征,表明它们可能形成于加厚陆壳的部分熔融。这些特征表明晚中生代中国东部高原的存在。     

Theoretical Calculation Model of Heat Transfer for Deep-derived Supercritical Fluids with a Case Study

Based on a set of equations established by Duan et al. (1992, 1996) for a geofluid system H2O-CO2-CH4(-N2), a formula is obtained to calculate the heat changes. Combining the geological T-P conditions (geothermal gradients and lithostatic and hydrostatic pressures), the enthalpy of some typical geofluids is figured out. Then the principles of heat transfer of deep-derived supercritical fluids are discussed. The result shows that deep-derived geofluids can bring a large amount of thermal heat and release most heat to the shallow surroundings as they move up, because the molar enthalpies vary very greatly from the deep to shallow, increasing with the increases of T and P. Generally, more than tens of kilojoules heat per molar can be released. Furthermore, the molar enthalpy is affected by the compositions of the geofluids, and the molar enthalpy of CO2, CH4, or N2 is greater than that of H2O, being twice, more than twice, and about 140% of H2O, respectively. Finally, a case study is conducted by investigat     

海拉尔盆地阿拉尔-罕达盖重磁电剖面深部结构特征及其地质意义

通过电磁场偏移成像处理技术,探索地震屏蔽层以下深部地质构造特征,揭示了海拉尔盆地深部存在似层状的电性异常,具有复式背斜的构造形态。盆地内各凹陷具有重力低、磁力高、电阻率低的重磁电特征;沉积地层为低频低幅度磁异常,岩浆岩为高频高强度的磁异常;剖面中东部电阻率存在低-高-低3层结构,岩浆岩呈高电阻率特征,古生界呈中低电阻率特征。德尔布干断裂与乌奴尔-鄂伦春断裂控制了深部古生界分布,古生界埋深为2～6 km,厚度为2～4 km;古生界与元古宇的接触界面呈复式背斜的构造形态,由3个背斜构造组成,对浅部凹陷分布有一定的控制作用。海拉尔地区晚古生代石炭纪发育泥岩、页岩、灰岩、板岩,推测盆地覆盖区可能具有一定的油气勘探前景。     

Changes in fluid geochemistry and physico-chemical conditions of geothermal systems caused by magmatic input: The recent abrupt outgassing off the island of Panarea (Aeolian Islands, Italy)

Hydrothermal systems and related vents can exhibit dramatic changes in their physico-chemical conditions over time as a response to varying activity in the feeding magmatic systems. Massive steam condensation and gas scrubbing processes of thermal fluids during their ascent and cooling cause further compositional changes that mask information regarding the conditions evolving at depth in the hydrothermal system. Here we propose a new stability diagram based on the CO₂-CH₄-CO-H₂ concentrations in vapor, which aims at calculating the temperatures and pressures in hydrothermal reservoirs. To filter gas scrubbing effects, we have also developed a model for selective dissolution of CO₂-H₂S-N₂-CH₄-He-Ne mixtures in fresh and/or air-saturated seawater.This methodology has been applied to the recent (November 2002) crisis that affected the geothermal field off the island of Panarea (Italy), where the fluid composition and fluxes have been monitored for the past two decades. The chemical and isotopic compositions of the gases suggest that the volatile elements originate from an active magma, which feeds a boiling saline solution having temperatures of up to 350°C and containing ≈12 mol% CO₂ in vapor. The thermal fluids undergo cooling and re-equilibration processes on account of gas-water-rock interactions during their ascent along fracture networks. Furthermore, steam condensation and removal of acidic species, partial dissolution in cold air-saturated seawater and stripping of atmospheric components, affect the composition of the geothermal gases at shallow levels. The observed geochemical variations are consistent with a new input of magmatic fluids that perturbed the geothermal system and caused the unrest event. The present-state evolution shows that this dramatic input of fluids is probably over, and that the system is now tending towards steady-state conditions on a time scale of months.     

Source processes of the thermal waters from the Phlegraean Fields (Naples, Italy) by means of the study of selected minor and trace elements distribution

The geochemical characteristics of hydrothermal waters from the Phlegraean Fields (P.F.) (Naples, Italy) were analysed for minor and trace elements, selectively mobilised in hydrothermal systems such as B, F, Hg, As, Pb and Tl.The water samples, collected from a shallow aquifer likely to be fed by deeper fluids, showed various geochemical features, resulting from the mixing of three components: (1) surface waters of meteoric origin; (2) hot deep waters deriving from water-rock interaction and including deep waters of marine origin; (3) magmatic fluids rising from the local magma chamber, lying a few kilometres below the town of Pozzuoli.This setting, although very complex, provides a reliable means of studying the distribution of the investigated trace elements. In particular, within the Phlegraean area, high contents of B (0.1-48 mg/l), F (0.5-8 mg/l), As (16-6050 μg/l) and Hg (0.7-232 μg/l) were observed. The levels of thallium in the springs close to Solfatara (about 7 μg/l) were in line with those normally recorded in hydrothermal areas, whereas high levels of this element (up to 23.3 μg/l) were identified in other wells of the study area. Lead (1.3 to 29.1 μg/l) appears to be anomalous with respect to its normal content in groundwater (about 1 μg/l), owing to the presence of high-density brines at depth, which enhance the solubility of Pb in volcanic rocks under hydrothermal conditions.The distribution of the investigated trace elements in the Phlegraean Fields thermal area is probably related to the different ascent pathways of the fluids. Clearly, apart from the influence exerted by anomalous thermal conditions, each element shows a different behaviour, depending on its geochemical affinity with mineral phases and as a consequence of the different enthalpy values, which determine ion partitioning in gaseous phases.Based on geochemical evidences and on the distribution of minor and trace elements, the source processes of the investigated hydrothermal waters were defined. Five main groups were identified: (1) acid sulphate waters, resulting from mixing of meteoric water with magmatic gases (mainly H₂S); (2) high sulphate-chloride waters, from a deep reservoir located in the major upflow zone; (3) waters associated with significant degassing of magmatic CO₂; (4) waters from a deep geothermal neutral chloride reservoir, resulting from heating of marine water modified by water-rock interaction processes; (5) cold waters from the inner area, influenced by low-temperature, water-rock interaction processes.     

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.     

Genesis of the Zhaxikang epithermal Pb-Zn-Sb deposit in southern Tibet,China: Evidence for a magmatic link

The Zhaxikang Pb-Zn-Sb deposit is one of the most important deposits in the Southern Tibet metallogenic belt. Based on field geology, petrography, melt- and fluid inclusions and C-H-O isotopes, we describe and discuss the mineralization, alteration, and their possible link with magmatic fluids. Our results show that the Zhaxikang deposit shares many geological and geochemical similarities with typical intermediate-sulfidation (IS) epithermal deposits. The Pb-Zn-Sb mineralization is closely related to Fe-Mn carbonate- and silicic alterations, which formed the outer rim around the greisen in the Cuonadong Dome. Orebodies occur mainly as structurally-controlled veins and breccia dikes, with major minerals include sphalerite, galena, pyrite, arsenopyrite, and Fe-Mn carbonates. Main stage ore-forming fluids were of medium temperature (214–292 °C), low salinity (2.6–5.3 wt.% NaCl eqv.) and CO₂-bearing.Melt/fluid inclusions in beryl and quartz from the pegmatite indicate that the primary magmatic fluids were derived from the melt-fluid immiscibility. The magmatic fluids were of low salinity (0.2–7.9 wt.% NaCl eqv.), high temperature (298–457 °C) and CO₂-rich, and contained minor CH₄, N₂, C₂H₆, C₃H₈ and C₆H₆. The presence of Mn-Fe carbonates and daughter gahnite minerals in the beryl-hosted inclusions indicates high Mn, Fe and Zn contents in the parental magma and related magmatic fluids. This implies a genetic link between magmatic fluids and the Pb-Zn-Sb mineralization, as also supported by Ar-Ar dating and H-O-C isotopic evidence. We suggest that the Zhaxikang is best classified as an IS epithermal deposit, and the ore-forming fluids are likely to be magma-derived. Boiling of the magmatic fluids led to high-salinity fluids and metal enrichment. High regional geothermal gradient caused by the thermal doming event may have facilitated long distance transportation of magmatic fluids, and led to the formation of a wide alteration zone and distal Pb-Zn-Sb mineralization. The temperature drop and meteoric water involvement may have precipitated the Pb-Zn-Sn minerals in the distal fault systems.     

O,H, and Sr isotope evidences of mixing processes in two geothermal fluid reservoirs at Yangbajing,Tibet, China

The Yangbajing geothermal field with the highest reservoir temperature among Chinese hydrothermal systems is located about 90 km northwest to Lhasa City, capital of Tibet, where high temperature geothermal fluids occur in two reservoirs: a shallow one at a depth of 180–280 m and a deep one at 950–1,850 m. In this study, Oxygen-18 and deuterium isotope compositions as well as ⁸⁷Sr/⁸⁶Sr ratios of water samples collected from geothermal wells, cold springs and surface water bodies were characterized to understand the genesis of geothermal fluids at Yangbajing. The results show that the deep geothermal fluid is the mixing product of both magmatic and infiltrating snow-melt water, whereas the shallow geothermal fluid is formed by the mixing of deep geothermal fluid with cold groundwater. Using a binary mixing model with deep geothermal fluid and cold groundwater as two endmembers, the mixing ratios of the latter in most shallow geothermal water samples were calculated to be between 40 and 50%. The combined use of O, H, and Sr isotopes proves to be an effective approach to depict the major sources of geothermal fluids and the mixing processes occurring in two reservoirs at Yangbajing.