Patterns of mineral transformations in clay gouge,with examples from low-angle normal fault rocks in the western USA

Neoformed minerals in shallow fault rocks are increasingly recognized as key to the behavior of faults in the elasto-frictional regime, but neither the conditions nor the processes which wall-rock is transformed into clay minerals are well understood. Yet, understanding of these mineral transformations is required to predict the mechanical and seismogenic behavior of faults. We therefore present a systematic study of clay gouge mineralogy from 30 outcrops of 17 low-angle normal faults (LANF's) in the American Cordillera to demonstrate the range and type of clay transformations in natural fault gouges. The sampled faults juxtapose a wide and representative range of wall rock types, including sedimentary, metamorphic and igneous rocks under shallow-crustal conditions. Clay mineral transformations were observed in all but one of 28 faults; one fault contains only mechanically derived clay-rich gouge, which formed entirely by cataclasis.Clay mineral transformations observed in gouges show four general patterns: 1) growth of authigenic 1M_d illite, either by transformation of fragmental 2M₁ illite or muscovite, or growth after the dissolution of K-feldspar. Illitization of fragmental illite–smectite is observed in LANF gouges, but is less common than reported from faults with sedimentary wall rocks; 2) ‘retrograde diagenesis’ of an early mechanically derived chlorite-rich gouge to authigenic chlorite–smectite and saponite (Mg-rich tri-octahedral smectite); 3) reaction of mechanically derived chlorite-rich gouges with Mg-rich fluids at low temperatures (50–150 °C) to produce localized lenses of one of two assemblages: sepiolite + saponite + talc + lizardite or palygorskite +/− chlorite +/− quartz; and 4) growth of authigenic di-octahedral smectite from alteration of acidic volcanic wall rocks. These transformation groups are consistent with patterns observed in fault rocks elsewhere. The main controls for the type of neoformed clay in gouge appear to be wall-rock chemistry and fluid chemistry, and temperatures in the range of 60–180 °C.     

Timing of brittle faulting and thermal events,Sydney region: association with the early stages of extension of East Gondwana

Structural studies in the Sydney region have revealed the presence of vertical to near-vertical, north-northeast-striking faults that are manifest as joint swarms and highly brecciated zones in which gouge of varying thickness is developed. Strike-slip movement accompanied by minor dip-slip, normal movement occurred on these faults. Timing of movement on these faults by K–Ar dating of illite and illite–smectite in fractions extracted from fault gouges, was attempted. These dates were compared with dates obtained from the host-rocks. K–Ar ages determined from the 2–10 μm to <0.1 μm fractions produced from the gouge and host-rocks, range from 159.5 ± 3.2 to 106.6 ± 2.1 Ma (n = 26). In <0.5 μm fractions extracted from the gouges that are less contaminated by detrital phases, K–Ar ages vary from 138 ± 4.4 to 106.5 ± 2.1 Ma (mean 121 Ma; n = 6) which are similar to ages obtained from host-rocks in the Sydney region. The similarity in age between the host rocks and gouge suggests that the K–Ar system has been reset. The resetting is attributed to a thermal event at ca 120 Ma related to the underplating of felsic intrusions associated with early stages of breakup of East Gondwana. Subsequent to this event, dykes of Early Eocene age (K–Ar whole-rock: 51.0 ± 1.1 Ma) exploited north-northeast-striking faults and subsequently developed brecciated margins. These observations and the fact that gouge formed before the thermal event suggests that movement took place on north-northeast-striking faults prior to 120 Ma and after 51 Ma.     

云南小湾断层泥矿物特征及其构造意义

通过显微镜观察、X射线衍射、红外光谱和化学分析等方法研究云南小湾断层泥中伊利石矿物特征,结果显示:(1)断层泥中的伊利石发育定向排列,其集合体呈扭折褶皱变形,有时呈流状构造充填在碎屑之间;(2)伊利石的X射线衍射特征为△[(002)-(001)]>8°,Ir>1,BB₁<4°,属ISII有序混层,膨胀层约占15%,晶胞参数b₀=8.993Å,1M多型结构;(3)层间阳离子2Ca+Na+K≈1,MgO含量变化1.05%-2.89%,结晶水(H₂O⁺)含量变化4.43%-5.23%。综合上述特征认为,断层泥伊利石不同于其它成因的伊利石,它是断层活动的直接产物,因此,根据它的特征可以推测断层活动机制。     

Volcanic Activity, Hydrothermal Alteration and Epithermal Gold-Silver Mineralization in the Ryuo Mine Area in the Kitami Metallogenic Province, Hokkaido, Japan

Abstract: Characterization of Neogene magmatism in the Ryuo mine area in the Kitami metallogenic province was carried out on the basis of K-Ar data for felsic–to–mafic terrestrial extrusive and intrusive volcanism from Late Miocene to Early Pliocene. The Ryuo epithermal gold-silver deposit occurs primarily in the felsic volcaniclastic rocks of the Ikutahara Formation and in Ryuo Rhyolite. The Ryuo mineralization age of 7. 7 – 8. 1 Ma coincides well with the hydrothermal alteration age (7. 7 Ma) of Ryuo Rhyolite hosting ore veins. It is concluded that the Ryuo mineralization was essentially accompanied by felsic volcanic activity during the sedimentation of the Ikutahara Formation, and was closely related both temporally and spatially to the intrusive activity of Ryuo Rhyolite. Hydrothermal alteration related to the epithermal gold-silver mineralization of the Ryuo deposit is primarily characterized by early regional and vein-related alterations, and late steam-heated alteration. Early regional alteration consists of a smectite halo (smectite+pyrite±quartz±opal–CT±mordenite°Clinoptilolite–heulandite series mineral). Early vein-related alteration is primarily marked by potassic alteration. This alteration halo can be subdivided into a K-feldspar halo (quartz+adular–ia+pyrite±illite±interstratified illite/smectite±smectite), an illite halo (quartz+illite + chlorite + pyrite ± interstratified illite/smec–tite±smectite) and an interstratified illite/smectite halo (quartz + interstratified illite/smectite+pyrite±smectite). Late steam-heated alteration characterized by kaolinite or alunite locally overprints the early K-feldspar halo. The style of the Ryuo gold-silver deposit is a low-sulfidation epithermal type. The gold–silver–bearing quartz vein precipitates during boiling of ore fluid. The origin of the ore fluid might be meteoric water. The temperature and sulfur fugacity conditions during precipitation of electrum and acanthite are estimated to be 206°– 238°C and 10^-13.5 – 10^-11.6 atm, respectively.     

Origin of Ore-forming Fluids Responsible for Gold Mineralization of the Pongkor Au-Ag Deposit, West Java, Indonesia: Evidence from Mineralogic, Fluid Inclusion Microthermometry and Stable Isotope Study of the Ciurug–Cikoret Veins

The Pongkor gold–silver mine is situated at the northeastern flank of the Bayah dome, which is a product of volcanism in the Sunda–Banda Arc. The hydrothermal alteration minerals in the Ciurug–Cikoret area are typical of those formed from acid to near‐neutral pH thermal waters. On the surface, illite/smectite mixed layer mineral (I/Sm), smectite and kaolinite, and spotting illite, I/Sm and K‐feldspar alteration occur at the top of the mineralized zone. Silicification, K‐feldspar and I/Sm zones are commonly formed in the wall rock, and gradually grade outwards into a propylitic zone. The mineralization of precious metal ore zone is constrained by fluid temperatures between 180 and 220°C, and with low salinity (<0.2 wt% NaCl equivalent) and boiling condition. The minimum depth of vein formation below the paleo‐water table is approximately 90–130 m for the hydrostatic column. Hydrogen and oxygen isotope data for quartz and calcite show relatively homogeneous fluid composition (?53 to ?68‰δD and ?5.7 to +0.3‰δ¹⁸O H₂O). There is no specific trend in the data with respect to the mineralization stages and elevation, which suggests that the ore‐forming fluids did not significantly change spatially during the vein formation. The stable isotope data indicate mixing between the hydrothermal fluids and meteoric water and interaction between the hydrothermal fluids and the host rock.     

Argillization processes at the El Berrocal analogue granitic system (Spain): mineralogy,isotopic study and implications for the performance assessment of radwaste geological disposal

The El Berrocal granite/U-bearing quartz vein (UQV) system has been studied as a natural analogue of a high-level radioactive waste repository. The main objective was to understand the geochemical behaviour of natural nuclides under different physicochemical conditions. Within this framework, the argillization processes related to fracturing and formation of the uranium–quartz vein were studied from a mineralogical and isotopic standpoint in order to establish their temperatures of formation and thus complete the geothermal history of the system. For this purpose, δ¹⁸O values were determined for pure mineral from the unaltered granite and quartz from the uranium–quartz vein, as well as for mixture samples from the hydrothermally altered granite (sericitised granite) and clayey samples from fracture fillings, including the clayey walls of the uranium–quartz vein. The isotopic signature of quartz from the uranium–quartz vein and the monophasic nature of its fluid inclusions led us to conclude that the isotopic signature of water in equilibrium with quartz was approximately in the range from −8.3‰ to −5.7‰ V-SMOV, its temperature of formation being around 85–120 °C. The δ¹⁸O values of pure sericite from the hydrothermally altered granite, calculated by means of the oxygen fraction molar method, indicate that its temperature of formation, in equilibrium with the aforementioned waters, is also in the range from 70 °C to approximately 120 °C. Clays from fracture fillings and clayey walls of the uranium–quartz vein are usually mixtures, in different proportions, of illite, approximately formed between 70 and 125 °C; two generations of kaolinite formed at approximately 90–130 °C and at around 25 °C, respectively; smectite, formed at ≤25 °C; and occasionally palygorskite, formed either between 30 and 45 °C or 19 and 32 °C, depending on the fractionation equation used. These data suggest that sericite from the hydrothermally altered granite, quartz from the uranium–quartz vein, illite and the first generation of kaolinite from the fracture fillings resulted from the same hydrothermal process affecting the El Berrocal granite in relation to fracturing. Under certain physicochemical conditions (T≈100 °C, pH≈8 and log [H₄SiO₄] between −4 and −3), illite and kaolinite can be paragenetic. As a result of weathering processes, smectite was formed from hydrothermal illite and inherited albite under alkaline weathering, while the second generation of kaolinite was formed from smectite, under acid conditions and close to the sulphide-rich uranium–quartz vein. Palygorskite is an occasional mineral formed probably either during the thermal tail of the above-described hydrothermal process or during weathering processes. In both cases, palygorskite must have formed from alkaline Si–Mg-rich solutions. Finally, these data and processes are discussed in terms of natural analogue processes, drawing some implications for the performance assessment of a deep geological radwaste repository (DGRR).     

Geological,geochemical, stable isotope,and fluid inclusion characteristics of epithermal gold mineralization,Velvet District,Nevada

Gold mineralization in the Velvet District occurs in an eastward dipping sequence of late Tertiary rhyolitic ash-flow tuffs, flows, and tuffaceous sediments in northwestern Nevada. Minor gold and silver concentrations are associated with irregular zones of brecciation, argillic alteration, and quartz veining along north-northeast trending normal faults. Reaction of mineralizing fluids with wallrock produced an argillic alteration assemblage of illite, mixed-layer clays, smectite, and kaolinite. Illite alteration and highest gold concentrations appear to be associated with zones of high water/rock ratios. Kaolinite, smectite, alunite, and opal are postulated to have formed during a steam-dominated episode of alteration.Fluid inclusion studies indicate that the quartz veins were deposited in the temperature range 230 to 280°C from fluids which had salinities equivalent to 0.2–0.8 weight percent NaCl. δ ¹⁸O of quartz veins varies from ?2.5 to $\text{+6.7 ‰}$ and indicates that the ore fluid must have been Tertiary meteroric water. Stable isotope data appear to define a zone of concentrated fluid flow and potential subsurface mineralization in the southeastern part of the district. Fluid inclusion and isotope studies can be used in combination with more standard geochemical, geophysical, and geological information to provide site-specific targets for epithermal metal concentrations.     

Mineralogy and chemical composition of the clay fraction of Neogene shales from the Surma Group in the Bengal basin,Bangladesh

Mineralogical and chemical investigations (<2μm clay separates) of shale samples from the Neogene-age Surma Group obtained from four wells (Habiganj-11, Shahbazpur-1, Titas-11, Titas-15) in the Bengal basin, Bangladesh, were carried out in order to reveal the clay mineral composition as reservoir exploration and exploitation requires a good understanding of the clay minerals. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM) and X-Ray fluorescence spectrometry (XRF). Mineralogically, the sub-surface Surma Group shales comprise predominantly quartz, plagioclase, illite, chlorite, kaolinite, with lesser amounts of K-feldspar, dolomite and smectite, and minor to trace amounts of calcite, siderite and pyrite. The chemical composition of the <2 μm clay separates also suggests an illite and chlorite-rich composition. With increasing burial depth, the Surma Group shales are enriched in illite. The gradual decreasing of the smectite clays with depth and ultimate disappearance at greater depths (≥ 3000 m) may have been responsible for the presence of the diagenetic illite. Based on the mineralogical composition it is most likely that the illite-chlorite associations together with quartz and feldspar were predominantly detrital in origin and thus reflect the presence of a rapidly-rising source terrain not subjected to intense weathering.     

Determination of volume loss and element mobility patterns associated with the development of the Copper Basin fault,Picacho State Recreation Area,SE California,USA

The fault zone architectural elements of the Copper Basin fault include a fault core, inner damage zone, and outer damage zone. Utilizing Yb as a reference frame element, significant elemental mass changes were documented across all three architectural zones, with the greatest change in the fault core. Porosity and volumetric strain both increase toward the principal slip surface reaching a maximum in the inner damage zone and then dropping significantly in the fault core. In the damage zone and unaffected wall rocks, smectite is the most prominent clay species, whereas illite dominates the fault core suggesting that temperatures may have reached ∼100–150 °C or more during the production of the fault core. A number of studies have interpreted similar mass changes and clay mineral reactions to indicate high water/rock ratios. Such interpretations imply that during rupture, permeability increased within the fault core allowing it to act as a pathway for hot, chemically reactive fluids. Then during and after rupture, CO₂ and SiO₂ rich fluids moved into the inner and outer damage zones where calcite and quartz precipitation healed the fractured and permeable rock.     

Diagenesis and Very Low‐grade Metamorphism of the Upper Permian Yangjiagou Formation in Eastern Changchun,China: Evidence from Clay Mineral Geothermobarometers

The metamorphic conditions of the Upper Permian Yangjiagou Formation in eastern Changchun, China, were evaluated based on the mineral assemblage, illite crystallinity, illite polytypism,the b dimension of illite, and the chemical composition of chlorite. The pelitic rocks in the Yangjiagou Formation are characterized by illite + kaolinite + chlorite ± mixed-layer chlorite/smectite and detrital quartz + plagioclase. Illite in the formation has a crystallinity of 0.38-0.55 and comprises mixed 2 M_1 and1 M_d polytypes, indicating a metamorphic temperature of 200℃. Based on the chemical composition of chlorite and the chlorite geothermometer, we estimated diagenetic to very low-grade metamorphic conditions with temperatures of 185℃～204℃. The b dimension of illite varies from 8.992 A to 9.005 A.We used a mathematical algorithm to extend Guidotti and Sassi's(1986) diagram relating illite b dimension with temperature and pressure, and used this diagram, together with illite crystallinity and chlorite chemical composition, to semi-quantitatively estimate the formation pressure at1.2 kbar. These reveal that the Yangjiagou Formation has experienced very low-grade metamorphism.     

Burial history determination of the Triassic succession of Central and Northern Tunisia using clay minerals

The Oued Belif 48 and Koudiat El Halfa 5 borehole samples have been analysed in order to reveal the mineralogical composition of the Triassic successions and their burial history within the geological evolution of the Tethysian southern margin. Oued Belif 48 borehole belongs to Nefza district which is a part of the “Nappe zone” (Tellian unit, north-western Tunisia). Koudiat El Halfa 5 borehole crosses the Koudiat El Halfa diapir (north–west of the north–south axis, Central Atlas). In this paper, the burial degree of evaporitic Triassic samples was determined by the “illite crystallinity” index and by the evolution of the other phyllosilicates, essentially chlorite, talc and illite/chlorite and illite/smectite mixed layers. The studied samples of the two boreholes are characterized by the presence of abundant clay minerals. The <2-μm grain-size fraction of the samples is mostly composed of illite, chlorite and smectite and may contain a slight percentage of swelling layers (illite/smectite and illite/chlorite). The illite crystallinity value measured on ethylene glycol solvated oriented mounts of the Oued Belif 48 samples oscillates globally between 1 and 2.5 characterizing the epizonal zone with a range of 300–400 °C temperatures. The measures of Koudiat El Halfa 5 samples crystallinity index show a value ranging from 2 to 4, which indicates the anchizone and early epizone burial stage (temperatures around 200 °C). These data can be explained by Miocene magmatic activities characterizing the Triassic material of Nefza district and also by burial phenomena effects.     

Clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin (Gulf of California)

The results of the study of clay mineral alterations in Upper Pleistocene sediments of the southern trough in the Guaymas Basin (Gulf of California) due to the influence of hydrothermal solutions and heat produced by sill intrusions are discussed. Core samples from DSDP Holes 477 and 477A were taken for the analysis of clay minerals. Application of the method of modeling X-ray diffraction patterns of oriented specimens of the finely dispersed particles made it possible to establish the phase composition of clay minerals, determine their structural parameters, and obtain reliable quantitative estimates of their contents in natural mixtures. The modeling data allowed us to characterize reliably the transformation of clay minerals in sediments of the hydrothermally active southern trough in the Guaymas Basin. In Upper Pleistocene sandy–clayey sediments of the southern trough, changes in the composition of clay minerals occurred under the influence of a long-living hydrothermal system. Its lower part (interval 170.0–257.5 m) with maximum temperatures (~300°C) was marked by the formation of chlorite. Terrigenous clay minerals are not preserved here. Saponite appears at a depth of 248 m in the chlorite formation zone. Higher in the sedimentary section, the interval 146–170 m is also barren of terrigenous clay minerals. Sediments of this interval yielded two newly formed clay minerals (chlorite and illite), which were formed at lower temperatures (above 180°C and below 300°C, approximately up to ~250°C), while the relatively low-temperature upper part (110–146 m) of the hydrothermal system (from ~140°C to ~180°C) includes the mixture of terrigenous and newly formed clay minerals. Terrigenous illite is preserved here. Illitization of the mixed-layer illite–smectite was subjected to illitization. The terrigenous montmorillonite disappeared, and chlorite–smectite with 5–10% of smectite layers were formed. In the upper interval (down to approximately 110 mbsf), the composition of terrigenous clay minerals remains unchanged. They are composed of the predominant mixed-layer illite–smectite and montmorillonite, the subordinate illite, mixed-layer chlorite–smectite with 5% of smectite layers, mixed-layer kaolinite–smectite with 30% of smectite layers, and kaolinite. This composition of clay minerals changed under the influence of sill intrusions into the sedimentary cover at 58–105 m in the section of Hole 477. The most significant changes are noted in the 8-m-thick member above the sill at 50–58 m. The upper part of this interval is barren of the terrigenous mixed-layer illite–smectite, which is replaced by the newly formed trioctahedral smectite (saponite). At the same time, the terrigenous dioctahedral smectite (montmorillonite) is preserved. The composition of terrigenous clay minerals remains unchanged at the top of the unit underlying the sill base.     

Characteristics and implication of clay minerals in the northern and southern parts of the Chelung-pu fault, Taiwan

In this study, we report the characteristics of clay minerals present in the Chelung-pu fault in Taiwan. In the 1999 Chi-Chi earthquake, different slip motions were recorded along the Chelung-pu fault in the northern and southern parts of the fault. The characteristics of clay minerals present in the fault zones can be attributed to the differences in motion. We analyzed the shallow drill core samples obtained from the northern and southern sites penetrating the fault. The clay minerals identified in most of the samples from both the sites are smectite, illite, and chlorite. There are illite–smectite mixed layers with a high illite content and no chlorite–smectite mixed layer. In some samples, no smectite is detected. We also examined the iron content and symmetry of iron and magnesium in the silicate and hydroxide layers in chlorite. At the northern site, the total iron content in chlorite of gouge is larger than that of the host rocks. On the other hand, at the southern site, the total iron content varies widely. It is hypothesized that the smectite consumption and differences in the characteristics of chlorite may be controlled by the differences in the lithology, fluid chemistry, fluid temperature, or fault activities (heating or breakage) between the northern and southern sites.     

Alterations of cretaceous siltstones and sandstones near basalt contacts (Nûgssuaq,Greenland)

The influence of the intrusion of basaltic dykes and sills was investigated on sandstones and siltstones of the Atane Formation (Turonian-Coniacian) from the Sarqaq area (Nûgssuaq peninsula, central West Greenland).In the unaltered rock sequence, the siltstones are dominated by kaolinite, quartz and feldspar. No cementation was observed. The sandstones which are prevalent in this formation are arkoses and lithic arkoses with quartz/feldspar ratios of about 1, with variable contents of rock fragments and with minor amounts of matrix. The matrix consists mainly of kaolinite, less frequently of illite-muscovite and smectite or interstratified illite-smectite. Cement minerals include calcite, Fe-calcite, both mainly in concretions, and subordinate Fe-oxide hydrates.The porosity of the sandstones and siltstones indicates a former maximum depth of burial of 1000 m in the Sarqaq region.Adjacent to thin dykes and sills (1–2 m) the above-described rocks are altered as follows. In sandstones albite (fibrous), quartzine, smectite, goethite were all formed at the expense of kaolinitic matrix, and aragonite cement. In siltstones, interstratified illite-smectite, illite, smectite and low-cristobalite replaced kaolinite. These minerals, especially smectite, exclude temperatures above 200°C; they were probably formed during a cooling period.Adjacent to thicker basalt intrusions—only sills, over 5 m thick, and no dykes are known from this area—the following alterations are observed. In sandstones two textural types of albite were formed in addition to: (1) fibrous albite mentioned above; (2) undulose lath-shaped albite; (3) coarse-twinned non-undulose replacement albite. Moreover, brownish luminescing undulose quartz, muscovite, chlorite, epidote, nontronite and anatase occur. In siltstones the mineral association muscovite-chlorite-pyrophyllite-albite occurs, suggesting temperatures in the range of 250–500°C. Additionally a 22–26 Å mixed-layer mineral (chlorite-muscovite?) formed. At the contacts of thick as well as thin basalt intrusions the detrital grains directly adjoining the basalt are partly fractured; potassium feldspar grains show also a chemical disintegration.The temperatures calculated by application of a cooling model are higher than those indicated by the mineral alterations observed. Convective heat transfer by pore water is suggested as an explanation.     

Characteristics and distribution of clay minerals and their effects on reservoir quality: Huagang Formation in the Xihu Sag,East China Sea Basin

Abstract

The characteristics and distribution of clay minerals and their effects on reservoir quality in the Huagang sandstones in the Xihu Sag, East China Sea Basin were studied by using X-ray diffraction, casting thin-sections, scanning electron microscopy, electron microprobe analysis, fluid inclusion analysis, constant-rate mercury injection and nuclear magnetic resonance. Clay minerals consist of kaolinite, chlorite, illite and illite–smectite mixed layer (I/S); kaolinite forms from dissolved feldspars, chlorite occurs as clay coatings that are transformed from clay precursors owing to the flocculation of suspended detrital clays or the crystallisation of pore fluids, and illite forms from the illitisation of detrital smectite, authigenic kaolinite and K-feldspars. Clay distribution is controlled by sedimentary environments, burial history and lithologies. Typical reservoirs in the western sub-sag are thin and developed in braided river facies at relatively shallow burial depths with clays dominated by kaolinite. However, typical reservoirs in the central inversion tectonic zone are thicker and developed in a braided delta front facies at deeper burial depths with clays mainly consisting of chlorite, illite and I/S. High-quality reservoirs are characterised by coarse granularity, high quartz content and low clay content with widespread development of chlorite coatings that inhibit quartz cements at low temperatures. At higher temperatures, the high-quality reservoirs develop more pores providing growth space for quartz cements and result in the coexistence of chlorite coatings and quartz cements. The high-quality reservoirs are controlled by their lithological characteristics rather than chlorite coatings. Illite and I/S clays create severe damage to reservoirs by reducing the size and connectivity of pore-throats.     

Fluid infiltration associated with seismic faulting: Examining chemical and mineralogical compositions of fault rocks from the active Chelungpu fault

In order to understand the fault zone architecture and mechanisms that caused the Chi-Chi earthquake, the Chelungpu drilling project was conducted during April 2000 through a collaborative project between Japan and Taiwan. In this study, chemical and mineralogical variations within the overall Chelungpu fault zone, including variations between less damaged host rocks, damaged zones, and fault cores caused by the Chi-Chi earthquake were examined. Slopes of TiO₂ immobile isocons were consistently > 1 for analyses comparing host rocks with rocks from damaged zones or with gouges from fault cores, indicating that volume loss occurred in damaged zones and the fault cores. These results strongly imply that pervasive fluid infiltration occurred within the fault zone. Volume loss within the damaged zone and fault core is interpreted to result from a two-stage process involving: (i) coseismic mechanical wearing and/or dissolution in the fault core, and (ii) fluid infiltration within the fault zone during postseismic and interseismic periods along cracks caused by seismic failure. Semi-quantitative XRD analysis indicates that the kaolinite content consistently increases from the less damaged host rocks to the damaged zone and gouges in each fault core. Mineralogic changes indicate that pervasive acidic fluid infiltration occurred within the fault zones and reacted with the feldspars or muscovite to form kaolinite. Enrichment of kaolinite and illite found in the fault zones of southern drilling site could play some role on the slipping behavior of the southern part of the Chelungpu fault. Greater volume loss in the fault core may have resulted from moderate permeability, combined with the very fine grain nature of pulverized material in the fault core, which enhanced chemical reactions including transformation of feldspars and muscovite to clay minerals. The study results indicate that pervasive fluid infiltration occurred and changed the mineralogical and chemical architecture of fault zones caused by the cyclic earthquakes.     

The Arinem Te‐Bearing Gold‐Silver‐Base Metal Deposit,West Java,Indonesia

The vein system in the Arinem area is a gold‐silver‐base metal deposit of Late Miocene (8.8–9.4 Ma) age located in the southwestern part of Java Island, Indonesia. The mineralization in the area is represented by the Arinem vein with a total length of about 5900 m, with a vertical extent up to 575 m, with other associated veins such as Bantarhuni and Halimun. The Arinem vein is hosted by andesitic tuff, breccia, and lava of the Oligocene–Middle Miocene Jampang Formation (23–11.6 Ma) and overlain unconformably by Pliocene–Pleistocene volcanic rocks composed of andesitic‐basaltic tuff, tuff breccia and lavas. The inferred reserve is approximately 2 million tons at 5.7 g t^?1 gold and 41.5 g t^?1 silver at a cut‐off of 4 g t^?1 Au, which equates to approximately 12.5t of Au and 91.4t of Ag. The ore mineral assemblage of the Arinem vein consists of sphalerite, galena, chalcopyrite, pyrite, marcasite, and arsenopyrite with small amounts of pyrrhotite, argentite, electrum, bornite, hessite, tetradymite, altaite, petzite, stutzite, hematite, enargite, tennantite, chalcocite, and covellite. These ore minerals occur in quartz with colloform, crustiform, comb, vuggy, massive, brecciated, bladed and calcedonic textures and sulfide veins. A pervasive quartz–illite–pyrite alteration zone encloses the quartz and sulfide veins and is associated with veinlets of quartz–calcite–pyrite. This alteration zone is enveloped by smectite–illite–kaolinite–quartz–pyrite alteration, which grades into a chlorite–smectite–kaolinite–calcite–pyrite zone. Early stage mineralization (stage I) of vuggy–massive–banded crystalline quartz‐sulfide was followed by middle stage (stage II) of banded–brecciated–massive sulfide‐quartz and then by last stage (stage III) of massive‐crystalline barren quartz. The temperature of the mineralization, estimated from fluid inclusion microthermometry in quartz ranges from 157 to 325°C, whereas the temperatures indicated by fluid inclusions from sphalerite and calcite range from 153 to 218 and 140 to 217°C, respectively. The mineralizing fluid is dilute, with a salinity <4.3 wt% NaCl equiv. The ore‐mineral assemblage and paragenesis of the Arinem vein is characteristically of a low sulfidation epithermal system with indication of high sulfidation overprinted at stage II. Boiling is probably the main control for the gold solubility and precipitation of gold occurred during cooling in stage I mineralization.     

Alteration of the Callovo–Oxfordian clay from Meuse-Haute Marne underground laboratory (France) by alkaline solution. I. A XRD and CEC study

The reaction of the clay fraction of the Callovo–Oxfordian hard shale formation hosting the French underground laboratory site, with high pH NaOH, KOH and Ca(OH)₂ solutions has been investigated through closed system experiments at 60, 90 and 120 °C over 6, 24 and 168 h. The mineralogical composition of the run samples has been determined using X-ray diffraction (XRD) of randomly oriented powders showing the formation of different species of zeolites (analcime, chabazite, phillipsite) and Ca silicates (tobermorite, katoite). The phyllosilicates were studied using XRD of oriented preparations and cation exchange capacity measurements. Detrital or diagenetic mica and chlorite in the <2 μm fraction remain unchanged. On the contrary, the smectite and random illite–smectite mixed layer minerals are strongly reactive. The expandable layers of montmorillonite type are selectively dissolved while beidellitic ones survive or are transitionally formed.     

Evidence of multi-stage faulting by clay mineral analysis: Example in a normal fault zone affecting arkosic sandstones (Annot sandstones)

Fault affecting silicoclastic sediments are commonly enriched in clay minerals. Clays are sensitive to fluid–rock interactions and deformation mechanisms; in this paper, they are used as proxy for fault activity and behavior. The present study focuses on clay mineral assemblages from the Point Vert normal fault zone located in the Annot sandstones, a Priabonian-Rupelian turbidite succession of the Alpine foredeep in SE France. In this area, the Annot sandstones were buried around 6–8 km below the front of Alpine nappes soon after their deposition and exhumed during the middle-late Miocene. The fault affects arkosic sandstone beds alternating with pelitic layers, and displays throw of about thirty meters. The fault core zone comprises intensely foliated sandstones bounding a corridor of gouge about 20 cm thick. The foliated sandstones display clay concentration along S–C structures characterized by dissolution of K-feldspar and their replacement by mica, associated with quartz pressure solution, intense microfracturation and quartz vein precipitation. The gouge is formed by a clayey matrix containing fragments of foliated sandstones and pelites. However, a detailed petrographical investigation suggests complex polyphase deformation processes. Optical and SEM observations show that the clay minerals fraction of all studied rocks (pelites and sandstones from the damage and core zones of the fault) is dominated by white micas and chlorite. These minerals have two different origins: detrital and newly-formed. Detrital micas are identified by their larger shape and their chemical composition with a lower Fe–Mg content than the newly-formed white micas. In the foliated sandstones, newly-formed white micas are concentrated along S–C structures or replace K-feldspar. Both types of newly formed micas display the same chemical composition confirmed microstructural observations suggesting that they formed in the same conditions. They have the following structural formulas: Na_0.05 K_0.86 (Al _1.77 Fe_0.08 Mg_0.15) (Si_3.22 Al_0.78) O₁₀ (OH)_2. They are enriched in Fe and Mg compared to the detrital micas. Newly-formed chlorites are associated with micas along the shear planes. According to microprobe analyses, they present the following structural formula: (Al_1,48 Fe_2,50 Mg_1,84) (Si_2,82 Al_1,18) O₁₀ (OH)₈. All these data suggest that these clay minerals are synkinematic and registered the fault activity. In the gouge samples, illite and chlorite are the major clay minerals; smectite is locally present in some samples.In the foliated sandstones, Kubler Index (KI) ((001) XRD peak width at half height) data and thermodynamic calculations from synkinematic chlorite chemistry suggest that the main fault deformation occurred under temperatures around 220 °C (diagenesis to anchizone boundary). KI measured on pelites and sandstones from the hanging and footwall, display similar values coherent with the maximal burial temperature of the Annot sandstones in this area. The gouge samples have a higher KI index, which could be explained by a reactivation of the fault at lower temperatures during the exhumation of the Annot sandstones formation.     

Epithermal Gold-Silver Mineralization of the Asachinskoe Deposit in South Kamchatka, Russia

The Asachinskoe epithermal Au‐Ag deposit is a representative low‐sulfidation type of deposit in Kamchatka, Russia. In the Asachinskoe deposit there are approximately 40 mineralized veins mainly hosted by dacite–andesite stock intrusions of Miocene–Pliocene age. The veins are emplaced in tensional cracks with a north orientation. Wall‐rock alteration at the bonanza level (170–200 m a.s.l.) consists of the mineral assemblage of quartz, pyrite, albite, illite and trace amounts of smectite. Mineralized veins are well banded with quartz, adularia and minor illite. Mineralization stages in the main zone are divided into stages I–IV. Stage I is relatively barren quartz–adularia association formed at 4.7 ± 0.2 Ma (K‐Ar age). Stage II consists of abundant illite, Cu‐bearing cryptomelane and other manganese oxides and hydroxides, electrum, argentite, quartz, adularia and minor rhodochrosite and calcite. Stage III, the main stage of gold mineralization (4.5–4.4 ± 0.1–3.1 ± 0.1 Ma, K‐Ar age), consists of a large amount of electrum, naumannite and Se‐bearing polybasite with quartz–adularia association. Stage IV is characterized by hydrothermal breccia, where electrum, tetrahedrite and secondary covellite occur with quartz, adularia and illite. The concentration of Au+Ag in ores has a positive correlation with the content of K₂O + Al₂O₃, which is controlled by the presence of adularia and minor illite, and both Hg and Au also have positive correlations with the light rare‐earth elements. Fluid inclusion studies indicate a salinity of 1.0–2.6 wt% NaCl equivalent for the whole deposit, and ore‐forming temperatures are estimated as approximately 160–190°C in stage III of the present 218 m a.s.l. and 170–180°C in stage IV of 200 m a.s.l. The depth of ore formation is estimated to be 90–400 m from the paleo‐water table for stage IV of 200 m a.s.l., if a hydrostatic condition is assumed. An increase of salinity (>C_NaCl≈ 0.2 wt%) and decrease of temperature (>T ≈ 30°C) within a 115‐m vertical interval for the ascending hydrothermal solution is calculated, which is interpreted as due to steam loss during fluid boiling. Ranges of selenium and sulfur fugacities are estimated to be logfSe2 = ?17 to ?14.5 and logfS2 = ?15 to ?12 for the ore‐forming solution that was responsible for Au‐Ag‐Se precipitation in stage III of 200 m a.s.l. Separation of Se from S‐Se complex in the solution and its partition into selenides could be due to a relatively oxidizing condition. The precipitation of Au‐Ag‐Se was caused by boiling in stage III, and the precipitation of Au‐Ag‐Cu was caused by sudden decompression and boiling in stage IV.