Tourmaline geochemistry and δ<Superscript>11</Superscript>B variations as a guide to fluid–rock interaction in the Habachtal emerald deposit,Tauern Window,Austria

Tourmalines from the Habachtal emerald deposit in the Eastern Alps formed together with emerald in a ductile shear zone during blackwall metasomatism between pelitic country rocks and a serpentinite body. Electron microprobe and secondary ion mass spectrometric (SIMS) analyses provide a record of chemical and B-isotope variations in tourmalines which represent an idealized profile from metapelites into the blackwall sequence of biotite and chlorite schists. Tourmaline is intermediate schorl-dravite in the country rock and become increasingly dravitic in the blackwall zones, while F and Cr contents increase and Al drops. Metasomatic tourmaline from blackwall zones is typically zoned optically and chemically, with rim compositions rich in Mg, Ti, Ca and F compared with the cores. The total range in δ¹¹B values is −13.8 to −5.1‰ and the within-sample variations are typically 3–5‰. Both of these ranges are beyond the reach of closed-system fractionation at the estimated 500–550°C conditions of formation, and at least two boron components with contrasting isotopic composition are indicated. A key observation from tourmaline core analyses is a systematic shift in δ¹¹B from the country rock (−14 to −10‰) to the inner blackwall zones (−9 to −5‰). We suggest that two separate fluids were channeled and partially mixed in the Habachtal shear zone during blackwall alteration and tourmaline-emerald mineralization. A regional metamorphic fluid carried isotopically light boron as observed in the metapelite country rocks. The other fluid is derived from the serpentinite association and has isotopically heavier boron typical for MORB or altered oceanic crust. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Fluid and Element Cycling in Subducted Serpentinite: a Trace-Element Study of the Erro-Tobbio High-Pressure Ultramafites (Western Alps, NW Italy)

The oceanic serpentinization of peridotites and the influenceof such an alteration on element cycling during their subductiondewatering are here investigated in a mantle slice (Erro–Tobbioperidotite), first exposed to oceanic serpentinization and laterinvolved in alpine subduction, partial dewatering and formationof a high-pressure olivine + titanian-clinohumite + diopside+ antigorite assemblage in the peridotites and in veins. Previouswork indicates that high-pressure veins include primary brines,representing a residue after crystallization of the vein assemblageand containing recycled oceanic Cl and alkalis. To reconstructthe main changes during oceanic peridotite serpentinizationand subsequent subduction, we analysed samples in profiles fromserpentinized oceanic peridotites to high-pressure serpentinites,and from high-pressure ultramafites to veins. Here we presentresults indicating that the main features of the oceanic serpentinizationare immobility of rare earth elements (REE), considerable waterincrease, local CaO decrease and uptake of trace amounts ofSr, probably as a function of the intensity of alteration. Srentered fine-grained Ca phases associated with serpentine andchlorite. Trace-element analyses of mantle clinopyroxenes andhigh-pressure diopsides (in country ultramafites and veins),highlight the close similarity in the REE compositions of thevarious clinopyroxenes, thereby indicating rock control on thevein fluids and lack of exotic components carried by externallyderived fluids. Presence of appreciable Sr contents in vein-formingdiopside indicates cycling of oceanic Sr in the high-pressurefluid. This, together with the recognition of pre-subductionCl and alkalis in the vein fluid, indicates closed-system behaviourduring eclogitization and internal cycling of exogenic components.Diopside and Ti-clinohumite are the high-pressure minerals actingas repositories for REE and Sr, and for high field strengthelements (HFSE), respectively. The aqueous fluid equilibratedwith such an assemblage is enriched in Cl and alkaline elementsbut strongly depleted in REE and HFSE (less than chondrite abundances).Sr is low [(0·2–1·6) x chondrites], althoughselectively enriched relative to light REE. KEY WORDS: eclogite facies; fluid; trace elements; serpentinite; subduction     

Mg-metasomatism of oceanic gabbros and its control on Ti-clinohumite formation during eclogitization

In the high-pressure meta-ophiolites of Western Liguria (Italy), serpentinized ultramafites host bodies of eclogite, metarodingite and Ti-clinohumite ± Ti-chondrodite-bearing rocks. The latter contain relics of augite, ilmenite and apatite, which suggest derivation from pristine Fe-Ti-rich gabbros. The composition of relict mantle clinopyroxene in the host serpentinites indicates primary depleted peridotite compositions. Compared with their inferred protoliths, the Ti-clinohumite dikelets and the host serpentinites display significant changes in their major and trace element concentrations, indicating element exchange between the two rock systems. In particular, the Fe-Ti-rich gabbros were depleted in CaO and FeO and were strongly enriched in MgO. Analogous compositional variations are shown by altered gabbros enclosed in serpentinized peridotites from the obducted ophiolite sequences of the Northern Apennine. This evidence suggests that the observed Mg-enrichment recorded by the Ti-clinohumite metagabbros occurred in oceanic environments as the result of diffusive exchange between ultramafites and gabbros in presence of fluids related to serpentinization of the ultramafic country rocks. Alteration of the gabbro and concomitant Mg-uptake mostly caused extensive chloritization of the igneous plagioclase. Survival of igneous ilmenite and augite and their reaction with the hydrothermal chlorite during high-pressure metamorphism produced the observed Ti-clinohumite and Ti-chondrodite assemblages. The data presented thus indicate that crystallization of Ti-clinohumite assemblages was facilitated by a stage of oceanic alteration leading to Mg-enrichment of original Fe-Ti-rich gabbros. We suggest that during alteration, Mg-metasomatism occurred prior to rodingitization and was related to the earlier stages of peridotite serpentinization. Survival of oceanic chemical heterogeneities in the Ti-clinohumite rocks, indicates that element mobility during high-pressure recrystallization of these rocks was on a limited scale. This allowed preservation of their pre-subduction alteration features. Received: 13 July 1998 / Accepted: 3 November 1998     

Hydrothermal alteration, fluid flow and volume change in shear zones: the layered mafic–ultramafic Kettara intrusion (Jebilet Massif, Variscan belt, Morocco)

During emplacement and cooling, the layered mafic–ultramafic Kettara intrusion (Jebilet, Morocco) underwent coeval effects of deformation and pervasive fluid infiltration at the scale of the intrusion. In the zones not affected by deformation, primary minerals (olivine, plagioclase, clinopyroxene) were partially or totally altered into Ca‐amphibole, Mg‐chlorite and CaAl‐silicates. In the zones of active deformation (centimetre‐scale shear zones), focused fluid flow transformed the metacumulates (peridotites and leucogabbros) into ultramylonites where insoluble primary minerals (ilmenite, spinel and apatite) persist in a Ca‐amphibole‐rich matrix. Mass‐balance calculations indicate that shearing was accompanied by up to 200% volume gain; the ultramylonites being enriched in Si, Ca, Mg, and Fe, and depleted in Na and K. The gains in Ca and Mg and losses in Na and K are consistent with fluid flow in the direction of increasing temperature. When the intrusion had cooled to temperatures prevailing in the country rock (lower greenschist facies), deformation was still active along the shear zones. Intense intragranular fracturing in the shear zone walls and subsequent fluid infiltration allowed shear zones to thicken to metre‐scale shear zones with time. The inner parts of the shear zones were transformed into chlorite‐rich ultramylonites. In the shear zone walls, muscovite crystallized at the expense of Ca–Al silicates, while calcite and quartz were deposited in ‘en echelon’ veins. Mass‐balance calculations indicate that formation of the chlorite‐rich shear zones was accompanied by up to 60% volume loss near the centre of the shear zones; the ultramylonites being enriched in Fe and depleted in Si, Ca, Mg, Na and K while the shear zones walls are enriched in K and depleted in Ca and Si. The alteration observed in, and adjacent to the chlorite shear zones is consistent with an upward migrating regional fluid which flows laterally into the shear zone walls. Isotopic (Sr, O) signatures inferred for the fluid indicate it was deeply equilibrated with host lithologies.     

Uniformly mantle-like δ<Superscript>18</Superscript>O in zircons from oceanic plagiogranites and gabbros

Lower ocean crust is primarily gabbroic, although 1–2% felsic igneous rocks that are referred to collectively as plagiogranites occur locally. Recent experimental evidence suggests that plagiogranite magmas can form by hydrous partial melting of gabbro triggered by seawater-derived fluids, and thus they may indicate early, high-temperature hydrothermal fluid circulation. To explore seawater–rock interaction prior to and during the genesis of plagiogranite and other late-stage magmas, oxygen-isotope ratios preserved in igneous zircon have been measured by ion microprobe. A total of 197 zircons from 43 plagiogranite, evolved gabbro, and hydrothermally altered fault rock samples have been analyzed. Samples originate primarily from drill core acquired during Ocean Drilling Program and Integrated Ocean Drilling Program operations near the Mid-Atlantic and Southwest Indian Ridges. With the exception of rare, distinctively luminescent rims, all zircons from ocean crust record remarkably uniform δ¹⁸O with an average value of 5.2 ± 0.5‰ (2SD). The average δ¹⁸O(Zrc) would be in magmatic equilibrium with unaltered MORB [δ¹⁸O(WR) ~ 5.6–5.7‰], and is consistent with the previously determined value for equilibrium with the mantle. The narrow range of measured δ¹⁸O values is predicted for zircon crystallization from variable parent melt compositions and temperatures in a closed system, and provides no indication of any interactions between altered rocks or seawater and the evolved parent melts. If plagiogranite forms by hydrous partial melting, the uniform mantle-like δ¹⁸O(Zrc) requires melting and zircon crystallization prior to significant amounts of water–rock interactions that alter the protolith δ¹⁸O. Zircons from ocean crust have been proposed as a tectonic analog for >3.9 Ga detrital zircons from the earliest (Hadean) Earth by multiple workers. However, zircons from ocean crust are readily distinguished geochemically from zircons formed in continental crustal environments. Many of the >3.9 Ga zircons have mildly elevated δ¹⁸O (6.0–7.5‰), but such values have not been identified in any zircons from the large sample suite examined here. The difference in δ¹⁸O, in combination with newly acquired lithium concentrations and published trace element data, clearly shows that the >3.9 Ga detrital zircons did not originate by processes analogous to those in modern mid-ocean ridge settings.     

The importance of talc and chlorite “hybrid” rocks for volatile recycling through subduction zones; evidence from the high-pressure subduction mélange of New Caledonia

The transfer of fluid and trace elements from the slab to the mantle wedge cannot be adequately explained by simple models of slab devolatilization. The eclogite-facies mélange belt of northern New Caledonia represents previously subducted oceanic crust and contains a significant proportion of talc and chlorite schists associated with serpentinite. These rocks host large quantities of H₂O and CO₂ and may transport volatiles to deep levels in subduction zones. The bulk-rock and stable isotope compositions of talc and chlorite schist and serpentinite indicate that the serpentinite was formed by seawater alteration of oceanic lithosphere prior to subduction, whereas the talc and chlorite schists were formed by fluid-induced metasomatism of a mélange of mafic, ultramafic and metasedimentary rocks during subduction. In subduction zones, dehydration of talc and chlorite schists should occur at sub-arc depths and at significantly higher temperatures (∼ 800°C) than other lithologies (400–650°C). Fluids released under these conditions could carry high trace-element contents and may trigger partial melting of adjacent pelitic and mafic rocks, and hence may be vital for transferring volatile and trace elements to the source regions of arc magmas. In contrast, these hybrid rocks are unlikely to undergo significant decarbonation during subduction and so may be important for recycling carbon into the deep mantle. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Magmatic and structural controls on porphyry-style Cu–Au–Mo mineralization at Kemess South,Toodoggone District of British Columbia,Canada

Kemess South is the only Cu–Au–Mo mine in the Toodoggone district and a major Cu and Au producer in British Columbia. Porphyry-style Cu–Au–Mo mineralization is mainly hosted by the tabular, SW-plunging, 199.6 ± 0.6-Ma Maple Leaf granodiorite, which intrudes tightly folded, SW-dipping, Permian Asitka Group siltstone and limestone and homogeneous Triassic Takla Group basalt. Southwest-dipping 194.0 ± 0.4-Ma Toodoggone Formation conglomerate, volcaniclastic, and epiclastic rocks overlie the granodiorite and Asitka Group rocks. Minor Cu–Au–Mo mineralization is hosted by the immediate Takla Group basalt country rock, whereas low-tonnage high-grade Cu zones occur beneath a 30-m-thick leached capping in supergene-altered granodiorite and in exotic positions in overlying Toodoggone Formation conglomerate. Granodiorite has an intrusive contact with mineralized and altered Takla Group basalt but displays a sheared contact with unmineralized and less altered Asitka Group siltstone. The North Block fault is a deposit-scale, E-striking, steeply S-dipping normal fault that juxtaposes the granodiorite/basalt ore body against unmineralized Asitka Group rocks. Younger NW- and NE-striking normal–dextral faults cut all rock types, orebodies, and the North Block fault with displacements of up to 100 m and result in the graben-and-horst-style block faulting of the stratigraphy and ore body. Both basalt and granodiorite host comparable vein sequence and alteration histories, with minor variations in hydrothermal mineral assemblages caused by differing protolith chemistry. Early potassic alteration (and associated early-stage Cu ± Au ± Mo mineralization) is partly replaced by phyllic and intermediate argillic alteration associated with main-stage Cu–Au–Mo mineralization. Two main-stage veins have Re–Os molybdenite ages of 201.3 ± 1.2 and 201.1 ± 1.2 Ma. These mineralization ages overlap the 199.6 ± 0.6-Ma U–Pb zircon crystallization age for the Maple Leaf granodiorite. Late-stage pyrite-rich stringer veins and related phyllic alteration assemblages are cut by anhydrite-rich, carbonate-rich, and chlorite veins. Fluids and metals associated with early-, main-, and late-stage veins were probably derived principally from the same deep magma chamber as the Maple Leaf granodiorite. These magmatic-derived fluids interacted with Asitka and Takla Group country rocks and possibly with meteoric and metamorphic fluids prior to mineralization.     

Localization control for chlorite breccia deformation beneath Catalina detachment fault,Rincon Mountains,Tucson, Arizona

The structural location of an approximately 3-km stretch of the Catalina detachment fault zone appears to have been controlled by an ultramylonite shear zone within mylonites of the Catalina–Rincon metamorphic core complex. The Catalina detachment fault zone consists of the detachment fault surface, a 3–5 m interval of cataclasite and ultracataclasite, up to ∼50 m of chlorite breccia, and a discrete subdetachment fault. Beneath the subdetachment fault is a km-scale thickness of mylonites. Progressive ductile-to-brittle shear-zone evolution of the fault-rock stratigraphy started with mylonitization, was followed by overprinting of mylonites by chlorite brecciation, and culminated in the formation of the Catalina detachment fault and associated ultracataclasites. The detachment fault is cospatial with and subparallel to the zone of chlorite breccia. The subdetachment fault is subparallel to the interval of chlorite brecciation and to the detachment fault. The ‘plane’ of projection of the approximately 30-m thick ultramylonite shear zone within the mountain of mylonite, when followed downdip, coincides with the base of the ‘chlorite breccia’ brittle shear zone. Ultramylonite is preserved in places in the immediate lower plate of the subdetachment fault. The position and orientation of the subdetachment fault appears to have been controlled by an ultramylonite shear zone within the lower-plate mylonites. The rheological properties and orientation of this ultramylonite shear zone favored its reactivation as the brittle sole fault of the zone of chloritic brecciation.     

Characteristic Features of REE and Pb–Zn–Ag Mineralizations in the Na Son Deposit,Northeastern Vietnam

The Na Son deposit is a small‐scale Pb–ZnPb–Zn–Ag deposit in northeast Vietnam and consists of biotite–chlorite schist, reddish altered rocks, quartz veins and syenite. The biotite–chlorite schist is intruded by syenite. Reddish altered rocks occur as an alteration halo between the biotite–allanite‐bearing quartz veins and the biotite–chlorite schist. Allanite occurs in the biotite–allanite‐bearing quartz veins and in the proximal reddish altered rocks. Rare earth element (REE) fluorocarbonate minerals occur along fractures or at rim of allanite crystals. The later horizontal aggregates of sulfide veins and veinlets cut the earlier reddish altered rocks. The earlier Pb–Zn veins consist of a large amount of galena and lesser amounts of sphalerite, pyrite and molybdenite. The later Cu veins cutting the Pb–Zn veins include chalcopyrite and lesser amounts of tetrahedrite and pyrite. The occurrences of two‐phase H₂O–CO₂ fluid inclusions in quartz from biotite–allanite‐bearing quartz veins and REE‐bearing fluorocarbonate minerals in allanite suggest the presence of CO₂ and F in the hydrothermal fluid. The oxygen isotopic ratios of the reddish altered rocks, biotite–chlorite schist, and syenite range from +13.9 to +14.9 ‰, +11.5 to +13.3 ‰, and +10.1 to +11.6 ‰, respectively. Assuming an isotopic equilibrium between quartz (+14.6 to +15.8 ‰) and biotite (+8.6 ‰) in the biotite–allanite‐bearing quartz vein, formation temperature was estimated to be 400°C. At 400°C, δ¹⁸O values of the hydrothermal fluid in equilibrium with quartz and biotite range from +10.5 to +11.7 ‰. These δ¹⁸O values are consistent with fluid that is derived from metamorphism. Assuming an isotopic equilibrium between galena (+1.5 to +1.7 ‰) and chalcopyrite (+3.4 ‰), the formation temperature was estimated to be approximately 300°C. The formation temperature of the Na Son deposit decreased with the progress of mineralization. Based on the geological data, occurrence of REE‐bearing minerals and oxygen isotopic ratios, the REE mineralization is thought to result from interaction between biotite–chlorite schist and REE‐, CO₂‐ and F‐bearing metamorphic fluid at 400°C under a rock‐dominant condition.     

Multistage melt/fluid-peridotite interactions in the refertilized lithospheric mantle beneath the North China Craton: constraints from the Li–Sr–Nd isotopic disequilibrium between minerals of peridotite xenoliths

Elemental and Li–Sr–Nd isotopic data of minerals in spinel peridotites hosted by Cenozoic basalts allow us to refine the existing models for Li isotopic fractionation in mantle peridotites and constrain the melt/fluid-peridotite interaction in the lithospheric mantle beneath the North China Craton. Highly elevated Li concentrations in cpx (up to 24 ppm) relative to coexisting opx and olivine (<4 ppm) indicate that the peridotites experienced metasomatism by mafic silicate melts and/or fluids. The mineral δ⁷Li vary greatly, with olivine (+0.7 to +5.4‰) being isotopically heavier than coexisting opx (−4.4 to −25.9‰) and cpx (−3.3 to −21.4‰) in most samples. The δ⁷Li in pyroxenes are considerably lower than the normal mantle values and show negative correlation with their Li abundances, likely due to recent Li ingress attended by diffusive fractionation of Li isotopes. Two exceptional samples have olivine δ⁷Li of −3.0 and −7.9‰, indicating the existence of low δ⁷Li domains in the mantle, which could be transient and generated by meter-scale diffusion of Li during melt/fluid-peridotite interaction. The ¹⁴³Nd/¹⁴⁴Nd (0.5123–0.5139) and ⁸⁷Sr/⁸⁶Sr (0.7018–0.7062) in the pyroxenes also show a large variation, in which the cpx are apparently lower in ⁸⁷Sr/⁸⁶Sr and slightly higher in ¹⁴³Nd/¹⁴⁴Nd than coexisting opx, implying an intermineral Sr–Nd isotopic disequilibrium. This is observed more apparently in peridotites having low ⁸⁷Sr/⁸⁶Sr and high ¹⁴³Nd/¹⁴⁴Nd ratios than in those with high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd, suggesting that a relatively recent interaction existed between an ancient metasomatized lithospheric mantle and asthenospheric melt, which transformed the refractory peridotites with highly radiogenic Sr and unradiogenic Nd isotopic compositions to the fertile lherzolites with unradiogenic Sr and radiogenic Nd isotopic compositions. Therefore, we argue that the lithospheric mantle represented by the peridotites has been heterogeneously refertilized by multistage melt/fluid-peridotite interactions.     

The La Unión Au ± Cu prospect,Camagüey District,Cuba: fluid inclusion and stable isotope evidence for ore-forming processes

The Camagüey district, Cuba, is known for its epithermal precious metal deposits in a Cretaceous volcanic arc setting. Recently, the La Unión prospect was discovered in the southern part of the district, containing gold and minor copper mineralization interpreted as porphyry type. Mineralization is hosted in a 73.0 ± 1.5 Ma calc–alkaline I-type oxidized porphyry quartz diorite intrusive within volcanic and volcaniclastic rocks of the early Cretaceous Guáimaro Formation. The porphyry is affected by propylitic alteration and crosscut by a network of quartz and carbonate veinlets and veins. Chlorite, epidote, sericite, quartz, and pyrite are the main minerals in the early veins which are cut by late carbonate and zeolite veins. Late barite pseudomorphously replaces pyrite. Gold is associated with pyrite as disseminations in the altered quartz diorite and in the veins, occurring as inclusions or filling fractures in pyrite with 4 g/t Au in bulk samples, and up to 900 ppm Au in in pyrite. Fluid inclusion and oxygen isotope data are consistent with a H₂O–NaCl–(KCl) mineralizing fluid, derived from the quartz diorite magma, and trapped at least at 425°C and 1.2 kbar. This primary fluid unmixed into two fluid phases, a hypersaline aqueous fluid and a low-salinity vapor-rich fluid. Boiling during cooling may have played an important role in metal precipitation. Pyrite δ³⁴S values for the La Unión prospect range between 0.71‰ and 1.31‰, consistent with a homogeneous magmatic sulfur source. The fluids in equilibrium with the mineralized rocks have estimated δ¹⁸O values from 8‰ to 11.8‰, calculated for a temperature range of 480–505°C. The tectonic environment of the La Unión prospect, its high gold and low copper contents, the physical–chemical characteristics of the mineralizing fluids and the isotopic signature of the alteration minerals and fluids indicate that the La Unión gold mineralization is similar to the porphyry gold type, even though the ore-related epidote–chlorite alteration can be classified as propylitic and not the classic potassic and/or phyllic alteration. The low copper contents in the prospect could be due to a mineralizing fluid previously saturated in copper, which is indicated by trapped chalcopyrite crystals in high-temperature fluid inclusions. The low-temperature paragenesis, represented by carbonate, zeolite and barite, indicates epithermal overprint. The study shows the potential for other gold porphyry-type deposits in the Cretaceous volcanoplutonic arc of Cuba.     

Geochemistry of Khor Um-Safi ophiolitic serpentinites,central Eastern desert,Egypt: Implications for neoproterozoic arc-basin system in the Arabian-Nubian shield

Serpentinites in the Eastern Desert of Egypt are the most distinctive lithological unit in the Arabian–Nubian Shield (ANS) ophiolite sequence which associated with major suture zones. Khor Um-Safi (KUS) serpentinites represent dismembered fragments of ophiolitic rocks located in the central Eastern Desert (CED) of Egypt.KUS serpentinites exhibit affinity to the typical metamorphic peridotites with harzburgitic protolith compositions. Their opaque mineral assemblage (pentlandite, heazlewoodite and magnetite) is similar to that observed in oceanic serpentinites and implies serpentinization under highly reducing conditions. They have refractory major element compositions with Al₂O₃ contents comparable to oceanic and active margin peridotites as well as Pan-African serpentinites. The Cr and TiO₂ contents reflect evolution within a supra-subduction zone (SSZ) environment. This implication is confirmed by the Al₂O₃/SiO₂ and MgO/SiO₂ ratios which akin to ANS ophiolitic peridotites in fore-arc setting. Their enrichment in compatible trace elements (Cr, Ni and Co) reveals a depleted mantle peridotite protolith.Modelling trace elements indicates that they represent the mantle residues from 15 to 20 % melting of spinel peridotite at oxygen fugacity conditions of the QFM + 1 buffer. This range of melt extraction is consistent with the typical range of SSZ peridotite. Oxygen fugacity estimation suggests evolution under more oxidizing regime similar to modern fore-arc basin system. Moreover, this implication indicates that the KUS mantle represents arc lithosphere interacted with arc melt.     

Synchronous deformation and hydrothermal activity in the shear zone hosted high-sulphidation Au-Cu deposit at Peak Hill, NSW, Australia

Altered and mineralised rocks at Peak Hill, are confined to a 300–500 m wide, north-south striking, steeply dipping, shear zone that is flanked by the Mingelo Volcanics along its western side, and Cotton Formation siltstones along its eastern side. This shear zone is defined by extensive zones of cataclasite and strongly foliated micaceous schists in marked contrast to the largely undeformed nature of the adjacent rocks. Advanced argillic assemblages (quartz-kaolinite-pyrite ± alunite ± illite) occur throughout the core of the Peak Hill deposit. Propylitic assemblages, including albite, quartz, interlayered chlorite-smectite, illite and ankerite, and a narrow discontinuous zone of argillic (quartz-illite-pyrite) alteration are developed in the Mingelo Volcanics along the western side of the deposit. Propylitic, argillic and advanced argillic assemblages are overprinted by an internally zoned phase of phyllosilicate alteration that grades inwards from a peripheral sericite-clay-chlorite assemblage, through phyllic assemblages (muscovite/illite-pyrite ± paragonite) to a pyrophyllite-pyrite ± diaspore ± andalusite altered core. Au-Cu mineralisation is hosted by barite-pyrite veins that cut the advanced argillic assemblage, but pre-date the phyllosilicate-dominated alteration. Native Au (lacking Ag), calaverite, Te-rich tennantite-tetrahedrite (goldfieldite), chalcopyrite, covellite and chalcocite occur in the barite-pyrite veins. No ore-bearing minerals were detected in any of the alteration assemblages. The total gold content of the Peak Hill deposit is currently 720 K ounces and this includes 100 K ounces of unmined reserves. Within the shear zone phyllosilicate minerals are developed in strain shadows and partly define the stretching lineation associated with dip-slip movement. The zonation within the phyllosilicate assemblages mimics the geometry of bends in the shear zone and minor internal structures. These textures indicate that the phyllosilicate alteration developed synchronous with movement on the shear zone. Earlier advanced argillic alteration and mineralisation are developed in rocks derived from both sides of the shear zone. Hydrothermal activity associated with the earlier advanced argillic alteration was therefore either synchronous with juxtaposition of these distinct rock units, or occurred during a later phase of movement on the shear zone. Cross-cutting fibrous textures in the auriferous barite-pyrite veins indicate that repeated fracturing of the advanced argillic altered rocks accompanied development of successive generations of auriferous veins. Concentrations of auriferous veins are localised in steeply plunging shoots that are oriented parallel to the stretching lineation in the shear zone. These features all indicate movement on the host shear zone accompanied each phase of hydrothermal activity in the Peak Hill deposit. The location, alteration zonation and distribution of mineralised veins within the deposit are intimately controlled by deformation on the host shear zone synchronous with hydrothermal activity. The development of high-sulphidation hydrothermal systems synchronous with deformation along brittle-ductile shear zones is a predictable consequence of intrusive activity during deformation in areas characterised by a high geothermal gradient. The close relationship between tectonism and hydrothermal activity indicates that these deposits are likely to be located in the vicinity of regional-scale shear zones. Deposits are likely to be aligned parallel to the regional-scale structural “grain” and restricted to areas of conspicuous deformation as is the case at Peak Hill (and Temora, NSW). Aluminous alteration zones concentrated in the vicinity of regional-scale structures in the Carolina Slate Belt may be a further example of this style of hydrothermal activity. Received: 30 September 1996 / Accepted: 28 August 1997     

Formation of chlorite during thrust fault reactivation. Record of fluid origin and P–T conditions in the Monte Perdido thrust fault (southern Pyrenees)

The chemical and isotopic compositions of clay minerals such as illite and chlorite are commonly used to quantify diagenetic and low-grade metamorphic conditions, an approach that is also used in the present study of the Monte Perdido thrust fault from the South Pyrenean fold-and-thrust belt. The Monte Perdido thrust fault is a shallow thrust juxtaposing upper Cretaceous–Paleocene platform carbonates and Lower Eocene marls and turbidites from the Jaca basin. The core zone of the fault, about 6 m thick, consists of intensely deformed clay-bearing rocks bounded by major shear surfaces. Illite and chlorite are the main hydrous minerals in the fault zone. Illite is oriented along cleavage planes while chlorite formed along shear veins (<50 μm in thickness). Authigenic chlorite provides essential information about the origin of fluids and their temperature. δ¹⁸O and δD values of newly formed chlorite support equilibration with sedimentary interstitial water, directly derived from the local hanging wall and footwall during deformation. Given the absence of large-scale fluid flow, the mineralization observed in the thrust faults records the P–T conditions of thrust activity. Temperatures of chlorite formation of about 240°C are obtained via two independent methods: chlorite compositional thermometers and oxygen isotope fractionation between cogenetic chlorite and quartz. Burial depth conditions of 7 km are determined for the Monte Perdido thrust reactivation, coupling calculated temperature and fluid inclusion isochores. The present study demonstrates that both isotopic and thermodynamic methods applied to clay minerals formed in thrust fault are useful to help constrain diagenetic and low-grade metamorphic conditions.     

Mineralogical and stable isotope studies of gold–arsenic mineralisation in the Sams Creek peralkaline porphyritic granite, South Island, New Zealand

At Sams Creek, a gold-bearing, peralkaline granite porphyry dyke, which has a 7 km strike length and is up to 60 m in thickness, intrudes camptonite lamprophyre dykes and lower greenschist facies metapelites and quartzites of the Late Ordovician Wangapeka formation. The lamprophyre dykes occur as thin (< 3 m) slivers along the contacts of the granite dyke. δ¹⁸O_magma values (+5 to +8‰, VSMOW) of the A-type granite suggest derivation from a primitive source, with an insignificant mature crustal contribution. Hydrothermal gold–sulphide mineralisation is confined to the granite and adjacent lamprophyre; metapelite country rocks have only weak hydrothermal alteration. Three stages of hydrothermal alteration have been identified in the granite: Stage I alteration (high fO₂) consisting of magnetite–siderite±biotite; Stage II consisting of thin quartz–pyrite veinlets; and Stage III (low fO₂) consisting of sulphides, quartz and siderite veins, and pervasive silicification. The lamprophyre is altered to an ankerite–chlorite–sericite assemblage. Stage III sulphide veins are composed of arsenopyrite + pyrite ± galena ± sphalerite ± gold ± chalcopyrite ± pyrrhotite ± rutile ± graphite. Three phases of deformation have affected the area, and the mineralised veins and the granite and lamprophyre dykes have been deformed by two phases of folding, the youngest of which is Early Cretaceous. Locally preserved early-formed fluid inclusions are either carbonic, showing two- or three-phases at room temperature (liquid CO₂-CH₄ + liquid H₂O ± CO₂ vapour) or two-phase liquid-rich aqueous inclusions, some of which contain clathrates. Salinities of the aqueous inclusions are in the range of 1.4 to 7.6 wt% NaCl equiv. Final homogenisation temperatures (Th) of the carbonic inclusions indicate minimum trapping temperatures of 320 to 355°C, which are not too different from vein formation temperatures of 340–380°C estimated from quartz–albite stable isotope thermometry. δ¹⁸O values of Stage II and III vein quartz range from +12 and +17‰ and have a bimodal distribution (+14.5 and +16‰) with Stage II vein quartz accounting for the lower values. Siderite in Stage III veins have δ¹⁸O (+12 to +16‰) and δ¹³C values (−5‰, relative to VPDB), unlike those from Wangapeka Formation metasediments (δ¹³C_{bulk carbon} values of −24 to −19‰) and underlying Arthur Marble marine carbonates (δ¹⁸O = +25‰ and δ¹³C = 0‰). Calculated δ¹⁸O_water (+8 to +11‰, at 340°C) and (−5‰) values from vein quartz and siderite are consistent with a magmatic hydrothermal source, but a metamorphic hydrothermal origin cannot be excluded. δ³⁴S values of sulphides range from +5 to +10‰ (relative to CDT) and also have a bimodal distribution (modes at +6 and +9‰, correlated with Stage II and Stage III mineralisation, respectively). The δ³⁴S values of pyrite from the Arthur Marble marine carbonates (range from +3 to +13‰) and Wangapeka Formation (range from −4 to +9.5‰) indicate that they are potential sources of sulphur for sulphides in the Sams Creek veins. Another possible source of the sulphur is the lithospheric mantle which has positive values up to +14‰. Ages of the granite, lamprophyre, alteration/mineralisation, and deformation in the region are not well constrained, which makes it difficult to identify sources of mineralisation with respect to timing. Our mineralogical and stable isotope data does not exclude a metamorphic source, but we consider that the source of the mineralisation can best be explained by a magmatic hydrothermal source. Assuming that the hydrothermal fluids were sourced from crystallisation of the Sams Creek granite or an underlying magma chamber, then the Sams Creek gold deposit appears to be a hybrid between those described as reduced granite Au–Bi deposits and alkaline intrusive-hosted Au–Mo–Cu deposits.     

Geological and structural controls on gold mineralization in the Tanami District, Northern Territory

Gold mineralization in the Tanami district is hosted within moderately northwest dipping turbiditic sedimentary and basaltic volcanic rocks of the Paleoproterozoic Mt. Charles Formation. The gold occurs within a complex sinistral wrench-fault array and associated veins and alteration haloes. The main mineralized faults have a northerly trend and dip steeply east. Subsidiary structures trend at 030° and 070° and dip towards the southeast. Paleostress calculations based on fault striation populations and geometry (strike and dip) of faults indicate that at the time of the mineralizing event, σ ₁ was sub-horizontal and SE–NW directed with σ ₂ subvertical. Structural studies indicate that the mineralization occurred after the regional folding event and synchronous with the emplacement of felsic dykes into the mine sequence. Gold veins in the Tanami district are interpreted to be part of an outer thermal aureole gold system that formed during the emplacement of granitoids in the nearby ∼1,815 to ∼1,799 Ma Frankenia and/or Coomarie domes. Economic gold mineralization occurred late in the paragenetic history of the district. Gold is hosted by quartz-carbonate veins within shear zones, and also in the surrounding sericite- quartz- pyrite ± carbonate-altered wallrocks. Gold-mineralized veins precipitated at depths of 3 to 6 km from high temperature (∼300°C), low salinity (∼5 wt% NaCl equivalent) fluids with low CO₂ contents. Barren quartz, dolomite and calcite veins that occur in pre- and post-mineralization thrust faults formed from high salinity (∼20 wt% NaCl equivalent), low temperature (∼120–150°C) basinal brines. Pyrite in the gold mineralized veins and alteration halos has lower δ ³⁴S values (6.8 to 12.5‰) than local diagenetic pyrite (17.8 to 19.2‰) or pyrite in pre-mineralization thrust faults (31.7 to 37.1‰). The mineralizing fluids are inferred to have contained a well-homogenized mixture of magmatic and sedimentary-derived sulfur. Editorial handling: D. Huston     

内蒙古三河铅锌矿床的矿化特征及构造控矿规律

以内蒙三河铅锌矿床为研究对象,通过详细的野外和井下地质调研、 勘查资料综合分析、 构造地质测量、矿石和蚀变岩的岩石学和矿物学研究等,对矿区主要的构造类型、产状特征、脉体和蚀变的类型及矿化与断裂构造的关系进行了详细的研究.研究结果表明,矿区矿体主要呈脉状-网脉状产于北西西向断裂构造中.根据矿区断裂-脉体类型-蚀变的关系可...     

Mineralogical, fluid inclusion, and stable isotope constraints on mechanisms of ore deposition at the Samgwang mine (Republic of Korea)—a mesothermal, vein-hosted gold–silver deposit

The Samgwang mine is located in the Cheongyang gold district (Cheonan Metallogenic Province) of the Republic of Korea. It consists of eight massive, gold-bearing quartz veins that filled NE- and NW-striking fractures along fault zones in Precambrian granitic gneiss of the Gyeonggi massif. Their mineralogy and paragenesis allow two separate vein-forming episodes to be recognized, temporally separated by a major faulting event. The ore minerals occur in quartz and calcite of stage I, associated with fracturing and healing of veins. Hydrothermal wall-rock alteration minerals of stage I include Fe-rich chlorite (Fe/(Fe+Mg) ratios 0.74-0.81), muscovite, illite, K-feldspar, and minor arsenopyrite, pyrite, and carbonates. Sulfide minerals deposited along with electrum during this stage include arsenopyrite, pyrite, pyrrhotite, sphalerite, marcasite, chalcopyrite, galena, argentite, pyrargyrite, and argentian tetrahedrite. Only calcite was deposited during stage II. Fluid inclusions in quartz contain three main types of C–O–H fluids: CO₂-rich, CO₂–H₂O, and aqueous inclusions. Quartz veins related to early sulfides in stage I were deposited from H₂O–NaCl–CO₂ fluids (1,500–5,000 bar, average 3,200) with T _htotal values of 200°C to 383°C and salinities less than about 7 wt.% NaCl equiv. Late sulfide deposition was related to H₂O–NaCl fluids (140–1,300 bar, average 700) with T _htotal values of 110°C to 385°C and salinities less than about 11 wt.% NaCl equiv. These fluids either evolved through immiscibility of H₂O–NaCl–CO₂ fluids as a result of a decrease in fluid pressure, or through mixing with deeply circulated meteoric waters as a result of uplift or unloading during mineralization, or both. Measured and calculated sulfur isotope compositions (δ³⁴S_H2S = 1.5 to 4.8‰) of hydrothermal fluids from the stage I quartz veins indicate that ore sulfur was derived mainly from a magmatic source. The calculated and measured oxygen and hydrogen isotope compositions (δ¹⁸O_H2O = −5.9‰ to 10.9‰, δD = −102‰ to −87‰) of the ore-forming fluids indicate that the fluids were derived from magmatic sources and evolved by mixing with local meteoric water by limited water–rock exchange and by partly degassing in uplift zones during mineralization. While most features of the Samgwang mine are consistent with classification as an orogenic gold deposit, isotopic and fluid chemistry indicate that the veins were genetically related to intrusions emplaced during the Jurassic to Cretaceous Daebo orogeny.     

河南省崤山地区金银矿床控矿构造特征与成矿模式

崤山位于华北陆块南缘,是河南省重要的有色金属成矿区。为进一步明确崤山地区控矿构造特征,分析探讨成矿就位机制,指导崤山地区中深部地质找矿工作,本文对崤山地区矿床地质特征、构造性质等要素进行了分析研究,将崤山地区控矿构造分为拆离断层控矿构造、韧性剪切带控矿构造和张扭性断裂控矿构造三类。①拆离断层沿太古界太华岩群的结晶基底与中元古界熊耳群盖层间发育,带内发育糜棱岩,崤山北部主要含矿石英脉多发育在紧靠拆离断层带下盘的太华岩群中,矿体就位于拆离剪切形成的拆离断层及其次级断裂带中;②韧性剪切带主要位于崤山中西部和北部,早期呈压扭特性,发育绿泥片岩质初糜棱岩、糜棱岩、花岗质超糜棱岩等,申家窑韧性剪切带晚期表现为张性特征,在其下盘发育有多组与其走向一致的羽列状次级断裂构造,矿体就位于韧性剪切带及其下盘羽状次级断裂带中;③张扭性断裂多发育于崤山中东部,断裂内充填有含金石英脉条带,围岩中多具绿泥石化、绿帘石化、钾化、黄铁矿化等,矿体就位于张扭性断裂带中。按照岩体、构造对成矿的作用关系,建立了崤山地区以深源岩浆为流体、以构造侵位为空间的"双控"成矿模式,指出韧性剪切带、拆离断层带中深部及其次级断裂带是寻找脉型金银矿床的有利地段,燕山期中酸性侵入岩体周缘有斑岩型铜钼矿成矿潜力。     

Hydrothermal alteration,fluid inclusions and stable isotope systematics of the Alvo 118 iron oxide–copper–gold deposit,Carajás Mineral Province (Brazil): Implications for ore genesis

The Alvo 118 iron oxide–copper–gold (IOCG) deposit (170 Mt at 1.0 wt.% Cu, 0.3 g/t Au) lies in the southern sector of the Itacaúnas Shear Belt, Carajás Mineral Province, along a WNW–ESE-striking, 60-km-long shear zone, close to the contact of the ~2.76-Ga metavolcano-sedimentary Itacaiúnas Supergroup and the basement (~3.0 Ga Xingu Complex). The Alvo 118 deposit is hosted by mafic and felsic metavolcanic rocks and crosscutting granitoid and gabbro intrusions that have been subjected to the following hydrothermal alteration sequence towards the ore zones: (1) poorly developed sodic alteration (albite and scapolite); (2) potassic alteration (biotite or K-feldspar) accompanied by magnetite formation and silicification; (3) widespread, pervasive chlorite alteration spatially associated with quartz–carbonate–sulphide infill ore breccia and vein stockworks; and (4) local post-ore quartz–sericite alteration. The ore assemblage is dominated by chalcopyrite (~60%), bornite (~10%), hematite (~20%), magnetite (10%) and subordinate chalcocite, native gold, Au–Ag tellurides, galena, cassiterite, F-rich apatite, xenotime, monazite, britholite-(Y) and a gadolinite-group mineral. Fluid inclusion studies in quartz point to a fluid regime composed of two distinct fluid types that may have probably coexisted within the timeframe of the Cu–Au mineralizing episode: a hot (>200°C) saline (32.8‰ to 40.6 wt.% NaCl eq.) solution, represented by salt-bearing aqueous inclusions, and a lower temperature (<200°C), low to intermediate salinity (<15 wt.% NaCl eq.) aqueous fluid defined by two-phase (L_H2O + V_H2O) fluid inclusions. This trend is very similar to those defined for other IOCG systems of the Carajás Mineral Province. δ ¹⁸O_H2O values in equilibrium with calcite (−1.0‰ to 7.5‰ at 277°C to 344°C) overlap the lower range for primary magmatic waters, but the more ¹⁸O-depleted values also point to the involvement of externally derived fluids, possibly of meteoric origin. Furthermore, sulphide δ ³⁴S values (5.1‰ to 6.3‰), together with available boron isotope and Cl/Br–Na/Cl data provide evidence for a significant component of residual evaporative fluids (e.g., bittern fluids generated by seawater evaporation) in this scenario that, together with magma-derived brines, would be the main sources of the highly saline fluids involved in the formation Alvo 118 IOCG deposit. The restricted high temperature sodic alteration, the pervasive overprinting of the potassic alteration minerals by chlorite proximal to the ore zones, ore breccias with open-space filling textures in brittle structures, microthermometric and stable isotope data indicate, collectively, that the Alvo 118 IOCG system developed at structurally high levels and may be considered the shallower representative of the IOCG systems of the CMP.