Hydrogeology and geochemistry in the Curuksu (Denizli) hydrothermal field, western Turkey

 Curuksu is a low temperature hydrothermal system located within the upper sector of the B. Menderes Graben. The hydrologic structure of the Curuksu hydrothermal system is largely controlled by major graben faults where it is characterized by the presence of two thermal reservoirs. One is formed by Paleozoic quartzite, schist and marble units, and the second consists of Pliocene limestone-travertine units. The thermal conditions in the Curuksu region indicate that the regional tectonics and resulting local stress field control low temperatures activity. Temperatures of 30 springs emerging in the study area range between 15 and 55  °C. These springs are classified as cold fresh, warm mineral and thermal waters. Pamukkale, Karahayıt and Honaz springs are steam condensate waters, whereas Curuksu springs are commonly steam-heated waters with respect to the major anion concentrations. The reservoir temperatures have been estimated from chemical compositions by utilizing simultaneously, geothermometers and mixing models. According to these thermometric methods, the most probable subsurface temperature is in the range of 62–90  °C. However, the mixing models suggest a temperature level of 80  °C for the parent water. The system has low total dissolved solid (TDS) of ∼1000–1500 mg/l, which indicate that these waters undergo conductive cooling within the reservoir. Received: 9 September 1999 · Accepted: 14 February 2000     

Petrogenesis of collision-related plutonics in Central Anatolia, Turkey

Central Anatolia exhibits good examples of calc-alkaline and alkaline magmatism of similar age in a collision-related tectonic setting (continent–island arc collision). In the Central Anatolia region, late Cretaceous post-collisional plutonic rocks intrude Palaeozoic–Mesozoic metamorphic rocks overthrust by Upper Cretaceous ophiolitic units to make up the Central Anatolian Crystalline Complex.

In the complex, three different intrusive rock types may be recognised based on their geochemical characteristics: (i) calc-alkaline (Behrekdag, Cefalikdag, and Celebi); (ii) subalkaline-transitional (Baranadag); and (ii) alkaline (Hamit). The calc-alkaline and subalkaline plutonic rocks are metaluminous I-type plutons ranging from monzodiorite to granite. The alkaline plutonic rocks are metaluminous to peralkaline plutons, predominantly A-type, ranging from nepheline monzosyenite to quartz syenite.

All intrusive rocks show enrichment in LILE and LREE relative to HFSE, and have high ⁸⁷Sr/⁸⁶Sr and low ¹⁴³Nd/¹⁴⁴Nd ratios. These characteristics indicate an enriched mantle source region(s) carrying a subduction component inherited from pre-collision subduction events. The tectonic discrimination diagram of Rb vs. (Y+Nb) suggests that the calc-alkaline, subalkaline, and alkaline plutonic rocks have been affected by crustal assimilation combined with fractional crystallisation processes.

The coexistence of calc-alkaline and alkaline magmatism in the Central Anatolian Crystalline Complex may be attributed to mantle source heterogeneity before collision. The former carries a smaller intraplate component and pre-subduction enrichment compared to the latter. Either thermal perturbation of the metasomatised lithosphere by delamination of the thermal boundary layer (TBL), or removal of a subducted plate (slab breakoff) is the likely mechanism for the initiation of the post-collisional magmatism in the Complex.     

Low temperature alteration of magmatic Ni-Cu-PGE sulfides as a source for hydrothermal Ni and PGE ores: A quantitative approach using automated mineralogy

Magmatic Ni-Cu-PGE sulfide assemblages are almost ubiquitously comprised of pyrrhotite-pentlandite-chalcopyrite(-pyrite). Sulfide alteration is common during syn- or post-magmatic fluid interaction, usually replacing sulfides with amphiboles or serpentine. However, some are altered to a low temperature (<200 °C) hydrothermal assemblage of pyrite-millerite-chalcopyrite (PMC). An example is the Ni-Cu-PGE mineralisation in the Grasvally-Norite-Pyroxenite-Anorthosite (GNPA) Member, northern Bushveld Complex, which displays a continuum of mineralogical styles formed through progressive alteration: Style 1 primary pyrrhotite-pentlandite-chalcopyrite; which is altered to Style 2 pyrrhotite-pyrite-pentlandite-chalcopyrite; Style 3 pyrite-pentlandite-chalcopyrite; Style 4 pyrite-pentlandite-millerite-chalcopyrite; and Style 5 pyrite-millerite-chalcopyrite-cubanite. Modelling using CHILLER confirms this mineralogical sequence is thermodynamically possible at ∼200 °C. Quantitative characterisation using automated Energy-Dispersive X-ray spectroscopy mapping alongside in situ laser ablation analyses determined mineral proportions, major and trace element concentrations and deportments in each style. The early loss of pyrrhotite removes over half of the bulk Fe and S during the initial stages of PMC alteration, increasing Cu, Ni and PGE tenors of the remaining sulfides significantly. As water–rock interaction progresses, pyrrhotite is replaced by pyrite and pentlandite by millerite, with concurrent losses in Fe, S and Ni. Copper is lost throughout the alteration, and is most pronounced in the more advanced stages. The fluids responsible were most likely acidic and oxidised, with metals mobilised as chloride complexes. Using Rh as an immobile normalising element, the overall mass loss in the most altered samples is calculated to be up to 90%, consistent with textural relationships that indicate 40–90% volume loss from Styles 2–5, with sulfides replaced by secondary silicates, including phlogopite, quartz, chlorite, pyroxenes and minor amphiboles. Magnetite is not a significant alteration product and thus Fe is mobilised, or incorporated into silicates. Most trace elements present in the magmatic sulfide (the IPGE, Rh and Bi) remain in the sulfide phases, and are effectively transferred to pyrite during PMC alteration, except Pd, which remains in pentlandite, and is liberated from the sulfide assemblage when pentlandite disappears. Selenium tenors increase slightly with alteration, demonstrating that alteration decreases S/Se ratios. The significant mobilisation of Ni, Cu and Pd during PMC alteration produces fluids enriched in these elements that may represent a metal source for a number of enigmatic hydrothermal Ni deposits such as Avebury, Enterprise and Talvivaara, whose metal sources remain speculative. The PMC alteration of the GNPA Member may be specifically a source for the nearby Waterberg hydrothermal Pt deposit. Furthermore, this study has implications not only for magmatic ore deposits, but also for the general implications of sulfide transformation and metal transfer in ore systems in general.     

Ore petrology,hydrothermal alteration,fluid inclusions,and sulfur stable isotopes of the Milin Kamak intermediate sulfidation epithermal Au-Ag deposit in Western Srednogorie,Bulgaria

The Milin Kamak gold-silver deposit is located in Western Srednogorie zone, 50 km west of Sofia, Bulgaria. This zone belongs to the Late Cretaceous Apuseni-Banat-Timok-Srednogorie magmatic and metallogenic belt. The deposit is hosted by altered trachybasalt to andesitic trachybasalt volcanic and volcanoclastic rocks with Upper Cretaceous age, which are considered to be products of the Breznik paleovolcano. Milin Kamak is the first gold-silver intermediate sulfidation type epithermal deposit recognized in Srednogorie zone in Bulgaria. It consists of eight ore zones with lengths ranging from 400 to 1000 m, widths from several cm to 3–4 m, rarely to 10–15 m, an average of 80–90 m depth (a maximum of 200 m) and dip steeply to the south. The average content of gold is 5.04 g/t and silver – 13.01 g/t. The styles of alteration are propylitic, sericite, argillic, and advanced argillic. Ore mineralization consists of three stages. Quartz-pyrite stage I is dominated by quartz, euhedral to subhedral pyrite, trace pyrrhotite and hematite in the upper levels of the deposit. Quartz-polymetallic stage II is represented by major anhedral pyrite, galena, Fe-poor sphalerite; minor chalcopyrite, tennantite, bournonite, tellurides and electrum; and trace pyrrhotite, arsenopyrite, marcasite. Gangue minerals are quartz and carbonates. The carbonate-gold stage III is defined by deposition of carbonate minerals and barite with native gold and stibnite.Fluid inclusions in quartz are liquid H₂O-rich with homogenization temperature (T_h) ranging from 238 to 345 °C as the majority of the measurements are in the range 238–273 °C. Ice-melting temperatures (T_m) range from −2.2 to −4.1 °C, salinity – from 3.7 to 6.6 wt.% NaCl equiv. These measurements imply an epithermal environment and low- to moderate salinity of the ore-forming fluids.δ³⁴S values of pyrite range from −0.49 to +2.44‰. The average calculated δ³⁴S values are 1.35‰. The total range of δ³⁴S values for pyrite are close to zero suggesting a magmatic source for the sulfur.     

A new approximation in determination of zonation boundaries of ignimbrite by ground penetrating radar: Kayseri,Central Anatolia,Turkey

Ground penetrating radar (GPR) method is used as a tool to identify the zonation boundaries in ignimbrite series through their columnar section. Ignimbrites can be classified in terms of welding degree, colour, texture and mineralogical compositions. The research area comprises a part of İncesu (Kayseri) ignimbrite at Central Anatolia, Turkey. This ignimbrite is divided into three levels and each level has clear differences in terms of macroscopic and microscopic views. This paper presents the results of an application of GPR for the determination of zonation boundary within the ignimbrite flow unit in the view of their textural and petrological features. RAMAC CU II equipment was used with 250 MHz shielded antenna on parallel ten profiles to observe the physical difference among the ignimbrite levels of the study area. Two levels out of three have been defined at the İncesu ignimbrite and supported by field geology and petrographical studies. The first level, which is extremely fractured structure, is about 1.5 m thick and matches with middle level of the İncesu ignimbrite. The second level has an average 50–75 cm thickness and matches with lower level of the ignimbrite. In this manner, vertical lithological variations should be taken into consideration during petrological investigation of the ignimbrites.     

Determination of the origin of the Helvadere drinking springs by means of hydrochemical and isotopic techniques, Aksaray, Central Anatolia, Turkey

The main aquifer of the Helvadere springs that emerges on the strike-slip of the Hasanda?? fault set alongside the Tuzgölü (salt lake) fault zone, and trends in a NW–SE direction of Aksaray city, in the western part of Central Anatolia, is the exposed rocks of Hasanda?? which are volcanics that have distinct hydrogeological properties. The meteoric origin of the spring waters is deduced from hydrochemical and environmental isotope (¹⁸O, ²H, ³H) studies. The springs have high discharge (Q>100?l/s) and low ion concentrations because of fast circulation along the groundwater flow path in the aquifer. Furthermore, because it has Ca-Na-Mg-HCO₃ hydrochemical facies, it conforms to high standards of drinking and irrigation water.     

Nonsulfide and sulfide-rich zinc mineralizations in the Vazante, Ambrósia and Fagundes deposits, Minas Gerais, Brazil: Mass balance and stable isotope characteristics of the hydrothermal alterations

The Vazante Group hosts the Vazante nonsulfide zinc deposit, which comprises high-grade zinc silicate ore (ZnSiO₄), and late-diagenetic to epigenetic carbonate-hosted sulfide-rich zinc deposits (e.g. Morro Agudo, Fagundes, and Ambrósia). In the sulfide-rich deposits, hydrothermal alteration involving silicification and dolomitization was related with ground preparation of favorable zones for fluid migration (e.g. Fagundes) or with direct interaction with the metalliferous fluid (e.g. Ambrósia). At Vazante, hydrothermal alteration resulted in silicification and dolomite, siderite, jasper, hematite, and chlorite formation. These processes were accompanied by strong relative gains of SiO₂, Fe₂O_3(T), Rb, Sb, V, U, and La, which are typically associated with the nonsulfide zinc mineralization. All sulfide-rich zinc ores in the district display a similar geochemical signature suggesting a common metal source from the underlying sedimentary sequences.Oxygen and carbon isotope compositions of hydrothermally altered rocks reveal a remarkable alteration halo at the Vazante deposit, which is not a notable feature in the sulfide-rich deposits. This pattern could be attributed to fluid mixing processes involving the metalliferous fluid and channelized meteoric water, which may control the precipitation of the Vazante nonsulfide ore. Sulfide deposition resulted from fluid–rock interaction processes and mixing between the ascending metalliferous fluids and sulfur-rich tectonic brines derived from reduced shale units.     

Role of fluid mixing and wallrock sulfidation in gold mineralization at the Semna mine area, central Eastern Desert of Egypt: Evidence from hydrothermal alteration, fluid inclusions and stable isotope data

The Semna gold deposit is one of several vein-type gold occurrences in the central Eastern Desert of Egypt, where gold-bearing quartz veins are confined to shear zones close to the boundaries of small granitoid stocks. The Semna gold deposit is related to a series of sub-parallel quartz veins along steeply dipping WNW-trending shear zones, which cut through tectonized metagabbro and granodiorite rocks. The orebodies exhibit a complex structure of massive and brecciated quartz consistent with a change of the paleostress field from tensional to simple shear regimes along the pre-existing fault segments. Textural, structural and mineralogical evidence, including open space structures, quartz stockwork and alteration assemblages, constrain on vein development during an active fault system. The ore mineral assemblage includes pyrite, chalcopyrite, subordinate arsenopyrite, galena, sphalerite and gold. Hydrothermal chlorite, carbonate, pyrite, chalcopyrite and kaolinite are dominant in the altered metaggabro; whereas, quartz, sericite, pyrite, kaolinite and alunite characterize the granodiorite rocks in the alteration zones. Mixtures of alunite, vuggy silica and disseminated sulfides occupy the interstitial open spaces, common at fracture intersections. Partial recrystallization has rendered the brecciation and open space textures suggesting that the auriferous quartz veins were formed at moderately shallow depths in the transition zone between mesothermal and epithermal veins.Petrographic and microthermometric studies aided recognition of CO₂-rich, H₂O-rich and mixed H₂O–CO₂ fluid inclusions in the gold-bearing quartz veins. The H₂O–CO₂ inclusions are dominant over the other two types and are characterized by variable vapor: liquid ratios. These inclusions are interpreted as products of partial mixing of two immiscible carbonic and aqueous fluids. The generally light δ³⁴S of pyrite and chalcopyrite may suggest a magmatic source of sulfur. Spread in the final homogenization temperatures and bulk inclusion densities are likely due to trapping under pressure fluctuation through repeated fracture opening and sealing. Conditions of gold deposition are estimated on basis of the fluid inclusions and sulfur isotope data as 226–267 °C and 350–1100 bar, under conditions transitional between mesothermal and epithermal systems.The Semna gold deposit can be attributed to interplay of protracted volcanic activity (Dokhan Volcanics?), fluid mixing, wallrock sulfidation and a structural setting favoring gold deposition. Gold was transported as Au-bisulfide complexes under weak acid conditions concomitant with quartz–sericite–pyrite alteration, and precipitated through a decrease in gold solubility due to fluid cooling, mixing with meteoric waters and variations in pH and fO₂.     

Geochemical signature of orogenic hydrothermal activity in an active tectonic intersection zone,Alpine Fault,New Zealand

A highly faulted and fractured rock mass has developed at the intersection of the Alpine and Hope faults, two major active faults in the South Island, New Zealand. The Alpine Fault is an oblique dextral reverse fault at the late Cenozoic-Recent Pacific-Australian plate boundary. The Hope Fault is a strike-slip fault parallel to the plate convergence vector. Hydrothermal fluids driven by the active tectonic processes have passed through the fractured rock mass, causing localised rock alteration and vein formation. Mylonites in the Alpine Fault zone are crosscut by cm-scale veins of quartz and/or ankerite with minor sulphides, with cemented breccias in dilational jogs. Breccia clasts and immediate (cm-scale) host rocks have been variably impregnated with carbonates and quartz. This generation of veins, breccias and altered rocks is post-dated by cataclasite and fault gouge zones which have been cemented by calcite, illite, smectite and chamosite. Ankerite and calcite have ¹⁸O between +10 and +30, and ¹³C between 0 and –8. These minerals are inferred to have formed from water with variable components of both meteoric and crustally exchanged fluid. Rock alteration associated with ankerite–quartz veins has added arsenic (up to 200 ppm As), strontium, and some Y to the rocks. Host-rock mylonites (<2 ppm As) have been depleted in arsenic compared to their precursors (5–15 ppm As). This depletion of arsenic in the middle crust provides the source for arsenic in shallower-level vein systems.Editorial handling: N. White     

Variations in composition and abundance of white mica in the hydrothermal alteration system at Hellyer,Tasmania, as revealed by infrared reflectance spectroscopy

Short-wave infrared (SWIR) spectral reflectance of hydrothermally altered volcanic rocks in the footwall of the Hellyer massive sulfide deposit was measured with a portable PIMA-II infrared spectrometer. The Al–OH band was used to derive information on the octahedral Al content and the abundance of white mica (sericite) in the hydrothermal alteration and mineralization system. The range of the Al–OH band wavelength from 2192 nm to 2222 nm corresponds to the number of octahedral Al (Al^vi) in white mica approximately from 3.9 to 3.0 (based on 4 octahedral cations per formula). This Al^vi range represents a significant compositional variation, covering most of the compositional region between muscovite (Al^vi = 4.0) and phengite (Al^vi = 3.0). Furthermore, the spectral reflectance data show that the compositional variation of white mica is spatially related to hydrothermal alteration zoning, such that phengitic white mica tends to occur in 1) main upflow fluid channel, 2) intensely altered volcanic rocks, and 3) Pb–Zn mineralization, whereas muscovitic white mica was formed preferentially distal to massive sulfide mineralization on the margin of the footwall alteration system. The results suggest that the Al–OH band wavelength, and therefore the octahedral Al content, of white mica can be used as vectors to mineralization to map the hydrothermal system at Hellyer.     

The mechanism of cation and oxygen isotope exchange in alkali feldspars under hydrothermal conditions

The mechanism of re-equilibration of albite in a hydrothermal fluid has been investigated experimentally using natural albite crystals in an aqueous KCl solution enriched in ¹⁸O at 600°C and 2 kbars pressure. The reaction is pseudomorphic and produces a rim of K-feldspar with a sharp interface on a nanoscale which moves into the parent albite with increasing reaction time. Transmission electron microscopy (TEM) diffraction contrast and X-ray powder diffraction (XRD) show that the K-feldspar has a very high defect concentration and a disordered Al, Si distribution, compared to the parent albite. Raman spectroscopy shows a frequency shift of the Si-O-Si bending vibration from ~476 cm⁻¹ in K-feldspar formed in normal ¹⁶O aqueous solution to ~457 cm⁻¹ in the K-feldspar formed in ¹⁸O-enriched solution, reflecting a mass-related frequency shift due to a high enrichment of ¹⁸O in the K-feldspar silicate framework. Raman mapping of the spatial distribution of the frequency shift, and hence ¹⁸O content, compared with major element distribution maps, show a 1:1 correspondence between the reaction rim formed by the replacement of albite by K-feldspar, and the oxygen isotope re-equilibration. The textural and chemical characteristics as well as the kinetics of the replacement of albite by K-feldspar are consistent with an interface-coupled dissolution-reprecipitation mechanism.     

Effect of temperature on the dissolution and thermal alteration of combined amino acids fixed in natural sediment under simulated hydrothermal conditions

Seafloor sediment containing biogenic amino acids was heated with NaCl solutions at 50–200 °C for 240 h to investigate the dissolution process of amino acids and evaluate their stabilities under hydrothermal conditions. Dissolved amino acids in the combined phase (dissolved combined amino acids, DCAAs) and free phase (dissolved free amino acids, DFAAs) were rapidly released into the solution during heating. The amount of DCAAs in the solutions was 4–9 times higher than the amount of DFAAs at each temperature. When heated at ⩽ 100 °C, most of the total dissolved hydrolyzable amino acids (TDHAAs) were in the combined form (DCAAs/TDHAAs ratios > 0.9). The compositions of the DCAAs in solutions heated at ⩽ 100 °C were similar to that of the total hydrolyzable amino acids (THAAs) of the initial sediment, indicating that the DCAAs, which are derived from organisms and biodebris in the sediment, are barely altered during the hydrothermal reaction at these temperatures. On the other hand, the DCAAs/TDHAAs ratios were 0.72 and 0.57 at 150 and 200 °C, respectively, and the compositions of the DCAAs at 150 and 200 °C were significantly different from that of the initial THAAs. In addition, non-protein amino acids (β-alanine and γ-aminobutyric acid), which are sensitive biochemical indicators of the diagenetic alteration of natural organic matter, drastically increased to 80.9% of the DCAAs after heating at 200 °C. These results suggests that DCAAs are thermally unstable in the hydrothermal solutions at ⩾ 150 °C. These DCAA would be transformed into thermally stable geo-polymers such as humic-like substances and hydrolyzable kerogens.     

Use of micro-XRF chemical analysis for mapping volcanogenic massive sulfide related hydrothermal alteration: Application to the subaqueous felsic dome-flow complex of the Cap d'Ours section,Glenwood rhyolite,Rouyn-Noranda,Québec,Canada

A new analytical method using micro-X-ray fluorescence (XRF) is presented for the in situ analysis of major elements in rock samples. This approach has allowed for a separate study of hydrothermal alteration of matrix versus fragments in volcaniclastic material (i.e. flow breccia). This is particularly important for volcanogenic massive sulfide (VMS) exploration in subaqueous felsic dome-flow complexes, where brecciated facies are omnipresent and the imprint of hydrothermal alteration is typically heterogeneous. In this study, eleven elements are measured with a 1.7 by 1.3 mm window considered to be representative of each sample, based on replicate analyses. An average is calculated for the analyzed window and yields a nearly complete analysis with the exception of loss of ignition (LOI). Micro-XRF data were validated using whole rock XRF analyses performed on the same sample block. The application of this chemical method has been tested successfully on thin sections from the Cap d'Ours section of the Glenwood rhyolite in the Rouyn-Noranda region of Québec, Canada. With 58 samples spaced at approximately 50 m intervals, two styles of alteration zoning were recognized: (1) a lateral and concordant zoning expressed by vent-proximal silicification in the west grading toward vent-distal chlorite–sericite alteration to the east, and (2) vertical and discordant zoning expressed by stronger sericitization in the upper part of later volcanic quartz- and feldspar-phyric endogenous lobes. The former is typical of cooling induced by seawater interaction at the lava–water interface at temperatures greater than 400 °C, whereas the latter is related to lower temperature (< 300 °C) hydrothermal mineralization associated with endogenous lobe emplacement within the volcanic pile. The presented results clearly demonstrate the potential use of the micro-XRF data for characterizing weak to intense hydrothermal alteration in highly fragmented volcanic rocks.     

Formation and emplacement ages of the SSZ‐type Neotethyan ophiolites in Central Anatolia,Turkey: palaeotectonic implications

Isolated outcrops of ophiolitic rocks, termed the Central Anatolian Ophiolites, are found as allochthonous bodies in the Central Anatolian Crystalline Complex, that represent the metamorphosed passive northern edge of the Tauride–Anatolide Platform, central Turkey. In terms of pseudostratigraphic relationships of the magmatic units and their chemical designation, the Central Anatolian Ophiolites exhibit a supra‐subduction zone (fore‐arc) setting within the Vardar–İzmir–Ankara–Erzincan segment of the Neotethys. The epi‐ophiolitic sedimentary cover of the Central Anatolian Ophiolites is generally characterized by epiclastic volcanogenic deep‐sea sediments and debris flows intercalated with pelagic units. The richest and most significant planktonic foraminiferal association recorded from the lowest pelagic members infer a formation age of early–middle Turonian to early Santonian. K/Ar ages of post‐collisional granitoids (81–65 Ma) intruding the basement rocks as well as the Central Anatolian Ophiolites suggest a post‐early Santonian to pre‐middle Campanian emplacement age. The marked high volume of epiclastic volcanogenic sediments intercalated with the pelagics of the Central Anatolian Ophiolite is suggestive of rifting in a marginal sea adjacent to a volcanic arc. Penecontemporaneous tectonism is reflected in repetitions in the stratigraphy and in debris flows, which result from major slides and mass‐gravity reworking of pre‐existing units and of arc‐derived volcanics and sediments. Correlating the rock units and formation/obduction ages of the Central Anatolian Ophiolites with further supra‐subduction zone type ophiolites in the eastern (Turkey) and western (Greece) parts of the Vardar–İzmir–Ankara–Erzincan segment of Neotethys we conclude that the intraoceanic subduction in the east is definitely younger and the closure history of this segment is more complex than previously suggested. Copyright © 2000 John Wiley & Sons, Ltd.     

Hydrogeochemical and Isotopic Study of Groundwater in a Semi-arid Region: Yeniceoba Plain (Cihanbeyli-KONYA), Central Anatolia,Turkey

Groundwater is the most important source of water supply in the Yeniceoba Plain in Central Anatolia,Turkey.An understanding of the geochemical evolution of groundwater is important for the sustainable development of water resources in this region.A hydrogeochemical investigation was conducted in the Plio-Quaternary aquifer system using stable isotopes(δ~(18)O andδD),tritium(~3H),major and minor elements(Ca,Na,K,Mg,Cl,SO_4,NO_3,HCO_3 and Br)in order to identify groundwater chemistry patterns and the processes affecting groundwater mineralization in this system.The chemical data reveal that the chemical composition of groundwater in this aquifer system is mainly controlled by rock/water interactions including dissolution of evaporitic minerals,weathering of silicates,precipitation/dissolution of carbonates,ion exchange,and evaporation.Based on the values of Cl/Br ratio(300 mg/l)in the Plio-Quaternary groundwater,dissolution of evaporitic minerals in aquifer contributes significantly to the high mineralization.The stable isotope analyses indicate that the groundwater in the system was influenced by evaporation of rainfall during infiltration.Low tritium values(generally1 tritium units)of groundwater reflect a minor contribution of recent recharge and groundwater residence times of more than three or four decades.     

Textural,mineralogical and stable isotope studies of hydrothermal alteration in the main sulfide zone of the Great Dyke,Zimbabwe and the precious metals zone of the Sonju Lake Intrusion,Minnesota, USA

Stratigraphic offsets in the peak concentrations of platinum-group elements (PGE) and base-metal sulfides in the main sulfide zone of the Great Dyke and the precious metals zone of the Sonju Lake Intrusion have, in part, been attributed to the interaction between magmatic PGE-bearing base-metal sulfide assemblages and hydrothermal fluids. In this paper, we provide mineralogical and textural evidence that indicates alteration of base-metal sulfides and mobilization of metals and S during hydrothermal alteration in both mineralized intrusions. Stable isotopic data suggest that the fluids involved in the alteration were of magmatic origin in the Great Dyke but that a meteoric water component was involved in the alteration of the Sonju Lake Intrusion. The strong spatial association of platinum-group minerals, principally Pt and Pd sulfides, arsenides, and tellurides, with base-metal sulfide assemblages in the main sulfide zone of the Great Dyke is consistent with residual enrichment of Pt and Pd during hydrothermal alteration. However, such an interpretation is more tenuous for the precious metals zone of the Sonju Lake Intrusion where important Pt and Pd arsenides and antimonides occur as inclusions within individual plagioclase crystals and within alteration assemblages that are free of base-metal sulfides. Our observations suggest that Pt and Pd tellurides, antimonides, and arsenides may form during both magmatic crystallization and subsolidus hydrothermal alteration. Experimental studies of magmatic crystallization and hydrothermal transport/deposition in systems involving arsenides, tellurides, antimonides, and base metal sulfides are needed to better understand the relative importance of magmatic and hydrothermal processes in controlling the distribution of PGE in mineralized layered intrusions of this type.     

新疆阿克陶县苏巴什一带磁铁矿地质特征及成因浅析

新疆阿克陶县苏巴什一带具有优越的成矿地质条件,带内相继发现了多个铁矿床,并具有一定的空间连续性。本文通过总结对比带内不同铁矿床的地质特征、赋矿地层、构造变质变形等特征,并以带内典型的磁铁矿床为例,深入分析矿体地质特征、矿体形态、矿物组合及矿石结构构造特征,认为该地区的磁铁矿具有相似的矿床成因及成矿演化史,经历了原始沉积期、区域变质改造期和热液叠加改造期3个阶段,属于沉积变质型磁铁矿。通过物探磁测,明确了区内磁异常主要由磁铁矿（化）引起,并总结了带内磁铁矿找矿标志,为该区铁矿进一步勘探调查指明方向。     

Role of fluid mixing and wallrock sulfidation in gold mineralization at the Semna mine area,central Eastern Desert of Egypt: Evidence from hydrothermal alteration,fluid inclusions and stable isotope data

The Semna gold deposit is one of several vein-type gold occurrences in the central Eastern Desert of Egypt, where gold-bearing quartz veins are confined to shear zones close to the boundaries of small granitoid stocks. The Semna gold deposit is related to a series of sub-parallel quartz veins along steeply dipping WNW-trending shear zones, which cut through tectonized metagabbro and granodiorite rocks. The orebodies exhibit a complex structure of massive and brecciated quartz consistent with a change of the paleostress field from tensional to simple shear regimes along the pre-existing fault segments. Textural, structural and mineralogical evidence, including open space structures, quartz stockwork and alteration assemblages, constrain on vein development during an active fault system. The ore mineral assemblage includes pyrite, chalcopyrite, subordinate arsenopyrite, galena, sphalerite and gold. Hydrothermal chlorite, carbonate, pyrite, chalcopyrite and kaolinite are dominant in the altered metaggabro; whereas, quartz, sericite, pyrite, kaolinite and alunite characterize the granodiorite rocks in the alteration zones. Mixtures of alunite, vuggy silica and disseminated sulfides occupy the interstitial open spaces, common at fracture intersections. Partial recrystallization has rendered the brecciation and open space textures suggesting that the auriferous quartz veins were formed at moderately shallow depths in the transition zone between mesothermal and epithermal veins.Petrographic and microthermometric studies aided recognition of CO₂-rich, H₂O-rich and mixed H₂O–CO₂ fluid inclusions in the gold-bearing quartz veins. The H₂O–CO₂ inclusions are dominant over the other two types and are characterized by variable vapor: liquid ratios. These inclusions are interpreted as products of partial mixing of two immiscible carbonic and aqueous fluids. The generally light δ³⁴S of pyrite and chalcopyrite may suggest a magmatic source of sulfur. Spread in the final homogenization temperatures and bulk inclusion densities are likely due to trapping under pressure fluctuation through repeated fracture opening and sealing. Conditions of gold deposition are estimated on basis of the fluid inclusions and sulfur isotope data as 226–267 °C and 350–1100 bar, under conditions transitional between mesothermal and epithermal systems.The Semna gold deposit can be attributed to interplay of protracted volcanic activity (Dokhan Volcanics?), fluid mixing, wallrock sulfidation and a structural setting favoring gold deposition. Gold was transported as Au-bisulfide complexes under weak acid conditions concomitant with quartz–sericite–pyrite alteration, and precipitated through a decrease in gold solubility due to fluid cooling, mixing with meteoric waters and variations in pH and fO₂.     

Symplectite of Pyrite and Magnetite in the Massive Sulphide Ore of the Mashan Mine,Anhui Province

A symplectite of pyrite and magnetite in the massive sulphide ore of the Mashan mine,Anhui Province,is interpreted to have been formed by their replacing earlier pyrrhotite.The compositions of pyrrhotite,pyrite and magnetite related to this texture are given by electron microprobe analysis.Such a texture is likely to be formed when the ore-forming system reaches the three-phase point of pyrrhotite,pyrite and magnetite from the pyrrhotite stability field.The very small probability for the system to reach this point could be used to account for the rare occurrence of such symplectite in natural ores.