Hydrogeochemistry of the Koyna River basin,India

Hydrogeochemistry of the Koyna River basin, famous for the Koyna earthquake (magnitude 7) of 1967, has been studied. Basalt is the primary aquifer; laterites, alluvium, and talus deposits form aquifers of secondary importance. Groundwater generally occurs under water table conditions in shallow aquifers. Deeper aquifers are associated only with basalts. One hundred and 87 water samples were collected from various sources, such as dugwells, borewells, springs, and surface water, including 40 samples for analysis of iron. Only major constituents were analyzed. Analyses show that the concentrations of Ca²⁺ exceed that of Mg²⁺ in almost all water samples; the concentrations of Na⁺ are generally next to Ca²⁺ and are always higher than that of K⁺; and CO₃ ^2– and SO₄ ^2– are very low and are often negligible. Groundwater in borewells tapping deeper aquifers has higher mineralization compared to that in dugwells representing shallow aquifers. Majority of the water samples are dominated by alkaline earths (Ca²⁺, Mg²⁺) and weak acids (HCO₃ ⁻, CO₃ ^2–). Groundwater from shallow aquifers is generally calcium-bicarbonate type (53%) and calcium-magnesium-bicarbonate type (27%). In case of deeper aquifer, it is mostly calcium-magnesium-bicarbonate type (29%), sodium-bicarbonate type (24%), calcium-bicarbonate type (19%), calcium-magnesium-sodium-bicarbonate type (19%) and sodium-calcium-bicarbonate type (9%). Groundwater water is generally fit for drinking and irrigation purposes, except in the lower reaches of the Koyna River basin, which is affected by near water logging conditions.     

Groundwater resources of the middle and upper Odra River basin, southwestern Poland

 The total amount of groundwater resources in the middle and upper Odra River basin is 5200×10³ m³/d, or about 7.7% of the disposable groundwater resources of Poland. The average modulus of groundwater resources is about 1.4 L/s/km². Of the 180 'Major Groundwater Basins' (MGWB) in Poland, 43 are partly or totally located within the study area. The MGWB in southwestern Poland have an average modulus of groundwater resources about 2.28 L/s/km² and thus have abundant water resources in comparison to MGWB from other parts of the country. Several types of mineral waters occur in the middle and upper Odra River basin. These waters are concentrated especially in the Sudety Mountains. Carbon-dioxide waters, with yields of 414 m³/h, are the most widespread of Sudetic mineral waters. The fresh waters of the crystalline basement have a low mineralization, commonly less than 100 mg/L; they are a HCO₃–Ca–Mg or SO₄–Ca–Mg type of water. Various hydrochemical compositions characterize the groundwater in sedimentary rocks. The shallow aquifers are under risk of atmospheric pollution and anthropogenic effects. To prevent the degradation of groundwater resources in the middle and upper Odra River basin, Critical Protection Areas have been designated within the MGWB. Received, January 1995 Revised, May 1996, August 1997 Accepted, August 1997     

Hydrogeologic framework of the Deccan terrain of the Koyna River basin, India

The Koyna River basin in India drew the attention of geoscientists after an earthquake (magnitude 7) in 1967. Since then, detailed geological, tectonic, and seismic investigations of this river basin have been carried out by several workers. However, very little study has been done on its hydrogeological framework. The present work aims at filling this gap. Basalts, laterites, alluvium, soils, and talus deposits form shallow unconfined aquifers, with transmissivity of 27–135 m²/d and a regional specific yield of 0.012. In shallow basaltic aquifers, the lower part of the highly weathered and highly jointed horizon above, and the poorly weathered and highly jointed horizon below, form the most potential zone for groundwater occurrence. Well yields in the deeper basaltic aquifers are directly related to the occurrence of lineaments, whereas at a shallower level they are related to geomorphic features. Spring discharges are highly dependent on their source aquifers and areas of recharge. They have a mean winter discharge of 46 m³/d and a summer discharge of 28 m³/d. Chemically, groundwaters are dominated by alkaline earths (Ca²⁺, Mg²⁺) and weak acids (HCO₃ ^–, CO₃ ^–); they are calcium-bicarbonate type (53%) and calcium-magnesium-bicarbonate type (27%) at shallower levels; and calcium-magnesium-bicarbonate type (29%), sodium-bicarbonate type (24%), calcium-bicarbonate type (19%), and calcium-magnesium-sodium-bicarbonate type (19%) in deeper aquifers. The Koyna River basin is characterized by both scarcity and abundance of groundwater. In the water-scarce areas in the dissected plateaus, artificial recharge of aquifers through construction of several recharge structures at suitable locations is highly recommended. In the water-abundant areas in the central valley, on the other hand, expanded consumptive use of water resources is encouraged. Electronic Publication     

Genesis and distribution of mineral waters as a consequence of recent lithospheric dynamics: the Rhenish Massif,Central Europe

Three major, interdependent processes control the genesis and distribution of mineral and thermal waters in the Rhenish Massif, Central Europe: (a) Magmatic processes in the upper mantle provide most of the CO₂ to produce bicarbonate waters in shallow aquifers. (b) Extension of the brittle upper crust enables the ascent of sodium chloride waters. (c) Uplift and erosion shape the massif's relief, which determines the extent of flow systems and the distribution of thermal springs. The chemistry of mineral waters further depends on the aquifers' mineral composition. A comprehensive set of hydrological, chemical, tectonic and geophysical data on the Rhenish Massif has been compiled. It was used to classify the mineral waters and to map the spatial distribution of water properties. The composition of cuttings from several representative wells producing different water types shows that the hydrothermal alteration of the aquifer rocks consists mainly of kaolinization of chlorite and dissolution of feldspar. Numerical transport simulations favour two modes of groundwater flow: topography-driven flow and the pressure-driven ascent of basement brines along active faults. Thermal convection is less important.     

Arsenic content and groundwater geochemistry of the San Antonio-El Triunfo, Carrizal and Los Planes aquifers in southernmost Baja California, Mexico

 The San Antonio-El Triunfo mining district, located at a mountainous region 45 km south-east of La Paz, Baja California, has been worked since the late 1700s. Mine waste material produced during 200 years of mineral extraction area poses a risk of local groundwater pollution and eventually, regional pollution to the Carrizal (west basin) and the Los Planes (east basin) aquifers. There are different types of deposits in the mining area. These are dominated by epithermal veins, in which arsenopyrite is an important component. Carrillo and Drever (1998a) concluded that, even though the amount of mine waste is relatively small in comparison to the large scale area, significant As in groundwater derived from the mine waste piles is found locally in the groundwater. This paper shows the results of geochemical analyses of groundwater samples from the San Antonio-El Triunfo area and the Carrizal and Los Planes aquifers during several years of monitoring (1993–1997). The highest values of total dissolved solids (TDS) and As are in the mineralized area where the mining operations occurred (∼1500 ppm TDS and 0.41 ppm As). The lowest concentrations of TDS and As are, in general, away from the mineralized area (∼500 ppm TDS and 0.01 ppm As). Sulfate and bicarbonate (alkalinity) are, in general, high near the mineralized area and low away from it. The arsenic concentrations vary seasonally, especially after the heavy summer thunderstorms. Geochemical modeling (MINTEQA2 and NETPATH) and analysis of the regional geochemical evolution of the groundwater from the mining area towards the aquifer of Los Planes shows that the most likely hydrochemical processes include: dilution, precipitation of calcite, and adsorption of As onto surfaces of iron oxyhydroxides (ferrihydrite). These processes act as natural controls to the extent and amount of As pollution in the Carrizal and Los Planes aquifers. Received: 4 May 1999 · Accepted: 22 February 2000     

The chemical composition of the surface system of Peneos river, Thessaly/Central Greece

 Peneos is the mainstream for the drainage of Thessaly's basin. It contributes significantly in recharging the aquifers, as well as to the direct irrigation water, since there is intense agricultural activity in the basin of Thessaly. The investigation of the hydrochemical conditions of the surface water system of Peneos showed that the chemical composition is related to the lithology of the aquifers of the basin, the anthropogenic influence and the biological activity. The chemical composition of this system changes in time and space. The salinity decreases during the winter period, in contrast to the summer period when it increases drastically. The lower values of TDS appear in the upstream part of the river (95–124 mg/l) whereas downstream, the values of TDS increase significantly (400–632 mg/l). The hydrochemical type Ca-Mg-HCO₃ dominates the largest part of the river while it changes to NA-Cl in the estuary. The concentrations of the dissolved species in the main Peneos river are higher than in the spring waters. Peneos is the most polluted river in Greece. The concentration of the pollutants is higher at the downstream part of the river, but is lower than the accepted upper limits. The use of the surface water of the system of Peneos river for irrigation purposes based on the SAR factor is acceptable because the absorption ratio for Na and salinity are low and medium respectively. Received: 27 October 1997 · Accepted: 21 September 1998     

Geochemical evidence of seawater intrusion into a coastal geothermal field of central Greece: example of the Thermopylae system

Thermal water of Thermopylae and from other geothermal fields located in the southern part of the Sperchios basin (central Greece) are characterized by high salinity (total dissolved salts, or TDS, range from 1.2 to 30.3 g L⁻¹) associated with a degassing of CO₂. To determine the mineralization processes, geochemical and isotopic investigations (major elements, ¹⁸O, ²H and ¹³C) have been carried out upon 17 thermal waters from springs and boreholes. This study emphasizes that all the thermal waters result from the mixing of a seawater end-member, several fresh water components depending on the field location, and a mantle-derived CO₂ rising upward through an E–W fault system. The seawater identified in the thermal mixture is likely to be evolved Aegean seawater (ASW). Once intruded into the basin sediments, the trapped seawater has its chemical content modified by both water–rock interactions and massive dissolution of the deep CO₂ (pCO₂ of 10^0.5 atm). The modelling performed with PHREEQC indicates that the anomalous major ion ratios measured in the so-called evolved ASW are explained by the dissolution of calcite and dolomitization process associated to precipitation of gypsum within the thermal aquifer.     

Geochemical patterns and origin of alkaline thermal waters in Central Greece (Platystomo and Smokovo areas)

This study investigates the origin and chemical composition of the thermal waters of Platystomo and Smokovo areas in Central Greece as well as any possible relationships of them to the neighboring geothermal fields located in the south-eastern part of Sperchios basin. The correlations between different dissolved salts and the temperature indicate that the chemical composition of thermal waters are controlled by, the mineral dissolution and the temperature, the reactions due to CO₂ that originates possibly by diffusion from the geothermal fields of Sperchios basin and the mixing of thermal waters with fresh groundwater from karst or shallow aquifers. Two major groups of waters are recognized on the basis of their chemistry: thermal waters of Na–HCO₃–Cl type and thermal waters mixed with fresh groundwater of Ca–Mg–Na–HCO₃ type. All thermal waters of the study area are considered as modified by water–rock interaction rainwater, heated in depth and mixed in some cases with fresh groundwater when arriving to the surface. Trace elements present low concentrations. Lithium content suggests discrimination between the above two groups of waters. Boron geochemistry confirms all the above remarks. Boron concentration ranges from 60 μg L^?1 to 10 mg L^?1, while all samples’ constant isotopic composition (δ¹¹B ≈ 10 ‰) indicates leaching from rocks. The positive correlation between the chemical elements and the temperature clearly indicates that much of the dissolved salts are derived from water–rock interactions. The application of geothermometers suggests that the reservoir temperature is around 100–110 °C. Chalcedony temperatures are similar to the emergent temperatures and this is typical of convective waters in fault systems in normal thermal gradient areas.     

Hydrochemistry of formation water with implication to diagenetic reactions in Sanzhao depression and Qijia-gulong depression of Songliao Basin, China

The Sanzhao depression and Qijia-gulong depression are two of the most important hydrocarbon-bearing sub-depressions in the Songliao basin, dominated by Cretaceous fluvial and lacustrine strata with volcanic and volcaniclastic rocks. In this paper, the pressure distributions and hydrochemistry variations in those two depressions are investigated. It is found that the Qijia-gulong depression is dominated by overpressure, but the Sanzhao depression is dominated by underpressure, especially in the Quantou formation. The salinity of formation water ranges from 1.0 g/L to 20 g/L, with a mean of 4 g/L in most formations. Water composition is dominated by NaHCO₃ water type but varies greatly in salinity and ionic ratios in the different depressions. The results of mass balance calculation reveal that, fluid chemistry in the Qijia-gulong depression is dominated by dissolution of silicate minerals and halite, whereas in the Sanzhao depression it is dominated by silicate mineral dissolution, evaporite dissolution (halite and gypsum), carbonate mineral dissolution/precipitation, and cation exchange.     

A geochemical and geophysical approach to derive a conceptual circulation model of CO2-rich mineral waters: A case study of Vilarelho da Raia, northern Portugal

The Vilarelho da Raia-Chaves region, located in northern Portugal adjacent to the Spanish border, is characterized by both hot and cold CO₂-rich mineral waters issuing from springs and drilled wells. The present paper updates the conceptual circulation model of the Vilarelho da Raia cold CO₂-rich mineral waters. Vilarelho da Raia mineral waters, dominated by Na and HCO₃ ions, have formed mainly by interaction with CO₂ of deep-seated mantle origin. The δ ¹⁸O, δ ²H and ³H values indicate that these waters are the result of meteoric waters infiltrating into Larouco Mountain, NW of Vilarelho da Raia, circulating at shallow depths in granitic rocks and moving into Vilarelho da Raia area. The conceptual geochemical and geophysical circulation model indicates that the hot and cold CO₂-rich mineral waters of Chaves (76 °C) and Vilarelho da Raia (17 °C) should be considered manifestations of similar but not the same geohydrological systems. Electronic Publication     

Tufa and travertines of southern Italy: deep‐seated,fault‐related CO2 as the key control in precipitation

Continental carbonates of Quaternary age in southern Italy commonly exhibit the facies of calcareous tufa, often reported as related to shallow aquifers fed by meteoric waters and to organic processes. A close spatial relationship exists between the mappable tufa deposits and major Quaternary extensional faults. With respect to the Ca‐Mg‐HCO₃ composition of limestone aquifers’ springs, tufa‐depositing springs exhibit higher salinity and alkalinity, are slightly warmer, have lower pH and are enriched in SO₄ and CO₂. Their δ¹³C values are systematically positive and compatible with a deep‐seated carbon source. A clear input of soil‐derived organic carbon is indicated only for small, non‐mappable tufas deposited by perched springs. The dataset indicates that the large tufa deposits owe their origin to a supplementary source of CO₂ advected by degassing through active faults, as a necessary prerequisite for inducing a rise of total dissolved salts and alkalinity. Meteoric waters that have come from a shallow aquifer are able to precipitate only limited amount of carbonates.     

The impact of CO<Subscript>2</Subscript> on shallow groundwater chemistry: observations at a natural analog site and implications for carbon sequestration

In a natural analog study of risks associated with carbon sequestration, impacts of CO₂ on shallow groundwater quality have been measured in a sandstone aquifer in New Mexico, USA. Despite relatively high levels of dissolved CO₂, originating from depth and producing geysering at one well, pH depression and consequent trace element mobility are relatively minor effects due to the buffering capacity of the aquifer. However, local contamination due to influx of brackish waters in a subset of wells is significant. Geochemical modeling of major ion concentrations suggests that high alkalinity and carbonate mineral dissolution buffers pH changes due to CO₂ influx. Analysis of trends in dissolved trace elements, chloride, and CO₂ reveal no evidence of in situ trace element mobilization. There is clear evidence, however, that As, U, and Pb are locally co-transported into the aquifer with CO₂-rich brackish water. This study illustrates the role that local geochemical conditions will play in determining the effectiveness of monitoring strategies for CO₂ leakage. For example, if buffering is significant, pH monitoring may not effectively detect CO₂ leakage. This study also highlights potential complications that CO₂ carrier fluids, such as brackish waters, pose in monitoring impacts of geologic sequestration.     

Review: The potential impact of underground geological storage of carbon dioxide in deep saline aquifers on shallow groundwater resources

Underground geological storage of CO₂ in deep saline aquifers is considered for reducing greenhouse gases emissions into the atmosphere. However, some issues were raised with regard to the potential hazards to shallow groundwater resources from CO₂ leakage, brine displacement and pressure build-up. An overview is provided of the current scientific knowledge pertaining to the potential impact on shallow groundwater resources of geological storage of CO₂ in deep saline aquifers, identifying knowledge gaps for which original research opportunities are proposed. Two main impacts are defined and discussed therein: the near-field impact due to the upward vertical migration of free-phase CO₂ to surficial aquifers, and the far-field impact caused by large-scale displacement of formation waters by the injected CO₂. For the near-field, it is found that numerical studies predict possible mobilization of trace elements but concentrations are rarely above the maximum limit for potable water. For the far-field, numerical studies predict only minor impacts except for some specific geological conditions such as high caprock permeability. Despite important knowledge gaps, the possible environmental impacts of geological storage of CO₂ in deep saline aquifers on shallow groundwater resources appears to be low, but much more work is required to evaluate site specific impacts.     

A Geochemical study of the groundwater in the Misli basin and environmental implications

The aim of this study was to determine geochemical properties of groundwater and thermal water in the Misli Basin and to assess thermal water intrusion into shallow groundwater due to over-extraction. According to isotope and hydrochemical analyses results, sampled waters can be divided into three groups: cold, thermal, and mixed waters. Only a few waters reach water–rock chemical equilibrium. Thermal waters in the area are characterized by Na⁺–Cl⁻–HCO₃⁻, while the cold waters by CaHCO₃ facies. On the basis of isotope results, thermal waters in the Misli basin are meteoric origin. In particular, δ¹⁸O and δ²H values of shallow groundwater vary from −10.2 to −12.2‰ and −71.2 to −82‰, while those of thermal waters range from −7.8 to −10.1‰ and from −67 to −74‰, respectively. The tritium values of shallow groundwater having short circulation as young waters coming from wells that range from 30 to 70 m in depth vary from 10 to 14 TU. The average tritium activity of groundwater in depths more than 100 m is 1.59 ± 1.16, which indicates long circulation. The rapid infiltration of the precipitation, the recycling of the evaporated irrigation water, the influence of thermal fluids and the heterogeneity of the aquifer make it difficult to determine groundwater quality changes in the Misli Basin. Obtained results show that further lowering of the groundwater table by over-consumption will cause further intrusion of thermal water which resulted in high mineral content into the fresh groundwater aquifer. Because of this phenomenon, the concentrations of some chemical components which impairs water quality in terms of irrigation purposes in shallow groundwaters, such as Na⁺, B, and Cl⁻, are highy probably expected to increase in time.     

Interaction between deep and shallow groundwater systems in areas affected by Quaternary tectonics (Central Italy): a geochemical and isotope approach

Hydro- and isotope geochemistry are used to refine groundwater conceptual models in two areas of central Italy (Acque Albule Basin and Velino River Valley) affected by extensional Quaternary tectonics, where deep and shallow groundwater flow systems are interacting. The role of geology, of recent deposits filling the plains and of main tectonic features controlling groundwater flowpaths and deep-seated fluids emergences are investigated and discussed. Environmental isotopes (²H and ¹⁸O) confirm recharge in the surrounding carbonate aquifers, and meteoric origin of both shallow and deep groundwater. Major ion chemistry indicates a mixing between shallow Ca-HCO₃ groundwater from carbonate aquifers and deep Ca-HCO₃-SO₄ groundwater, characterised by higher salinity and temperature and high concentration in sulphates. Isotopic composition of dissolved sulphates (δ ³⁴S and δ ¹⁸O) and dissolved inorganic carbon (δ ¹³C), henceforth indicated as DIC, are used to verify the presence of different sources of groundwater, and to validate the mixing model suggested by the major ion analyses. Sulphate isotope composition suggests a marine origin for the groundwater characterised by elevated sulphate concentration, whose source is present in the deep buried sequences. Carbon isotope composition confirms the role of a DIC source associated to CO₂ degassing of a deep reservoir. Groundwater conceptual models are improved underlining the importance of Plio-Pleistocene sequences filling the tectonic depression. In the Acque Albule area, the travertine plateau represents a mixing stratified aquifer, where deep groundwater contribution is spread into the shallow aquifer. The alluvial–clastic–lacustrine leaky aquifer of Velino Valley enables a complete mixing of shallow and deep groundwater allowing spot-located discharge of deep groundwater along tectonic patterns and facilitating sulphate reduction in the lacustrine sediments, explaining locally the presence of H₂S.     

Hydrogeological conditions and quality of ground waters in northern Banat,Pannonian basin

Geological relationships, hydrogeology and chemical composition of ground water in northern Banat were studied through the period 2000–2004 using the available background data from published and unpublished sources. Northern Banat is the extreme northeastern part of the Republic of Serbia and a geotectonic part of the vast Pannonian depression. The source of domestic and industrial water supply is only groundwater from artesian and subartesian aquifers of Lower Pleistocene (Q₁¹) and Upper Pleistocene (Pl₃²) sand deposits. The ground water, “peculiar” in chemical composition, is the only source of drinking water in the arid area. A notable variation in the chemical composition of artesian waters within the same geotectonic unit (Pannonian basin), abstracted for municipal water supplies of Kikinda, Novi Knezevac and Djala, has attracted attention of these authors. Our paper attempts to interpret the variation in the chemical composition of ground water and the cause of the variation by the interaction of ground water and rocks forming the aquifers on the case example of the water supply sources for the three mentioned towns. With respect to the depth and lithology of the aquifers, we interpret the varied chemical compositions of waters in the mentioned sources as a consequence of natural factors (geological environment), geological relationships and hydrogeological conditions.     

Hydrogeologic and hydrochemical framework of the shallow groundwater system in the southern Voltaian Sedimentary Basin, Ghana

 The southern Voltaian Sedimentary Basin underlies an area of about 5000 km² in east-central Ghana. Groundwater in the basin occurs in fractures in highly consolidated siliciclastic aquifers overlain by a thin unsaturated zone. Aquifer parameters were evaluated from available aquifer-test data on 28 shallow wells in the basin. Hydraulic-conductivity values range from 0.04–3.6 m/d and are about two orders of magnitude greater than the hydraulic conductivity calculated using Darcy's Law and the average groundwater velocity estimated from carbon-14 dating. Linear-regression analysis of the transmissivity and specific-capacity data allowed the establishment of an empirical relationship between log transmissivity and log specific capacity for the underlying aquifers. Groundwater chemistry in the basin is controlled by the weathering of albitic plagioclase feldspar. The weathering rates of various minerals were estimated using ¹⁴C-derived average velocity in the basin. The weathering rate of albite was calculated to be 2.16 μmol L^–1 yr^–1 with the resulting formation of 3.3 μmol L^–1 yr^–1 of kaolinite and 0.047 μmol L^–1 yr^–1 of calcite. The low porosity and permeability of the aquifers in the basin are attributed to the precipitation of secondary minerals on fracture surfaces and interlayer pore spaces. Received, September 1997 Revised, July 1998, August 1998 Accepted, August 1998     

Review: Thermal water resources in carbonate rock aquifers

The current knowledge on thermal water resources in carbonate rock aquifers is presented in this review, which also discusses geochemical processes that create reservoir porosity and different types of utilisations of these resources such as thermal baths, geothermal energy and carbon dioxide (CO₂) sequestration. Carbonate aquifers probably constitute the most important thermal water resources outside of volcanic areas. Several processes contribute to the creation of porosity, summarised under the term hypogenic (or hypogene) speleogenesis, including retrograde calcite solubility, mixing corrosion induced by cross-formational flow, and dissolution by geogenic acids from deep sources. Thermal and mineral waters from karst aquifers supply spas all over the world such as the famous bath in Budapest, Hungary. Geothermal installations use these resources for electricity production, district heating or other purposes, with low CO₂ emissions and land consumption, e.g. Germany’s largest geothermal power plant at Unterhaching near Munich. Regional fault and fracture zones are often the most productive zones, but are sometimes difficult to locate, resulting in a relatively high exploration uncertainty. Geothermal installations in deep carbonate rocks could also be used for CO₂ sequestration (carbonate dissolution would partly neutralise this gas and increase reservoir porosity). The use of geothermal installations to this end should be further investigated.     

Replenishment conditions and regimen of underground waters in Carboniferous deposits of Moscow artesian basin

There are seven principal aquifers in the Carboniferous rocks of the Moscow basin. These are replenished by 1) precipitation on the outcrops, 2) water-bearing horizons in the overlying Mesozoic and Quaternary, and 3) directly from lakes and rivers in favorable situations. Total exchange time (time for complete recharge) is estimated at 85 years, which is remarkably short for a basin of that size and capacity. Water from these aquifers has been used for almost 100 years. Cones of depression in the Upper and Middle Carboniferous are 65–90 km across, with lowering of 25–50 m of the water table; in the Lower Carboniferous, 150–180 km in diameter, with lowering up to 70 m. In areas of direct recharge from a stream the cone of depression is very small and shallow. The authors believe that because of the favorable recharge situation water yield of the basin can be greatly increased. -- E. Ingerson.     

Hydrothermal fluid evolution and structural control of the Guarim gold mineralisation, Tapajós Province, Amazonian Craton, Brazil

Fluid inclusion and structural studies were carried out at the Guarim gold deposit in the Palaeoproterozoic Tapajós province of the Amazonian craton. Guarim is a fault-hosted gold deposit cutting basement granitoids. It consists of a quartz vein, which is massive in its inner portions, grading laterally either to a massive or to cavity-bearing quartz vein associated with hydrothermal breccias. The wallrock alteration comprises chlorite, carbonate, white mica and sulphide minerals, with free gold occurring within quartz grains and spatially associated with sulphide mineral grains. Petrographic, microthermometric and Laser Raman investigations recognised CO₂-rich, mixed H₂O–CO₂, and H₂O fluid inclusions. The coexisting CO₂ and H₂O–CO₂ inclusions were interpreted as primary immiscible fluids that formed the gold-bearing vein. The H₂O inclusions were considered a product of later infiltration of fluids unrelated to the mineralising episode. The mineralising fluid has CO₂ ranging typically from 5–10 mol%, contains traces of N₂, has salinities of ∼5 wt% NaCl equiv., and densities varying between 0.85 and 0.95 g/cm³. The P–T estimations bracket gold deposition between 270–320 °C and 0.86–2.9 kb; ƒ_O2–ƒ_S2–pH estimates suggest a reduced, near-neutral character for the fluid. Variations in the physico-chemical properties, as demonstrated by the fluid inclusion study, resulted from a combination of fluid immiscibility and pressure fluctuation. This interpretation, combined with textural and structural evidence, suggests the emplacement of the mineralised vein in an active fault and at a rather shallow level (4–7 km). The geological and structural setting, deposit-scale textures and structures, wallrock alteration and physico-chemical fluid properties are compatible with those of epizonal to mesozonal orogenic lode gold deposits. Received: 3 March 2000 / Accepted: 21 October 2000