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1.
《Chemical Geology》2002,182(2-4):637-654
The inner sector of the Eastern Carpathians displays a large number of Na–HCO3, CO2-rich, meteoric-originated cold springs (soda springs) and bore wells, as well as dry mofettes. They border the southern part of the Pliocene–Quaternary Calimani–Gurghiu–Harghita (CGH) calc-alkaline volcanic chain. Both volcanic rocks and CO2-rich emissions are situated between the eastern part of the Transylvanian Basin and the main east Carpathian Range, where active compression tectonics caused diapiric intrusions of Miocene halite deposits and associated saline, CO2-rich waters along active faults. The regional patterns of the distribution of CO2 in spring waters (as calculated pCO2) and the distribution pattern of the 3He/4He ratio in the free gas phases (up to 4.5 Rm/Ra) show their maximum values in coincidence with both the maximum heat-flow measurements and the more recent volcanic edifices. Moving towards the eastern external foredeep areas, where oil fields and associated brines are present, natural gas emissions become CH4-dominated. Such a change in the composition of gas emissions at surface is also recorded by the 3He/4He ratios that, in this area, assume ‘typical’ crustal values (Rm/Ra=0.02).In spite of the fact that thermal springs are rare in the Harghita volcanic area and that equilibrium temperature estimates based on geothermometric techniques on gas and liquid phases at surface do not suggest the presence of shallow active hydrothermal systems, a large circulation of fluids (gases) is likely triggered by the presence of mantle magmas stored inside the crust. If total 3He comes from the mantle or from the degassing of magmas stored in the crust, CO2 might be associated to both volcanic degassing and thermometamorphism of recently subducted limestones.  相似文献   

2.
This paper deals with the mineral springs feeding the Scrajo spa in the Sorrento peninsula southeast of Naples, approximately 6 km from Castellammare di Stabia, another spa location. The Scrajo mineral water is sulphureous, salt-bromine-iodic and CO2-rich. The two hydromineral areas fall within the groundwater basin of Mt. Faito formed chiefly by limestones. Due to the high permeability of the limestones, there is considerable rainwater infiltration which recharges a basal fresh groundwater resting on denser seawater. This groundwater body feeds the mineral springs of the Scrajo spa, the springs of Castellammare di Stabia and some submarine springs. All the data gathered for the Scrajo springs led to propose the following mineralisation scheme: (1) The basal fresh groundwater of Mt. Faito (on underlying seawater) receives endogenous contributions of CO2 and H2S which cause a “natural” seawater intrusion within the fresh groundwater; (2) The upwelling of gases would appear to occur via the major faults which bound Sorrento peninsula to the NW; (3) During the year, the chemistry of the springs changes according to different degrees of seawater intrusion: the minimum occurs in June and the maximum in November. The close interaction between the sea and the Scrajo’s mineral waters (but also those of Castellammare di Stabia) highlights their particular vulnerability not only to over-extraction of groundwater but also to climate change. Finally, a hypothesis is presented to explain the connection between the mineral waters rich in CO2 and H2S and the concentration of karst phenomena observed in the Scrajo area.  相似文献   

3.
腾冲新生代火山区温泉CO2气体排放通量研究   总被引：6，自引：6，他引：0  
近期研究表明,不仅火山喷发期会向当时的大气圈输送大量的温室气体,火山间歇期同样会释放大量的温室气体。在火山活动间歇期,火山区主要以喷气孔、温(热)泉以及土壤微渗漏等形式向大气圈释放温室气体。腾冲是我国重要的新生代火山区,同时也是重要的水热活动区,那里出露大量的温泉,然而目前未见腾冲火山区温泉气体排放通量的研究报道。本文利用数字皂膜通量仪测量了腾冲新生代火山区温泉中CO2的排放通量。研究结果表明,腾冲新生代火山区温泉向当今大气圈输送的CO2通量达3.58×103 t·a-1,相当于意大利锡耶纳Bassoleto地热区温泉中CO2的排放规模。腾冲火山区温泉的CO2释放通量主要受深部岩浆囊、断裂分布、地下水循环、围岩成分等多方面因素的影响。本文根据温泉中CO2的排放特征,将腾冲温泉分为南北两区,南区温泉CO2通量远高于北区的温泉,热海地热区的通量为腾冲CO2通量的最大值。在北温泉区,CO2通量主要受控于断裂的分布;而在南温泉区,除受到断裂控制外,热海地热区底部的岩浆囊及其与围岩的相互作用成为CO2气体的重要物质来源,同时高温的岩浆囊为温泉及CO2的形成提供了重要热源。  相似文献   

4.
Two springs (Cuihua Spring, Shuiqiuchi Spring) in Cuihua Mountain of the Qinling Mountains were observed and sampled monthly during 2004 and 2005 to trace their physical properties and chemical compositions with seasons. Although both pH values and cation (Ca2+, Mg2+, K+, and Na+) contents of Cuihua Spring are higher than those of Shuiqiuchi Spring, seasonal variations in both springs are obvious. The pH values of both spring waters are between 5.69 and 6.98, lower than that of rainwater during summer and autumn. From January to November, the pH values of both springs similarly vary from high to low and then to high again. Variations in electric conductivities of two spring waters are contrary, although their electric conductivities are positively correlative with the cation content respectively. This can be attributed to different water sources of the two springs or different acidic rocks they passed. The contents of HCO3 −, Ca2+, Mg2+, K+, and Na+ are low, indicating a low silicate weathering that the strata in this district are mainly composed of granite and schist of quartz and mica. Differing from change in spring water in karst regions of South China where abundant precipitation and dilution of rainwater cause low pH and electric conductivity in summer and autumn, the seasonal variations in the pH values and the electric conductivities of two springs in Qinling Mountains are attributed to seasonal changes in CO2 produced by microorganisms’ activity in soil within respective year, rather than rainfall. The microorganisms’ activity in soil produces more CO2 during summer and autumn. Therefore, the water nature of springs in silicate regions chiefly reflects the seasonal changes of CO2 produced by the microorganisms in soil.  相似文献   

5.
《Applied Geochemistry》2006,21(2):289-304
Mineral springs from Daylesford, Australia discharge at ambient temperatures, have high CO2 contents, and effervesce naturally. Mineral waters have high HCO3 and Na concentrations (up to 4110 and 750 mg/L, respectively) and CO2 concentrations of 620–2520 mg/L. Calcium and Mg concentrations are 61–250 and 44–215 mg/L, respectively, and Si, Sr, Ba, and Li are the most abundant minor and trace elements. The high PCO2 of these waters promotes mineral dissolution, while maintaining low pH values, and geochemical modelling indicates that the CO2-rich mineral water must have interacted with both sediments and basalts. Amorphous silica concentrations and silica geothermometry indicate that these waters are unlikely to have been heated above ambient temperatures and therefore reflect shallow circulation on the order of several hundreds of metres. Variations in minor and trace element composition from closely adjacent spring discharges indicate that groundwater flows within relatively isolated fracture networks. The chemical consistency of individual spring discharges over at least 20 a indicates that flow within these fracture networks has remained isolated over long periods. The mineral water resource is at risk from mixing with potentially contaminated surface water and shallow groundwater in the discharge areas. Increased δ2H values and Cl concentrations, and lower Na concentrations indicate those springs that are most at risk from surface contamination and overpumping. Elevated NO3 concentrations in a few springs indicate that these springs have already been contaminated during discharge.  相似文献   

6.
The mineral water deposits in Kiseljak are located in the central Dinarids, Bosnia and Herzegovina, in the southwestern edge of Sarajevo–Zenica basin that was formed in the zone of Busova?a fault. Busova?a fault reaches deep into the Earth’s crust and is characterised by the presence of mineral and thermomineral water enriched with CO2 and CO2 springs (mofetes) in the direction of Ilid?a–Kiseljak–Busova?a. Deposits are constructed of layers of Palaeozoic to Cretaceous age. Primary aquifer of mineral waters is Permian clastites and evaporites and secondary Anisian carbonates. Mineral water and CO2 are of different origin. The water is of atmospheric origin. Due to slow circulation, water descends in the primary aquifer where it becomes enriched with CO2 and minerals. Due to high pressure in the primary aquifer mineral water ascends along Busova?a fault, mounts into the secondary aquifer and rises at spring sources. Water is a mixture of two or more waters of different mineralization. Mixing of water occurs in the zone of secondary aquifer even at greater depths without the influence of contemporary climatic factors. Intensive water mixing is indicated by the high ratio of Ca/Sr, Na/Cl and Ca/SO4 and the mixing diagram. CO2 is thermometamorphic, arising from the catalytic activity of SiO2 on carbonates in the deeper layers of the Earth’s crust, where quartz porphyry broke through Palaeozoic formations.  相似文献   

7.
In this paper, we present the Starzach site, a region featuring numerous natural CO2 emission spots, such as mofettes, that reappeared after a longer period of extensive industrial CO2 mining. We discuss the results of a detailed literature study on the geological setting and the activities related to the gas mining in combination with own measurements to introduce the site as an example on how gas leakage from an insecure CCS reservoir could manifest at the surface. The site is in particular interesting for such investigations as the CO2 emissions started to replenish after the end of the CO2 mining and offers the unique possibility to investigate an increase in degassing activity as it might be expected for an active CCS site where leakage is suspected. Based on the geological setting and soil, gas emission, and isotope investigations, we further discuss the source of the CO2 emission and the gas ascent to the ground surface via deep-reaching faults, latter being so far excluded by previous work. The combination of our extensive literature review and recent field investigations allowed us to draw new geological conclusions for the site that were under discussion for a long time and to give insight into the site’s potential for CCS-related analog studies in the future.  相似文献   

8.
Presently many research projects focus on the reduction of anthropogenic CO2 emissions. It is intended to apply underground storage techniques such as flue gas injection in unminable coal seams. In this context, an experimental study has been performed on the adsorption of pure CO2 and preferential sorption behavior of flue gas. A coal sample from the Silesian Basin in Poland (0.68% V Rr), measured in the dry and wet state at 353 K has been chosen for this approach. The flue gas used was a custom class industrial flue gas with 10.9% of CO2, 0.01% of CO, 9% of H2, 3.01% of CH4, 3.0% of O2, 0.106% of SO2 and nitrogen as balance.Adsorption isotherms of CO2 and flue gas were measured upto a maximum of 11 MPa using a volumetric method. Total excess sorption capacities for CO2 on dry and wet Silesia coal ranged between 1.9 and 1.3 mmol/g, respectively. Flue gas sorption capacities on dry and wet Silesia coal were much lower and ranged between 0.45 and 0.2 mmol/g, respectively, at pressures of 8 MPa. The low sorption capacity of wet coal has resulted from water occupying some of the more active adsorption sites and hence reducing the heterogeneity of adsorption sites relative to that of dry coal. Desorption tests with flue gas were conducted to study the degree of preferential sorption of the individual components. These experiments indicate that CO2 is by far the prefered sorbing component under both wet and dry conditions. This is followed by CH4. N2 adsorbs very little on the coal in the presence of CO2 and CH4. It is also observed that the adsorption of CO2 onto coal is not significantly hindered by the addition of other gases, other than dilution effect of the pressure.In addition to the sorption experiments, the density of the flue gas mixture has been determined up to 18 MPa at 318 K. A very good precision of these measurements were documented by volumetric methods.  相似文献   

9.
This paper reviews various coal seam gas (CSG) models that have been developed for the Sydney Basin, and provides an alternative interpretation for gas composition layering and deep-seated CO2 origins. Open file CSG wells, supplemented by mine-scale information, were used to examine trends in gas content and composition at locations from the margin to the centre of the basin. Regionally available hydrochemistry data and interpretations of hydrodynamics were incorporated with conventional petroleum well data on porosity and permeability. The synthesised gas and groundwater model presented in this paper suggests that meteoric water flow under hydrostatic pressure transports methanogenic consortia into the subsurface and that water chemistry evolves during migration from calcium-rich freshwaters in inland recharge areas towards sodium-rich brackish water down-gradient and with depth. Groundwater chemistry changes result in the dissolution and precipitation of minerals as well as affecting the behaviour of dissolved gases such as CO2. Mixing of carbonate-rich waters with waters of significantly different chemistries at depth causes the liberation of CO2 gas from the solution that is adsorbed into the coal matrix in hydrodynamically closed terrains. In more open systems, excess CO2 in the groundwater (carried as bicarbonate) may lead to precipitation of calcite in the host strata. As a result, areas in the central and eastern parts of the basin do not host spatially extensive CO2 gas accumulations but experience more widespread calcite mineralisation, with gas compositions dominated by hydrocarbons, including wet gases. Basin boundary areas (commonly topographic and/or structural highs) in the northern, western and southern parts of the basin commonly contain CO2-rich gases at depth. This deep-seated CO2-rich gas is generally thought to derive from local to continental scale magmatic intrusions, but could also be the product of carbonate dissolution or acetate fermentation.  相似文献   

10.
《Applied Geochemistry》2000,15(9):1345-1367
Rare Earth Elements (REEs), and Sr and Nd isotope distributions, have been studied in mineralized waters from the Massif Central (France). The CO2-rich springs are characterized by a neutral pH (6–7) associated with total dissolved solids (TDS) from 1 to 7 g l−1. The waters result from the mixing of very mineralized water pools, thought to have equilibrated at a temperature of around 200°C with superficial waters. These two mineral water pools evidenced by Sr isotopes and dissolved REEs could reflect 2 different stages of water–rock interaction and an equilibrium with different mineral assemblages.The concentrations of individual dissolved REEs and total dissolved REEs (ΣREE), in the mineral waters examined, vary over several orders of magnitude but are not dependent on the main parameters of the waters (TDS, T°C, pH, Total Organic C). The dissolved REE concentrations presented as upper continental crust normalized patterns show HREE enrichment in most of the samples. The time evolution of REE patterns does not show significant fluctuations except in 1 borehole, located in the Limagne d’Allier area, which was sampled on 16 occasions over an 18 month period. Ten samples are HREE-enriched, whereas 6 samples show flat patterns.The aqueous speciation of REEs shows that CO2−3 complexes dominate (>80%) over the free metal, F−, SO2−4 and HCO−3 complexes. The detailed speciation demonstrates that the fractionation of REEs (i.e. the HREE enrichment) in CO2-rich and pH neutral fluids is due essentially to the predominance of the CO2−3 complexes.The Sr isotopic composition of the mineral waters in the Massif Central shows different mixing processes; in the Cézallier area at least 3 end-member water types exist. The most dilute end-member is likely to originate as poorly mineralized waters with minimal groundwater circulation. Two other mineralized end-members are identified, although the link between the geographical location of spring outflow and the mixing proportion between the 2 end-members is not systematic. The range in ϵNd(0) for mineralized waters in the Massif Central correlates well with that of the known parent rocks except for 4 springs. One way to explain the ϵNd(0) in these instances is a contribution from drainage of volcanic rocks. The isotopic systematics help to constrain the hydrogeological models for this area.  相似文献   

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