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1.
Impacts of subsurface heat storage on aquifer hydrogeochemistry   总被引：3，自引：3，他引：0  
The use of shallow aquifers for subsurface heat storage in terms of energy management and building climatisation can lead to a temperature rise in the aquifer to 70 °C and above. The influence of temperature changes on individual mineral and sorption equilibria, reaction kinetics and microbial activity is largely known. However, the impact of heating to temperatures as high as 70 °C on the aquifer overall system has not been quantified yet. Temperature-related changes in sediment ion exchange behaviour, dimension and rates of mineral dissolution and precipitation as well as microbially enhanced redox processes were studied in column experiments using aquifer sediment and tap water at 10, 25, 40, and 70 °C. At 70 °C, a change in sediment sorption behaviour for cations and organic acids was postulated based on temporal changes in pH, magnesium, and potassium concentration in the experimental solution. No clear changes of pH, TIC and major cations were found at 10–40 °C. Redox zoning shifted from oxic conditions towards nitrate and iron(III) reducing conditions at 25 and 40 °C and sulphate reducing conditions at 70 °C. This was attributed to (a) a temperature-related increase in microbial reduction activity, and (b) three times higher release of organic carbon from the sediment at 70 °C compared to the lower temperatures. The findings of this study predict that a temperature increase in the subsurface up to 25 °C and above can impair the usability of ground water as drinking and process water, by reducing metal oxides and thus possibly releasing heavy metals from the sediment. Generally, at 70 °C, where clear cation and organic carbon desorption processes were observed and sulphate reducing conditions could be achieved, a site-specific assessment of temperature effects is required, especially for long-term operations of subsurface heat storage facilities.  相似文献   

2.
Aquifer thermal energy storage in urban and industrial areas can lead to an increase in subsurface temperature to 70 °C and more. Besides its impacts on mineral and sorption equilibria and chemical reaction kinetics in an aquifer, temperature sensitively influences microbial activity and thus redox processes, such as sulphate reduction. Microorganism species can only operate within limited temperature ranges and their adaptability to temperature is a crucial point for the assessment of the environmental consequences of subsurface heat storage. Column experiments with aquifer sediment and tap water at 10, 25, 40, and 70 °C showed that under the constant addition of acetate sulphate reduction could be initiated after 26–63 pore volumes exchanged at all temperatures. Fastest initiation of sulphate reduction with the highest reduction rates was found at 40 °C. Maximum rate constants during experimental run-time were 0.56 h?1 at 40 °C and 0.33, 0.36, and 0.25 h?1 at 10 and, 25, and 70 °C, respectively. Hence, microbial activity was enhanced by a temperature increase to 40 °C but was significantly lowered at 70 °C. At 25 °C methane was found in solution, indicating the presence of fermenting organisms; at 10, 40, and 70 °C no methane production was observed. It could be shown that redox processes in an aquifer generally can adapt to temperatures significantly higher than in situ temperature and that the efficiency of the reduction process can be enhanced by temperature increase to a certain limit. Enhancement of sulphate reduction in an aquifer due to temperature increase could also allow enhanced degradation of organic ground water contaminants such as BTEX, where sulphate is an important electron acceptor.  相似文献   

3.
T. Praharaj  D. Fortin   《Applied Geochemistry》2008,23(12):3728-3740
Several studies have shown that SO4-reducing bacteria (SRB) are active in acidic sulfide-rich mine tailings and sediments impacted by mining activities. SRB activity in acidic tailings has been shown to vary with seasons as a result of fluctuating in situ physico-chemical conditions. Iron-reducing bacteria (FeRB) also play an important role in Fe cycling in sediments impacted by mining activities, but their activity in mine tailings is poorly understood, despite the fact that geochemical evidence indicates that they might be active. The present study was undertaken to assess the seasonal changes in SRB and FeRB abundance and activity in alkaline Pb–Zn mine tailings (Calumet tailings) located near Ottawa, ON, Canada. Results showed that FeRB and SRB populations were present throughout the year at two different sampling sites at the Calumet tailings, but SO4 reduction rates (SRR) were lower in the spring than in the summer, indicating that SRB activity was affected by organic C availability and/or temperature. Surface agricultural runoff at one site provided ample nutrients and organic C to the tailings, but SRB activity remained lower than the site not impacted by nutrient runoff, suggesting that the type of organic C was different between the two sites and that less labile organic substrates were available to SRB in the organic-rich site. High SRB activity in the site containing low organic C inhibited the abundance of FeRB, and possibly their activity, as a result of abiotic reduction of Fe(III)-rich minerals by biogenic sulfides, which lowered the pool of final electron acceptors. The abiotic reduction pathway was consistent with the porewater data which showed that sulfide was consumed and SO4 produced, along with Fe(II). These results show a strong interdependence between SRB and FeRB activity, as observed in other environments, such as saltmarsh sediments. Low temperature did not appear to hinder FeRB abundance in alkaline tailings. Finally, despite evidence that SRB populations were active at both sites, the |S isotopic composition of the AVS and CRS fractions were not representative of biogenic sulfides, indicating that the overall S-isotope signature of mine tailings is more representative of abiotic sulfides originating from the ore body.  相似文献   

4.
The rate of palagonitization of three chemically different types of basaltic glasses has been determined experimentally as a function of temperature (20–90 ° C) and time (3.5–14 months) in both fresh and saline water. Between ca. 40 ° C and 70 ° C there is a marked increase in the rate of transformation of the glasses, especially those of alkali basalt composition. The alteration process also accelerates after ca. 10 months at temperature higher than 70 ° C. These phenomena are possibly related to stepwise losses of the major elements, and minimum activation temperatures for the oxide/ion—water metasomatism.  相似文献   

5.
The use of renewable energy can be enhanced by utilising groundwater reservoirs for heating and cooling purposes. The urbanisation effect on the peak heating and peak cooling capacity of groundwater in a cold groundwater region was investigated. Groundwater temperatures were measured and energy potentials calculated from three partly urbanised aquifers situated between the latitudes of 60° 25′N and 60° 59′N in Finland. The average groundwater temperature below the zone of seasonal temperature fluctuations was 3–4 °C higher in the city centres than in the rural areas. The study demonstrated that due to warmer groundwater, approximately 50–60 % more peak heating power could be utilized from populated areas compared with rural areas. In contrast, approximately 40–50 % less peak cooling power could be utilised. Urbanisation significantly increases the possibility of utilising local heat energy from groundwater within a wider region of naturally cold groundwater. Despite the warming in urban areas, groundwater still remains attractive as a source of cooling energy. More research is needed in order to determine the long-term energy capacity of groundwater, i.e. the design power, in urbanised areas of cold regions.  相似文献   

6.
The Laguna Lagunillas basin in the arid Andes of northern Chile exhibits a shallow aquifer and is exposed to extreme air temperature variations from 20 to ?25 °C. Between 1991 and 2012, groundwater levels in the Pampa Lagunillas aquifer fell from near-surface to ~15 m below ground level (bgl) due to severe overexploitation. In the same period, local mean monthly minimum temperatures started a declining trend, dropping by 3–8 °C relative to a nearby reference station. Meanwhile, mean monthly maximum summer temperatures shifted abruptly upwards by 2.7 °C on average in around 1996. The observed air temperature downturns and upturns are in accordance with detected anomalies in land-surface temperature imagery. Two major factors may be causing the local climate change. One is related to a water-table decline below the evaporative energy potential extinction depth of ~2 m bgl, which causes an up-heating of the bare soil surface and, in turn, influences the lower atmosphere. At the same time, the removal of near-surface groundwater reduces the thermal conductivity of the upper sedimentary layer, which consequently diminishes the heat exchange between the aquifer (constant heat source of ~10 °C) and the lower atmosphere during nights, leading to a severe dropping of minimum air temperatures. The observed critical water-level drawdown was 2–3 m bgl. Future and existing water-production projects in arid high Andean basins with shallow groundwater should avoid a decline of near-surface groundwater below 2 m bgl and take groundwater-climate interactions into account when identifying and monitoring potential environmental impacts.  相似文献   

7.
Fluid inclusion studies in combination with hydrogen, oxygen and sulphur isotope data provide novel insights into the genesis of giant amethyst-bearing geodes in Early Cretaceous Paraná continental flood basalts at Amestita do Sul, Brazil. Monophase liquid inclusions in colourless quartz, amethyst, calcite, barite and gypsum were analysed by microthermometry after stimulating bubble nucleation using single femtosecond laser pulses. The salinity of the fluid inclusions was determined from ice-melting temperatures and a combination of prograde and retrograde homogenisation temperatures via the density maximum of the aqueous solutions. Four mineralisation stages are distinguished. In stage I, celadonite, chalcedony and pyrite formed under reducing conditions in a thermally stable environment. Low δ34SV-CDT values of pyrite (?25 to ?32?‰) suggest biogenic sulphate reduction by organotrophic bacteria. During the subsequent stages II (amethyst, goethite and anhydrite), III (early subhedral calcite) and IV (barite, late subhedral calcite and gypsum), the oxidation state of the fluid changed towards more oxidising conditions and microbial sulphate reduction ceased. Three distinct modes of fluid salinities around 5.3, 3.4 and 0.3 wt% NaCl-equivalent characterise the mineralisation stages II, III and IV, respectively. The salinity of the stage I fluid is unknown due to lack of fluid inclusions. Variation in homogenisation temperatures and in δ18O values of amethyst show evidence of repeated pulses of ascending hydrothermal fluids of up to 80–90 °C infiltrating a basaltic host rock of less than 45 °C. Colourless quartz and amethyst formed at temperatures between 40 and 80 °C, while the different calcite generations and late gypsum precipitated at temperatures below 45 °C. Calculated oxygen isotope composition of the amethyst-precipitating fluid in combination with δD values of amethyst-hosted fluid inclusions (?59 to ?51?‰) show a significant 18O-shift from the meteoric water line. This 18O-shift, high salinities of the fluid inclusions with chloride-sulphate composition, and high δ34S values of anhydrite and barite (7.5 to 9.9?‰) suggest that sedimentary brines from deeper parts of the Guaraní aquifer system must have been responsible for the amethyst mineralisation.  相似文献   

8.
Sandstone alterations triggered by fire-related temperatures   总被引：1，自引：1，他引：0  
The aim of the study was to identify and describe changes in two different sandstone types when undergoing different environmental and extreme temperature regimes to assess the possibility of finding insolation weathering and how these sandstones would behave during and after a fire. The first step was the simulation in the laboratory of temperature regimes up to 60 °C which would correspond to extreme events that could be found in insolation cycles even in Central Europe and the second one was the temperature above 200 °C simulating in laboratory conditions the thermal regime of a potential fire situation at temperatures up to 200, 400, 600 and 800 °C. Heating the samples above 400 °C led to gradual changes in mineral composition, colour, surface roughness and physical properties reaching, eventually, total rock breakdown through spalling and granular disaggregation. The different behaviour of sandstones exposed to high temperatures is mainly caused by their different mineral composition with various ratios of minerals that are more or less chemically stable at high temperatures as well as by the differences in the porosity.  相似文献   

9.
The Cuatrociénegas area is useful for the investigation of the effect of groundwater extraction in the Chihuahuan freshwater xeric ecoregion. It has been investigated at this time using a selection of geochemical indicators (major, minor and trace elements) and δ34S data, to characterize the origin of groundwater, the main geochemical processes and the mineral/groundwater interactions controlling the baseline geochemistry. The area is composed of limestones of Mesozoic age, with a composite thickness of about 500 m, overlaid by basin fill (poorly consolidated young sediments). Substantial water extraction and modification of natural discharges from the area along the last century have produced a detrimental impact on ecosystem structure and function. Water–rock interactions, mixing and evaporative processes dominate the baseline groundwater quality. Natural recharge is HCO3–Ca type in equilibrium with calcite, low salinity (TDS?<?500 mg/L), Cl? lower than 11 mg/L and average Li+ concentration of 0.005 mg/L. Along the groundwater flow systems, δ34S evidence and mass transfer calculations indicate that Cretaceous gypsum dissolution and dedolomitization reactions adjust water composition to the SO4–Ca type. The increase of water–rock interaction is reflected by Cl? values increase (average 68 mg/L), TDS up to about 1500 mg/L and an average Li+ concentration of 0.063 mg/L. Calculations with chemical geothermometers indicate that temperature at depth could be at maximum of 15–20 °C higher than field-measured temperature for pozas. After groundwater is discharged to the surface, chemical evolution continues; water evaporation, CO2 degassing and precipitation of minerals such as gypsum, calcite and kaolinite represent the final processes and reactions controlling water chemical composition.  相似文献   

10.
《Geochimica et cosmochimica acta》1999,63(19-20):3247-3259
The rate of Si release from dissolving bytownite feldspar in abiotic batch reactors increased as temperatures increased from 5° to 35°C. Metabolically inert subsurface bacteria (bacteria in solution with no organic substrate) had no apparent effect on dissolution rates over this temperature range. When glucose was added to the microbial cultures, the bacteria responded by producing gluconic acid, which catalyzed the dissolution reaction by both proton- and ligand-promoted mechanisms. The metabolic production, excretion, and consumption of gluconic acid in the course of glucose oxidation, and therefore, the degree of microbial enhancement of mineral dissolution, depend on temperature. There was little accumulation of gluconic acid and therefore, no significant enhancement of mineral dissolution rates at 35°C compared to the abiotic controls. At 20°C, gluconate accumulated in the experimental solutions only at the beginning of the experiment and led to a twofold increase in dissolved Si release compared to the controls, primarily by the ligand-promoted dissolution mechanism. There was significant accumulation of gluconic acid in the 5°C experiment, which is reflected in a significant reduction in pH, leading to 20-fold increase in Si release, primarily attributable to the proton-promoted dissolution mechanism. These results indicate that bacteria and microbial metabolism can affect mineral dissolution rates in organic-rich, nutrient-poor environments; the impact of microbial metabolism on aluminum silicate dissolution rates may be greater at lower rather than at higher temperatures due to the metabolic accumulation of dissolution-enhancing protons and ligands in solution.  相似文献   

11.
Annual abstraction of 2.6?×?109 m3 of groundwater in the 53,000 km2 Konya Closed Basin of central Turkey has caused a head decline of 1 m/year over the last few decades. Therefore, understanding the hydrogeology of this large endorheic basin, in a semi-arid climate, is important to sustainable resource management. For this purpose, the groundwater’s radiocarbon age distribution has been investigated along a 150-km transect parallel to regional flow. Results show that the groundwater ranges in age from Recent at the main recharge area of the Taurus Mountains in the south, to about 40,000 years around the terminal Salt Lake located in the north. In this predominantly confined flow system, radiocarbon ages increase linearly by distance from the main recharge area and are in agreement with the hydraulic ages. The mean velocity of regional groundwater flow (3 m/year) is determined by the rate of regional groundwater discharge into the Salt Lake. Calcite dissolution, dedolomitization and geogenic carbon dioxide influx appear to be the dominant geochemical processes that determine the carbon isotope composition along the regional flow path. The groundwater’s oxygen-18 content indicates more humid and cooler paleorecharge. A maximum drop of 5°C is inferred for the past recharge temperature.  相似文献   

12.
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.  相似文献   

13.
Groundwater at the Azores archipelago is a strategic resource for the freshwater supply. Freshwater, mineral and thermal water discharges occur in the archipelago, and especially at the Fogo and Furnas volcanoes (São Miguel). These discharges provide data for case studies of groundwater chemistry from volcanic monitoring due to the stable composition of the sampled waters. The mineral and thermal discharges are mainly of sodium bicarbonate types and present a large range of temperatures, from cold springs to waters at about 90 °C. Some boiling discharges have a sulfate-dominated composition, suggesting a steam-heating mechanism. Geochemical studies on these mineral and thermal waters began in the 19th century. Data gathered since these earlier studies provide a baseline for pH, temperature, CO2 and major-element composition. Weekly measurements of pH and temperature also denote a rather stable behavior.  相似文献   

14.
A set of experiments have been performed on volcanic materials from Etna, Stromboli and Vesuvius in order to evaluate how the exposure to thermal and redox conditions close to that of active craters affects the texture and composition of juvenile pyroclasts. Selected samples were placed within a quartz tube, in presence of air or under vacuum, and kept at T between 700 and 1,130 °C, for variable time (40 min to 12 h). Results show that reheating reactivates the melt, which, through processes of chemical and thermal diffusion, reaches new equilibrium conditions. In all the experiments performed at T = 700–750 °C, a large number of crystal nuclei and spherulites grows in the groundmass, suggesting conditions of high undercooling. This process creates textural heterogeneities at the scale of few microns but only limited changes of groundmass composition, which remains clustered around that of the natural glasses. Reheating at T = 1,000–1,050 °C promotes massive groundmass crystallization, with a different mineral assemblage as a function of the redox conditions. Morphological modifications of clasts, from softening to sintering as temperature increases, occur under these conditions, accompanied by progressive smoothing of external surfaces, and a reduction in size and abundance of vesicles, until the complete obliteration of the pre-existing vesicularity. The transition from sintering to welding, characteristic of high temperature, is influenced by redox conditions. Experiments at T = 1,100–1,130 °C and under vacuum produce groundmass textures and glass compositions similar to that of the respective starting material. Collapse and welding of the clasts cause significant densification of the whole charge. At the same temperature, but in presence of air, experimental products at least result sintered and show holocrystalline groundmass. In all experiments, sublimates grow on the external surfaces of the clasts or form a lining on the bubble walls. Their shape and composition is a function of temperature and fO2 and the abundance of sublimates shows a peak at 1,000 °C. The identification of the features recorded by pyroclasts during complex heating–cooling cycles allows reconstructing the complete clasts history before their final emplacement, during weakly explosive volcanic activity. This has a strong implication on the characterization of primary juvenile material and on the interpretation of eruption dynamics.  相似文献   

15.
Environmental protection has mentioned the need to cut out all of fuels sulfur compounds. One of the most important processes that affect sulfur removal in atmospheric condition is the interaction of liquid fuels with solid sulfur removal adsorbents such as zeolites. To investigate the nano-AgX-zeolite efficiency for the sulfur adsorption process, a set of experimental tests was arranged and conducted by Box–Behnken design software, in an adsorption laboratory setup. The selected variables comprised metal percent, adsorption temperature and calcination temperature. The parameter levels were 0.5–10 %, 30–120 and 200–500 °C, respectively. The experiment results were used to find the statistical model. The results demonstrate that the sulfur concentration level is 48.36 ppm in the last product at 83 °C for adsorption temperature, 5.53 % for metal percent and 436 °C for calcination temperature in constant pH and constant process time.  相似文献   

16.
This study focused on typical injection layers of deep saline aquifers in the Shiqianfeng Formation used in the Carbon Capture and Sequestration Demonstration Projects in the Ordos Basin, Northwest China. The study employed experiments and numerical simulations to investigate the mechanism of CO2 mineral sequestration in these deep saline aquifers. The experimental results showed that the dissolved minerals are plagioclase, hematite, illite–smectite mixed layer clay and illite, whereas the precipitated minerals are quartz (at 55, and 70 °C) and kaolinite (at 70 °C). There are rare carbonate mineral precipitations at the experimental time scale, while the precipitation of quartz as a product of the dissolution of silicate minerals and some intermediate minerals rich in K and Mg that transform to clay minerals, reveals the possibility of carbonate precipitation at the longer time scale. These results are consistent with some results previously reported in the literature. We calibrated the kinetic parameters of mineral dissolution and precipitation by these experimental results and then simulated the CO2 mineral sequestration under deep saline aquifer conditions. The simulation results showed that the dissolved minerals are albite, anorthite and minor hematite, whereas the precipitated minerals are calcite, kaolinite and smectite at 55 and 70 °C. The geochemical reaction of illite is more complex. At 55 °C, illite is dissolved at the relatively lag time and transformed to dawsonite; at 70 °C, illite is precipitated in the early reaction period and then transformed to kaolinite. Based on this research, sequestrated CO2 minerals, which are mainly related to the temperature of deep saline aquifers in Shiqianfeng Fm., are calcite and dawsonite at lower temperature, and calcite at higher temperature. The simulation results also establish that calcite could precipitate over a time scale of thousands of years, and the higher the temperature the sooner such a process would occur due to increased reaction rates. These characteristics are conducive, not only to the earlier occurrence of mineral sequestration, but also increase the sequestration capacity of the same mineral components. For a sequestration period of 10,000 years, we determined that the mineral sequestration capacity is 0.786 kg/m3 at 55 °C, and 2.180 kg/m3 at 70 °C. Furthermore, the occurrence of mineral sequestration indirectly increases the solubility of CO2 in the early reaction period, but this decreases with the increase in temperature.  相似文献   

17.
Northeastern Morocco is characterised by a large number of surface geothermal manifestations. Thermal waters are hosted within sedimentary rocks, and in particular the Liassic dolomitic limestones act as a reservoir. The presence of geothermal waters is closely related to important fault systems. Meteoric water infiltrates along those fractures and faults, gets heated, and then returns to the surface through hydrothermal conduits. Most of the thermal waters are of Na–Cl and Ca–Mg–HCO3 types. In this paper different geochemical approaches were applied to infer the reservoir temperature. Na–K–Mg1/2 ternary diagram points to temperatures ranging from 100 to 180 °C. Cation geothermometers suggest an average reservoir temperature of about 100 °C. Mineral solution equilibria analysis yields temperatures ranging from 50 to 185 °C. The silica enthalpy mixture model gives an average value (about 110 °C) higher than that inferred from cation geothermometers.  相似文献   

18.
Irrigation with diluted seawater would be an alternative water resource which can play an important role under scarce resources of freshwater for promoting agricultural production in coastal areas. Salvadora persica Linn. was irrigated with different concentrations of seawater (0, 10, 20, 40, 60, 80 and 100 % seawater), and their effect on plant growth, nutrient contents in soil and plants, shift in soil microbial community structure (phospholipid fatty acid; PLFA) and community-level physiological profiling (CLPP, Biolog ECO MicroPlate) were studied. Plant dry matter was significantly increased with all seawater treatments, and highest increase was at 20 % seawater treatment. Sodium and chloride contents were significantly increased, whereas ratios of K/Na and Ca/Na were significantly decreased in plants with seawater irrigation. Soil electrical conductivity (EC), available K and Na were significantly increased with increasing the concentration of seawater. Total PLFA concentration and PLFA profile of soils were used as indices of total microbial biomass and community composition, respectively. The concentrations of total PLFA, gram-positive, gram-negative and actinomycetes biomarker PLFAs were significantly reduced at 20, 40, 80 and 40 % concentrations of seawater, respectively. The application of different concentrations of seawater induced a clear shift in the soil microbial community structure toward the bacterial abundance. The microbial community structure and community-level physiological profiling in seawater irrigation treatments had significantly differentiated. It can be concluded that irrigation with different concentrations of seawater had significant impact on soil chemical and microbial properties which is attributed due to the salinity stress.  相似文献   

19.
This study investigated the thermal regime of shallow groundwater in the Turin area (NW Italy), where the large energy demand has motivated a new interest for renewable sources, such as the use of ground-source heat pumps for domestic heating and cooling. The vertical variability of the groundwater temperature between the ground surface and 10–20 m was detected: deeper temperatures were higher than shallow temperatures in spring, while a decrease with depth occurred in autumn. These variations are connected with the heating and cooling cycles of the ground surface due to the seasonal temperature oscillation. Variations below the seasonal oscillation are likely to be connected with the presence of advective heat transport due to the groundwater flow, according to the hydraulic features of a shallow aquifer. Temperature values mostly ranged between 12 and 14 °C in rural areas, while the values were between 14 and 16 °C below the Turin city. This groundwater warming is attributed to a widespread urban heat island phenomenon linked to warmer land surface temperatures in Turin city. Sparse warm outliers are connected with point heat sources and site-specific conditions of land and subsurface use, which may cause the aquifer temperature to rise. A relatively stable temperature below the seasonal fluctuation zone combined with high productivity and legislated limits for deeper groundwater use represent favourable conditions for a large-scale diffusion of groundwater heat pumps within the shallow aquifer. Moreover, this heat surplus should be regarded as a resource for future geothermal installations.  相似文献   

20.
Stromatolites forming today on a small scale in hydrothermal environments are chemical and biological analogues of much larger Precambrian formations. Carbon isotopic composition varied as a function of CO2 concentration, pH, and species composition. Stratiform, layered stromatolites grew in silica-depositing springs at 55° to 70°C; they consisted mainly of a unicellular alga, Synechococcus, and a filamentous, photosynthetic bacterium, Chloroflexus. These thermophiles become enriched in 12C as the concentration of carbon dioxide in the effluent waters increases. At a concentration of 40 ppm total inorganic C, and δ13C of organic carbon was ～ ?12%., whereas at 900 ppm total inorganic C, the δ13C of similar species was ～ ?25%.. Conical stromatolites or conophytons (principally a filamentous, blue-green alga Phormidium and Chloroflexus) grew at 40°-55°C. In older, broader conophytons, Chloroflexus was the dominant organism. Their δ13C values were ～ ?18%. in a variety of hot springs. In carbonate-depositing springs, i.e., carbon dioxide saturated, conophytons and stromatolites consisting of a variety of blue-green algae and photosynthetic bacteria had the most negative δ13C values (to ?30%.). These carbon isotope ratios are directly comparable to carbon isotope ratios of kerogen from Precambrian stromatolites. The presence and activity of methanogenic bacteria or heterotrophic, aerobic and anaerobic bacteria did not alter significantly the δ13C of the original organic matter.The hydrogen isotopic fractionation between thermophilic organisms and water is 0 to ?74 for temperatures of 85° to 46°C, respectively. Acidophilic algae fractionated hydrogen isotopes to a lesser extent than did the photosynthetic organisms inhabiting neutral pH springs. Because organic matter retains some of its original isotopic signature, relationships of CO2 levels, pH, temperature, and species composition between modern stromatolites and their environment and those of the Precambrian can be inferred.  相似文献   

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