Origin and history of hydrothermal fluids of the Reykjanes and Krafla geothermal fields,Iceland

The Reykjanes and Krafla geothermal fields are both examples of active high temperature systems and show similar assemblages of alteration minerals, but the fluid at Reykjanes is dominantly sea water whereas that at Krafla is meteoric. Oxygen isotope analyses of surface rock and of drill chip samples from different depths are presented, together with results for the Krafla fluid, which is close to local precipitation (δ ¹⁸ O = ?11.9‰, δD= ?86.8‰). Calcite in both systems is apparently in equilibrium with the present deep fluid at the present field temperature, except for the upper 250 m at Reykjanes where the fluid may be more meteoric than at depth. Feldspar gives similar results. Quartz separates at Reykjanes are anomalously lighter than coexisting feldspar and give exceptionally high quartz-fluid temperatures. It is suggested that quartz originally grew when the fluid was more nearly meteoric (? glacial period) and has not re-equilibrated. Bulk-rock ¹⁸ O depletion supports this interpretation of the history of the Reykjanes system. Quartz in the Krafla system is mostly in equilibrium at the present field conditions but anomalies occur near the boundary between the upper and lower parts of the system, suggesting that this is not entirely stable. A high fluid:rock ratio (10–100 minimum) is indicated for the Krafla field.     

Composition of geothermal minerals from saline and dilute fluids — Krafla and Reykjanes, Iceland

In high temperature geothermal areas (T.200°C) in Iceland the alteration minerals formed show a regular zoning with increasing temperature i.e. smectite, chlorite, epidote and actinolite. To test the effect of varying composition of the hydrothermal circulation fluid drillhole chips from two contrasting areas were analyzed in detail. The Reykjanes area is fed with sea water while Krafla is fed with meteoric water and has a Cl⁻ concentration of 28 ppm. Both areas have tholeiitic basalts, lavas and hyaloclastites as original reservoir rocks.

Although both systems have the same sequence of alteration minerals the actual composition of the minerals differs between systems reflecting the different chemical composition of the circulating waters. In Reykjanes, with its brine fluid, the composition of the original rock appears not to affect the composition of the alteration minerals while the reverse appears to be the case in Krafla.     

The geochemistry of trace elements in geothermal fluids,Iceland

Trace element geochemistry was studied in geothermal fluids in Iceland. The major and trace element compositions of hot springs, sub-boiling, and two-phase (liquid and vapor) wells from 10 geothermal areas were used to reconstruct the fluid composition in the aquifers at depth. Aquifer fluid temperatures ranged from 4 to 300 °C, pH values between 4.5 and 9.3, and fluids typically contained total dissolved solids <1000 ppm, except in geothermal areas that have seawater and seawater-meteoric water mixtures. Trace alkali elements Li, Rb and Cs are among the most mobile elements in aquifer fluids, with concentrations in the range of <1 ppb to 3.49 ppm Li, <0.01 to 57 ppb Cs, and <1 ppb to 3.77 ppm Rb. Their chemistry is thought to be dominated by rock leaching and partitioning into Na- and K-containing major alteration minerals. Arsenic, Sb, Mo and W are typically present in concentrations in the range of 1–100 ppb. They are relatively mobile, yet Mo may be limited by molybdenite solubility. The alkaline earth elements Ba and Sr are quite immobile with concentrations in the range of <0.1–10 ppb Ba and <1–100 ppb Sr in the dilute fluids, but up to 5.9 ppm Ba and 8.2 ppm Sr in saline fluids. These elements show a systematic relationship with Ca, possibly due to substitution for Ca in Ca-containing major alteration minerals like calcite, epidote and anhydrite. Incorporation into major Ca-minerals may also be important for Mn. Many metals including Fe, Cr, Ni, Zn, Cu, Co, Pb and Ag have low mobility and concentrations, typically <1 ppb for Ag, Cd, Co, Cr, Cu, Ni, and Pb, <10 ppb for Zn and < 100 ppb for Fe, although for some metals higher concentrations are associated with saline fluids. Based on the metals assessed, saturation is approached with respect to many sulfide minerals and in some cases oxide minerals but Cu, Ni and Pb minerals are slightly but systematically undersaturated, and Ag phases significantly undersaturated. Evaluation of mineral-fluid equilibria for these metals is problematic due to their low concentrations, problems associated with assessing the aqueous species distribution by thermodynamic calculations, and uncertainties concerning the exact minerals possibly involved in such reactions. Reaction path calculations, poor comparison of concentrations measured in the samples collected at the wellhead and published downhole data as well as boiling, cooling and mass precipitation calculations suggest removal of many metals due to changes upon depressurization boiling and conductive cooling of the aquifer fluids as they ascend in wells. These results imply that processes such as mass precipitation upon fluid ascent may be highly important and emphasize the importance of considering mass movement in geothermal systems.     

Gas pressures and redox reactions in geothermal fluids in Iceland

The gas and redox chemistry of 100–300 °C geothermal fluids in Iceland has been studied as a function of fluid temperature and fluid composition. The partial pressures of CO₂ in dilute (mCl<500 ppm) and saline (mCl>500 ppm) geothermal fluids above 200 °C are controlled by the mineral buffer clinozoisite+prehnite+calcite+quartz. Two buffers are considered to control the H₂S and H₂ partial pressures above 200 °C depending on fluid salinity, epidote+prehnite+pyrite+pyrrhotite for dilute fluids and pyrite+prehnite+quartz+magnetite+anhydrite+clinozoisite+quartz for saline fluids. Below 200 °C, the partial pressures of CO₂, H₂S and H₂ also seem to be buffered but other minerals must be involved. Zeolites are expected to replace prehnite and epidote. Redox potential calculated on the assumption of equilibrium for the H⁺/H₂ redox couple decreases in dilute geothermal fluids with increasing temperature from about −0.5 V at 100 °C to −0.8 V at 300 °C, whereas saline geothermal fluids at 250 °C display a redox potential of about −0.45 V. A systematic discrepancy between redox couples of about 0.05–0.09 V is observed in the redox potential for the dilute geothermal fluids, whereas redox potentials agree within 0.02–0.04 V for saline geothermal waters. The discrepancies in the calculated redox potential for dilute geothermal fluids are thought to be due to a general lack of equilibrium between CH₄, CO₂ and H₂ and between H₂S, SO₄ and H₂. It is, accordingly, concluded that an overall equilibrium among redox species has not been reached for dilute geothermal fluids whereas it appears to be more closely approached for the saline geothermal fluids. The latter conclusion is based on limited database and should be treated with care. Since the various redox components are not in an overall equilibrium in geothermal fluids in Iceland these fluids cannot be characterised by a unique hydrogen fugacity, oxygen fugacity or redox potential at a given temperature and pressure.     

Aquifer chemistry of four high-temperature geothermal systems in Iceland

The deep water feeding wet-steam wells in four high-temperature geothermal areas in Iceland have highly variable salinity as reflected in the chlorine concentrations which vary from 20 to 19000 ppm. Using available values for equilibrium constants, the activities of 26 chemical species involving the major components of the reservoir water have been calculated and quantitative evaluations of solute/ solute, mineral/solute chemical equilibria in these geothermal systems have been made.The unflashed reservoir water is just saturated with calcite. The saline geothermal waters, which represent heated sea-water, are just saturated with anhydrite, but the dilute waters, which are of meteoric origin, are somewhat undersaturated with this mineral. The fluoride mobility is thought to be limited by an ionic exchange reaction where F^? replaces some of the OH^? in the layered silicates. The pH of the unflashed reservoir water is governed by ionic exchange equilibrium in which all the major cations participitate. At a given temperature it seems likely that the activity of one cation fixes the activities of all the other major cations and hydrogen ion. If this is so and we take all the other chemical equilibria which have been demonstrated to exist for granted, it turns out that the major element composition of the unflashed high-temperature geothermal waters is controlled by two independent variables only. These variables are the temperature and the supply to the water of the incompatible element chlorine, incompatible indicating that this element is not incorporated in the geothermal minerals.     

西藏羊八井热田地热流体成因及演化的惰性气体制约栽

地热流体中惰性气体的相对丰度和同位素组成,不仅可以揭露热田的热源性质,而且还能够揭示深、浅层地热流体的内在联系和演化过程等.在西藏羊八井热田的地热气体中,已检测出大量的4He组分,3He/4He值是大气的0.087～0.259倍,表明深部地壳物质的局部熔融为热田提供能量.浅层地热流体的3He/4He值自西北向东南呈降低趋势,与热储温度的变化相一致,反映出侧向运移时补充了更多的壳源氦.热田北区深层地热流体具有稍高的3He/4He值,是浅层地热流体的母源.气体中氪和氙的相对丰度具有大气降水成因的特征.结合现有的实际资料,建立了热田地热流体的概念模型.     

Helium isotopes in geothermal systems: Iceland,The Geysers,Raft River and Steamboat Springs

Helium isotope ratios have been measured in geothermal fluids from Iceland, The Geysers, Raft River, Steamboat Springs and Hawaii. These ratios have been interpreted in terms of the processes which supply He in distinct isotopic ratios (i.e. magmatic He, ~10 R_a; atmospheric He, R_a; and crustal He, ~0.1 R_a) and in terms of the processes which can alter the isotopic ratio (hydrologic mixing, U-Th series alpha production and weathering release of crustal He, magma aging and tritiugenic addition of ³He). Using this interpretational scheme, Iceland is found to be an area of hot-spot magmatic He implying an active volcanic source although the data are suggestive of high-temperature weathering release of crustal He incorporated in the geothermal fluids. By comparison to fumarolic gases from Hawaii and Juan De Fuca and Cayman Trench basaltic glass samples, The Geysers contains MOR type magmatic He again implying an active volcanic source possibly a “leaky” transform related to the San Andreas Fault System. Raft River contains only crustal He indicating no active volcanic sources. Steamboat Springs He isotope ratios are distinctly less than typical plate margin volcanics but must still have a magmatic source. A preliminary assessment of the cause for this low ratio is made assuming an “aging” magma source.     

Surface effects of triggered fault slip on Reykjanes Peninsula, SW Iceland

Three large earthquakes (M_w>4.5) were triggered within 5 min, 85 km west of a M_w 6.5 earthquake in the South Iceland Seismic Zone (SISZ). We report on surface effects of these triggered earthquakes, which include fresh rupture, widespread rockfall, disrupted rockslides and block slides. Field data confirm that the earthquakes occurred along N-striking right-lateral strike-slip faults. Field data also support the conclusion from modeling of InSAR data that deformation from the second triggered event was more significant than for the other two. A major hydrological effect was the draining of water through an open fissure on a lake bed, lowering the lake level by greater than 4 m. Field relationships suggest that a component of aseismic slip could have been facilitated by water draining into the fault zone.     

Application of radium isotopes to determine crustal residence times of hydrothermal fluids from two sites on the Reykjanes Peninsula, Iceland

Radium isotopes were used to determine the crustal residence times of hydrothermal fluids from two geothermal wells (Svartsengi and Reykjanes) from the Reykjanes Peninsula, Iceland. The availability of rock samples from the subsurface (to depths of 2400 m) allowed direct comparison of the radium isotopic characteristics of the fluids with those of the rocks within the high temperature and pressure reaction zone. The ²²⁶Ra activity of the Svartsengi fluid was ∼one-fourth of the Reykjanes fluid and the ²²⁸Ra/²²⁶Ra ratio of the Svartsengi fluid was ∼twice that of Reykjanes. The fluid isotopic characteristics were relatively stable for both sites over the 6 years (2000-2006) of the study. It was determined, using a model that predicts the evolution of the fluid ²²⁸Ra/²²⁶Ra ratio with time, that both sites had fluid residence times, from the onset of high temperature water-rock reaction, of less than 5 years. Measurement of the short-lived ²²⁴Ra and ²²³Ra allowed estimation of the recoil input parameter used in the model. The derived timescale is consistent with results from similar studies of fluids from submarine systems, and has implications for the use of terrestrial systems in Iceland as an exploited energy resource.     

西藏羊八井热田地热流体成因及演化的惰性气体制约

地热流体中惰性气体的相对丰度和同位素组成，不仅可以揭露热田的热源性质，而且还能够揭示深，浅层地热流体的内在联系和演化过程等。在西藏羊八井热田的地热气体中，已检测出大量的^4He组分，3He/^4He值是大气的0．087－0．259倍，表明深部地壳物质的局部熔融为热田提供能量，浅层地热流体的3He/4He 值自西北向东南呈降低趋势，与热储温度的变化相一致，反映出侧向运移时补充了更多的壳源氦，热田北区深层地热流体具有稍高的3He/4He值，是浅层地热流体的母源，气体中氪和氙的相对丰度具有大气降水成因的特征，结合现有的实际资料，建立了热田地热流体的概念模型。     

Sulfur isotope systematics in icelandic geothermal systems and influence of seawater circulation at Reykjanes

Pyrite from altered basalts from Nàmafjall and Krafla high-temperature fields and deep zones at Reykir, Leira and other low-temperature fields, and aqueous sulfides from Nàmafjall, have δ³⁴S values of 0 to 2.6%. These values are close to those for postglacial basaltic lavas from the Reykjanes Peninsula. The major source of sulfur in these meteoric hydrothermal systems is the upper-mantle or basalt. At the low-temperature fields, however, the δ³⁴S values of sulfide decrease with decreasing depth, suggesting the presence of a light sulfur source in the shallower aquifers.In contrast, in the Reykjanes and Svartsengi geothermal fields, where seawater contributes to the hydrothermal systems, sulfide sulfur is distinctly enriched in ³⁴S at all depths except for one Reykjanes pyrite from 84 m depth. The enrichment is about 8%. at the deepest core (1734 m) of Reykjanes and decreases with decreasing depth. These enrichments are most likely due to seawater sulfate being involved in the hydrothermal systems. However, in the Reykjanes fluid, dissolved heavy sulfates are not in isotopic equilibrium with sulfide. Disequilibrium between sulfate and sulfide is also demonstrated in all other Icelandic geothermal systems studied.     

Erosional effects on terrestrial resources over the last millennium in Reykjanes, southwest Iceland

The study presents the effect of soil erosion on vegetation, soil accumulation (SA), SA rate (SAR), soil quality, soil mass, and the soil organic carbon (SOC) pool in Brown Andosols and Histosols in a 24-km² area in southwest Iceland. Undisturbed prehistoric soils were distinguished from disturbed historic soils using tephrochronology. Soil erosion has been severe during historic time (last 1135 yr), resulting in the increase of the soil mass deposited in soils covered by vegetation by a factor of 7.3-9.2 and net loss of soil in unvegetated areas. The SAR correlated positively with SOC sequestration. SOC is easily transported and, given the extensive accumulation of soil, the net effect of burial and subsequent reduction in decomposition is to increase SOC storage. Nevertheless, the increased accumulation and soil depletion has decreased soil quality, including the SOC, and reduced soil resistance to erosion with the depleted SOC contributing to enrichment of atmospheric CO₂. The initial terrestrial disturbance was triggered by anthropogenic land use during the Medieval Warm Period, followed by volcanic activity approximately three centuries later. The combination of harsh climate during the Little Ice Age and drastic anthropogenic perturbations has led to land degradation at a catastrophic scale.     

CO2 emissions and heat flow through soil,fumaroles, and steam heated mud pools at the Reykjanes geothermal area,SW Iceland

Carbon dioxide emissions and heat flow through soil, steam vents and fractures, and steam heated mud pools were determined in the Reykjanes geothermal area, SW Iceland. Soil diffuse degassing of CO₂ was quantified by soil flux measurements on a 600 m by 375 m rectangular grid using a portable closed chamber soil flux meter and the resulting data were analyzed by both a graphical statistical method and sequential Gaussian simulations. The soil temperature was measured in each node of the grid and used to evaluate the heat flow. The heat flow data were also analyzed by sequential Gaussian simulations. Heat flow from steam vents and fractures was determined by quantifying the amount of steam emitted from the vents by direct measurements of steam flow rate. The heat loss from the steam heated mud pools was determined by quantifying the rate of heat loss from the pools by evaporation, convection, and radiation. The steam flow rate into the pools was calculated from the observed heat loss from the pools, assuming that steam flow was the only mechanism of heat transport into the pool. The CO₂ emissions from the steam vents and mud pools were determined by multiplying the steam flow rate from the respective sources by the representative CO₂ concentration of steam in the Reykjanes area. The observed rates of CO₂ emissions through soil, steam vents, and steam heated mud pools amounted to 13.5 ± 1.7, 0.23 ± 0.05, and 0.13 ± 0.03 tons per day, respectively. The heat flow through soil, steam vents, and mud pools was 16.9 ± 1.4, 2.2 ± 0.4, and 1.2  ± 0.1 MW, respectively. Heat loss from the geothermal reservoir, inferred from the CO₂ emissions through the soil amounts to 130 ± 16 MW of thermal energy. The discrepancy between the observed heat loss and the heat loss inferred from the CO₂ emissions is attributed to steam condensation in the subsurface due to interactions with cold ground water. These results demonstrate that soil diffuse degassing can be a more reliable proxy for heat loss from geothermal systems than soil temperatures. The soil diffuse degassing at Reykjanes appears to be strongly controlled by the local tectonics. The observed diffuse degassing defines 3–5 elongated N–S trending zones (000–020°). The orientation of the diffuse degassing structures at Reykjanes is consistent with reported trends of right lateral strike slip faults in the area. The natural CO₂ emissions from Reykjanes under the current low-production conditions are about 16% of the expected emissions from a 100 MWe power plant, which has recently been commissioned at Reykjanes.     

Historic magmatism on the Reykjanes Peninsula,Iceland: a snap-shot of melt generation at a ridge segment

We present new compositional data on a suite of historic lava flows from the Reykjanes Peninsula, Iceland. They were erupted over a short time period between c. 940 and c. 1340 ad and provide a snap-shot view of melt generation and evolution processes beneath this onshore, 65 km long, ridge segment. The lavas are tholeiitic basalts (MgO 6.5–9.2 wt%) and sparsely (≪5%) olivine and/or plagioclase phyric (±trace clinopyroxene). Individual eruptive events show remarkable compositional homogeneity. Despite a limited variation in Sr–Nd isotope compositions, high-precision double-spike Pb isotope data show tight coherent arrays that, together with correlations with incompatible trace element ratios, indicate control by binary mixing processes. Poor correlations with elemental abundances require that this mixing took place prior to extensive fractional crystallisation. Olivines in the historic lavas have light δ¹⁸O values (+4.2 to +4.3‰), which is likely to be a feature of the enriched mantle source to Reykjanes Peninsula lavas. High precision Pb isotope analyses of other post-glacial Reykjanes Peninsula lavas show significant variability in ²⁰⁷Pb/²⁰⁴Pb and ²⁰⁸Pb/²⁰⁴Pb at lower ²⁰⁶Pb/²⁰⁴Pb values than in the historic lavas. This variation demonstrates that at least three compositionally distinct components within the mantle are required to explain the Pb isotope variations within the Reykjanes Peninsula as a whole. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Changing compositions in the Iceland plume; Isotopic and elemental constraints from the Paleogene Faroe flood basalts

Elemental and Sr, Nd, Hf and high precision Pb isotopic data are presented from 59 low-Ti and high-Ti lavas from the syn-break up part of the Faroe Flood Basalt Province. The depleted MORB-like low-Ti lavas erupted in the rift zone between the Faroe Islands and central East Greenland around the time of break up of the North Atlantic have isotopic end-member compositions different from the depleted Iceland lavas. We suggest that the main low-Ti mantle component is NAEM (North Atlantic End-Member (Ellam and Stuart, 2000, J. Petrol. 41, 919) and that the ²⁰⁷Pb/²⁰⁴Pb value of the component should be 15.35 and ε_Hf = + 16.5. NAEM is the main depleted component in the early Iceland plume. This is supported by high mantle potential temperatures (up to 1550 °C) calculated for the source of the low-Ti basalts. The unique mantle isotopic composition of NAEM with low ²⁰⁶Pb/²⁰⁴Pb (17.5) and Δ7/4Pb (? 3.8) precludes a derivation from recycled MORB lithosphere. Instead we suggest that NAEM represents a plume component of recycled depleted Archean lithospheric mantle that was further depleted ~ 500 Ma ago, possibly in connection with the recycling process. Two other isotopic end-members are required to explain the variation of the Faroe low-Ti basalts: (1) The Faroe depleted component (FDC), with ⁸⁷Sr/⁸⁶Sr = 0.7025, ε_Nd = + 11, ε_Hf = + 19.5, ²⁰⁶Pb/²⁰⁴Pb = 18.2, ²⁰⁷Pb/²⁰⁴Pb = 15.454 and ²⁰⁸Pb/²⁰⁴Pb = 37.75, which is similar in composition to some Atlantic MORB and is regarded as a local upper mantle source. (2) An enriched EM-type component similar in geochemistry to the Icelandic Öræfajökull lavas. This component is believed to be recycled pelagic sediments in the plume but it can alternatively be a local crustal or lithospheric mantle component. The enriched Faroe high-Ti lavas erupted inland from the rift have isotopic compositions very similar to the enriched Icelandic neo-volcanics and these lava suites apparently share the two enriched plume end-members IE1 and IE2 (Geochim. Cosmochim. Acta 68, 2, 2004). The lack of mixing between high and low-Ti melts at the time of break up, is explained by a zoned plume where only low-Ti sources were present beneath the rift zone surrounded by high-Ti sources on both sides of the rift. The enriched plume components in the high-Ti lava sequences on the Faroe Islands and central East Greenland changed rapidly on a ka-scale which implies, from geophysical modelling, that this area was positioned above the center of the plume, and that the Iceland plume was centered under the Atlantic ridge already from the Paleocene.     

Isotopic constraints on the genesis and age of autochthonous glaucony in the Oligo-Miocene Torquay Group, south-eastern Australia

The Oligo‐Miocene Torquay Group at Bird Rock in south‐eastern Australia comprises a sequence of fine‐grained skeletal carbonates and argillaceous and glauconitic sandstones, deposited in a cool‐water, mid‐shelf environment. The Bird Rock glaucony is autochthonous and consists predominantly of randomly interstratified glauconitic smectite, which constitutes bioclast infills and faecal pellet replacements. The results of Rb–Sr and oxygen isotopic analysis of samples taken from a single glauconitic horizon (the BW horizon) indicate that the glaucony developed through a series of simultaneous dissolution–crystallization reactions, which occurred during very early diagenesis in a closed or isochemical system, isolated from the ambient marine environment. The constituent ions of the glaucony were derived primarily from terrigenous clay minerals, but considerable potassium may have been sourced indirectly from sea water, through potassium enrichment of clay precursors. The pore fluids associated with glauconitization were marine derived, but progressively modified by the dissolution–crystallization of detrital clay minerals and autochthonous glaucony. Rb–Sr data for the BW horizon indicate that dating glauconies may be somewhat problematic, as co‐genetic glauconitic minerals can show a range of initial strontium compositions, which reflect the incorporation of strontium derived from mineralogical precursors and/or contemporaneous sea water. Rb–Sr isochrons indicate that the glaucony of the BW horizon formed at 23 ± 3 Ma. This age is in good agreement with both the established biostratigraphy and a ⁸⁷Sr/⁸⁶Sr age for the horizon (23 ± 1 Ma), but could only be determined using the independent age constraint and the estimate of the ⁸⁷Sr/⁸⁶Sr ratio of contemporaneous sea water provided by analysis of associated biogenic carbonate.     

Isotopic composition of noble gases in geothermal fluids of the Krušné Hory Mts., Czechoslovakia,and the nature of the local geothermal anomaly

The contents and isotopic composition of all noble gases in the fluids from two localities (Karlovy Vary and Franti?kovy Lázně) in Western Czechoslovakia are given. The data show: (1) atmospheric Ne, Ar, Kr and Xe, which indicates meteoric recharge; (2) excess He, attributed to radiogenic contributions; (3) a small excess of Ne, but the data shed no light on its origin. Even though there is no evidence of any juvenile component in these mineral waters, part of the dissolved He is believed to be of deep (mantle) origin.Correlation between the ratio ${}^3\text{He}{}^4$He and heat flow has been reported in the literature: our data enabled a direct test of this relationship and proved its fairly good validity. The combined interpretation of the heat flow and isotopic composition shows that the local heat flow anomaly in the Kru?né Hory graben is of deep origin and was produced by the mass outflow which occurred during the Alpine activation of the Bohemian Massif.     

北京市通州区地热流体水化学和同位素特征及其地热学意义

通过对北京市通州区蓟县系岩溶热储中地热流体的水化学组分、2H、18O、3H、14C、锶同位素组成的研究,论述了区域内地热系统中水的补给径流循环特征和地温分布特征。研究区内蓟县系热储中地热水的出水温度分布在35~91 ℃范围内,补给来源为北京市西北部或北部山区大气降水,平均补给高程为1510m。热储中地热水年龄和热储温度均呈现出明显的构造控制特点。通州区西部,大兴迭隆起构造单元内,热水年龄从西北（18ka）向东南（27ka）增加,运移速度约1.5m/a,热储温度从57.4 ℃增至86.5 ℃。东南部的夏垫断裂是一个导水导热断裂,其上地热水年龄减小至8.4ka,同时热储温度增至107.8 ℃。地热水中锶含量和锶同位素值均沿着地下水的径流方向增加,揭示了两个过程的叠加影响：蓟县系碳酸盐岩中锶的溶解与87Rb的衰减,后者呈现出明显的时间累积效应,在研究区东南部体现的更明显。     

北京市通州区地热流体水化学和同位素特征及其地热学意义

通过对北京市通州区蓟县系岩溶热储中地热流体的水化学组分、2H、18O、3H、14C、锶同位素组成的研究,论述了区域内地热系统中水的补给径流循环特征和地温分布特征.研究区内蓟县系热储中地热水的出水温度分布在35～91℃范围内,补给来源为北京市西北部或北部山区大气降水,平均补给高程为1510 m.热储中地热水年龄和热储温度...     

Br/Cl ratio,Zn and radon constraints on the origin and fate of geothermal fluids in the coastal region of southeastern China

Low-to-medium temperature geothermal fluids in the granite regions of southeastern China are an important renewable energy resource, but they are also a source of contamination containing highly toxic elements such as fluoride and arsenic. This study analyzed the origin of the geothermal fluids in a regional-scale hydrogeological unit in the city of Xiamen, China, based on isotope and hydrochemical analyses. The Br/Cl ratios suggested that the inland geothermal fluid is merely recharged by rainwater from the mountain edge, while the coastal geothermal fluid is originally recharged by the seawater and later mixed with rain-derived groundwater. The geothermal water featured high SiO₂ and detectable Zn concentrations. The former reflects the significant water–granite interaction along the flow path, and the latter indicates the active hydraulic connection between surface waters, shallow aquifers and deep geothermal fluids. High radon content was detected near the deep conductive fault adjacent to a geothermal well, demonstrating that the fault damage zone acts as a major conduit for upward transport of the deep geothermal fluid. As a result, the fault damage zones developed in the granite are necessary for the formation of geothermal water, which leads to the uneven distribution of geothermal water in the subsurface. High-temperature geothermal water can be found in those regions with fairly sparse fault damage zones. In contrast, in the region with high-density fault activities, the active communication between shallow cool water and deep geothermal fluids can decrease the water temperature.