Pseudosection analysis for talc-Na pyroxene-bearing piemontite-quartz schist in the Sanbagawa Belt, Japan

Abstract Various modes of occurrence of talc were identified in piemontite‐quartz schists collected from schist and eclogite units in the Kotsu area of the Sanbagawa Belt, eastern Shikoku, Japan. They can be classified into the following types: (A) matrix and (B) pull‐apart talc. The matrix talc is associated with aegirineaugite or glaucophane in the eclogite unit and with albite or chlorite in the schist unit. The pull‐apart talc is developed at the pull‐apart of microboudin structures of Na‐amphibole, along with albite or chlorite in samples from both units, suggesting that the pull‐apart talc was formed by Na‐amphibole consuming reactions in both units. The talc–aegirineaugite–phengite association is found in a thin layer (a few millimetres thick), with higher Na₂O/(Na₂O + Al₂O₃ + MgO) ratio in the ANM (Al₂O₃–Na₂O–MgO) diagram projected from phengite, epidote and other minerals, in the eclogite unit. Crystals of aegirineaugite have decreased jadeite content [= 100 × Al/(Na + Ca)] and increased aegirine content [= 100 × (Na – Al)/(Na + Ca)] from the core (ca Jd₄₀Aeg₄₀Di₂₀) to the rim (ca Jd₂₃Aeg₅₃Di₂₄), and are replaced by winchite and albite in varying degrees at the crystal margins. Na‐amphibole is glaucophane/crossite, commonly rimmed by Al‐poor crossite or winchite at the margin in the eclogite unit, although it is relatively homogeneous crossite in the schist unit. These textures suggest that the talc‐phengite‐(aegirineaugite or glaucophane) assemblage equilibrated during an early stage of metamorphism and the pull‐apart talc was formed at a later stage in the eclogite unit. A plausible petrogenetic grid in the NCKFe³⁺MASH system with excess piemontite (regarded as epidote), hematite, quartz and water, pseudosection analysis for the aegirineaugite‐bearing layer and the observed mineral assemblages suggest that the talc‐aegirineaugite‐phengite assemblage is stable under high pressure conditions (ca 560–580°C and 18–20 kbar). The pull‐apart talc was formed at ca 565–580°C and 9.5–10.5 kbar by the reaction of glaucophane/crossite + paragonite = talc + albite during the decompression stage, suggesting that the piemontite‐quartz schist in the eclogite unit experienced high‐pressure metamorphism at ca 50–60 km depth and was then exhumed to ca 30 km depth under nearly adiabatic conditions.     

Thermodynamic conditions of framework grain dissolution of clastic rocks and its application in Kela 2 gas field

Feldspar and clastic debris are the most important constituent framework grains of sedimentary clastic rocks and their chemical dissolution plays an essential role in the formation and evolution of the secondary pore in the reservoir rocks. On the basis of thermodynamic phase equilibrium, this study investigates the chemical equilibrium relationships between fluid and various plagioclase and K-feldspar in diagenesis of the sediments, particularly, the impact of temperature and fluid compositions (pH, activity of K+, Na+, Ca2+ and so on) on precipitation and dissolution equilibria of feldspars. Feldspar is extremely easily dissolved in the acid pore water with a low salinity when temperature decreases. The dissolution of anorthite end-member of plagioclase is related to the Ca content of the mineral and the fluid, higher Ca either in the mineral or in the fluid, easier dissolution of the feldspar. Moreover, the dissolution of albite end-member of plagioclase is related to Na of both the mineral and fluid,     

Experimental study on supercritical phenomena of WO_3 solubility in NaCl-H_2O system

The singular behavior of supercritical fluids was found more than one hundred years ago. In 1879, English scientists Hannay and Hogarth[1] firstly studied the properties of supercritical fluids collectively and discovered that ethanol and carbon tetrachlo…     

Viscosity and structural changes of albite (NaAlSi3O8) melt at high pressures

Viscosity of anhydrous albite melt, determined by the falling-sphere method in the solid-media, piston-cylinder apparatus, decreases with increasing pressure from 1.13 × 10⁵ P at 1 atm to 1.8 × 10⁴ P at 20 kbar at 1400°C. The rate of decrease in viscosity is larger between 12 and 15 kbar than in other pressure ranges examined. The density of the quenched albite melt increases with increasing pressure of quenching from 2.38 g/cm³ at 1 atm to 2.53 g/cm³ at 20 kbar. The rate of increase in density is largest at pressures between 15 and 20 kbar. The melting curve of albite shows an inflexion at about 16 kbar. These observations strongly suggest that structural changes of albite melt would take place effectively at pressures near 15 kbar. Melt of jadeite (NaAlSi₂O₆) composition shows very similar changes in viscosity and density and a melting curve inflexion at pressures near 10 kbar. Difference in pressure for the suggested effective structural changes of albite and jadeite melts is 5–6 kbar, which is nearly the same as that between the subsolidus reaction curves nepheline + albite= 2jadeite and albite=jadeite + quartz. The structural changes of the melts are, however, continuous and begin to take place at pressures lower than those of the crystalline phases.     

Experimental constraints on the genesis of Jadeite quartzite from Shuanghe, Dabie Mountain ultra-high pressure metamorphic terrane

Jadeite quartzite,essentially a two-phase rock made up of jadeite and quartz,is one of the most important UHP lithologies occurring in the Dabie Mountain ultrahigh pressure metamorphic belt and forms layers in biotite-plagioclase gneiss.High pressurehigh temperature studies on natural albite from the country rock gneiss were undertaken to reveal the—in parts—complex mineralogical changes that occur in the jadeite quartzite during prograde metamorphism.Experiments were conducted at 800–1200°C,in the pressure range of 2.0–3.5 GPa.One of the most intriguing results shows that the low pressure boundary of the jadeite+coesite stability field is located between about 3.2 GPa at 1000°C and 3.4 GPa at 1200°C,thus about(0.2–0.3)±0.1GPa higher than the quartz-coesite transition curve,given the uncertainty in the present study.Minor amounts of sodium and aluminum entering the structure of quartz and the intimate intergrowth texture of the run products may contribute to the observed pressure shift.Combined petrological and mineralogical studies on the run products and the natural rocks yield the following prograde reaction sequence to have occurred:The protolith of the jadeite-quartzite from Dabie Mountain is an albitized siltstone/greywacke characterized by an albite+quartz assemblage.During prograde metamorphism albite breaks down to form jadeite+quartz and thus at this stage two types of quartz can be distinguished whereas type-I-quartz already existed in the protolith,type-II-quartz represents a newly formed reaction product of albite.During further P-T-increase the pure type-I-quartz was transformed to coesite,whereas type-II-quartz(together with jadeite)was still present as a stable phase because of its impurities of Na and Al.At a later stage during further subduction,type-II-quartz also decomposes to form coesite.These studies represent an important puzzlement for a better understanding of the evolution of jadeite-quartzite from the Dabie Mountain during continental crust subduction and thus contribute to a more complete knowledge of the formation of the Dabie Mountain UHP orogenic belt in general.     

Zircon saturation revisited: temperature and composition effects in a variety of crustal magma types

Hydrothermal experiments in the temperature range 750–1020°C have defined the saturation behavior of zircon in crustal anatectic melts as a function of both temperature and composition. The results provide a model of zircon solubility given by: In D_Zr^zircon/melt= ?3.80?[0.85(M?1)]+12900/T where D_Zr^zircon/melt is the concentration ratio of Zr in the stoichiometric zircon to that in the melt, T is the absolute temperature, and M is the cation ratio (Na + K + 2Ca)/(Al · Si). This solubility model is based principally upon experiments at 860°, 930°, and 1020°C, but has also been confirmed at temperatures up to 1500°C for M = 1.3. The lowest temperature experiments (750° and 800°C) yielded relatively imprecise, low solubilities, but the measured values (with assigned errors) are nevertheless in agreement with the predictions of the model.For M = 1.3 (a normal peraluminous granite), these results predict zircon solubilities ranging from ～ 100 ppm dissolved Zr at 750°C to 1330 ppm at 1020°C. Thus, in view of the substantial range of bulk Zr concentrations observed in crustal granitoids (～ 50–350 ppm), it is clear that anatectic magmas can show contrasting behavior toward zircon in the source rock. Those melts containing insufficient Zr for saturation in zircon during melting can have achieved that condition only by consuming all zircon in the source. On the other hand, melts with higher Zr contents (appropriate to saturation in zircon) must be regarded as incapable of dissolving additional zircon, whether it be located in the residual rocks or as crystals entrained in the departing melt fraction. This latter possibility is particularly interesting, inasmuch as the inability of a melt to consume zircon means that critical geochemical “indicators” contained in the undissolved zircon (e.g. heavy rare earths, Hf, U, Th, and radiogenic Pb) can equilibrate with the contacting melt only by solid-state diffusion, which may be slow relative to the time scale of the melting event.     

Characteristics and quantitative of negative ion in salt aqueous solution by Raman spectroscopy at -170℃

The results from Raman spectroscopy analysis of salt aqueous solutions at -170℃ demonstrate that for those clearly sharp iron peaks whose Raman wavenumber is close to each other such as and , their original shape could be restorable by the stripping technique, and that ice's sharp characteristic peak (3090-3109 cm-1) is steady, while the spectrum band of the complex compound (nCl--[H+-OH-]n) chlorine ion combined chemically with water molecule is 3401-3413 cm-1. On the other hand, the research shows that the higher the negative iron concentration, the stronger its Raman characteristic peak intensity and the smaller the ice's. Based on the number of data and theoretical work, the strong correlation of the molar concentration of negative ion with the band area ratio is built up. Moreover, the developed Raman method is successfully used in the component analysis of the field fluid inclusions from Silurian sandstone in Tarim basin.     

Geochemical evolution of groundwater in hard-rock aquifers of South India using statistical and modelling techniques

ABSTRACT

Multivariate statistical analysis and inverse geochemical modelling techniques were employed to deduce the mechanism of groundwater evolution in the hard-rock terrain of Telangana, South India. Q-mode hierarchical cluster analysis (HCA) and principal component analysis (PCA) were used to extract the hydrogeochemical characteristics and classify the groundwater samples into three principal groups. Use of thermodynamic stability diagrams and inverse geochemical modelling in PHREEQC identified the chemical reactions controlling hydrogeochemistry of each of the groups obtained from statistical analysis. The model output showed that a few phases are governing the water chemistry in this area and the geochemical reactions responsible for evolution of groundwater chemistry along the flow path are (i) dissolution of evaporite minerals (dolomite, halite); (ii) dissolution of primary silicate minerals (albite, anorthite, K-feldspar, biotite); (iii) precipitation of secondary silicate minerals (kaolinite, quartz, gibbsite, Ca-montmorillonite) along with anhydrite and calcite; and (iv) reverse ion exchange processes.     

Kyanite far from equilibrium dissolution rate at 0–22℃ and pH of 3.5–7.5

Kyanite is an important and slow-dissolving mineral. Earlier work has measured its dissolution rate at high temperature and acidic pH, but experimental measurements at low temperature and near neutral p H were lacking. The rate equation by Palandri and Kharaka(A compilation of rate parameters of water–mineral interaction kinetics for application to geochemical modeling. US Geological Survey, Open File Report 2004-1068, 2004) indicates that the rate of kyanite dissolution at room temperature and near neutral pH is on the order of 10^-17 mol m^-2 s^-1, orders of magnitudes slower than most common silicate minerals such as albite and quartz. This study used an externallystirred mixed-flow reactor, which allows high solid:solution ratios, to measure the dissolution rate of kyanite at 0–22 ℃ and pH of 3.5–7.5. The measured dissolution rate of kyanite is 4.6–7.6 9 10-13 mol m^-2 s^-1 at 22℃, and the apparent activation energy is 73.5 kJ mol^-1. This dissolution rate is close to the rate of quartz dissolution and four orders of magnitude faster than the prediction by rate equation of Palandri and Kharaka(2004).Based on our new experimental data, we recommend the following rate equation for modeling the dissolution of kyanite at ambient temperatures.r=ke(-Ea)/R(1/T-1/(298.15))where k = 5.08 9 10-13 mol m^-2 s^-1, and Ea= 73.5 kJ mol^-1. Review of literature data(Carroll in The dissolution behavior of corundum, kaolinite, and andalusite: a surface complex reaction model for the dissolution of aluminosilicate minerals in diagenetic and weathering environs. Dissertation, Northwestern University, 1989) led to a recommended rate equation for andalusite as for T = 25℃ and pH = 2–10:r=k1aH+^n1+k2+k3aH^+^n3where k1= 4.04 9 10^-10 mol m^-2 s^-1, k2= 7.95×10^-10 mol m^-2 s^-1, k3= 1.01×10^-17 mol m^-2 s^-1, n1= 1.2 and n3=-0.6.     

Iron oxidation state in lower mantle mineral assemblages: I. Empirical relations derived from high-pressure experiments

The oxidation state of iron can significantly influence the physical and chemical properties of lower mantle minerals. To improve methods for estimation of Fe³⁺/∑Fe, synthetic assemblages of (Mg,Fe)(Si,Al)O₃ perovskite and (Mg,Fe)O ferropericlase were synthesised from oxide starting mixtures in Re or Fe capsules at 26 GPa and 1650-1850 °C using a multianvil press. (Mg,Fe)(Si,Al)O₃ majorite was also present in some of the run products. Both electron energy loss spectra (EELS) and Mössbauer spectra were measured for each run product, and a robust fitting method was developed for Mössbauer spectra using EELS results as a standard that enabled Fe³⁺/∑Fe of (Mg,Fe)(Si,Al)O₃ perovskite to be determined from Mössbauer spectra of multiphase assemblages. There is a close to linear variation between Fe³⁺/∑Fe and Al concentration in (Mg,Fe)(Si,Al)O₃ perovskite, independent of oxygen fugacity. The concentration of Fe³⁺ in (Mg,Fe)O increases with increasing iron concentration along curves of constant oxygen fugacity, where higher oxygen fugacity stabilises greater Fe³⁺ concentrations. Fe²⁺/Mg partition coefficients calculated from chemical composition data corrected for measured Fe³⁺/∑Fe showed values nearly identical within experimental error for all samples, and independent of Al concentration and oxygen fugacity. Simple empirical relations were derived to calculate Fe³⁺/∑Fe in (Mg,Fe)(Si,Al)O₃ perovskite and (Mg,Fe)O ferropericlase samples for which no Mössbauer or EELS data were available, and tested by applying them to calculation of Fe²⁺/Mg partition coefficients from literature data for (Mg,Fe)(Si,Al)O₃ perovskite-(Mg,Fe)O assemblages where only total iron concentrations had been measured. Results showed Fe²⁺/Mg partition coefficients that were equal to existing values within experimental error, hence confirming the validity of the empirical relations.     

Metasomatism of the peridotites from southern Mariana fore-arc:Trace element characteristics of clinopyroxene and amphibole

Modal composition and mineral composition of harzburgites from the southern Mariana fore-arc show that they are highly refractory. There are a few modals of clinopyroxene (0.7 vol %) in harzburgites. Two types of amphibole are found in these harzburgites: magnesiohornblende accompanied by clinopy-roxene with higher Al2O3 content (>7%) and lower Mg#; tremolite around orthopyroxene with lower Al2O3 content (< 2%) and higher Mg#. Trace element of clinopyroxene and two types of amphibole are ana-lyzed. Primitive mantle-normalised REE patterns for clinopyroxene and magnesio hornblende are very similar and both show HREE enrichment relative to LREE,while magnesiohornblende has higher con-tent of trace element than clinopyroxene. The contents of trace element of tremolite are much lower than those of magnesiohornblende. Clinopyroxene shows enrichment of most of the trace element except HREE and Ti relative to clinopyroxene in abyssal peridotites. Petrology and trace element characteristic of clinopyroxene and two types of amphibole indicate that southern Mariana fore-arc harzburgites underwent two stages of metasomatism. The percolation of a hydrous melt led to mobility of Al,Ca,Fe,Mg,Na,and large amounts of trace element. LILE and LREE can be more active in hydrous melt than HREE and Ti,and the activities of most of the trace element except some of LILE are influ-enced by temperature and pressure.     

Titanium solubility in coexisting garnet and clinopyroxene at very high pressure: the significance of exsolved rutile in garnet

Exsolution microstructures including ilmenite±garnet in clinopyroxene and rutile in garnet are common in clinopyroxenite and eclogite from the Sulu ultrahigh-pressure (UHP) terrane. In order to understand the phase relations and Ti solubility in both garnet and clinopyroxene in a natural TiO₂-bearing system, several experiments at 5-15 GPa, 1000-1400°C were carried out using the multianvil high-pressure apparatus. The Hujianlin ilmenite-rich garnet clinopyroxenite showing exsolution microstructure was selected as starting material, because it closely approaches a composition lying in the TiO₂-CaO-MgO-FeO-Al₂O₃-SiO₂ system. Except for minor melt in one experiment at 1400°C and 5 GPa, other run products contain majoritic garnet+clinopyroxene±ilmenite (or rutile) and exhibit neoblastic texture. With increasing pressure, Ti and Ca, Mg and Si contents of neoblastic garnet increase with decreasing Al. The principal coupled substitutions are Ca²⁺Ti⁴⁺→2Al³⁺ and Si⁴⁺Mg²⁺→2Al³⁺ responding to majorite component increase. Titanium solubility (0.8-4.5 wt% as TiO₂) in garnet and Grt_Ti/Cpx_Ti ratio have a pronounced positive correlation with pressure between 5 and 15 GPa. On the other hand, the coexisting clinopyroxene contains low Ti (0.17-0.53 wt% as TiO₂), and shows no significant pressure effect. Rutile exsolution in garnet is coupled to that of pyroxene exsolution; both are exsolved from majoritic garnet on decompression. Therefore, the amount of such exsolved lamellae is a potential indicator of high-pressure metamorphism in exhumed rocks, whereas the TiO₂ content of clinopyroxene coexisting with garnet is not sensitive to pressure change.     

Transformations of runoff chemistry in the Arctic tundra,Northwest Territories,Canada

The transformation of snowmelt water chemical composition during melt, elution and runoff in an Arctic tundra basin is investigated. The chemistry of the water flowing along pathways from the surface of melting snow to the 95·5 ha basin outlet is related to relevant hydrological processes. In so doing, this paper offers physically based explanations for the transformation of major ion concentrations and loads of runoff water associated with snowmelt and rainfall along hydrological pathways to the stream outlet. Late‐lying snowdrifts were found to influence the ion chemistry in adjacent reaches of the stream channel greatly. As the initial pulse of ion‐rich melt water drained from the snowdrift and was conveyed through hillslope flowpaths, the concentrations of most ions increased, and the duration of the peak ionic pulse lengthened. Over the first 3 m of overland flow, the concentrations of all ions except for NO increased by one to two orders of magnitude, with the largest increase for K⁺, Ca²⁺ and Mg²⁺. This was roughly equivalent to the concentration increase that resulted from percolation of relatively dilute water through 0·25 m of unsaturated soil. The Na⁺ and Cl^? were the dominant ions in snowmelt water, whereas Ca²⁺ and Mg²⁺ dominated the hillslope runoff. On slopes below a large melting snowdrift, ion concentrations of melt water flowing in the saturated layer of the soil were very similar to the relatively dilute concentrations found in surface runoff. However, once the snowdrift ablated, ion concentrations of subsurface flow increased above parent melt‐water concentrations. Three seasonally characteristic hydrochemical regimes were identified in a stream reach adjacent to late‐lying snowdrifts. In the first two stages, the water chemistry in the stream channel strongly resembled the hillslope drainage water. In the third stage, in‐stream geochemical processes, including the weathering/ion exchange of Ca²⁺ and Mg²⁺, were the main control of streamwater chemistry. Copyright © 2006 John Wiley & Sons, Ltd.     

Holocene calcrete crust deposits on the moraine of Batura Glacier, northern Pakistan

Abstract   Calcretes can be observed on the surface of old moraines around Batura Glacier in the upper Hunza Valley, Karakoram Mountains, Pakistan. They develop as a calcareous crust cementing small gravels under boulders. In order to understand the genesis of the calcrete crust, a variety of methods were employed: (i) study of mineralogy and geochemistry of a calcrete crust precipitated on the lateral moraine using X-ray diffractometer and electron probe microanalysis; (ii) analysis of solute chemistry of surface water and ice bodies around the Batura Glacier; and (iii) accelerator mass spectrometry ¹⁴C dating of the crust itself. The results indicate that the calcrete crust has definite laminated layers composed of a fine-grain and compact calcite layer, and a mineral fragment layer. The chemical composition of the calcite layer is approximately 60% CaO and 1% MgO. The mineral fragment layer consists of rounded grain materials up to 0.2 mm in diameter. It shows a graded bedding structure with fine grains of quartz, albite and muscovite. Meanwhile, as the Paleozoic Pasu limestone is distributed around the terminal of Batura Glacier, Ca cations dissolve in the melt water of the glacier. Accordingly, the calcrete crust is precipitated by decreases in CO₂ partial pressure from glacier ice and evaporation of the melt water, including high concentration of Ca²⁺ at ephemeral streams and small ponds stagnating between the moraine and glacial ice. On the basis of the AMS ¹⁴C age, the calcrete is considered to have formed approximately 8200 calibrated years bp under the Batura glacial stage.     

Two stages of isotopic exchanges experienced by the Ertaibei granite pluton, northern Xinjiang, China

¹⁸O/¹⁶O and D/H of coexisting feldspar, quartz, and biotite separates of twenty samples collected from the Ertaibei granite pluton, northern Xinjiang, China are determined. It is shown that the Ertaibei pluton experienced two stages of isotopic exchanges. The second stage of¹⁸O/¹⁶O and D/H exchanges with meteoric water brought about a marked decrease in the δ¹⁸O values of feldspar and biotite from the second group of samples. The D/H of biotite exhibits a higher sensitivity to the meteoric water alteration than its¹⁸O/¹⁶O. However, the first stage of¹⁸O/¹⁶O exchange with the¹⁸O-rich aqueous fluid derived from the dehydration within the deep crust caused the Δ¹⁸O_{Quartz-Feldspar} reversal. It is inferred that the dehydration-melting may have been an important mechanism for anatexis. It is shown that the deep fluid encircled the Ertaibei pluton like an envelope which serves as an effective screen to the surface waters.     

Sedimentary geochemistry and provenance of the Lower and Middle Devonian Laojunshan Formation,the North Qilian Orogenic Belt

The Laojunshan Formation is a suite of molasse formed during the rapid uplift of the North Qilian Orogenic Belt (NQOB). Forty-one samples of sandstone have been collected from the Sunan and Minle sections in the western sector and the Gulang and Jingyuan sections in the eastern sector of the NQOB belt. Geochemical analyses of those samples indicated: 1) The MgO+Fe2O3T and Al2O3/SiO2 values are higher, and K2O/Na2O ratios are lower in the western sector than those in the eastern sector. 2) All of them are de...     

Heterogeneous Nucleophilic Transformation of Metolachlor by Bisulfide on Alumina Surface

The present research elucidates the accelerating effect of alumina minerals on metolachlor transformation using sulfur nucleophiles and also determines the metolachlor transformation mechanisms in the heterogeneous reaction systems. Metolachlor transformation was first systematically investigated under different conditions. Then, the Fourier transform infrared (FTIR) spectra were used to characterize the changes in the surface bonds of the aluminas. The transformation products were qualitatively identified using LC/MS. The results showed that bisulfide can produce efficient metolachlor transformation rates, and the presence of the aluminas can further accelerate the transformation by achieving complete transformation in <21 days. In addition, a higher pH and higher bisulfide concentration are more favorable for metolachlor transformation. When normalized to the surface area, the metolachlor transformation rates were found to follow the order of α‐Al₂O₃>γ‐AlOOH>γ‐Al₂O₃ in the presence of different aluminas. FTIR results indicated that the enhancement of metolachlor transformation rates by bisulfide with aluminas can be attributed to the surface active nucleophiles on alumina surfaces formed through Al? S and Al? O bonds. The substitution of chlorine on the metolachlor followed the S_N2 mechanism by bisulfide with accelerated rate through mediating the heterogeneous reactions with aluminas.     

Hydrogeochemistry of Water in Coal Measures during Grouting Treatment of Taoyuan Mine,China

Permian coal measure sandstone fissure water (referred to as “coal measure water,” that is, water in coal measures) is one of the important water sources for industrial and agricultural activities in mining areas. However, the regional high-pressure grouting, one of the most widely used floor control methods, may affect the coal measure water which is connected with limestone aquifer. This study used Taoyuan mine, a typical coal mine in Huaibei coalfield, as the research area to study the influencing mechanism of a grouting treatment on the hydrogeochemical evolution of coal measure water. The hydrogeochemical characteristics and water-rock interaction mechanism of the coal measure water before and during the treatment were evaluated using a Piper trigram, ion combination ratio, and hydrogen-oxygen stable isotope. The anions and cations in the coal measure water before and during the treatment had the same trends at SO₄²⁻ > HCO₃⁻ > Cl⁻ and Na⁺ > Ca²⁺ > Mg²⁺, respectively. Hydrochemical types of coal measure water before treatment were mainly SO₄·Cl-Ca·Mg, SO₄·Cl-Na, and HCO₃-Na, and during treatment they were mainly SO₄·Cl-Na and HCO₃-Na. The formation of chemical components of coal measure water before treatment was mainly caused by carbonate dissolution, sulfate dissolution, and pyrite oxidation. During the treatment, sulfate dissolution and pyrite oxidation were the main geochemical processes, and ion exchange was enhanced. Atmospheric precipitation was the source of all water samples, and all showed an obvious ¹⁸O drift.     

Characteristics of soil moisture in permafrost observed in East Siberian taiga with stable isotopes of water

Soil moisture and its isotopic composition were observed at Spasskaya Pad experimental forest near Yakutsk, Russia, during summer in 1998, 1999, and 2000. The amount of soil water (plus ice) was estimated from volumetric soil water content obtained with time domain reflectometry. Soil moisture and its δ¹⁸O showed large interannual variation depending on the amount of summer rainfall. The soil water δ¹⁸O decreased with soil moisture during a dry summer (1998), indicating that ice meltwater from a deeper soil layer was transported upward. On the other hand, during a wet summer (1999), the δ¹⁸O of soil water increased due to percolation of summer rain with high δ¹⁸O values. Infiltration after spring snowmelt can be traced down to 15 cm by the increase in the amount of soil water and decrease in the δ¹⁸O because of the low δ¹⁸O of deposited snow. About half of the snow water equivalent (about 50 mm) recharged the surface soil. The pulse of the snow meltwater was, however, less important than the amount of summer rainfall for intra‐annual variation of soil moisture. Excess water at the time just before soil freezing, which is controlled by the amount of summer rainfall, was stored as ice during winter. This water storage stabilizes the rate of evapotranspiration. Soil water stored in the upper part of the active layer (surface to about 120 cm) can be a water source for transpiration in the following summer. On the other hand, once water was stored in the lower part of the active layer (deeper than about 120 cm), it would not be used by plants in the following summer, because the lower part of the active layer thaws in late summer after the plant growing season is over. Copyright © 2002 John Wiley & Sons, Ltd.     

Characterization of lake water and ground water movement in the littoral zone of Williams Lake,a closed‐basin lake in north central Minnesota

Williams Lake, Minnesota is a closed‐basin lake that is a flow‐through system with respect to ground water. Ground‐water input represents half of the annual water input and most of the chemical input to the lake. Chemical budgets indicate that the lake is a sink for calcium, yet surficial sediments contain little calcium carbonate. Sediment pore‐water samplers (peepers) were used to characterize solute fluxes at the lake‐water–ground‐water interface in the littoral zone and resolve the apparent disparity between the chemical budget and sediment data. Pore‐water depth profiles of the stable isotopes δ¹⁸O and δ²H were non‐linear where ground water seeped into the lake, with a sharp transition from lake‐water values to ground‐water values in the top 10 cm of sediment. These data indicate that advective inflow to the lake is the primary mechanism for solute flux from ground water. Linear interstitial velocities determined from δ²H profiles (316 to 528 cm/yr) were consistent with velocities determined independently from water budget data and sediment porosity (366 cm/yr). Stable isotope profiles were generally linear where water flowed out of the lake into ground water. However, calcium profiles were not linear in the same area and varied in response to input of calcium carbonate from the littoral zone and subsequent dissolution. The comparison of pore‐water calcium profiles to pore‐water stable isotope profiles indicate calcium is not conservative. Based on the previous understanding that 40–50 % of the calcium in Williams Lake is retained, the pore‐water profiles indicate aquatic plants in the littoral zone are recycling the retained portion of calcium. The difference between the pore‐water depth profiles of calcium and δ¹⁸O and δ²H demonstrate the importance of using stable isotopes to evaluate flow direction and source through the lake‐water–ground‐water interface and evaluate mechanisms controlling the chemical balance of lakes. Published in 2003 by John Wiley & Sons, Ltd.