Application of carbon isotopes to detect seepage out of coalbed natural gas produced water impoundments

Coalbed natural gas (CBNG) production from coal bed aquifers requires large volumes of produced water to be pumped from the subsurface. The produced water ranges from high quality that meets state and federal drinking water standards to low quality due to increased salinity and/or sodicity. The Powder River Basin of northeastern Wyoming is a major coalbed natural gas producing region, where water quality generally decreases moving from the southeastern portion of the basin towards the center. Most produced water in Wyoming is disposed into impoundments and other surface drainages, where it may infiltrate into shallow groundwater. Groundwater degradation caused by infiltration of CBNG produced water holding impoundments into arid, soluble salt-rich soils is an issue of immense importance because groundwater is a major source for stock water, irrigation, and drinking water for many small communities in these areas. This study examines the potential of using stable C isotope signatures of dissolved inorganic C (δ¹³C_DIC) to track the fate of CBNG produced water after it is discharged into the impoundments. Other geochemical proxies like the major cations and major anions were used in conjunction with field water quality measurements to understand the geochemical differences between CBNG produced waters and ambient waters in the study area. Samples were collected from the CBNG discharge outfalls, produced water holding impoundments, and monitoring wells from different parts of the Powder River Basin and analyzed for δ¹³C_DIC. The CBNG produced waters from outfalls and impoundments have positive δ¹³C_DIC values that fall within the range of +12‰ to +22‰, distinct from the ambient regional surface and groundwaters with δ¹³C_DIC values ranging from −10‰ to −14‰. The results from the study demonstrate that these contrasting δ¹³C_DIC signatures can be used to trace seepage out of CBNG produced water impoundments into shallow groundwaters.     

The effect of naturally acidified irrigation water on agricultural volcanic soils. The case of Asembagus, Java, Indonesia

Acid water from the Banyuputih river (pH  3.5) is used for the irrigation of agricultural land in the Asembagus coastal area (East Java, Indonesia), with harmful consequences for rice yields. The river water has an unusual composition which is caused by seepage from the acidic Kawah Ijen crater lake into the river. This unique irrigation setting allows the study of soil acidification in situ. This paper assesses the effects of volcanogenically contaminated irrigation water on the chemical properties of the agricultural soils.The changes in soil properties were evaluated by comparing samples taken from the topsoil and sub-soil (1–3 m depth) from areas irrigated with acid water and areas irrigated with neutral water. The field survey thus resulted in four soil categories. Bulk soil composition, organic matter content, moisture content and particle size distribution were determined. Reactive phases were quantified with the selective extractions 1 M KCl, 0.1 M Na-pyrophosphate and 0.2 M acid ammonium oxalate (AAO).By comparing the four soil categories it is shown that the use of the naturally polluted irrigation water has had a large influence on the chemical composition of the topsoil. The composition of the soil solution has changed over the entire investigated soil profile. Furthermore the acid irrigation water has strongly modified the composition of the reactive phases, extracted as KCl, pyrophosphate, and AAO extractable elements, and also the bulk soil composition has been significantly modified. Overall this has resulted in the net dissolution of some elements and the net precipitation of others. The changes in the reactive phases and bulk soil composition are only apparent in the topsoil (0–20 cm) but not in the deeper soil.     

Potassium leaching in undisturbed soil cores following surface applications of gypsum

Displacement studies on leaching of potassium (K⁺) were conducted under unsaturated steady state flow conditions in nine undisturbed soil columns (15.5 cm in diameter and 25 cm long). Pulses of K⁺ applied to columns of undisturbed soil were leached with distilled water or calcium chloride (CaCl₂) at a rate of 18 mm h⁻¹. The movement of K⁺ in gypsum treated soil leached with distilled water was at a similar rate to that of the untreated soil leached with 15 mM CaCl₂. The Ca²⁺ concentrations in the leachates were about 15 mM, the expected values for the dissolution of the gypsum. When applied K⁺ was displaced with the distilled water, K⁺ was retained in the top 10–12.5 cm depth of soil. In the undisturbed soil cores there is possibility of preferential flow and lack of K⁺ sorption. The application of gypsum and CaCl₂ in the reclamation of sodic soils would be expected to leach K⁺ from soils. It can also be concluded that the use of sources of water for irrigation which have a high Ca²⁺ concentration can also lead to leaching of K⁺ from soil. Average effluent concentration of K⁺ during leaching period was 30.2 and 28.6 mg l⁻¹ for the gypsum and CaCl₂ treated soils, respectively. These concentrations are greater than the recommended guideline of the World Health Organisation (12 mg K⁺ l⁻¹).     

Use of Sr isotopes as a tool to decipher the soil weathering processes in a tropical river catchment,southwestern India

River water composition (major ion and ⁸⁷Sr/⁸⁶Sr ratio) was monitored on a monthly basis over a period of three years from a mountainous river (Nethravati River) of southwestern India. The total dissolved solid (TDS) concentration is relatively low (46 mg L⁻¹) with silica being the dominant contributor. The basin is characterised by lower dissolved Sr concentration (avg. 150 nmol L⁻¹), with radiogenic ⁸⁷Sr/⁸⁶Sr isotopic ratios (avg. 0.72041 at outlet). The composition of Sr and ⁸⁷Sr/⁸⁶Sr and their correlation with silicate derived cations in the river basin reveal that their dominant source is from the radiogenic silicate rock minerals. Their composition in the stream is controlled by a combination of physical and chemical weathering occurring in the basin. The molar ratio of SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotopic ratio show strong seasonal variation in the river water, i.e., low SiO₂/Ca ratio with radiogenic isotopes during non-monsoon and higher SiO₂/Ca with less radiogenic isotopes during monsoon season. Whereas, the seasonal variation of Rb/Sr ratio in the stream water is not significant suggesting that change in the mineral phase being involved in the weathering reaction could be unlikely for the observed molar SiO₂/Ca and ⁸⁷Sr/⁸⁶Sr isotope variation in river water. Therefore, the shift in the stream water chemical composition could be attributed to contribution of ground water which is in contact with the bedrock (weathering front) during non-monsoon and weathering of secondary soil minerals in the regolith layer during monsoon. The secondary soil mineral weathering leads to limited silicate cation and enhanced silica fluxes in the Nethravati river basin.     

Changes in soil quality indicators under long-term sewage irrigation in a sub-tropical environment

Though irrigation with sewage water has potential benefits of meeting the water requirements, the sewage irrigation may mess up to harm the soil health. To assess the potential impacts of long-term sewage irrigation on soil health and to identify sensitive soil indicators, soil samples were collected from crop fields that have been irrigated with sewage water for more than 20 years. An adjacent rain-fed Leucaena leucocephala plantation system was used as a reference to compare the impact of sewage irrigation on soil qualities. Soils were analyzed for different physical, chemical, biological and biochemical parameters. Results have shown that use of sewage for irrigation improved the clay content to 18–22.7%, organic carbon to 0.51–0.86% and fertility status of soils. Build up in total N was up to 2,713 kg ha⁻¹, available N (397 kg ha⁻¹), available P (128 kg ha⁻¹), available K (524 kg ha⁻¹) and available S (65.5 kg ha⁻¹) in the surface (0.15 m) soil. Long-term sewage irrigation has also resulted a significant build-up of DTPA extractable Zn (314%), Cu (102%), Fe (715%), Mn (197.2), Cd (203%), Ni (1358%) and Pb (15.2%) when compared with the adjacent rain-fed reference soil. Soils irrigated with sewage exhibited a significant decrease in microbial biomass carbon (−78.2%), soil respiration (−82.3%), phosphatase activity (−59.12%) and dehydrogenase activity (−59.4%). An attempt was also made to identify the sensitive soil indicators under sewage irrigation, where microbial biomass carbon was singled out as the most sensitive indicator.     

Evaluation of diffuse and preferential flow pathways of infiltrated precipitation and irrigation using oxygen and hydrogen isotopes

Subsurface-water flow pathways in three different land-use areas (non-irrigated grassland, poplar forest, and irrigated arable land) in the central North China Plain were investigated using oxygen (¹⁸O) and hydrogen (²H) isotopes in samples of precipitation, soils, and groundwater. Soil water in the top 10 cm was significantly affected by both evaporation and infiltration. Water at 10–40 cm depth in the grassland and arable land, and 10–60 cm in poplar forest, showed a relatively short residence time, as a substantial proportion of antecedent soil water was mixed with a 92-mm storm infiltration event, whereas below those depths (down to 150 cm), depleted δ¹⁸O spikes suggested that some storm water bypassed the shallow soil layers. Significant differences, in soil-water content and δ¹⁸O values, within a small area, suggested that the proportion of immobile soil water and water flowing in subsurface pathways varies depending on local vegetation cover, soil characteristics and irrigation applications. Soil-water δ¹⁸O values revealed that preferential flow and diffuse flow coexist. Preferential flow was active within the root zone, independent of antecedent soil-water content, in both poplar forest and arable land, whereas diffuse flow was observed in grassland. The depleted δ¹⁸O spikes at 20–50 cm depth in the arable land suggested the infiltration of irrigation water during the dry season. Temporal isotopic variations in precipitation were subdued in the shallow groundwater, suggesting more complete mixing of different input waters in the unsaturated zone before reaching the shallow groundwater.

     

A new simple approach to evaluate pedogenic clay transformation in a Vertic Calcisol

The aim of this study is to characterize the pedogenic clay minerals by using simple approach: mixing mineralogical and geochemical findings.The fine clay fractions (< 0.1 μm) of a Vertic Cambisol profile were studied by means of X-ray diffraction (XRD), infrared spectroscopy (FTIR) and cation exchange capacity (CEC).Qualitative and quantitative mineralogical compositions of the clay mixture were determined.Moreover, chemical equilibria and thermodynamic stabilities of minerals (calcite, gypsum, kaolinite, smectites and illites) were studied using results of ionic activities obtained from total concentration of various aqueous species in water extracts from soil-saturated pastes.XRD analysis shows a good homogeneity in the mineralogical composition of the soil material, with depth of soil profiles. The identified clay minerals are mainly illite–smectite mixed layers (I/S) and kaolinite. The chemical analysis of saturated paste extracts with clay minerals shows a slight undersaturation of the illitic phase while smectites and also calcite and gypsum reach the thermodynamic equilibrium along the soil profile.     

Effects of biochar, cow bone, and eggshell on Pb availability to maize in contaminated soil irrigated with saline water

Toxicity of heavy metals adversely affects environment and human health. Organic materials derived from natural matters or wastes have been applied to soils to reduce the mobility of contaminants such as heavy metals. However, the application of cow bone powder (CB), biochar (BC), and eggshell powder (ES) is rarely investigated for the reduction of Pb bioavailability in soils irrigated with saline water. The objective of this study was to assess the effectiveness of CB, BC, and ES additions as immobilizing substances on Pb bioavailability in shooting range soil irrigated with deionized and saline water. Each additive of CB, BC, and ES at 5 % (w/w) was mixed with soils and then the deionized and saline water were irrigated for 21 days. With deionized water irrigation, the soils treated with CB, BC, and ES exhibited higher pH when compared with saline water irrigation. With saline water irrigation, the electrical conductivity, water-soluble anions, and cations were significantly increased in soils treated with CB, BC, and ES. The water-soluble Pb in soils treated with CB, BC, and ES was significantly decreased with saline water irrigation. On the other hand, the water-soluble Pb in soil treated with CB was increased with deionized water irrigation. Only BC with saline water irrigation decreased the Pb concentration in maize shoots.     

Shallow groundwater and soil chemistry response to 3 years of subsurface drip irrigation using coalbed-methane-produced water

Disposal of produced waters, pumped to the surface as part of coalbed methane (CBM) development, is a significant environmental issue in the Wyoming portion of the Powder River Basin, USA. High sodium adsorption ratios (SAR) of the waters could degrade agricultural land, especially if directly applied to the soil surface. One method of disposing of CBM water, while deriving beneficial use, is subsurface drip irrigation (SDI), where acidified CBM waters are applied to alfalfa fields year-round via tubing buried 0.92 m deep. Effects of the method were studied on an alluvial terrace with a relatively shallow depth to water table (～3 m). Excess irrigation water caused the water table to rise, even temporarily reaching the depth of drip tubing. The rise corresponded to increased salinity in some monitoring wells. Three factors appeared to drive increased groundwater salinity: (1) CBM solutes, concentrated by evapotranspiration; (2) gypsum dissolution, apparently enhanced by cation exchange; and (3) dissolution of native Na–Mg–SO₄ salts more soluble than gypsum. Irrigation with high SAR (～24) water has increased soil saturated paste SAR up to 15 near the drip tubing. Importantly though, little change in SAR has occurred at the surface.     

Environmental evaluation of elemental cesium and strontium contents and their isotopic activity concentrations in different soils of La Mancha (Central Spain)

Cesium and Strontium concentrations were analyzed in eight pedogenetic soil profiles developed on different rocks from a semiarid mediterranean region: La Mancha (Central Spain). Concentration activities of ¹³⁷Cs and ⁹⁰Sr, as for some soil properties, were also measured. The results are presented in this document: Cs concentrations range between 0.4 and 18.3 mg kg⁻¹ and Sr varies widely between 11.0 and 3,384 mg kg⁻¹. Therefore, it is clear that there is a broad range of concentrations and there are also values significantly higher than the average values stated by several authors. Concentrations of long-life artificial radionuclides (¹³⁷Cs, ⁹⁰Sr) were determined in some of the same soils. The activity concentration mean values (Bq kg⁻¹) were ranging between 0.82 and 21.76 for ¹³⁷Cs and ⁹⁰Sr variations range between 6.73 and 0.35. There were no significant correlations between radionuclides and stable trace elements. The data indicate that the soils do not show significant radioactivity of these elements and therefore they do not pose a danger. By the same token, no risk of contamination by this activity was detected. Finally, spatial patterns seem to be affected by the soil type and some soil properties.     

Sensitivity assessment of strontium isotope as indicator of polluted groundwater for hydraulic fracturing flowback fluids produced in the Dameigou Shale of Qaidam Basin

Hydrogeochemical processes that would occur in polluted groundwater and aquifer system, may reduce the sensitivity of Sr isotope being the indicator of hydraulic fracturing flowback fluids(HFFF) in groundwater. In this paper, the Dameigou shale gas field in the northern Qaidam Basin was taken as the study area, where the hydrogeochemical processes affecting Sr isotope was analysed. Then, the model for Sr isotope in HFFF-polluted groundwater was constructed to assess the sensitivity of Sr isotope as HFFF indicator. The results show that the dissolution can release little Sr to polluted groundwater and cannot affect the εSr(the deviation of the 87 Sr/86 Sr ratio) of polluted groundwater. In the meantime, cation exchange can considerably affect Sr composition in the polluted groundwater. The Sr with low εSr is constantly released to groundwater from the solid phase of aquifer media by cation exchange with pollution of Quaternary groundwater by the HFFF and it accounts for 4.6% and 11.0% of Sr in polluted groundwater when the HFFF flux reaches 10% and 30% of the polluted groundwater, respectively. However, the Sr from cation exchange has limited impact on Sr isotope in polluted groundwater. Addition of Sr from cation exchange would only cause a 0.2% and 1.2% decrease in εSr of the polluted groundwater when the HFFF flux reaches 10% and 30% of the polluted groundwater, respectively. These results demonstrate that hydrogeochemical processes have little effect on the sensitivity of Sr isotope being the HFFF indicator in groundwater of the study area. For the scenario of groundwater pollution by HFFF, when the HFFF accounts for 5%(in volume percentage) of the polluted groundwater, the HFFF can result in detectable shifts of εSr(ΔεSr=0.86) in natural groundwater. Therefore, after consideration of hydrogeochemical processes occurred in aquifer with input of the HFFF, Sr isotope is still a sensitive indicator of the Quaternary groundwater pollution by the HFFF produced in the Dameigou shale of Qaidam Basin.     

Effects of long-term irrigation with treated wastewater. Part I: Evolution of soil physico-chemical properties

The long-term impact of irrigation on a Mediterranean sandy soil irrigated with Treated wastewater (TWW) since 1980 was evaluated. The main soil properties (CEC, pH, size distribution, exchangeable cations and chloride, hydraulic conductivity) as well as the organic matter and Cu, Cr and Pb speciation in an irrigated soil and a non-irrigated control soil at various soil depths were monitored and compared during a 2 years experiment. In this first part, the evolution of the physico-chemical soil properties was described. The irrigation with TWW was beneficial with regard to water and nutrient supplying. All the exchangeable cations other than K⁺ were higher in the irrigated soil than in the reference one. A part of the exchangeable cations was not fixed on the exchange complex but stored as labile salts or in concentrated soil solution. Despite the very sandy soil texture, both saturated and unsaturated hydraulic conductivity exhibited a significant diminution in the irrigated soil, but remained high enough to allow water percolation during rainy periods and subsequent leaching of accumulated salts, preventing soil salinization. In the irrigated soil, exchangeable sodium percentage (ESP) exhibited high values (20% on average) and the soil organic C was lower than in the reference. No significant effect was noticed on soil mineralogical composition due to irrigation.     

Isotopic evidence for the source of Ca and S in soil gypsum, anhydrite and calcite in the Atacama Desert, Chile

The origin of pedogenic salts in the Atacama Desert has long been debated. Possible salt sources include in situ weathering at the soil site, local sources such as aerosols from the adjacent Pacific Ocean or salt-encrusted playas (salars), and extra-local atmospheric dust. To identify the origin of Ca and S in Atacama soil salts, we determined δ³⁴S and ⁸⁷Sr/⁸⁶Sr values of soil gypsum/anhydrite and ⁸⁷Sr/⁸⁶Sr values of soil calcite along three east-west trending transects. Our results demonstrate the strong influence of marine aerosols on soil gypsum/anhydrite development in areas where marine fog penetrates inland. Results from an east-west transect located along a breach in the Coastal Cordillera show that most soils within 90 km of the coast, and below 1300 m in elevation, are influenced by marine aerosols and that soils within 50 km, and below 800 m in elevation, receive >50% of Ca and S from marine aerosols (δ³⁴S values > 14‰ and ⁸⁷Sr/⁸⁶Sr values >0.7083). In areas where the Coastal Cordillera is >1200 m in elevation, however, coastal fog cannot penetrate inland and the contribution of marine aerosols to soils is greatly reduced. Most pedogenic salts from inland soils have δ³⁴S values between +5.0 to +8.0‰ and ⁸⁷Sr/⁸⁶Sr ratios between 0.7070 and 0.7076. These values are similar to average δ ³⁴S and ⁸⁷Sr/⁸⁶Sr values of salts from local streams, lakes, and salars (+5.4 ±2‰ δ³⁴S and 0.70749 ± 0.00045 ⁸⁷Sr/⁸⁶Sr) in the Andes and Atacama, suggesting extensive eolian reworking of salar salts onto the surrounding landscape. Ultimately, salar salts are precipitated from evaporated ground water, which has acquired its dissolved solutes from water-rock interactions (both high and low-temperature) along flowpaths from recharge areas in the Andes. Therefore, the main source for Ca and S in gypsum/anhydrite in non-coastal soils is indirect and involves bedrock alteration, not surficially on the hyperarid landscape, but in the subsurface by ground water, followed by eolian redistribution of ground-water derived salar salts to soils. The spatial distribution of high-grade nitrate deposits appears to correspond with areas that receive the lowest fluxes of local marine and salar salt, supporting arguments for tropospheric nitrogen as the main source for soil nitrate.     

The influence of sulfur deposition rates on sulfate retention patterns and mechanisms in aerated forest soils

Stable isotope ratios were used as a tracer for S flow and transformations in an irrigation experiment with 5 different German forest soils. Seventy-five lysimeters constructed from soil cores, 15 from each site, were irrigated over 20 months with SO₄-rich artificial canopy throughfall, simulating 3 different S input levels: 35 kg S ha⁻¹ in treatment I, 63 kg S ha⁻¹ in treatment II, and 131 kg S ha⁻¹ in treatment III. The δ³⁴S value of the irrigation SO₄ was more than 22‰ higher than those of total S in the untreated soils. Mass and isotope balances for different soil S compounds were used to assess the patterns and mechanisms of S retention in individual soil horizons and their dependence on S deposition levels. Independent of the S deposition level, on average 12±5 kg ha⁻¹ of the applied S were bound organically by the microbial biomass in all soils. Immobilization of irrigation SO₄ occurred predominantly in the topsoil horizons with the formation of C-bonded S being more prevalent than the synthesis of organic sulfates. Tracer retention via formation of organic soil S compounds accounted for up to 50% of the irrigation SO₄ in treatment I, from 16 to 25% in treatment II, and less than 20% in treatment III. The dominant process of inorganic S retention in the soils appeared to be adsorption of SO₄, but precipitation of aluminum hydroxy sulfate minerals constituted a second potential inorganic retention process in some soils. Sulfate adsorption increased with increasing sesquioxide content of the soils and with increasing S deposition rates. In soils with high sesquioxide contents, typically more than 70% of the irrigated S was retained inorganically, whereas in the soil with the lowest sesquioxide content, generally less than 50% of the labeled irrigation S was detected in inorganic form. In the latter soil, the sesquioxide content was not high enough to fully adsorb the elevated SO₄ inputs in treatments II and III. Consequently, increased tracer S export with the seepage water SO₄ was observed in the experimental variants with elevated SO₄ deposition rates. In soils with high sesquioxide contents, the elevated SO₄ inputs in treatments II and III were fully retained in the soil horizons in inorganic form during the 20 months of the experiment and thus increased seepage water export of labeled SO₄ was not observed. The ability to inorganically retain tracer S in the mineral soil horizons was identified as the major factor regulating the extent of tracer S export with the seepage water at 60 cm depth. The high retention of labeled S in all soils combined with the comparatively low recovery of irrigation SO₄ with the seepage water implies that the mean transit time of S in the uppermost 60 cm of the acid forest soils varies between several years and many decades, much longer than previously thought.     

Sr and Nd isotopes as tracers in pedogenic studies: Evidence for Saharan dust contribution to the soils of Muravera (Sardinia,Italy)

Sr and Nd isotopes were applied to 5 soil profiles from the Muravera area, in south-eastern Sardinia.All the soils, which have developed during the Quaternary on the Lower Paleozoic metamorphic basement except for one on Eocene carbonates, are located far from major sources of pollution. Therefore, they are suitable for testing pedogenic processes and geochemical evolution to benefit for environmental studies.The Sr isotopic ratios range largely (δ⁸⁷Sr = 1.7–65.9‰), even in each soil profile. In particular, the observed increase of δ⁸⁷Sr with depth in the most of the metamorphic rock-based soils can be accounted for by the downward decrease of Sr contributions from organic matter and Saharan dust, both displaying lower isotopic ratios than the soil bedrocks. The carbonate rock-based soil exhibits δ⁸⁷Sr higher (1.7–18.1‰) than the bedrock, indicating a significant contribution of radiogenic Sr from the siliciclastic fraction of the soil, and probably from dust input. The Nd isotopic ratios are slightly variable through the profiles (ɛ_Nd from −7.8 to −14.5), confirming little mobility of Nd and Sm during the pedogenesis. Among the minerals present in the soils, phosphates, albite, and calcite are those important in providing low radiogenic Sr and Nd to organic matter of the soils.Lastly, this isotopic study has in particular allowed for evaluating the potential proportion of contribution of Saharan dust to south-eastern Sardinia, thus corroborating the findings of other studies related to soils from the central-western Mediterranean.     

87Sr/86Sr as an indicator of flowpaths and weathering rates in the Plynlimon experimental catchments,Wales, U.K.

A knowledge of the processes involved in streamflow generation are critical to an understanding of solute transport and weathering rates in upland catchments. The determination of specific flow pathways and the formulation of process-based models have proved difficult in such terrains, largely due to the heterogeneous nature of catchments and the necessary limitations of bulked parameter models. Natural geochemical tracers have proved invaluable in developing conceptual models of catchment functioning and for constraining weathering processes and geochemical cycling. Strontium isotopes have been used as a natural tracer to calculate weathering rates for Sr and Ca, and to constrain the dominant flow pathways in two upland forested sub-catchments (Afon Hafren and Afon Hore) of the River Severn at Plynlimon in Central Wales. The dominant source of Sr in the catchments is considered to be from the weathering of silicate minerals. Weathering rates for Sr and Ca in the Afon Hafren, calculated using Sr isotopes, were similar to those derived from mass balance studies. The rates for the Afon Hore were similar for Ca, but significantly different for Sr. The reason for the difference is unclear, but may be due to additional sources (calcite) in the catchment. Strontium isotope ratios for different input sources and compartments within the catchment were characterised and helped to identify potential flow pathways. The data suggest an important role for groundwater inputs in contrast to previous models which indicated a dominant role for soil waters.     

海平面升降中的元素地球化学响应--以塔中地区奥陶纪为例

海相岩石自生矿物中的锶同位素组成可反映其沉积时期的海平面波动趋势。塔中地区奥陶系87Sr／87Sr分析表明,在早奥陶世海平面总体呈下降趋势,而在中晚奥陶世海平面则持续上升并保持在奥陶纪平均海平面之上。氧同位素分析表明,塔中地区下奥陶统的白云岩主要为低海平面期高盐度环境沉积的准同生白云岩。微量元素分析结果支持同位素研究结论。分析测试表明,锶、氧同位素及一些微量元素均对海平面升降波动具有敏感的反应。     

Silicon isotopes in allophane as a proxy for mineral formation in volcanic soils

Weathering of basaltic ash in volcanic areas produces andosols, rich in allophane and ferrihydrite. Since the rate of mineral formation is very useful in climate and geochemical modelling, this study investigates Si isotope compositions of allophane as a proxy for mineral formation. Allophane formed in contrasting conditions in five Icelandic soil profiles displays silicon isotope signatures lighter than the basalt in less weathered soils (?0.64 ± 0.15‰), and heavier in more weathered organic-rich soils (+0.23 ± 0.10‰). The fate of the dissolved Si in those volcanic soils strongly depends on Al availability. In organic-rich soils, most of Al is humus-complexed, and the results support that Si precipitates as opaline silica by super-saturation, leaving an isotopically heavier dissolved Si pool to form allophane with uncomplexed Al. This study highlights that Si isotopes can be useful to record successive soil processes involved in mineral formation, which is potentially useful in environmental paleo-reconstruction.     

Organic compounds in produced waters from coalbed natural gas wells in the Powder River Basin,Wyoming, USA

The organic composition of produced water samples from coalbed natural gas (CBNG) wells in the Powder River Basin, WY, sampled in 2001 and 2002 are reported as part of a larger study of the potential health and environmental effects of organic compounds derived from coal. The quality of CBNG produced waters is a potential environmental concern and disposal problem for CBNG producers, and no previous studies of organic compounds in CBNG produced water have been published. Organic compounds identified in the produced water samples included: phenols, biphenyls, N-, O-, and S-containing heterocyclic compounds, polycyclic aromatic hydrocarbons (PAHs), aromatic amines, various non-aromatic compounds, and phthalates. Many of the identified organic compounds (phenols, heterocyclic compounds, PAHs) are probably coal-derived. PAHs represented the group of organic compounds most commonly observed. Concentrations of total PAHs ranged up to 23 μg/L. Concentrations of individual compounds ranged from about 18 to <0.01 μg/L. Temporal variability of organic compound concentrations was documented, as two wells with relatively high organic compound contents in produced water in 2001 had much lower concentrations in 2002.     

Evidence for mass-dependent isotopic fractionation of strontium in a glaciated granitic watershed

The stable isotope composition of strontium (expressed as δ^88/86Sr) may provide important constraints on the global exogenic strontium cycle. Here, we present δ^88/86Sr values and ⁸⁷Sr/⁸⁶Sr ratios for granitoid rocks, a 150 yr soil chronosequence formed from these rocks, surface waters and plants in a small glaciated watershed in the central Swiss Alps. Incipient chemical weathering in this young system, whether of inorganic or biological origin, has no resolvable effect on the ⁸⁷Sr/⁸⁶Sr ratios and δ^88/86Sr values of bulk soils, which remain indistinguishable from bedrock in terms of Sr isotopic composition. Although due in part to the chemical heterogeneity of the forefield, the lack of a resolvable difference between soil and bedrock isotopic composition indicates that these soils have thus far witnessed minimal net loss of Sr; a low degree of chemical weathering is also implied by bulk soil chemistry. The isotopic composition of Sr in streamwater is more radiogenic than median soil, reflecting the preferential weathering of biotite in the catchment; streamwater δ^88/86Sr values, however, are indistinguishable from bulk soil δ^88/86Sr values, implying that no resolvable fractionation of Sr isotopes takes place during release to the weathering flux in the Damma forefield. Analyses of plant tissue reveal that plants (Rhododendron and Vaccinium) preferentially assimilate the lighter isotopes of Sr such that their δ^88/86Sr values are significantly lower than those of the soils in which they grow. Additionally, δ^88/86Sr values of foliar and floral tissues are lower than those of roots, contrary to observations for Ca, for which Sr is often used as an analogue in weathering studies. We suggest that processes that discriminate against Sr in favour of Ca, due to the different nutritional requirement of plants for these two elements, are responsible for the observed contrast.