Origin of sulphate in the unsaturated zone and groundwater of a loess aquifer

The use of the sulphate mass balance (SMB) between precipitation and soil water as a supplementary method to estimate the diffuse recharge rate assumes that the sulphate in soil water originated entirely from atmospheric deposition; however, the origin of sulphate in soil and groundwater is often unclear, especially in loess aquifers. This study analysed the sulphur (δ³⁴S-SO₄) and oxygen (δ¹⁸O-SO₄) isotopes of sulphate in precipitation, water-extractable soil water, and shallow groundwater samples and used these data along with hydrochemical data to determine the sources of sulphate in the thick unsaturated zone and groundwater of a loess aquifer. The results suggest that sulphate in groundwater mainly originated from old precipitation. When precipitation percolates through the unsaturated zone to recharge groundwater, sulphates were rarely dissolved due to the formation of CaCO₃ film on the surface of sulphate minerals. The water-extractable sulphate in the deep unsaturated zone (>10 m) was mainly derived from the dissolution of evaporite minerals and there was no oxidation of sulphide minerals during the extraction of soil water by elutriating soil samples with deionized water. The water-extractable concentration of SO₄ was not representative of the actual SO₄ concentration in mobile soil water. Therefore, the recharge rate cannot be estimated by the SMB method using the water-extractable concentration of SO₄ in the loess areas. This study is important for identifying sulphate sources and clarifying the proper method for estimating the recharge rate in loess aquifers.     

Evolution of the Subsurface K‐Rich Brines in the Triassic Carbonates in the Sichuan Basin of China

Subsurface K‐rich brines are important mineral resources for fertilizer production while the evolution of such brines is poorly documented. In the Sichuan Basin in southwest China, they are found mainly in the Middle and Lower Triassic marine carbonate aquifers. Total dissolved solids of the brines range from 176 to 378 g/L and K concentrations, from 1.9 to 53.3 g/L. We found that the brines are mainly of Cl‐Na type, while Ba is absent in the brines. Comparison of the brine samples with both the trajectories of ions and the newly proposed trajectories of ion ratios of evaporated seawater suggests that the brines are enriched in Ca, Sr, Li, and I, depleted in SO₄ and Mg, and neither enriched nor depleted in Cl and Na. These brines underwent four evolutionary periods: (1) deposition of marine rocks, (2) deposition of continental clastics, (3) tectonic deformation, and (4) rock erosion. Precipitation of salt minerals, dolomitization, sulfate reduction, and recrystallization during the first two periods are responsible for the enrichment and depletion of the chemical constituents of the brines. Extremely high K concentrations in two wells, both tapping the Middle Triassic Leikoupo carbonate aquifers, are attributed to the subsurface dissolution of potash salts during the migration of the brines to the anticlines formed during the third period in the Paleogene age. Saline and salty springs emanate from the outcropping carbonates in the river valleys in some anticlines in the eastern basin due to incongruent dissolution of the salt‐bearing carbonates during the fourth period.     

High sulphate concentrations in squeezed Boom Clay pore water: evidence of oxidation of clay cores

Pore water has been extracted from Boom Clay by mechanical squeezing. Clay cores were obtained from various boreholes, all drilled at the SCK·CEN domain (Mol, Belgium).In contrast to pore water collected from piezometers, high sulphate concentrations are measured in the squeezed pore water. The lowest sulphate concentrations (<60 mg/l) were measured in pore waters squeezed immediately after drilling. Higher sulphate concentrations were often measured in the pore water when the clay cores were preserved for some time (generally <500 mg/l SO₄²⁻, but sometimes up to 20,000 mg/l SO₄²⁻). Nevertheless, a relation between preservation time and sulphate content could not be retrieved. However, major ion concentrations were obviously correlated with the sulphate content in the squeezed waters. The observed evolution in chemical composition were explained by water–rock interactions considering the pyrite oxidation and the subsequent ion exchange and mineral dissolution reactions.     

A study on hydrological series of the Niger River

Abstract

The Hubert segmentation procedure has been applied to historical series of annual average discharges of the Niger River at Koulikoro (Mali), Niamey (Niger) and Lokoja (Nigeria) stations. The breaks, especially those identified at Koulikoro and Niamey, match well with those identified in the Senegal River series at Bakel using the same procedure. Lokoja departs from this regional pattern, as it shows in the late 1980s a return to wetter conditions much earlier than the other three stations. The magnitudes of the variation of the inter-annual means between the alternating wet and dry periods are significant and similar. These results seem to suggest that phenomena causing non-stationarity in hydrological series can have a sub-continental impact or, in contrast, may be more limited in their spatial coverage.

Editor Z.W. Kundzewicz; Associate editor H. Aksoy

Citation Abrate, T., Hubert, P., and Sighomnou, D., 2013. A study on hydrological series of the Niger River. Hydrological Sciences Journal, 58 (2), 271–279.     

Origin and chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta,Botswana

The origin and the chemical and isotopic evolution of dissolved inorganic carbon (DIC) in groundwater of the Okavango Delta in semi-arid Botswana were investigated using DIC and major ion concentrations and stable oxygen, hydrogen and carbon isotopes (δD, δ¹⁸O and δ¹³C_DIC). The δD and δ¹⁸O indicated that groundwater was recharged by evaporated river water and unevaporated rain. The river water and shallow (<10 m) groundwater are Ca–Na–HCO₃ type and the deep (≥10 m) groundwater is Na–K–HCO₃ to HCO₃–Cl–SO₄ to Cl–SO₄–HCO₃. Compared to river water, the mean DIC concentrations were 2 times higher in shallow groundwater, 7 times higher in deep groundwater and 24 times higher in island groundwater. The δ¹³C_DIC indicate that DIC production in groundwater is from organic matter oxidation and in island groundwater from organic matter oxidation and dissolution of sodium carbonate salts. The ionic and isotopic evolution of the groundwater relative to evaporated river water indicates two independent pools of DIC.     

Hydrologic and biogeochemical controls on the spatial and temporal patterns of nitrogen and phosphorus in the Kuparuk River,arctic Alaska

Nitrogen (N) and phosphorus (P) dynamics in the Kuparuk River in arctic Alaska were characterized in a 3‐year study using routine samples near the mouth of the river at the Arctic Ocean, synoptic whole‐river surveys, and temporally intense sampling during storms in three headwater basins. The Lower Kuparuk River has low nitrate concentrations (mean [NO₃]‐N] = 17 µg l^?1 ± 1·6 SE) and dissolved inorganic N (DIN, mean [N] = 31 µg l^?1 ± 1·2 SE) compared with rivers in more temperate environments. Organic forms constituted on average 90% of the N exported to the Arctic Ocean, and high ratios of dissolved organic N (DON) to total dissolved N (TDN) concentrations (mean 0·92) likely result from waterlogged soils formed by reduced infiltration due to permafrost and low hydrologic gradients. Annual export of TDN, DON, and particulate N averaged 52 kg km^?2, 48 kg km^?2, and 4·1 kg km^?2 respectively. During snowmelt, the high volume of runoff typically results in the highest nutrient loads of the year, although high discharge during summer storms can result in substantial nutrient loading over short periods of time. Differences in seasonal flow regime (snowmelt versus rain) and storm‐driven variation in discharge appear to be more important for determining nutrient concentrations than is the spatial variation in processes along the transect from headwaters towards the ocean. Both the temporal variation in nitrate:DIN ratios of headwater streams and the spatial variation in nitrate:DIN between larger sub‐basins and smaller headwater catchments is likely controlled by shifts in nitrification and soil anoxia. Copyright © 2008 John Wiley & Sons, Ltd.     

Multiple-indicator study of the response of groundwater recharge sources to highly turbid river water after a landslide in the Tedori River alluvial fan,Japan

The large volume of groundwater stored in the Tedori River alluvial fan, Ishikawa Prefecture, Japan, is an important source of local drinking and industrial water. The Tedori River was observed to be highly turbid from the beginning of May 2015 to at least November 2017 due to a landslide in the upper reach of the river. After the landslide, the groundwater level was drawn down by several to 10 m near the middle river section during paddy irrigation periods in 2015 and 2016. This study addresses the impacts of the highly turbid water on groundwater recharge from the river and paddy fields. In 2016, we sampled groundwater, river water, paddy irrigation water, paddy ponding water, and precipitation five times at 2-month intervals. We analysed the H, O, and Sr stable isotopic compositions and major dissolved ion (and Sr) concentrations and compared our data to previous data obtained in June 2011. Ca, Sr, Cl, SO₄, and TN concentrations and δ¹⁸O values were higher in June 2016 than in June 2011; these increases were more extreme along the left bank of the Tedori River than along the right bank. We explored the mixing of Tedori River water with groundwater using a two-endmember mixing model based on their Sr concentrations and isotopic compositions. Compared to June 2011, mixing ratios were decreased near the Tedori River in 2016, and larger decreases were observed along the left bank and in the middle stream area. These results confirm that the contribution to groundwater recharge from the river decreased during the turbidity event, particularly along the left bank.     

Hydrochemical and isotopic characterization of groundwater in the southeastern part of the Plateaux Region,Togo

Hydrochemical, inverse geochemical modelling and isotopic approaches are used to assess the hydrogeochemical evolution of groundwater from the basement aquifers in the southeastern part of the Plateaux Region, Togo. Groundwater originates from present-day rainwater infiltration and is mostly fresh and slightly acidic to neutral. Hydrochemical facies are predominantly mixed cations-HCO₃ associated with Ca/Mg-Cl, Na-HCO₃ and Na-Cl water types in equilibrium with kaolinite and Ca/Mg-smectites. They are related to silicates hydrolysis, anthropogenic contamination, nitrification/denitrification, mixing along flowpaths and dissolution/precipitation of secondary minerals. The pattern of flow paths is in accordance with an increasing trend in total dissolved solids (TDS) toward the potentiometric depression located in the central and southern parts of the aquifer system. Inverse geochemical modelling using the NETPATH-WIN model showed the relative importance of biotite, plagioclase and amphibole weathering and dissolution of secondary carbonate minerals along the flowpath, suggesting that an abundance of minerals is not necessarily the main factor controlling the groundwater chemistry evolution.     

Water Quality Assessment and Resource Potentials: the Case of Aba–Urban and its Environs,Niger Delta Basin

The quest for improved water supply to cater for the ever increasing population has given rise to the assessment of water quality and resource potentials in Aba-Urban and its environments. The area, which lies within the Niger Delta Basin is underlain by the Benin Formation that is highly aquiferous. Samples of sands and water were subjected to sedimentological and hydrochemical analysis, respectively. Result reveals that the aquifer is thick (over 100 m) and unconfined. The computed aquifer parameters indicate high yielding clean-sands with hydraulic conductivity values ranging from 1.13 × 10^–4 to 5.70 × 10^–3 m/s. The specific discharge is about 14.2 m/year while the average linear groundwater velocity is calculated to be 53.46 m/year. Hydrochemical investigations carried out on water samples from Aba River and the groundwater system revealed low dissolved geochemical constituents. Although, there is a slight increase from the north to the southern part along the flow path. In general, the groundwater is relatively enriched in Ca, Mg?HCO^-₃ions and is predominantly of bicarbonate constituents. However, in some places Cl^? ions dominate over HCO^-₃ions. This is common where the water has come in contact with domestic sewage. This kind of contamination is also accompanied by elevated concentration of NO^-₃ions. Generally, the groundwater in most cases meets the standard for human consumption and is a better alternative to surface water. Consequently an increase exploitation of the prolific Benin aquifer through more hygienic and safe methods will surely be the best way of improving the domestic water supply situation in Aba City.     

Hydrogeochemical Evolution of Interaction Between Surface Water and Groundwater Affected by Exploitation

Hydrogeochemical evolution of interactions between surface water and groundwater is crucial for guaranteeing water supply quality in a riverside water source area. This study focuses on the seasonal and spatial characteristics of hydrogeochemical evolution affected by groundwater exploitation in the Hulan water source area using hydrochemical analyses and stable isotope tracers. Results show that the concentrations of major ions and total dissolved solids (TDS) increase considerably during the dry season. A bicarbonate water type is primarily produced by the dissolution of calcite, dolomite and gypsum, as well as the cation exchange and human activities. Along the typical infiltration path, the proportions of surface water increase with proximity to the river from 8%-63% during the wet season to 11%-84% during the dry season, which are attributed to an increased hydraulic gradient by exploitation. The typical path is classified into two zones. The first is the intensive mixing zone (within 1 km) with increasing concentrations of major ions and TDS due to mixing effect. The second is the exploitation influence zone (1-3.3 km) with increased concentrations of Ca²⁺, Mg²⁺, SO₄²⁻, and HCO₃⁻ during the dry season due to two reasons of seasonal variations in evaporation, stronger water-rock interactions and mixing effects with increased surface water by exploitation.     

Behaviour of Different Molecular-weight Fractions of DOC of Elbe River Water during River Bank Infiltration

This paper reports changes in dissolved organic carbon concentration β(DOC) and the relation between UV-active and non-UV-active components determined for Elbe river water and river bank infiltrate in the Torgau river basin between 1992 and 1994. Using an ultrafiltration method, the fractionation of the DOC content was obtained for the fractions > 10 000 g/mol, 1 000…10 000 g/mol, and < 1 000 g/mol. The spectral absorption coefficient at 254 nm a₂₅₄ of the molecular-weight fractions was also measured. The mean total DOC concentration of Elbe river water decreased from 6.0 mg/L to below 3.9 mg/L along two investigated flowpaths. Two thirds of the decrease occurred within the first few metres of the river bed and one third along the 350 m length of the groundwater flowpaths. The a₂₅₄ values showed a significant decrease from 14.8 1/m in Elbe river water to 7.8 1/m in the aquifer. Along a flowpath, the proportion of low-molecular weight fraction of DOC increased, the proportion of high-molecular weight fraction decreased, and the proportion of the 1 000…10 000 g/mol molecular-weight fraction remained relatively stable. The Elbe river water contained the main portion of UV-active compounds in the fraction 1 000…10 000 g/mol, and this was also the case for samples of river infiltrate. For the high-molecular weight fraction, mainly non-UV-active compounds were attenuated in the river bed sediment.     

Temporal variation of chemical and mechanical weathering in NE Iceland: Evaluation of a steady-state model of erosion

This study critically assesses the temporal sensitivity of the steady-state model of erosion that has been applied to chemical and mechanical weathering studies of volcanic islands and the continents, using only one sample from each catchment. The model assumes a geochemical mass balance between the initially unweathered rock of a drainage basin and the dissolved and solid loads of the river.Chemical composition of 178 samples of suspended and dissolved inorganic river constituents, collected in 1998–2002, were studied from five basaltic river catchments in NE Iceland. The Hydrological Service in Iceland has monitored the discharge and the total suspended inorganic matter concentration (SIM) of the glacial rivers for ~ four decades, making it possible to compare modelled and measured SIM fluxes.Concentration of SIM and grain size increased with discharge. As proportion of clay size particles in the SIM samples increased, concentrations of insoluble elements increased and of soluble decreased. The highest proportion of altered basaltic glass was in the clay size particles.The concentration ratio of insoluble elements in the SIM was used along with data on chemical composition of unweathered rocks (high-Mg basalts, tholeiites, rhyolites) to calculate the pristine composition of the original catchment rocks. The calculated rhyolite proportions compare nicely with area-weighted average proportions, from geological maps of these catchments.The calculated composition of the unweathered bedrock was used in the steady-state model, together with the chemical composition of the suspended and dissolved constituents of the river. Seasonal changes in dissolved constituent concentrations resulted in too low modelled concentrations of SIM_mod at high discharge (and too high SIM_mod at low discharge). Samples collected at annual average river dissolved load yielded SIM_mod concentrations close to the measured ones. According to the model, the studied rivers had specific mechanical denudation rates of 1.3–3.0 kg/m²/yr whereas the average measured rates were 0.8–3.5 kg/m²/yr which are among the highest on Earth.This study validates the use of a steady-state model of erosion to estimate mechanical weathering rates at the scale of a river catchment when the collected riverine dissolved load represents the average chemical composition over a mean hydrological year.     

Identifying spatio-temporal variation and controlling factors of chemistry in groundwater and river water recharged by reclaimed water at Huai River,North China

Reclaimed water is efficiently used to recover the dry river, but river water and groundwater may be impacted considering the water quality. Thus, it is critical to study the factors controlling water chemistry. Samples of reclaimed water, river and groundwater were collected monthly from January to September in 2010, in Huai River (North China). And samples were analyzed for major 15 physio-chemical parameters. Using hierarchical cluster analysis, 9 months are divided into two distinct groups, which show the clear temporal variation. In reclaimed water and river water, one group includes February, while the other includes other months. In shallow and deep groundwater, one group includes months from January to April, while the other encompasses others. Monitoring stations are classified into three groups. Group A with high value of ions and nitrogen (order: NH₄-N > NO₃-N > NO₂-N) includes reclaimed water and river water. Group B with moderate concentration and nitrogen (order: NO₃-N > NH₄-N > NO₂-N) includes all shallow groundwater and one deep groundwater. Group C with the low value and nitrogen (order: NO₃-N > NO₂-N > NH₄-N), includes two deep groundwater. Using multivariate analysis and ionic relationships, river water chemistry is found to be controlled by reclaimed water and evaporation process; chemistry in shallow groundwater and one deep groundwater, with type of Na–Ca(Mg)–HCO₃–Cl, is controlled by dissolution of calcite, carbonate weathering. Additionally, reactions of nitrification, denitrification and cation exchange occur in the infiltration of reclaimed water; chemistry in the other deep groundwater, with type of Ca–Mg–HCO₃–Cl, is controlled by dissolution of calcite, carbonate weathering and denitrification.     

Uranium and thorium isotopes in the rivers of the Amazonian basin: hydrology and weathering processes

Two expeditions (October 1989 and May 1992) were carried out to two points of the main Amazon River channel and four tributaries. The Solimões and Madeira rivers, taking their origin in the Andes, are whitewater rivers. The Negro River is a typical acid, blackwater river. The Trombetas River flows through bauxite‐rich areas, and is characterized by low concentrations of dissolved humic substances. The ²³⁸U, ²³⁴U, ²³²Th and ²³⁰Th activities were recorded from dissolved, suspended particulate phases and river bank sediments. The latter were analysed for their ²²⁶Ra, ²²⁸Ra and ²¹⁰Pb contents, and also subjected to leaching with 0·2 M hydroxylamine–hydrochloride solution to determine the concentrations of radionuclides bound to amorphous Fe hydroxides and Mn oxides and hydroxides. The dissolved U average concentration in the Amazon system is ten times lower than the mean world river concentration. The uranium concentration observed at Óbidos in the lower Amazon (0·095 µg L^?1), where the U content in the river bank sediments and suspended matter is lowest, suggests U release from the solid phase during river transport. About 485 t of U are transported annually to the Amazon delta area in dissolved form, and 1943 t bound to suspended particulate matter. Total U and Th concentrations in the river bank sediments ranged from 1·59 to 7·14 µg g^?1 and from 6·74 to 32 µg g^?1, respectively. The highest concentrations were observed in the Trombetas River. The proportion extracted by means of the hydroxylamine solution (HL) was relatively high for U in the Trombetas river bank sediment (31%) and for Th in the Solimões sediment (30%). According to the alpha recoil effects, the ²³⁴U/²³⁸U activity ratios of the Andean river waters and downstream Amazon water (Óbidos) were >1, but were <1 in the Negro River (at Manaus). The activity ratios of dissolved U correlate with pH and also with the U activity ratios in the river bank sediment hydroxylamine extracts. As expected, the ²³⁴U/²³⁸U activity ratios in river bank sediments were <1 in the Andean rivers and in the downstream Amazon, but they were >1 in the Trombetas and Negro rivers. Such ratios probably result from the binding of dissolved uranium to solid sediment. The ²²⁸Th/²³²Th ratios of river bank sediments were close to unity (except for the Negro River, where it is lower), suggesting no significant Th exchanges between the river water and the sediment. The ²²⁶Ra/²³²Th activity ratios were <1, and the ²²⁶Ra/²²⁸Ra activity ratios generally were significantly higher than the activity ratios of their respective parents. This perhaps is the result of easier leaching of the ²²⁶Ra parent, ²³⁰Th, from solid material (owing to the alpha recoil effect) than of the ²²⁸Ra parent. Uranium and thorium isotopes were used as tools to evaluate the chemical weathering rate of rocks in the Amazon system, which was estimated to be 2·7 cm 1000 year^?1 s^?1. Copyright © 2002 John Wiley & Sons, Ltd.     

Sources and fate of nutrients in a subtropical reservoir

This study examined the sources and fate of nutrient inputs from two principal tributaries to the eutrophic subtropical Wivenhoe reservoir: an unregulated river and a dammed river with regular releases, during a period of declining reservoir water levels. Nutrient budgets were constructed over a period of 6 years, and combined with short-term data on nutrient concentrations and forms, and δ¹⁵N stable isotope data. Our study found that over a 6 year period, there was net retention of phosphorus (P) in the reservoir, with 60% of inputs retained. Most of the P input load came from the unregulated river, with an agricultural catchment, during periods of high flow. During one event half of the total TP load from the unregulated river in the study period was delivered in only 12 days. Much of the P was dissolved inorganic P (DIP) and was derived from high P concentrations in soils and sediments. This highlights the importance of appropriate catchment management practices to reduce P losses from terrestrial systems because retention of P in reservoir sediments reduces the availability of this nutrient for agricultural production. In contrast, there was negligible retention of nitrogen (N). The unregulated river was an important source of N derived from N fixation in the river and adjacent soils, while the source from the dammed river was mostly reprocessed N. The high retention of P relative to N is consistent with relatively higher accumulation of P in sediments.     

Controls on Methane Occurrences in Aquifers Overlying the Eagle Ford Shale Play,South Texas

Assessing natural vs. anthropogenic sources of methane in drinking water aquifers is a critical issue in areas of shale oil and gas production. The objective of this study was to determine controls on methane occurrences in aquifers in the Eagle Ford Shale play footprint. A total of 110 water wells were tested for dissolved light alkanes, isotopes of methane, and major ions, mostly in the eastern section of the play. Multiple aquifers were sampled with approximately 47 samples from the Carrizo‐Wilcox Aquifer (250‐1200 m depth range) and Queen City‐Sparta Aquifer (150‐900 m depth range) and 63 samples from other shallow aquifers but mostly from the Catahoula Formation (depth <150 m). Besides three shallow wells with unambiguously microbial methane, only deeper wells show significant dissolved methane (22 samples >1 mg/L, 10 samples >10 mg/L). No dissolved methane samples exhibit thermogenic characteristics that would link them unequivocally to oil and gas sourced from the Eagle Ford Shale. In particular, the well water samples contain very little or no ethane and propane (C1/C2+C3 molar ratio >453), unlike what would be expected in an oil province, but they also display relatively heavier δ¹³C_methane (>?55‰) and δD_methane (>?180‰). Samples from the deeper Carrizo and Queen City aquifers are consistent with microbial methane sourced from syndepositional organic matter mixed with thermogenic methane input, most likely originating from deeper oil reservoirs and migrating through fault zones. Active oxidation of methane pushes δ¹³C_methane and δD_methane toward heavier values, whereas the thermogenic gas component is enriched with methane owing to a long migration path resulting in a higher C1/C2+C3 ratio than in the local reservoirs.     

Application of Ultrafiltration for Characterization of the DOC of Elbe River Water

An ultrafiltration methodology and the results of its application on Elbe river water are presented. Compared with other methods, Ultrafiltration allows fractionation of the molecular-weight fractions of DOC for higher volumes of solution in a shorter time. To characterize the molecular-weight fractions, the sum parameter DOC (β(DOC)) and the absorption coefficient at 254 nm a₂₅₄ were measured, together with determination of a₂₅₄/ β(DOC) for further characterization of the DOC fractions and to provide information about changes in parts of the UV-active substances of the total dissolved organic material. In the period May 1992 to November 1994, the DOC molecular-weight composition of 65 samples of Elbe river water were determined. At two sampling locations (Torgau-East and Meissen), the DOC content β(DOC) was approximately 6 mg/L. The high-molecular weight fraction (> 10000 g/mol) gave a mean of 13% of the total DOC content β₀(DOC). The measurements showed that the molecular composition of DOC in the Elbe does not greatly differ. There was also no clear seasonal influence on the molecular-weight composition of the DOC content. During the period of investigation, the percentage part of β(DOC) and a₂₅₄/β(DOC) of the high-molecular weight fraction of the total dissolved organic material increased, while the a₂₅₄/β(DOC) values of the middle molecular-weight fraction remained fairly constant. The dependence of β(DOC) on discharge of the Elbe river is low. Changes in molecularweight composition of DOC were only observed during the steepest increase in river discharge during a flood event, with another spectrum of substances responsible for the increase in β(DOC) when compared with the β(DOC) for low or middle water level.     

Evaluation of CO2 solubility-trapping and mineral-trapping in microbial-mediated CO2–brine–sandstone interaction

Evaluation of CO₂ solubility-trapping and mineral-trapping by microbial-mediated process was investigated by lab experiments in this study. The results verified that microbes could adapt and keep relatively high activity under extreme subsurface environment (pH < 5, temperature > 50 °C, salinity > 1.0 mol/L). When microbes mediated in the CO₂–brine–sandstone interaction, the CO₂ solubility-trapping was enhanced. The more biomass of microbe added, the more amount of CO₂ dissolved and trapped into the water. Consequently, the corrosion of feldspars and clay minerals such as chlorite was improved in relative short-term CO₂–brine–sandstone interaction, providing a favorable condition for CO₂ mineral-trapping. Through SEM images and EDS analyses, secondary minerals such as transition-state calcite and crystal siderite were observed, further indicating that the microbes played a positive role in CO₂ mineral trapping. As such, bioaugmentation of indigenous microbes would be a promising technology to enhance the CO₂ capture and storage in such deep saline aquifer like Erdos, China.     

淮北临涣矿采煤沉陷区不同水体水化学特征及其影响因素

为研究淮北临涣矿采煤沉陷区不同水体的补给水源及溶质来源,在现场调查的基础上,系统采集丰水期、平水期、枯水期沉陷区积水、地表河水和浅层地下水样进行测试分析,采用Piper三线图、Gibbs图和因子分析方法,对不同水体水化学特征及其影响因素进行讨论.结果表明:地表水水体总溶解性固体(TDS)质量浓度表现为枯水期丰水期平水期,浅层地下水表现为枯水期平水期丰水期,地表水TDS质量浓度明显高于浅层地下水.地表水中主要阴阳离子为Na~+、Cl~-和SO_4~(2-),水化学类型主要为SO_4~(2-)-Cl~--Na~+型;浅层地下水离子以HCO_3~-、Ca~(2+)和Mg~(2+)为主,表现为HCO_3~--Ca~(2+)-Mg~(2+)型.结合Gibbs图和因子分析可知,地表水受蒸发作用、地表径流以及采煤活动等因素影响,浅层地下水在一定程度上体现出大气降水和地表水补给的特点,受岩石风化作用影响较为明显.