Impact of regional geology, land use and flow path on stream water chemistry in a small watershed

Stream water chemistry is dependent on the physical, chemical and biological processes occurring in the watershed. Understanding the governing mechanism of the stream water chemistry in a watershed is the first step for the water quality management. The study area drains a total catchment area of 1.46 km^2 and consists of forest （80%）, upland （15%） and rice paddy field （5%）. The studied area has two distinctive bedrocks, quartzite and schist. We periodically collected the stream water samples at mainstream and tributaries and the pH, electrical conductivity （EC）, alkalinity and the concentrations of cations and anions of the collected stream water samples were determined in the field and laboratory. The all collected water samples were nearly neutral and the EC and concentrations of Na, K, Ca, Sr, Si and HCO3 of the stream water samples collected from the schist terrain had greater values than those from the quartzite terrain. The mainstream running along the boundary of schist and quartzite terrains had the intermediate values of the tributaries. The stream water samples collected in and near the upland showed a high concentration of NO3^- than those of forest regardless the lithology. The stream pathway was also directly reflected on the chemistry of stream water. The stream water drained in the forest of quartzite terrain had the lowest values of alkalinity, EC and concentrations of cations and anions but the stream water drain in the upland of schist terrain had the highest values of EC and concentrations of cations and anions, especially NO3^-.     

Assessment of Rock-Eval Tmax Data in Bambra-2 Well of Barrow Sub-basin, North West Shelf of Australia： A Case Study of Contaminated Rock-Eval Data

The contamination of cuttings and side-wall core (SWC) samples in the Bambra-2 well by drilling-mud additives and natural hydrocarbons may cause Ruek-Eval Tmax (℃) data to be suspect, and affect its utility in the assessment of thermal maturity. The Rock-Eval results of 284 cuttings samples, 31 side-wall core samples and conventional core samples from the Jurassic-Cretaceous sedimentary sequences in the Bambra-2 well are presented in this paper. Significantly lower Tmax values from cuttings samples compared with Tmax values from conventional core samples and solvent extracted SWC samples, from the deeper and higher maturity interval, are thought to have been caused by contamination by diesel and other drilling-mud additives. The cuttings samples in the Barrow Group of Cretaceous may be contaminated by natural hydrocarbons, resulting their Tmax values to be 2-10℃ lower than a regularly increased Tmax trend from core samples. This study indicates that more reliable Rock-Eval Tmax data are obtained from the conventional core samples and solvent extracted SWC samples. This study also indicates that the Tmax values from some SWC samples were also affected by free hydrocarbons, due to the use of diesel as a mud additive as well.     

Composition of Kerogen in Kupferschiefer from Southwest Poland

Thirty-seven Kupferschiefer samples from southwestern Poland were analyzed by microscopy, Rock-Eval approach and instrumental neutron activation analysis to understand the geochemical and morphological characteristics of kerogen present in the samples. The analytical results indicate that there are two different types of kerogens. One type was only subjected to thermal alteration processes, and the other was further oxidized after deposition of the sediment.In the oxidized samples migrabitumen was transformed into pyrobitumen. Rock-Eval analyses show a significant decrease in HI values in the oxidized samples and an increase in OI values in relation to the samples that were not influenced by oxidation. Variations in S2 versus Corg contents indicate a change in kerogen from Type II to Type III with progressing oxidation. The presence of pyrobitumen and the depletion of hydrogen in the altered kerogen allow one to conclude that the kerogen was used as hydrogen donor for thermochemical sulfate reduction(TSR).     

Isotopic composition of dissolved boron and its geochemical behavior in a freshwater-seawater mixture at the estuary of the Changjiang （Yangtze） River

The isotopic composition of dissolved boron, in combination with the elemental concentrations of B, Cl and salinities in freshwater-seawater mixed samples taken from the estuary of the Changjiang River, the largest one in China, was investigated in detail in this study. Brackish water and seawater samples from the estuary of the Changjiang River were collected during low water season in November, 1998. Boron isotopic compositions were determined by the Cs2BO^＋2-graphite technique with a analytical uncertainty of 0.2‰ for NIST SRM 951 and an average analytical uncertainty of 0.8‰ for the samples. The isotopic compositions of boron, expressed in δ^11B, and boron concentrations in the Changjiang River at Nanjing and seawater from the open marine East Sea, China, are characterized by δ^11B values of -5.4‰ and 40.0‰, as well as 0.0272 and 4.43 mg B/L, respectively. Well-defined correlations between δ^11B values, B concentrations and Cl concentrations are interpreted in terms of binary mixing between fiver input water and East Sea seawater by a process of straightforward dilution. The offsets of δ^11B values are not related to the contents of clastic sediment and to the addition of boron. These relationships favor a conservative behavior of boron at the estuarine of the Changjiang River.     

The O and H isotope characteristics of water from major rivers in China

Isotopic compositions of the water sources and evapotranspiration in large rivers of China are not well explored. In this investigation, d18 O and dD values of water from major large rivers of China are integrated to understand the spatial and temporal variations in the isotopes of water and d-excess. River water samples were collected from the channels and tributaries of the Changjiang, Yellow, Songhua and Liao Rivers in China. Water from upstream was generally enriched with light isotopes relative to that from downstream areas. Water from the Songhua River and upper reach of the Changjiang River has relatively negative isotopic values impacted by latitude and altitude effects, respectively. The spatial pattern showed that d18O-H2 O values in rivers mainly ranged from-9 to-7 % in most of China based on roughly mapped contours, and rivers enriched in light isotopes were primarily located in the Tibetan Plateau and northeast China The slopes of linear regression from the Yellow and Liao Rivers suggested that the loss of water by direct evaporation shifted the isotopes of water, especially in some small tributaries. Additionally, there was a narrow range of low d18OH2 O values from the main channel of rivers during the lowflow season relative to the high-flow season due to influence of the monsoon climate. No distinct spatial variation of d-excess values was found in the rivers of China. However, water samples in some rivers with low d-excess values had high d18 O values, indicating that evaporation in the tributaries has led to significant water loss, especially in tributaries of the Yellow and Liao Rivers.     

Identifying the Sources of Solutes in Karst Groundwater in Chongqing,China: a Combined Sulfate and Strontium Isotope Approach

Groundwater from karst subterranean streams is among the world’s most important sources of drinking water supplies, and the hydrochemical characteristics of karst water are impacted by both natural environment and people. Therefore, the study of hydrochemistry and its solutes’ sources is very important to ensure the normal function of life support systems. In this paper, thirty?five representative karst groundwater samples were collected from different aquifers (limestone and dolomite) and various land use types in Chongqing to trace the sources of solutes and relative hydrochemical processes. Hydrogeochemical types of karst groundwater in Chongqing were mainly of the Ca?HCO3 type or Ca (Mg)?HCO3 type. However, some hydrochemical types of karst groundwater were the K+Na+Ca?SO4 type (G25 site) or Ca?HCO3+SO4 type (G26 and G14 site), indicating that the hydrochemistry of these sites might be strongly influenced by anthropogenic activities or unique geological characteristics. The dissolved Sr concentrations of the studied groundwater ranged from 0.57 to 15.06 μmmol/L, and the 87Sr/86Sr varied from 0.70751 to 0.71627. The δ34S?SO42? fell into a range of ?6.8‰?21.5‰, with a mean value of 5.6‰. The variations of both 87Sr/86Sr and Sr values of the groundwater samples indicated that the Sr element was controlled by the weathering of limestone, dolomite and silicate rock. However, the figure of 87Sr/86Sr vs. Sr2+/[K++Na+] showed that the anthropogenic inputs also obviously contributed to the Sr contents. For tracing the detailed anthropogenic effects, we traced the sources of solutes collected karst groundwater samples in Chongqing according to the δ34S value of potential sulfate sources. The variations of both δ34S and 1/SO42? values of the groundwater samples indicated that the atmospheric acid deposition (AAD), dissolution of gypsum (GD), oxidation of sul?de mineral (OS) or anthropogenic inputs (SF: sewage or fertilizer) have contributed to solutes in karst groundwater. The influence of oxidation of sul?de mineral, atmospheric acid deposit and anthropogenic inputs to groundwater in Chongqing karst areas was much widespread.     

Biomarker Compounds as Indicators of Paleoenvironments

In an attempt to assess the paleoenvironments of terrestrial sediments,some twenty-two representa-tive Chinese non-marine sediment samples were studied using the molecular organic geochemistry method.The sediment samples stuied include oilshale,shale,mudstone and glauber salt from Tertiary to Cretaceous in age.Judging from geological/geochemical data and paleosalinity data,the samples studied are of lacustrine sedimentary origin and can be divided into three different types:fresh water,brackish and saline/hypersaline lake sediments.The aliphatic fractions were separated from the extracts of the samples and analysed by means of GC and GC/MS instruments,giving a number of parameters such as relative abundances of alkanes and cycloalkanes as shown in the mass chromatograms.     

Strontium isotope composition of the Arno River Valley waters （Tuscany, Italy） as a natural tracer of water-rock interaction and mixing processes

Sr isotope studies of surficial waters have highlighted that differences in the ^87Sr/^86Sr ratio and Sr concentration are primarily caused by mixing of waters of various origins with specific isotopic and chemical characteristics, resulting from water-rock interaction processes. In this paper we reported the first Sr isotopic ratios, coupled with water chemistry, the measurement was carried out on samples related to （1） the Amo River （Tuscany, central-northern Italy）, between the source and the mouth, （2） the most important tributaries and to （3） the thermal water discharges seeping out in the southern part of the basin. The main goals are： a） to use the ^87Sr/^86Sr ratio as a discriminative parameter of source areas, b） to define its variation along both the main course and principal tributaries, and c） to estimate the effects of the mixing process of the different end-embers. The outcropping rocks in the Amo River Basin are predominantly sedimentary, mainly made up of Mesozoic limestones, Oligocene sandstones and Plio-Pleistocene marine-lacustrine formations. Triassic and Mesosinian evaporites crop out in the Elsa and Era reaches, whereas Paleozoic quartzitic formations occur in the Mrs. Pisani area. Strontium isotopic composition is generally controlled by lithology and does not seem to be affected by anthropic input and flow rate. The ^87Sr/^86Sr ratios in the Arno Basin vary between 0.707963 and 0.712743, the highest ratios being related to waters circulating in the Palezoic rocks and Oligocene sandstone formations. Less radiogenic values pertain to the Elsa and Era tributaries where contributions related to the dissolution of evaporitic sequences, and mixing processes with the thermal discharges have been distinguished. The tributaries show that water samples in the pristine area have higher ^87Sr/^86Sr ratios than the respective tributaries from which water samples were collected near the confluence. Eventually, water samples collected along the Arno River, close to the mouth, tend to have Sr isotopic ratios similar to those of the present seawater.     

REE geochemistry of Chaohu and Longgan lakes, eastern China

The rare-earth elements （REEs） are a series of elements including lanthanides with atomic numbers from 57 to 71, as well as Y with an atomic number of 39. The REEs are commonly used as geochemical tracers in the study of many geologic processes because of their unique and chemically coherent behavior. The main purpose of this research is to understand the effect of water-particle interaction on trace metal transport, the distribution and chemical species of the REEs in water through case studies on geochemical behavior of the REEs in the Chaohu and Longgan lakes, eastern China. Concentrations of the dissolved REEs were detected by ICP-MS （Inductively Coupled Plasma-Mass Spectrometry）. Before ICP-MS measurement, REEs were concentrated from water samples by using solvent extraction and back extraction with a mixture 65% HDEHP （2-etheylhexyl hydrogen phosphate） and 35% H2MEHP （2-ehtylhexyl dihydrogen phosphate）. The results showed that the average concentrations of dissolved REEs in summer are higher than in winter for Chaohu Lake： they were 162.6 ng/kg and 86.5 ng/kg, respectively. On the country, the REE contents of winter samples were higher than those of summer water samples for Longganhu Lake： they were 111.1 ng/kg and 44.0 ng/kg, respectively. The contents of suspended particulate matter and pH are the two important factors controlling the concentrations of dissolved REE in the lakes. The contents of the REEs decrease with increasing pH in the Longgan and Chaohu lakes. The suspended particulate matter shows different sorption/desorption toward the dissolved REEs in the two water bodies. Most lake water samples have a fiat NASC-normalized REE pattern, and the others have heavy REE-enrichment patterns relative to NASC, which may imply that the dissolved REEs were mainly present in the form of fine colloids in the Chaohu and Longgan lakes.     

Thermal properties of harzburgite and dunite at 0.8–3 GPa and 300–823 K and implications for the thermal evolution of Tibet

Thermal diffusivity(D)and thermal conductivity(κ)of harzburgite and dunite from Luobusha ophiolite were simultaneously measured up to 3 GPa and 823 K using the transient plane-source method in a multi anvil apparatus.The results show that the values of D andκof both samples systematically decrease with increasing temperature and increase with increasing pressure.By combination of the thermal physical data of rocks and minerals and geophysical constraints,we performed numerical simulation on the thermal evolution of Tibet vary over depth,distance and geologic ages.The present results provide new constraints on occurrence of partial melting and its geophysical significance beneath Tibetan crust.     

The effect of acid deposition on base cation cycling in a karstic-forested catchment： Evidence from strontium isotopes

Bedrock weathering and atmospheric deposition are the two primary sources of base cations （K^＋, Na^＋, Ca^2＋ and Mg^2＋） to forest ecosystems. Therefore, the key problem is to understand the relative inputs from these two sources and the cycling in the ecosystem. This study focuses on the effects of acid deposition on cation cycling in a small-forested karstic catchment in Guizhou Province. Sr isotope ratios were used as a tracer for understanding the transport process between the different cation pools： rock, soil, surface water, atmospheric deposition and plant. The samples of wet deposition, total deposition, throughfall, surface and ground waters, vegetation, and soil were monthly collected. The exchangeable Sr^2＋ and Ca^2＋ in soil samples were extracted by using 1 M ammonium acetate. The leaf-tissue samples were ashed at 550℃, and the residue was digested in ultrapure HClO4 and HNO3. All water samples were filtrated through 0.45 μm aperture filter paper. Base cation concentrations and Sr isotopic composition were analyzed for all the samples. The results show that acid deposition （average pH 4.9） frequently occurred in the studied region. Cation abundance follows an increasing manner from rainwater, throughfall, to surface water or ground water samples, suggesting that acid deposition at first eiuviates Ca^2＋ , Mg^2＋ and Sr^2＋ from leaf, then the exchangeable cations from soil, and at last cations accumulate in surface water or ground water.     

Stable isotopes （S, Cl） and hydrochemical variations in a karstic ground water system, Guiyang, SW China

A groundwater system in a karstic terrain is easily subject to pollution and its remediation is difficult once contaminated by human activities. The groundwater samples collected in both winter and summer seasons at Guiyang, SW China, show a wide range of variations in chemical composition and dominance of Ca^2＋, Mg^2＋, SO4^2-, and HCO3^- ions. The anthropogenic inputs include Cl^-, NO3^-, SO4^2-, Na^＋, and K^＋, as judged from the relationships between different elemental ratios and sewage samples. Cl^- concentrations of all water samples in the study area vary from 0 to 3.9 mmol/L in winter and are higher than in summer. In most of the samples, SO4^2- concentrations are high, ranging from 0.1 to 11 mmol/U The studies show that the cycling of sulfur plays an important role in controlling water chemistry and fate of contaminants in groundwater. In order to understand the source of SO4^2- and the geochemical cycling of some elements in the karstic groundwater environment, we have carried out a study on the variations of S and Cl isotope compositions, in addition to other isotopic tracers such as ^87Sr/^86Sr and δ^13C studied previously. The δ^37Cl values of the groundwater samples present a seasonal variation, ranging from 0.00‰ to ＋2.03‰ in winter and from -1.46‰ to ＋0.29‰ in summer. The surface water samples show a similar range of variations as observed for groundwater. Two rainwater samples collected at Guiyang have a distinct isotopic signature （mean value is -3‰） compared to the δ^37Cl values reported in literature. These results indicate that ground water is mainly derived from precipitation and suggest a fast recharge of the karst system by surface water.     

Stable Carbon Isotope Variations in Cave Percolation Waters and their Implications in Four Caves of Guizhou, China

Monitoring and sampling of main plants,soil CO2,soil water,bedrock,spring water,drip water and its corresponding speleothem were performed at four cave systems of Guizhou,Southwest China,from April 2003 to May 2004,in order to understand stable carbon isotope ratios variations of dissolved inorganic Carbon(DIC) in cave percolation waters(δ13CDIC) and their implications for paleoclimate.Stable carbon isotopic compositions and ions(Ca,Mg,Sr,SO4,Cl etc.) were measured for all samples.The results indicate that there are significant differences among the δ13CDIC values from inter-cave,even inter-drip of intra-cave in the four caves.The δ13CDIC values from the Liangfeng Cave(LFC) is lightest among the four caves,where vegetation type overlying the cave is primary forest dominated by tall trees with lighter average δ13C value(–29.9‰).And there are remarkable differences in δ13CDIC values of different drip waters in the Qixing Cave(QXC) and Jiangjun Cave(JJC),up to 6.9‰ and 7.8‰,respectively.Further analyses show that the δ13CDIC values in cave drip waters are not only controlled by vegetation biomass overlying the cave,but also hydro-geochemical processes.Therefore,accurate interpreting of δ13C recorded in speleothems cannot be guaranteed if these effects of the above mentioned factors are not taken into consideration.     

Arsenic Distribution Pattern in Different Sources of Drinking Water and their Geological Background in Guanzhong Basin,Shaanxi, China

To study arsenic(As) content and distribution patterns as well as the genesis of different kinds of water, especially the different sources of drinking water in Guanzhong Basin, Shaanxi province, China, 139 water samples were collected at 62 sampling points from wells of different depths, from hot springs, and rivers. The As content of these samples was measured by the intermittent flowhydride generation atomic fluorescence spectrometry method(HG-AFS). The As concentrations in the drinking water in Guanzhong Basin vary greatly(0.00–68.08 μg/L), and the As concentration of groundwater in southern Guanzhong Basin is different from that in the northern Guanzhong Basin. Even within the same location in southern Guanzhong Basin, the As concentrations at different depths vary greatly. As concentration of groundwater from the shallow wells(50 m deep, 0.56–3.87 μg/L) is much lower than from deep wells(110–360 m deep, 19.34–62.91 μg/L), whereas As concentration in water of any depth in northern Guanzhong Basin is 10 μg/L. Southern Guanzhong Basin is a newly discovered high-As groundwater area in China. The high-As groundwater is mainly distributed in areas between the Qinling Mountains and Weihe River; it has only been found at depths ranging from 110 to 360 m in confined aquifers, which store water in the Lishi and Wucheng Loess(Lower and Middle Pleistocene) in the southern Guanzhong Basin. As concentration of hot spring water is 6.47–11.94 μg/L; that of geothermal water between 1000 and 1500 m deep is 43.68–68.08 μg/L. The high-As well water at depths from 110 to 360 m in southern Guanzhong Basin has a very low fluorine(F) value, which is generally 0.10 mg/L. Otherwise, the hot springs of Lintong and Tangyu and the geothermal water in southern Guanzhong Basin have very high F values(8.07–14.96 mg/L). The results indicate that highAs groundwater in depths from 110 to 360 m is unlikely to have a direct relationship with the geothermal water in the same area. As concentration of all reservoirs and rivers(both contaminated and uncontaminated) in the Guanzhong Basin is 10 μg/L. This shows that pollution in the surface water is not the source of the high-As in the southern Guanzhong Basin. The partition boundaries of the high- and low-As groundwater area corresponds to the partition boundaries of the tectonic units in the Guanzhong Basin. This probably indicates that the high-As groundwater areas can be correlated to their geological underpinning and structural framework. In southern Guanzhong Basin, the main sources of drinking water for villages and small towns today are wells between 110–360 m deep. All of their As contents exceed the limit of the Chinese National Standard and the International Standard(10 μg/L) and so local residents should use other sources of clean water that are 50 m deep, instead of deep groundwater(110 to 360 m) for their drinking water supply.     

Geochemical Characteristics of Gases from the Wudalianchi Volcanic Area,Northeastern China

The origins of gases in springs, pools and wells from the Wudalianchi (WDLC) volcanic area are discussed based upon molecular and isotope compositions of the gases. Nine gas and water samples were collected from bubbles and water of the springs and pools in the WDLC volcanic area, Northeastern China, in August 1997. The molecular components were measured with a MAT-271 mass spectrometer (MS), helium isotope ratios with a VG-5400 MS, and (13C with a MAT-251 MS in the Lanzhou Institute of Geology. The gases are enriched in CO2 , and most of the CO2 concentrations are over 80% (V). The helium and methane concentrations have relatively wide ranges of 0.7 to 380×10-6 and 4 to 180×10-6, respectively. The 3He/4He ratios are between 1.05 Ra and 3.1 Ra (Ra = 1.4×10-6); the 4He/20Ne values are between 0.45 and 1011, larger than the atmospheric value (0.32). The (13C (PDB) values of carbon dioxide range from (9.6 to (4.2‰. These geochemical data demonstrate that the spring water is from aquifers at different depths, and that helium and carbon dioxide are derived from the mantle, and are contaminated by crust gases during deep fluid migration. Also, there are larger fluxes of deep-earth matter and energy in the WDLC volcanic area.     

Distribution and Influence of Iron Phases on the Physico—Chemical Properties of Phyllosilicates

Clay minerals from different Cretaceous stratigraphic successions of Egypt were investigated using XRD,DTA,dissolution analysis(DCB),IR,Moessbauer and X-band Electron Spin Resonance(ESR) spectroscopies.The purity of the samples and the degree of structural order were determined by XRD.The location of Fe in the octahedral sheet is characterized by absorption bands at-875cm^-1 assigned as Al-OH-Fe which is present after chemical dissolution of free iron.The Moessbauer spectra of these clays sow two doublets with isomer shift and quadrupole splitting typical of octahedral coordinated Fe^3 ,in addition to third doubler with hyperfine parameter typical of Fe^2 in the spectra of Abu-Had kaolinite (H)sample.6-lines magnetic hyperfine components which are consistent with those of hematite are confirmed in the spectra of both Isel and Rish kaolinite samples.Goethite was confirmed by both IR and DTA.Multiple nature of ESR of these clays suggested structural Fe in distorted octaedral symmetry and as non-structural Fe.Little dispersion and low swelling indices as well as incomplete activaiton of investigated montmorillonite samples by NaCO3 appear to be due to incomplete disaggregation of montmorillonite particles.This can be explained by the ability of Fe-gel to aggregate the montmorillonite into pseudo-particles and retard the rigid-gel structure.However,extraction of this ferric amorphous compound by dithonite treatment recovers the surface properties of the montmorillonite samples.On the other hand,amounts and site occupation of Fe associated with kaolinite samples show a negative correlation with the parameters used to describe the degree of crystalline perfection,color,brightness and vitrification range of these kaolinite samples.     

Special and seasonal variations of trace metals in PM10 in Chongqing

Nineteen trace metals in PM10 were measured by X-ray fluorescence spectroscopy （XRF） at three sites in Chongqing. The special and seasonal variations of trace metals in PM10 samples collected in the downtown were different from those in the background area of Jinyunshan. The source identification indicated that particulate materials were contributed mainly by two sources.     

Distribution and Influence of Iron Phases the Physico—Chemical Properties of Phyllosilicates

Clay minerals from different Cretaceous stratigraphic successions of Egypt were investigated using XRD,DTA,dissolution analysis(DCB),IR,Moessbauer and X-ray Electron Spin Resonance(ESR) spectroscopes.The purity of the samples and the degree of their structural order were determined by XRD.The location of Fe in the octahedral sheet is characterized by absorption bands at-875cm^-1 assigned as Al-OH-Fe which persist after chemical dissolution of free iron.The Moessbauer spectra of these clays show two doublets with isomer shift and quadrupole splitting typical of octahedrally coordinated Fe^3 ,in addition to third doublet with hyperfine parameter typical of Fe^2 in the spectra of Abu-Had kaolinite (H) sample.Six-lines magnetic hyperfine components which are consistent with those of hematite are confirmed in the spectra of both Isel and Rish kaolinite samples.Goethite was confirmed by both IR and DTA.Multiple nature of ESR of these clays suggested structural Fe in distorted octahedral symmetry as well as non-structural Fe.Little dispersion and low swelling indices as well as incomplete activation of the investigated montmorillonite samplas by NaCO3 appear to be due to incomplete disaggregation of montmorillonite particles.This can be explained by the ability of Fe-gel to aggregate the montmorillonite into pseudo-particles and retard the rigid-gel structure.However,extraction of this ferric amorphous compound by dithonite treatment recovers the surface properties of the montmorillonite samples.On the other hand,the amount and site occupation of Fe associated with kaolinite samples show an inverse correlation with the parameters used to describe the degree of crystallinity perfection,color,brightness and vitrification range of these kaolinite samples.     

Seasonal variations in sulfur isotopic composition of dissolved SO<Subscript>4</Subscript><Superscript>2−</Superscript> in the Aha Lake,Guiyang and their implications

The Aha Lake is a seasonal anoxic water system in the southwest of Guiyang City, Guizhou Province, China. Seasonal variations in SO42- concentrations and their isotopic compositions in lake water as well as in the tributaries were investigated in this study. The results showed that sulfate concentrations in river water range from 0.94 to 6.52 mmol/L and their δ34S values range from -14.9‰ and 0.9‰, while lake water has sulfate concentrations ranging from 1.91 to 2.79 mmol/L, and δ34S values from -9.8‰ to -5.9‰. It is suggested that coal mining drainage is the major source of SO42- in the Aha Lake. Rainfall, sewage discharge, sulfide oxidation and gypsum dissolution have made only limited contributions. Different depth-dependent distributions of dissolved SO42- and δ34S were de-veloped for both DB and LJK in summer and winter. Due to water overturn, δ34S values display homogenous vertical distributions in winter and spring. While in summer and autumn, significant positive shifts of δ34S were clearly ob-served in epilimnion and bottom strata as a result of water stratification. High δ34S values in epilimnion may result from the retention of rainwater during water stratification. Dissimilatory sulfate reduction by bacteria was thought to be responsible for the increase of δ34S value in hypolimnion.     

Grains Containing Oil Inclusions in Different Hydrocarbon Production and Show Types of Sandstone Reservoirs from the Central Junggar Basin, Northwest China

The values of grains containing oil inclusions (GOI) in 120 reservoir sandstone samples from the central Junggar Basin of Northwest China were investigated. The sandstones are characterized by different types of hydrocarbon production and shows. The values range from 0.015% to 19.9%, and show a fairly good correlation with the hydrocarbon production/shows, which are qualitatively suggestive of reservoir hydrocarbon abundance and petroleum migration. Thus, it may be implied that the values can reflect hydrocarbon migration, being not controlled mainly by the other influencing factors. Further correlation between the values and the reservoir hydrocarbon production and show types indicates that the GOI method can be used in hydrocarbon migration study when the petroleum type of a reservoir is normal oil or gas alone, but it should be used with caution when light oil charges the reservoirs or a complex hydrocarbon migration event takes place. The case study in the central Junggar Basin using the method presents some new understanding on hydrocarbon migration. Thus, the method may help to solve specific petroleum geological problems, and can be treated as a routine tool in hydrocarbon migration study.