Streamwater chemistry and flow dynamics along vegetation-soil gradient in a subalpine Abies fabri forest watershed, China

Streamwater chemistry and spatial flow dynamics from a subalpine Abies fabri forest in an experimental watershed located in the east slope of Gongga Mountain were analyzed to gain insights into the gradient effect of primary community succession on the stream biogeochemical process. Results showed that high sand content(exceeding 80%) and porosity in the soil(exceeding 20% in A horizon and 35% in B horizon), as well as a thick humus layer on the soil surface, made the water exchange quickly in the Huangbengliu(HBL) watershed. Consequently, no surface runoff was observed, and the stream discharge changed rapidly with the daily precipitation. The flow trends of base ions in the stream water were influenced by the Abies fabri succession gradient. Ca 2+ , HCO - 3 and SO 2- 4 were the dominant anions in the streamwater in this region. A significant difference of Ca 2+ , HCO - 3 and SO 2- 4 concentration exported between the succession stages in the watershed can be found. But they had the similar temporal change in the stream flow. Ca 2+ , HCO - 3 and SO 2- 4 showed significantly negative correlations with the daily precipitation and the stream discharge. \;Concentrations of Cl -, Na +, K +, and Mg 2+ were low in all streamwaters monitored and we observed no differences along the Abies fabri succession gradient. Low ratios of Na:(Na+Ca) (range from 0.1 to 0.2) implied cations were from bedrock weathering(internal source process in the soil system) in this region. But, a variance analysis showed there were almost no differences between rainwater and streamwaters for Mg 2+ , Na +, K +, and Cl - concentrations. This indicated that they might be come from rainfall inputs(external source). The highly mobile capacity, rapid water exchange between precipitation and discharge, and long-term export lead to this observed pattern were suggested.

Changes of water chemistry from rainfall to stream flow in Obagbile Catchment, Southwest Nigeria

Water chemistry changes when it flows through different pathways.This study aims to characterize the differences of water(including rainwater,overland flow,soil water,groundwater,and stream water)chemistry of five kinds of water in Obagbile Catchment in Southwest Nigeria,determine the changes in water chemistry that occur as the water moves from one pathway to another,and identify the factors responsible for the water chemistry changes.To do these,we collected 50 water samples from 10 heavy storms that received equal to or more than 10 mm of rain within an hour to test the changes of water chemical properties across various pathways in this study.The results show that overland flow had the highest p H and electrical conductivity(EC)and rainwater had the lowest values of the two parameters.Ca^(2+),Mg^(2+),Cl^(ˉ),and HCOO^(ˉ) were found to have their highest concentrations in stream water;meanwhile,NO_(3)^(–),NH_(4)^(+),and SO_(4)^(2–) were found to have almost the same low concentrations in all the water samples.K+was only dominant in stream water;while dissolved organic carbon(DOC)was lowest in rainwater,same in overland flow,soil water,and groundwater samples,and highest in stream flow.Principal component analysis(PCA)showed that for all the water samples from different pathways,two factors mainly accounted for the total variances.The two factors were related to the crustal and anthropogenic sources in rainwater,suggesting that the high loadings of major cations(e.g.,Ca^(2+) and Mg^(2+)) in rainwater samples are soil-derived.The PCA for the overland flow and soil water showed strong correlations among pH,EC,and the concentrations of Na^(+),Mg^(2+),HCOO^(-),and CH_(3)COO^(-),while the high loadings of all the parameters and the strong correlations among each other were evident in the stream water.In conclusion,the chemical constituents found in water are also the components of pathways through which the water flows.The major factors responsible for the change in the chemical properties of water in Obagbile Catchment are weathering and anthropogenic activities.

Chronological Study of Coal-seam Water and its Implication on Gas Production in the South Qinshui Basin

The knowledge of the residence time of formation water is fundamental to understanding the subsurface flow and hydrological setting.To better identify the origin and evolution of coal seam water and its impact on gas storage and production,this study collected coalbed methane co-produced water in the southeast Qinshui Basin and detected chemical and isotopic compositions,especially 36Cl and 129I concentrations.The calculated tracer ages of 129I(5.2–50.6 Ma)and 36Cl(0.13–0.76 Ma)are significantly younger than the age of coal-bearing formation(Pennsylvanian-Cisuralian),indicating freshwater recharge after coal deposition.The model that utilises 129I/I and 36Cl/Cl ratios to constrain the timing of recharge and the proportion of recharge water reveals that over 60%of pre-anthropogenic meteoric water entered coal seams since 10 Ma and mixed with residue initial deposition water,corresponding to the basin inversion in Cenozoic.The spatial distribution of major ion concentrations reveals the primary recharge pathway for meteoric water from coal outcrops at the eastern margin to the basin center.This study demonstrates the occurrence of higher gas production rates from wells that accept water recharge in recent times and suggests the possible potential of the non-stagnant zones for high gas production.

Identified the hydrochemical and the sulfur cycle process in subsidence area of Pingyu mining area using multi-isotopes combined with hydrochemistry methods

Groundwater serves as an important water source for residents in and around mining areas.To achieve scientific planning and efficient utilization of water resources in mining areas,it is essential to figure out the chemical formation process and the ground water sulfur cycle that transpire after the coal mining activities.Based on studies of hydrochemistry and D,^(18)O-H_(2)O,^(34)S-SO_(4)isotopes,this study applied principal component analysis,ion ratio and other methods in its attempts to reveal the hydrogeochemical action and sulfur cycle in the subsidence area of Pingyu mining area.The study discovered that,in the studied area,precipitation provides the major supply of groundwater and the main water chemistry effects are dominated by oxidation dissolution of sulfide minerals as well as the dissolution of carbonate and silicate rocks.The sulfate in groundwater primarily originates from oxidation and dissolution of sulfide minerals in coal-bearing strata and human activities.The mixed sulfate formed by the oxidation of sulfide minerals and by human activities continuously recharges the groundwater,promoting the dissolution of carbonate rock and silicate rock in the process.

Thermochemical Sulfate Reduction in the Tazhong District,Tarim Basin,Northeast China:Evidence from Formation Water and Natural Gas Geochemistry

Systematic analyses of the formation water and natural gas geochemistry in the Central Uplift of the Tarim Basin （CUTB） show that gas invasion at the late stage is accompanied by an increase of the contents of HeS and CO2 in natural gas, by the forming of the high total dissolved solids formation water, by an increase of the content of HCO3^-, relative to Cl^-, by an increase of the 2nd family ions （Ca^2＋, Mg^2＋, Sr^2＋ and Ba^2＋） and by a decrease of the content of SO4^2-, relative to Cl^-. The above phenomena can be explained only by way of thermochemicai sulfate reduction （TSR）. TSR often occurs in the transition zone of oil and water and is often described in the following reaction formula： ∑CH＋CaSO4＋H-2O→H2S＋CO2＋CaCO3. （1） Dissolved SO4^2- in the formation water is consumed in the above reaction, when HeS and CO2 are generated, resulting in a decrease of SO4^2- in the formation water and an increase of both HeS and CO2 in the natural gas. If formation water exists, the generated CO2 will go on reacting with the carbonate to form bicarbonate, which can be dissolved in the formation water, thus resulting in the enrichment of Ca^2＋ and HCO3^-. The above reaction can be described by the following equation： CO2＋HeO＋CaCO3→Ca^2＋＋2HCO3^-. The stratigraphic temperatures of the Cambrian and lower Ordovician in CUTB exceeded 120℃, which is the minimum for TSR to occur. At the same time, dolomitization, which might be a direct result of TSR, has been found in both the Cambrian and the lower Ordovician. The above evidence indicates that TSR is in an active reaction, providing a novel way to reevaluate the exploration potentials of natural gas in this district.

Water chemistry controlled aggregation and photo-transformation of silver nanoparticles in environmental waters

The inevitable release of engineered silver nanoparticles（Ag NPs） into aquatic environments has drawn great concerns about its environmental toxicity and safety. Although aggregation and transformation play crucial roles in the transport and toxicity of Ag NPs, how the water chemistry of environmental waters influences the aggregation and transformation of engineered Ag NPs is still not well understood. In this study, the aggregation of polyvinylpyrrolidone（PVP） coated Ag NPs was investigated in eight typical environmental water samples（with different ionic strengths, hardness, and dissolved organic matter（DOM） concentrations） by using UV–visible spectroscopy and dynamic light scattering. Raman spectroscopy was applied to probe the interaction of DOM with the surface of Ag NPs. Further, the photo-transformation and morphology changes of Ag NPs in environmental waters were studied by UV–visible spectroscopy, inductively coupled plasma mass spectrometry, and transmission electron microscopy. The results suggested that both electrolytes（especially Ca2＋and Mg2＋） and DOM in the surface waters are key parameters for Ag NP aggregation, and sunlight could accelerate the morphology change, aggregation, and further sedimentation of Ag NPs. This water chemistry controlled aggregation and photo-transformation should have significant environmental impacts on the transport and toxicity of Ag NPs in the aquatic environments.

Effect of pore water chemistry on anisotropic behavior of clayey soil and possible application in underground construction

The effect of pore water chemistry on anisotropic behavior of consolidation and shear strength of reconstituted Ariake clay has been investigated experimentally.Two types of chemicals added into the pore water of the soil for enhancing flocculation microstructure of soil particles are sodium chloride(salt)(NaCl),and calcium chloride(CaCl_(2));and two dispersants added are sodium triphosphate(Na_(5)-P_(3)O_(10))and sodium hexametaphosphate(Na_(6)P_(6)O_(18)),respectively.The concentrations of these chemicals in pore water were 2-3%.Degrees of anisotropy of the coefficient of consolidation and undrained shear strength decreased with adding NaCl and CaCl_(2),but increased with adding the dispersants.Degree of anisotropy also increased with one-dimensional(1D)deformation and the samples with dispersive additives had higher increase rate.It has been confirmed qualitatively by scanning electron microscopy(SEM)images that adding dispersive chemicals promoted the formation of dispersive microstructure and increased the degree of anisotropy,and the chemicals enhancing flocculent microstructure had an inverse effect.The possible application of the findings to underground construction has been discussed also.

Role of water chemistry on estrone removal by nanofiltration with the presence of hydrophobic acids

Hydrophobic acid organic matter （HpoA） extracted from treated effluent has been known to improve the rejection of steroid hormone estrone by reverse osmosis （RO） and nanofiltration （NF） membranes. In this study, the effects of solution chemistry （solution pH and ionic strength） on the estrone rejection by NF membrane with the presence of HpoA were systematically investigated. Crossflow nanofiltration experiments show that the presence of HpoA significantly improved estrone rejection at all pH and ionic strength levels investigated. It is consistently shown that the ＂enhancement effect＂ of HpoA on estrone rejection at neutral and alkaline pH is attributed to the binding of estrone by HpoA macromolecules via hydrogen bonding between phenolic functional groups in feed solutions, which leads to an increase in molecular weight and appearance of negative charge. The membrane exhibited the best performance in terms ofestrone rejection at pH 10.4 （compared to pH 4 and pH 7） as a result of strengthening the electrostatic repulsion between estrone and membrane with the presence of HpoA. At neutral pH level, the ability of HpoA macromolecules to promote estrone rejection became stronger with increasing ionic strength due to their more extended conformation, which created more chances for the association between estrone and HpoA. The important conclusion of this study is that increasing solution pH and salinity can greatly intensify the ＂enhancement effect＂ of HpoA. These results can be important for NF application in direct/indirect potable water reuse.

Hydrogeochemistry of River Water in the Upper Reaches of the Datong River Basin,China:Implications of Anthropogenic Inputs and Chemical Weathering

This research investigated anthropogenic inputs and chemical weathering in the upper reaches of the Datong River Basin,a tributary of the upper Yellow River,NW China.Multiple approaches were applied to data from 52 water and 12 soil samples from the Muli,Jiangcang,and Mole basins to estimate the chemical component concentrations and to analyze hydrochemical characteristics,distribution patterns,and origins in this coal mining-affected river basin.Coal mining has enhanced the weathering of the lithosphere in the study region.The total dissolved solids in the river range from 145.4 to 701.9 mg/L,which is higher than the global average for rivers.Ion concentration spatial distributions increase around mining areas.River geochemistry is mainly controlled by coal mining activity,carbonate weathering,and silicate weathering,with variances of 33.4%,26.2%,and 21.3%,respectively.Ca^(2+),Mg^(2+),and HCO_(3)^(-)are mainly due to the dissolution of carbonate minerals(calcite>dolomite);Si and K+are mainly from potassium(sodium)feldspar weathering;and Na+and SO_(4)^(2-)mainly from coal mine production.A conceptual model of the river water ion origins from the study area is presented and management implications for improving the adverse effects of coal mining are proposed.These results provide an important standard reference for water resource and environmental management in the study region.

Trace-element ions in snow,ice and water from Antarctic and Arctic with reference of their water vapor chemistry

The some trace elements in the Antarctic and Arctic snow, ice, water were studied using the methodology and theory of water vapor chemistry. The concentrations of ions Zn 2+ , Cd 2+ , Pb 2+ , Cu 2+ , Sn 4+ , Bi 3+ in Antarctic and Arctic snow a significant spatial similarity; they are also close to those defined elsewhere on the basic of studies of water vapor chemistry: on average Zn 2+ 5.0 μg/L, Cd 2+ 0.080 μg/L, Pb 2+ 0.030 μg/L, Cu 2+ 0.70 μg/L, Sn 4+ 0.99 μg/L, Bi 3+ 0.18 μg/L. Apparently, the ion concentration in the Antarctic and Arctic region represent natural baseline values and are controlled by natural water cycles.

Origin, Flow of Formation Water and Hydrocarbon Accumulation in the Zhenwu Area of the North Jiangsu Basin, China

In order to understand the origin and flow of formation water and to evaluate the hydrocarbon accumulation and preservation conditions, the properties of formation water chemistry and dynamics of the Zhenwu area in the southern Gaoyou Sag, North Jiangsu Basin, China, have been investigated. The results show that Xuzhuang oilfield is infiltrated discontinuously by meteoric water under gravity, which consequently leads to the desalination of formation water. Formation water in the Zhenwu and Caozhuang oilfields is less influenced by meteoric water infiltration, and the origin is interpreted to be connate water. Hydrocarbon migration, accumulation and preservation are closely related to the hydrodynamic field of formation water. Formation water concentrates gradually during the process of centrifugal flow released by mudstone compaction and the centripetal flow of meteoric water infiltration, leading to the high salinity of the central part. The geological conditions of the southern fault-terrace belt are poor for hydrocarbon accumulation and preservation as meteoric water infiltration, leaching and oxidation, while the central part, i.e., northern Zhenwu and Caozhuang oilfields is beneficial for an abundance of hydrocarbon accumulation. Most of the large scale oil-~as fields locate herein.

Chemical and Isotopic Characters of the Water and Suspended Particulate Materials in the Yellow River and Their Geological and Environmental Implications

The chemical and isotopic characteristics of the water and suspended particulate materials （SPM） in the Yellow River were investigated on the samples collected from 29 hydrological monitoring stations in the mainstem and several major tributaries during 2004 to 2007. The JD and δ^18O values of the Yellow River water vary in large ranges from -32%0 to -91‰ and from -3.1‰ to -12.5‰, respectively. The characters of H and O isotope variations indicate that the major sources of the Yellow River water are meteoric water and snow melting water, and water cycle in the Yellow River basin is affected strongly by evaporation process and human activity. The average SPM content （9.635 g/L） of the Yellow River is the highest among the world large rivers. Compared with the Yangtze River, the Yellow River SPM has much lower clay content and significantly higher contents of clastic silicates and carbonates. In comparison to the upper crust rocks, the Yellow River SPM contains less SiO2, CaO, K2O and Na2O, but more TFe203, Co, Ni, Cu, Zn, Pb and Cd. The abnormal high Cd contents found in some sample may be related to local industrial activity. The REE contents and distribution pattern of the Yellow River SPM are very close to the average value of the global shale. The average δ^30Sisp in the Yellow River （-0.11‰） is slightly higher than the average value （-0.22‰） of the Yangtze River SPM. The major factors controlling the δ^30Si SPM of the Yellow River are the soil supply, the isotopic composition of the soil and the climate conditions. The TDS in the Yellow River are the highest among those of world large rivers. Fair correlations are observed among Cl, Na^＋, K^＋, and Mg^2＋ contents of the Yellow River water, indicating the effect of evaporation. The Ca^2＋ and Sr^2＋ concentrations show good correlation to the SO42 concentration rather than HCO3-concentration, reflecting its origin from evaporates. The NO3-contents are affected by farmland fertilization. The Cu, Zn and Cd contents in dissolved load of the Yellow River water are all higher than those of average world large rivers, reflecting the effect of human activity. The dissolved load in the Yellow River water generally shows a REE distribution pattern parallel to those for the Yangtze River and the Xijiang River. The δ^30Si values of the dissolved silicon vary in a range from 0.4%0 to 2.9%0, averaging 1.34%o. The major processes controlling the Dsi weathering process of silicate rocks, growth of and δ^30SiDiss of the Yellow River water are the phytolith in plants, evaporation, dissolution of phytolith in soil, growth of fresh water diatom, adsorption and desorption of aqueous monosilicic acid on iron oxide and human activities. The average δ^30^SiDiss value of the Yellow River is significantly lower than that of the Nile River, Yangtze River and Siberia rivers, but higher than those of other rivers, reflecting their differences in chemical weathering and biological activity. The δ^34SSO4 values of the Yellow River water range from -3.8%0 to 14.1%o, averaging 7.97%0. There is some correlation between SO4^2- content and δ^34SSO4. The factors controlling the δ^34SSO4 of the Yellow River water are the SO4 in the meteoric water, the SO4 from gypsum or anhydrite in evaporite rocks, oxidation and dissolution of sulfides in the mineral deposits, magmatic rocks and sedimentary rocks, the sulfate reduction and precipitation process and the sulfate from fertilizer. The ^87Sr/^86Sr ratios of all samples range from 0.71041 to 0.71237, averaging 0.71128. The variations in the ^87Sr/^86Sr ratio and Sr concentration of river water are primarily caused by mixing of waters of various origins with different 87Sr/S6Sr ratios and Sr contents resulting from water-rock interaction with different rock types.

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 tg/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 high As 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.

Chemical and Isotopic Characteristics of the Water and Suspended Particulate Materials in the Yangtze River and Their Geological and Environmental Implications

The chemical and isotopic characteristics of the water and suspended particulate materials（SPM） in the Yangtze River were investigated on the samples collected from 25 hydrological monitoring stations in the mainsteam and 13 hydrological monitoring stations in the major tributaries during 2003 to 2007. The water samples show a large variation in both δD（ 30‰ to 112‰） and δ18O（ 3.8‰ to 15.4‰） values. Both δD and δ18O values show a decrease from the river head to the Jinsha Jiang section and then increase downstream to the river mouth. It is found that the oxygen and hydrogen isotopic compositions of the Yangtze water are controlled by meteoric precipitation, evaporation, ice（and snow） melting and dam building. The Yangtze SPM concentrations show a large variation and are well corresponded to the spatial and temporal changes of flow speed, runoff and SPM supply, which are affected by the slope of the river bed, local precipitation rate, weathering intensity, erosion condition and anthropogenic activity. The Yangtze SPM consists of clay minerals, clastic silicate and carbonate minerals, heavy minerals, iron hydroxide and organic compounds. From the upper to lower reaches, the clay and clastic silicate components in SPM increase gradually, but the carbonate components decrease gradually, which may reflect changes of climate and weathering intensity in the drainage area. Compared to those of the upper crust rocks, the Yangtze SPM has lower contents of SiO2, CaO, K2 O and Na2 O and higher contents of TFe2 O3 and trace metals of Co, Ni, Cu, Zn, Pb and Cd. The ΣREE in the Yangtze SPM is also slightly higher than that of the upper crust. From the upper to lower reaches, the CaO and MgO contents in SPM decrease gradually, but the SiO2 content increases gradually, corresponding to the increase of clay minerals and decrease of the carbonates. The δ30SiSPM values（ 1.1‰ to 0.3‰） of the Yangtze SPM are similar to those of the average shale, but lower than those of the granite rocks（ 0.3‰ to 0.3‰）, reflecting the effect of silicon isotope fractionation in silicate weathering process. The δ30SiSPM values of the Yangtze SPM show a decreasing trend from the upper to the middle and lower reaches, responding to the variation of the clay content. The major anions of the river water are HCO 3, SO 4 2, Cl, NO 3, SiO 4 4 and F and the major cations include Ca2＋, Na＋, Mg2＋, K＋ and Sr2＋. The good correlation between HCO3-content and the content of Ca2＋may suggest that carbonate dissolution is the dominate contributor to the total dissolved solid（TDS） of the Yangtze River. Very good correlations are also found among contents of Cl, SO4 2, Na＋, Mg2＋, K＋and Sr2＋, indicating the important contribution of evaporite dissolution to the TDS of the Yangtze River. High TDS contents are generally found in the head water, reflecting a strong effect of evaporation in the Qinghai-Tibet Plateau. A small increase of the TDS is generally observed in the river mouth, indicating the influence of tidal intrusion. The F and NO3 contents show a clear increase trend from the upstream to downstream, reflecting the contribution of pesticides and fertilizers in the Chuan Jiang section and the middle and lower reaches. The DSi shows a decrease trend from the upstream to downstream, reflecting the effect of rice and grass growth along the Chuan Jiang section and the middle and lower reaches. The dissolved Cu, Zn and Cd in the Yangtze water are all higher than those in world large rivers, reflecting the effect of intensive mining activity along the Yangtze drainage area. The Yangtze water generally shows similar REE distribution pattern to the global shale. The δ30SiDiss values of the dissolved silicon vary from 0.5‰ to 3.7‰, which is the highest among those of the rivers studied. The δ30SiDiss values of the water in the Yangtze mainsteam show an increase trend from the upper stream to downstream. Its DSi and δ30SiDiss are influenced by multiple processes, such as weathering process, phytolith growth in plants, evaporation, phytolith dissolution, growth of fresh water diatom, adsorption and desorption of aqueous monosilicic acid on iron oxide, precipitation of silcretes and formation of clays coatings in aquifers, and human activity. The δ34SSO4 values of the Yangtze water range from 1.7‰ to 9.0‰. The SO4 in the Yangtze water are mainly from the SO4 in meteoric water, the dissolved sulfate from evaporite, and oxidation of sulfide in rocks, coal and ore deposits. The sulfate reduction and precipitation process can also affect the sulfur isotope composition of the Yangtze water. The87Sr/86Sr ratios of the Yangtze water range from 0.70823 to 0.71590, with an average value of 0.71084. The87Sr/86Sr ratio and Sr concentration are primary controlled by mixing of various sources with different87Sr/86Sr ratios and Sr contents, including the limestone, evaporite and the silicate rocks. The atmospheric precipitation and anthropogenic inputs can also contribute some Sr to the river. The δ11B values of the dissolved B in the Yangtze water range from 2.0‰ to 18.3‰, which is affected by multifactors, such as silicate weathering, carbonate weathering, evaporite dissolution, atmospheric deposition, and anthropogenic inputs.

Potential hydraulic connectivity of coal mine aquifers based on statistical analysis of hydrogeochemistry

Mining activities interfere with the natural groundwater chemical environment,which may lead to hydrogeochemical changes of aquifers and mine water inrush disasters.This study analyzed the hydrochemical compositions of 80 water samples in three aquifers and developed a water source identification model to explore the control factors and potential hydraulic connection of groundwater chemistry in a coal mine.The results showed that the hydrochemical types of the three aquifers were different.The main hydrochemical compositions of the loose-layer,coal-bearing,and limestone aquifers were HCO_(3)·Cl-Na,SO_(4)·HCO_(3)-Na,and SO_(4)-Na·Ca,respectively.The correlation,Unmix,and factor an-alyses showed that the hydrochemical composition of groundwater was controlled by the dissolution of soluble minerals(such as calcite,dolomite,gypsum,and halite)and the weathering of silicate minerals.The factor score plot combined with Q-mode cluster analysis demon-strated no remarkable hydraulic connection among the three aquifers in the study area.The water source identification model effectively identified the source of inrush water.Moreover,the mixing ratio model rationally quantified the contributions of the three aquifers to inrush water.

Chemical Characteristics of Stream Draining fromDudu Glacier: An Alpine Meltwater Stream inGanga Headwater, Garhwal Himalaya

The EC (electrical conductivity), pH and concentrations of major anions, cations and dissolved silica were determined in the stream meltwater draining from the glacier. Stream meltwater samples were sampled during June and October 1997 from Dudu glacier, Bhngirathi valley, Garhwal Himalaya. This study is an attempt to reveal the hydrochemical processes operating in the glacialized regime of Garhwal Himalaya. The results show that the abundance order of cations and anions in the meltwater is c(Ca2+ )>c(Na+ )>c(Mg2+ ) >c(K+ ) and c(SO42- ) >c>(HCO3-) >c(NO3- ) >c(CI- ). The rock weathering is the most important mechanism controlling the water chemistry in the basin. Pyrite oxidation and carbonation are the main hydrogen ion supply reactions contributing to the chemical weathering in the basin. There is a distinct difference between the solute concentrations in samples collected during June and October.

Characterization of groundwater in the Ejina Basin,northwest China:hydrochemical and environmental isotopes approaches

To characterize the groundwater in the Ejina Basin,surface and groundwater samples were collected in May and October of 2002.On-site analyses included temperature,electrical conductance(EC),total alkalinity(as HCO 3) by titration,and pH.Chemical analyses were undertaken at the Geochemistry Laboratory of the Cold and Arid Region Environmental and Engineering Institute,Chinese Academy of Sciences,Lanzhou,China.The pH of the groundwater ranged from 7.18 to 8.90 with an average value of 7.72,indicating an alkaline nature.The total dissolved solids(TDS) of the groundwater ranged from 567.5 to 5,954.4 mg/L with an average of 1,543.1 mg/L and a standard deviation of 1,471.8 mg/L.According to the groundwater salinity classification of Robinove et al.(1958),47.4 percent of the samples were brackish and the remainder were fresh water.The ion concentration of the groundwater along the riverbed and near the southern margin of the basin were lower than those farther away from the riverbed.The groundwater in the study area was of Na +-HCO 3 type near the bank of the Heihe River and in the southern margin of the basin,while Na +-SO 4 2-Cl type samples were observed in the terminal lake region.In the desert area the groundwater reached a TDS of 3,000-6,000 mg/L and was predominantly by a Na +-Cl chemistry.Br/Cl for the water of Ejina Basin indicates an evaporite origin for the groundwater with a strongly depleted Br/Cl ratio(average 0.000484).The surface water was slightly enriched in Br/Cl(average 0.000711) compared with groundwater.The calculated saturation index(SI) for calcite and dolomite of the groundwater samples range from 0.89 to 1.31 and 1.67 to 2.67 with averaged 0.24 and 0.61,respectively.About 97 percent of the groundwater samples were kinetically oversaturated with respect to calcite and dolomite,and all the samples were below the equilibrium state with gypsum.Using isotope and hydrochemical analyses,this study investigated the groundwater evolution and its residence time.The groundwater content was mainly determined by the dissolutions of halite,gypsum,and Glauber’s salt(Na 2 SO 4),as well as Na + exchange for Ca 2+,and calcite and dolomite precipitation.With the exception of a few locations,most of the groundwater samples were suitable for irrigation uses.Most of the stable isotope compositions in the groundwater sampled plotted close to the Global Meteoric Water Line(GMWL),indicating that the groundwater was mainly sourced from meteoric water.There was evidence of enrichment of heavy isotopes in the groundwater due to evaporation.Based on the tritium content in atmospheric precipitation and by adopting the exponential-piston model(EPM),the mean residence time of the unconfined aquifer groundwater was evaluated.The results show that these groundwaters have low residence time(12 to 48 years) and are renewable.In contrast,the confined groundwater had 14 C ages estimated by the Pearson model between 4,087 to 9,364 years BP.Isotopic signatures indicated formation of deep confined groundwaters in a colder and wetter climate during the late Pleistocene and Holocene.

Variation of nutrient fluxes by rainfall redistribution processes in the forest canopy of an urban larch plantation in northeast China

Atmospheric deposition(dry and wet deposition)is one of the primary sources of chemical inputs to terrestrial ecosystems and replenishes the nutrient pool in forest ecosystems.Precipitation often acts as a primary transporting agent and solvent;thus,nutrient cycles in forests are closely linked to hydrological processes.We collected precipitation data during a growing season to explore variations in nutrient cycling and nutrient balances in the rainfall redistribution process(wet deposition)in a larch plantation in northeast China.We measured nutrient(NO_(3)^(-),PO_(4)^(3−),Cl^(−),K,Ca,Na,and Mg)inputs via bulk precipitation,throughfall and stemfl ow,and used a canopy budget model to estimate nutrient fl uxes via canopy exchange.Our results suggest that the average concentrations of the base cation(K,Ca,Na,and Mg)showed the following order:stemfl ow>throughfall>bulk precipitation.Throughfall and stemfl ow chemistry dramatically fl uctuated over the growing season when net fl uxes(throughfall+stemfl ow—bulk precipitation)of NO−3,PO3−4,SO2−4,Cl−,K,Ca,Na,and Mg were−6.676 kg·ha^(-1),−1.094 kg·ha^(-1),−2.371 kg·ha^(-1),1.975 kg·ha^(-1),0.470 kg·ha^(-1),−5.202 kg·ha^(-1),−0.336 kg·ha^(-1),and 1.397 kg·ha^(-1),respectively.These results suggest that NO−3,PO3−4,SO2−4,Ca,and Na were retained,while Cl−,K,and Mg were washed off by throughfall and stemfl ow.

Damming effects on dissolved inorganic carbon in different kinds of reservoirs in Jialing River,Southwest China

To assess the effects of river damming on dissolved inorganic carbon in the Jialing River, a total of 40 water samples, including inflow, outflow, and stratified water in four cascade reservoirs(Tingzikou, Xinzheng,Dongxiguan, Caojie) were collected in January and July,2016. The major cations, anions, and δ^(13)C_(DIC) values were analyzed. It was found that the dissolved compositions are dominated by carbonate weathering, while sulfuric acids may play a relatively important role during carbonate weathering and increasing DIC concentration. Different reservoirs had variable characteristics of water physiochemical stratification. The DIC concentrations of reservoir water were lower in summer than those in winter due to the dilute effects and intensive aquatic photosynthesis, as well as imported tributaries. The δ^(13)C_(DIC) values in Tingzikou Reservoir were higher during summer than those in winter,which indicated that intensive photosynthesis increased the δ^(13)C_(DIC) values in residual water, but a similar trend was not obvious in other reservoirs. Except for in Xinzheng Reservoir, the δ^(13)C_(DIC) values in inflow and outflow reservoir water were lower than those in the surface water of stratified sampling in summer. For stratified sampling, it could be found that, in summer, the Tingzikou Reservoir δ^(13)C_(DIC) values significantly decreased with water depthdue to the anaerobic breakdown of organic matter. The significant correlation(p<0.01 or 0.05) between the DIC concentrations, the δ^(13)C_(DIC) values and anthropogenic species(Na^++K^+, Cl~–, SO_4^(2-) and NO_3^-) showed that the isotope composition of DIC can be a useful tracer of contaminants. In total, Tingzikou Reservoir showed lacustrine features, Xinzheng Reservoir and Dongxiguan Reservoir had "transitional'' features, and Caojie Reservoir had a total of "fluvial'' features. Generally, cascade reservoirs in the Jialing River exhibited natural river features rather than typical lake features due to characteristics of reservoir water in physiochemical stratification, spatiotemporal variations of DIC concentrations and isotopic compositions. It is evident that the dissolved inorganic carbon dynamics of natural rivers had been partly remolded by dam building.

Binding of Pyrene to Different Molecular Weight Fractions of Dissolved Organic Matter:Effects of Chemical Composition and Steric Conformation

The binding constant（KDOM） of pyrene onto different molecular weight（Mw） fractions of a dissolved organic matter（DOM） extract from an estuarine sediment was measured via a fluorescence quenching method,and the possible binding mechanisms were discussed.The influence of water chemical parameters on pyrene binding was studied to elucidate the effects of DOM steric conformation.DOM fraction with larger M w（14000） showed a greater KDOM（2.02×10 5） than that with smaller Mw did,and the KDOMs were 1.16×105 and 1.13×105 for the fractions with M w of 1000―14000 and 1000,respectively.The K DOM s of different M w DOM fractions were correlated positively with the atomic ratio of C/H and absorbance at 280 nm;while a negative correlation existed between K DOM and（O＋C）/N（atomic ratio）,and K DOM and O-containing groups.These correlations indicate the positive influence of aromatic structure and the negative effect of polarity on DOM binding capacity.Infrared spectroscopy revealed that specific interactions existed between pyrene and the DOM fraction with larger M W besides hydrophobic partition,i.e.,NH-π interaction in DOM moiety（1000―14000） and π-π electron donor acceptor（EDA） forces in DOM moiety（14000）.KDOM varied in a complex pattern with increasing cation concentration and pH,which could be explained by the change in DOM steric conformation.Formed aggregates favored the lipophilic partition of pyrene.However,the accessibility to some interior binding sites became low when the aggregate was too large,leading to a reduced KDOM.