藏南羊卓雍错流域水化学主离子特征及其控制因素

水化学主离子特征是流域湖泊的一个重要特征,对气候以及河流所经地区的环境具有指示作用.本文对藏南羊卓雍错流域水化学主离子组成特征及其控制因素进行分析,结果显示流域内不同水体(湖水、河水、地下水)之间的主离子组成以及水化学类型差异显著.其中,羊卓雍错的水化学类型为SO24--HCO3--Mg2+-Na+,巴纠错为SO24--Mg2+-Na+,沉错为SO24--Na+-Mg2+-Ca2+,普莫雍错为HCO3--SO24--Mg2+-Ca2+,空姆错为HCO3--SO24--Ca2+;流域河水中主要阴离子为HCO3-和SO24-,Ca2+为绝对优势阳离子;流域地下水化学类型则为HCO3--Ca2+.究其原因,流域水体化学组成主要受岩石风化作用控制;除此,羊卓雍错、巴纠错和沉错水化学组成亦受自身蒸发-结晶作用的影响.就入湖河水而言,羊卓雍错入湖河水整体受碳酸盐岩石风化的影响较大,蒸发岩溶解的影响次之;沉错和空姆错入湖河流(卡鲁雄曲)的蒸发岩来源则略大于碳酸盐岩来源;而硅酸盐对流域内河水的水化学性质影响较小.与入湖河水相比,羊卓雍错和沉错湖水的Mg2+、Na+和SO24-含量较高,而Ca2+和HCO3-含量较低.这应该与湖水蒸发强烈使得湖水中Ca2+和HCO3-析出并沉积到湖底有关.而空姆错由于湖泊面积小、入湖河水流量大,致使其湖水与入湖河水的主离子组成差异不显著.     

Chemical weathering and CO2 consumption in the glaciated Karuxung River catchment,Tibetan Plateau

Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO₂ balance, it is important to identify the characteristics and driving factors of chemical weathering and CO₂ consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO₂, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km⁻² yr⁻¹, respectively, in maximum) and potential net release of CO₂ (with an upper constraint of 35.6 and 35.2 t km⁻² yr⁻¹, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.     

Factors controlling the major ion chemistry of streams in the blue ridge and valley and ridge physiographic provinces of Virginia and Maryland

The factors controlling the chemistry of 69 low-order streams in the Blue Ridge and Valley and Ridge physiographic provinces of Virginia and Maryland were studied over a 13-month period. Principal component analysis was used to examine regional patterns in stream chemistry and to examine the degree to which the chemistry of low-order streams is controlled by the bedrock upon which they flow. Streams clustered into regionally isolated groups, strongly related to bedrock type, with SO^2?₄ and HCO^?₃ the chemical variables of most importance. Sulphate concentrations appear to be strongly controlled by climate and hydrology, and sorption in the soils within the watershed. Much of the atmospherically derived SO^2?₄ accumulates in watersheds during the growing season and is later flushed out. Weathering reactions were found to be particularly important in the production of HCO^?₃, accounting for 91 per cent on an annual basis, and export of divalent cations from these watersheds, accounting for 48–50 per cent on an annual basis. About half of non-anthropogenic Na⁺ was derived from weathering of silicates, whereas nearly all K⁺ was identified with leaching by SO^2?₄. Water chemistry was strongly related to the rock type in the watershed and the weatherability of the component minerals. Rock type is not a randomly distributed function; instead, it is controlled by geologic factors that result in clusters of similar rock types in a given region. When planning large synoptic studies, it is extremely important to consider that a sampling scheme based on random sampling of a non-randomly distributed function May, not provide the most accurate representation of the variables of interest. Instead, a hierarchical sampling scheme May, be indicated. Our results also suggest that, although one sample in time May, be sufficient to characterize the primary geochemical factors controlling stream chemistry throughout the year, it May, not be sufficient to detect subtle, flow-related alterations in chemistry.     

Mass‐balance modeling of mineral weathering rates and CO2 consumption in the forested,metabasaltic Hauver Branch watershed,Catoctin Mountain,Maryland, USA

Mineral weathering rates and a forest macronutrient uptake stoichiometry were determined for the forested, metabasaltic Hauver Branch watershed in north‐central Maryland, USA. Previous studies of Hauver Branch have had an insufficient number of analytes to permit determination of rates of all the minerals involved in chemical weathering, including biomass. More equations in the mass‐balance matrix were added using existing mineralogic information. The stoichiometry of a deciduous biomass term was determined using multi‐year weekly to biweekly stream‐water chemistry for a nearby watershed, which drains relatively unreactive quartzite bedrock. At Hauver Branch, calcite hosts ~38 mol% of the calcium ion (Ca²⁺) contained in weathering minerals, but its weathering provides ~90% of the stream water Ca²⁺. This occurs in a landscape with a regolith residence time of more than several Ka (kiloannum). Previous studies indicate that such old regolith does not typically contain dissolving calcite that affects stream Ca²⁺/Na⁺ ratios. The relatively high calcite dissolution rate likely reflects dissolution of calcite in fractures of the deep critical zone. Of the carbon dioxide (CO₂) consumed by mineral weathering, calcite is responsible for approximately 27%, with the silicate weathering consumption rate far exceeding that of the global average. The chemical weathering of mafic terrains in decaying orogens thus may be capable of influencing global geochemical cycles, and therefore, climate, on geological timescales. Based on carbon‐balance calculations, atmospheric‐derived sulfuric acid is responsible for approximately 22% of the mineral weathering occurring in the watershed. Our results suggest that rising air temperatures, driven by global warming and resulting in higher precipitation, will cause the rate of chemical weathering in the Hauver Branch watershed to increase until a threshold temperature is reached. Beyond the threshold temperature, increased recharge would produce a shallower groundwater table and reduced chemical weathering rates. Copyright © 2013 John Wiley & Sons, Ltd.     

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.     

Effect of water excess on soil carbon dioxide,seepage water chemistry,and calcite speleothem growth: An experimental and modelling approach

The effect of the water excess in soil on soil gaseous carbon dioxide concentrations (c_CO2) was studied based on field experiments. The gradual water addition of 15 and 30 L m⁻² to leptosols and anthrosols, simulating 15 and 30 mm precipitation, respectively, caused the overall c_CO2 increase of 1.53 × 10⁻¹ mol m⁻³ (increase by 60%) and 1.61 × 10⁻¹ mol m⁻³ (increase by 112%) in the soil airs. The effect of the c_CO2 increment on seepage water, cave dripwater chemistry, and calcite speleothem overgrowths was deduced from geochemical modelling. It showed that the c_CO2 increments may lead to the increments in total dissolved carbon, aqueous calcium, and dissolved solids of 1.10 × 10⁻³ mol L⁻¹ (increase by 35%), 4.45 × 10⁻⁴ mol L⁻¹ (increase by 30%), and 1.55 × 10⁻³ mol L⁻¹ (increase by 34%), respectively. After the total degassing of CO₂ in the cave, the increment in the saturation index of dripwater, SI, could reach up to ΔSI = 0.31, which means an increase by hundreds of percent. The water excess of 5 L m⁻² following a dry period would cause the increment in saturation index ΔSI = 0.17. The modelling further showed that the c_CO2 increase associated with the 30 L m⁻² water excess could induce the calcite overgrowth up to 1 μm thick per 1 m² surface area. The effect of water excess with additional water supplies gradually weakens, probably due to reduced CO₂ diffusivity and soil microorganism activity. It can be assumed that the most contrasting peaks in dripwater chemistry are associated with the individual precipitation events after short dry periods. The increased supersaturation of dripwater is expected to lead to faster growth of speleothem and changes in calcite textures.     

Fluoride enrichment in aquifers of the Thar Desert: controlling factors and its geochemical modelling

The groundwater is the only source of drinking water in the Jaisalmer district of Rajasthan, India. The study area is a part of the Thar Desert. It has low and scattered population and no industries; hence, the possibility of anthropogenic input of fluoride is almost negligible. Thus, the enrichment of fluoride is only possible due to geochemical processes taking place in the groundwater of the region. A total of 100 groundwater samples, 34 samples from Jaisalmer and 66 samples from the Pokharan administrative blocks, were collected. It was observed that the concentration of fluoride ranged from 0.08 mg/l to 4.56 mg/l in the groundwater of Jaisalmer and from 0.56 mg/l to 6.60 mg/l in the samples of the Pokharan block. The alkaline condition (average pH, 7.7 ± 0.22 and 8.01 ± 0.25 in Jaisalmer and the Pokharan administrative block, respectively) in the region favours fluorite dissolution. Ion exchange, dissolution of calcite, semi‐arid climate, alkaline conditions and weathering are responsible for fluoride enrichment in the groundwater of the study area. Copyright © 2012 John Wiley & Sons, Ltd.     

Using multivariate statistical techniques and geochemical modelling to identify factors controlling the evolution of groundwater chemistry in a typical transitional area between Taihang Mountains and North China Plain

Identifying the key factors controlling groundwater chemical evolution in mountain-plain transitional areas is crucial for the security of groundwater resources in both headwater basins and downstream plains. In this study, multivariate statistical techniques and geochemical modelling were used to analyse the groundwater chemical data from a typical headwater basin of the North China Plain. Groundwater samples were divided into three groups, which evolved from Group A with low mineralized Ca-HCO₃ water, through Group B with moderate mineralized Ca-SO₄-HCO₃ water, to Group C with highly saline Ca-SO₄ and Ca-Cl water. Water-rock interaction and nitrate contamination were mainly responsible for the variation in groundwater chemistry. Groundwater chemical compositions in Group A were mainly influenced by dissolution of carbonates and cation exchange, and suffered less nitrate contamination, closely relating to their locations in woodland and grassland with less pronounced human interference. Chemical evolution of groundwater in Groups B and C was gradually predominated by the dissolution of evaporites, reverse ion exchange, and anthropogenic factors. Additionally, the results of the inverse geochemical model showed that dedolomitization caused by gypsum dissolution, played a key role in the geochemical evolution from Group A to Group B. Heavy nitrate enrichment in most groundwater samples of Groups B and C was closely associated with the land-use patterns of farmland and residential areas. Apart from the high loads of chemical fertilizers in irrigation return flow as the main source for nitrate contamination, the stagnant zones, flood irrigation pattern, mine drainage, and groundwater-exploitation reduction program were also important contributors for such high mineralization and heavy NO₃⁻ contents in Group C. The important findings of this work not only provide the conceptual framework for the headwater basin but also have important implications for sustainable management of groundwater resources in other headwater basins of the North China Plain.