Land-use change versus natural controls on stream water chemistry in the Subandean Amazon,Peru

This study evaluates the effects of deforestation and land-use change, as compared to natural controls, on stream water chemistry in the Subandean Amazon. Dissolved major and trace elements were determined near the stream outlet of 48 independent watersheds with varying morphology, bed rock composition and intactness of forest cover (pristine to highly exploited). Geomorphological characteristics were derived from a digital elevation model, geological formations from digitalized maps and forest cover from digital classification of SPOT satellite images. Partial least square regression and multiple linear regression showed that watershed average elevation, which ranged between 396 and 1649 m, was the strongest control on stream water chemistry, explaining >70% of the variation in K and a considerable part also for Mn, U, Mg and HCO₃ with near exponential concentration increases down the altitude gradient. Forest cover, which ranged between 7% and 99%, correlated strongly with average elevation (Spearman correlation coefficient, r_s = 0.8), but had no statistically significant impact on stream solute concentrations. Thus, in the studied Subandean region, watershed scale deforestation has not resulted in measurable impacts on stream water chemistry which is dominated by the spatial variation in natural controls.     

Geochemical controls on lead concentrations in stream water and sediments

The equilibrium distribution of lead in solution and adsorbed on cation exchange sites in sediment theoretically may be calculated from equations representing selectivities of substrate for lead over H⁺, Ca²⁺ and Na⁺, and the stabilities of lead solute species. Such calculations include consideration of total concentrations of major ions, cation exchange capacity (CEC) of substrate, and pH, at values expected in various natural systems. Measurements of CEC and selectivity coefficients were made for synthetic halloysite, a finely divided amorphous 1:1 clay prepared by precipitation from a mixture of solutions of aluminum and silica. Where suspended sediment having the same properties is present in concentrations of 10-1,000 mg/1 at pH 6–8, more than 90% of the lead present can be adsorbed on sediment surfaces. The cation exchange behavior of lead and other minor cationic species in natural systems could be predicted by this type of model if enough other supporting information were available. Information of the type needed describing natural stream sediments, however, is presently inadequate for accurate predictions.     

Mineralogical controls on porosity and water chemistry during O2-SO2-CO2 reaction of CO2 storage reservoir and cap-rock core

Reservoir and cap-rock core samples with variable lithology's representative of siliciclastic reservoirs used for CO₂ storage have been characterized and reacted at reservoir conditions with an impure CO₂ stream and low salinity brine. Cores from a target CO₂ storage site in Queensland, Australia were tested. Mineralogical controls on the resulting changes to porosity and water chemistry have been identified. The tested siliciclastic reservoir core samples can be grouped generally into three responses to impure CO₂-brine reaction, dependent on mineralogy. The mineralogically clean quartzose reservoir cores had high porosities, with negligible change after reaction, in resolvable porosity or mineralogy, calculated using X-ray micro computed tomography and QEMSCAN. However, strong brine acidification and a high concentration of dissolved sulphate were generated in experiments owing to minimal mineral buffering. Also, the movement of kaolin has the potential to block pore throats and reduce permeability. The reaction of the impure CO₂-brine with calcite-cemented cap-rock core samples caused the largest porosity changes after reaction through calcite dissolution; to the extent that one sample developed a connection of open pores that extended into the core sub-plug. This has the potential to both favor injectivity but also affect CO₂ migration. The dissolution of calcite caused the buffering of acidity resulting in no significant observable silicate dissolution. Clay-rich cap-rock core samples with minor amounts of carbonate minerals had only small changes after reaction. Created porosity appeared mainly disconnected. Changes were instead associated with decreases in density from Fe-leaching of chlorite or dissolution of minor amounts of carbonates and plagioclase. The interbedded sandstone and shale core also developed increased porosity parallel to bedding through dissolution of carbonates and reactive silicates in the sandy layers. Tight interbedded cap-rocks could be expected to act as baffles to fluids preventing vertical fluid migration. Concentrations of dissolved elements including Ca, Fe, Mn, and Ni increased during reactions of several core samples, with Mn, Mg, Co, and Zn correlated with Ca from cap-rock cores. Precipitation of gypsum, Fe-oxides and clays on seal core samples sequestered dissolved elements including Fe through co-precipitation or adsorption. A conceptual model of impure CO₂-water-rock interactions for a siliciclastic reservoir is discussed.     

Mineralogical and geochemical characterization of precipitates on stream receiving acid mine water, Korea

Seasonal variations of water chemistry occurred in acid mine drainage receiving mine and leachate water. Sulfate and metal concentrations were low in winter but high in spring and summer. Mine waters were highly acidic (up to pH 3.4) in nature with high concentrations of manganese, copper and zinc but high electrical conductivity and sulfate in leachate. The blue and brownish yellow precipitates were formed under different chemical environments of acid mine drainage. Brownish yellow (Munsell color 7.5YR 8/12), blue (Munsell color 2.5B 9/7) and light blue (Munsell color 2.5B 9/3) precipitates deposited on the stream bottom receiving acid mine water. The brownish yellow precipitates formed in the acid mine water, whereas the blue and light blue precipitates formed in the leachate water. The brownish yellow precipitates consisted mainly of ferrihydrite, whereas the blue and light blue precipitates consisted of glaucocerinite and/or woodwardite.     

Temporal and spatial differences in salinity and water chemistry in SW Florida estuaries: Effects of human-impacted watersheds

Three estuaries near Naples, Florida with variably modified watersheds have been investigated to understand the chemical consequences of altering drainage patterns. Blackwater River (near natural drainage, control site), Henderson Creek (moderately modified watershed), and Faka-Union Canal (severe channelization) were sampled for temperature, salinity, δ¹⁸O, δ¹³C of dissolved inorganic carbon (DIC), molality of CO₂ (ΣCO₂), and Mg:Ca and Sr:Ca ratios between freshwater and marine water end members over a 17-mo period. Carbon isotope composition followed similar seasonal patterns as salinity. Freshwater and seawater end members are more negative than the global average, likely reflecting equilibration with local carbon sources derived from mangrove leaf litter and groundwater. δ¹³C responds to differences in primary productivity between estuaries. Henderson Creek has higher primary productivity than Blackwater River (probable due to higher sewage input and agricultural runoff) and has more positive δ¹³C and lower ΣCO₂. δ¹⁸O is affected by seasonal input of freshwater from atmospheric precipitation, evaporation, and groundwater. Late summer and fall rains lower the δ¹⁸O of estuarine water, whereas evaporative conditions in the dry season elevate δ¹⁸O to values that can be more positive upstream than those from the Gulf of Mexico (estuarine inversion). Evaporation produces water in the Gulf of Mexico that is >1‰ more positive than the global sea surface average most of the year. The very negative δ¹⁸O values in Blackwater River and Henderson Creek likely reflect atmospheric and groundwater contribution. Mg:Ca and Sr:Ca ratios of Gulf water from all three estuaries are similar to global averages at low latitudes. Freshwater end members among estuaries are different in that Blackwater River has higher ratios, suggesting a groundwater contribution. Dolomitic rocks in the subsurface likely provide a source of Mg ions.     

Weathering and anthropogenic influences on the water and sediment chemistry of Wular Lake,Kashmir Himalaya

This paper presents a study on the Wular Lake which is the largest fresh water tectonic lake of Kashmir Valley, India. One hundred and ninety-six (196) water samples and hundred (100) sediment samples (n = 296) have been collected to assess the weathering and Anthropogenic impact on water and sediment chemistry of the lake. The results showed a significant seasonal variability in average concentration of major ions being highest in summer and spring and lower in winter and autumn seasons. The study revealed that lake water is alkaline in nature characterised by medium total dissolved solids and electrical conductivity. The concentration of the major ion towards the lake central showed a decreasing trend from the shore line. The order of major cations and anions was Ca²⁺ > Mg²⁺ > Na⁺ > K⁺ and HCO₃ ^? > SO₄ ^2? > Cl^?, respectively. The geochemical processes suggested that the chemical composition lake water is mostly influenced by the lithology of the basin (carbonates, silicates and sulphates) which had played a significant role in modifying the hydrogeochemical facies in the form of Ca–HCO₃, Mg–HCO₃ and hybrid type. Chemical index of alteration values of Wular Lake sediments reflect moderate weathering of the catchment area. Compared to upper continental crust and the post-Archean Shale, the sediments have higher Si, Ti, Mg and Ca contents and lower Al, Fe, Na, K, P, Zn, Pb, Ni, Cu content. Geoaccumulation index (Igeo) and US Environmental Protection Agency sediment quality standards indicated that there is no pollution effect of heavy metals (Zn, Mn, Pb, Ni and Co).The study also suggested that Wular Lake is characterised by both natural and anthropogenic influences.     

Chemical weathering and related controls on surface water chemistry in the Absaroka Mountains,Wyoming

Chemical relationships among surface waters, soils and rocks were investigated in the drainage basin of the North Fork of the Shoshone River in northwestern Wyoming. The area is underlain entirely by andesitic volcanic rocks. Smectite is the only clay mineral forming in soils over much of the area, although minor kaolinite occurs in a few areas of higher-than-average rainfall.Mass-balance calculations relating stream water chemistry to rock alteration indicate that controls on the chemistry of surface waters take place not in the soil zone but in the altered rock zone. The dominant weathering process which controls the water chemistry is slight alteration of large volumes of rock, rather than development of chemical equilibria involving secondary phases in the soil zone. The altered rock is enriched in feldspars and depleted in ferromagnesian minerals compared to fresh rock. The high rate of physical erosion of the area is enough to remove the residue, reexpose the bedrock, and continue the weathering process.     

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^-.     

湖南金船塘锡铋矿床矿物化学特征及其地质意义

金船塘锡铋矿床是东坡矿田内一以锡铋为主的大型矽卡岩型多金属矿床,迄今为止对其矽卡岩矿物学特征的系统研究较少。本文以金船塘锡铋矿床主要矽卡岩矿物为研究对象,利用电子探针技术对该矿矽卡岩矿物学特征进行了研究。电子探针分析结果表明:金船塘锡铋矿床的矽卡岩中的石榴子石主要为钙铝榴石-钙铁榴石系列,含少量的锰铝榴石,辉石为透辉石-钙铁辉石系列,角闪石主要为铁镁钙闪石,其次为钙镁闪石、阳起石和透闪石,表明该区的矽卡岩为钙质矽卡岩,含少量的锰质矽卡岩。同时,根据矽卡岩矿物学特征的研究,笔者进一步探讨了该矿床锡石的沉淀机制:早期矽卡岩阶段的氧逸度较高,Sn主要以Sn4+的形式替代Fe3+存在于石榴子石中,而在晚期矽卡岩阶段由于氧逸度的降低,Sn主要以Sn2+的形式呈氯的络合物在流体中迁移,由于流体的温度、盐度、pH和氧逸度的变化,Sn2+被氧化成Sn4+,导致锡石沉淀。     

Impacts of environmental flow controls on the water table and groundwater chemistry in the Ejina Delta,northwestern China

The impacts of environmental flow controls on the water table and chemistry of groundwater in the Ejina Delta, an arid inland river basin in northwest China, were investigated with field observations in 2001 and 2009. The results indicate that the shallow groundwater level rose by 0–2 m in the upper reaches of the east tributary of the Heihe River and in the areas of Saihantaolai—Dalaikubu during the period of environmental flow controls. The chemical constituents of the groundwater show a distinct spatial heterogeneity with the total dissolved solids (TDS) in the groundwater increasing from the periphery towards the depocenter of the Ejina Basin. In addition, the rate of groundwater cycling in the south of the Ejina Delta increased, and the mineralization of groundwater declined, while the overall mineralization and salinity increased in the northern regions, especially in the depocenter of the Ejina Basin. Since shallow groundwater is important to the ecology of arid regions, and because understanding the changes in the shallow groundwater environment (groundwater level and hydrochemistry) in response to environmental flow controls is essential for the sustainable improvement of the ecological environment, the results of this paper can be used as a reference for watershed water resources planning and management to help maintain the health and proper function of rivers in arid regions.     

Major-element chemistry and micromorphology of Mn-oxide coatings on stream alluvium

The Mn-oxide coatings on alluvium of six small streams in the eastern U.S.A. have been studied using a scanning electron microscope equipped with an energy dispersive X-ray analyzer. Low magnification surface analyses show that Mn is generally the most abundant followed by either Fe or Si. Several percent each of Ca and Al also occur. The Mn/Fe ratios range from 0.29 to 7.69 but average 2.37. Point analyses of coating cross sections show considerable variation in Mn/Fe ratios but no evidence of regular layering or microchemical laminations such as occurs in rock varnish. Two micromorphologies predominate: roughly circular structures which have a cellular appearance and spherical structures. The cellular structures are remarkably similar to porous Mn-oxide precipitated by bacteria in cultures prepared by Mustoe, suggesting that Mn-oxidizing bacteria are important in forming stream Mn-oxide precipitates.     

Hydrologic controls on water chemistry and mercury biotransformation in a closed river system: The Carson River,Nevada

The Carson River flows in a closed basin system and the total flow of the river water decreases downstream due to both evaporation and consumptive uses. This river system is fed primarily by snow pack in the Sierra Nevada during the winter, which flows down gradient following melting in spring and summer. Water loss through evaporation in the Carson River results in a downstream buildup of conservative elements such as Cl⁻ and certain oxyanion forming elements including Se, Mo and W, which are known to interfere with the transformation of Hg within the S cycle. In addition to these naturally occurring hydrologic processes and the resulting affects on water chemistry, the Carson River Basin has been historically impacted by Au and Ag mining that used Hg amalgamation techniques. Contamination of Hg in the Carson River system is now well documented and published Hg concentrations in different environmental compartments are extremely high. In this study, hydrologically driven changes in water chemistry of the river system and the resulting effects on Hg cycling were examined. Results show that periods of low water flow correspond to high water pH (up to 8.3), relatively high concentrations of oxyanion forming elements (e.g., As, Se, Mo and W), and low Hg methylation potential in sediment. In contrast, periods of high flow bring about dilution, which results in lower pH (∼7), lower concentrations of oxyanion forming elements, but higher Hg methylation potential. Overall, changes in flow regimes likely affect rates of methyl-Hg (MeHg) production through a combination of factors such as high pH, which favors MeHg demethylation, and the occurrence of relatively high concentrations of Group VI oxyanions that could interfere with microbial SO₄ reduction and MeHg production.     

Short-term changes in water chemistry in the Baccu Locci stream (Sardinia,Italy) affected by past mining

Short-term changes in water chemistry, and especially in dissolved trace element concentrations, associated with diel cycles during base-flow conditions at a specific sampling station in the Baccu Locci stream draining the homonymous old mine area in Sardinia (Italy) were investigated. Diel fluctuations in pH and alkalinity were correlated with the temperature-dependent CO₂ solubility and the biologically-induced CO₂ production, both of which were higher during the night. Adsorption/desorption to/from streambed material, in particular ferrihydrite, is believed to be the main in-stream mechanism causing the observed diel variations in dissolved concentrations of As and Zn. Arsenic was mainly affected by the dual action of temperature and competing carbonate ions, whereas pH seemed less important. Temperature acted in accordance with the exothermic feature of anion sorption onto hydrous metal oxide surfaces; aqueous carbonate species exerted their competitive effect in relation to alkalinity variation. Zinc was primarily affected by temperature, in accordance with the endothermic feature of metal cation sorption onto hydrous metal oxide surfaces, and secondly by pH. Co-precipitation of As and Zn with calcite is another possible mechanism, which requires further investigation involving examination of inorganic and biological materials coating the streambed. All these processes potentially controlling the diel cycles of trace elements should be carefully considered to assess the effectiveness of remediation actions currently in progress at Baccu Locci. A normalization method for data from asynchronous sampling has been developed and proposed in order to eliminate or at least attenuate the effect of sampling time and provide an additional tool to identify the processes/mechanisms involved in trace element concentration fluctuations observed along a contaminated stream during base-flow conditions.     

Mineralogical controls on mine drainage of the abandoned Ervedosa tin mine in north-eastern Portugal

The Ervedosa Mine, in north-eastern Portugal, has Sn-bearing quartz veins containing cassiterite and sulphides that cut Silurian schists and a Sn-bearing muscovite granite. These veins were mined for Sn and As₂O₃ until 1969. Cassiterite, the main Sn ore, has alternate lighter and darker growth-zones. The darker zones are richer in Fe, Nb, Ta and Ti, but poorer in Sn than the adjoining lighter zones. Exsolution blebs of ferrocolumbite, manganocolumbite, Ti ixiolite, rutile, ilmenite and rare wolframite were found in the darker zones. Arsenopyrite is the most abundant sulphide and contains inclusions of pyrrhotite, bismuth, bismuthinite and matildite. Other sulphides are pyrite, sphalerite, chalcopyrite and stannite. Secondary solid phases consisting mainly of hydrate sulphate complexes of Al, Fe, Ca and Mg (aluminocopiapite, copiapite, halotrichite, pickeringite, gypsum and alunogen, meta-alunogen) occur at the surface of the Sn-bearing quartz veins and their wall rocks (granite and schist), while oxides, hydroxides, arsenates and residual mineral phases (albite, muscovite and quartz) occur in mining tailings. Toxic acid mine waters (acid mine drainage AMD), which have high conductivity and significant concentrations of As, SO₄ and metal (Cu, Zn, Pb, Fe, Mn, Cd, Ni and Co), occur in an area directly affected by the mine. Surface stream waters outside this area have low conductivity and a pH that is almost neutral. Metal and As concentrations are also lower. Stream waters within the impact area have an intermediate composition, falling between that of the AMD and the natural stream waters outside impact area. Waters associated directly with mineralised veins must not be used for human consumption or agriculture.     

Establishment of background water quality conditions in the Great Zab River catchment: influence of geogenic and anthropogenic controls on developing a baseline for water quality assessment and resource management

The Great Zab River catchment is a major left-bank tributary of the River Tigris and drains a substantial part of the Kurdistan Region, an autonomous region of Northern Iraq. Within Kurdistan, the water resources of the Great Zab River catchment are under pressure from population increase and are utilized for potable, domestic and agricultural and industrial supply. As with many parts of the world, effective management of water resources within Kurdistan is hindered by a lack of water quality data and established background concentrations. This study therefore represents the first regional survey of river water chemistry for the Great Zab River catchment and presents data on the spatial and temporal trends in concentrations of As, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, Li, Mn, Mo, Ni, Pb, Sr, Zn, NO₃^?, SO₄^2?, F^?, Cl^? and PO₄^3?, in addition to pH, electrical conductivity, dissolved oxygen and turbidity. As a tool for underpinning the management and monitoring of water quality, background concentrations were defined for the Great Zab catchment using three methods. The influences of geogenic and anthropogenic controls upon spatial and temporal trends in water chemistry are also evaluated. The influence of geogenic loading from underlying bedrock was identifiable within the observed spatial trends, with the most notable differences found between waters sampled from the relatively more volcanic-rich Zagros zone to the north and those sampled from the lower catchment underlain by younger clay-, sand- and siltstones. The greatest anthropogenic influence, identifiable through elements such as Cl^? and NO₃^?, is present in the more highly populated lower catchment. The background concentrations identified in the Great Zab catchment would be those expected as a result of geogenic loading with some anthropogenic influence and represent a more conservative value when compared to those such as the World Health Organization Maximum Admissible Concentration. However, background concentrations represent a powerful tool for identifying potential anthropogenic impacts on water quality and informing management of such occurrences.     

Composition of water and suspended sediment in streams of urbanized subtropical watersheds in Hawaii

Urbanization on the small subtropical island of Oahu, Hawaii provides an opportunity to examine how anthropogenic activity affects the composition of material transferred from land to ocean by streams. This paper investigates the variability in concentrations of trace elements (Pb, Zn, Cu, Ba, Co, As, Ni, V and Cr) in streams of watersheds on Oahu, Hawaii. The focus is on water and suspended particulate matter collected from the Ala Wai Canal watershed in Honolulu and also the Kaneohe Stream watershed. As predicted, suspended particulate matter controls most trace element transport. Elements such as Pb, Zn, Cu, Ba and Co exhibit increased concentrations within urbanized portions of the watersheds. Particulate concentrations of these elements vary temporally during storms owing to input of road runoff containing elevated concentrations of elements associated with vehicular traffic and other anthropogenic activities. Enrichments of As in samples from predominantly conservation areas are interpreted as reflecting agricultural use of fertilizers at the boundaries of urban and conservation lands. Particulate Ni, V and Cr exhibit distributions during storm events that suggest a mineralogical control. Principal component analysis of particulate trace element concentrations establishes eigenvalues that account for nearly 80% of the total variance and separates trace elements into 3 factors. Factor 1 includes Pb, Zn, Cu, Ba and Co, interpreted to represent metals with an urban anthropogenic enrichment. Factor 2 includes Ni, V and Cr, elements whose concentrations do not appear to derive from anthropogenic activity and is interpreted to reflect mineralogical control. Another, albeit less significant, anthropogenic factor includes As, Cd and U and is thought to represent agricultural inputs. Samples collected during a storm derived from an offshore low-pressure system suggest that downstream transport of upper watershed material during tradewind-derived rains results in a 2-3-fold dilution of the particulate concentrations of Pb, Zn and Cu in the Ala Wai canal watershed.     

中国流域水污染控制分区方法与应用

针对中国以往的流域分区方法主观性较强,尤其是对水污染控制单元的划分方法不统一,划分依据不充分等特点,提出了"流域-控制区-控制单元"三级分区体系,采取定性和定量分析相结合的方法进行流域水污染控制分区研究,重点在控制单元层面构建了层次分析模型,以区县为单元基于汇水特征、城镇布局、工业布局和农业布局4个因素进行评分比较,筛选区县主导排污去向,作为将其划入某一或某几个控制单元的依据。以松花江流域为例,将松花江流域划为三大控制区,33个控制单元,其中莫力达瓦达斡尔族自治旗在内的10个区县被拆分到两个或两个以上的单元,基于流域自然汇水特征,且充分体现流域水污染防治重点和方向,重点落实地方政府治污目标、责任和任务,为中国流域水污染防治规划的科学制定与实施提供重要依据。     

Heavy metal assessment and water quality values in urban stream and rain water

Water quality monitoring in developing countries is inadequate, especially in stream water affected by urban effluents and runoff. The purpose of this study was to investigate heavy metal contaminants in the Nakivubo Stream water in Kampala, Uganda. Water samples Nakivubo Channelized Stream, tributaries and industrial effluents that drain into the stream were collected and analysed for the total elemental concentration using flame atomic absorption spectrophotometer. The results showed that: 1) the wastewater was highly enriched with lead and manganese above the maximum permissible limit; 2) the levels of dissolved oxygen were below the maximum permissible limit, while the biological oxygen demand was above the maximum permissible limit. All industrial effluents/wastewater were classified as strong (> 220 mg/L). Factor analysis results reveal two sources of pollutants; 1) mixed origin or chemical phenomena of industrial and vehicular emissions and 2) multiple origin of lead (vehicular, commercial establishment and industrial). In conclusion, Nakivubo Channelized Stream water is not enriched with heavy metals. These heavy metals (lead, cadmium and zinc) were rapidly removed by co-precipitation with manganese and iron hydroxides and total dissolved solids into stream sediments. This phenomena is controlled by pH in water.