Water and nutrient fluxes in a cool temperate rainforest at the Cordillera de la Costa in southern Chile

Water and nutrient fluxes were studied during a 12-month period in an alerce (Fitzroya cupressoides) forest, located in a remote site at the Cordillera de la Costa (40°05′S) in southern Chile. Measurements of precipitation, throughfall, stemflow, effective precipitation, soil infiltration and stream flow were carried out in an experimental, small watershed. Simultaneously, monthly water samples were collected to determine the concentrations and transport of organic-N, NO₃-N, total-P, K⁺, Ca²⁺, Na⁺ and Mg²⁺ in all levels of forest. Concentration of organic-N, NO₃-N, total-P and K⁺ showed a clear pattern of enrichment in the throughfall, stemflow, effective precipitation and soil infiltration. For Ca²⁺ and Mg²⁺, enrichment was observed in the effective precipitation, soil infiltration and stream flow. Annual transport of K⁺, Na⁺, Ca²⁺ and Mg²⁺ showed that the amounts exported from the forest via stream flow (K⁺=0·95, Na⁺=32·44, Ca²⁺=8·76 and Mg²⁺=7·16 kg ha⁻¹ yr⁻¹) are less than the inputs via precipitation (K⁺=6·39, Na⁺=40·99, Ca²⁺=15·13 and Mg²⁺=7·61 kg ha⁻¹ yr⁻¹). The amounts of organic-N and NO₃-N exported via stream flow (organic-N=1·04 and No₃-N=3·06 kg ha⁻¹ yr⁻¹) were relatively small; however, they represented greater amounts than the inputs via precipitation (organic-N=0·74 and NO₃-N=0·97 kg ha⁻¹ yr⁻¹), because of the great contribution of this element in the superficial soil horizon, where the processes of decomposition of organic material, mineralization and immobilization of the nutrients occurs. © 1998 John Wiley & Sons, Ltd.     

Lithological and hydrological controls on water composition: evaporite dissolution and glacial weathering in the south central Andes of Argentina (33°–34°S)

Lithological and hydrological influence on fluvial physical and chemical erosion was studied in a glacierized sedimentary basin with high evaporite presence. Suspended particulate matter (SPM), total dissolved solids (TDS) and major ion concentrations were analysed for 2 years of different hydrologic condition: (i) 2009–2010, Q = 100% average; and (ii) 2010–2011, Q = 60% average. Annual hydrograph was simple regime‐type with one peak in summer related to snow melting. The intra‐annual SPM and TDS variations were directly and inversely associated to Q, respectively. Snow chemistry showed continental influence (Na⁺/Ca²⁺ = 0.17), and atmospheric input of TDS was <1% of the total exported flux. River water was highly concentrated in Ca²⁺ and SO₄²⁻ (~4 mmol l⁻¹) and in Na⁺ and Cl⁻ (~3 mmol l⁻¹). Ca²⁺/SO₄²⁻ and Na⁺/Cl⁻ molar ratios were ~1 and related to Q, directly and inversely, respectively. Major ion relationships suggest that river chemistry is controlled by evaporite (gypsum and halite) dissolution having a summer input from sulfide oxidation and carbonate dissolution, and a winter input from subsurface flow loaded with silicate weathering products. This variation pattern resulted in nearly chemostatic behaviour for Ca⁺, Mg²⁺ and SO₄²⁻, whereas Na⁺, Cl⁻ and SiO₂ concentrations showed to be controlled by dilution/concentration processes. During the 2009–2010 hydrological year, the fluxes of water, SPM and TDS registered in the snow melting–high Q season were, respectively, 71%, 92% and 67% of the annual total, whereas for equal period in 2010–2011, 56% of water, 86% of SPM and 54% of TDS annual fluxes were registered. The SPM fluxes for 2009–2010 and 2010–2011 were 1.19 × 10⁶ and 0.79 × 10⁶ t year⁻¹, whereas TDS fluxes were 0.68 × 10⁶ and 0.55 × 10⁶ t year⁻¹, respectively. Export rates for 2009–2010 were 484 t km² year⁻¹ for SPM and 275 t km² year⁻¹ for TDS. These rates are higher than those observed in glacierized granite basins and in non‐glacierized evaporite basins, suggesting a synergistic effect of lithology and glaciers on physical and chemical erosion. Copyright © 2014 John Wiley & Sons, Ltd.     

粤东五华河流域的化学风化与CO2吸收

基于对粤东五华河干流和支流水体的物理、化学组成测试数据,应用质量平衡法和相关分析法探讨湿热山地丘陵地区岩石化学风化过程对大气CO₂的吸收.结果表明:五华河水体的总溶解性固体含量(77.11 mg/L)接近于世界河流的平均值(65 mg/L);离子组成以Ca²⁺、Na⁺和HCO₃^-为主,可溶性Si次之.五华河流域化学径流组成主要源自硅酸盐矿物化学风化过程的贡献,碳酸盐矿物的贡献较少;大气和土壤CO₂是流域内岩石化学风化的主要侵蚀介质.与同一气候带其他河流相比较,五华河流域岩石化学风化过程对大气CO₂的吸收通量(2.14×105mol/(km²·a))较低,这主要是由于流域内缺乏碳酸盐岩所导致.     

A study on the reaction kinetics of mineral surface adsorption in mix system

The experimental results on adsorption of ions pb²⁺, Zn²⁺ and Ag⁺ onto mineral surfaces in a mix system show that the reaction kinetics of adions adsorbed onto mineral surfaces was mainly controlled by their diffusion rates in solution. The concentration variations can be fit for the second-order rate equation with good determined coefficients r = 0.800 5—0.979 7. In the near neutral solution, the concentration of exchanged ions K⁺ and Na⁺ related to reaction time can be described by the fint-order rate equation with r = 0.855 7–0.997 7. Meanwhile, the complex diffusionexchange rate equation is suitable for describing the ca^{2 +} concentration variation, as ions Pb^{2 +} and Zn²⁺ were adions. Experimental data show that the amount of ions K⁺, Na⁺and Ca²⁺ release is much more than that of adion decrement in solution. This fact may suggest that the complexstion reaction of adions Pb²⁺, Z²⁺ and Ag⁺ with the mineral surfaces was the major reaction process while adions were not entering the phyllosilicate interlayers or CaCO₃ lattice to exchange the ions K⁺, Na⁺ and Ca²⁺ at room temperature. Project supported by the National Natural Science Foundation of China (Grant No. 49773206) and the Natural Science Foundation of Guangdong Province (Grant No. 960504)     

Fifty-year variations in water ionic composition in small tributaries of the Southern Baikal

Concentrations of major ions in surface waters of the rivers of Khara-Murin and Snezhnaya are compared based on data of many-year observations carried out in the 1950s and 2000s. The concentrations of HCO ₃ ^? , Cl^?, Ca²⁺, Mg²⁺, Na⁺ + K⁺ are shown to be stable. A considerable increase in SO ₄ ^?2 concentration was revealed.     

Ion Chemistry of the Ionosphere at E- and F-Region Altitudes: A Review

The current state of knowledge of E- and F-region ion chemistry is reviewed. Considerable attention is given to the progress in the chemistry of unexcited N₂ ⁺, O₂ ⁺, NO⁺, O⁺(⁴S), N⁺, H⁺, He⁺, Fe⁺, Mg⁺, Na⁺, Ca⁺, and K⁺ ions and electronically excited O⁺(²D), O⁺(²P), O⁺(⁴P), and $ {\text{O}}^{ + } (^{2} {\text{P}}^{*} ) $ ions. Achievements in our understanding of the role of vibrationally excited N₂ ⁺, O₂ ⁺, and NO⁺ ions in the ionosphere are discussed.     

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

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

Hydrochemical characteristics and salinization processes of groundwater in the shallow aquifer of Eastern Laizhou Bay,China

Groundwater salinization has become a crucial environmental problem worldwide and is considered the most widespread form of groundwater contamination in the coastal zone. In this study, a hydrochemical investigation was conducted in the eastern coastal shallow aquifer of Laizhou Bay to identify the hydrochemical characteristics and the salinity of groundwater using ionic ratios, deficit or excess of each ions, saturation indices and factor analysis. The results indicate that groundwater in the study area showed wide ranges and high standard deviations for most of hydrochemical parameters and can be classified into two hydrochemical facies, Ca²⁺‐Mg²⁺‐Cl^‐ facies and Na⁺‐Cl^‐ facies. The ionic ratio, deficit or excess of each ions and SI were applied to evaluate hydrochemical processes. The results obtained indicate that the salinization processes in the coastal zones were inverse cation exchange, dissolution of calcite and dolomite, and intensive agricultural practices. Factor analysis shows that three factors were determined (Factor 1: TDS, EC, Cl^‐, Mg²⁺, Na⁺, K⁺, Ca²⁺ and SO₄^2‐; Factor 2: HCO₃^‐ and pH; Factor 3: NO₃^‐ and pH), representing the signature of seawater intrusion in the coastal zone, weathering of water–soil/rock interaction, and nitrate contamination, respectively. Copyright © 2011 John Wiley & Sons, Ltd.     

Seasonal evolution of penitente glaciochemistry at Tapado Glacier,Northern Chile

This study uses stable isotopes and major ions to examine the seasonal evolution of penitentes on the surface of Tapado Glacier, in the Norte Chico region of the Chilean Andes. A snow pit was sampled in November 2011, and penitentes were sampled during the summer (December 2011 and January 2012). The major ion load of the winter snowpack is dominated by Ca²⁺ (60%), SO₄^2? (16%) and NO₃^? (13%), and there is little influence from marine air masses at the site, with most SO₄^2?, Mg²⁺, Ca²⁺ and Na⁺, derived from non‐sea salt sources. During the early ablation season we observe increases in stable isotope ratios and major ion concentrations (particularly lithic ions Na⁺, Mg²⁺ and Ca²⁺) in the upper reaches of penitentes, which is attributed to sublimation and the aeolian deposition of dust particles. In the late‐summer, melt replaces sublimation as the dominant ablation process and results in smoothing of the stable isotope profile and the elution of major ions within the penitente snow and ice matrix. Copyright © 2015 John Wiley & Sons, Ltd.     

Hydrochemical characteristics of throughfall and stemflow in a Moso‐bamboo (Phyllostachys pubescens) forest

To investigate the impacts of the invasion by bamboo on fluxes of nutrients and pollutants, the nutrient/pollutant fluxes and canopy interactions, including neutralization of acidity, leaching and uptake of nitrogen (N), were characterized in conjunction with rainfall partitioning in a Moso‐bamboo (Phyllostachys pubescens) forest. Measurements of precipitation volume, pH, major ions, and silicate (SiO₂) in rainfall, throughfall and stemflow were collected weekly in a Moso‐bamboo forest located in Munakata City, Western Japan for 1 year. Results showed that rainfall partitioning into stemflow was larger than that for other types of forest, which may be due to the properties of Moso‐bamboo forest structure, such as a straight and smooth culm. Inorganic N (NO₃⁻ + NH₄⁺) and S (SO₄²⁻) fluxes of throughfall and stemflow were approximately 1·6 and 1·3 times higher than that of rainfall, respectively. Contribution of stemflow flux to inorganic N and S fluxes to the forest floor was high. This could be due to lower uptake of inorganic N through culm and a higher rainfall partitioning into stemflow than that for other types of forest. The Moso‐bamboo canopy neutralized rainfall acidity, reducing the fluxes of potentially acidifying compounds via throughfall and stemflow. Canopy leaching of K⁺ was distinctly higher than that of Mg²⁺ and Ca²⁺ and could be related to the high mobility of K⁺ in plant tissues. Cl⁻ and SiO₂ were readily leached as for K⁺. The impact of the invasion by bamboo on nutrient cycling was discussed. Copyright © 2010 John Wiley & Sons, Ltd.     

The Enrichment Process of Groundwater Fluorine in Sea Water Intrusion Area of Gaomi City,China

A typical area, Gaomi City in China, was chosen to discuss the enrichment process of groundwater fluorine in sea water intrusion area. The groundwater had fluorine levels of 0.09–10.99 mg/L, with an average concentration of 1.38 mg/L. The high-fluorine groundwater was mainly distributed in the unconsolidated Quaternary sediments, where concentrations in 83.6% of the samples exceeded the national limit of 1.0 mg/L. The groundwater in the Quaternary sediments also had higher levels of Cl⁻, TDS, Mg²⁺, and pH and lower levels of Ca²⁺, Co, Ni, and Cu than that in the bedrock. The groundwater fluorine levels in the Quaternary sediments are positively correlated with Cl⁻, TDS, Mg²⁺, pH, and negatively correlated with Ca²⁺, γCa²⁺/γMg²⁺, Co, Ni, Cu. Geochemical indices of Cl⁻ and TDS indicate sea water intrusion in the Quaternary high-fluorine groundwater area (F⁻ > 1.0 mg/L), while they do not indicate any intrusion in the bedrock area. The chemical weathering of minerals was intensified with the intrusion of sea water. Cation exchange was confirmed to occur in the Quaternary sediments and was promoted by sea water intrusion. Cation exchange consumes part of groundwater Ca²⁺ and permits more F⁻ dissolving. Consequently, in the Quaternary sediments, the groundwater was supersaturated with CaF₂ minerals and undersaturated with MgF₂ minerals when F⁻ > 1.0 mg/L, while CaF₂ and MgF₂ minerals both are undersaturated when F⁻ < 1.0 mg/L. Thus, the chemical weathering of minerals and cation exchange caused by sea water intrusion are the crucial processes controlling the groundwater fluorine levels, which should be considered when the groundwater fluorine enrichment mechanism is discussed along coastal zones.     

Hydrogeochemical characteristics of surface water and groundwater in the karst basin,southwest China

Groundwater is a very significant water source used for irrigation and drinking purposes in the karst region, and therefore understanding the hydrogeochemistry of karst water is extremely important. Surface water and groundwater were collected, and major chemical compositions and environmental isotopes in the water were measured in order to reveal the geochemical processes affecting water quality in the Gaoping karst basin, southwest China. Dominated by Ca²⁺, Mg²⁺, HCO₃^? and SO₄^2?, the groundwater is typically characterized by Ca? Mg? HCO₃ type in a shallow aquifer, and Ca? Mg? SO₄ type in a deeper aquifer. Dissolution of dolomite aquifer with gypsiferous rocks and dedolomitization in karst aquifers are important processes for chemical compositions of water in the study basin, and produce water with increased Mg²⁺, Ca²⁺ and SO₄^2? concentrations, and also increased TDS in surface water and groundwater. Mg²⁺/Ca²⁺ molar ratios in groundwater decrease slightly due to dedolomitization, while the mixing of discharge of groundwater with high Mg²⁺/Ca²⁺ ratios may be responsible for Mg²⁺/Ca²⁺ ratios obviously increasing in surface water, and Mg²⁺/Ca²⁺ ratios in both surface water and groundwater finally tending to a constant. In combination with environmental isotopic analyses, the major mechanism responsible for the water chemistry and its geochemical evolution in the study basin can be revealed as being mainly from the water–rock interaction in karst aquifers, the agricultural irrigation and its infiltration, the mixing of surface water and groundwater and the water movement along faults and joints in the karst basin. Copyright © 2009 John Wiley & Sons, Ltd.     

Sampling strategy to describe the temporal hydrochemical characteristics of an alpine proglacial stream

A hierarchical sampling programme (including continuous monitoring, twice-daily sampling and sampling at hourly intervals over selected 24 hour periods) was devised to support hydrochemical and hydrological research programmes on an alpine proglacial stream. The rationale for the research and for the sampling programme are explained and the hydrochemical time series generated over an ablation season are analysed to assess the degree to which they support the study aims. It appears that there is no satisfactory substitute for the chemical analysis of at least two water samples taken at approximately maximum and minimum discharge every day, if seasonal variations in meltwater chemistry are to be effectively characterized. Such time series data can be used to estimate Box-Jenkins transfer function-noise models between particular solutes (SO²⁻₄, Ca²⁺, Mg²⁺, Na⁺ and possibly K⁺) and either discharge or electrical conductivity, which can then be used to fill any short gaps in the data. This approach is not satisfactory even for filling short gaps in the twice-daily determinations of pH, HCO⁻₃ and NO⁻₃. At the diurnal time-scale (based on hourly determinations over 24 hour periods) electrical conductivity seems to provide a good surrogate for most of the solutes studied. HCO⁻₃, SO²⁻₄, Ca²⁺ and Mg²⁺ were found to be particularly strongly related to electrical conductivity and there was little if any significant serial autocorrelation in the residuals from all of the simple linear regression relationships that were estimated between individual species and conductivity. It is concluded that the hierarchical sampling design was suitable for the purposes of the study, and that the continuous monitoring of electrical conductivity provides excellent supporting information to the chemical analysis of water samples if it is used carefully as a means of short term calibration and interpolation of the solute record.     

土地利用结构与景观格局对鄱阳湖流域赣江水质的影响

于2015年1月和7月采集赣江干流及支流34个采样点水样,测定电导率、水化学离子、无机氮等水质指标.利用赣江流域2014年30 m分辨率的土地利用数据,以流域景观类型占比表征土地利用结构,景观指数表征景观格局;采用Pearson相关分析、Bioenv分析、Mantle检验与方差分解等方法分析流域土地利用结构与景观格局对赣江水质的影响.结果表明:上游Cl~-、Na~+浓度最高,中游电导率、Cl~-、Na~+、K~+、Ca~(2+)等水质指标最低,下游电导率、HCO_3~-、SO_4~(2-)、Mg~(2+)、Ca~(2+)、NO_3~--N等水质指标最高.居民建设用地是对水质影响最显著的单一土地利用类型.林地、水田与居民建设用地是对水质影响最显著的土地利用类型组合.平均最近邻体指数是对水质影响最显著的单一景观指数,斑块个数、斑块聚集度指数、平均最近邻体指数是对水质影响最显著的景观指数组合.枯水期土地利用结构和景观格局对水质的贡献率分别为41.1%和17.2%,景观格局对水质的贡献率(17.2%)均为和土地利用结构的交互作用,无独立贡献部分;丰水期二者对水质贡献率分别为51%、53%,交互作用部分为37%.以上结果表明,土地利用结构与景观格局都对赣江水质有较大影响,二者的交互作用在该影响中占有重要地位,且枯水期景观格局对水质的影响涵盖在与土地利用结构的交互作用中.     

Changes in Water Hydrochemistry in Bays of the Bratsk Reservoir Caused by Forest Harvesting Operations

For the first time, the results of studying the hydrochemical characteristics of bays in the Bratsk Reservoir, subject to the effect of forest harvesting operations are given. The obtained data include the concentrations of NO₃^?, NO₂^?, NH₄⁺, PO₄^-3, SiO₂, phenols, oil products, and organic matter and the oxygen regime of water in the bays. The concentration and distribution in water of biogenic elements and O₂-typical of wood decay processes-demonstrate the high self-purification capacity of ecosystems in the majority of bays. At the same time, water of some bays shows signs of eutrophication and high concentrations of phenols and oil products.     

Rainfall intensity affects runoff responses in a semi-arid catchment

The source and hydrochemical makeup of a stream reflects the connectivity between rainfall, groundwater, the stream, and is reflected to water quantity and quality of the catchment. However, in a semi-arid, thick, loess covered catchment, temporal variation of stream source and event associated behaviours are lesser known. Thus, the isotopic and chemical hydrographs in a widely distributed, deep loess, semi-arid catchment of the northern Chinese Loess Plateau were characterized to determine the source and hydrochemical behaviours of the stream during intra-rainfall events. Rainfall and streamflow were sampled during six hydrologic events coupled with measurements of stream baseflow and groundwater. The deuterium isotope (²H), major ions (Cl⁻, SO₄²⁻, NO₃⁻, Ca²⁺, K⁺, Mg²⁺, and Na⁺) were evaluated in water samples obtained during rainfall events. Temporal variation of ²H and Cl⁻ measured in the groundwater and stream baseflow prior to rainfall was similar; however, the isotope compositions of the streamflow fluctuated significantly and responded quickly to rainfall events, likely due to an infiltration excess, overland dominated surface runoff during torrential rainfall events. Time source separation using ²H demonstrated greater than 72% on average, the stream composition was event water during torrential rainfall events, with the proportion increasing with rainfall intensity. Solutes concentrations in the stream had loglinear relationships with stream discharge, with an outling anomaly with an example of an intra-rainfall event on Oct. 24, 2015. Stream Cl⁻ behaved nonconservative during rainfall events, temporal variation of Cl⁻ indicated a flush and washout at the onset of small rainfall events, a dilution but still high concentration pattern in high discharge and old water dominated in regression flow period. This study indicates rainfall intensity affects runoff responses in a semi-arid catchment, and the stored water in the thick, loess covered areas was less connected with stream runoff. Solute transport may threaten water quality in the area, requiring further analysis of the performance of the eco-restoration project.     

Soluble salt deposit in the Nihewan beds and its environmental significance

Observation and experimental analysis of soluble salt deposit along four profiles across the strata deposited in Nihewan paleolake basin enabled us to recognize the nature and evolution stages of the Nihewan paleolake and its significance in stratigraphical division and pa-leo-environmental reconstruction. The Nihewan paleolake was at least a weak-saline to semi-saline lake and represents an intracontinental lake in the semi-arid region. The lower member of sedimentary strata in the paleolake contains gypsum layer and gypsum lamellae. Soluble salt is mainly composed of SO ₄ ^2- and Ca²⁺ ions, representing a trend of the paleolake evolving into a stage of sulfate lake. The upper member of the strata has predominantly Cl^-, K⁺, and Na⁺ ions in soluble salt, indicating a starting development of the paleolake to chlorite lake, but no salt rock was deposited, indicating a drying trend of the area.     

Chemical Composition of Dew Resulting from Radiative Cooling at a Semi-arid Site in Agra, India

Dew samples were collected between October 2007 and February 2008 from a suburban site in Agra. pH, conductivity, major inorganic ions (F^?, Cl^?, NO ₃ ^? , SO ₄ ^2? , Na⁺, K⁺, Ca²⁺, Mg²⁺, and NH ₄ ⁺ ), and some trace metals (Cr, Sn, Zn, Pb, Cd, Ni, Mn, Fe, Si, Al, V, and Cu) were determined to study the chemistry of dew water. The mean pH was 7.3, and the samples exhibited high ionic concentrations. Dew chemistry suggested both natural and anthropogenic influences, with acidity being neutralized by atmospheric ammonia and soil constituents. Ion deposition flux varied from 0.25 to 3.0?neq?m^?2?s^?1, with maximum values for Ca²⁺ followed by NH ₄ ⁺ , Mg²⁺, SO ₄ ^2? , Cl^?, NO ₃ ^? , Na⁺, K⁺, and F^?. Concentrations of trace metals varied from 0.13 to 48?μg?l^?1 with maximum concentrations of Si and minimum concentration of Cd. Correlation analysis suggested their contributions from both crustal and anthropogenic sources.     

Water quality and hydrogeochemical characteristics of the River Buyukmelen,Duzce, Turkey

The River Buyukmelen is located in the province of Duzce in northwest Turkey and its water basin is approximately 470 km². The Aksu, Kucukmelen and Ugursuyu streams flow into the River Buyukmelen. It flows into the Black Sea with an output of 44 m³ s⁻¹. The geological succession in the basin comprises limestone and dolomitic limestone of the Yılanlı formation, sandstone, clayey limestone and marls of the Akveren formation, clastics and volcano‐clastics of the Caycuma formation, and cover units comprised of river alluvium, lacutrine sediments and beach sands. The River Buyukmelen is expected to be a water source that can supply the drinking water needs of Istanbul until 2040; therefore, it is imperative that its water quality be preserved. The samples of rock, soil, stream water, suspended, bed and stream sediments and beach sand were collected from the Buyukmelen river basin. They were examined using mineralogical and geochemical methods. The chemical constituents most commonly found in the stream waters are Na⁺, Mg²⁺, SO²⁻₄, Cl⁻ and HCO₃⁻ in the Guz stream water, Ca²⁺ in the Abaza stream water, and K⁺ in the Kuplu stream water. The concentrations of Na⁺, K⁺, Ca²⁺, Mg²⁺, SO²⁻₄, HCO⁻₃, Cl⁻, As, Pb, Ni, Mn, Cr, Zn, Fe and U in the Kuplu and Guz stream waters were much higher than the world average values. The Dilaver, Gubi, Tepekoy, Maden, Celik and Abaza streams interact with sedimentary rocks, and the Kuplu and Guz streams interact with volcanic rocks. The amount of suspended sediment in the River Buyukmelen in December 2002 was 120 mg l⁻¹. The suspended and bed sediments in the muddy stream waters are formed of quartz, calcite, plagioclase, clay (kaolinite, illite and smectite), muscovite and amphibole minerals. As, Co, Cd, Cr, Pb, Ni, Zn and U have all accumulated in the Buyukmelen river‐bed sediments. The muddy feature of the waters is related to the petrographic features of the rocks in the basin and their mineralogical compositions, as most of the sandstones and volcanic rocks (basalt, tuffite and agglomerate) are decomposed to a clay‐rich composition at the surface. Thus, the suspended sediment in stream waters increases by physical weathering of the rocks and water–rock interaction. Owing to the growing population and industrialization, water demand is increasing. The plan is to bring water from the River Buyukmelen to Istanbul's drinking‐water reservoirs. According to the Water Pollution Regulations, the River Buyukmelen belongs to quality class 1 based on Hg, Cd, Pb, As, Cu, Cr, Zn, Mn, Se, Ba, Na⁺, Cl⁻, and SO²⁻₄; and to quality class 3 based on Fe concentration. The concentration of Fe in the River Buyukmelen exceeds the limit values permitted by the World Health Organization and the Turkish Standard. Because water from the River Buyukmelen will be used as drinking water, it will have an adverse effect on water quality and humans if not treated in advance. In addition, the inclusion of Mn and Zn in the Elmali drinking‐water reservoir of Istanbul and Fe in the River Buyukmelen water indicates natural inorganic contamination. Mn, Zn and Fe contents in the waters are related to geological origin. Moreover, the River Buyukmelen flow is very muddy in the rainy seasons and it is inevitable that this will pose problems during the purification process. Copyright © 2005 John Wiley & Sons, Ltd.     

Acidification recovery in a changing climate: Observations from thirty-five years of stream chemistry monitoring in forested headwater catchments at the Turkey Lakes watershed,Ontario

Long-term ecosystem studies are valuable for understanding integrated ecosystem response to global changes in atmospheric deposition and climate. We examined trends for a 35-year period (1982/83–2017/18) in concentrations of a range of solutes in precipitation and stream water from nine headwater catchments spanning elevation and surficial geology gradients at the Turkey Lakes watershed (TLW) in northeastern Ontario, Canada. Average annual water year (WY, October to September) concentrations in precipitation significantly declined over the period for sulphate (SO₄²⁻), nitrate (NO₃⁻) and chloride (Cl⁻), while calcium (Ca²⁺) and potassium (K⁺) concentrations increased, resulting in a significant pH increase from 4.2 to 5.7. Trends in stream chemistry through time are generally consistent with expectations associated with acidification recovery. Concentration of many stream water solutes (SO₄²⁻, Cl⁻, calcium [Ca²⁺], magnesium [Mg²⁺] and NH₄⁺ generally decreased, while others (silica [SiO₂] and dissolved organic carbon [DOC]) generally increased. Increases were also observed for alkalinity (six of nine catchments), acid neutralizing capacity ([ANC]; six of nine catchments) and pH (eight of nine catchments), while conductivity declined (six of nine catchments). Variability in trends among catchments are associated with differences in surficial geology and wetland cover. While absolute solute concentrations were generally lower at bedrock dominated high-elevation catchments compared to till dominated lower elevation catchments, the rate of change of concentration was often greater for high elevation catchments. This study confirms continued, but non-linear stream chemistry recovery from acidification, particularly at the less buffered high and moderate elevation sites. The heterogeneity of responses among catchments highlights our incomplete understanding of the relative importance of different mechanisms influencing stream chemistry and the consequences for downstream ecosystems.