Weathering of sulfidic shale and copper mine waste: secondary minerals and metal cycling in Great Smoky Mountains National Park,Tennessee, and North Carolina,USA

Metal cycling via physical and chemical weathering of discrete sources (copper mines) and regional (non-point) sources (sulfide-rich shale) is evaluated by examining the mineralogy and chemistry of weathering products in Great Smoky Mountains National Park, Tennessee, and North Carolina, USA. The elements in copper mine waste, secondary minerals, stream sediments, and waters that are most likely to have negative impacts on aquatic ecosystems are aluminum, copper, zinc, and arsenic because these elements locally exceed toxicity guidelines for surface waters or for stream sediments. Acid-mine drainage has not developed in streams draining inactive copper mines. Acid-rock drainage and chemical weathering processes that accompany debris flows or human disturbances of sulfidic rocks are comparable to processes that develop acid-mine drainage elsewhere. Despite the high rainfall in the mountain range, sheltered areas and intermittent dry spells provide local venues for development of secondary weathering products that can impact aquatic ecosystems.Electronic Supplementary Material  Supplementary material is available for this article if you access the article at . A link in the frame on the left on that page takes you directly to the supplementary material.

Analyses of trace elements on quartz surfaces in sulfidic mine tailings from Kristineberg (Sweden) a few years after remediation

Laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) has been applied to determine the elemental composition of the surface layer, as well as of the first interior layer, of quartz grains from the mine tailings from Kristineberg (northern Sweden) in order to determine concentration gradients between these two layers. The quartz grains were collected from the oxidized and unoxidized zones within the tailings. The aim of this study is to assess the role of quartz surfaces as sites for the attenuation of solutes from the mine-tailings porewater. Concentrations of Cu, Ag, Sb, Pb and Bi are highest near the surface of each grain and decrease towards the interior. The surface concentration of Cu, Zn and Pb is more pronounced within the unoxidized than within the oxidized zone of the tailings. Cu exhibits a distinct concentration peak at the surface of the quartz grains below the pre-remediation oxidation front. For Zn and Ce the trend of high surface concentration is less pronounced than for Cu or Pb. Silver, Bi and As are preferably adsorbed within the uppermost layers of the oxidized zone where the pH is as high as 6.2. The conversion of intensity signals of the elements to concentration values in ppm was done by using external standards (NIST silicate glass).     

GIS-based hazard mapping and zonation of debris flows in Xiaojiang Basin,southwestern China

Debris flow sites were identified at 140 locations in the Xiaojiang Basin in Yunnan province, southwestern China. Their spatial distribution and catchment characteristics are described in detail on the basis of previous research, air photo interpretation, field investigation and mapping using Geographical Information Systems (GIS). Using a statistical approach, a quantitative model of hazards assessment and zonation was developed through synthesis analysis of basin areas, gradients, and the relative reliefs of these debris flow sites. In terms of debris flow hazard assessment, areas within the Xiaojiang Basin can be classified as severe, heavy and light hazard regions.     

The importance of hydrogeological and hydrological investigations in the residential area: a case study in Burdur,Turkey

Water resources in residential areas are negatively affected by floods. In addition, many aquifers are contaminated as a result of urbanization. Great damage caused during earthquakes are partly attributed to the residential pattern which ignores the potential effect of groundwater. Hydrogeological and hydrological surveys must be carried out in the residential areas to determine the interaction between water and residential development of all types.Recent hydrogeological and hydrological investigations regarding the impact of urbanization were made for the city of Burdur (Turkey). To evaluate the effect of earthquakes on groundwater, groundwater isohypse and groundwater isopach maps were prepared showing most of the buildings within the Burdur city boundaries, which are in the areas where groundwater depth is less than 10 m. This is considered a critical depth for liquefaction during an earthquake. Lowering of the groundwater table has to be considered as one of the alternatives in reducing earthquake hazards. The chemical makeup of groundwater was also determined to consider its relationship to contamination and possible effects upon the foundations. Streams flowing across the Burdur residential area formed a flooding risk. Results of the peak flow analysis can be used to design improvements for the city. Maps of the best residential development areas have been prepared by using hydrological and hydrogeological results.     

Geophysical response of filled sinkholes,soil pipes and associated bedrock fractures in thinly mantled karst,east-central Illinois

Karst aquifers are often protected by a thin mantle of unconsolidated sediment. Soil pipes and sinkholes may breach this natural protective barrier and open pathways for contaminants to quickly reach bedrock aquifers. Geophysical surveys offer a quick and noninvasive way to identify these features; such surveys may also be sequenced to reveal increasing detail in critical areas. At a study site in east-central Illinois, electromagnetic (EM) surveys mapped high conductivity anomalies over filled sinkholes and soil pipes that penetrated the unconsolidated cover. Two-dimensional inverted resistivity sections, made over these anomalies, depict filled sinkholes and soil pipes as conductive zones above deeply weathered bedrock fractures. Borings verified the geophysical models and suggest high conductivities associated with the filled sinkholes are the result of enhanced moisture near active soil pipes. EM surveys also identified conductive zones in the overburden above a probable bedrock fracture linking sinkhole areas 0.5 km apart. Resistivity and EM methods, used in a phased and sequential manner, thus proved useful in mapping filled sinkholes and in delineating the vertical and lateral connections between soil pipes and hydraulically active bedrock fractures.     

Sequential extraction procedure in columns. Part 1: Development and description of a new method

A sequential extraction procedure was carried out in columns using reagents that are known to be reliable from batch tests. The intention was to distinguish between different chemical forms of iron and heavy metals in samples from reduced porous aquifers, which demands anaerobic conditions for the extraction procedure and the determination of small amounts of reactive mineral phases in a quartz dominated sediment system. By means of the developed method, anaerobic conditions can be guaranteed in the columns, which could not be realized to full satisfaction in batch tests that were carried out in a glove box. In order to distinguish between the fractions that were water soluble, exchangeable, bound to carbonates and bound to hydroxides, different reagents were pumped through the sediments and sampled after passage of the columns. Sediment samples of 10 kg each were investigated in this way. The extraction steps were known to be complete when analyses revealed that no further major and trace elements were leached out of the columns. This approach enabled well-adjusted amounts of reagents to be used. By means of the sequential extraction procedure in columns the composition of even small amounts of reactive mineral phases can be determined successfully, which contributes to a deeper understanding of the hydrogeochemical processes in aquifers. In batch tests this accuracy cannot be reached because of the surplus of the extraction solution in relation to the amount of sediment (higher solution-sediment ratio). Furthermore, larger samples are much more representative of the composition of the aquifers than smaller ones and the heterogeneity of the sediment does not limit the accuracy of the results as much as in batch tests. In addition, the technique of flushing sediment in a column is much more typical for the situation in an aquifer than suspending a few grams of a sample in the extracting reagents in batch extraction tests. In order to demonstrate the methodical improvements and field applications, the newly developed method was used to investigate the changing binding forms and mobility of iron and trace metals in samples from a lignite overburden dump, which are influenced by pyrite oxidation processes (acidification) followed by the addition of crushed limestone (neutralization) (see "Sequential extraction procedure in columns. Part 2: Application of a new method").     

Evaluation of aluminum speciation in surface waters in China and its environmental risk assessment

As the ongoing global research on acid precipitation is developing in depth, more and more attention has been paid to the ecological effects of aluminum (Al) due to its toxicity to plants and animals, which is caused by acid precipitation. As a very serious problem of terrestrial and aquatic environmental acidification occurs in China, especially in southwestern China, a systematic investigation of Al speciation in these regions is very important. In this paper, the Al speciation results of surface waters in China are reported and its ecological impacts is evaluated. More than 100 water samples were collected from about twenty provinces of China. Driscoll's Al speciation scheme combined with the modified MINQEL computer model is used for speciation of Al. This study shows that the ecological impacts of acidification are quite different between China and Western countries, because of different geographical environments and geological settings. In Western countries, acidification is mainly caused by NO₂^-. Due to low concentrations of K⁺, Na⁺, Ca²⁺, Mg²⁺, the buffer capacities of soil and water are weak. Therefore, natural waters can be acidified to pH<5 very easily, resulting in a considerable mobilization of Al and worsening of the ecological environment. In China, acid precipitation is mainly in the form of sulfuric acid. In northwestern China, concentrations of K⁺, Na⁺, Ca²⁺, Mg²⁺ are high in soil and surface waters. This leads to much higher capacity and a high resistance ability to acidification. The pH values of waters in this region are high (around 7) and no serious Al toxicity is found at present. However, in northeastern and southeastern China, the soil is rich in Al (unsaturated aluminosilicates in northeastern China, saturated aluminosilicates in north and central China, aluminum-rich soil in southeastern and southwestern China). The concentrations of K⁺, Na⁺, Ca²⁺, Mg²⁺ in soil and waters are lower than those of northwestern China. Therefore the buffer capacity is limited. Numerous surface waters have already been acidified and pH values declined to 5. The impacts of Al toxicity on ecological systems in these regions are very serious, especially in Jiangxi, Hubei Provinces and Chongqing Municipality.     

Modeling Biogeochemistry,the Key for Understanding Environmental Chemistry of a Semi－Arid Soil in Egypt

1IntroductionThecomponentsoftheenvironmentaredamagedbyagriculturalpractices.Soilslosstheirfer tilityandwaterdeterioratesduetopollution .Chemicalweatheringofmineralandsoiloccursattheinterfacesbetweentheliquidandsolidphases;consequentlythesurfaceareaandcompositionofthemineralsplayanimportantroleinthisprocess.GarrelsandMackenzie ( 1 96 7)suggestedthatincon gruentweatheringreactionswouldproducedissolvedspeciesandnewsolidsthataremorestableintheweatheringenvironmentthantheoriginalbedrockminerals.Ro…     

The distribution of meteoric <Superscript>36</Superscript>Cl/Cl in the United States: a comparison of models

The natural distribution of ³⁶Cl/Cl in groundwater across the continental United States has recently been reported by Davis et al. (2003). In this paper, the large-scale processes and atmospheric sources of ³⁶Cl and chloride responsible for controlling the observed ³⁶Cl/Cl distribution are discussed.The dominant process that affects ³⁶Cl/Cl in meteoric groundwater at the continental scale is the fallout of stable chloride from the atmosphere, which is mainly derived from oceanic sources. Atmospheric circulation transports marine chloride to the continental interior, where distance from the coast, topography, and wind patterns define the chloride distribution. The only major deviation from this pattern is observed in northern Utah and southern Idaho where it is inferred that a continental source of chloride exists in the Bonneville Salt Flats, Utah.In contrast to previous studies, the atmospheric flux of ³⁶Cl to the land surface was found to be approximately constant over the United States, without a strong correlation between local ³⁶Cl fallout and annual precipitation. However, the correlation between these variables was significantly improved (R ²=0.15 to R ²=0.55) when data from the southeastern USA, which presumably have lower than average atmospheric ³⁶Cl concentrations, were excluded. The total mean flux of ³⁶Cl over the continental United States and total global mean flux of ³⁶Cl are calculated to be 30.5±7.0 and 19.6±4.5 atoms m^–2 s^–1, respectively.The ³⁶Cl/Cl distribution calculated by Bentley et al. (1986) underestimates the magnitude and variability observed for the measured ³⁶Cl/Cl distribution across the continental United States. The model proposed by Hainsworth (1994) provides the best overall fit to the observed ³⁶Cl/Cl distribution in this study. A process-oriented model by Phillips (2000) generally overestimates ³⁶Cl/Cl in most parts of the country and has several significant local departures from the empirical data.

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Resumen Davis et al. (2003) han informado de la distribución natural de la proporción ³⁶Cl/Cl en las aguas subterráneas de la parte continental de los Estados Unidos de América [EUA]. En este artículo, se discute cuáles son los procesos a gran escala y las fuentes atmosféricas del ³⁶Cl y del cloruro que dan lugar a la distribución observada de ³⁶Cl/Cl.El proceso dominante que afecta a la relación ³⁶Cl/Cl en las aguas subterráneas de origen meteórico a escala continental es el aporte de cloruro estable desde la atmósfera, que procede principalmente de los océanos. La circulación atmosférica transporta el cloruro marino hacia el interior, donde la distancia a la costa, topografía y corrientes del viento definen la distribución del cloruro. La única desviación principal de este esquema tiene lugar al norte de Utah y en el sur de Idaho, donde se deduce que existe una fuente continental de cloruro en los Rellanos Salados de Bonneville (Salt Flats).En contraste con estudios previos (Knies et al. 1994; Phillips 2000), se ha descubierto que el flujo atmosférico de ³⁶Cl hacia la superficie terrestre es aproximadamente constante en todos los estados, sin deducirse una correlación fuerte entre el aporte de ³⁶Cl y la precipitación anual. Sin embargo, la correlación entre estas variables se ve mejorada de forma significativa, con coeficientes de regresión comprendidos entre 0,15 y 0,55, cuando se excluyen los datos recogidos en el sudeste de los EUA, que tienen concentraciones de ³⁶Cl atmosférico presuntamente inferiores a la media. El flujo medio total de ³⁶Cl calculado en la zona continental de los Estados Unidos vale 30,5±7,0 átomos por metro cuadrado y segundo, mientras que el flujo total global de ³⁶Cl es de 19,6±4,5 átomos por metro cuadrado y segundo.La distribución de ³⁶Cl/Cl calculada por Bentley et al. (1986) infravalora la magnitud y variabilidad observada en los valores medidos a lo largo de los Estados Unidos. El modelo propuesto por Hainsworth (1994) proporciona el mejor ajuste conjunto a la distribución observada de ³⁶Cl/Cl en este estudio. El modelo orientado a procesos de Phillips (2000) sobreestima por lo general la distribución de ³⁶Cl/Cl en la mayoría del país y difiere significativamente de algunos valores locales empíricos.

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Résumé La distribution naturelle du rapport ³⁶Cl/Cl dans les eaux souterraines des États-Unis a été récemment présentée par Davis et al. (2003). Dans ce travail, les processus à grande échelle et les sources atmosphériques de ³⁶Cl et de chlorure responsables du contrôle de la distribution observée du rapport ³⁶Cl/Cl sont discutés. Le processus dominant qui affecte le rapport ³⁶Cl/Cl dans les eaux souterraines dorigine météorique à léchelle continentale est lapport atmosphérique de chlorure stable, qui provient pour lessentiel de sources océaniques. La circulation atmosphérique transporte des chlorures marins vers lintérieur des continents, où la distribution de chlorure est définie par la distance à la côte, la topographie et les régimes des vents. La seule exception majeure à ce schéma est observée dans le nord de lUtah et le sud de lIdaho où lon suppose quil existe une source continentale de chlorure dans les bas-fonds salés de Bonneville. Au contraire de précédentes études (Knies et al. 1994; Phillips 2000), on trouve que le flux atmosphérique de ³⁶Cl vers le sol est approximativement constant sur lensemble des États-Unis, sans forte corrélation entre la retombée locale de ³⁶Cl et les précipitations annuelles. Cependant, la corrélation entre ces variables devient significative (R ²=0.15 à 0.55) lorsquon supprime les données du sud-est des États-Unis, dont on pense quelles présentent des concentrations en ³⁶Cl atmosphérique inférieures à la moyenne. Le flux total moyen de ³⁶Cl sur les États-Unis continentaux et le flux moyen global de ³⁶Cl sont respectivement évalués à 30.5 ± 7.0 et 19.6 ± 4.5 atomes.m^–2.s^–1. La distribution du rapport ³⁶Cl/Cl calculée par Bentley et al. (1986) sous-estime lordre de grandeur et la variabilité observés pour la distribution mesurée du rapport ³⁶Cl/Cl sur les États-Unis continentaux. Le modèle proposé par Hainsworth (1994) fournit le meilleur ajustement densemble à la distribution du rapport ³⁶Cl/Cl observée dans cette étude. Un modèle orienté vers les processus proposé par Phillips (2000) surestime dans lensemble le rapport ³⁶Cl/Cl dans la plupart des régions du pays et présente plusieurs désaccords locaux avec les données empiriques.

     

Importance of water quality to nekton habitat use in a North Carolina Branch estuary

Nekton abundance and water quality were examined over 8 yr (1986–1993) in Isaac Creek, a small (2.5 km long), shallow (1–2 m), estuarine creek draining to Adams Creek (Neuse River system), North Carolina, United States. Water quality and nekton were sampled at 8 to 12 stations at 2–3 wk intervals from April to October (76 dates). The nekton assemblage, sampled by trawl, included 42 taxa but was dominated by 11 species (7 fish and 4 decapod crustaceans). Nekton and water quality (temperature, salinity, dissolved oxygen [DO], salinity gradient) data were grouped and analyzed by three (upper, middle, and lower) creek zones to determine if estimated abundance was correlated with water quality. Potentially stressful water quality conditions for salinity (<5 ppt), temperature (>30°C in morning), and DO (<2 mg 1⁻¹) mainly occurred in the upper and middle zones. The most frequent occurrence of potentially stressful conditions for salinity was in the spring and for dissolved oxygen and temperature in middle to late summer. The frequency of potentially stressful conditions increased during a 3-yr period following timber harvest of a large portion of the watershed. Canonical correspondence analysis (CCA) suggested little correlation between the top 11 species and water quality and indicated an assemblage with regular seasonal changes. Comparison of nekton use of the middle and upper zones of the creek for 3-yr pre- and post-harvest periods showed an increase in proportion of nekton caught in those zones, despite the higher frequency of potentially stressful water quality conditions. This observation suggests that a complex set of factors, including water quality, influence the pattern of nekton use in Isaac Creek.