Distinguishing between natural and anthropogenic sources of metals entering the Irish Sea

International agreements (e.g. OSPAR) on the release of hazardous substances into the marine environment and environmental assessments of shelf seas require that concentrations and bioavailability of metals from anthropogenic sources can be distinguished from those originating as a result of natural geological processes. The development of a methodology for distinguishing between anthropogenic and natural sources of metals entering the Irish Sea through river inputs is described. The geochemistry of stream, river and estuarine sediments has been used to identify background geochemical signatures, related to geology, and modifications to these signatures by anthropogenic activities. The British Geological Survey (BGS) geochemical database, based on stream sediments from 1 to 2 km² catchments, was used to derive the background signatures. Where mining activity was present, the impact on the signature was estimated by comparison with the geochemistry of sediments from a geologically similar, but mining free, area. River sediment samples taken upstream and downstream of major towns were used respectively to test the validity of using stream sediments to estimate the chemistry of the major river sediment and to provide an indication of the anthropogenic impact related to urban and industrial development. The geochemistry of estuarine sediments from surface samples and cores was then compared with river and offshore sediment chemistry to assess the importance of riverine inputs to the Irish Sea. Studies were undertaken in the Solway, Ribble, Wyre and Mersey estuaries. The results verify that catchment averages of stream sediments and major river samples have comparable chemistry where anthropogenic influences are small. Major urban and industrial (including mining) development causes easily recognised departures from the natural multi-element geochemical signature in river sediment samples downstream of the development and enhanced metal levels are observed in sediments from estuaries with industrial catchments. Stream sediment chemistry coupled with limited river and estuarine sampling provides a cost-effective means of identifying anthropogenic metal inputs to the marine environment. Investigations of field and laboratory protocols to characterise biological impact (bioaccumulation) of metals in sediments of the Irish Sea and its estuaries show that useful assessments can be made by a combination of surveys with bioindicator species such as clams Scrobicularia plana, selective sediment measurements that mimic the ‘biologically available’ fractions, and laboratory (mesocosm) studies.     

Geochemical mapping based on geological units: a case study from the Marnoso-arenacea formation (Northern Apennines,Italy)

Geochemical maps can provide us with much information on geology, earth surface processes and anthropogenic pressure and are valuable tools for ore prospecting and land management. Stream sediments represent an integral of the various possible sources of sediments upstream from the sampling point therefore there can be multiple signal sources but generally the prevailing signal source is the one related to bedrock geology. Stream sediments collected from active second-order channels including singular geological units, were selected in order to determine the geochemical characteristics of each unit. The aim of this study was to analyze their potential for using them to integrate geological interpretation and produce a geologically-oriented geochemical map. From the 770 samples collected for a regional geochemical mapping program, we selected 149 samples whose catchment basin included only one of the members recognized within the Marnoso-arenacea formation. This middle–upper Miocene (Langhian–Tortonian) turbiditic unit forms the backbone of the Romagna Apennines and has been subdivided into 14 members according to age and lithostratigraphic criteria. The results indicate that there are marked differences in the composition of the members of the Marnoso arenecea formation which indicate the provenance of the sediment and the palaeogeographic evolution of the units. By means of univariate and multivariate statistical analyses (Factor analyzes) two main types of sediment compositions are identified: Tortonian members are characterized by sialic coarse grain-sediments while the Langhian–Serravallian members are richer in carbonate fraction, slightly enriched in a mafic contribution. This study elaborated the geochemical data from a geological point of view by integrating the information available in literature to spatially extend the interpretation based on limited site observation as for petrographic studies. In general, the geochemical map based on a geological unit could be a useful tool for carrying out the geological reconstruction of a complex area.     

A comparison of regional geochemical data from lakes and streams in northern Labrador; implications for mixed-media geochemical mapping

Labrador has been covered by reconnaissance-scale geochemical surveys under the National Geochemical Reconnaissance program. Lake sediment and water were the chief sample media, but stream sediment and water were employed in the mountainous terrain of northern Labrador. The main objective of these surveys was mineral resource assessment, but the data are also relevant to geological and environmental studies, and would be most useful to the non-specialist if the data from the two drainage types could be combined to produce unified element distribution maps for the whole region.A comparison of stream and lake data for a 5,700-km² area where both drainage types were sampled suggests that only the pH of the lake and stream waters are directly comparable, showing a common range and similar spatial distribution. Comparing the two types of sediment, most elements show obvious differences in either median content or range or both, indicating that stream and lake sediment are geochemically distinct media, and their element contents cannot be compared directly. The distribution patterns of Cu, Ni and U reflect similar bedrock features in both sediment types. In contrast, Co, F, Fe, Hg, Mn, V and Zn show little or no spatial correlation between stream and lake sediment, but are strongly intercorrelated in the stream sediment data set.The sediments collected from lakes in Labrador represent disturbed column, about 40 cm in length, of organic debris that accumulated over the past several hundred years. Metal accumulation in the sediment is largely through fixation from inflowing surface and groundwater by microorganisms, coprecipitation with hydrous Fe and Mn oxides, sorption by clay minerals and chemical and biochemical processes at and just below the sediment/water interface. The stream sediments in this study were collected from active sediment, and represent principally the mechanical-weathering products of bedrock, with variable amounts of organic matter and hydrous Fe and Mn oxides. Considering the difference in the two sediment types, it is probably not surprising that there is rather limited spatial correlation between the geochemistry of the two sediment types indicating that to a large extent each medium reflects a different facet of the bedrock geochemistry. Only for a few elements should the data sets be merged. The degree of spatial correlation for U, Ni and Cu increases as the data are generalized by averaging into larger blocks, suggesting that the combined data sets will be more successful in defining broad crustal geochemical features rather than local details. The implication of this study for international geochemical mapping is that geochemical patterns for many elements are strongly dependent on the sample medium chosen. Therefore, when it is necessary to change sample media in passing from one terrain type to another, a comparative study must be carried out to determine how the geochemistry of the different sample media compare spatially.     

Spatial variations and distributions of phosphorus and nitrogen in bottom sediments from a typical north-temperate lake,China

Concentrations and vertical distributions of total nitrogen (TN), total phosphorus (TP) and their different forms in sediments obtained from nine locations of Lake Dalinouer in September 2008 were analyzed. The results demonstrated that TP in surface sediments ranged from 0.493 to 0.904 g/kg, and inorganic phosphorus was the main fraction of total phosphorus, ranging from 335 to 738 mg/kg. Simultaneously, the autogenetic calcium phosphorus (ACa-P) was the main fraction of inorganic phosphorus, ranging from 145.4 to 543.2 mg/kg. Vertical distribution of different phosphorus forms in different sediment cores was distinguishing, and most of them tended to increase toward the surface sediment, indicated that the phosphorus concentration was related to the humanity with a certain extent. The relationships between TP and occluded phosphorus and ACa-P were significant. Nitrogen in the sediment was composed mainly of organic nitrogen, accounting for grater than 80 % of TN. NO₃ ^?-N was the dominate fraction of inorganic nitrogen in the surface sediment, ranging between 51 and 346 mg/kg (151.1 ± 104.4 mg/kg), and accounting for between 2.2 and 17.7 % of total sediment nitrogen (6.2 ± 5.6 %). The ratio of organic carbon and TN in sediment was in range of 6.0–25.8 and presented a tendency of lake centre >lake sides, indicating that nitrogen accumulated in the sediments from lake sides came mainly from terrestrial source and nitrogen was mainly autogenetic in lake centre. Ratio of N:P in all sampling sites was below 14, indicated that N was the limiting nutrient for algal growth in this lake.     

Land use,sediment loads and dispersal pathways from two catchments at the southern end of Lake Tanganyika,Africa: implications for lake management

Increasing sediment loads entering the Lake Tanganyika ecosystem are hastening the need for improved understanding of the linkages between catchment characteristics and influent sediment transport and loading. Sediment loads of two catchments at the southern end of the lake were estimated for October 1998–December 1999, and catchment characteristics determined using GIS. It was found that both sediment yields and loads were higher from the catchment of the Lunzua River (19.8 t km^?2 and 20,114 t, respectively) compared with that of the Kalambo (4.1 t km^?2 and 12,197 t) in 1999. These differences were both attributed to the smaller size and higher road density of the Lunzua catchment, and suggest that previous recommendations regarding the positioning of underwater lake reserves fail to take into account the low sediment retention capacity of small mountainous rivers. Differences between the study rivers in the transport of suspended sediments, organic matter, and bedload sediments into the lake were also found, the latter determined by the novel application of the 'McLaren Model'.     

Regional geochemical baseline concentration of potentially toxic trace metals in the mineralized Lom Basin,East Cameroon: a tool for contamination assessment

The distribution of trace metals in active stream sediments from the mineralized Lom Basin has been evaluated. Fifty-five bottom sediments were collected and the mineralogical composition of six pulverized samples determined by XRD. The fine fraction (<?150 µm) was subjected to total digestion (HClO₄?+?HF?+?HCl) and analyzed for trace metals using a combination of ICP-MS and AAS analytical methods. Results show that the mineralogy of stream sediments is dominated by quartz (39–86%), phyllosilicates (0–45%) and feldspars (0–27%). Mean concentrations of the analyzed metals are low (e.g. As?=?99.40 µg/kg, Zn?=?573.24 µg/kg, V?=?963.14 µg/kg and Cr?=?763.93 µg/kg). Iron and Mn have significant average concentrations of 28.325 and 442 mg/kg, respectively. Background and threshold values of the trace metals were computed statistically to determine geochemical anomalies of geologic or anthropogenic origin, particularly mining activity. Factor analysis, applied on normalized data, identified three associations: Ni–Cr–V–Co–As–Se–pH, Cu–Zn–Hg–Pb–Cd–Sc and Fe–Mn. The first association is controlled by source geology and the neutral pH, the second by sulphide mineralization and the last by chemical weathering of ferromagnesian minerals. Spatial analysis reveals similar distribution trends for Co–Cr–V–Ni and Cu–Zn–Pb–Sc reflecting the lithology and sulphide mineralization in the basin. Relatively high levels of As were concordant with reported gold occurrences in the area while Fe and Mn distribution are consistent with their source from the Fe-bearing metamorphic rocks. These findings provide baseline geochemical values for common and parallel geological domains in the eastern region of Cameroon. Although this study shows that the stream sediments are not polluted, the evaluation of metal composition in environmental samples from abandoned and active mine sites for comparison and environmental health risk assessment is highly recommended.     

Biomarker Compounds as Indicators of Paleoenvironments

In an attempt to assess the paleoenvironments of terrestrial sediments,some twenty-two representa-tive Chinese non-marine sediment samples were studied using the molecular organic geochemistry method.The sediment samples stuied include oilshale,shale,mudstone and glauber salt from Tertiary to Cretaceous in age.Judging from geological/geochemical data and paleosalinity data,the samples studied are of lacustrine sedimentary origin and can be divided into three different types:fresh water,brackish and saline/hypersaline lake sediments.The aliphatic fractions were separated from the extracts of the samples and analysed by means of GC and GC/MS instruments,giving a number of parameters such as relative abundances of alkanes and cycloalkanes as shown in the mass chromatograms.     

Assessment of heavy metal pollution in lake sediments of Katedan Industrial Development Area,Hyderabad, India

Spatial distribution and temporal trends studies were carried out at Katedan Industrial Development Area (KIDA) near Hyderabad, capital of Andhra Pradesh state, India under Indo-Norwegian Institutional Cooperation Program, to find out the extent of contamination in streams and lake sediments from the discharge of industrial effluents. Stream and lake sediment samples were collected from the five lakes in the study area and connecting water streams. The samples were analyzed by XRF spectrometer for toxic elements. The studies reveal that the stream sediments with in the KIDA and the impounded Noor Mohammed Lake down stream have high concentration of some of the toxic elements like chromium, nickel, lead, arsenic, zinc etc. The geology of the area indicates that the study area consists of residual soil of acidic rocks, which are predominantly of Archaean gneisses and granites having low to medium concentrations of chromium and nickel. The source of these high concentration of elements like lead 2,300 mg/kg, copper 1,500 mg/kg, arsenic 500 mg/kg, chromium 500 mg/kg etc. cannot be derived from the surrounding acidic rocks and may be attributed to the industrial effluents released in the ditches and random dumping of hazardous solid waste. It was observed that the metal concentrations increased in the streams during the dry season (pre-monsoon period). After the monsoon rains, the metal concentrations in the streams were reduced by half which may be due to dilution. The eroded sediments are deposited in the lake where very high concentrations were encountered. Overflowing of the lake will spread the contamination further downstream. The lake sediments will remain as a major source of contamination by desorption to the water phase regardless of what happens to the effluent discharge in the KIDA. However, some samples showed enrichment of lead, arsenic and nickel during post-monsoon, which were collected near the dumpsite due to the leaching of toxic elements from the dump site to the lakes. Some of the toxic elements like nickel and copper have not shown any dilution but have increased after the rains, which could be due to the leaching of arsenic from the dumpsite to the lake along with rainwater. Geochemical maps showing the distribution of heavy/trace elements in streams and lakes are prepared and presented in this paper. Effect of toxic elements on the health of the residents in the surrounding residential areas is also discussed.     

Environmental geochemistry of high arsenic groundwater at western Hetao plain, Inner Mongolia

Environmental geochemistry of high arsenic groundwater at Hetao plain was studied on the basis of geochemical survey of the groundwater and a core sediment. Arsenic concentration in groundwater samples varies from 76 to 1093 μg/L. The high arsenic groundwater mostly appears to be weakly alkaline. The concentrations of NO₃⁻ and SO₄²⁻ are relatively low, while the concentrations of DOC, NH₄⁺, dissolved Fe and sulfide are relatively great. Analysis of arsenic speciation in 21 samples shows that arsenic is present in the solution predominantly as As(III), while particulate arsenic constitutes about 10% of the total arsenic. Methane is detected in five samples with the greatest content being 5107 μg/L. The shallow aquifer in Hangjinhouqi of western Hetao plain is of strongly reducing condition. The arsenic content in 23 core sediment samples varies from 7.7 to 34.6 mg/kg, with great value in clay and mild clay layer. The obvious positive relationship in content between Fe₂O₃, Mn, Sb, B, V and As indicates that the distribution of arsenic in the sediments may be related to Fe and Mn oxides, and the mobilization of Sb, B and V may be affected by similar geochemical processes as that of As.     

Areal versus linear evaluation of relationship between drainage basin lithology and geochemistry of stream and overbank sediments in low-order mountainous drainage basins

The comparison of two multiple regression models is based on the assumption that geochemical composition of the drainage basin alluvial sediments is derived primarily from the underlying bedrock lithology. The parent material is integrated with both stream sediment and overbank sediment geochemistry via the two essentially different approaches as regards the drainage basin geomorphological data: (1) as the relative area of influence representing a portion of the catchment basin occupied by a specific rock type and (2) as the relative “line” of influence representing a narrow zone of the underlying bedrock traversed by the perennial streams which form the active stream network. The model comparison is established on the goodness-of-fit test for both experimental designs and for the same set of data. Both experiments converge on the linear approach as the more appropriate model in evaluating the lithologic influence on the analysed sample media in small mountainous watersheds.     

Vertical geochemical variations and arsenic mobilization in the shallow alluvial aquifers of the Chapai-Nawabganj District, northwestern Bangladesh: implication of siderite precipitation

Core sediments from three disturbed boreholes (JOR, GHAT, and RAJ) and two undisturbed boreholes (DW1 and DW2) were collected in the study area of the Chapai-Nawabganj district of northwestern Bangladesh for geochemical analyses. In the study area, groundwater samples from fourteen As-contained private wells and five nested piezometers at both the DW1 and DW2 boreholes were also collected and analyzed. The groundwater arsenic concentrations in the uppermost aquifer (10–40 m of depth) range from 3 to 315 μg/L (mean 47.73 ± 73.41 μg/L), while the arsenic content in sediments range from 2 to 14 mg/kg (mean 4.36 ± 3.34 mg/kg). An environmental scanning electron microscope (ESEM) with an energy dispersive X-ray spectrometer was used to investigate the presence of major and trace elements in the sediments. Groundwaters in the study area are generally the Ca–HCO₃ type with high concentrations of As, but low levels of Fe, Mn, NO₃ ^? and SO ₄ ^?2 . The concentrations of As, Fe, Mn decrease with depth in the groundwater, showing vertical geochemical variations in the study area. Statistical analysis clearly shows that As is closely associated with Fe and Mn in the sediments of the JOR core (r = 0.87, p < 0.05 for Fe and r = 0.78, p < 0.05 for Mn) and GHAT core (r = 0.95, p < 0.05 for Fe and r = 0.93, p < 0.05 for Mn), while As is not correlated with Fe and Mn in groundwater. The comparatively low Fe and Mn concentrations in some groundwater and the ESEM image revealed that siderite precipitated as a secondary mineral on the surface of the sediment particles. The correlations along with results of sequential extraction experiments indicated that reductive dissolution of FeOOH and MnOOH represents a mechanism for releasing arsenic into the groundwater.     

Arsenic associations in sediments from shallow aquifers of northwestern Hetao Basin,Inner Mongolia

Understanding the mechanism of arsenic mobilization from sediments to groundwater is important for water quality management in areas of endemic arsenic poisoning, such as the Hetao Basin in Inner Mongolia, northern China. Aquifer geochemistry was characterized at three field sites (SH, HF, TYS) in Hangjinhouqi County of northwestern Hetao Basin. The results of bulk geochemistry analysis of sediment samples indicated that total As concentrations have a range of 6.8–58.5 mg/kg, with a median of 14.4 mg/kg. The highest As concentrations were found at 15–25 m depth. In the meanwhile, the range of As concentration in the sediments from background borehole is 3–21.8 mg/kg, with a median value of 9 mg/kg. The As sediments concentrations with depth from the SH borehole were correlated with the contents of Fe, Sb, B, V, total C and total S. Generally, the abundance of elements varied with grain size, with higher concentrations in finer fractions of the sediments. Distinct lithology profile and different geochemical characteristics of aquifer sediments indicate the sediments are associated with different sources and diverse sedimentary environments. Up to one third of arsenic in the sediments could be extracted by ammonium oxalate, suggesting that Fe oxyhydroxides may be the major sink of As in the aquifer. Sequential extraction results indicate that arsenic occurs as strongly adsorbed on and/or co-precipitated with amorphous Fe oxyhydroxides in sediments accounting for 35 and 20%, respectively, of the total contents of arsenic. The release of As into groundwater may occur by desorption from the mineral surface driven by reductive dissolution of the Fe oxide minerals. Furthermore, small proportions of As associated with iron sulfides occur in the reductive sediments.     

Metal transport, partition and fixation in drainage waters and sediments in carbonate terrain in Southeastern Ontario

Lake sediment composition as an indicator of mineralization within the catchment area has found widespread application in recent years, particularly in Canada. Results have indicated, however, the existence of varying relationships between lake sediment composition and mineralization resulting from local features of the limnological environment. Accordingly it was considered appropriate to examine the nature of metal transport in the lake and stream environment, the partitioning of metal between the stream waters and stream sediments and between lake waters and lake sediments to obtain some understanding of the factors that affect the lake sediment-mineralization relationship. This investigation was carried out over an area containing Pb-Zn occurrences of supposed “Mississippi-Valley type” in Grenville and Paleozoic bedrock in southeastern Ontario.The headwater drainage systems comprise active streams, swamps, beaver ponds and small lake-bog systems giving way downstream to open lakes. The beaver swamps and seasonal swamps act as drainage sinks for metals, restricting the extent of geochemical dispersion in drainage systems adjacent to mineralization. Selective extraction analysis of bog, stream and lake sediments indicates that metals are preferentially concentrated with amorphous iron oxides, which readily adsorb and complex lead and zinc and are stable in the alkaline environment common in swamps adjacent to carbonate-hosted lead-zinc mineralization. The accumulation of lead and zinc with amorphous iron oxides combined with the adsorbing and chelating action of organic matter on lead and zinc makes organic-rich sediments from these small swampy areas an excellent sample medium for reflecting local mineralization. Down drainage anomalies of these elements can be accentuated by selective analysis for the amorphous iron oxide-held metal, involving selective extraction techniques.In contrast, within larger lake systems, the analysis of water samples indicates that geochemical dispersion in surface waters in the high pH environment (pH = 8.0) associated with the carbonate-hosted lead-zinc deposits is extremely restricted. In this environment, anomalous metal contents in lake water were not evident in lakes adjacent to mineralization, while anomalous lake sediment compositions exist only in lakes immediately adjacent to Pb-Zn mineralization and do not extend down the drainage system. The restricted dispersion necessitates basing geochemical reconnaissance surveys on collection and analysis of samples from the headwater organic-rich swamps at a higher sample density and resulting higher cost than in areas where a lower sample density is acceptable due to a wider dispersion.     

Heavy metal contamination in surface sediments of Gökçekaya Dam Lake,Eskişehir,Turkey

The present study to find seasonal (September 2010–June 2011) heavy metal (Cd, Pb, Cr, Co, Ni, Zn, Cu, Fe, As) contamination and the origins thereof in surface sediments of Gökçekaya Dam Lake, as constructed on Sakarya River, the third-longest river in Turkey and the largest river of the Northwestern Anatolia. Upon analyses for the purpose thereof, heavy metal contamination in annual average concentrations in the lake sediment varied, respectively, as Fe > Zn > Cr > Ni > Cu > Pb > Co > As > Cd. Statistical assessments performed in order to see whether the average values of the heavy metal contamination as measured at stations placed in the lake changed by seasonal periods. There found statistically significant differences especially in Cd, Zn, and Pb between seasonal periods. In accordance with the Sediment Quality Index, Gökçekaya Dam Lake sediment was classified as “highly polluted” in terms of the amount of anthropogenic contaminants of As, Cr, Cu, Ni, Pb, and Zn. Enrichment factor and geoaccumulation index values (I _geo) were calculated in order to geochemically interpret the source of contamination due to heavy metal concentration in the lake sediment and the level of pollution. The As, Co, Cr, Cu, Ni Pb, and Zn values demonstrated that the sediment was rich for anthropogenic contaminants. The lake was found especially rich for arsenic (14.97–34.70 mg/kg) and lead (68.75–98.65 mg/kg) in accordance with annual average values. In general the lake was geochemically characterized as “moderately contaminated” in terms of As, Co, Cr, Cu, Ni, Pb, and Zn content.     

Heavy metal contamination in sediments of Balanagar industrial area,Hyderabad, Andra Pradesh,India

Environmental geochemical studies were carried out to find out the extent of contamination in sediments due to heavy metals in Balanagar industrial area, Hyderabad, Andhra Pradesh, India. The industrial area consisting of 350 small and large industries manufacturing battery, steel planting, pharmaceutical chemicals, metal plating, etc. The present study was undertaken on sediment contamination in Balanagar industrial area, to determine extent and distribution of heavy metals (Cu, Cr, Ni, Pb, Zn, As) and to delineate the source. There is no treatment plant in the industrial area, and many industries release the effluents into nearby nalas and lakes. Solid waste from the industries is also being dumped along the roads and near the open grounds due to which heavy metals migrate from solid waste to the groundwater. The sediments samples were collected from the study area in clean polythene covers and were analyzed for their heavy metals by X-ray fluorescence spectrometry. The concentration ranges of different heavy metals were Cr, 96.2–439.6 mg/kg; Cu, 95.7–810 mg/kg; Ni, 32.3–13,068.2 mg/kg; Pb, 59.2–512 mg/kg; Zn, 157.1–4,630.5 mg/kg; Co, 1.8–48.3 mg/kg; and V, 35.2–308.5 mg/kg. High concentration of heavy metals in sediments can be attributed to some pharmaceutical and metal industries in the study area. Based on the results obtained, suitable remedial measures can be adopted such as phytoremediation and bio-remediation for reduction of heavy metals in sediments.     

Arsenic content, fractionation, and ecological risk in the surface sediments of lake

The Nansi Lake has been seriously affected by long-term intensive industrial and urban activities. The objectives of this study were to determine the content, distribution, and ecological risk of arsenic and investigate the geochemical relationships between arsenic forms and sediment mineral phases of the Nansi Lake. Twenty samples of surface sediments were collected and analyzed for arsenic contents and chemical forms. Results indicated that total content of arsenic in the sediment samples averaged 13.45?mg/kg and ranged from 8.27 to 21.75?mg/kg. The arsenic was mostly associated with iron oxides (67.3%), followed by the association with the residual fraction (19.2%). In addition, total content of arsenic was positively correlated with the organic matter and iron contents in the sediment. The molar ratios of iron oxide bound arsenic content to iron content are lower than the maximal molar ratios of arsenic to iron for natural hematite, magnetite, and goethite. The total content of arsenic in the sediment samples was usually higher than threshold effect concentration of 9.79?mg/kg, but lower than probable effect concentration of 33.0?mg/kg for arsenic in freshwater sediments. Adverse effects or toxicity to the aquatic organisms, caused by arsenic in the sediments of the Nansi Lake, will likely occur at these levels of arsenic contamination.     

Vertical distribution of bacterial populations associated with arsenic mobilization in aquifer sediments from the Hetao plain, Inner Mongolia

To understand the mechanism of arsenic mobilization from sediment to groundwater mediated by microorganism, vertical distribution of bacterial populations in aquifer sediments of the Hetao plain, Inner Mongolia was investigated by a two-step nested PCR-DGGE and 16S rRNA gene clone libraries, combined with sediment geochemistry. A borehole to 30 m depth was drilled and 11 sediment samples were collected. Lithological profile and different geochemical characteristics of sediments indicated a distinct transition of oxidizing–reducing environment along the depth of the sediment core. As(III) and Fe(II) concentrations elevated progressively from 10 m, simultaneously coupling with decrease of As(V) and Fe(III) concentrations, implying that reductive dissolution of arsenic-rich Fe(III) oxyhydroxides led to arsenic release. Results of DGGE displayed that sediment samples with higher concentrations of total arsenic and total organic carbon had lower population diversity, which suggested total arsenic concentrations were important to determine the population diversity of sediments. Bacterial communities of a sediment sample with the highest diversity and ratio of As(III) to total As were dominated by aerobic and facultative anaerobic bacteria and belonged to Alpha-, Beta-, and Gammaproteobacteria and Firmicutes group. Most of the retrieved sequences were closely related to high arsenic-resistance organisms, sulfide/thiosulfate oxidizers, denitrifiers, and aromatic hydrocarbon degraders. Thiobacillus distinctly predominated in clone library, which suggested that arsenic might be released by oxidized dissolution of sulfide minerals coupled to arsenate reduction or nitrate reduction in anaerobic condition. These data have important implications for understanding the microbially mediated arsenic mobilization in aquifers.     

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.     

Geochemical characteristics of fine and coarse fractions of sediments in the Yarlung Zangbo River Basin (southern Tibet,China)

Tracing sources of aeolian sediment is key to reconstructing earth surface processes in arid areas and interpreting the paleoenvironmental significance of aeolian sequences. However, the difference of geochemical characteristics between different fractions of sediments in the Yarlung Zangbo River Basin (YZRB) is still unclear, so we want to identify which fraction of sediments is more suitable for tracing sediment sources. Considering the long distance between different wide valleys in the YZRB, we wonder whether there is any difference between these wide valleys in terms of geochemical characteristics of sediments. Forty-three surface sediment samples in the YZRB are collected, and the grain-size distributions and the major-element composition for 37 samples and the trace and rare earth element composition for the coarse (75–500 μm) and fine (<?75 μm) fractions of all samples are determined. The results reveal the following: (1) the fine fractions of the deposits contain more environmental information, suggesting that the fine fractions cannot be directly compared between different climate zones for provenance identification and that appropriate coarse fractions, based on the grain-size distribution of the targeted sediments, are more ideal for tracing sediment sources; and (2) geochemical characteristics of various sediment types show spatial heterogeneity. The coarse and fine fractions of the loose sediment samples can be divided into two regional groups based on geochemical characteristics: the Maquanhe zone in the upper reach, the Xigaze, Shannan and Mainling zone in the middle reach, which is consistent with the geological background of the YZRB; (3) aeolian deposits in the YZRB are a local origin and predominantly derived from the adjacent loose sediments, and fluvial sediments in the upper reach contribute little to the aeolian sands in the middle reach.     

Interrelationship between geochemical elements of sediment and groundwater at Samrak Park Delta of Nakdong River Basin in Korea: multivariate statistical analyses and artificial neural network approaches

This research was conducted at Samrak Park Delta of Nakdong River Basin in Busan Metropolitan City, Korea. The main objective of this study was to evaluate the interrelationship of geochemical elements in sediments and groundwater through multivariate statistical analyses and a multilayer perceptron artificial neural network model. The mean concentrations of chemical elements were Si (46%), Fe (16.9%), Al (15.7%), K (7.5%) and Ca (4.5%) in sediments, and Na (8650 mg/L), Mg (999 mg/L), Ca (432 mg/L), K (293 mg/L) and Cl (17,640 mg/L) in groundwater, respectively. The principal component analysis produced 3 kinds of factors with the variances of 63.37, 27.02 and 9.62%, respectively. It is suggested that the chemical components of sediments and groundwater were mainly originated from source rocks and seawater intrusion, with the minor impacts of irrigation and industry. Cluster analysis also showed that chemical elements were mainly controlled by the natural geogenic sources and seawater intrusion. Multilayer perceptron of artificial neural network (ANN) presented the good interrelationship between sediment and groundwater. The determination coefficients (R ²) between ANN predicted values and observed values in groundwater showed the high values of 0.61–0.97 except Mg, Mn and Sr. It is revealed that the chemical components of sediment and groundwater were derived from local geological origin and from the minor impact of anthropogenic sources. Multivariate analyses and ANN contributed to the identification of the mutual relationship between the geochemical elements of sediment and those of groundwater.