A study of oxygen isotopic fractionation during bio-induced calcite precipitation in eutrophic Baldeggersee,Switzerland

In order to better understand environmental factors controlling oxygen isotope shifts in autochthonous lacustrine carbonate sequences, we undertook an extensive one-year study (March, 1995 to February, 1996) of water-column chemistry and daily sediment trap material from a small lake in Central Switzerland. Comparisons between calculated equilibrium isotope values, using the fractionation equation of Friedman and O’Neil, (1977) and measured oxygen isotope ratios of calcite in the sediment-traps reveal that oxygen isotopic values of autochthonous calcite (δ¹⁸O) are in isotopic equilibrium with ambient water during most of the spring and summer, when the majority of the calcite precipitates. In contrast, small amounts of calcite precipitated in early-spring and again in late-autumn are isotopically depleted in ¹⁸O relative to the calculated equilibrium values, by as much as 0.8‰. This seasonally occurring apparent isotopic nonequilibrium is associated with times of high phosphorous concentrations, elevated pH (∼8.6) and increased [CO₃²⁻] (∼50 μmol/l) in the surface waters. The resulting weighted average δ¹⁸O value for the studied period is −9.6‰, compared with a calculated equilibrium δ¹⁸O value of −9.4‰. These data convincingly demonstrate that δ¹⁸O of calcite are, for the most part, a very reliable proxy for temperature and δ¹⁸O of the water.     

Diagenetic control on arsenic partitioning in sediments of the Meghna River delta,Bangladesh

A stratigraphic profile of solid phase As was measured to investigate the diagenetic cycling of arsenic and related elements in fluvial sediments of the Meghna River delta plain. The distributions of Fe, Mn, and Al are typically characterized by surficial solid phase enrichment, and As is distributed down to 36.6 m showing similar alternate layers of maxima and minima with Fe, Mn and TOC, which reflects the diagenetic remobilization and periodical differences in source materials of As. Lithological characteristics and geochemical data suggest that elevated levels of As are found in organic-matter-rich clay and silty sand rather than sand samples, with occasionally enriched As content in iron-oxyhydroxide-coated sand grains. Arsenic demonstrates a positive and significant co-variation with total organic carbon in sediments, which suggests the important role of particulate and colloidal organic matter and biological activity in controlling the distribution of arsenic in the Bengal delta. However, the concentrations of Fe and Mn weakly correlate with As contents, whereas Al contents show no relationship with As. The results of this study suggest that reactive oxides or hydroxides of Fe and Mn, rather than Fe and Mn with other minerals, might control arsenic distribution.     

Diagenetic cycling of trace elements in the bottom sediments of the Swan River Estuary,Western Australia

Teflon strips were used in-situ in the bottom sediments at two sites in the Swan River Estuary to collect diagenetic Fe–Mn oxyhydroxides and monitor monthly changes in their morphology and trace element geochemistry. This study demonstrates that substantial concentrations of trace elements accumulate at the redox front during the formation of diagenetic Fe–Mn oxyhydroxides. It is likely that the Fe–Mn oxyhydroxides initially nucleate and grow on the Teflon strips via bacterial activity. Trace element geochemistry of the diagenetic Fe–Mn oxyhydroxides is influenced by changes in the supply of trace elements from either the bottom sediments and/or water column or changes in the physico-chemical status of bottom and porewaters. If sufficient diagenetic Fe–Mn oxyhydroxides are preserved in the upper layer(s) of the bottom sediment it is possible that diagenetic (secondary) trace element enrichment profiles may be produced which modify the historical input of natural or anthropogenic trace element sources. Alternatively, partial or complete dissolution of the diagenetic Fe–Mn oxyhydroxides in response to temporal changes in the redox status of the bottom sediment may lead to a substantial underestimate of trace element fluxes in historical bottom sediment profiles. This study highlights that considerable care must be taken when interpreting short- to long-term geochemical profiles in bottom sediments due to the possible occurrence of rapid, seasonally mediated diagenetic processes.     

A biogeochemical study of sediments from the eutrophic Lake Lugano and the oligotrophic Lake Brienz,Switzerland

The biomarker composition and stable isotope (C, O) ratio values of organic matter (OM) and carbonate from sediment cores from the oligotrophic Lake Brienz and the eutrophic Lake Lugano (both in Switzerland) are compared, in order to obtain information about OM sources and transformation processes. Eutrophic conditions at Lake Lugano are reflected in elevated total organic carbon (TOC) content and hydrogen index (HI) values, as well as higher lipid concentrations. Parallel down core trends in δ¹³C values of TOC and calcite in the Lake Lugano sediments reflect bioproductivity cycles. Variations in δ¹⁸O values of calcite are consistent with changes in mean summer temperature over the time interval covered by the core. In contrast, such a correlation does not exist for Lake Brienz and there the stable isotope composition of calcite reflects its allochthonous origin. In the sediments of both lakes, fatty acid (FA) distributions and the composition of n-alkanols and n-alkanes indicate highly variable proportions of autochthonous OM sources (algae, zooplankton, bacteria) and OM from land plants. Enhanced in situ microbial synthesis during sediment deposition in Lake Lugano is suggested by the higher TOC-normalised concentrations of branched chain FAs (C₁₅–C₁₇), hopanoic acids and triterpenoid alcohols (i.e. tetrahymanol, diplopterol). Variations in the concentrations of cholesterol are related to contributions from zooplankton and/or green algae, while sitosterol concentrations reflect the input of vascular plants. Periods of increased input of OM from diatoms are evidenced by high 24-methylcholesta-5,22-dien-3β-ol (either epibrassicasterol or brassicasterol) and/or highly branched isoprenoid (HBI) alkenes concentrations. High relative concentrations of diplopterol in Lake Lugano sediments are consistent with the predominance of cyanobacteria commonly observed in eutrophic lakes. The presence of archeol and hydroxyarcheol in very low concentrations in the Lugano sediments argues for the activity of methanogens and/or anaerobic methanotrophs.Differences in OM degradation processes are reflected in higher chlorin index values in the Brienz sediments but higher saturated vs. unsaturated n-FAs in the core from Lugano. Higher concentrations of branched chain FAs and 16:1ω7 n-FA, as well as enhanced 18:1ω7/18:1ω9 n-FA, are consistent with enhanced bacterial biomass in the Lugano water column or sediments. The preservation of phytol seems to be enhanced in sediments with a high relative contribution of land plant OM. Major factors affecting OM accumulation in the lakes are differences in OM sources (i.e. terrestrial OM vs. autochthonous production), extent of bacterial activity and most likely oxygen availability in the water column.     

Diagenetic mobilization of manganese in Peru Basin sediments

The Mn contents and sedimentation rates of two cores from different areas of the Peru Basin have been determined. The southern core is associated with Mn nodules of conventional slow accretion rates (~ mm/10⁶ yr) while the northern one accompanies nodules with very high growth rates (~10² mm/10⁶ yr). The depletion of Mn observed within the top 40 cm of the cores is interpreted as resulting from a diagenetic remobilization of Mn⁺² due to the oxidative characteristics of the sedimentary column. In both cores, the calculated flux of Mn provided by the sediment is higher than the total Mn recovered in the overlying nodules. This indicates that the Mn content of the Peru Basin nodules can be supplied by diagenetic processes from the sediment, not only for the slowly growing nodules but also for the extremely fast growing concretions found in the north of the basin.     

Biogeochemical redox cycling of arsenic in mine-impacted lake sediments and co-existing pore waters near Giant Mine,Yellowknife Bay,Canada

Lacustrine sediments, submerged tailings, and their pore waters have been collected at several sites in Yellowknife Bay, Great Slave Lake, Canada, in order to investigate the biogeochemical controls on the remobilization of As from mining-impacted materials under different depositional conditions. Radiometric dating confirms that a mid-core enrichment of Pb, Zn, Cu and Sb corresponds to the opening of a large Au mine 60 a ago. This was evident even in a relatively remote site. Arsenic was enriched at mid-core, coincident with mining activity, but clearly exhibited post-depositional mobility, migrating upwards towards the sediment water interface (SWI) as well as down-core. Deep-water (15 m) Yellowknife Bay sediments that contain buried mine waste are suboxic, relatively organic-rich and abundant in microbes with As in pore waters and sediments reaching 585 μg/L and 1310 mg/kg, respectively. Late summer pore waters show equal proportions of As(III) and As(V) (16–415 μg/L) whereas late winter pore waters are dominated by As(III) (284–947 μg/L). This can be explained by As(III) desorption mechanisms associated with the conversion of FeS to FeS₂ and the reduction of As(V) to As(III) through the oxidation of dissolved sulfide, both microbially-mediated processes. Processes affecting As cycling involve the attenuating efficiency of the oxic zone at the SWI, sediment redox heterogeneity and the reductive dissolution of Fe(hydr)oxides by labile organic matter, temporarily and spatially variable.     

Phosphorus distribution in the sediments of a shallow eutrophic lake,Lake Chaohu,China

In this study, the sediment profiles of total phosphorus (TP), inorganic phosphorus (P_i), organic phosphorus (P_o), C/P and N/P were used to investigate time-dependent P distribution changes in Lake Chaohu. The characteristics of P_i and P_o fractions in the surface sediments were studied and the difference between east and west lake region was also discussed. The P_i and P_o contents displayed a clear gradient from east to west in sediments of Lake Chaohu, and the P_o/P ratios were lower in sediments with industrial and urban pollution sources input in west lake region. The study indicated that different sediments area had diverse concentrations and distributions of P_o fractions due to their different drainage basin and pollution sources. The profile distribution of the C/P and N/P ratios decreased with increasing depths and stayed relatively constant ratios at the depths of 15–30 cm. The C/P and N/P ratios were always below Redfield ratios in sediment profile, indicating P enrichment but likely due to the preferential loss of carbon in respect to phosphorus. The rank order of P_i-fractions extracted was HCl-P_i > NaOH-P_i > NaHCO₃-P_i in surface sediments. The relative distribution of NaHCO₃-P_i and HCl-P_i was in agreement with the trophic conditions of the regions studied. Among the sequentially extracted P_o forms, the rank order of P_o fractions was residual P_o > HCl-P_o > fulvic acid-P > humic acid-P > NaHCO₃-P_o, with mean relative proportion of 5.4:3.4:2.2:1.1:1.0.     

Late quaternary sediments in Lake Zürich,Switzerland

Lake Zürich occupies a glacially overdeepened perialpine trough in the northern Middlelands of Switzerland. A total of 154.4 m of Quaternary sediments and 47.3 m of Tertiary Molasse bedrock has been cored from the deepest part of the lake, some 10 km south of the city of Zürich. Some 16.8 m of gravels and sands directly overlying the bedrock include basal till and probably earliest subglacial fluvial and lacustrine deposits. These are overlain by 98.6 m of fine-grained, glacial-aged sediments comprising completely deformed proglacial and/or subglacial lacustrine muds, separated by four basal mud tills. The lack of interglacial sediments, fossils, and other datable material, and the presence of severe sediment deformation and unknown amounts of erosion prevent the establishment of an exact chronostratigraphy for sediments older than the upper mud till. Above it some 8.6 m of lacustrine muds were deposited, folded, faulted, and tilted during the final opening of the lake at about 17,500–17,000 years ago. Superimposed are 30.4 m of final Würm and post-glacial sediments comprising (from oldest): cyclic proglacial mud, thick-bedded and laminated mud, a complex transition zone, laminated carbonate, laminated marl, and diatom-calcite varves. These sediments reflect changing catchment and lacustrine conditions including: glacial proximity, catchment stability, lake inflow characteristics, thermal structure, chemistry, and bed stability. Average sedimentation rates ranged from 11 cm yr⁻¹ immediately after glacier withdrawal, to as low as 0.4 mm yr⁻¹ as the environment stabilized. The lack of coarse outwash deposits separating the fine-grained glaciolacustrine sediments from a corresponding underlying basal till suggests that deglaciation of the deep northern basin of Lake Zürich was by stagnation-zone retreat rather than by retreat of an active ice-front.     

Diagenetic migration of sulfides in sediments accumulated in different sedimentation settings

Migration and accumulation of sulfides at the contact of lithologically and geochemically different layers are considered. The possible mechanisms (gravitational, diffusion, elision, and electrogeochemical) for sulfide transportation during diagenesis are discussed. Data are presented to explain the localization of sulfide minerals at the boundary of reduced and oxidized sediments. The paper considers examples of stratiform sulfide concentrations of not only ore grade, but also lower grade, which, however, are of great significance for understanding the formation conditions of some geochemical anomalies. Link between the diagenetic migration of sulfides and the formation of iridium anomaly is substantiated.     

Diagenetic metal profiles in recent sediments of a scottish freshwater Loch

Integrated total elemental, phase-specific, and pore-water analyses of sediment cores from Loch Ba, Scotland, show that early diagenetic processes have promoted extensive metal enrichment immediately beneath the sediment-water interface. The accumulation of Mn, Pb, Zn, Cu, and Co in sedimentary solids upward of 3 cm depth is accompanied by an increasing residence of these elements in adsorbed and hydrous oxide phases. Such phases are formed through oxidative precipitation from the interstitial pore fluids, following the upward migration of metals from more deeply buried, anaerobic sectors of the sediment pile. There is good evidence that Fe and Ni are subject to similar influences, although their total abundances near the sediment surface are less conspicuously modified. In the Loch Ba sediments, the oxic conditions promoting metal precipitation are entirely confined to strata of postindustrial age. In the absence of fully diagnostic pore-water and sequential chemical data, similar diagenetic profiles could plausibly be misinterpreted as the product of anthropogenic contamination.     

Geographical distribution of arsenic in sediments within the Rio Conchos Basin,Mexico

Arsenic (As) content of sediments from the Rio Conchos and Rio San Pedro in northern Mexico were measured to determine if this toxic metalloid had accumulated to unsafe levels to humans and aquatic life. The spatial distribution of As in each of the six clusters of river and arroyo sediments was analyzed to determine variations with respect to background levels and to infer about potential As sources and sinks. In the northern part of the study area, background concentrations varied little throughout the area and concentrations in river sediments were close to background levels. In the southern part, however, the content of As in arroyo sediment contained a wider range of values and anomalous concentrations. The latter could be traced in part to the presence of mine tailings. As concentrations were below the limit in all studied river stretches and thus do not pose an immediate threat to the river environment, but As content in reservoir sediments exceeded the guideline values. Reservoirs seem to act as a sink for As, warranting closer observation and monitoring.     

Microbial mercury cycling in sediments of the San Francisco Bay-Delta

Microbial mercury (Hg) methylation and methylmercury (MeHg) degradation processes were examined using radiolabled model Hg compounds in San Francisco Bay-Delta surface sediments during three seasonal periods: late winter, spring, and fall. Strong seasonal and spatial differences were evident for both processes. MeHg production rates were positively correlated with microbial sulfate reduction rates during late winter only. MeHg production potential was also greatest during this period and decreased during spring and fall. This temporal trend was related both to an increase in gross MeHg degradation, driven by increasing temperature, and to a build-up in pore water sulfide and solid phase reduced sulfur driven by increased sulfate reduction during the warmer seasons. MeHg production decreased sharply with depth at two of three sites, both of which exhibited a corresponding increase in reduced sulfur compounds with depth. One site that was comparatively oxidized and alkaline exhibited little propensity for net MeHg production. These results support the hypothesis that net MeHg production is greatest when and where gross MeHg degradation rates are low and dissolved and solid phase reduced sulfur concentrations are low.     

Diagenetic alteration of smectite in argillaceous sediments of the Rhinegraben (SW Germany)

Clay minerals of about 600 samples from drill cores in the Tertiary shales of the Rhinegraben, were analysed by X-ray diffraction methods. It was found that the abundance of smectite decreases with increasing amounts of mixed layer clays and illites, suggesting a diagenetic alteration of smectite with increasing temperatures of the sediments as was also observed in other sedimentary basins. As for the relation between smectite alteration and temperatures as measured in sample depths, in the marine Graue Schichtenfolge (Middle Oligocene) when temperatures reach 70°C and over, smectite no longer is to be found. In the limnic Bunte Niederröderner Schichten (Upper Oligocene) the maximum temperature of smectite occurrence is about 80°C. These temperatures also fit the results of former field studies of the thermal stability of smectite. In the brackish to limnic Obere and Untere Hydrobienschichten (Lower Miocene) however, smectite seems to have disappeared already at a temperature of over 30°C. Although the smectite distribution in the latter formations may depend partly on its inhomogenous deposition there is also evidence for the diagenetic alteration of smectite in these formations. The rapid disappearance of smectite in these formations was possibly caused by a greater availability of potassium ions since high permeability of these strata provide extraordinarily good mobility of the pore solutions. In the older Lymnäenmergel formation (Upper Eocene) a more advanced stage of smectite alteration is found as compared to the other formations at corresponding temperatures. This is considered to be the consequence of the longer duration of diagenesis and the rock salt inclusions of this saline formation which might have enriched the pore solutions with potassium ions.     

太湖底泥的空间分布和富营养化特征

太湖是一个大型的浅水湖泊,周围有数十条入湖河流,陆地风化物质被携带入湖即形成了底泥.由于湖底地形的差异,底泥在湖中的分布并不均匀.根据浅地层剖面仪的测量,在湖的西部存在一条南北向分布、宽度不等的古河道,底泥主要分布于古河道,在湖的沿岸和东太湖也有分布.根据估算,太湖底泥的蓄积量约为13.5亿m3.太湖周围人口密集,工农业发达,二十多年来经济的快速发展引起了湖泊的富营养化,太湖底泥中的营养元素不断增高,并在一定的条件下向水体释放,加剧了水体的富营养化,引起连续多年春夏季节的蓝藻爆发.经过政府的源头控制和治理,目前富营养化状况初步得到遏止,并有改善的迹象.但底泥中的营养元素可以在很长时间内释放,因此富营养化的治理将是一个长期的过程.     

Volatile fatty acid cycling in organic-rich marine sediments

Volatile fatty acid (VFA) apparent turnover rates were determined by measuring whole sediment VFA concentrations and the corresponding reaction rate constants. The following ranges of VFA concentrations were measured in Cape Lookout Bight, N.C. sediments (μmole·l_s^?1): acetate 54–660, propionate 1–24, butyrate <0.5–22, iso-butyrate <0.5–6. Apparent turnover rates measured over a one-year period ranged from 18–600 μmole·l_s^?1·h^?1 for acetate and 0.7–7 μmole·l_s^?1·h^?1 for the carboxyl carbon of propionate. Methane production was observed only with acetate and only in sulfatedepleted sediments; total acetate turnover attained approximately the same maximum value in both sulfate-reducing and sulfate-depleted sediments.Apparent turnover rates for acetate and propionate appeared to be controlled by similar factors: in sulfate-reducing (surface) sediments the turnover rates were stimulated by autumn storm-mediated deposition/resuspension events; in deeper sulfate-depleted sediments the turnover rates followed changes in the ambient temperature. Changes in VFA poolsizes were proportionally much larger than changes in corresponding rate constants. The ratio of CO₂ to CH₄ produced from acetate vs. depth suggested that non-methanogenic bacteria accounted for 60% of the acetate turnover in sulfate-depleted sediments.VFA concentrations were much lower in N.C. continental slope mud than in Cape Lookout sediments; acetate was the only VFA detectable throughout the top 40 cm of the slope sediments. The estimated production rate of CO₂ from acetate decreased rapidly with depth. The surface rate was approximately 20 times less than that measured at similar temperatures in sulfate-reducing Cape Lookout sediments.     

Natural enrichment of arsenic in Loch Lomond sediments

Concentrations of arsenic in surface or near-surface sediment in 12 of 13 cores from the three major basins of Loch Lomond are substantially enhanced, up to 675 mg/kg compared with background values of 15–50 mg/kg. Sedimentary As profiles are attributed to post-depositional enrichment processes since there are no recent significant sources of environmental As contamination, anthropogenic or natural, in the Loch Lomond area. The enrichments can be interpreted in terms of post-depositional diagenetic remobilization processes in sediment reducing zones, followed by upward migration of As through interstitial waters and oxidation/adsorption/precipitation reactions in near-surface oxidizing layers. Confirmation of the diagenetic/adsorption hypothesis is provided directly by the analysis of As species (1.5–81 μg/l) in pore water and indirectly via comparison with sedimentary phosphorus.     

Heavy metal and arsenic distributions in sediments of the Elba-Argentario basin, southern Tuscany, Italy

 Arsenic, chromium, cobalt, copper, lead, nickel, vanadium and zinc distributions in surficial and core sediments of the Elba-Argentario marine basin (southern Tuscany, central-western Italy) are reported. Analysis of such distributions compared with grain size and mineralogical data allowed the identification of areas showing trace element enrichments with respect to natural background. These enrichments are moderate and essentially restricted to Pb and Zn; only As shows a widespread, though not high, positive anomaly. This general pattern is in good agreement with the minor industrialization affecting the basin's watershed. An unexpected anomaly, concerning Co, Pb, and As, as well as Fe and Ti, has been pointed out close to Montecristo Island. This has been ascribed to illegal local dumping of chemical waste. Received: 12 January 1996 / Accepted: 9 September 1996     

Diagenetic processes in Holocene carbonate sediments: Florida Bay mudbanks and islands

The sedimentology, mineralogy and pore fluid chemistry of seven cores from the Holocene sediments of Florida Bay were studied to determine the physical processes and diagenetic reactions affecting the sediments. The cores were taken in a transect from a shallow mudbank onto a small adjacent island, Jimmy Key. Steady state models of pore fluid chemistry are used to estimate the rates of various reactions. In the mudbank sediments, little carbonate mineral diagenesis is taking place. No change in sediment mineralogy is detectable and pore water profiles of Ca²⁺, Mg²⁺ and Sr²⁺ show only minor variation. Chloride concentrations indicate substantial biological mixing of seawater from the bay into the sediments in one of the cores. Pore water analyses of sulphate and alkalinity show only a low degree of sulphate depletion and a decreasing extent of sulphate reduction downcore. Models of sulphate reduction in the mudbank show that there is substantial chemical exchange between the sediment pore fluids and water from the bay probably as a result of bio-irrigation. The sulphate and alkalinity data also suggest that the underlying Pleistocene rocks contain water of near normal seawater composition. Stratigraphic analysis and δ¹³C analyses of the organic carbon in the sediments of the island cores show that the sediments were primarily deposited in a subtidal mudbank setting; only the upper 20–30 cm is supratidal in origin. Nevertheless, island formation had a significant effect on pore fluid chemistry and the types of diagenetic reactions throughout the sediment column. Chloride in the sediment pore fluids is more than twice the normal seawater concentrations over most of the depth of the cores. The constant, elevated chloride concentrations indicate that hypersaline fluids which formed in ponds on the island are advected downward through the sediments. Models of the chloride profiles yield an estimate of 2·5 cm yr^?1 as a minimum advective velocity. Changes in pore water chemistry with depth are interpreted as indicating the following sequence of reactions: (1) minor high-Mg calcite dissolution and low-Mg calcite precipitation, from 0 to 35 cm; (2) Ca- or Mg-sulphate dissolution and low-Mg calcite precipitation, from 5 to 35 cm; (3) dolomite or magnesite precipitation together with sulphate reduction, from 35 to 55 cm; and (4) little reaction below 55 cm. In addition, one or more as yet unidentified reactions must be taking place from 5 to 55 cm depth as an imbalance in possible sources and sinks of alkalinity is observed. The imbalance could be explained if chloride is not completely conservative. Despite the pore fluid chemical evidence for diagenetic reactions involving carbonate minerals, no changes in sediment mineralogy were detected in X-ray diffraction analyses, probably because of the comparatively young age of the island.     

Transformation of arsenic compounds in modern intertidal sediments of Iriomote Island, Japan

The arsenic accumulation process in intertidal sediments of Iriomote Island, Japan, is analyzed as a naturally balanced arsenic-fixation system. Major and minor element chemistry is analyzed by X-ray fluorescence photometry, mineralogy is investigated by X-ray diffractometry, and four arsenic compounds are characterized by hydrogen-generated atomic absorption photometry. It is found that arsenic is accumulated by iron hydroxides/oxides precipitated following the decomposition of humic acids in the shallower sediment, and is subsequently incorporated into iron sulfide minerals at depth. The arsenic is immobile during incorporation into arsenic-bearing phases, suggesting that arsenic is unlikely to be released into the porewater under natural conditions in early diagenesis. The formation and decomposition of arsenic-bearing organic compounds appear to be associated with the formation and decomposition of arsenic in oxyhydroxides/oxides, suggesting that microbial activity may play an important role in controlling the behavior of arsenic and arsenic-bearing phases in the sediment column.     

Characterization of arsenic occurrence in the water and sediments of the Okavango Delta,NW Botswana

Detailed chemical analyses were performed on surface water, groundwater and sediment samples collected from the Okavango Delta between February and November 2003 in order to examine the distribution and geochemistry of naturally occurring As in the area. Surface water in the Okavango Delta, which is neutral to slightly acidic and has high dissolved organic C (DOC), was found to be slightly enriched in As when compared to a global value for stream water. Of the 20 new borehole analyses from this project, six were found to have values exceeding 10 μg/L, the current World Health Organization provisional guideline value for As. The results from field speciation indicate that As(III) is slightly more predominant than As(V). There is a positive correlation between As and pH and between As and DOC in the groundwater samples. For the sediment samples, there is a positive correlation between As and Co, As and Fe, As and loss on ignition (LOI) and between As and the percent fines in the sample. Reductive dissolution of oxides and hydroxides in the sediments with organic C as an electron acceptor is the likely mechanism for the release of As from the sediments into the groundwater.