Partition of arsenic in soils sediments and the origin of naturally elevated concentrations in groundwater of the southern pampa region (Argentina)

Excessive arsenic concentrations above the Argentinean and WHO guidelines for drinking water (10 μg L⁻¹) affects shallow aquifers of the southern Pampean Plain (Argentina) hosted in the Pampean and the Post Pampean formations (loess and reworked loess; Plio-Pleistocene–Holocene). Health problems related to high As concentrations in drinking waters are known as Endemic Regional Chronic Hydroarsenicism. Hydrochemistry of shallow groundwaters and soil geochemistry were investigated aiming to (1) understand the partition of As in the solid phase and its relationship with unacceptable As concentrations in waters, (2) identify the provision source of As to groundwaters. Only 5% of the samples had As concentrations <10 μg L⁻¹; in 27% As concentrations ranged from 10 to 50 μg L⁻¹ and in 58% it reached 60–500 μg L⁻¹. The coarse fraction (50–2,000 μm) hosts about 27% of the total As in the solid phase, being positively correlated to Ba (p < 0.01; r ² = 0.93). About 70% is included in the <2 μm fraction and had positive correlations of As–Fe (p < 0.05; r ² = 0.85) and As–Cr (p < 0.05; r ² = 0.68). Soils and sediment sand fractions of vadose zones are the primary sources of As in shallow groundwater while adsorption–desorption processes, codisolution–coprecipitation, and evaporation during the dry seasons raise As concentrations in waters exceeding the guideline value for drinking water.     

Geo-chemical Behavior of Uranium in the Sambhar Salt Lake, Rajasthan (India): Implications to "Source" of Salt and Uranium "Sink"

Among several salt lakes in the Thar Desert of western India, the Sambhar is the largest lake producing about 2 × 10⁵ tons of salt (NaCl) annually. The “lake system” (lake waters, inflowing river waters, and sub-surface brines) provides a unique setting to study the geo-chemical behavior of uranium isotopes (²³⁸U, ²³⁴U) in conjunction with the evolution of brines over the annual wetting and evaporation cycles. The concentration of ²³⁸U and the total dissolved solids (TDS) in lake water increase from ~8 μg L⁻¹ and ~8 g L⁻¹ in monsoon to ~1,400 μg L⁻¹ and 370 g L⁻¹, respectively, during summer time. The U/TDS ratio (~1 μg g⁻¹ salt) and the ²³⁴U/²³⁸U activity ratio (1.65 ± 0.05), however, remain almost unchanged throughout the year, except when U/TDS ratio approaches to 3.8 at/or beyond halite crystallization. These observations suggest that uranium behaves conservatively in the lake waters during the annual cycle of evaporation. Also, uranium and salt content (TDS) are intimately coupled, which has been used to infer the origin and source of salt in the lake basin. Furthermore, near uniform ratios in evaporating lake waters, when compared to the ratio in seawater (~0.1 μg g⁻¹ salt and 1.14 ± 0.02, respectively), imply that aeolian transport of marine salts is unlikely to be significant source of salt to the lake in the present-day hydrologic conditions. This inference is further consistent with the chemical composition of wet-precipitation occurring in and around the Sambhar lake. The seasonal streams feeding the lake and groundwaters (within the lake’s periphery) have distinctly different ratios of U/TDS (2–69 μg g⁻¹ salt) and ²³⁴U/²³⁸U (1.15–2.26) compared to those in the lake. The average U/TDS ratio of ~1 μg g⁻¹ salt in lake waters and ~19 μg g⁻¹ salt in river waters suggest dilution of the uranium content by the recycled salt and/or removal processes presently operating in the lake during the extraction of salt for commercial use. Based on mass-balance calculations, a conservative estimate of "uranium sink" (in the form of bittern crust) accounts for ~5 tons year⁻¹ from the lake basin, an estimate similar to its input flux from rivers, i.e., 4.4 tons year⁻¹.     

Nitrogen-15 Isotope Enrichment in Benthic Boundary Layer Gases of a Stratified Eutrophic Iron and Manganese Rich Lake

The applicability of the natural abundance of nitrogen gas isotope ratios was used to indicate the spatial distribution of nitrogen transformations in the water column and sediment pore waters of Lake Ngapouri, a small (area 0.19 km²), monomictic, eutrophic lake in the Taupo Volcanic Zone, North Island, New Zealand. Samples were collected from the epilimnion, hypolimnion, benthic boundary layer and at 5-cm intervals from the sediment pore waters at monthly intervals for 1 year. Values of δ¹⁵N [N₂] ranged from −1 to 0.28‰ in the epilimnion, −1.5 to 1.25‰ in the hypolimnion, −1.8 to 12.2‰ in the benthic boundary layer and −0.7 to 3.5‰ in sediment pore waters. Values of δ¹⁵N [N₂] showed a strong seasonal pattern that was related to the loss of dissolved oxygen in the hypolimnion during seasonal stratification. Increases in ¹⁵N-enriched dinitrogen take place in the benthic boundary layer during the periods of anoxia (taken to be dissolved oxygen concentrations <6.3 μM) and may be related to abundant ammonium substrate (up to 275 μM) to support denitrification. Nitrate concentrations increased up to 36 μM with increasing duration of anoxia. We hypothesise that an alternative electron acceptor besides oxygen is required to support the nitrification needed for the production of nitrate. Iron and manganese hydroxides and oxides from material sedimenting out of the water column may have induced chemo-nitrification sufficient to oxidise ammonium in the anoxic benthic boundary layer. The nitrate formed would mostly be rapidly denitrified so that the δ¹⁵N [N₂] would continue to become enriched during the presence of anoxia, as observed in hypolimnion and benthic boundary layer of Lake Ngapouri. The changes in δ¹⁵N [N₂] values indicate the potential use of isotope ratios to identify and quantify potential chemo-nitrification/denitrification in the water column and sediment pore waters of lakes.     

Stable Carbon Isotope Biogeochemistry and Anthropogenic Impacts on Karst Ground Water, Zunyi, Southwest China

Natural and anthropogenic impacts on karst ground water, Zunyi, Southwest China, are discussed using the stable isotope composition of dissolved inorganic carbon and particulate organic carbon, together with carbon species contents and water chemistry. The waters can be mainly characterized as HCO₃–Ca type, HCO₃ · SO₄–Ca type, or HCO₃ · SO₄–Ca · Mg type, according to mass balance considerations. It is found that the average δ¹³C_DIC values of ground waters are higher in winter (low-flow season) than in summer (high-flow season). Lower contents of dissolved inorganic carbon (DIC) and lower values of δ¹³C_DIC in summer than in winter, indicate that local rain events in summer and a longer residence time of water in winter play an important role in the evolution of ground water carbon in karst flow systems; therefore, soil CO₂ makes a larger contribution to the DIC in summer than in winter. The range of δ¹³C_DIC values indicate that dissolved inorganic carbon is mainly controlled by the rate of carbonate dissolution. The concentrations of dissolved organic carbon and particulate organic carbon in most ground water samples are lower than 2.0 mg C L⁻¹ and 0.5 mg C L⁻¹, respectively, but some waters have slightly higher contents of organic carbon. The waters with high organic carbon contents are generally located in the urban area where lower δ¹³C_DIC values suggest that urbanization has had an effect on the ground water biogeochemistry and might threaten the water quality.     

The Geochemistry of Supraglacial Streams of Canada Glacier,Taylor Valley (Antarctica), and their Evolution into Proglacial Waters

We have investigated the geochemistry of supraglacial streams on the Canada Glacier, Taylor Valley, Antarctica during the 2001–2002 austral summer. Canada Glacier supraglacial streams represent the link between primary precipitation (i.e. glacier snow) and proglacial Lake Hoare. Canada Glacier supraglacial stream geochemistry is intermediate between glacier snow and proglacial stream geochemistry with average concentrations of 49.1 μeq L⁻¹ Ca2+, 19.9 μeq L⁻¹ SO₄²⁻, and 34.3 μeq L⁻¹ HCO₃⁻. Predominant west to east winds lead to a redistribution of readily soluble salts onto the glacier surface, which is reflected in the geochemistry of the supraglacial streams. Western Canada Glacier supraglacial streams have average SO₄²⁻:HCO₃⁻ equivalent ratios of 1.0, while eastern supraglacial streams average 0.5, suggesting more sulfate salts reach and dissolve in the western supraglacial streams. A graph of HCO₃⁻ versus Ca2+ for western and eastern supraglacial streams had slopes of 0.87 and 0.72, respectively with R2 values of 0.84 and 0.83. Low concentrations of reactive silicate (> 10 μmol L⁻¹) in the supraglacial streams suggested that little to no silicate weathering occurred on the glacier surface with the exception of cryoconite holes (1000 μmol L⁻¹). Therefore, the major geochemical weathering process occurring in the supraglacial streams is believed to be calcite dissolution. Proglacial stream, Anderson Creek, contains higher concentrations of major ions than supraglacial streams containing 5 times the Ca²⁺ and 10 times the SO₄²⁻. Canada Glacier proglacial streams also contain higher concentrations (16.6–30.6 μeq L⁻¹) of reactive silicate than supraglacial streams. This suggests that the controls on glacier meltwater geochemistry switch from calcite and gypsum dissolution to both salt dissolution and silicate mineral weathering as the glacier meltwater evolves. Our chemical mass balance calculations indicate that of the total discharge into Lake Hoare, the final recipient of Canada Glacier meltwater, 81.9% is from direct glacier runoff and 19.1% is from proglacial Andersen Creek. Although during a typical, low melt ablation season Andersen Creek contributes over 40% of the water added to Lake Hoare, its overall chemical importance is diluted by the direct inputs from Canada Glacier during high flow years. Decadal warming events, such as the 2001–2002 austral summer produce supraglacial streams that are a major source of water to Lake Hoare.     

Phytoplankton Biomass and Production in Subtropical Hong Kong Waters: Influence of the Pearl River Outflow

The size-fractionated phytoplankton biomass and primary production were investigated in four contrasting areas of Hong Kong waters in 2006. Phytoplankton biomass and production varied seasonally in response to the influence of the Pearl River discharge. In the dry season, the phytoplankton biomass and production were low (<42 mg chl m⁻² and <1.8 g C m⁻² day⁻¹) in all four areas, due to low temperatures and dilution and reduced light availability due to strong vertical mixing. In contrast, in the wet season, in the river-impacted western areas, the phytoplankton biomass and production increased greater than five-fold compared to the dry season, especially in summer. In summer, algal biomass was 15-fold higher than in winter, and the mean integrated primary productivity (IPP) was 9 g C m⁻² day⁻¹ in southern waters due to strong stratification, high temperatures, light availability, and nutrient input from the Pearl River estuary. However, in the highly flushed western waters, chl a and IPP were lower (<30 mg m⁻² and 4 g C m⁻² day⁻¹, respectively) due to dilution. The maximal algal biomass and primary production occurred in southern waters with strong stratification and less flushing. Spring blooms (>10 μg chl a L⁻¹) rarely occurred despite the high chl-specific photosynthetic rate (mostly >10 μg C μg chl a ⁻¹ day⁻¹) as the accumulation of algal biomass was restricted by active physical processes (e.g., strong vertical mixing and freshwater dilution). Phytoplankton biomass and production were mostly dominated by the >5-μm size fraction all year except in eastern waters during spring and mostly composed of fast-growing chain-forming diatoms. In the stratified southern waters in summer, the largest algal blooms occurred in part due to high nutrient inputs from the Pearl River estuary.     

Determining Spatial and Temporal Inputs of Freshwater,Including Submarine Groundwater Discharge,to a Subtropical Estuary Using Geochemical Tracers,Biscayne Bay,South Florida

Geochemical mixing models were used to decipher the dominant source of freshwater (rainfall, canal discharge, or groundwater discharge) to Biscayne Bay, an estuary in south Florida. Discrete samples of precipitation, canal water, groundwater, and bay surface water were collected monthly for 2 years and analyzed for salinity, stable isotopes of oxygen and hydrogen, and Sr²⁺/Ca²⁺ concentrations. These geochemical tracers were used in three separate mixing models and then combined to trace the magnitude and timing of the freshwater inputs to the estuary. Fresh groundwater had an isotopic signature (δ ¹⁸O = −2.66‰, δD −7.60‰) similar to rainfall (δ ¹⁸O = −2.86‰, δD = −4.78‰). Canal water had a heavy isotopic signature (δ ¹⁸O = −0.46‰, δD = −2.48‰) due to evaporation. This made it possible to use stable isotopes of oxygen and hydrogen to separate canal water from precipitation and groundwater as a source of freshwater into the bay. A second model using Sr²⁺/Ca²⁺ ratios was developed to discern fresh groundwater inputs from precipitation inputs. Groundwater had a Sr²⁺/Ca²⁺ ratio of 0.07, while precipitation had a dissimilar ratio of 0.89. When combined, these models showed a freshwater input ratio of canal/precipitation/groundwater of 37%:53%:10% in the wet season and 40%:55%:5% in the dry season with an error of ±25%. For a bay-wide water budget that includes saltwater and freshwater mixing, fresh groundwater accounts for 1–2% of the total fresh and saline water input.     

Chemical and isotopic variations in the Wiśniówka Mała mine pit water,Holy Cross Mountains (south-central Poland)

In 2005 and 2006, hydrogeochemical study was carried out in the bipartite Wiśniówka Mała pit lake of the Holy Cross Mountains (south-central Poland). This is the largest acidic water body in Poland. This report presents the element concentrations in the water and sediment, stable sulfur and oxygen isotope ratios in the soluble sulfates, and stable oxygen isotope ratio in the water. The scope of the investigation also encompassed mineralogical examinations (scanning electron microscope, X-ray diffraction) of the sediment. The results of this study show that there is a spatial and temporal variability in concentrations of most elements and sulfur isotope ratios in the examined pit lake. The water of the western pond displayed a lower pH with a mean of 3.73 and higher conductivity (390 μS cm⁻¹) as well as higher concentrations of sulfates (156 mg L⁻¹) and most of the cations and anions. The concentrations of Fe²⁺ and Fe³⁺ averaged 0.8 and 0.4 mg·L⁻¹. In contrast, the eastern pond water revealed a higher pH (mean of 4.36), lower conductivity (293 μS cm⁻¹) and lower sulfate (90 mg L⁻¹) and trace metal levels. Similar variations were recorded in the stable sulfur isotope ratios. The δ³⁴S_V-CDT(SO₄ ²⁻) values in the water of the western pit pond were in the range of −6.7 to −4.6‰ (mean of −5.6‰), whereas that in the eastern pit pond ranged from −2.2 to −0.9‰ (−1.6‰). The alkalinity of the entire lake water was below 0.1 mg·L⁻¹ CaCO₃. No distinct difference in the δ¹⁸O_V-SMOW(SO₄ ²⁻) was noted between the western and eastern pit ponds. Compared to the Purple Pond in the Sudetes (Poland) and similar sites throughout the world, the examined pit lake is highlighted by distinctly low concentrations of sulfates, iron and other trace metals. Based on this and other studies performed in the Holy Cross Mountains, a conclusion can be drawn that the SO₄ ²⁻ in the Wiśniówka Mała pit lake water is a mixture of SO₄ ²⁻ derived from the following sources: (1) pyrite oxidation (especially in the western pond water), (2) leaching of soluble sulfates from soils and waste material, as well as (3) subordinate deposition of airborne sulfate precipitation.     

Hydrogeochemical and isotopic investigation of the Bursa-Oylat thermal waters, Turkey

The Oylat spa is located 80 km southeast of Bursa and 30 km south of Ineg?l in the Marmara region. With temperature of 40°C and discharge of 45 l/s, the Oylat main spring is the most important hot water spring of the area. Southeast of the spa the Forest Management spring has a temperature of 39.4°C and discharge of 2 l/s. The G?z spring 2 km north of the spa, which is used for therapy of eye disease, and cold waters of the Saadet village springs with an acidic character are the further important water sources of the area. EC values of Main spring and Forest Management hot spring (750–780 μS/cm) are lower than those of Saadet and G?z spring waters (2,070–1,280 μS/cm) and ionic abundances are Ca > Na + K > Mg and SO₄ > HCO₃ > Cl. The Oylat and Sızı springs have low Na and K contents but high Ca and HCO₃ concentrations. According to AIH classification, these are Ca–SO₄–HCO₃ waters. Based on the results of δ¹⁸O, ²H and ³H isotope analyses, the thermal waters have a meteoric origin. The meteoric water infiltrates along fractures and faults, gets heated, and then returns to surface through hydrothermal conduits. Oylat waters do not have high reservoir temperatures. They are deep, circulating recharge waters from higher enhanced elevations. δ¹³C_DIC values of the Main spring and Forest Management hot spring are −6.31 and −4.45‰, respectively, indicating that δ¹³C is derived from dissolution of limestones. The neutral pH thermal waters are about +18.7‰ in δ³⁴S while the sulfate in the cold waters is about +17‰ (practically identical to the value for the neutral pH thermal waters). However, the G?z and Saadet springs (acid sulfate waters) have much lower δ³⁴S values (~+4‰).     

Distribution of Hydrogen and Oxygen Isotopes in Salt Lakes of the Qinghai—Xizang Plateau,China

The Qinghai-Xizang Plateau is an area where a large number of salt lakes are distributed. We have collected several hundred samples of natural waters over the Plateau since 1976 and carried out researches on their hydrogen and oxygen isotopes. The results indicate that the^δD and δ¹⁸O values of the salt lake waters over the Plateau range from −64.1 to +12.4‰ and from −11.19 to +8.62‰, respectively. From the different types of surfaces, ground and lake waters of various salinities it is inferred that the compositions of H and O isotopes in the initial water of Qinghai Lake are^δD=−55.0‰ and {ie336-1}; and those in the original water from the lakes in northern Xizang, are^δD=−116.0‰ and {ie336-2}. Brines in the salt lakes are derived from rain water through prolonged circulation. Oilfield water also makes some contribution to the salt lakes in the Qaidam Basin. Similar slopes of evaporation lines of water isotopes are noticed for the Qinghai Lake area and northern Xizang. This is attributed to the evolution of the isotopes in these water bodies in an environment of middle latitude and high elevation.     

Primary productivity in the German Bight (1994–1996)

Within the KUSTOS program (Coastal Mass and Energy Fluxes-the Land-Sea Transition in the Southeastern North Sea) 28 to 36 German Bight stations were seasonally surveyed (summer 1994, spring 1995, winter 1995–1996) for light conditions, dissolved inorganic nutrient concentrations, chlorophylla (chla), and photosynthesis versus light intensity (P:E) parameters. Combining P:E curve characteristics with irradiance, attenuation, and chlorophyll data resulted in seasonal estimates of the spatial distribution of total primary production. These data were used for an annual estimate of the total primary production in the Bight. In winter 1996 the water throughout the German Bight was well mixed. Dissolved inorganic nutrient concentrations were relatively high (nitrogen [DIN], soluble reactive phosphorus [SRP], and silicate [Si]: 23, 1, and 10 μM, respectively). Chla levels generally were low (< 2 μg l⁻¹) with higher concentrations (4–16 μg l⁻¹) in North Frisian coastal waters. Phytoplankton was limited by light. Total primary production averaged 0.2 g C m⁻² d⁻¹. Two surveys in April and May 1995 captured the buildup of a strong seasonal thermo-cline accompained by the development of a typical spring diatom bloom. High nutrient levels in the mixed layer during the first survey (DIN, SRP, and Si: 46, 0.45, and 11 μM, respectively) decreased towards the second survey (DIN, SRP, and Si: 30.5, 0.12, and 1.5 μM, respectively) and average nutrient ratios shifted further towards highly imbalanced values (DIN:SRP: 136 in survey 1, 580 in survey 2; DIN:Si: 13.5 in survey 1, 96 in survey 2). Chla ranged from 2 to 16 μg l⁻¹ for the first survey and rose to 12–50 μg l⁻¹ in the second survey. Phytoplankton in nearshore areas continued to be light limited during the second survey, while data from the stratified regions in the open German Bight indicates SRP and Si limitation. Total primary production ranged from 4.0 to 6.3 g C m⁻² d⁻¹. During summer 1994 a strong thermal stratification was present in the German Bight proper and shallow coastal areas showed unusually warm (up to 22°C), mixed waters. Chla concentrations ranged from 2 to 18 μg l⁻¹. P:E characteristics were relatively high despite the low nutrient regime (DIN, SRP, and Si: 2, 0.2, and 1.5 μM, respectively), resulting in overall high total primary production values with an average of 7.7 g C m⁻² d⁻¹. Based on the seasonal primary production estimates of the described surveys a budget calculation yielded a total annual production of 430 g C m⁻² yr⁻¹ for the German Bight.     

δ<Superscript>18</Superscript>O shifts of geothermal waters in the central of Weihe Basin,NW China

The thermal-waters resources in Weihe Basin of Shaanxi province, NW China are historically classified as middle- to low- temperature thermal-waters in China. Recent exploitation of the deep thermal reservoir in the centre part of the basin (i.e. Xi’an and Xianyang) had observed plentiful supply of thermal fluid with higher measured maximum temperature (120°C) and higher hydraulic pressure (80.50 MPa) in the deeper (more than 4,000 m deep) sedimentary basin. A recent isotope study shows that deep geothermal waters in the cities of Xi’an and Xianyang are characterized by an observable horizontal oxygen-18 (δ¹⁸O) shift and minor deuterium (²H) enrichment. The considerable oxygen shift is possibly due to the following four reasons: water–rock interaction at high temperature, slow circulation rate of water, low water-to-rock ratio, and old age. On the end number of the δ¹⁸O shift, minor δ²H enrichment occur when there is higher concentrations of H₂S, CH₄, I and Br with lower rate of rSO₄ ²⁻/rCl⁻ and r _Na⁺/r _Cl⁻ suggesting relatively isolated geological environment. In a few thermal waters points, r\textNa^\text+ \text/r\textCl^-r{\text{Na}}^{{\text{+}}} {\text{/}}r{\text{Cl}}^{-} < 0.85. This shows possible presence of formation waters. Combining the results from isotopic study and chemical analysis, we can classify the types of geothermal waters into three groups, the shallow and fast circulating system, the semi-circulating system and the deep and slow circulating system.     

Stable isotope characterisation of co-existing carbonates from the Holocene Gallocanta lake (NE Spain): palaeolimnological implications

The sedimentary succession of Gallocanta lake, a closed saline lake located in the Iberian Range (NE Spain), documents two successive lacustrine stages: (1) brackish lake stage and (2) shallow saline lake stage. The saline stage corresponds to the present-day situation in which the lake water properties are mainly controlled by a strongly negative annual water balance. The carbonates of the brackish lake stage have relatively constant δ¹⁸O values, however, they are rather high (δ¹⁸O_Do = 2.4‰ and δ¹⁸O_Cc = 4.5‰ mean values) suggesting a hydrologically closed lake with a long residence time of the waters. δ¹⁸O values of carbonates from the saline stage vary greatly, and are lighter than in the previous stage (δ¹⁸O_Do = 0.5‰, δ¹⁸O_Cc = −0.7‰, δ¹⁸O_Mgs = −2.3‰ mean values). These carbonates also precipitated in a hydrologically closed lake, but in equilibrium with a lake water of more variable isotopic composition. The δ¹³C values for carbonates of both stages reflect a mixing of different pools of carbon, but during saline stage δ¹³C values have been more controlled by the equilibrium of the lake waters with atmospheric CO₂. During the current stage, calcite and dolomite precipitate in Gallocanta lake mainly during spring and summer, although dolomite precipitation is more favoured towards the summer. Magnesite precipitates at the beginning of autumn, when the first rainfall re-dissolves the saline surface crust, producing saline waters with a high Mg²⁺ content. The isotopic composition of lake waters sampled in 2005 are far higher than those calculated from the carbonates. It is considered that this could be due to two factors: either because there have not been many extremely dry years (like the year 2005) during the development of the lake, or because the physical and chemical characteristics of the lake waters in such conditions are not appropriate for the development of these minerals.     

Biogeochemistry of the Russian Arctic. Kara Sea: Research results under the SIRRO project, 1995–2003

The Kara Sea is an area uniquely suitable for studying processes in the river-sea system. This is a shallow sea into which two great Siberian rivers, Yenisei and Ob, flow. From 1995 to 2003, the sea was studied by six international expeditions aboard the R/V Akademik Boris Petrov. This publication summarizes the results obtained, within the framework of this project, at the Vernadsky Institute of Geochemistry and Analytical Chemistry, Russian Academy of Sciences. Various hydrogeochemical parameters, concentrations and isotopic composition of organic and carbonate carbon of the sediments, plankton, particulate organic matter, hydrocarbons, and dissolved CO₂ were examined throughout the whole sea area at more than 200 sites. The δ¹³C varies from −22 and −24‰ where Atlantic waters enter the Kara Sea and in the North-eastern part of the water area to −27‰ in the Yenisei and Ob estuaries. The value of δ¹³C of the plankton is only weakly correlated with the δ¹³C of the organic matter from the sediments and is lower by as much as 3–4‰. The paper presents the results obtained from a number of meridional river-sea profiles. It was determined from the relations between the isotopic compositions of plankton and particulate matter that the riverwaters carry material consisting of 70% detrital-humus matter and 30% planktonogenic material in the river part, and the material contained in the off-shore waters consists of 30% terrigenous components, with the contribution of bioproducers amounting to 70%. The carbon isotopic composition of the plankton ranges from −29 to −35‰ in the riverine part, from −28 to −27‰ in the estuaries, and from −27.0 to −25% in the marine part. The relative lightness of the carbon isotopic composition of plankton in Arctic waters is explained by the temperature effect, elevated CO₂ concentrations, and long-distance CO₂ supply to the sea with riverwaters. The data obtained on the isotopic composition of CO₂ in the surface waters of the Kara Sea were used to map the distribution of δ¹³C_{CO 2}. The complex of hydrocarbon gases extracted from the waters included methane, C₂–C₅, and unsaturated C₂₌–C₄₌ hydrocarbons, for which variations in the concentrations in the waters were studied along river-estuary-sea profiles. The geochemistry of hydrocarbon gases in surface fresh waters is characterized by comparable concentrations of methane (0.3–5 μl/l) and heavier hydrocarbons, including unsaturated ones. Microbiological methane with δ¹³C from −105 to −90‰ first occurs in the sediments at depths of 40–200 cm. The sediments practically everywhere display traces of methane oxidation in the form of a shift of the δ¹³C of methane toward higher values and the occurrence of autogenic carbonate material, including ikaite, enriched in the light isotope. Ikaite (δ¹³C from −25 to −60‰) was found and examined in several profiles. The redox conditions in the sediments varied from normal in the southern part of the sea to highly oxidized along the Novaya Zemlya Trough. Vertical sections through the sediments of the latter exemplify the complete suppression of the biochemical activity of microorganisms. Our data provide insight into the biogeochemistry of the Kara Sea and make it possible to specify the background values needed for ecological control during the future exploration operations and extraction of hydrocarbons in the Kara Sea. Original Russian Text ? E.M. Galimov, L.A. Kodina, O.V. Stepanets, G.S. Korobeinik, 2006, published in Geokhimiya, 2006, No. 11, pp. 1139–1191.     

Effect of source water quality on arsenic (V) removal from drinking water by coagulation/microfiltration

The effect of the source water quality on As(V) removal by coagulation/microfiltration (C/MF) was investigated systematically using a jar test and a lab-scale test; the results of the lab-scale test coincide with those of the jar test. It showed that the increase of dissolved organic carbon (DOC), HPO₄ ²⁻ and HCO₃ ⁻ concentrations would moderately decrease As(V) removal, and the residual As(V) concentration in treated water is no more than 10 μg L⁻¹ when the concentration of DOC, HPO₄ ²⁻ and HCO₃ ⁻ in raw water is not beyond 9.22 mg L⁻¹, 1.6 mg L⁻¹ and 300 mg L⁻¹, respectively. Other co-ions, such as Cl⁻, NO₃ ⁻, F⁻, SO₄ ²⁻, and counter-ions including K⁺, Ca²⁺ and Mg²⁺, have little effect on As(V) removal. Both results of the jar test and the lab-scale test demonstrate that Fe³⁺ dose of 6 mg L⁻¹ is enough to eliminate the influence of HCO₃ ⁻ whose concentration changes from 350 mg L⁻¹ to 450 mg L⁻¹. In the lab-scale test, As(V) removal ranged from 92.8 to 98.2% at Fe³⁺ dose of 4 mg L⁻¹ and 5 mg L⁻¹ when As(V) concentration in raw water was about 100 μg L⁻¹. The results obtained in this study suggest that As(V) removal by C/MF process is sensitive to the quality of raw water, and a jar test needs to be done before C/MF process is used for arsenic removal from drinking water.     

Wetland-water column exchanges of carbon, nitrogen, and phosphorus in a southern Everglades dwarf mangrove

We used enclosures to quantify wetland-water column nutrient exchanges in a dwarf red mangrove, (Rhizophora mangle L.) system near Taylor River, an important hydraulic linkage between the southern Everglades and eastern Florida Bay, Florida, USA. Circular enclosures were constructed around small (2.5–4 m diam) mangrove islands (n=3) and sampled quarterly from August 1996 to May 1998 to quantify net exchanges of carbon, nitrogen, and phosphorus. The dwarf mangrove wetland was a net nitrifying environment with consistent uptake of ammonium (6.6–31.4 μmol m⁻² h⁻¹) and release of nitrite +nitrate (7.1–139.5 μmol m⁻² h⁻¹) to the water column. Significant flux of soluble reactive phosphorus was rarely detected in this nutrient-poor, P-limited environment. We did observe recurrent uptake of total phosphorus and nitrogen (2.1–8.3 and 98–502 μmol m⁻² h⁻¹, respectively), as well as dissolved organic carbon (1.8–6.9 μmol m⁻² h⁻¹) from the water column. Total organic carbon flux shifted unexplainably from uptake, during Year 1, to export, during Year 2. The use of unvegetated (control) enclosures during the second year allowed us to distinguish the influence of mangrove vegetation from soil-water column processes on these fluxes. Nutrient fluxes in control chambers typically paralleled the direction (uptake or release) of mangrove enclosure fluxes, but not the magnitude. In several instances, nutrient fluxes were more than twofold greater in the absence of mangroves, suggesting an influence of the vegetation on wetland-water column processes. Our findings characterize wetland nutrient exchanges, in a mangrove forest type that has received such little attention in the past, and serve as baseline data for a system undergoing hydrologic restoration.     

Stable water isotope climate archives in springs from the Olympic Mountains,Washington

The ¹⁸O and ²H (HDO) compositions are summarized for sampled springs (n = 81) within the Elwha watershed (≈692 km²) on the northern Olympic Peninsula. Samples, collected during 2001–2009, of springs (n = 158), precipitation (n = 520), streams (n = 176), and firn (n = 3) assisted the determinations for meteoric composition of recharge waters. The local mean water line (LMWL) is defined as δ²H = 8.2δ¹⁸O − 9.3 for the watershed. Recharge history is surmised from groundwater ages ranging from 5 ± 3 years (apparent ⁸⁵Kr) to 9,490 ± 420 ¹⁴C cal years BP. About 56% of the springs were recharged over the last 1,000 years while 13% of springs were recharged over 5,000 years ago. Spring HDO values fluctuate between −11.8 to −15.6‰ δ¹⁸O and −90.9 to −119.4‰ δ²H. Deuterium excess values predominate around 4–6‰. The HDO proxy records from springs suggest a pronounced paleoclimate shift in air masses near 5,000 year BP on the Peninsula.     

Transmission of <Emphasis Type="Italic">δ</Emphasis><Superscript>13</Superscript>C signals and its paleoclimatic implications in Liangfeng Cave system of Guizhou Province,SW China

A series of samples, including vegetation, soil organic matter, soil waters, spring, bedrock, pool water, drip waters (upper-drip waters and ground-drip waters) and their corresponding speleothems were collected at Liangfeng Cave (LFC) system of Guizhou Province, southwest of China, respectively, from 2003 to 2004 year, then their stable carbon isotopes were measured and analyzed. Results reveal that vegetation is C₃ type in LFC system; cave overlying δ ¹³C signals, including values and variations, could be transmitted to drip water (speleothem); speleothem δ ¹³C mainly shows a biogenic δ ¹³C value character (soil CO₂ from plant respiration and decay); and there are remarkable seasonal variations of δ ¹³C values for drip water TDIC (speleothem), which are lighter at least 2.0‰ in the rainy seasons than in the dry ones. So, it could be feasible to reconstruct high-resolution changes of paleoecology and paleoclimate by using speleothem δ ¹³C values.     

Hydrogeology and hydrogeochemistry of Günyüzü semi-arid basin (Eski?ehir, Central Anatolia)

Groundwater is often the only water source in semi-arid regions of Turkey. Günyüzü Basin, located in the Sakarya River basin, SW of Eskişehir, exhibits semi-arid conditions. The study area is composed of Paleozoic metamorphic rocks, Eocene granitic rocks, Neogene sedimentary rocks, and Quaternary alluvium. In the basin, Paleozoic Marbles are the main reservoir rocks for hot and cold water, bordered by impermeable diabases dykes at the sides and by impermeable granites and schists. Neogene-aged limestones, conglomerates and alluvium represent the other significant aquifers. Water samples chosen to exemplify the aquifer characteristics, were collected from springs and wells in both the dry and the wet seasons. The cation and anion permutation of the samples show that carbonates are the dominant lithology in the formation of chemical composition. δ¹⁸O (−11.2 to −8.9‰) and δ²H (−79 to −60‰) isotopic values show that all waters (thermal and cold) are meteoric in origin. The hydrological, hydrochemical, and isotopic properties of the waters reveal that there exist two main groups of groundwater systems; one of these is deep circulating, while the other one is shallow. Tritium values, 0–4 TU (Tritium Unit) indicate the presence of old, static water in these aquifer systems.     

Biogeochemistry of Major Redox Elements and Mercury in a Tropical Reservoir Lake (Petit Saut,French Guiana)

The hydroelectric reservoir of Petit Saut, French Guiana, was created in 1994–1995 by flooding 350 km² of tropical forest. When sampled in 1999, the lake exhibited a permanent stratification separating the 3–5 m thick, oxygenated epilimnion from the anoxic hypolimnion. The rate of anaerobic organic carbon mineralization below the oxycline was on the order of 1 μmol C m⁻² s⁻¹ and did not show a pronounced difference between wet and dry seasons. Methanogenesis accounted for 76–83% of anaerobic carbon mineralization, with lesser contributions of sulfate reduction and dissimilatory iron reduction. Upward mixing of reduced inorganic solutes explained 90% of the water column O ₂ demand during the dry season, while most O ₂ consumption during the wet season was coupled to aerobic respiration of organic matter synthesized in the surface waters. Inorganic mercury species represented 10–40% of total dissolved mercury in the epilimnion, but were of relatively minor importance (≤10%) in the anoxic portion of the water column. Net production of soluble organic mercury compounds in the flooded soils and anoxic water column did not vary significantly between wet and dry seasons. Methylmercury accounted for about 15% of total dissolved mercury below the oxycline. Its estimated net production rate, 0.04 mg m⁻² yr⁻¹, is of the same order of magnitude as values reported for contaminated lakes and flooded terrestrial ecosystems.