The supply and accumulation of silica in the marine environment

Rivers and submarine hydrothermal emanations supply 6.1 × 10¹⁴g SiO₂/yr to the marine environment. Approximately two-thirds of the silica supplied to the marine environment can be accounted for in continental margin and deep-sea deposits. Siliceous deep-sea sediments located beneath the Antarctic Polar Front (Convergence) account for over a fourth (1.6 × 10¹⁴g SiO₂/yr) of the silica supplied to the oceans. Deep-sea sediment accumulation rates beneath the Polar Front are highest in the South Atlantic with values as large as 53cm/kyr during the last 18.000 yr. Siliceous sediments in the Bering Sea, Sea of Okhotsk, and Subarctic North Pacific accumulate 0.6 × 10¹⁴g SiO₂/yr or 10% of the dissolved silica input to the oceans. The accumulation of biogenic silica in estuarine deposits removes a maximum of 0.8 × 10¹⁴g SiO₂/yr. Although estuarine silica versus salinity plots indicate extensive removal of riverine silica from surface waters, the removal rates must be considered as maximum values because of dissolution of siliceous material in estuarine sediments and bottom waters. Siliceous sediments from continental margin upwelling areas (e.g. Gulf of California, Walvis Bay, or Peru-Chile coast) have the highest biogenic silica accumulation rates in the marine environment (69 g SiO₂ cm²/kyr). Despite the rapid accumulation of biogenic silica, upwelling areas account for less than 5% of the silica supplied to the marine environment because they are confined laterally to such small areas.     

Geochemistry of the Onyx River (Wright Valley,Antarctica) and its role in the chemical evolution of Lake Vanda

The Onyx River (Wright Valley, Antarctica) is a dilute meltwater stream originating in the vicinity of the Wright Lower Glacier. It acquires a significant fraction of its salt content when glacial meltwaters contact Wright Valley soils at Lake Brownworth and the concentrations of all ions increase with distance along the 28-km channel down to Lake Vanda. Average millimolar concentrations of major ions at the Vanda weir during the 1980–1981 flow season were: Ca = 0.119; Mg = 0.061; Na = 0.212; K = 0.033; Q = 0.212; SO₄ = 0.045; HCO₃ = 0.295; and SiO₂ = 0.049. Based on the flow measurements of Chinn (1982), this amounts to an annual flux (in moles) to Lake Vanda of: Ca = 0.238 × 10⁶; Mg = 0.122 × 10⁶; Na = 0.424 × 10⁶; K = 0.066 × 10⁶; Cl = 0.424 × 10⁶; SO₄ = 0.09 × 10⁶; HCO₃ = 0.59 × 10⁶; SiO₂ = 0.098 × 10⁶.In spite of the large salt input from this source, equilibrium evaporation of Onyx River water would have resulted in early calcite deposition and in the formation of a Na-Mg-Cl-HCO₃ brine rather than in the Ca-Na-Mg-Cl waters observed in Lake Vanda. The river alone could not have produced a brine having the qualitative geochemical features of the lower saline waters of Lake Vanda.It is proposed that the Vanda brine is instead the result of past ( > 1200 yrs BP) mixing events between Onyx River inflows and calcium chloride-rich deep groundwaters derived from the Don Juan Basin. The mixing model presented here shows that the Onyx River is the major contributor of K, HCO₃, SO₄, and (possibly) Mg found in the lake and a significant contributor (approximately one half) of the observed Na. Calcium and Cl, on the other hand, came largely from deep groundwater sources in the Don Juan Basin. All concentrations except Mg are well predicted by this model. The chemical composition of the geologically recent upper lake is explained in terms of ionic diffusion from the pre-formed brine, coupled with Onyx River inflow. Ionic ratios calculated from this latter model are in very good agreement with those observed in the lake at 35 meters.     

Seepage measurements from Long Lake,Indiana Dunes National Lakeshore

 Long Lake, located near Lake Michigan within the dune-complexes of Indiana Dunes National Lakeshore, USA, was formed some time during the Pleistocene and Holocene epochs. A surficial aquifer underlies Long Lake, which is either a source or sink for the later. The hydrologic processes in the lakeshore and surrounding environs have been significantly altered during the agricultural, municipal, and industrial development of the region. Limited data suggest that the organisms of Long Lake have elevated levels of several contaminants. This study attempts to quantify seepage within the lake to assess the potential threat to groundwater quality. Seepage measurements and minipiezometric tests were used to determine seepage within the lake. Seepage measurements and minipiezometric tests suggest that water seeps out of Long Lake, thus recharging the groundwater that flows southwest away from the lake. There is a great deal of variability in the seepage rate, with a mean of 11.5×10^–4±11.2×10^–4 m d^–1. The mean seepage rate of 0.3 m yr^–1 for Long Lake is greater than the 0.2 m yr^–1 recharge rate estimated for the drainage basin area. The Long Lake recharge volume of 2.5×10⁵ m³ yr^–1 is approximately 22% of the volume of the lake and is significant when compared to the total surface recharge volume of 4.8×10⁵ m³ yr^–1 to the upper aquifer of the drainage area. There is a potential for contamination of the groundwater system through seepage from the lake from contaminants derived from aerial depositions. Received: 16 August 1995 · Accepted: 18 September 1995     

Dissolved silica budget in the North basin of Lake Lugano

We studied the dissolved silica cycle in the water column of the North basin of Lake Lugano, Switzerland/Italy. Lake Lugano is a meromictic, eutrophic lake, permanently stratified below 100-m depth. A one-box model was used to calculate a silica mass-balance over 1993, based on various lake measurements, such as sediment traps, sediment cores, water analysis and biota countings. We found that the North basin of Lake Lugano is at steady state as far as dissolved silica is concerned. The primary source of dissolved silica in the lake is river input (about 80%), with diffusion from bottom sediments and groundwater input also playing a role. Atmospheric input is negligible. The main export of dissolved silica occurs via biogenic uptake by diatoms and final burial of their frustules in the bottom sediment. Loss of dissolved silica through the lake outflow only represents 15% of the total output. Of the total amount of Si exported to the lake bottom through diatom sinking, less than 20% is re-supplied to the surface water by diffusion. Thus, the lake acts as an important permanent sink for silica. The long residence time of dissolved silica in the lake (7 years) is related to the strong physical stratification of the lake. Only about 10% of the standing stock are available to phytoplankton uptake.     

Chesapeake Bay nutrient and plankton dynamics: III. The annual cycle of dissolved silicon

Silicic acid (H₄SiO₄) flux from the sediment, H₄SiO₄ concentration and river flow were used to obtain an annual dissolved silicon budget for Chesapeake Bay. H₄SiO₄ concentrations vary seasonally in the estuary: for a 12-year period, mean H₄SiO₄ concentrations in the mesohaline region were high both in spring and in late summer to early fall, and were low in late spring—occasionally approaching levels potentially limiting to diatom growth. Most of the annual allochthonous H₄SiO₄ supply to the estuary derives from the three major rivers, but regenerative H₄SiO₄ flux from the sediment to the water column exceeds the total riverine input by a factor of at least five. Sediment H₄SiO₄ efflux exhibits seasonality and averages approximately 2–3 mol Si m^?2 yr^?1. The high rates of sediment dissolution and efflux appear to maintain high levels of H₄SiO₄ in the mesohaline region, and Si-limitation of diatom growth there seems unlikely. The relative rates of biogenic silica formation and dissolution do not vary synchronously: seasonal variations in diatom productivity, sedimentary release of H₄SiO₄ and river flow all contribute to the observed late winter and late summer seasonal maxima and late spring minimum in water column H₄SiO₄ concentrations. If the only source of Si to support sedimentary H₄SiO₄ efflux is biogenic particulate silica recently deposited from the water column and this silica in turn was produced by diatoms in a ratio of 8C:1 Si, the minimum annual primary production by diatoms is at least 260 g C m^?2, approximately half of annual total plankton primary production. This estimate would be revised upwards according to the amount of particulate biogenic silica dissolving in the water column. Burial of biogenic silica amounts to from 2 to 84% of the sediment efflux of H₄SiO₄, depending on location in the bay. On an annual basis, burial represents from 60 to 100% of fluvial H₄SiO₄-Si inputs.     

Spatial and temporal distribution of methane in an extensive shallow estuary, South India

Sedimentary methane (CH₄) fluxes and oxidation rates were determined over the wet and dry seasons (four measurement campaigns) in Pulicat lake, an extensive shallow estuary in south India. Dissolved CH₄ concentrations were measured at 52 locations in December 2000. The annual mean net CH₄ flux from Pulicat lake sediments was 3.7 × 10⁹ g yr^-1 based on static chamber measurements. A further 1.7 × 10⁹g yr_-1 was estimated to be oxidized at the sediment-water interface. The mean dissolved concentration of CH₄ was 242nmol |^-1 (ranging between 94 and 501 nmol |^-1) and the spatial distribution could be explained by tidal dynamics and freshwater input. Sea-air exchange estimates using models, account only for ∼13% (0.5 × 10⁹ g yr-1) of the total CH₄ produced in sediments, whereas ebullition appeared to be the major route for loss to the atmosphere (∼ 63% of the net sediment flux). We estimated the total atmospheric source of CH₄ from Pulicat lake to be 0.5 to 4.0 × 10⁹g yr^-1.     

Dissolution of quartz into dilute alkaline solutions at 90°C: A kinetic study

The rate of dissolution of Fontainebleau sand (pure quartz) into sodium hydroxide solutions (from 0.001 M to 0.5 M) has been determined at 90°C in well-stirred vessels. Dissolution leads to an equilibrium state, controlled by the solubility of quartz in pure water as undissociated silicic acid H₄SiO₄. As long as the initial molality of sodium hydroxide does not exceed 0.02 mol · kg⁻¹, the dissolution leads only to the formation of the three monomeric species H₄SiO₄, H₃SiO₄⁻ and H₂SiO₄²⁻, while polymers appear in the silica-rich solutions obtained in more alkaline media. The rate of dissolution can be represented by an adaptation of Stöber's model to alkaline solutions; the basic assumption is that the quartz surface is partially covered by a layer of adsorbed silicate ions, which represent an intermediate species between solid and dissolved silica.     

Oxidation of methane in the water column of Lake Baikal

The rate of aerobic oxidation of methane was calculated based on average profiles of the tritiumhelium age of the Baikal waters and concentrations of the dissolved methane in the water column. In the deep lake zone (>200 m), the intensity of oxidation vertically decreases and is (2–0.3) × 10^?2 nl CH₄l^?1 days^?1 in southern and central Baikal and (2.8–1.0) × 10^?2 nl CH₄ l^?1 days^?1 in northern Baikal. The effective coefficient of the oxidation rate in the lake depressions is 3.6 × 10^?4, 3.3 × 10^?4, and 3.7 × 10^?4 days^?1, respectively. At current methane concentrations in the water column, about 80 t of methane is oxidized per year. Oxidation of the dissolved methane in the water column was estimated at a possible increase of its concentration.     

Gas buildup in Lake Nyos,Cameroon: The recharge process and its consequences

The gases dissolved in Lake Nyos, Cameroon, were quantified recently (December 1989 and September 1990) by two independent techniques: in-situ measurements using a newly designed probe and laboratory analyses of samples collected in pre-evacuated stainless steel cylinders. The highest concentrations of CO₂ and CH₄ were 0.30 mol/kg and 1.7 mmol/kg, respectively, measured in cylinders collected 1 m above lake bottom. Probe measurements of in-situ gas pressure at three different stations showed that horizontal variations in total dissolved gas were negligible. Total dissolved-gas pressure near the lake bottom is 1.06 MPa (10.5 atm), 50% as high as the hydrostatic pressure of 2.1 MPa (21 atm). Comparing the CO₂ profile constructed from the 1990 data to one obtained in May 1987 shows that CO₂ concentrations have increased at depths to below 150 m. Based on these profiles, the average rate of CO₂ input to bottom waters was 2.6 × 10⁸ mol/a. Increased deep-water temperatures require an average heat flow of 0.32 MW into the hypolimnion over the same time period. The transport rates of CO₂, heat, and major ions into the hypolimnion suggest that a low-temperature reservoir of free CO₂ exists a short distance below lake bottom and that convective cycling of lake water through the sediments is involved in transporting the CO₂ into the lake from the underlying diatreme. Increased CH₄ concentrations at all depths below the oxycline and a high¹⁴C content (41% modern) in the CH₄ 4 m above lake bottom show that much of the CH₄ is biologically produced within the lake. The CH₄ production rate may vary with time, but if the CO₂ recharge rate remains constant, CO₂ saturation of the entire hypolimnion below 50 m depth would require ∼140a, given present-day concentrations.     

Processes of supply and removal of dissolved silicon in the oceans

A critical assessment has been made of the processes of supply and removal of dissolved silicon in the ocean. The only sources of importance appear to be continental drainage (supplying 4.3 × 10¹⁴ g SiO₂/yr), Antarctic weathering and migration from sediment pore waters. The magnitudes of the last two processes are uncertain but there is evidence that they may add significantly to the river input. The total input appears to lie uncertainly within the range of 5.12 × 10₁₄ g SiO₂/yr.Estimates of removal in estuarine mixing processes (less than 1 × 10₁₄ g SiO₂/yr) and in pelagic siliceous oozes (less than 2 × 10₁₄ g SiO₂/yr) suggest that deposition by these processes may not balance the input. Other removal processes could include biological deposition in coastal waters, but the hypothesis that some removal in the sea occurs by inorganic processes, such as reverse weathering reactions, cannot be discounted.     

Holocene hydrological variability of Lake Ladoga,northwest Russia,as inferred from diatom oxygen isotopes

This article presents a new comprehensive assessment of the Holocene hydrological variability of Lake Ladoga, northwest Russia. The reconstruction is based on oxygen isotopes of lacustrine diatom silica (δ¹⁸O_diatom) preserved in sediment core Co 1309, and is complemented by a diatom assemblage analysis and a survey of modern isotope hydrology. The data indicate that Lake Ladoga has existed as a freshwater reservoir since at least 10.8 cal. ka BP. The δ¹⁸O_diatom values range from +29.8 to +35.0‰, and relatively higher δ¹⁸O_diatom values around +34.7‰ between c. 7.1 and 5.7 cal. ka BP are considered to reflect the Holocene Thermal Maximum. A continuous depletion in δ¹⁸O_diatom since c. 6.1 cal. ka BP accelerates after c. 4 cal. ka BP, indicating Middle to Late Holocene cooling that culminates during the interval 0.8–0.2 cal. ka BP, corresponding to the Little Ice Age. Lake‐level rises result in lower δ¹⁸O_diatom values, whereas lower lake levels cause higher δ¹⁸O_diatom values. The diatom isotope record gives an indication for a rather early opening of the Neva River outflow at c. 4.4–4.0 cal. ka BP. Generally, overall high δ¹⁸O_diatom values around +33.5‰ characterize a persistent evaporative lake system throughout the Holocene. As the Lake Ladoga δ¹⁸O_diatom record is roughly in line with the 60°N summer insolation, a linkage to broader‐scale climate change is likely.     

Cadmium deposition and mobility in the sediments of an acidic oligotrophic lake

A dated core from the profoundal zone in a pristine oligotrophic acidic lake was analyzed for Cd as well as for Al, Ca, Fe, Mg, Mn, Pb, Ti and total carbon and nitrogen. Overlying water and porewater samples were also obtained on six occasions at the same site, and yielded vertical profiles of pH and dissolved Cd, Ca, Fe, Mg, Mn, sulfide, SO₄⁻², organic and inorganic carbon concentrations. These extensive porewater and sediment geochemical data were used, together with information on infaunal benthos, to decipher the sedimentary record of Cd contamination. Depth variation of sediment Ca concentrations indicate that the lake suffered from progressive acidification starting about 1950. The present-day accumulation rate of Cd (J_acc^Cd = 5.4 ± 0.4 × 10⁻¹¹ mol cm⁻² yr⁻¹) in the sediments is the sum of the flux of Cd deposited with settling particles (J_S^Cd = 3.3 ± 0.2 × 10⁻¹¹ mol cm⁻² yr⁻¹) and the fluxes of dissolved Cd across the sediment-water interface due to molecular diffusion (J_D^Cd = 1.8 ± 0.3 × 10⁻¹¹ mol cm⁻² yr⁻¹), bioturbation (J_B^Cd = 1.1 ± 0.2 × 10⁻¹⁴ mol cm⁻² yr⁻¹) and bioirrigation (J_I^Cd = 0.27 ± 0.05 × 10⁻¹¹ mol cm⁻² yr⁻¹). Biological mixing of the sediments was negligible. The shape of the vertical profile of total Cd concentration with depth in the sediment appears to be determined more by its input history than by post-depositional mobilization and redistribution in the sediment column.     

Zeolitic diagenesis of late Quaternary fluviolacustrine sediments and associated calcrete formation in the Lake Bogoria Basin, Kenya Rift Valley

Late Quaternary fluviolacustrine siltstones, mudstones and claystones (Loboi Silts) on the northern margins of the saline, alkaline Lake Bogoria in the Kenya Rift Valley contain up to c. 40% authigenic analcime and minor natrolite. The zeolitic sediments are reddish brown and up to 1 m thick. The amount of analcime increases upward in the profile, but decreases with distance from the lake. The altered sediments show many pedogenic features including zeolitic root mats, rootmarks, concretions and carbonate rhizoliths. Residual patches of calcrete locally cap the zeolitic rocks. The profile is interpreted as an exhumed palaeosol and land surface on the former margins of the lake. The analcime occurs as submicroscopic (0–5–2–5 μ.m) subhedral and euhedral crystals, which have an average Si/A 1 ratio of 2–33 (as determined by X-ray microanalysis) or 2–18 (d-value of 639 analcime peak). The analcime formed in lake marginal sediments (soils) by reaction of silicate detritus with Na₂CO₃ rich pore waters concentrated close to the land surface by evaporative pumping and evapotranspiration. Poorly ordered clay minerals were probably the main reactants. Authigenic illite may have been a by-product of the reactions. Chemical analyses suggest that pore waters supplied some of Na⁺, and possibly K⁺ and SiO₂. The associated calcrete and rhizoliths were formed during or shortly after the main period of zeolitic alteration. The Ca²⁺ may have originated from infiltrating dilute runoff and groundwater. Authigenic smectite was precipitated in open porosity following analcime formation. The zeolitic alteration at Lake Bogoria provides a relatively recent analogue for lake marginal zeolites found in many ancient saline, alkaline lake sediments.     

Uranium geochemistry on the Amazon shelf: Evidence for uranium release from bottom sediments

In Amazon-shelf waters, as salinity increases to 36.5 × 10⁻³, dissolved uranium activities increase to a maximum of 4.60 dpm 1⁻¹. This value is much higher than the open-ocean value (2.50 dpm 1⁻¹), indicating a source of dissolved uranium to shelf waters in addition to that supplied from open-ocean and riverine waters. Uranium activities are much lower for surface sediments in the Amazon-shelf seabed (mean: 0.69 ±.09 dpm g⁻¹) than for suspended sediments in the Amazon River (1.82 dpm g⁻¹). Data suggest that the loss of particulate uranium from riverine sediments (and the consequent input of dissolved uranium to shelf waters) is probably the result of uranium desorption from the ferric-oxyhydroxide coatings on sediment particles, and/or uranium release by mobilization of the ferric oxyhydroxides. The total flux (i.e., riverine flux plus desorbed-remobilized particulate flux) of dissolved ²³⁸U from the Amazon shelf (about 1.2 × 10¹⁵ dpm yr⁻¹) constitutes about 15% of uranium input to the world ocean, commensurate to the Amazon River's contribution to world river-water discharge (approximately 18%). Measurement of only the riverine flux of dissolved ²³⁸U underestimates, by a factor of about 5, the flux of dissolved²³⁸U from the Amazon shelf to the open ocean.     

Geochemistry of organic-rich river waters in Amazonia: Insights on weathering processes of intertropical cratonic terrain

In this study, eight organic-rich rivers that flow through the Brazilian craton in the southwestern Amazon rainforest are investigated. This investigation is the first of its type in this area and focuses on the effects of lithology, long-term weathering, thick soils, forest cover and hydrological period on the dissolved load compositions in rivers draining cratonic terrain. The major dissolved ion concentrations, alkalinity (TAlk), SiO₂, trace element concentrations, and Sr isotope contents in the water were determined between April 2009 and January 2010. In addition, the isotopic values of oxygen and hydrogen were determined between 2011 and 2013. Overall, the river water is highly dilute and dominated by the major dissolved elements TAlk, SiO₂ and K⁺ and the major dissolved trace elements Al, Fe, Ba, Mn, P, Zn and Sr, which exhibit large temporal and spatial variability and are closely correlated with the silicatic bedrock and hydrology. Additionally, rainwater and recycled water vapor and the size of the basin contribute to the geochemistry of the waters. The total weathering flux estimated from our results is 2–4 t km⁻².yr⁻¹, which is one of the lowest fluxes in the world. The CO₂ consumption rate is approximately 21–61 10³ mol km⁻² yr⁻¹, which is higher than expected given the stability of the felsic to basic igneous and metamorphic to siliciclastic basement rocks and the thick tropical soil cover. Thus, weathering of the cratonic terrain under intertropical humid conditions is still an important consumer of CO₂.     

Short-term biogeochemical influence of a diatom bloom on the nutrient and trace metal concentrations in South San Francisco Bay microcosm experiments

Two laboratory microcosm experiments were conducted to mimic an annual spring diatom bloom in South San Francisco Bay by isolating the phytoplankton community from the benthic grazing pressure to induce a phytoplankton bloom. The purpose of these experiments was to isolate the impact of a spring diatom bloom on the nutrient and trace metal geochemical cycling. Microcosms were created in 2.5 L incubation bottles and subjected to one of 4 treatments (control, copper [Cu] addition, manganese [Mn] addition, and both Cu and Mn addition) to investigate the toxicity of Cu on the resident plankton and the potential antagonistic effects of Mn on reducing Cu toxicity. Dissolved macronutrient (nitrate + nitrite, phosphate, and silicate), and dissolved and particulate trace metal (Cu, Ni, Mn) concentrations were monitored in the grow-out incubations on a daily basis. Chlorophylla concentrations were also monitored over the course of the experiment and used to calculate diatom-specific growth rates. In the experiments containing ambient South San Francisco Bay surface waters, average specific growth rates were on the order of 1.1 d^?1. The induced diatom blooms resulted in significant removal of macronutrients from the microcosms over the course of the experiments. Our research supports previous suggestions that dissolved Ni and Cu concentrations in South San Francisco Bay have a very low biological availability as a result of organic chelation. Ni(EDTA)^2? has been found to be the dominant dissolved Ni species by other researchers and Cu speciation analyses from this study and others indicate that > 99% of the dissolved Cu in South San Francisco Bay is strongly chelated as CuL₁. The free cupric ion concentration was on the order of 10^?12 M. Marked removal of dissolved Mn was observed in the control treatments, well exceeding expected dissolved Mn removal by diatom uptake. Additions of 375 nM Cu resulted in the complete titration of the chelating ligand (L₁) concentrations. The elevated [Cu²⁺] (≈10^?8MM) appeared to have a toxic effect on the diatom community observed in the significant decreases in their specific growth rates (μ=0.4 d^?1). The suppression of dissolved Mn removal from solution was also observed in treatments spiked with high levels of dissolved Cu, providing support that Mn precipitation was due to biologically mediated oxidation not phytoplankton assimilation. The observed geochemical behavior in the concurrent Cu and Mn addition treatments provide evidence in support of Mn alleviation of Cu toxicity. The biological role in the ambient short-term biogeochemical cycling of Cu and Ni in South San Francisco Bay appears to be minimal due to the inert character of the organic ligand-metal complexes. A significant portion of the annual macronutrient and Mn cycling occurs as a result of spring diatom blooms in South San Francisco Bay.     

Authigenic mineralogy, depositional environments and evolution of fault-bounded lakes of the Yunnan Plateau, south-western China

The Dianchi, Erhai and Fuxian lakes lie in faulted basins in a subtropical humid region of the Yunnan Plateau, China. Three groups of authigenic minerals have been recognized in their recent sediments - carbonate minerals, Fe-bearing minerals and silica minerals. The main authigenic minerals are goethite, calcite, aragonite, siderite and quartzine. Goethite is chemically precipitated from a colloidal suspension. Calcite is a widespread chemical precipitate that is present in deep parts of the lakes and in shallow areas associated with aquatic macrophytes. Aragonite is mainly biochemical in origin, and commonly associated with shallow benthos. Siderite forms in reducing environments, associated with pore waters with a high P_CO2 that resulted from microbial degradation of organic matter. It forms mainly in deep-water environments. Quartzine, which occurs mainly in delta front and prodeltaic sites, forms from diatom dissolution and dissolved silica introduced by streams. Six authigenic mineral associations are recognized, each of which can be related to depositional setting within the lake and the stage of lake development. The same associations can also be recognized in a 480-m-long core recovered from Dianchi Lake. Strong reducing environments and migrating pore fluids with high P_CO2 have led to the early diagenetic alteration of some of the initial authigenic minerals. Using the mineral associations from the modern lakes, the Pliocene to Recent history of Dianchi Lake has been interpreted, and is in general agreement with palaeoenvironmental reconstructions based upon palaeontological and other evidence.     

Chemical and Strontium Isotopic Compositions of the Hanjiang Basin Rivers in China: Anthropogenic Impacts and Chemical Weathering

The Hanjiang River, the largest tributaries of the Changjiang (Yangtze) River, is the water source area of the Middle Route of China’s South-to-North Water Transfer Project. The chemical and strontium isotopic compositions of the river waters are determined with the main purpose of understanding the contribution of chemical weathering processes and anthropogenic inputs on river solutes, as well as the associated CO₂ consumption in the carbonate-dominated basin. The major ion compositions of the Hanjiang River waters are characterized by the dominance of Ca²⁺ and HCO₃ ⁻, followed by Mg²⁺ and SO₄ ²⁻. The increase in TDS and major anions (Cl⁻, NO₃ ⁻, and SO₄ ²⁻) concentrations from upstream to downstream is ascribed to both extensive influences from agriculture and domestic activities over the Hanjiang basin. The chemical and Sr isotopic analyses indicate that three major weathering sources (dolomite, limestone, and silicates) contribute to the total dissolved loads. The contributions of the different end-members to the dissolved load are calculated with the mass balance approach. The calculated results show that the dissolved load is dominated by carbonates weathering, the contribution of which accounts for about 79.4% for the Hanjiang River. The silicate weathering and anthropogenic contributions are approximately 12.3 and 6.87%, respectively. The total TDS fluxes from chemical weathering calculated for the water source area (the upper Hanjiang basin) and the whole Hanjiang basin are approximately 3.8 × 10⁶ and 6.1 × 10⁶ ton/year, respectively. The total chemical weathering (carbonate and silicate) rate for the Hanjiang basin is approximately 38.5 ton/km²/year or 18.6 mm/k year, which is higher than global mean values. The fluxes of CO₂ consumption by carbonate and silicate weathering are estimated to be 56.4 × 10⁹ and 12.9 × 10⁹ mol/year, respectively.     

Hydrogeochemistry of two river main floodplain lakes,Hessia, FR Germany

Two lakes, Lake Gänseweiher (LGW) and Lake Fechenheimer Weiher (LFW) occupy groundwater filled abandoned gravel pits which serve as fishing grounds and are part of recreational areas, respectively.Both lakes are cut into a near-surface groundwater aquifer, which is located in the pleistocene River Main gravel terrace t₆. They are sealed at the base by miocene clays and above by overlying flood deposits of the River Main. The latter provide protection from pollutants derived from wet and dry deposition of atmospheric contaminants.Groundwater chemistry determines the pool of dissolved constituents in lake water. The temporal and spatial distribution patterns of chemical compounds in lake water are brought about by endo-biogenic processes, of which the indicators are nitrate-nitrogen and dissolved silica. The latter illustrates an instantaneous response to pulses of diatom blooms.Both lakes are eutrophic (polytrophic) according to the classification guidelines presented in literature.     

Geochemical,isotopic and hydrological mass balance approaches to constrain the lake water–groundwater interaction in Dal Lake,Kashmir Valley

It is important to have qualitative as well as quantitative understanding of the hydraulic exchange between lake and groundwater for effective water resource management. Dal, a famous urban fresh water lake, plays a fundamental role in social, cultural and economic dynamics of the Kashmir Valley. In this paper geochemical, isotopic and hydrological mass balance approaches are used to constrain the lake water–groundwater interaction of Dal Lake and to identify the sources of lake water. Water samples of precipitation (n = 27), lake water (n = 18) and groundwater (n = 32) were collected across the lake and its catchment for the analysis of δ¹⁸O and δ²H. A total of 444 lake water samples and 440 groundwater samples (springs, tube wells and dug wells) were collected for the analysis of Ca²⁺, Mg²⁺, HCO₃ ^?, SO₄ ^2?, Cl^?, NO₃ ^?, Na⁺ and K⁺. Water table and lake water level were monitored at 40 observation locations in the catchment. Water table map including pH and EC values corroborate and verify the gaining nature of the Dal Lake. Stable isotopes of lake water in Boddal and Gagribal basins showed more deviation from the global meteoric water line than Hazratbal and Nigeen basins, indicating the evaporation of lake water. The isotopic and geochemical mass balance suggested that groundwater contributes a significant proportion (23–40%) to Dal Lake. The estimated average groundwater contribution to Dal Lake ranged from 31.2 × 10³ to 674 × 10³ m³ day^?1 with an average of 276 × 10³ m³ day^?1. The study will be useful to delineate the possible sources of nutrients and pollutants entering the lake and for the management of lake water resources for sustainable development.