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1.
Concentrations of Se in the pore-water and in the solid phase, and the concentrations of other diagenetic constituents (Fe, Mn, phosphate, ammonium and I) in pore-water, were determined in a sediment core from a 350-m deep station in the lower St. Lawrence Estuary. The concentration of dissolved Se in pore-water was 2.1 nmol kg−1 at the surface of the core, increasing to a maximum of 7.6 nmol kg−1 at a depth of 12 cm, and thereafter decreasing gradually with depth. This profile is similar to the profiles of Fe and phosphate, whose concentration maxima occur around 10 cm. The concentration of total sedimentary Se remained almost constant with depth (≈ 0.75 mg kg−1); however, a significant enrichment of oxalate-leachable Se was observed in the top 2 cm. The sedimentary cycling of Se appears to be closely related to that of Fe: adsorption of Se onto Fe oxyhydroxide at or near the sediment-water interface, release of the adsorbed Se by the reduction of Fe oxyhydroxide, and removal by formation of ferroselite (FeSe2) at depth. The pore-water flux of Se was estimated by two different methods, firstly from the pore-water gradient, and secondly by applying a box model to the oxalate-leachable solid-phase Se data. The methods agree well both giving values for the flux of 0.11 nmol cm−2 year−1. This agreement suggests that the loss of labile Se in the sediment is balanced by the upward flux of dissolved Se. 相似文献
2.
Cross-flow ultrafiltration (CFF) is often used to obtain separation and concentration of colloids from bulk natural water samples. Application of the ultrafiltration permeation model allows the quantitative determination of the low molecular weight material (LMW, < 1 kDa) and colloids in bulk dissolved organic matter (DOM) from measurements of time series permeate samples obtained from CFF. Detailed analysis of a Yukon River water sample shows that DOM absorption coefficient and fluorescence follow the permeation model and that the complex spectral optical properties of LMW DOM can be reconstructed from CFF data. A combination of measured and modeled data indicates that the LMW contribution to bulk DOM optical properties obtained from CFF can be grossly underestimated by the use of a low concentration factor (CF, the ratio of initial sample volume to retentate volume). Even at a relatively high CF of 19, optical properties of LMW DOM calculated from measurements of the retentate or integrated permeate would underestimate true values by 5–36%. In the Yukon River sample, LMW dissolved organic carbon represented 26% of the bulk concentration, but only 3–14% of the colored DOM was in the LMW fraction while 31–33% of bulk DOM florescence was due to LMW DOM. The contrasting optical properties of LMW and colloidal DOM support the concept that analysis of bulk DOM absorption and fluorescence properties reveals information about DOM molecular weight. 相似文献
3.
John A. E. Gibson Warwick F. Vincent Patrick Van Hove Claude Belzile Xioawa Wang Derek Muir 《Aquatic Geochemistry》2002,8(2):97-119
The geochemical processes occurring within meromictic Lake A (maxdepth 120 m) on northern Ellesmere Island, Canada, were investigated to determinethe history of the lake and to provide a baseline for future studies. The lake contained seawaterdiluted by freshwater input that had been mixed prior to the lake's isolation from tidalaction. Input of freshwater after isolation of the lake created vertical stratification resultingin the creation of distinct oxic, suboxic and anoxic zones. Dissolved oxygen was present to 13 m,and sulphide beneath 32 m. Manganese and iron cycling dominated the redox chemistrybetween these depths. Total manganese concentrations reached 176 M, higher thanin most other natural stratified lake or marine environments. 相似文献
4.
Bacterial dominance of phototrophic communities in a High Arctic lake and its implications for paleoclimate analysis 总被引：1，自引：1，他引：0
Dermot Antoniades Julie Veillette Marie-Josée Martineau Claude Belzile Jessica Tomkins Reinhard Pienitz Scott Lamoureux Warwick F. Vincent 《Polar Science》2009,3(3):147-161
The phototrophic communities in meromictic, perennially ice-covered Lake A, on Ellesmere Island in the Canadian High Arctic, were characterized by pigment analysis using high performance liquid chromatography. Samples were taken to determine the vertical changes down the water column as well as a variation between years. These analyses showed that Lake A had distinct phototrophic communities in its oxic and anoxic layers. The pigment analyses indicated that phototrophic biomass in the upper, oxic waters was dominated by picocyanobacteria, while in the lower, anoxic layer photosynthetic green sulphur bacteria were dominant. Interannual variation in pigment concentrations was related to the penetration of photosynthetically active radiation in the water column, suggesting that light availability may be limiting the net accumulation of photosynthetic bacterial biomass in Lake A. Pigment analysis of the surface sediments indicated that deposition was dominated by the photosynthetic sulphur bacterial contribution. The sedimentary record of bacterial pigments in polar meromictic lakes offers a promising tool for the reconstruction of past changes in ice cover and therefore in climate. 相似文献
5.
Sediment diffusive fluxes of Fe,Mn, and P in a eutrophic lake: Contribution from lateral vs bottom sediments 总被引：3，自引：0，他引：3
Nelson Belzile Jaime Pizarro Montserrat Filella Jacques Buffle 《Aquatic Sciences - Research Across Boundaries》1996,58(4):327-354
Water column data and porewater profiles are used to study the chemical evolution with time and with depth of a eutrophic lake. By using different approaches, diffusion fluxes for dissolved iron, manganese and phosphate are calculated and used to describe the processes occurring at the sediment-water interface as well as in the hypolimnion of the lake. These data are used in the elaboration of a qualitative model to describe the chemical behaviour of the sedimentary interface of an anoxic lake with emphasis on the Fe/P/S system. Acorona model is proposed to explain the evolution with time of the diffusion process by estimating the relative contribution of bottom and lateral sediment surfaces to the total fluxes of dissolved elements diffusing from the sediment to the overlying water. As the hypolimnion becomes more anoxic, it has been observed that lateral sediment surfaces (16 to 10 meters in depth) represents a larger supplier of diffusing dissolved components than the bottom sediment portion (bottom to 18 meters). 相似文献
6.
Antimony in the environment: A review focused on natural waters. III. Microbiota relevant interactions 总被引：1，自引：0，他引：1
Antimony is ubiquitously present in the environment as a result of natural processes and human activities. Antimony is not considered to be an essential element for plants or animals. In this third review paper on the occurrence of antimony in natural waters, the interactions of antimony with microbiota are discussed in relation to its fate in natural waters. This paper covers the following aspects: occurrence in microbiota, uptake transport mechanisms, pathways of Sb(III) removal from cells involved in antimony tolerance, oxidation and reduction of antimony by living organisms, phytochelatin induction and biomethylation. This review is based on a careful and systematic examination of a comprehensive collection of papers on the above mentioned aspects of the subject. All data are quoted from the original sources. Relatively little existing information falls within the strict scope of this review and, when relevant, discussion on the interactions of antimony with reference microorganisms, such as Escherichia coli, Saccharomyces cerevisiae and different protozoan parasites of the genus Leishmania, has been included. 相似文献
7.
对采自新疆尉犁蛭石矿、河南灵宝-陕西潼关蛭石矿的工业蛭石矿物样品进行了可交换性阳离子与交换容量研究，发现新疆尉犁蛭石矿金云母-蛭石中可交换性阳离子主要为Na^ 和Ca^2 ，其次为Mg^2 、K^ 、Ba^2 和Sr^2 ；而河南灵宝-陕西潼关蛭石矿工业蛭石样品的可交换性阳离子主要为Ca^2 和Mg^2 ，其次为Na^ 、K^ 等。金云母-蛭石和绿泥石-蛭石间层矿物的阳离子交换容量随间层结构中蛭石晶层的含量增加而增大，一般在56．92～98．95mmol／100g之间，仅为蛭石最大阳离子交换容量的一半。金云母-蛭石样品阳离子交换容量大小与K2O含量呈负相关关系，与(Na2O CaO)含量呈正相关关系。 相似文献
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9.
The vertical distributions of dissolved Se species [Se(IV), Se(VI) and organic Se] and diagenetic constituents [Fe(II) and Mn(II)] were obtained in porewater samples of two Sudbury area lakes (Clearwater and McFarlane). The sedimentary concentration profiles of total Se, Se species bound to Fe–Mn oxyhydroxides and to organic matter, and of elemental Se were also determined along with the concentrations of Fe, Mn and S in different extractable fractions. Results indicated that the concentrations of total dissolved Se in porewater samples were very low, varying from around 2.0 nM to a maximum level of 6.5 nM, while the concentrations of total Se species in the solid phase varied between 2 and 150 nmol/g on a dry weight basis. The two lakes showed striking differences in the presence of Se(IV) and Se(VI) at the sediment–water interface (SWI). In Clearwater Lake, Se(VI) was present at this interface and Se(IV) was not detectable, whereas the opposite was found in McFarlane Lake. This suggests that reducing conditions might have existed near the SWI of McFarlane Lake at the sampling time; this hypothesis was confirmed by several other measured chemical parameters. The profiles of total dissolved Se of both lakes suggest upward and downward diffusion of dissolved Se species along the concentration gradients. Assuming that no precipitation occurred at the SWI, the fluxes of dissolved Se species across the SWI in Clearwater and McFarlane lakes were estimated to be 0.108 and 0.034 nmol cm−2 a−1, respectively. These values do not include the possible losses of volatile Se species due to microbial methylation. In the reducing sediments of both lakes, the formation of elemental Se and pyritic Se were found to be important mechanisms for controlling the solubility of Se in this environment. The main geochemical processes involving Se identified in this study are: the adsorption of Se onto Fe–Mn oxyhydroxides at or near the SWI, the release of adsorbed Se by the reduction of the same oxyhydroxides and the mineralization of organic matter, and the removal of Se from porewaters to form elemental Se and a S mineral phase such as Se–pyrite or pure ferroselite. 相似文献
10.
Temperature, pH, total alkalinity, dissolved oxygen, silicate, nitrate, phosphate and the Mn, Fe and Al contents of suspended particulate matter (SPM) were measured in the Rimouski River estuary as functions of chlorinity during the period May—September 1980.At any given time, total alkalinity (TA) is conservative within the estuary with respect to chlorinity. However, the total alkalinity (TA) of the freshwater is related to river flow. This is attributed to dilution of the river water with bicarbonate-poor rainwater.Generally, pH follows the same pattern observed for TA in freshwater. Dissolved oxygen is usually more concentrated in freshwater and decreases linearly with increasing chlorinity. Freshwater is always saturated or supersaturated with respect to O2. Seasonal fluctuations are attributed to temperature variations.There is no evidence for removal of soluble silicate from the freshwater entering the sea. The concentration of silicate in the freshwater is strongly influenced by rainfall. Soil leaching, conditioned by high rainfall increases the concentration of soluble silicate in freshwater. Nitrate behaves similarly whereas phosphate is complicated by the presence of sewage.Analysis of the Mn, Fe and Al contained in the SPM indicates dilution of river-borne particles rich in Mn by others less rich in this element. A decrease in Mn content with increasing chlorinity and SPM concentration as well as increasing concentrations of SPM with increasing chlorinity indicate that the composition is controlled primarily by physical mixing of material from two sources rather than by chemical processes. Within the analytical precision the Fe/Al ratio does not vary with the chlorinity. 相似文献