Geochemical records of the sediments and their significance in Dongping Lake Area,the lower reach of Yellow River,North China

Dongping Lake area, located in the lower reaches of Yellow River, is an ideal place to study the changes of modern river and lake sedimentary environment. The sediment samples of Dawen River, Yellow River, and Dongping Lake were collected, and the major elements, trace elements and organic matter geochemical composition of the samples were analyzed. Cluster analysis, characteristic element ratio method and graphic method were used to explore the geochemical characteristics of sediments and their environmental implication. The results show that the contents of SiO_2, Na_2O, TiO_2 and Zr in sediments of Dawen River and Yellow River are relatively high, and the contents of iron and manganese oxides, organic matter, CaO, P_2O_5 and Sr in lake sediments are relatively high. That reveals the differences of sedimentary environments between the rivers and the lake. The contents of Sr and Zr in Dawen River are affected by the rapid migration of clastic materials in the upstream carbonate source area during the flood season; the δCe,ΣREE and REE's ratios in the sediments of the Yellow River reflect the influence of the Loess source; and the distribution of elements changes along the flow direction during the flood season. The characteristics of p H, element composition and LREE HREE fractionation of the lake sediments indicate that the sediment source is complex, and the lake environment is affected by the flood season. The study shows that the geochemical content and its variation characteristics of sediments effectively reveal the sedimentary environment, material composition and characteristics of flood season of rivers and the lake in the study area.     

Water chemistry and sedimentological observations in littlefield lake,michigan: Implications for lacustrine marl deposition

A combination of both water chemistry and sedimentological information was used to investigate the carbonate-producing mechanism in Littlefield Lake, a small lake located in Isabella County, central Michigan. Data on temperature, dissolved oxygen, pH, calcium carbonate (CaCO₃) saturation, alkalinity, calcium, and magnesium were obtained on a monthly basis over a 13-month period, with each parameter determined at 1m intervals over a depth range of 20m. The loss of dissolved carbon dioxide (CO₂) from warm surface waters during direct degassing, and to a lesser extent during photosynthetic uptake by lacustrine macrophytes and phytoplankton during the summer, results in massive precipitation of the low-magnesium calcite which predominates in all Littlefield Lake sedimentary facies However, despite the fact that carbonate precipitation in this rather typical temperate-region marl lake is directly related to, and may be driven by, seasonal variation in these physiochemical parameters, most calcite forms as encrustations around cyanophytic and chlorophytic macrophytes. Such relationships demonstrate that carbonate precipitation in marl lakes may result from complex interactions between both biochemical and physiochemical processes. As such, marl formation in this, and probably many other calcareous lake systems, can not be simply ascribed to one or the other of these two general mechanisms.     

Biogeochemistry of trace metals (Mn, Sr, Rb, Ba, Cu, Zn, Pb and Cd) in a river-wetland-lake system (Balaton Region, Hungary)

Mn, Sr, Ba, Rb, Cu, Zn, Pb and Cd concentrations have been measured seasonally in the water and deposited sediments of the system comprising: Zala river (main input) — Lakes Kis-Balaton 1 and 2 (small artificial lakes created in a former bay of Lake Balaton) — Keszthely bay (hypertrophic part of Lake Balaton). The concentrations of the trace elements together with pH, alkalinity, dissolved cations (Ca²⁺, Mg²⁺, Na⁺, and K⁺), dissolved inorganic ligands (Cl^–, SO₄ ^2–), particulate Al, Ca, inorganic and organic carbon are used to assess the contamination of the study area and biogeochemical processes controlling trace element concentrations. Thermodynamic speciation calculations have also been utilized to enhance our understanding of the system. In the sediments Rb, Ba, Cu and Zn concentrations were mainly controlled by the abundance of the aluminosilicate fraction. Strontium was mainly associated with the calcium carbonate fraction. The aluminosilicate fraction constitutes a major sink for Mn and Cd but the concentration of these elements are also strongly related to calcite precipitation. The main processes that control the dissolved distribution of trace elements in the Balaton system were: solid phase formation (carbonate) for Mn; coprecipitation with calcite for Sr, Ba, Rb and possibly Mn and Cd; adsorption/desorption processes (pH dependent) for Zn and Pb; solubilization of Mn and precipitation of Cd and Cu in reed covered wetland areas where anoxic conditions were probably existing during the warm season. A preliminary budget of atmospheric and river input to Lake Balaton has also been outlined. Although Lake Balaton, is subjected to anthropogenic inputs mainly from agricultural and domestic activities, their impact on trace element concentrations in the Balaton system is very limited due to the efficiency of removal processes (i.e. adsorption and co-precipitation) and to high sedimentation rates and strong sediment re-suspension. Anthropogenic inputs are only detected for Pb.     

Using Mg Isotopes to Trace Cyanobacterially Mediated Magnesium Carbonate Precipitation in Alkaline Lakes

This study assesses the potential use of Mg isotopes to trace Mg carbonate precipitation in natural waters. Salda Lake (SW Turkey) was chosen for this study because it is one of the few modern environments where hydrous Mg carbonates are the dominant precipitating minerals. Stromatolites, consisting mainly of hydromagnesite, are abundant in this lake. The Mg isotope composition of incoming streams, groundwaters, lake waters, stromatolites, and hydromagnesite-rich sediments were measured. Because Salda Lake is located in a closed basin, mass balance requires that the Mg isotopic offset between Lake Salda water and precipitated hydromagnesite be comparable to the corresponding offset between Salda Lake and its water inputs. This is consistent with observations; a ??²⁶Mg offset of 0.8?C1.4??? is observed between Salda Lake water and it is the incoming streams and groundwaters, and precipitated hydromagnesite has a ??²⁶Mg 0.9?C1.1??? more negative than its corresponding fluid phase. This isotopic offset also matches closely that measured in the laboratory during both biotic and abiotic hydrous Mg carbonate precipitation by cyanobacteria (Mavromatis, V., Pearce, C., Shirokova, L. S., Bundeleva, I. A., Pokrovsky, O. S., Benezeth, P. and Oelkers, E.H.: Magnesium isotope fractionation during inorganic and cyanobacteria-induced hydrous magnesium carbonate precipitation, Geochim. Cosmochim. Acta, 2012a. 76, 161?C174). Batch reactor experiments performed in the presence of Salda Lake cyanobacteria and stromatolites resulted in the precipitation of dypingite (Mg₅(CO₃)₄(OH)₂·5(H₂O)) and hydromagnesite (Mg₅(CO₃)₄(OH)₂·4H₂O) with morphological features similar to those of natural samples. Concurrent abiotic control experiments did not exhibit carbonate precipitation demonstrating the critical role of cyanobacteria in the precipitation process.     

Searching of toxic metal pollution by using geospatial technology on the Kodaikanal Lake—near industrial area

The present study investigates the anthropogenic metal input into the lake system, the toxic metal pollution in the sediments of Kodaikanal Lake. Surface sediment samples were collected at seven locations to represent its spatial variability within the lake. Samples were subjected to analyze for Fe, Co, Cr, Mn, Ni, Zn, Cd, Cu, Ag, Pb, Hg, and As by energy dispersive X-ray fluorescence (EDXRF) and their concentrations in lake sediments range from 102,000–109,000, 561–2699, 292–544, 211–482, 79–163, 57–265, 57–74, 37–92, 46–59, 20–97, 19–30, to 13–24 mg/kg, respectively. The sources of pollution were inferred through spatial and statistical analyses. Most of the toxic metal contents in the sediments are found to exceed the background concentration in all locations. The enrichment factor (EF) and index of geoaccumulation (I _geo) of Hg, Co, Cd, and Ag showed that sediments of Kodaikanal Lake exhibit the probability of anthropogenic influence. The significant Pearson’s correlation coefficient is also suggesting that they probably originated from the same source of occurrence. The contamination factor and degree of contamination of the Kodaikanal Lake sediments are strongly polluted in terms of most of the examined metals. The study also provides environmentally significant information about anthropogenic influence on the lake sediments.     

Distribution of cadmium among multimedia in Lake Qinghai,China

Lake Qinghai in the Qinghai-Tibet plateau is the largest lake in China. This study firstly reported the geochemistry of Cd in the lake. Water samples were collected from Lake Qinghai (n = 69) and Buha River (n = 12), while sediment (n = 22) and topsoil (n = 45) samples were collected from the lake and around the lake area, respectively. In addition, pore water samples (n = 20) were separated from sediment samples. Water samples were analyzed for pH, K, Na, Ca, Mg, Cl, S, and Cd, while sediment and topsoil samples were analyzed for K, Na, Ca, Mg, Al, Fe, Mn, S, Sc, and Cd. The average concentration of Cd was 0.014 μg L^?1 in the water of Lake Qinghai and 0.007 μg L^?1 in the water of Buha River. However, the average concentration of Cd was 0.320 μg L^?1 in the sediment pore water, much higher than that in the lake water and river water. Cadmium concentration in the lake water might be mainly controlled by salinity, while it in the pore water might be mainly controlled by carbonate minerals. Cadmium concentration in the river water might be controlled by alkalinity and pH. The average concentration of Cd in the sediment was 0.284 mg kg^?1. The enrichment of Cd in the lake sediment was significantly higher than that in the topsoil around the lake. Anthropogenic atmospheric deposition of Cd did not led to the increase in dissolved Cd level in the lake water, but led to its enrichment in the lake sediment.     

Controls on uranium distribution in lake sediments

Uranium geochemistry has been investigated in three acid lakes located on the Canadian Shield and one circumneutral lake in the Appalachian Region of Eastern Canada. In all Shield lakes, dissolved U concentrations were higher in the porewater than in the overlying water. In one of them, whose hypolimnion is perennially oxic, U released to porewater at depths of Fe remobilization was removed from the porewater at depths of Fe oxyhydroxides precipitation; these similarities in the U and Fe profiles indicate that part of the U becomes associated to Fe oxyhydroxides. The dissolved U and Fe profiles in the other two Shield lakes, whose hypolimnions were anoxic when sampled, did not show any significant recycling of these elements in the vicinity of the sediment-water interface and both elements diffused from the sediment to the overlying water. In contrast, in the Appalachian Lake, dissolved U concentrations were higher in the overlying water than in porewater, strongly decreased at the vicinity of the sediment-water interface and then remained relatively constant with sediment depth. Diagenetic modeling of the porewater U profiles, assuming steady-state, reveals that authigenic U always represented ?3% of the total U concentration in the sediments of all lakes. This observation indicates that diagenetic reactions involving U are not quantitatively important and that most of the U was delivered to the sediments at our study sites as particulate U and not through diffusion across the sediment-water interface, as is seen in continental margin sediments. Comparison of the U:C_org and U:Fe molar ratios in diagenetic material collected across the sediment-water interface with Teflon sheets and in surface sediments (0-0.5 cm) of the lake having a perennially oxic hypolimnion suggest that solid phase U was mainly bound to organic matter originating from the watershed; a strong statistical correlation between sediment non-lithogenic U and C_org in the Appalachian Lake supports this contention. Thermodynamic calculations of saturation states suggest that dissolved U was not removed from porewater through precipitation of UO_2(s), U₃O_7(s) and U₃O_8(s) as previously proposed in the literature.     

The significance of Chara vegetation in the precipitation of lacustrine calcium carbonate

A significant portion of calcium carbonate is deposited in lake sediments as a result of biological processes related to the photosynthetic activity of phytoplankton in the pelagic realm and, in addition, macrophytes in the littoral zone. Lake Wigry, one of the largest lakes in Poland (north‐east Poland), is characterized by: (i) carbonate sediments with a CaCO₃ content exceeding 80% within the littoral zone; and (ii) large areas of submerged vegetation dominated by charophytes (macroscopic green algae, Characeae family). It is claimed that charophytes are highly effective in utilizing HCO₃^? and forming thick CaCO₃ encrustations. Thus, this study was aimed at evaluating the CaCO₃ production by dense Chara stands overgrowing the lake bottom reaching a depth of 4 m. In late July 2009, the fresh and dry mass of plants, the percentage contribution of calcium carbonate and the production of CaCO₃ per 1 m² were investigated along three transects at three depths (1 m, 2 m and 3 m, with each sample area equal to 0·0625 m²) per transect. The composition and structure of phytoplankton and the physico‐chemical properties of the water analysed in both the littoral and pelagic zones served as the environmental background and demonstrated moderately low fertility in the lake. The greatest dry plant mass exceeded 1000 g m^?2 and CaCO₃ encrustations constituted from 59% to over 76% of the charophyte dry weight. Thus, the maximum and average values of carbonates precipitated by charophytes were 685·5 and 438 g m^?2, respectively, which exceeded previously reported results. A correlation of carbonate production with the depth of Chara stands was detected, and intermediate depths offered the most favourable conditions for carbonate precipitation (589 g m^?2 on average). As precipitated carbonates are ultimately stored in bottom deposits, the results highlight the significance of charophytes in lacustrine CaCO₃ sedimentation.     

Climate implications of major geochemical elements in the Holocene sediments of the North and East China monsoonal regions

Two Holocene sediment cores were retrieved respectively from the enclosed Lake Daihai in the monsoon/arid transition zone of North China and the Taihu Lake coast in the monsoonal area of the Yangtze delta, Eastern China. Distribution of major geochemical elements and their ratios were employed to reveal the characteristics of Holocene climate and associated environmental implications in the two regions. It is suggested that the temporal distribution of major elements serve as a useful indicator to denote the variations of monsoon effective precipitation for the enclosed lake area. High values of resistant elements such as Al₂O₃, SiO₂, TiO₂, (FeO + Fe₂O₃), MnO in the lake sediments correspond to the depressed chemical weathering and weakened mon-soon effective precipitation, while the highs of mobile and easy soluble elements such as MgO, CaO, Na₂O reflect the enhanced chemical weathering and increased monsoon effective precipitation in the lake basin. In comparison, the behaviors of the major elements in sediments of the Taihu Lake coast were largely controlled by the changes both in sea transgression in the different Holocene time periods and the monsoon precipitation. The relatively highs of Al₂O₃, TiO₂, (FeO + Fe₂O₃), in marine-influenced sediments suggest relatively strong coastal hydrodynamics and chemical weathering, and vice versa. Meanwhile, the lows of SiO₂, Na₂O and CaO in the non-marine-influenced sediments also denote relatively strong hydrodynamics and chemical weathering due to enhanced monsoon precipitation, and vice versa. Sedimentary environment should be taken into account when achieving a full understanding of their climate implications.     

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.     

Composition and origin of organic matter in surface sediments of Lake Sarbsko: A highly eutrophic and shallow coastal lake (northern Poland)

We present an organic geochemical study of surface sediments of Lake Sarbsko, a shallow coastal lake on the middle Polish Baltic coast. The aim was to provide evidence concerning the origin of the organic matter (OM) and its compositional diversity in surface deposits of this very productive, highly dynamic water body. The content and composition of the OM in the bottom sediments were investigated at 11 sampling stations throughout the lake basin. OM sources were assigned on the basis of bulk indicators [total organic carbon (TOC), total nitrogen (TN), δ¹³C_TOC and δ¹⁵N and extractable OM yield], biomarker composition of extractable OM and compound-specific C isotope signatures. The source characterization of autochthonous compounds was verified via phytoplankton analysis. The distribution of gaseous hydrocarbons in the sediments, as well as temporal changes in lake water pH, the concentration of DIC (dissolved inorganic carbon) and δ¹³C_DIC were used to trace OM decomposition.The sedimentary OM is composed mainly of well preserved phytoplankton compounds and shows minor spatial variability in composition. However, the presence of CH₄ and CO₂ in the bottom deposits provides evidence for microbial degradation of sedimentary OM. The transformation of organic compounds in surface, bottom and pore waters via oxidative processes influences carbonate equilibrium in the lake and seasonally favours precipitation or dissolution of CaCO₃.The data enhance our understanding of the relationships between the composition of sedimentary OM and environmental conditions within coastal ecosystems and shed light on the reliability of OM proxies for environmental reconstruction of coastal lakes.     

Comparison of metal(loid) concentrations in water, sediments and fish from two large shallow lakes

Hulun Lake and Taihu Lake are both large shallow lakes in China. In summer and winter of 2009, water, sediments and fish samples were collected from the two lakes and the concentrations of metal(loids) were analyzed. The results demonstrated that aqueous concentrations of arsenic (As), chromium (Cr), cadmium (Cd), nickel (Ni) and copper (Cu) in Hulun Lake were significantly higher than those in Taihu Lake. Especially, the As concentrations (about 130 μg/L) in Hulun Lake dramatically exceeded the permissible level of drinking water. Compared with Taihu Lake, metal(loid) concentrations in the sediments of Hulun Lake were significantly lower, which might have less impacts on the metal exchanges between water and sediments. In contrast, concentrations of the measured metal(loids) (including As) in fish from Hulun Lake and Taihu Lake were comparable, suggesting that the dramatic difference in aqueous and sediment metal(loid) concentrations had less influence on the metal(loid) bioavailability. The higher concentrations of dissolved organic carbon (DOC) and cations (e.g., Na⁺, K⁺ and Mg²⁺) in lake water might contribute to the reduced metal(loid) bioavailability to fish in Hulun Lake.     

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.     

Hydrochemistry of the Lake Magadi basin,Kenya

New and more complete compositional data are presented for a large number of water samples from the Lake Magadi area, Kenya. These water samples range from dilute inflow (<0.1 g/kg dissolved solids) to very concentrated brines (>300 g/kg dissolved solids). Five distinct hydrologic stages can be recognized in the evolution of the water compositions: dilute streamflow, dilute ground water, saline ground water (or hot spring reservoir), saturated brines, and residual brines. Based on the assumption that chloride is conserved in the waters during evaporative concentration, these stages are related to each other by the concentration factors of about 1:28:870:7600:16,800.Dilute streamflow is represented by perennial streams entering the Rift Valley from the west. All but one (Ewaso Ngiro) of these streams disappear in the alluvium and do not reach the valley floor. Dilute ground water was collected from shallow pits and wells dug into lake sediments and alluvial channels. Saline ground water is roughly equivalent to the hot springs reservoir postulated by Eugster (1970) and is represented by the hottest of the major springs. Saturated brines represent surficial lake brines just at the point of saturation with respect to trona (Na₂CO₃.NaHCO₃.2H₂O), while residual brines are essentially interstitial to the evaporite deposit and have been subjected to a complex history of precipitation and re-solution.The new data confirm the basic hydrologic model presented by Eugster (1970) which has now been refined, particularly with respect to the early stages of evaporative concentration. Budget calculations show that only bromide is conserved as completely as chloride. Sodium follows chloride closely until trona precipitation, whereas silica and sulfate are largely lost during the very first concentration' step (dilute streamflow-dilute ground water). A large fraction of potassium and all calcium plus magnesium are removed during the first two concentration steps (dilute streamflow-dilute ground water-saline ground water). Carbonate and bicarbonate are the dominant anions, and mechanisms by which they are extracted from the solution include precipitation of alkali and alkaline-earth carbonates, and degassing, as well as precipitation and re-solution of efflorescent crusts. Much sulfate is apparently lost from solution by sorption as well as subsurface reduction.Seasonal runoff, principally from the valley floor north of Lake Magadi, is considered to be the principal recharge to the Magadi ground water system. Evaporative concentration is the overall process responsible for the chemical evolution of the brines. This includes not only simple evaporation, but also mineral precipitation as films and cements in the unsaturated zone, re-solution, and reprecipitation of efflorescent crusts, with consequent recycling of salts. In fact, a large fraction of the solutes are acquired through dissolution of efflorescent crusts.Data were obtained for borehole brines from as deep as 297 m. They show the existence of two distinct brine bodies below the present lake, one shallow, coexistent with bedded salts, and highly concentrated (260 g/kg average dissolved solids), and the other deeper in lacustrine sediments or fractured lavas, and only half as concentrated.     

Characterizing Major Controls on Spatial and Seasonal Variations in Chemical Composition of Surface and Pore Brine of Maharlu Lake,Southern Iran

Maharlu Lake with Na–Cl water type is the terminal point of a closed basin in southern Iran. A total of 10 water samples from two rivers discharging to the lake and 78 water samples of surface and pore brine of Maharlu Lake have been collected from different depths (surface, 20, 50 and 100 cm) of four sampling stations along the lake during a period of lake water-level fluctuation (November 2014–July 2015). To investigate chemical interaction between lake surface water and shallow pore water and to understand the major factors governing chemical composition of Maharlu brine, concentrations of major and minor (boron, bromide and lithium) solutes, pH and total dissolved solids have been measured in collected water samples. Saturation indices of evaporite minerals in collected water samples have been also calculated. The chemical behavior of dissolved solutes and evaporative evolution of the lake brine during a hydrological period have been simulated using PHREEQC. The results of our investigations indicated that chemical composition of lake surface water and pore brine of Maharlu Lake are mainly connected with lake water-level fluctuations and distance from input rivers (and depth), respectively. Hydrochemical investigations and statistical analysis showed that the brines chemistry of Maharlu is mainly controlled by three processes: brine evaporative evolution, dissolution–precipitation and diagenetic evolution of secondary carbonates.     

Seasonally chemical weathering and CO<Subscript>2</Subscript> consumption flux of Lake Qinghai river system in the northeastern Tibetan Plateau

The major cation and anion compositions of waters from the Lake Qinghai river system (LQRS) in the northeastern Tibetan Plateau were measured. The waters were collected seasonally from five main rivers during pre-monsoon (late May), monsoon (late July), and post-monsoon (middle October). The LQRS waters are all very alkaline and have high concentrations of TDS (total dissolved solids) compared to rivers draining the Himalayas and the southeastern Tibetan Plateau. Seasonal variations in the water chemistry show that, except the Daotang River, the TDS concentration is high in October and low in July in the LQRS waters. The forward models were used to quantify the input of three main rivers (Buha River, Shaliu River, and Hargai River) from rain, halite, carbonates, and silicates. The results suggest that (1) atmospheric input is the first important source for the waters of the Buha River and the Shaliu River, contributing 36–57% of the total dissolved cations, (2) carbonate weathering input and atmospheric input have equal contribution to the Hargai River water, (3) carbonate weathering has higher contribution to these rivers than silicate weathering, and (4) halite is also important source for the Buha River. The Daotang River water is dominated by halite input owing to its underlying old lacustrine sediments. The water compositions of the Heima River are controlled by carbonate weathering and rainfall input in monsoon season, and groundwater input may be important in pre-monsoon and post-monsoon seasons. After being corrected the atmospheric input, average CO₂ drawdown via silicate weathering in the LQRS is 35 × 10³ mol/km² per year, with highest in monsoon season, lower than Himalayas and periphery of Tibetan Plateau rivers but higher than some rivers draining shields.     

Silica in Lake Superior: mass balance considerations and a model for dynamic response to eutrophication

The dissolved silica concentration in waters of Lake Superior probably is in a steady state because it is not influenced significantly by man, and the climate, topography and vegetation in the drainage area of the lake have been stable for the past 4000 years. Therefore the rate at which dissolved silica is introduced to the lake should equal the output rate.The primary inputs are: tributaries (4.1–4.6 × 10⁸kgSiO₂/yr), diffusion from sediment pore waters (0.21?0.78 × 10⁸kgSiO₂/yr) and atmospheric loading (0.26 × 10⁸kgSiO₂/yr). Silica is lost from the lake waters by: outflow through the St. Marys River, diatom deposition, adsorption onto particulates in the sediments, and authigenic formation of new silicate minerals. Tributary outflow accounts for less than one half the annual input of silica, and diatom deposition and silica adsorption withdraw less than 10% of the annual input. Therefore the formation of new silicate phases must be the dominant sink for dissolved silica in Lake Superior. The specific phases formed are not identified in the bottom sediments. X-ray diffraction studies suggest that smectite is one product, and amorphous ferroaluminum silicates may be another product.Mathematical modeling of the dissolved silica response to lake eutrophication suggests that the phosphate loading to Lake Superior would have to increase by about 250-fold to cause a silica depletion rate equal to that reported for Lake Michigan, assuming no change in the rate of upwelling of deep waters.     

太湖流域土壤重金属元素污染历史的重建:以Pb、Cd为例

太湖是位于长江下游的一个大型浅水湖泊,通过对4个代表太湖不同沉积环境的湖底沉积剖面的137Cs和210Pb沉积定年,重建太湖湖底沉积物和太湖来水流域土壤Cd、Pb的污染历史。结果显示:1980年以前,太湖底积物中Cd、Pb含量与流域内的自然背景含量相当,1980年以后,湖底沉积物中的Cd、Pb含量显著增高,这与我国大规模工业化进程的起始时间基本一致,推测工业化进程是湖底沉积物中Cd、Pb含量增加的主要原因。1900年以来太湖湖底沉积物中累积含有Cd和Pb分别为146t和25980t,其中苕溪来水提供的Cd和Pb分别为40t、6777t,宜溧河来水提供的Cd、Pb分别为36t、6023t,其他来水(洮、滆、运河)提供的Cd、Pb分别为71t、13179t,其他来水是太湖Cd、Pd累积的主要输入途径。Cd、Pb累积的高峰期为20世纪80—90年代,1980年以来,运河来水Cd、Pb的输出通量为28.26t、3419t;苕溪流域Cd、Pb的输出总量分别为13.70t、1585t,其中人为源的Cd、Pb为8.90t、610t,人为源输出的Cd、Pb通量占总输出量的64.96%和38.47%;宜溧河流域Cd、Pb的输出总量分别为10.09t、1063t,人为源的Cd、Pb分别6.96t和500t,人为源输出的Cd、Pb通量占总输出量的68.68%和47.08%,表明太湖流域人类活动所导致的Cd已超过自然剥蚀过程,因此削减工业化进程中的Cd、Pb排放总量,控制太湖运河来水的输出通量是改善太湖底积物Cd、Pb环境质量的关键措施。     

Modern sediments and sedimentary processes in Lake Rudolf (Lake Turkana) eastern Rift Valley, Kenya

Tertiary sediments around Lake Rudolf (now Lake Turkana) in the East African Rift Valley have yielded abundant palaeontological and palaeoanthropological remains. The present study provides a basis for interpreting the ancient lake environment and furthering our knowledge of rift valley lacustrine deposits. Bottom sediments in Lake Rudolf are fine-grained (average 71% clay) well laminated and have montmorillonite, kaolinite and illite as the principal clay minerals. The sediments are relatively poor in silica (40–45%) but rich in Fe₂O₃ (10%). Both mineral proportions and chemical composition change systematically over the area of the lake and delineate four sedimentological provinces: (1) iron-rich, silty kaolinitic muds (Omo Delta); (2) iron-rich, fine-grained montmorillonite muds (North Basin); (3) silty montmorillonite muds rich in Na₂O and K₂O (Central Delta); and (4) argillaceous calcite silts (South Basin). Omo Delta and North Basin sediments are derived from the volcanics of the Ethiopian plateau; the source of Central Delta sediments is the Precambrian metamorphic terrain of the rift valley margin; the South Basin has a restricted detrital input. The water in the lake is alkaline (pH 9.2) and moderately saline (TDS = 2500 p.p.m.). Comparisons with influent water from the Omo River indicate a 200-fold concentration for the lake water. Models based on equilibrium between sediments and water column account for most of the non-conservative chemical components in the lake water. Sedimentation rates are high (about 1 m per 1000 years) and the dominance of detrital sediments makes Lake Rudolf unusual in comparison with other closed-basin lakes in the African Rift Valley although some similarities with ancient rift valley deposits are suggested.     

Biogeochemical controls on reaction of sedimentary organic matter and aqueous sulfides in holocene sediments of Mud Lake, Florida

The distribution and quantity of organic sulfur and iron sulfur species were determined in the Holocene sediments from Mud Lake, Florida. The sediments of this shallow, sinkhole lake are characterized by high sulfur and organic carbon contents as well as active sulfate reduction. They record a shift from a basal peat (below 2 m) comprised of water lily-dominated organic matter to the present cyanobacterial/algal-dominated lake deposit (upper 1 m). This shift in depositional environment and subsequent organic matter source was accompanied by variation in the amount of reactive iron delivered to the sediments, which in turn influenced the type and extent of organic matter sulfurization. Extractable intramolecular organic sulfur is principally found as C₂₅ highly branched isoprenoid (HBI) thiolanes. Extractable polysulfide-linked lipids, determined by selective chemical cleavage with MeLi/MeI and analyzed as methylthioethers (MTE), are dominated by n-alkanes with sulfur attachments at position 1 and 2, as well as lower amounts of C₂₅ HBI-MTE. The δ¹³C values and carbon-chain length distribution of both series of n-alkylMTE indicate that they are derived from distinct biological precursors. Among the n-alkylMTE with sulfur attachment at position 1 there are three homologous series: one saturated and two with both cis and trans enethiol isomers. The identification of the enethiol in the sulfur-linked macromolecules indicates that n-alkylaldehydes are precursors lipids. The intervals of high concentration of bulk organic sulfur and sulfurized lipids coincide with the intervals of high mineral sulfur content (acid volatile sulfide and chromium reducible sulfur). We suggest that the main control on the enhanced addition of sulfur to the organic matter in Mud Lake was the increased formation of polysulfides during the reduction of iron hydroxides and the subsequent reaction of those polysulfides with mildly oxidized sedimentary organic matter.