Dissolved trace elements and heavy metals from the shallow lakes in the middle and lower reaches of the Yangtze River region,China

Dissolved trace elements and heavy metals of waters and sediments in the ten shallow lakes in the middle and lower reaches of the Yangtze River region were determined to identify their composition and spatial distribution, and to assess the extent of their environmentally detrimental effects by comparison with water and sediment quality guidelines. Results indicated that As and Pb were the main pollutants in lake waters and Mn and Hg the potential ones, while As, Cu and Pb were the main pollutants in lake sediments. Their spatial distribution indicated that Daye Lake was seriously polluted by metals, which was corroborated by cluster analysis. Higher concentrations of trace elements have been found in lakes downstream of the Yangtze River delta, and higher concentrations of metals have been recorded in sediments of upstream lakes, suggesting that metals in water were more sensitive to anthropogenic activities and that metals in sediment were mainly controlled by minerals. Correlation analyses demonstrated that there were stronger associations among metals in lake sediments than those in lake waters, and their good relationships suggested the common sources. Further research on the subject will help develop water quality management with the aim of restoring shallow lakes in the Yangtze River.     

Acidification and Trace Metals of Lakes in Taiwan

One hundred and eighty lakes, ponds and reservoirs in Taiwan, and the offshore islands have been investigated since 1985. Effects such as warming/cooling, mixing, photosynthesis and respiration on pH have been identified. These effects were found to be less profound than those resulting from the geology. Since there is little rain or lake water pH data available prior to 1970, it was necessary to use proxy data in order to ascertain the history of lake acidification. In this study, we present data based on diatoms in a sediment core collected from a lake in the remote subalpine region of southern Taiwan. The acidity of this lake water was found to have increased since 1900. We measured the concentrations of 55 chemical species in lake water samples. In addition, concentrations of 26 chemical species were obtained from sediments. Conductivity, alkalinity (HCO₃ ^?), most other major and minor chemical species, as well as the non sea-salt SO₄/Na ratio in lake water clearly decrease with elevation. Distribution of pH is similar, although the trend is less clear. Distribution of trace metals, however, shows a different trend as anthropogenic pollution, diagenetic reduction and lake acidification are at play.     

Distribution and isotopic composition of sulfur in lake sediments of northern Ontario

Sediments from unpolluted and highly polluted lakes in northern Ontario have been fractionated into acid volatile sulfide, HCl-soluble sulfur, elemental sulfur, pyrite sulfur, ester sulfate and carbon-bonded sulfur and the isotopic composition of each fraction determined. In general, reduced inorganic S constitutes 25–50% of the total S in the polluted surficial sediments, but is <20% in the unpolluted samples, with pyrite formation being a minor process of S diagenesis in lake sediment ecosystems. Organic S in the form of ester sulfate and carbon-bonded S predominates and both the C/S ratios and the isotopic data suggest that, in unpolluted lakes, plant detritus can be a major contributor of organic-S to the sediments. The depth profiles observed suggest that the more labile ester sulfate is diagenetically converted to the carbon-bonded form. For the polluted sediments from the Sudbury basin, the isotopic data suggest that (a) the elemental S is derived from the oxidation of acid volatile sulfide in the aerobic surficial sediments, and (b) the isotopically light reduced S species are incorporated into the organic material. S diagenesis in lake sediments generally results in the release of ³⁴S to the overlying water. The suggestion is made that sulfate concentrations over 5 mg/1 accompanied by an enrichment of surficial sediments with isotopically different S may signal significant inputs of pollutant S into the lake and its basin.     

Analysis of arsenic speciation in mine contaminated lacustrine sediment using selective sequential extraction,HR-ICPMS and TEM

In order to determine how As speciation in lacustrine sediment changes as a function of local conditions, sediment cores were taken from three lakes with differing hydrologic regimes and subjected to extensive chemical and TEM analysis. The lakes (Killarney, Thompson and Swan Lakes) are located within the Coeur d’ Alene River system (northern Idaho, USA), which has been contaminated with trace metals and As, from over 100 a of sulfide mining. Previous analyses of these lakebed sediments have shown an extensive amount of contaminant metals and As associated with sub-μm grains, making them extremely difficult to analyze using standard methods (scanning electron microscopy, X-ray diffraction). Transmission electron microscopy offers great advantages in spatial resolution and can be invaluable in determining As speciation when combined with other techniques. Data indicate that because of differences in local redox conditions, As speciation and stability is dramatically different in these lakes. Killarney and Thompson Lakes experience seasonal water-level fluctuations due to drawdown on a downstream dam, causing changes in O₂ content in sediment exposed during drawdown. Swan Lake has relatively constant water levels as its only inlet is dammed. Consequently, Killarney and Thompson Lakes show an increase in labile As-bearing phases with depth, while Swan Lake data indicate stable As hosts throughout the sediment profile. Based on these observations it can be stated that As in lakebed sediments is much less mobile, and therefore less bioavailable, when water is kept at a constant level.     

Modern carbon burial in Lake Qinghai,China

The quantification of carbon burial in lake sediments, and carbon fluxes derived from different origins are crucial to understand modern lacustrine carbon budgets, and to assess the role of lakes in the global carbon cycle. In this study, we estimated carbon burial in the sediment of Lake Qinghai, the largest inland lake in China, and the carbon fluxes derived from different origins. We find that: (1) The organic carbon burial rate in lake sediment is approximately 7.23 g m⁻² a⁻¹, which is comparable to rates documented in many large lakes worldwide. We determined that the flux of riverine particulate organic carbon (POC) is approximately 10 times higher than that of dissolved organic carbon (DOC). Organic matter in lake sediments is primarily derived from POC in lake water, of which approximately 80% is of terrestrial origin. (2) The inorganic carbon burial rate in lake sediment is slightly higher than that of organic carbon. The flux of riverine dissolved inorganic carbon (DIC) is approximately 20 times that of DOC, and more than 70% of the riverine DIC is drawn directly and/or indirectly from atmospheric CO₂. (3) Both DIC and DOC are concentrated in lake water, suggesting that the lake serves as a sink for both organic and inorganic carbon over long term timescales. (4) Our analysis suggests that the carbon burial rates in Lake Qinghai would be much higher in warmer climatic periods than in cold ones, implying a growing role in the global carbon cycle under a continued global warming scenario.     

The onset of anthropogenic activity recorded in lake sediments in the vicinity of the Horne smelter in Quebec,Canada: Sulfur isotope evidence

Contents and δ³⁴S values of several S compounds, enumerations of S-reducing bacteria (SRB) and Fe-reducing bacteria (IRB), and Fe, Pb and In concentrations were determined for ²¹⁰Pb-dated sediment cores from two lakes in Quebec, Canada. Both lakes are located approximately 70 km downwind of the Horne smelter and refinery in Rouyn-Noranda. Increases in Fe, Pb and In concentrations and a decrease in the δ³⁴S values of total S in both lake sediment cores coincide with the start-up of the smelter in 1927. The shift towards more negative δ³⁴S values was primarily caused by an increase in the extent of S isotope fractionation during bacterial (dissimilatory) SO₄ reduction due to SO₄ loading of the lakes after smelting began. Consequently, an enhanced accumulation of ³²S-enriched reduced inorganic S compounds is evident in the sediments. δ³⁴S values of organic S in the sediments decreased only slightly due to the smelter emissions between 1930 and 1980. Hence, due to the sulfide depositing mechanisms, S isotope ratios constitute a useful tracer recording the onset of S pollution in sediments of the two previously SO₄-limited lakes investigated. In contrast, total S concentrations alone are not reliable indicators for anthropogenic S loading in lake sediment records.     

Behavior of heavy metals in sulfide mine tailings and bottom sediment (Salair,Kemerovo region,Russia)

The given work focused on solving the problem of environmental geochemistry related to investigation of element speciation, their mobility, and migration in polluted areas. The purpose was to describe quantitatively migration, distribution, and redistribution of heavy metals by the example of the old tailings (Talmovaya sands) of the Lead Zinc Concentration Plant (Salair, Kemerovo region, Russia) and technogenic bottom sediments of the Malaya Talmovaya river. Contents of elements in the sulfide tailings range in the following limits: Zn: 1,100–27,000 ppm, Cd: 1.3–240 ppm, Pb: 0.01–0.81 ppm, Cu: 220–960 ppm, As: 15–970 ppm, Fe: 19,000–76,000 ppm, and Ba: 80,000–1,00,000 ppm. Element concentrations in the river sediment are proportional to the element contents in the sulfide tailings. Element speciations in the sulfide tailings and technogenic bottom sediments were investigated by the modified sequential extraction procedure. Chemical forms of heavy metals in pore water and surface water were calculated by WATEQ4F software. Principles of heavy metal migration in the sulfide tailings and technogenic bottom deposits were established. The obtained results about element species in the sulfide tailings and sediment explain the main principles of element migration and redeposition. In the mine waste and technogenic bottom deposits, there is vertical substance transformation with formation of geochemical barriers.     

Heavy metal and anionic contamination in the water and sediments in Al-Mujib reservoir,central Jordan

Sixty-five sediment samples and 25 water samples were collected from Al-Mujib reservoir, central Jordan, in order to investigate the heavy metal and ionic contamination assessment. Therefore, to achieve this aim, water and sediment samples were collected during winter and summer seasons (2007) from Al-Mujib reservoir and the areas surrounding it. The study shows that there are elevated levels of SO₄ ²⁻, Cl⁻ and Na⁺ in reservoir water, which might originate from anthropogenic activities in the reservoir catchment area. In addition, the reservoir water has higher total hardness (TH) values together with high Ca and Mg contents. This might be attributed to pH of reservoir water and the nature of the rocks exposed in the catchment area. The average levels of heavy metals in reservoir sediments are Fe = 14,888.1, Cu = 17.8, Zn = 88.6, Ni = 38.7, Cd = 4.4, Mn = 337.9 and Pb = 6.1 mg/kg, which are lower than that observed in Wadi Al-Arab reservoir, northern Jordan. The values of enrichment factor are Cd = 35.5, Ni = 3.02, Zn = 2.54, Cu = 1.26, Mn = 1.2 and Pb = 0.57; these values indicate that heavy metals in sediments of Al-Mujeb reservoir have a different anthropogenic incrimination inputs. The study showed that the sediments are polluted with Cd, relatively contaminated with Ni and Zn and uncontaminated with respect to Mn, Pb and Cu.     

Assessment of metal concentrations in lake sediments of southwest Japan based on sediment quality guidelines

Geochemical analysis of the bottom sediments of Lakes Banryoko, Onbe, Hamahara and Kijima in Shimane prefecture of southwest Japan was carried out to determine their metal concentrations, and to assess the potential for ecological harm by comparison with sediment quality guidelines. The work conducted includes water quality measurement, and analyses of trace and major elements and rare earth element (REE) of sediments. Results showed that water quality of the lakes contrasts slightly between their upper and lower parts. Average abundances of As, Pb, Zn, Cu, Ni, and Cr in Banryoko sediments were 27, 33, 90, 27, 25, and 46 ppm, respectively, compared to 31, 52, 175, 44, 44, and 75 ppm at Onbe, 11, 26, 96, 13, 13, and 35 ppm at Hamahara, and 24, 43, 193, 31, 12, and 30 ppm at Kijima. These concentrations exceeded the lowest effect level that has moderate impact on aquatic organisms as proposed by the New York State Department of Environmental conservation. Pb and Cu abundances are comparable to the Coastal Ocean Sediment Database threshold, while As and Zn exceed this value, indicating the concentrations of these metals are potentially toxic. Increases in the abundances of these metals in lake sediments are probably related to the reducing condition of the sediments, anthropogenic sources and surface soil erosion. The REE patterns of sediments in the study areas are broadly comparable to the average upper continental crust, but show some contrast between lakes due to differing source litho type. Significant positive correlations between Fe₂O₃ and As, Pb, Zn, and Cu were found in the sediments, suggesting these metals may be adsorbed on Fe oxides in the lake sediments.     

Water quality and sediment geochemistry in lakes of Yunnan Province, southern China

 Yungui Plateau lakes in southwestern China are economically important, although few have been studied previously. Water and sediments of 24 lakes throughout Yunnan Province were sampled in October 1994. We describe the chemical and physical characteristics of Yunnan lakes, and address effects of regional geology and human influences on water quality and sediment type. Water quality differs between deep Yunnan lakes of tectonic origin and shallow solution basins. Shallow lakes generally have higher nutrient concentrations and appear to be more susceptible to riparian disturbance than deeper lakes. Shallow lakes with high macrophyte standing crops, nevertheless, exhibit nutrient-poor waters. Principal ions Ca²⁺, Mg²⁺, and HCO₃ ^– reflect regional carbonate geology, except in Cheng Hai, which is a sodium bicarbonate lake. Specific conductance and δ¹⁸O are positively correlated, indicating that evaporation concentrates both solutes and ¹⁸O. Large, shallow lakes in southeastern Yunnan exhibit ¹⁸O-enriched waters because of substantial evaporation, whereas small, deep lakes are ¹⁸O-depleted. Lake waters are ¹⁸O-depleted in small, shallow basins that receive substantial rainwater input relative to their small volumes. ¹⁸O enrichment in Cheng Hai suggests that a recent 5-m water-level decline in this lake was caused by increased evaporation or diversion of freshwater inflow. Yunnan watersheds have undergone substantial deforestation, agricultural cultivation, soil erosion, and industrialization. Limnetic nutrient concentrations indicate that human activities have affected water quality. Organic matter content is low in sediments because of increased non-carbonate, clastic sediment yield from watersheds. Environmental policies are needed to balance ecological contraints with economic activities that impact water quality. Received: 1 July 1996 / Accepted: 2 October 1996     

Variations in the isotopic composition of molybdenum in freshwater lake systems

Variations in molybdenum isotopic composition, spanning the range of ∼ 2.3‰ in the terms of ⁹⁷Mo/⁹⁵Mo ratio, have been measured in sediment cores from three lakes in northern Sweden and north-western Russia. These variations have been produced by both isotopically variable input of Mo into the lakes due to Mo isotopic heterogeneity of bedrock in the drainage basins and fractionation in the lake systems due to temporal variations in limnological conditions. Mo isotope abundances of bedrock in the lake drainage basins have been documented by analysis of Mo isotope ratios of a suite of molybdenite occurrences collected in the studied area and of detrital fractions of the lake sediment cores. The median δ⁹⁷Mo value of the investigated molybdenites is 0.26‰ with standard deviation of 0.43‰ (n = 19), whereas the median δ⁹⁷Mo value of detrital sediment fractions from two lakes is − 0.40‰ with standard deviation of 0.36‰ (n = 15).The isotopic composition of Mo in the sediment cores has been found to be dependent on redox conditions of the water columns and the dominant type of scavenging phases. Hydrous Fe oxides have been shown to be an efficient scavenger of Mo from porewater under oxic conditions. Oxidative precipitation of Fe(II) in the sediments resulted in co-precipitation of Mo and significant authigenic enrichment at the redox boundary. In spite of a pronounced increase in Mo concentration associated with Fe oxides at the redox boundary the isotopic composition of Mo in this zone varies insignificantly, suggesting little or no isotope fractionation during scavenging of Mo by hydrous Fe oxides. In a lake with anoxic bottom water a chironomid-inferred reconstruction of O₂ conditions in the bottom water through the Holocene indicates that increased O₂ concentrations are generally associated with low δ⁹⁷Mo/⁹⁵Mo values of the sediments, whereas lowered O₂ contents of the bottom water are accompanied by relatively high δ⁹⁷Mo/⁹⁵Mo values, thus confirming the potential of Mo isotope data to be a proxy for redox conditions of overlying waters. However, it is pointed out that other processes including input of isotopically heterogeneous Mo and Mn cycling in the redox-stratified water column can be a primary cause of variations in Mo isotopic compositions of lake sediments.     

Assessment of branched GDGTs as temperature proxies in sedimentary records from several small lakes in southwestern Greenland

This study of five small (<3.0 ha) lakes in southwestern Greenland examines the veracity of branched glycerol dialkyl glycerol tetraethers (br GDGTs) as a temperature proxy in lacustrine systems. The proximity (<5 km) of the lakes suggests that their temperature history, and thus their br GDGT records, should be similar. Distributions of br GDGTs in (i) surface sediments from all five lakes, (ii) ¹⁴C-dated sediment cores from two lakes (Upper and Lower EVV Lakes) and (iii) soil samples from the area surrounding the lakes were examined. The temporal records of br GDGT-based temperature for the two cores exhibited both similarities and major discrepancies. The differences between the paleotemperature records for the two lakes suggest that br GDGTs are not solely soil-derived, reflecting air temperature, but also indicate an additional br GDGT contribution from another source. Among the broader suite of lake sediments, there was a strong correlation (R² 0.987) between br GDGT-based surface sediment temperatures and measured summer bottom water temperatures for the four lakes with hypoxic/anoxic bottom waters, including Upper EVV Lake. The correlation suggests production of br GDGTs by anaerobic bacteria within the bottom water and/or sediment–water interface, reflecting environmental temperature for the individual lakes and augmenting the uniform, soil-derived signal. Hence, assessment of br GDGTs in Greenland lake sediments provides evidence for their origin from anaerobic autochthonous bacteria and indicates that interpretation of lacustrine br GDGT-based paleotemperature records requires contextual knowledge of individual lake systems and potential source(s) of sedimentary br GDGTs.     

Sulfur isotope studies to quantify sulfate components in water of flooded lignite open pits – Lake Goitsche,Germany

A system of connected lignite mining pits (part of the former Goitsche mining complex, Germany) was flooded with river water between 1999 and 2002. A considerable accumulation of acid associated with oxidized sulfides in sediments was seen as a critical point for the development of the lake water. To characterize the components contributing to the supply of dissolved lake water SO₄ hydro-chemical and isotope investigations with respect to groundwater, pore water in the sulfide bearing sediments, river water and lake water were performed. δ³⁴S of pore water SO₄ that was dominated by oxidized pyrites ranges around −25‰ VCDT and differs strongly from river water SO₄ with about +4.4‰. Thus, interactions between lake water and sediments were particularly pronounced during the first phase of flooding. For this period, a more quantitative estimation of the SO₄ components in the lake water was difficult because of the heterogeneous SO₄ distributions between the different sub-basins of the lake and according to the flooding process itself. Later, a component separation was attempted following mixing of the whole lake, which first occurred in spring 2002. A very heterogeneous groundwater environment with respect to highly variable SO₄ concentrations and δ³⁴S values and changing interaction with the forming lakes proved to be one of the most important limitations in the calculations of the mixing.     

Biogeochemical reactive–diffusive transport of heavy metals in Lake Coeur d’Alene sediments

Decades of runoff from precious-metal mining operations in the Lake Coeur d’Alene Basin, Idaho, have left the sediments in this lake heavily enriched with toxic metals, most notably Zn, Pb and Cu, together with As. The bioavailability, fate and transport of these metals in the sediments are governed by complex biogeochemical processes. In particular, indigenous microbes are capable of catalyzing reactions that detoxify their environments, and thus constitute an important driving component in the biogeochemical cycling of these metals. Here, the development of a quantitative model to evaluate the transport and fate of Zn, Pb and Cu in Lake Coeur d’Alene sediments is reported. The current focus is on the investigation and understanding of local-scale processes, rather than the larger-scale dynamics of sedimentation and diagenesis, with particular emphasis on metal transport through reductive dissolution of Fe hydroxides. The model includes 1-D inorganic diffusive transport coupled to a biotic reaction network including consortium biodegradation kinetics with multiple terminal electron acceptors and syntrophic consortium biotransformation dynamics of redox front. The model captures the mobilization of metals initially sorbed onto hydrous ferric oxides, through bacterial reduction of Fe(III) near the top of the sediment column, coupled with the precipitation of metal sulfides at depth due to biogenic sulfide production. Key chemical reactions involve the dissolution of ferrihydrite and precipitation of siderite and Fe sulfide. The relative rates of these reactions play an important role in the evolution of the sediment pore-water chemistry, notably pH, and directly depend on the relative activity of Fe and SO₄ reducers. The model captures fairly well the observed trends of increased alkalinity, sulfide, Fe and heavy metal concentrations below the sediment–water interface, together with decreasing terminal electron acceptor concentrations with depth, including the development of anoxic conditions within about a centimeter below the lake bottom. This effort provides insights on important biogeochemical processes affecting the cycling of metals in Lake Coeur d’Alene and similar metal-impacted lacustrine environments.     

Geochemistry of Manasbal lake sediments,Kashmir: Weathering,provenance and tectonic setting

This paper presents a detailed sediment chemistry investigation of the Manasbal lake, Srinagar, Jammu and Kashmir, India, which is one of the high altitude lakes in the Kashmir valley. 22 lake floor sediment samples covering the entire lake were collected and analyzed for textural characteristics, CaCO₃, organic matter, TOC, TN contents, C/N ratio, major and trace element chemistry. These analyses were conducted to trace the provenance of the sediments. Textural parameters reveal that the lake sediments consist predominantly clay and silt fractions. The C/N ratio of the sediments indicates a mixed source of TOC, both autochthonous and allochthonous in origin. The log (Fe₂O₃/K₂O) Vs. log (SiO₂/ Al₂O₃) graph of the sediments discriminates the rock types of the catchment area that are Fe-shale, Fe-sand, wacke, shale and litharenite. The Chemical Index of Alteration (CIA) falls between 59.11 to 90.16% and Chemical Index of Weathering (CIW) between 63.97 to 99.68% and these values are higher than the Post-Archaean Australian Shale (PAAS), indicating moderate to highly chemically weathered lake floor sediments. Plagioclase Index of Alteration (PIA) values (60.74-99.63%) suggests the occurrence of plagioclase feldspars in the lake floor sediments. Geochemical characteristics signify a mixed-nature of provenance of the lake floor sediments due to the tectonic settings of the lake basin in a complex catchment area.     

Application of equilibrium partitioning approach to derive sediment quality criteria for heavy metals in a shallow eutrophic lake, Lake Chaohu, China

In this study, the equilibrium partitioning approach was used to derive the sediment quality criteria (SQC) recommended values of eight heavy metals (Cr, Cu, Pb, Zn, Cd, As, Fe and Mn) for surface sediments taken from Lake Chaohu. The concentration of the heavy metal in the interstitial water (C _IW) was determined by the film diffusion gradient technology to obtain the metal partitioning coefficient (K _P). Moreover, the metal fractionation of the sediments were analyzed using European Community Bureau of Reference sequential extraction procedure and the partitioning of bound phases including total organic carbon (TOC), grain sizes and acid volatile sulfide (AVS) were also investigated. The values of K _P for Cr, Cu, Pb, Zn, Cd, As, Fe and Mn were 3,924.84, 2,276.23, 17,811.30, 738.35, 10,986.54, 718.74, 5,875.34 and 341.20 L/kg, respectively. Sediment quality criteria were normalized on the basis of fine materials, AVS, TOC and the residual metals (M _R). SQC values for Cr, Cu, Pb, Zn, Cd, As, Fe and Mn based on Chinese surface water quality criteria were derived with the values of 78.53, 56.95, 362.93, 74.68, 23.90, 71.84, 3,546.53 and 68.42 mg/kg, respectively. The suggested SQC values in this study were compared SQCs from different countries and areas, which indicated SQCs from different countries or regions appeared to have great discrepancies attributed to the difference of the physical and chemical characteristics of sediments.     

Environmental pollution impact on water and sediments of Kumaun lakes, Lesser Himalaya, India: a comparative study

A study of the water and sediment chemistry of the Nainital, Bhimtal, Naukuchiyatal and Sattal Lakes of Kumaun, has shown that the water of these lakes are alkaline and that electrical conductivity, total dissolved solid and bicarbonate HCO ₃ ⁻ are much higher in Nainital than in the other three lakes. The weathering of limestone lithology and anthropogenic pollution, the latter due to the very high density of population in the Nainital valley, are the primary sources of enhanced parameters. The low pH of Nainital Lake water is due to low photosynthesis and enhanced respiration, increasing CO₂ in the water and the consequent enhancement of Ca²⁺ and HCO ₃ ⁻ . The dissolved oxygen in Nainital Lake is less compared to other lakes, indicating anoxic conditions developing at the mud–water interface at depth. The PO ₄ ³⁻ content in Nainital is higher (124 μg/l), showing an increasing trend over time leading to eutrophic conditions. The trace metals (Cu, Co, Zn, Ni, Mn, and Sr) are present in greater amounts in the water of Nainital Lake than in the other three lakes, though Fe and Cr are high in Bhimtal and Fe in Naukuchiyatal. The higher abundance is derived from the leaching of Fe–Mg from metavolcanic and metabasic rocks. Most of the heavy metals (Cr, Ni, Cu, Mn, Fe, Sr, and Zn) significantly enrich the suspended sediments of the lakes compared to the bed sediments which due to their adsorption on finer particles and owing to multiple hydroxide coating and organic content, except for Fe, which is enriched in the bed sediments. The high rate of sedimentation, 11.5 mm/year in Nainital, compared to Bhimtal with 4.70 mm/year, Naukuchiyatal with 3.72 mm/year, and Sattal with 2.99 mm/year, has resulted in shorter residence time, poor sorting of grains, and lesser adsorption of heavy metals, leading consequently, their depletion in the bed sediments of Nainital Lake.     

Geochemical and equilibrium trends in mine pit lakes

Chemical composition and equilibrium trends in mine pit lakes were examined to provide guidance for the application of geochemical models in predicting future lake water quality at prospective open pit mines. Composition trends show that elevated solute levels generally occur only at the extremes of acidic and alkaline pH conditions. Concentrations of cationic metals (Al, Cd, Cu, Fe, Mn, Pb, and Zn) are elevated only in acidic pit lakes, whereas anionic metalloids (As and Se) are generally elevated only in alkaline pit lakes. These trends are indicative of sulfide mineral oxidation and evapoconcentration for acidic and alkaline conditions, respectively.For nearly all pit lakes, SO₄ is the dominant solute, but is limited by gypsum solubility. Fluorite, calcite, and barite are also important solubility controls. Well-defined solubility controls exist for the major metals (Al, Fe, Mn), including jurbanite and alunite for Al, ferrihydrite for Fe, and manganite, birnessite, and, possibly, rhodochrosite for Mn. Determinations of definite controls for the minor metals are less distinct, but may include otavite for Cd, brochantite and malachite for Cu, cerrusite and pyromorphite for Pb, and hydrozincite and Zn silicates for Zn. Concentrations of As and Se appear to be limited only by adsorption, but this control is sharply diminished by increased pH and SO₄ concentration. In general, the concentrations of minor metals in pit lakes are not well represented by the theoretical solubilities of pure-phase minerals contained in the thermodynamic databases. Hence, modeling efforts will generally have to rely on empirical data on the leaching characteristics of pit wall-rocks to predict the concentrations of minor metals (Cd, Cu, Pb, Zn) in mine pit lakes.Methodologies for predicting pit lake water chemistry are still evolving. Geochemical and equilibrium trends in existing pit lakes can provide valuable information for guiding the development and application of predictive models. However, mineralogical studies of pit lake sediments, suspended particles, and alteration assemblages and studies of redox transformations are still needed to validate and refine the representations of geochemical processes in water quality models of mine pit lakes.     

Dinosterol δD values in stratified tropical lakes (Cameroon) are affected by eutrophication

In freshwater settings, dinosterol (4α,23,24-trimethyl-5α-cholest-22E-en-3β-ol) is produced primarily by dinoflagellates, which encompass various species including autotrophs, mixotrophs and heterotrophs. Due to its source specificity and occurrence in lake and marine sediments, its presence and hydrogen isotopic composition (δD) should be valuable proxies for paleohydrological reconstruction. However, because the purity required for hydrogen isotope measurements is difficult to achieve using standard wet chemical purification methods, their potential as a paleohydrological proxy is rarely exploited. In this study, we tested δD values of dinosterol in both particulate organic matter (POM) and sediments of stratified tropical freshwater lakes (from Cameroon) as a paleohydrological proxy, the lakes being characterized by variable degrees of eutrophication. In POM and sediment samples, the δD values of dinosterol correlated with lake water δD values, confirming a first order influence of source water δD values. However, we observed that sedimentary dinosterol was D enriched from ca. 19 to 54‰ compared with POM dinosterol. The enrichment correlated with lake water column conditions, mainly the redox potential at the oxic–anoxic interface (E_h OAI). The observations suggest that paleohydrologic reconstruction from δD values of dinosterol in the sediments of stratified tropical lakes ought to be sensitive to the depositional environment, in addition to lake water δD values, with more positive dinosterol δD values potentially reflecting increasing lake eutrophication. Furthermore, in lake sediments, the concentration of partially reduced vs. non-reduced C₃₄ botryococcenes, stanols vs. stenols, and bacterial (diploptene, diplopterol and ββ-bishomohopanol) vs. planktonic/terrestrial lipids (cholesterol, campesterol and dinosterol) correlated with E_h OAI. We suggest using such molecular proxies for lake redox conditions in combination with dinosterol δD values to evaluate the effect of lake trophic status on sedimentary dinosterol δD values, as a basis for accurately reconstructing tropical lake water δD values.