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1.
《Applied Geochemistry》2006,21(11):1837-1854
Total dissolved and total particulate Hg mass balances were estimated during one hydrological period (July 2001–June 2002) in the Thur River basin, which is heavily polluted by chlor-alkali industrial activity. The seasonal variations of the Hg dynamics in the aquatic environment were assessed using total Hg concentrations in bottom sediment and suspended matter, and total and reactive dissolved Hg concentrations in the water. The impact of the chlor-alkali plant (CAP) remains the largest concern for Hg contamination of this river system. Upstream from the CAP, the Hg partitioning between dissolved and particulate phases was principally controlled by the dissolved fraction due to snow melting during spring high flow, while during low flow, Hg was primarily adsorbed onto particulates. Downstream from the CAP, the Hg partitioning is controlled by the concentration of dissolved organic and inorganic ligands and by the total suspended sediment (TSS) concentrations. Nevertheless, the particulate fluxes were five times higher than the dissolved ones. Most of the total annual flux of Hg supplied by the CAP to the river is transported to the outlet of the catchment (total Hg flux: 70 μg m−2 a−1). Downstream from the CAP, the bottom sediment, mainly composed of coarse sediment (>63 μm) and depleted in organic matter, has a weak capacity to trap Hg in the river channel and the stock of Hg is low (4 mg m−2) showing that the residence time of Hg in this river is short. 相似文献
2.
B,As, and F contamination of river water due to wastewater discharge of the Yangbajing geothermal power plant,Tibet, China 总被引：5，自引：0，他引：5
Thermal waters from the Yangbajing geothermal field, Tibet, contain high concentrations of B, As, and F, up to 119, 5.7 and
19.6 mg/L, respectively. In this paper, the distribution of B, As, and F in the aquatic environment at Yangbajing was surveyed.
The results show that most river water samples collected downstream of the Zangbo River have comparatively higher concentrations
of B, As, and F (up to 3.82, 0.27 and 1.85 mg/L, respectively), indicating that the wastewater discharge of the geothermal
power plant at Yangbajing has resulted in B, As, and F contamination in the river. Although the concentrations of B, As, and
F of the Zangbo river waters decline downstream of the wastewater discharge site due to dilution effect and sorption onto
bottom sediments, the sample from the conjunction of the Zangbo River and the Yangbajing River has higher contents of B, As,
and F as compared with their predicted values obtained using our regression analysis models. The differences between actual
and calculated contents of B, As, and F can be attributed to the contribution from upstream of the Yangbajing River. Water
quality deterioration of the river has induced health problems among dwellers living in and downstream of Yangbajing. Effective
measures, such as decontamination of wastewater and reinjection into the geothermal field, should be taken to protect the
environment at Yangbajing. 相似文献
3.
西藏羊八井地热电厂产生的高氟废水直接排入了流经羊八井热田的藏布曲（河）。利用离子色谱仪（IC）测定了藏布曲水样的氟浓度;通过浸提实验提取了藏布曲河床沉积物中的总氟和各种存在形态的氟,并确定了其含量。藏布曲河水的氟浓度明显受到地热废水排放的影响,河床沉积物中水溶态氟和可交换态氟的分布也与地热电厂排污口的位置有明显的对应关系。然而,河床沉积物中的铁锰结合态氟、有机束缚态氟、残余态氟和总氟的分布与地热废水排放无显著联系,表明地热废水来源氟在进入藏布曲后主要向河床沉积物中的水溶态氟和可交换态氟转化。藏布曲河床沉积物是地热废水来源氟的一个汇。 相似文献
4.
《Applied Geochemistry》2006,21(3):515-527
Dissolved and particulate Hg fluxes in the Lot–Garonne–Gironde fluvial-estuarine system were obtained from observation of daily discharge and suspended particulate matter (SPM) concentrations. In addition to the measurements of the total dissolved (<0.45 μm) and particulate Hg (>0.45 μm), called HgTD and HgTP respectively, the dissolved inorganic Hg species (HgRD) were determined monthly. Geochemical background values for HgTP in sediments and SPM were similar to crustal values and to typical concentrations in SPM of non-contaminated river systems, respectively. The Riou Mort watershed already known as the origin of important historical polymetallic (e.g., Cd, Zn) pollution was identified as an important Hg point source. In the downstream Lot River, Hg concentrations were clearly higher than those in other moderately contaminated systems. The mean relative contribution of HgRD to HgTD in the Lot River and in the Garonne River was close to 25% and 50%, respectively, and showed no correlation with water discharge or SPM concentration. Depending on the origin and nature of SPM, HgTP concentrations were correlated or not with particulate organic C (POC). Maximum HgTP concentrations were measured in samples containing low POC concentrations and were attributed to sediment resuspension. In contrast, high POC concentrations (6–17%) during algal blooms were associated with low/moderate HgTP concentrations (<0.5 mg kg−1) at different sites, suggesting that Hg concentrations in fluvial phytoplankton may be limited by bioavailability of dissolved Hg and/or physiologically controlled Hg accumulation. Mercury was mostly (up to 98%) transported in the particulate phase with estimated annual Hg fluxes at the outlet of the Lot River system ranging from 35 to 530 kg a−1 for the past decade. The minimum anthropogenic component (58–84% of total Hg fluxes) could not be explained by present Riou Mort point source contributions, suggesting important Hg release from contaminated sediment as a major source and from downstream point sources (e.g., coal-fired power plants and/or metal processing industries). HgTP concentrations and fluxes were strongly related to hydrologic variations and were clearly increased by riverbed dredging during lock construction. Therefore, the estimated Hg stocks in the Lot River sediment (5–13 tons) represent an important potential Hg source for the downstream fluvial-estuarine system. 相似文献
5.
The pollution and deterioration of most important vital rivers in the Katanga region, Democratic Republic of Congo (DRC) are mainly due to the discharge of untreated industrial effluents as well as to the mining and artisanal mineral exploitation activities. In this study, the concentrations of metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Mo, Ag, Sn, and Pb) and major elements (Na, Mg, and K) in mining effluents, water and sediment samples of two main rivers of the district of Kolwezi (Katanga, DRC) were subjected to analysis by Inductive Coupled Plasma-Mass Spectroscopy (ICP-MS). The results showed that, in general, the metal concentrations in the sampling sites from the mining effluent and river waters exceed largely the World Health Organization and the Aquatic Quality Guidelines for the Protection of Aquatic Life recommendation limits. The highest metal concentrations in water and sediment samples were detected surrounding the mining effluents discharge. In the surface sediments of Luilu River, the values of 47,468 and 13,199 mg kg−1 were observed for Cu and Co, respectively. For the sediment samples from Musonoie River, the maximum values of 370.8 and 240.6 mg kg−1 for Cu and Co, respectively were observed. The results of this study suggest that the mining effluents being discharged into the rivers and the accumulation of pollutants in sediments might represent a source of toxicity for aquatic living organisms and could pose significant human health risks. The measures to establish a monitoring program and the application of wastewater treatment techniques to the mining effluents prior to discharge are recommended to reduce the load of contaminants into the receiving systems. 相似文献
6.
The Yellow, Yangtze and Pearl Rivers supply over 90% of the sediment flux from China to the western Pacific Ocean. Trends and abrupt changes in the water discharge and sediment load of the three rivers were examined and compared based on data updated to the year 2011 at the seasonal and annual scales. The total water discharge from the three rivers shows a statistically insignificant decreasing trend with a rate of 0.62 × 109 m3/a, and the total sediment load shows a statistically significant decreasing trend at a rate of 31.12 × 106 t/a from the 1950s to 2011. The water discharge of the entire Yellow River and the upstream portion of the Yangtze River shows significant decreasing trends, and that of the mid-lower stream of Yangtze River and the entire Pearl River shows insignificant trends. The sediment loads in the three river basins all show significant decreasing trends at the annual and seasonal scales, and a dramatic decrease in the 2000s resulted in a more obvious decreasing trend over the studied period. From the 1950s to the 2000s, the contribution of sediment flux from the Yellow River to the ocean decreased from 71.8% to 37.0%, and the contributions of the Yangtze and Pearl Rivers increased from 24.2% and 4.0% to 53.0% and 10.0%, respectively. Inter-annual variations in water discharge and sediment load were affected by climate oscillations, such as the El Niño/Southern Oscillation, and the long-term decreasing trend in sediment load was primarily caused by human activities. Dam constructions and soil conservation projects were the major causes of sediment reduction. From the 1970s to the 2000s, the decrease in total sediment load from the three rivers caused by climate change and human activities was 2.24 × 108 t/a (23.0%) and 7.5 × 108 t/a (77.0%), respectively. In the coming decades, the sediment flux from the three rivers into the sea will decrease further with intensifying human activities, resulting in many challenges for the management of river basins and river deltas. 相似文献
7.
Many studies have proposed that silicic acid and phosphate (PV) can displace arsenic sorbed to iron oxides leading to elevated As concentrations in aquatic systems. While surface complexation models are adept at quantifying sorption to synthetic oxides in laboratory systems their application to complex natural systems remains challenging. In this study we provide a systematic approach to developing a robust use of models for understanding AsV distribution in natural systems in which hydrated iron oxides are the main adsorptive phase. The Waikato River provides a useful laboratory for this work because it contains high H4SiO4, AsV and PV loadings due to geothermal and agricultural inputs. A 15 min oxalate extraction and a 48 h ethylenediaminetetraacetic acid (EDTA) extraction of river sediment contained the same ratios of As:Fe, P:Fe and Si:Fe. Both of these extracts target the poorly ordered iron oxide phases (typically ferrihydrite) and by following the release of elements over time in the EDTA extraction it was possible to demonstrate that the extracted As, P, and Si were associated with the ferrihydrite. This demonstrates for the first time that a single oxalate extraction can quantify ferrihydrite sorbed H4SiO4, As and PV and provides a basis to quantify the role of these ligands in inhibiting AsV sorption to sediments. The measured concentrations of ferrihydrite sorbed AsV, PV and H4SiO4 for the Waikato River suspended sediment allow for the informed selection of appropriate model parameters for applying the Diffuse Layer Model to the system. In this way it was possible to quantify the effect of the individual components in the river water on AsV sorption. This study provides an explanation for the observation that the proportion of sorbed As in the Waikato River is generally significantly lower than that observed in rivers closer to the world average concentrations. More generally the study provides a method to quantify the role of individual water chemistry components on AsV distribution in natural systems. 相似文献
8.
Dissolved and particulate Zn and Ni concentrations were determined at 76 locations along the Yangtze River basin from the headwaters to the estuary during flood and dry seasons. Spatial and temporal variations of Zn and Ni were investigated and six major source zones were identified. The Three Gorges Dam (TGD) blocked most of the suspended loads and extremely low concentration of Zn and Ni were observed downstream of the dam. Dissolved (ranging from 0.062 to 8.0 μg L−1) and particulate (ranging from 12 to 110 mg kg−1) Ni showed similar levels of concentrations during flood and dry seasons, whereas dissolved (ranging from 0.43 to 49 μg L−1) and particulate (ranging from 54 to 1100 mg kg−1) Zn were slightly and much lower in the flood season than dry season, respectively. This was attributed to the increased water discharge during the flood season causing a dilution effect and sediment resuspension. In the flood season, average concentrations of Zn and Ni were higher in the main channel than in tributaries, due to soil erosion and mining activities providing the dominant inputs. The situation was opposite in the dry season, attributed to the contribution of municipal sewage, industrial activities, and waste disposal. During the flood season, dissolved Zn and Ni concentrations were negatively correlated with pH. Water and suspended particulate matter (SPM) from the upper reaches, middle reaches, and lower reaches of the Yangtze River were characterized by their Zn and Ni concentrations. The Panzhihua, Nanling and Tongling mining areas were considered as the most important source zones of particulate Zn and Ni. The Chongqing region, Wuhan region and the Yangtze River Delta provided most of the dissolved Zn and Ni inputs into the river. Annual net flux of Zn (10–72 × 105 kg a−1) and Ni (5.0–19 × 105 kg a−1) in each source zone were estimated according to their respective influent and effluent fluxes. Contributions of the source zones to Zn and Ni transport decreased from the upper reaches to the lower reaches. 相似文献
9.
《Applied Geochemistry》2006,21(11):1955-1968
Elemental Hg–Au amalgamation mining practices are used widely in many developing countries resulting in significant Hg contamination of surrounding ecosystems. The authors examined for the first time Hg contamination in air, water, sediment, soil and crops in the Tongguan Au mining area, China, where elemental Hg has been used to extract Au for many years. Total gaseous Hg (TGM) concentrations in ambient air in the Tongguan area were significantly elevated compared to regional background concentrations. The average TGM concentrations in ambient air in a Au mill reached 18,000 ng m−3, which exceeds the maximum allowable occupational standard for TGM of 10,000 ng m−3 in China. Both total and methyl-Hg concentrations in stream water, stream sediment, and soil samples collected in the Tongguan area were elevated compared to methyl-Hg reported in artisanal Au mining areas in Suriname and the Amazon River basin. Total Hg concentrations in vegetable and wheat samples ranged from 42 to 640 μg kg−1, all of which significantly exceed the Chinese guidance limit for vegetables (10 μg kg−1) and foodstuffs other than fish (20 μg kg−1). Fortunately, methyl-Hg was not significantly accumulated in the crops sampled in this study, where concentrations varied from 0.2 to 7.7 μg kg−1. 相似文献
10.
Qaidam Basin is a hyperarid inland basin with an area of 121 × 103 km2 located on the northern Tibetan Plateau. Today, one fourth of the basin is covered by playas and hypersaline lakes. Nearly 80% of brine lithium found in China is contained in four salt lakes: Bieletan (BLT), DongTaijinaier (DT), XiTaijinaier (XT) and Yiliping (YLP). In the past decade, great attention was paid to improving the technology for the extraction of lithium from the brine deposits, but studies on origin and mode of formation of the brine deposits remained limited. Our recent investigations found that: (1) ~ 748.8 t of lithium was transported annually into the lower catchment of the four salt lakes via the Hongshui–Nalinggele River (H–N River), the largest river draining into the Qaidam Basin, (2) Li+-rich brines are formed only in salt lakes associated with inflowing rivers with Li+ concentrations greater than 0.4 mg/L, and (3) the water Li+ concentration is positively correlated with both the inflowing river and the associated subsurface brine, including saline lakes with low lithium concentrations. These findings clearly indicate that long-term input of Li+ from the H–N River controls the formation of lithium brine deposits. Here we determine that the source of the lithium is from hydrothermal fields where two active faults converge in the upper reach of the Hongshui River. The hydrothermal fields are associated with a magmatic heat source, as suggested by the high Li+ and As3 + content water from geysers. Based on the assumption of a constant rate of lithium influx, we estimate that the total reserves of lithium were likely formed since the postglacial period. Our data indicate that lithium reserves in each of the four salt lakes depend on the influx of Li+-bearing water from the H–N River. The data also suggest that during the progradation of the alluvial Fan I, the H–N River drained mostly into the BLT salt lake until the Taijinaier River shifted watercourse to the north and began to feed the salt lakes of the DT, XT and YLP, alongside with the Fan II progradation. The inference is consistent with stratigraphic evidence from the sediment cores of the four salt lakes. One of the major findings of our work is the importance of the contrasting hydroclimatic conditions between the high mountains containing ice caps and the terminal salt lakes. The greater than 4000 m of relief in the watershed enables a massive amount of ions, such as K+, to be weathered and transported together with detrital material from the huge, relatively wet alpine regions to the hyperarid terminal basins, where intense evaporation rapidly enriches the lake water, resulting in evaporite deposition and associated K+- and Li+-rich brine deposits. 相似文献
11.
《Applied Geochemistry》2005,20(11):1985-2002
Elevated levels of dissolved arsenic (∼300 μg L−1) have been detected beneath and in groundwater plumes extending away from a closed landfill in southern Maine. This study sought to determine the source of arsenic to the aquifer, the processes responsible for arsenic mobilization, and to evaluate the effectiveness of remediation efforts that have occurred at this site. The As appears to originate in the natural (glacial) aquifer solids, which contain ∼5 mg kg−1 As on a dry weight basis. This conclusion is supported by the relatively uniform distribution of As in sediment samples, results of laboratory batch incubation experiments, and comparisons with groundwaters in nearby wetlands, which also have high levels of dissolved As that do not appear to originate within the landfill. The As is mobilized in the subsurface by strongly reducing conditions beneath the landfill and in nearby wetlands. In the aquifer beneath the landfill, the average oxidation–reduction potential (ORP) is −95 mV (Eh + 105 mV), and these reducing conditions were primarily induced by landfill leachate. Remediation efforts at this site have included installation of a low permeability clay cap; groundwater extraction, oxidation, and re-injection; and subsurface oxidation by injection of magnesium peroxide. The natural source of arsenic within the aquifer solids, coupled with widespread reducing conditions, has severely limited the effectiveness of these interventions on groundwater arsenic concentrations. 相似文献
12.
Trace element geochemistry was studied in geothermal fluids in Iceland. The major and trace element compositions of hot springs, sub-boiling, and two-phase (liquid and vapor) wells from 10 geothermal areas were used to reconstruct the fluid composition in the aquifers at depth. Aquifer fluid temperatures ranged from 4 to 300 °C, pH values between 4.5 and 9.3, and fluids typically contained total dissolved solids <1000 ppm, except in geothermal areas that have seawater and seawater-meteoric water mixtures. Trace alkali elements Li, Rb and Cs are among the most mobile elements in aquifer fluids, with concentrations in the range of <1 ppb to 3.49 ppm Li, <0.01 to 57 ppb Cs, and <1 ppb to 3.77 ppm Rb. Their chemistry is thought to be dominated by rock leaching and partitioning into Na- and K-containing major alteration minerals. Arsenic, Sb, Mo and W are typically present in concentrations in the range of 1–100 ppb. They are relatively mobile, yet Mo may be limited by molybdenite solubility. The alkaline earth elements Ba and Sr are quite immobile with concentrations in the range of <0.1–10 ppb Ba and <1–100 ppb Sr in the dilute fluids, but up to 5.9 ppm Ba and 8.2 ppm Sr in saline fluids. These elements show a systematic relationship with Ca, possibly due to substitution for Ca in Ca-containing major alteration minerals like calcite, epidote and anhydrite. Incorporation into major Ca-minerals may also be important for Mn. Many metals including Fe, Cr, Ni, Zn, Cu, Co, Pb and Ag have low mobility and concentrations, typically <1 ppb for Ag, Cd, Co, Cr, Cu, Ni, and Pb, <10 ppb for Zn and < 100 ppb for Fe, although for some metals higher concentrations are associated with saline fluids. Based on the metals assessed, saturation is approached with respect to many sulfide minerals and in some cases oxide minerals but Cu, Ni and Pb minerals are slightly but systematically undersaturated, and Ag phases significantly undersaturated. Evaluation of mineral-fluid equilibria for these metals is problematic due to their low concentrations, problems associated with assessing the aqueous species distribution by thermodynamic calculations, and uncertainties concerning the exact minerals possibly involved in such reactions. Reaction path calculations, poor comparison of concentrations measured in the samples collected at the wellhead and published downhole data as well as boiling, cooling and mass precipitation calculations suggest removal of many metals due to changes upon depressurization boiling and conductive cooling of the aquifer fluids as they ascend in wells. These results imply that processes such as mass precipitation upon fluid ascent may be highly important and emphasize the importance of considering mass movement in geothermal systems. 相似文献
13.
A detailed investigation of the fluvial geochemistry of the Han River system allows to estimate the rates of chemical weathering and the consumption of CO2. The Han River drains approximately 26,000 km2 and is the largest river system in South Korea in terms of both water discharge and total river length. It consists of two major tributaries: the North Han River (NHR) and the South Han River (SHR). Distinct differences in basin lithology (silicate vs. carbonate) between the NHR and SHR provide a good natural laboratory in which to examine weathering processes and the influence of basin geology on water quality. The concentrations of major elements and the Sr isotopic compositions were obtained from 58 samples collected in both summer and winter along the Han River system in both 2000 and 2006. The concentrations of dissolved loads differed considerably between the NHR and SHR; compared with the SHR, the NHR had much lower total dissolved solids (TDS), Sr, and major ion concentrations but a higher Si concentration and 87Sr/86Sr ratio. A forward model showed that the dissolved loads in the NHR came primarily from silicate weathering (55 ± 11%), with a relatively small portion from carbonates (30 ± 14%), whereas the main contribution to the dissolved loads in the SHR was carbonate weathering (82 ± 3%), with only 11 ± 4% from silicates. These results are consistent with the different lithologies of the two drainage basins: silicate rocks in the NHR versus carbonate rocks in the SHR. Sulfuric acid derived from sulfide dissolution in coal-containing sedimentary strata has played an important role in carbonate weathering in the SHR basin, unlike in the NHR basin. The silicate weathering rate (SWR) was similar between the NHR and SHR basins, but the rate of CO2 consumption in the SHR basin was lower than in the NHR basin due to an important role of sulfuric acid derived from pyrite oxidation. 相似文献
14.
Pedo-sedimentological fieldwork were carried out in the Lajia Ruins within the Guanting Basin along the upper Yellow River valley. In the eolian loess-soil sections on the second river terrace in the Lajia Ruins, we find that the land of the Qijia Culture (4.20–3.95 ka BP) are fractured by several sets of earthquake fissures. A conglomerated red clay covers the ground of the Qijia Culture and also fills in the earthquake fissures. The clay was deposited by enormous mudflows in association with catastrophic earthquakes and rainstorms. The aim of this study is to provide a luminescence chronology of the sediment stratigraphy of the Lajia Ruins. Eight samples were taken from an eolian loess-soil section (Xialajia section) in the ruins for optically stimulated luminescence (OSL) dating. The OSL ages are in stratigraphic order and range from (31.94 ± 1.99) ka to (0.76 ± 0.02) ka. Combined OSL and 14C ages with additional stratigraphic correlations, a chronological framework is established. We conclude that: (1) the second terrace of the upper part of Yellow River formed 35.00 ka ago, which was followed by the accumulation of the eolian loess-soil section; and (2) the eolian loess-soil section is composed of the Malan Loess of the late last glacial (MIS-2) and Holocene loess-soil sequences. 相似文献
15.
《Applied Geochemistry》1998,13(3):293-304
Distributions of 15 elements with depth in two sediment cores from Puck Bay in the Gulf of Gdansk show that Ag, Cd, Pb, Zn and possibly Cu and Ni are anthropogenically enriched in the sediments there. The concentrations of these elements decrease sharply with depth in the sediment column and the elements are preferentially enriched in the <2 μm size fraction of the sediment. The sequence of element enrichment depends on whether the enrichment factor (EF) and the anthropogenic factor (AF) are used to calculate the element enrichment. By contrast, the anthropogenic elements show no systematic decrease in concentration with depth in a sediment core taken from near the mouth of the Vistula River. This reflects the higher sedimentation rate there such that the entire upper 20 cm of the core was deposited during the major, post-war period of industrialization in Poland. In addition, these elements are enriched in the 2–63 μm fraction compared to the <2 μm fraction in these sediments. This suggests that the heavy metals are mainly adsorbed on Fe oxyhydroxide particles with diameters greater than 2 μm at the hydrological front where Vistula river water mixes with brackish Baltic water. It appears that heavy-metal pollution of sediments in parts of Puck Bay may be greater than that near the mouth of the Vistula River which may reflect, in part, the higher sedimentation rate near the mouth of the Vistula River. The mode of incorporation of heavy-metals into the sediments in the two areas may also be different. 相似文献
16.
Documenting whether surface water catchments are in net chemical mass balance is important to understanding hydrological systems. Catchments that export significantly greater volumes of solutes than are delivered via rainfall are not in hydrologic equilibrium and indicate a changing hydrological system. Here an assessment is made of whether a saline catchment in southeast Australia is in chemical mass balance based on Cl. The upper reaches of the Barwon River, southeast Australia, has total dissolved solids, TDS, concentrations of up to 5860 mg/L and Cl concentrations of up to 3370 mg/L. The high river TDS concentrations are due to the influxes of groundwater with TDS concentrations of up to 68,000 mg/L. Between 1989 and 2011, the median annual Cl flux from the upper Barwon catchment was 17.8 × 106 kg (∼140 kg/a/ha). This represents 340–2230% of the annual Cl input by rainfall to the catchment. Major ion and stable isotope geochemistry indicate that the dominant source of solutes in the catchment is evapotranspiration of rainfall, precluding mineral dissolution as a source of excess Cl. The upper Barwon catchment is not in chemical mass balance and is a net exporter of solutes. The chemical imbalance may reflect the transition within the last 100 ka from an endorheic lake system where solutes were recycled producing shallow groundwater with high TDS concentrations to a better drained catchment. Alternatively, a rise in the regional water table following land clearing may have increased the input of groundwater with high TDS concentrations to the river system. 相似文献
17.
《Applied Geochemistry》2005,20(8):1546-1559
Total Hg concentrations and Hg speciation were determined in bottom sediments of Marano lagoon to investigate the consequences of Hg phases on fish farms and shellfish cultivation areas. Mercury phases were separated into cinnabar (HgS) and non-cinnabar compounds, via a thermo-desorption technique, in surface and core sediments; both of which had been contaminated by industrial wastes and mining activity residues. The former are due to an industrial complex, which has been producing cellulose, chlor-alkali and textile artificial fibres since 1940. Processing and seepage wastewaters, which were historically discharged into the Aussa-Corno river system and therefore into the lagoon, have been significantly reduced since 1984 due to the construction of wastewater treatment facilities. The second source is the Isonzo River, which has been the largest contributor of Hg into the northern Adriatic Sea since the 16th century due to Hg mining at the Idrija mine (western Slovenia). Red cinnabar (HgS) derived from the mining area is mostly stable and insoluble under current environmental conditions. In contrast, organically bound Hg, such as Hg bound to humic acids, has the potential to be transformed into bioavailable Hg compounds (for example, methylmercury). The presence of the two Hg forms permitted each Hg source to be quantified. It also allowed the areas with the highest risk of Hg contamination from Hg-rich sediment to be identified; thus potentially avoiding the transfer of Hg from the sediment into the water column and eventually into living biota. The results show that Hg Enrichment Factors in bottom sediments exceed values of 10 and cinnabar dominates the central sector near the main tidal channel where tidal flux is more effective. Non-cinnabar compounds were found to be enriched in fine grained material and organic matter. In fact, up to 98% of total Hg at the Aussa-Corno river mouth and in the inner margin of the basin occurred in an organic form. This evidence, combined with the high contents of total Hg (4.1–6.6 μg g−1 and EF > 10) measured in surface sediments, suggest that Hg in Marano lagoon is involved in biogeochemical transformations (e.g., methylation). 相似文献
18.
Ronald L. Bruhn Francis H. Brown Patrick N. Gathogo Bereket Haileab 《Journal of African Earth Sciences》2011,59(2-3):295-312
The distribution of hominin fossil sites in the Turkana Basin, Kenya is intimately linked to the history of the Omo River, which affected the paleogeography and ecology of the basin since the dawn of the Pliocene. We report new geological data concerning the outlet channel of the Omo River between earliest Pliocene and final closure of the Turkana Basin drainage system in the latest Pliocene to earliest Quaternary. Throughout most of the Pliocene the Omo River entered the Turkana Basin from its source in the highlands of Ethiopia and exited the eastern margin of the basin to discharge into the Lamu embayment along the coast of the Indian Ocean. During the earliest Pliocene the river’s outlet was located in the northern part of the basin, where a remnant outlet channel is preserved in basalts that pre-date eruption of the Gombe flood basalt between 4.05 and 3.95 Ma. The outlet channel was faulted down to the west prior to 4.05 Ma, forming a natural dam behind which Lake Lonyumun developed. Lake Lonyumun was drained between 3.95 and 3.9 Ma when a new outlet channel formed north of Loiyangalani in the southeastern margin of the Turkana Basin. That outlet was blocked by Lenderit Basalt lava flows between 2.2 and 2.0 Ma. Faulting that initiated either during or shortly after eruption of the Lenderit Basalt closed the depression that is occupied by modern Lake Turkana to sediment and water.Several large shield volcanoes formed east of the Turkana Basin beginning by 2.5–3.0 Ma, volcanism overlapping in time, but probably migrating eastward from Mount Kulal on the eastern edge of the basin to Mount Marsabit located at the eastern edge of the Chalbi Desert. The mass of the volcanic rocks loaded and depressed the lithosphere, enhancing subsidence in a shallow southeast trending depression that overlay the Cretaceous and Paleogene (?) Anza Rift. Subsidence in this flexural depression guided the course of the Omo River towards the Indian Ocean, and also localized accumulations of lava along the margins of the shield volcanoes. Lava flows at Mount Marsabit extended across the Omo River Valley after 1.8–2.0 Ma based on estimated ages of fossils in lacustrine and terrestrial deposits, and possibly by as early as 2.5 ± 0.3 Ma based on dating of a lava flow. During the enhanced precipitation in latest Pleistocene and earliest Holocene (11–9.5 ka) this flexural depression became the site of Lake Chalbi, which was separated from Lake Turkana by a tectonically controlled drainage divide. 相似文献
19.
《Applied Geochemistry》2006,21(10):1760-1780
Sulfide-rich mine tailings in Adak that are exposed to weathering cause acid mine drainage characterized by low pH (2–4) and high SO4 (up to 800 mg L−1). Surface water, sediment and soil samples collected in this study contain higher concentrations of As, Cu, Fe and Zn, compared to the target and/or intervention limits set by international regulatory agencies. In particular, high As concentrations in water (up to 2900 μg L−1) and sediment (up to 900 mg kg−1) are of concern. There is large variability in trace element concentrations, implying that both physical (grain size) and chemical factors (pH, secondary phases as sulfides, Al-oxides or clay minerals) play an important role in their distribution. The low pH keeps the trace elements dissolved, and they are transported farther downstream. Trace element partition coefficients are low (log Kd = 0.3–4.3), and saturation indices calculated with PHREEQC are <0 for common oxide and sulfidic minerals. The sediment and soil samples indicate an enhanced pollution index (up to 17), and high enrichment factors for trace elements (As up to 38,300; Zn up to 800). Finally, leaves collected from different plant types indicate bioaccumulation of several elements (As, Al, Cu, Fe and Zn). However, some of the plants growing in this area (e.g., Salix, Equisétum) are generally resistant to metal toxicity, and hence, liming and phytoremediation could be considered as potential on-site remediation methods. 相似文献
20.
Arsenic species including arsenite, arsenate, and organic arsenic were measured in the porewaters collected from Poyang Lake, the largest freshwater lake of China. The vertical distributions of dissolved arsenic species and some diagenetic constituents [Fe(II), Mn(II), S(−II)] were also obtained in the same porewater samples in summer and winter. In sediments the concentration profiles of total As and As species bound to Fe–Mn oxyhydroxides and to organic matter were also determined along with the concentrations of Fe, Mn and S in different extractable fractions. Results indicate that, in the summer season, the concentrations of total dissolved As varying from 3.9 to 55.8 μg/L in sediments were higher than those (5.3–15.7 μg/L) measured in the winter season, while the concentrations of total As species in the solid phase varied between 10.97 and 25.32 mg/kg and between 7.84 and 30.52 mg/kg on a dry weight basis in summer and winter, respectively. Seasonal profiles of dissolved As suggest downward and upward diffusion, and the flux of dissolved As across the sediment–water interface (SWI) in summer and winter were estimated at 3.88 mg/m2 a and 0.79 mg/m2 a, respectively. Based on porewater profiles and sediment phase data, the main geochemical behavior of As was controlled by adsorption/desorption, precipitation and molecular diffusion. The solubility and migration of inorganic As are controlled by Fe–Mn oxyhydroxides in summer whereas they appear to be more likely controlled by both amorphous Fe–Mn oxyhydroxides and sulfides in winter. A better knowledge of the cycle of As in Poyang Lake is essential to a better management of its hydrology and for the environmental protection of biota in the lake. 相似文献