首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 765 毫秒
1.
Four 2–3 m sediment cores were taken at the sites on the periphery of mussel raft concentrations in the subtidal zone of the inner Ría de Vigo (Galicia, NW Spain) with a view to evaluate the potential risk to mariculture from sediment-borne trace elements (As, Cd, Cr, Cu, Mn, Ni, Pb and Zn). The distribution of each of these elements in reactive, organic, pyrite and silicate-bound fractions was determined at 64 samples, and these data were used to calculate the degree of trace metal pyritization (DTMP) of each metal/metalloid. In the top 10–20 cm, relatively oxic conditions led to As, Cd, Cu, Pb and Zn having large reactive fractions due to their association with Fe and Mn oxyhydroxides. At lower levels, anoxic conditions favoured by intense diagenesis led to the precipitation of trace metals and metalloids as sulphides, with or without association with pyrite. Particularly large pyrite fractions in the 20–100 cm layer are attributed to the organic matter of this layer being more marine in origin than that of deeper sediments. DTMP was greatest for Cu and As, and least for Pb, Zn and Cr. The risk of trace element toxicity in the event of disturbances instituting oxic conditions in these sediments is discussed.  相似文献   

2.
Pore water has been extracted from Boom Clay by mechanical squeezing. Clay cores were obtained from various boreholes, all drilled at the SCK·CEN domain (Mol, Belgium).In contrast to pore water collected from piezometers, high sulphate concentrations are measured in the squeezed pore water. The lowest sulphate concentrations (<60 mg/l) were measured in pore waters squeezed immediately after drilling. Higher sulphate concentrations were often measured in the pore water when the clay cores were preserved for some time (generally <500 mg/l SO42−, but sometimes up to 20,000 mg/l SO42−). Nevertheless, a relation between preservation time and sulphate content could not be retrieved. However, major ion concentrations were obviously correlated with the sulphate content in the squeezed waters. The observed evolution in chemical composition were explained by water–rock interactions considering the pyrite oxidation and the subsequent ion exchange and mineral dissolution reactions.  相似文献   

3.
Mariculture is an important economic activity in shallow marine areas of the Rías Baixas (Galicia, NW Spain). The maintenance of high product quality requires surveillance of environmental quality, including the risk of metal toxicity. In this study the redox status of intertidal sediments in the Bay of San Simón, and the risk of toxicity posed by their As, Cd, Cr, Cu, Mn, Ni, Pb and Zn contents, were evaluated by determination of operationally defined reactive, silicate-bound, organic and pyrite-related fractions of these elements and of Fe. The large silicate-bound fractions of most of these metals indicate their lithogenic origin; the main exception is Pb, which in all respects exhibits singular behaviour associated with its predominantly anthropogenic origin in a ceramics factory. In sediments with larger fine-grained particle contents, which are oxic only in the top few centimetres, greater proportions of the trace elements are present as sulphides or associated with sulphide minerals: the degree of pyritization of Fe (DOP) is 46% overall, and the pyrite fraction of some elements doubtless increases at the expense of the reactive fraction, most overall degrees of trace metal pyritization (DTMPs) lying in the range 10-50%. A decline in pyrite genesis at depths below about 18 cm in these sediments is attributed to the exhaustion of organic matter susceptible to metabolization by sulphide-generating bacteria. In coarse-grained, oxic sediments the oxidation of sulphides makes pyrite-related fractions very small, and reactive and silicate-bound fractions are negatively correlated; reactive fractions associated with Fe-Mn oxyhydroxides are large, and DOP and DTMPs are low (generally much lower than in mud-rich sediments), except for Pb. Most of the elements studied are mainly present in forms that are neither bioavailable nor potentially bioavailable, and so do not constitute a significant environmental threat. However, the high DTMPs of Cu and Pb indicate significant potential bioavailability, which should be taken into account in evaluations of environmental quality and the risk to bivalve cultures.  相似文献   

4.
The distributions of 16 polycyclic aromatic hydrocarbons (PAHs) were determined in the aqueous phase, suspended particulate matter (SPM), sediment, and pore water of the Daliao River Estuary in Liaodong Bay, Bohai Sea (China). Total PAH concentrations ranged from 139.16 to 1717.87 ng L−1 in surface water, from 226.57 to 1404.85 ng L−1 dry weight in SPM, from 276.26 to 1606.89 ng g−1 dry weight in sediments, and from 10.20 to 47.27 μg L−1 in pore water. PAH concentrations were at relatively moderate levels in water, SPM, sediment and pore water in comparison with those reported for other estuary and marine systems around the world. Sedimentary PAH concentrations decreased offshore owing to active deposition of laterally-transported river-borne particles. PCA analysis of the possible PAH source suggested petrogenic and pyrolytic PAH inputs in the studied region.  相似文献   

5.
A critical evaluation of literature values for the solubility products, K sp NBS = [Fe2+][HS–] Fe2+ HS– (H NBS + )–1, of various iron sulphide phases results in consensus values for the pKs of 2.95 ± 0.1 for amorphous ferrous sulphide, 3.6 ± 0.2 for mackinawite, 4.4 ± 0.1 for greigite, 5.1 ± 0.1 for pyrrhotite, 5.25 ± 0.2 for troilite and 16.4 ± 1.2 for pyrite.Where the analogous ion activity products have been measured in anoxic freshwaters in which there is evidence for the presence of solid phase FeS, the values lie within the range of 2.6–3.22, indicating that amorphous iron sulphide is the controlling phase. The single value for a groundwater of 2.65 (2.98 considering carbonate complexation) agrees. In seawater four values range between 3.85 to 4.2, indicating that mackinawite or greigite may be the controlling phase. The single low value of 2.94 is in a situation where particularly high fluxes of Fe (II) and S (–II) may result in the preferential precipitation of amorphous iron sulphide. Formation of framboidal pyrite in these sulphidic environments may occur in micro-niches and does not appear to influence bulk concentrations. Calculations show that the formation of Fe2S2 species probably accounts for very little of the iron or sulphide in most natural waters. Previously reported stability constants for the formation of Fe (HS)2 and (Fe (HS)3)– are shown to be suspect, and these species are also thought to be negligible in natural waters. In completely anoxic pore waters polysulphides also have a negligible effect on speciation, but in tidal sediments they may reach appreciable concentrations and lead to the direct formation of pyrite. Concentrations of iron and sulphide in pore waters can be controlled by the more soluble iron sulphide phase. The change in the IAP with depth within the sediment may reflect ageing of the solid phase or a greater flux of Fe (II) and S (–II) nearer the sediment surface. This possible kinetic influence on the value of IAPs has implications for their use in geochemical studies involving phase formation.  相似文献   

6.
Annual variations in concentrations of Fe forms in the bottom water (0–70 cm from the bottom, by layers), pore water, and in solid phase of silts (25 cm, by layers) of the Krasnovidovo Pool channel area of the Mozhaisk Reservoir are studied. A drastic increase in the concentration and ratio of Fesusp/Fedis in the water layer 0–20 cm from the bottom is detected. Fe(II) dominates in dissolved and suspended forms. The concentrations of Fe(III) reaching 2–3 mg/l were for the fist time revealed in the pore water of silts (Eh ～ ?120 mV). The factors responsible for this phenomenon are discussed. Fe flux from sediments is tentatively assessed as 0.2–0.6 mg Fe m2/day.  相似文献   

7.
The artificial reservoir Lagoa da Pampulha in central Brazil has been increasingly affected by sediment deposition and pollution from urban and industrial sources. This study investigates water chemistry and heavy metal concentrations and their fractionation in the lake sediment using ICP-OES, ICP-MS, and XRD analyses. Fractionation analysis was done by sequential extraction under inert gas as well as after oxidation. The lake exhibits a permanent stratification with an oxygen-free hypolimnion below 2 m depth. Nutrient concentrations are enriched for phosphorous components (SRP, PO4). In the sediment it was not possible to detect oxygen. Carbon, sulfur, and most of the analyzed heavy metals are enriched in the top sediment layer with a pronounced downward decrease, indicating the presence of an anthropogenic influence. Statistical analysis, including correlations and a Principal Component Analysis (PCA) of depth-related total concentration data, helps to distinguish presumably anthropogenic heavy metals from geogenic components. Some samples with high element concentrations in the sediment also show elevated concentrations in their pore water. Analyses of element distribution between sediment and pore water suggest a strong bonding of heavy metals to the anoxic sediment. The trend towards elevated solubility in the pore water of oxidized samples is clear for most of the analyzed elements. Fractionation analysis reveals characteristic associations of selected elements to specific mineral bonding forms. In addition, it indicates that the behavior of heavy metals in the sediment is strongly influenced by organic substances. These substances provide buffering against oxidation, acidification, and metal release. The high nutrient loading causes reducing conditions in the lake sediment. These conditions trigger the accumulation of sediments rich in S2−, which stabilizes the fixation of heavy elements. In the future, care must be taken to reduce the supply of contaminants and to prevent the release of heavy metals from sediments dredged for remediation purposes.  相似文献   

8.
Limited information exists on one of the mechanisms governing sediment input to streams: streambank erosion by ground water seepage. The objective of this research was to demonstrate the importance of streambank composition and stratigraphy in controlling seepage flow and to quantify correlation of seepage flow/erosion with precipitation, stream stage and soil pore water pressure. The streambank site was located in Northern Mississippi in the Goodwin Creek watershed. Soil samples from layers on the streambank face suggested less than an order of magnitude difference in vertical hydraulic conductivity (Ks) with depth, but differences between lateral Ks of a concretion layer and the vertical Ks of the underlying layers contributed to the propensity for lateral flow. Goodwin Creek seeps were not similar to other seeps reported in the literature, in that eroded sediment originated from layers underneath the primary seepage layer. Subsurface flow and sediment load, quantified using 50 cm wide collection pans, were dependent on the type of seep: intermittent low‐flow (LF) seeps (flow rates typically less than 0·05 L min?1), persistent high‐flow (HF) seeps (average flow rate of 0·39 L min?1) and buried seeps, which eroded unconsolidated bank material from previous bank failures. The timing of LF seeps correlated to river stage and precipitation. The HF seeps at Goodwin Creek began after rainfall events resulted in the adjacent streambank reaching near saturation (i.e. soil pore water pressures greater than ?5 kPa). Seep discharge from HF seeps reached a maximum of 1·0 L min?1 and sediment concentrations commonly approached 100 g L?1. Buried seeps were intermittent but exhibited the most significant erosion rates (738 g min?1) and sediment concentrations (989 g L?1). In cases where perched water table conditions exist and persistent HF seeps occur, seepage erosion and bank collapse of streambank sediment may be significant. Copyright © 2007 John Wiley & Sons, Ltd.  相似文献   

9.
Both evergreen and deciduous forests (Efs and Dfs) are widely distributed under similar climatic conditions in tropical monsoon regions. To clarify the hydraulic properties of the soil matrix in different forest types and their effects on soil water storage capacity, the soil pore characteristics (SPC) were investigated in Ef and Df stands in three provinces in Cambodia. Soils in the Ef group were characterized in common by large amounts of coarse pores with moderate pore size distribution and the absence of an extremely low Ks at shallow depths, compared to Df group soils. The mean available water capacity of the soil matrix (AWCsm) for all horizons of the Ef and Df group soils was 0·107 and 0·146 m3 m?3, respectively. The mean coarse pore volume of the soil matrix (CPVsm) in the Ef and Df groups was 0·231 and 0·115 m3 m?3, respectively. A water flow simulation using a lognormal distribution model for rain events in the early dry season indicated that variation in SPC resulted in a larger increase in available soil water in Ef soils than in Df soils. Further study on deeper soil layers in Ef and each soil type in Df is necessary for the deeper understanding of the environmental conditions and the hydrological modelling of each forest ecosystem. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

10.
Waters and sediments from the Potiguar Basin (NE Brazilian coast) were investigated for the presence and nature of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons. The region receives treated produced waters through a submarine outfall system serving the industrial district. The total dispersed/dissolved concentrations in the water column ranged from 10-50 ng L−1 for ∑16PAH and 5-10 μg L−1 for total aliphatic hydrocarbons. In the sediments, hydrocarbon concentrations were low (0.5-10 ng g−1for ∑16PAH and 0.01-5.0 μg g−1 for total aliphatic hydrocarbons) and were consistent with the low organic carbon content of the local sandy sediments. These data indicate little and/or absence of anthropogenic influence on hydrocarbon distribution in water and sediment. Therefore, the measured values may be taken as background values for the region and can be used as future reference following new developments of the petroleum industry in the Potiguar Basin.  相似文献   

11.
During the high water season, the flooding reduces environmental heterogeneity in aquatic ecosystems of the Pantanal wetland. When the water level recedes, lakes and channels are formed as individual systems. Therefore, we expected the spatial heterogeneity during the low water phase resulting in changes on biological communities leading to high phytoplankton abundance, biomass and diversity within and between habitats. To test this hypothesis, we analyzed eight freshwater systems (five oxbow lakes, two channels, and the river) during the low water period. Phytoplankton biomass, abundance, diversity (alpha, beta, gamma) and diversity metrics as richness (species per sample), Shannon diversity (H′) and evenness were measured in all systems along with nutrient concentrations, zooplankton and bacteria abundances. We found 97 species as gamma diversity. The alpha diversity was unexpectedly low in comparison to most other South American floodplain systems (38 species in river, 24 in channels and 29 in lakes). Also, the systems are relatively similar in composition (beta diversity, 28%). Connectivity differences between systems highlighted differences in phytoplankton abundance and biomass (fresh weight) ranging from 1428 ind mL−1 (river) to 3710 ind mL−1 (lakes) and from 0.71 mg L−1 (river) to 2.9 mg L−1 (lakes), respectively. However, our results did not indicate significant differences in phytoplankton species richness between the systems during the low water. Our main conclusions are that local factors may be responsible for changes on phytoplankton community and the time of isolation during the low water phase was not sufficient to promote changes in phytoplankton diversity between the habitats.  相似文献   

12.
Kawah Putih is a summit crater of Patuha volcano, West Java, Indonesia, which contains a shallow, 300 m-wide lake with strongly mineralized acid–sulfate–chloride water. The lake water has a temperature of 26–34°C, pH=<0.5–1.3, Stot=2500–4600 ppm and Cl=5300–12 600 ppm, and floating sulfur globules with sulfide inclusions are common. Sulfur oxyanion concentrations are unusually high, with S4O62−+S5O62−+S6O62−=2400 – 4200 ppm. Subaerial fumaroles (<93°C) on the lake shore have low molar SO2/H2S ratios (<2), which is a favorable condition to produce the observed distribution of sulfur oxyanion species. Sulfur isotope data of dissolved sulfate and native sulfur show a significant 34S fractionation (ΔSO4–Se of 20‰), probably the result of SO2 disproportionation in or below the lake. The lake waters show strong enrichments in 18O and D relative to local meteoric waters, a result of the combined effects of mixing between isotopically heavy fluids of deep origin and meteoric water, and evaporation-induced fractionation at the lake surface. The stable-isotope systematics combined with energy-balance considerations support very rapid fluid cycling through the lake system. Lake levels and element concentrations show strong seasonal fluctuations, indicative of a short water residence time in the lake as well.Thermodynamic modeling of the lake fluids indicates that the lake water is saturated with silica phases, barite, pyrite and various Pb, Sb, Cu, As, Bi-bearing sulfides when sulfur saturation is assumed. Precipitating phases predicted by the model calculations are consistent with the bulk chemistry of the sulfur-rich bottom sediments and their identified mineral phases. Much of the lake water chemistry can be explained by congruent rock dissolution in combination with preferential enrichments from entering fumarolic gases or brines and element removal by precipitating mineral phases, as indicated by a comparison of the fluids, volcanic rocks and lake bed sediment.Flank springs on the mountain at different elevations vary in composition, and are consistent with local rock dissolution as a dominant factor and pH-dependent element mobility. Discharges of warm sulfate- and chloride-rich water at the highest elevation and a near-neutral spring at lower level may contain a small contribution of crater-lake water. The acid fluid-induced processes at Patuha have led to the accumulation of elements that are commonly associated with volcano-hosted epithermal ore deposits. The dispersal of heavy metals and other potentially toxic elements from the volcano via the local drainage system is a matter of serious environmental concern.  相似文献   

13.
Natural concentrations of 238U and δ234U values were determined in estuarine surface waters and pore waters of the Amazon and Fly (Papua New Guinea) Rivers to investigate U transport phenomena across river-dominated land–sea margins. Discharge from large, tropical rivers is a major source of dissolved and solid materials transported to the oceans, and are important in defining not only oceanic mass budgets, but also terrestrial weathering rates.On the Amazon shelf, salinity-property plots of dissolved organic carbon, pH and total suspended matter revealed two vastly contrasting water masses that were energetically mixed. In this mixing zone, the distribution of uranium was highly non-conservative and exhibited extensive removal from the water column. Uranium removal was most pronounced within a salinity range of 0–16.6, and likely the result of scavenging and flocculation reactions with inorganic (i.e., Fe/Mn oxides) and organic colloids/particles. Removal of uranium may also be closely coupled to exchange and resuspension processes at the sediment/water interface. An inner-shelf pore water profile indicated the following diagenetic processes: extensive (1 m) zones of Fe(III)—and, to a lesser degree, Mn(IV)—reduction in the absence of significant S(II) concentrations appeared to facilitate the formation of various authigenic minerals (e.g., siderite, rhodocrosite and uraninite). The pore water dissolved 238U profile co-varied closely with Mn(II). Isotopic variations as evidenced in δ234U pore waters values from this site revealed information on the origin and history of particulate uranium. Only after a depth of about 1 m did the δ234U value approach unity (secular equilibrium), denoting a residual lattice bound uranium complex that is likely an upper-drainage basin weathering product. This suggests that the enriched δ234U values represent a riverine surface complexation product that is actively involved in Mn–Fe diagenetic cycles and surface complexation reactions.In the Fly River estuary, 238U appears to exhibit a reasonably conservative distribution as a function of salinity. The absence of observed U removal does not necessarily imply non-reactivity, but instead may record an integration of concurrent U removal and release processes. There is not a linear correlation between δ234U vs. 1/238U that would imply simple two component mixing. It is likely that resuspension of bottom sediments, prolonged residence times in the lower reaches of the Fly River, and energetic particle–colloid interactions contribute to the observed estuarine U distribution. The supply of uranium discharged from humid, tropical river systems to the sea appears to be foremost influenced by particle/water interactions that are ultimately governed by the particular physiographic and hydrologic characteristics of an estuary.  相似文献   

14.
Depth profiles of solute chemistry and sulfate isotopic compositions are presented for groundwater and pore water in a sequence of Quaternary glacial outwash sediments. Sand units show evidence for hydraulic connection to the surface and thus modern sources of solutes. Finer‐grained sediments show a general pattern of increasing solute concentrations with depth, with sulfate derived from ancient rainwater and pyrite oxidation in the soil/drift. In these sediments sulfate has undergone bacterial sulfate reduction (BSR) to produce biogenic sulfide. In clay sediments, with d10 ≤ 1·6 µm, high concentrations of sulfate and acetate now co‐exist, implying that BSR is inhibited. The correlation with smaller sediment grain size indicates that this is due to pore size exclusion of the sulfate reducing bacteria. Mechanical restriction of microbial function thus provides a fundamental limitation on microbial respiration in buried clay‐rich sediments, which acts as a control on the chemical evolution of their pore waters. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

15.
To remove chromate from a wastewater, a porous permeable reactive barrier system (PRBS), using pyrite and biotite, was adapted. This study included bench‐scale column experiments to evaluate the efficiency of the PRBS and investigate the reaction process. The total chromium concentration of the effluent from the biotite and pyrite columns reached the influent concentration of 0·10 mM after passing through more than 150 pore volumes (PVs) and 27 PVs respectively, and remained constant thereafter. The CrVI concentration in the effluent from the biotite column became constant at about 0·08 mM , accounting for approximately 80% of the influent concentration, after passing through 200 PVs. Moreover, in the pyrite column, the CrVI concentration remained at about 0·01 mM , 10% of the input level, after passing through 116 PVs. This shows that both columns maintained their levels of chromate reduction once the CrVI breakthrough curves (BTCs) had reached the steady state, though the steady‐state output concentration of total chromium had reached the influent level. The variances of the iron concentration closely followed those of the chromium. The observed data for both columns were fitted to the predicted BTCs calculated by CXTFIT, a program for estimating the solute transport parameters from experimental data. The degradation coefficient µ of the total chromium BTCs for both columns was zero, suggesting the mechanisms for the removal of chromate limit the µ of the CrVI BTCs. The CrVI degradation of the pyrite column (6·60) was much greater than that of the biotite column (0·27). In addition, the CrVI retardation coefficient R of the pyrite column (253) was also larger than that of the biotite column (125). The R values for the total chromium BTCs from both columns were smaller than those of the CrVI BTC. Whereas the total chromium BTC for the pyrite column showed little retardation (1·5), the biotite column showed considerable retardation (80). The results for the 900 °C heat‐treated biotite column were analogous to those of the control column (quartz sand). This suggests that the heat‐treated biotite played no role in the retardation and removal of hexavalent chromium. The parameters of the heat‐treated biotite were calculated to an R of 1·2 and µ of 0·01, and these values confirmed quantitatively that the heated biotite had little effect on the transport of CrVI. These solute transport parameters, calculated by CXTFIT from the data obtained from the column tests, can provide quantitative information for the evaluation of bench‐ or field‐scale columns as a removal technology for CrVI in wastewater or contaminated groundwater. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

16.
Water is a limiting factor for life in the McMurdo Dry Valleys (MDV), Antarctica. The active layer (seasonally thawed soil overlying permafrost) accommodates dynamic hydrological and biological processes for 10–16 weeks per year. Wetted margins (visually wetted areas with high moisture content) adjacent to lakes and streams are potential locations of great importance in the MDV because of the regular presence of liquid water, compared with the rest of the landscape where liquid water is rare. At 11 plots (four adjacent to lakes, seven adjacent to streams), soil particle size distribution, soil electrical conductivity, soil water content and isotopic signature, width of the wetted margin, and active layer thaw depth were characterised to determine how these gradients influence physicochemical properties that determine microbial habitat and biogeochemical cycling. Sediments were generally coarse‐grained in wetted margins adjacent to both lakes and streams. Wetted margins ranged from 1·04 to 11·01 m in average length and were found to be longer at lakeside sites than streamside. Average thaw depths ranged from 0·12 to 0·85 m, and were found to be deepest under lake margins. Lake margins also had much higher soil electrical conductivity, steeper topographic gradients, but more gradual soil moisture gradients than stream margins. Patterns of soil water δ18O and δD distribution indicate capillary action and evaporation from wetted margins; margin pore waters generally demonstrated isotopic enrichment with distance from the shore, indicating evaporation of soil water. Lake margin pore waters were significantly more negative in DXS (DXS = δD‐8δ18O) than streamside pore waters, indicating a longer history of evaporation there. Differences between lake and stream margins can be explained by the more consistent availability of water to lake margins than stream margins. Differences in margin characteristics between lakes and streams have important consequences for the microbial habitat of these margins and their functional role in biogeochemical cycling at these terrestrial–aquatic interfaces. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

17.
地震荷载作用下发生滑坡的滑动带通常由粗颗粒与细颗粒组成。滑带土的动力性质及动孔隙水压力的发展对边坡的稳定性至关重要。对掺细料砾石混合土进行动三轴试验来探讨细料(粒径小于0.5mm)含量对砾石(粒径6~20mm)混合土的动孔压特性的影响,进行细料含量为0%、20%和40%的三组试样的动三轴试验,采用固结围压为100kPa、固结应力比为1.0、频率为1.0Hz,施加轴向动应力分别为0.50、0.55、0.60和0.65kN,得到动孔压的变化规律。试验发现:(1)相同激振力作用下,随着细料含量的增加,动孔隙水压力增长速度逐渐变缓;相同细料含量时,随着激振力的增大,动孔隙水压力增长速度变快。(2)激振力较大和细料含量较少时,动孔隙水压力在较少的振次下达到较大值并趋于稳定。(3)细料含量为20%的砾石混合土试样在试验终止时的振动次数最大,细料含量为40%的砾石混合土在试验终止时的振动次数最小。(4)当细粒含量为0%和20%时,试验终止时最终的孔压都可以接近固结围压;当细粒含量为40%,激振力较大时,试验终止时最终的孔压才接近固结围压,而激振力较小时最终的孔压远远没有达到固结围压。  相似文献   

18.
The ‘Chicken Creek’ artificial catchment area, Welzow-South, E Germany, created to study processes and structures of initial ecosystem development, discharges into a small experimental lake (A=3805 m2, V=3992 m3, zmax=2.4 m). This lake was man-made in 2005 and filled by natural surface runoff until January 2006. In summer 2006 and 2008, the actual development of sediments and the evolution of the phosphorus (P) cycle were studied. 19.7% of the original lake volume was filled by sediment within the first 3 years. A fine-grained sediment representing silt (6.3-63 μm) accumulated at high accretion rates at the deepest point (200 mm a−1, 0-24 mm week−1) due to massive erosion in the catchment. The sediment is low in organic matter (2.5-5.2%) and total P (TP, 0.31-0.97 mg g−1). Low amounts of P associated with degradable organic matter and surplus of metal hydroxides (Fe:P∼40, Al:P∼20) favor an efficient P binding and low dissolved P concentrations in pore water (1-107 μg l−1). Hence, the mineral sediment quality and the low rates of P release (0.06 mg m−2 d−1) revealed that a lake at an initial stage of development has essentially no sedimentary P cycle compared to eutrophic shallow lakes. However, the increasing emersed and submersed macrophyte growth will control further lake succession by intensifying the internal nutrient cycling. The macrophytes drive the evolution of a sedimentary P cycle by mobilizing and translocating P, by accumulating carbon and thus by stimulating microbial and redox processes.  相似文献   

19.
Observations are presented on dilution and dispersion rates of ballast water discharged under normal operational conditions at the semi-enclosed port of Goderich, Ontario. The ballast water was tagged with Rhodamine-WT dye and microscopic magnetically-attractive tracer particles. Maximum concentrations of dye immediately after discharge were diluted to 1-5% of initial ballast tank concentrations, and within 3 days had decreased to less than 0.1% of initial concentrations. Inside the harbor, there was 10-20% of the ballast water still present after 2 days, consistent with a flushing rate of 0.8-1.15 day−1. Magnetic particles were collected up to 7.5 km outside the harbor after one day, consistent with a dilution factor of order 105 outside the harbor. The results of this study are discussed in the context of ballast water discharge standards proposed by the International Maritime Organization to minimize the introduction of aquatic nonindigenous species through ships’ ballast water and sediments.  相似文献   

20.
Climate factors play critical roles in controlling chemical weathering, while chemically weathered surface material can regulate climate change. To estimate global chemical weathering fluxes and CO2 balance, it is important to identify the characteristics and driving factors of chemical weathering and CO2 consumption on the Tibetan Plateau, especially in glaciated catchments. The analysis of the hydro-geochemical data indicated that silicate weathering in this area was inhibited by low temperatures, while carbonate weathering was promoted by the abundant clastic rocks with fresh surfaces produced by glacial action. Carbonate weathering dominated the riverine solute generation (with a contribution of 58%, 51%, and 43% at the QiangYong Glacier (QYG), the WengGuo Hydrological Station (WGHS), and the lake estuary (LE), respectively). The oxidation of pyrite contributed to 35%, 42%, and 30% of the riverine solutes, while silicate weathering contributed to 5%, 6%, and 26% of the riverine solutes at the QYG, WGHS, and LE, respectively. The alluvial deposit of easily weathering fine silicate minerals, the higher air temperature, plant density, and soil thickness at the downstream LE in comparison to upstream and midstream may lead to longer contact time between pore water and mineral materials, thus enhancing the silicate weathering. Because of the involvement of sulfuric acid produced by the oxidation of pyrite, carbonate weathering in the upstream and midstream did not consume atmospheric CO2, resulting in the high rate of carbonate weathering (73.9 and 75.6 t km−2 yr−1, respectively, in maximum) and potential net release of CO2 (with an upper constraint of 35.6 and 35.2 t km−2 yr−1, respectively) at the QYG and WGHS. The above results indicate the potential of the glaciated area of the Tibetan Plateau with pyrite deposits being a substantial natural carbon source, which deserves further investigation.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号