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1.
《Geochimica et cosmochimica acta》1999,63(19-20):3321-3336
Dissolved and particulate trace metal (Al, Cd, Cu, Pb, and Zn) concentrations were determined over a 21 month time period at four streamwater sites in the Pinelands (New Jersey, USA), a coastal plain region characterized by low-pH waters and highly weathered soils. Al and Zn were also determined at two sites over a 5 day period following a major precipitation event. In the Batsto River (pH 4.4–6.3), a representative Pinelands stream draining a largely forested watershed moderately impacted by agriculture, discharge-weighted mean concentrations of dissolved metals were (in nM): Al = 4610; Cd = 0.39; Cu = 4.6; Pb = 1.0; and Zn = 149. Dissolved Cd, Cu, and Zn in the undeveloped Bass River (pH 4.1–4.8) are in a similar range, but Pb concentration is 2–3 times greater. Dissolved metals show highly significant positive correlations to discharge, and weaker inverse relationships to pH over both the long- and short-term time series. Overall, seasonal and short-term variability in dissolved metal concentrations is most consistent with control by hydrologic flow path changes during high discharge, when shallow groundwaters mobilize anthropogenic metals stored in near-surface soil horizons and bypass potential metal removal processes in bordering wetlands. The data also suggest that in-stream metal removal driven by summertime biological productivity may further reduce low-discharge metal concentrations, as a secondary effect. For these metals, the particulate fraction is generally minor, and variations in solution/particle partitioning are unimportant to spatial/temporal variations dissolved concentrations, except for Pb. Estimates of atmospheric input can account for riverine fluxes of these metals, and suggest that Zn retention is minimal in this system, while Pb, Cu and Cd are more strongly retained. The positive relationship between discharge and metals concentration, and the unusually high concentrations in Pinelands streams compared to other world rivers, suggest that riverine effects on metals distributions in the estuary and nearby coastal ocean will be measurable and strongly seasonal.  相似文献   

2.
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.  相似文献   

3.
杨小平 《第四纪研究》2002,22(2):97-104
本文阐述了巴丹吉林沙漠丘间地湖泊及其周围浅层地下水的水化学特征。在研究地区湖泊中的TDS变化范围较大,介于1.2g/L和398.2g/L之间。微咸湖泊属于Na(Ca)(Mg)Cl(SO4)(HCO3)类型,而含盐量高的湖泊则属于Na(K)Cl(CO3)(SO4)类型。文章根据同位素分析结果,提出了浅层地下水年龄都较年轻的观点。结合对古湖岸地貌与沉积的研究,文章还指出巴丹吉林沙漠地区湖泊在全新世发生过明显变化,湖水矿化度的增高和水域面积的快速萎缩是由于全新世中期以来出现的干旱化所造成的。  相似文献   

4.
波浪扰动对太湖底泥磷释放影响模拟   总被引：7，自引：0，他引：7       下载免费PDF全文
为揭示波浪扰动对湖泊底泥磷释放的影响,在波浪水槽中模拟了不同波高情况下扰动对水体、水土界面、底泥间隙水的磷、溶解氧等的影响.结果显示,在大波扰动下,沉积物大量悬浮,水体总磷随之增加,溶解性磷增加却不显著;波浪扰动显著增加了水体和沉积物界面的溶解氧浓度,并增加了溶解氧在沉积物的侵蚀深度;波浪扰动降低了沉积物表层10 cm内间隙水中的磷浓度,而10 cm以下沉积物中间隙水中磷浓度基本保持不变.研究表明,波浪扰动可迅速增加水体中颗粒态的营养盐,但是对于溶解态营养盐,尤其是水体中活性磷浓度的影响,则受沉积物性质、水-沉积物间隙水磷浓度差,以及水-沉积物中氧含量等多方面因素的影响.  相似文献   

5.
Multivariate statistical techniques, such as cluster analysis, principal component analysis (PCA) and factor analysis (FA) were applied to evaluate and interpret the water quality data set for 13 parameters at 10 different sites of the three lakes in Kashmir, India. Physicochemical parameters varied significantly (p?<?0.05) among the sampling sites. Hierarchical cluster analysis grouped 10 sampling sites into three clusters of less polluted, moderately polluted and highly polluted sites, based on similarity of water quality characteristics. FA/PCA applied to data sets resulted in three principal components accounting for a cumulative variance of 69.84, 65.05 and 71.76% for Anchar Lake, Khushalsar Lake and Dal Lake, respectively. Factor analysis obtained from principal components (PCs) indicated that factors responsible for accelerated eutrophication of the three lakes are domestic waste waters, agricultural runoff and to some extent catchment geology. This study assesses water quality of three lakes through multivariate statistical analysis of data sets for effective management of these lakes.  相似文献   

6.
Major Ion Geochemistry of Nam Co Lake and its Sources, Tibetan Plateau   总被引：4，自引：0，他引：4  
The major cations and anions from lake water samples and its sources, including glacier snow, precipitation, stream, and swamp water in the Nam Co basin, central Tibetan Plateau, were studied. The concentrations of the major ions varied significantly in the five environmental matrices. Generally, the mean concentrations of most ions are in the order of lake water > swamp water > stream water > precipitation > snow. Rock weathering is the dominant process controlling the chemical compositions of the stream and swamp waters, with carbonate weathering being the primary source of the dissolved ions. The Nam Co lake water is characterized by high Na+ concentration and extremely low Ca2+ concentration relative to other ions, resulting from evapoconcentration and chemical precipitation within the lake. Comparison with the water chemistry of other lakes over the Tibetan Plateau indicated that Nam Co is located in a transition area between non-saline lakes and highly saline lakes. The relatively low concentration of total dissolved solids is possibly due to the abundant inflow of glacial meltwater and relatively high annual precipitation.  相似文献   

7.
《Applied Geochemistry》2004,19(1):153-162
In aquatic systems, the bioavailability of an element to microorganisms is greatly influenced by its chemical speciation. The goal of this work was to assess metal toxicity to a green algae (Pseudokirchneriella subcapitata) and a bacterium (Vibrio fisheri) as a function of size fractionation and chemical speciation (using the program MINTEQA2) in contaminated water of the Upper Vistula River. Water samples were collected at 1 reference site, 4 polluted sites and one polluted site on the Vistula's main tributary, the Przemsza River. Toxicity measurements were performed on unfiltered samples and, total dissolved (<1.2 μm), and truly dissolved (<1 kDa) fractions. Trace metal (Cd, Co, Cr, Cu, Mn, Pb, Zn) concentrations were measured in these samples and also in the colloidal fraction (1 kDa–1.2 μm). At the reference site, the low metal concentrations were in agreement with the absence of measurable toxicity. In the polluted section of the river, free metal concentrations were largely below the potential toxic levels for bacteria, which was in agreement with the absence of toxicity. Although Zn2+ was at potentially toxic-level concentrations in total dissolved and truly dissolved fractions in the polluted riverine section, toxicity for algae was observed, only in truly dissolved fractions from two stations. The absence of toxicity in most samples was related to metal association with particles and with low molecular weight ligands as well as the presence of organic ligands (phenol). The reason for toxic effects in two ultrafiltered samples is not clear, but may be related to the elimination of the colloidal organic fraction and thus the eradication of its protective effect occurring in natural samples.  相似文献   

8.
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.  相似文献   

9.
The hydrogeochemistry of the Lake Waco drainage basin,Texas   总被引：1，自引：0，他引：1  
The origin of surface water chemistry in highly impacted drainage basins must be investigated on a drainage-basin scale if the causes of the pollution are to be elucidated. This study characterizes and deciphers the surface water chemistry of a nutrient polluted river system in central Texas. Four tributaries of the Lake Waco reservoir were chemically characterized temporally and spatially in order to gain a complete understanding of the nature and origin of dissolved solids being transported into the lake. Temporal chemical variations measured at the base of each of the drainage basins are repetitive and seasonal. The most periodic and well-defined variation is exhibited by nitrate concentrations although many of the other solutes show seasonal changes as well. These temporal chemical changes are controlled by seasonal precipitation. During rainy seasons, the shallow aquifer is recharged resulting in stream discharge that is high in nitrate, calcium, and bicarbonate. When the shallow flow system is depleted in the summer, stream waters are dominated by deeper groundwater and become rich in sodium. Spatial variations in the chemistry of South Bosque surface waters were characterized using the snapshot technique. The spatial distribution of nitrate in surface waters is controlled by fertilizer application to row crops and the location of a munitions factory. The concentrations of naturally derived solutes such as Ca+, Na+, Cl–, and SO4–2are controlled by underlying lithologies.  相似文献   

10.
Generation of dust particles from the Owens Lake playa creates a severe air pollution hazard in the western United States. Much of the dust produced from the dry lakebed is derived from salts formed by evaporation of saline groundwater that often contains high concentrations of dissolved arsenic (As). The objectives of this research were to study the spatial distribution of dissolved arsenic in the shallow groundwater, and to examine factors affecting arsenic solubility and speciation. Evapoconcentration, redox potential, pH, and mineral solubility were examined as factors regulating arsenic biogeochemistry. Dissolved arsenic concentrations ranged from 0.1 to 96 mg L−1 and showed a general increase from the shoreline to the center of the lakebed. Arsenic concentrations were strongly correlated to electrical conductivity (EC) and δD suggesting that evapoconcentration is an important process regulating total As concentrations. Arsenite [As(III)] was the dominant form of inorganic arsenic at Eh values less than about −170 mV while arsenate [As(V)] was predominant at higher Eh values. Organic arsenic was negligible (<0.21%) in all shallow groundwater samples. Dissolved arsenic concentrations do not appear to be strongly regulated by solid-phase reactions. Solid-phase arsenic concentrations generally ranged between 4.0 and 42.6 mg kg−1 and a maximum concentration range (20 to 40 mg kg−1) was reached as solution concentration increased up to 80 mg L−1, indicating minimal sorption and/or precipitation of arsenic. Chemical equilibrium modeling indicated that orpiment (As2S3) was the only solid phase with a positive saturation index (indicating over-saturation), but only at high arsenic and sulfide concentrations. The findings of this research are important for assessing the potential environmental impacts of elevated arsenic concentrations on dust mitigation efforts taking place at Owens Dry Lake.  相似文献   

11.
Concentrations of nutrients (NO3 ?, NO2 ?, NH4 +, PO4 3?, and dissolved SiO2) were examined in three North China estuaries—the Luanhe, Shuangtaizihe, and Yalujiang. These riverine-estuarine systems provide distinct geographic and hydrodynamic conditions, that is, a shallow water zone embraced by shoals and sandbars (Luanhe), the confluence of two streams in the upper estuary with different water and sediment loads, and a turbidity maximum in the upper estuarine mixing zone (Yalujiang). Nutrient element concentrations in these rivers are high in comparison with large, less disturbed systems but similar to those from polluted and/or eutrophic European and North American rivers. This is attributed to intensive weathering and erosion and extensive use of chemical fertilizers. In the fresh-marine waters mixing zone, nutrient species can behave either conservatively or nonconservatively, or both. Wherever nonconservative behaviours of nutrient elements are observed, remobilization from solid phases is probably the predominant mechanism. The extrapolation of dilution curves to the fresh water end-members gives estimated riverine concentrations, which can be between two and ten times higher than those from field observations. Taking into account the high N:P ratios (102–104) from North China rivers and very low concentrations of nitrogen species in the Northwest Pacific coastal oceans (e.g., Yellow Sea), the estuaries in this study may act as regions in which production is limited by phosphorus to regions in which production is limited by nitrogen.  相似文献   

12.
Natural observations were analyzed to study the distribution of dissolved species of major and trace elements in the Onega and Mezen’ mouth areas and the tendencies in the chemical transformations of the is continental runoff in the river mouths of the White Sea drainage system. It is shown that the migration of major ions and dissolved species of Li, Rb, Cs, Sr, B, F and Mo is consistent with a conservative behavior and is controlled by hydrodynamic processes. The amounts of uranium and barium additionally supplying in the Mezen’ mouth exceed those removed with a continental runoff, whereas the Onega, Severnaya Dvina, and other rivers of the White Sea drainage system are characterized by the conservative behavior of uranium, while barium desorption from particulate matter reaches no more than 33% of its content in the riverine waters. The growth of concentrations of these elements in the Mezen’ mouth is caused by the long-term interaction of solid matters of the continental runoff with saline waters in the tide-affected estuary. 28–59, 12–63, 25–67 and 20–63% of concentrations of iron, aluminum, lanthanum, and cerium are removed from the riverine waters in the mouth areas of all studied rivers of the White Sea drainage system mainly owing to the coagulation and flocculation of organic and organomineral colloids. The distribution of dissolved species of mineral phosphorus and silicon in the Mezen’ mouth is presumably controlled by the remineralization of the organic matter in the bottom sediments, which due to the hydrological features of estuary are regularly stirred up and interact with vertically mixing water sequence. Up to 20–46% of dissolved phosphates and 3–22% of silicon are removed from the continental runoff during vegetation period in the mouths of the Onega, Severnaya Dvina, and other rivers of the White Sea drainage system mainly owing to their biological consumption.  相似文献   

13.
The viscous behaviour of laterite slurries was characterized by measurements of shear stress at constant and changing shear rates. Steady state stresses were obtained after accounting for the settling solids: the values show that the fluids possess viscosities of order 100 mPa s and are moderately shear-thinning, for solid volume fractions from 0.06 to 0.18 and for shear rates between 10 and 1000 s−1. Transient stress measurements were made for steps down in shear rate and for ramps down and up in shear rate. It was found that the Bingham–Maxwell model provides good fits to the transient data, both at low concentrations, where yield behaviour is dominant, and at high concentrations, where elasticity is dominant. For volume fractions of 0.10 or greater, relaxation times were found from step tests to be of order 10 s, but relaxation times found from the ramp tests were generally several times higher.  相似文献   

14.
In the present paper the factors controlling river water chemistry are described and their significance is evaluated, including: climate, petrography, soils/sediments, geomorphology of the catchment area, hydrography, pollution, biological activity of rivers, and rainwater composition. The results of this study indicate that the dominant factors influencing riverwater chemistry are the climate and the petrography of the catchment area. In the case of heavily polluted rivers, pollution appears to be the dominant factor.The approach followed is based on the watershed information, e.g., climatic, geomorphological, petrographical (percentage distribution of geochemical important petrographic units), soil/sediment composition, rainwater composition, as well as the hydrographic and the hydrochemical data of the rivers.In order to achieve a better understanding of the nature of the factors influencing river water composition as well as to specify them quantitatively, multivariate statistical analyses (factor and cluster analyses) were performed on the rain-corrected hydrochemical and petrographic information of the watersheds.  相似文献   

15.
In order to assess the pollution levels of selected heavy metals, 45 bottom sediment samples were collected from Al-Kharrar lagoon in central western Saudi Arabia. The concentrations of the heavy metals were recorded using inductively coupled plasma-mass spectrometer (ICP-MS). The results showed that the concentrations of Pb and Cd exceeded the environmental background values. However, the heavy metal contents were less than the threshold effect level (TEL) limit. The concentrations of heavy metals in lagoon bottom sediments varied spatially, but their variations showed similar trends. Elevated levels of metals were observed in the northern and southern parts of the lagoon. Evaluation of contamination levels by the sediment quality guidelines (SQG) of the US-EPA revealed that sediments were non-polluted-moderately to heavily polluted with Pb; non-polluted to moderately polluted with Cu; and non-polluted with Mn, Zn, Cd, and Cr. The geoaccumulation index showed that lagoon sediments were unpolluted with Cd, Mn, Fe, Hg, Mo, and Se; unpolluted to moderately polluted with Zn and Co; and moderately polluted with Pb, Cr, Cu, and As. The high enrichment factor values for Pb, As, Cu, Cr, Co, and Zn (>2) indicate their anthropogenic sources, whereas the remaining elements were of natural origins consistent with their low enrichment levels. The values of CF indicate that the bottom sediments of Al-Kharrar lagoon are moderately contaminated with Mn and Pb.  相似文献   

16.
The vertical distributions of dissolved Se species [Se(IV), Se(VI) and organic Se] and diagenetic constituents [Fe(II) and Mn(II)] were obtained in porewater samples of two Sudbury area lakes (Clearwater and McFarlane). The sedimentary concentration profiles of total Se, Se species bound to Fe–Mn oxyhydroxides and to organic matter, and of elemental Se were also determined along with the concentrations of Fe, Mn and S in different extractable fractions. Results indicated that the concentrations of total dissolved Se in porewater samples were very low, varying from around 2.0 nM to a maximum level of 6.5 nM, while the concentrations of total Se species in the solid phase varied between 2 and 150 nmol/g on a dry weight basis. The two lakes showed striking differences in the presence of Se(IV) and Se(VI) at the sediment–water interface (SWI). In Clearwater Lake, Se(VI) was present at this interface and Se(IV) was not detectable, whereas the opposite was found in McFarlane Lake. This suggests that reducing conditions might have existed near the SWI of McFarlane Lake at the sampling time; this hypothesis was confirmed by several other measured chemical parameters. The profiles of total dissolved Se of both lakes suggest upward and downward diffusion of dissolved Se species along the concentration gradients. Assuming that no precipitation occurred at the SWI, the fluxes of dissolved Se species across the SWI in Clearwater and McFarlane lakes were estimated to be 0.108 and 0.034 nmol cm−2 a−1, respectively. These values do not include the possible losses of volatile Se species due to microbial methylation. In the reducing sediments of both lakes, the formation of elemental Se and pyritic Se were found to be important mechanisms for controlling the solubility of Se in this environment. The main geochemical processes involving Se identified in this study are: the adsorption of Se onto Fe–Mn oxyhydroxides at or near the SWI, the release of adsorbed Se by the reduction of the same oxyhydroxides and the mineralization of organic matter, and the removal of Se from porewaters to form elemental Se and a S mineral phase such as Se–pyrite or pure ferroselite.  相似文献   

17.
INTRODUCTIONZibo lies in the center of Shandong Province,China.Thetopography of Zibo is high in the south and low in the north.Zibo is characterized by hills in the east,the south and thewest,and a wide plain in the north(Fig.1) .The annual rain-fall is 5 0 0 - 70 0 mm .The coal resources are very abundant in Zibo.There areXiazhuang,Xihe and Hongshan coal mines in the researcharea.The m ining sewage,about 0 .844 2× 10 8m3/ a,accountsfor about80 % of runoff of the Xiaofu River.The X…  相似文献   

18.
Daqing Oilfield is located in the northeast of Songnen Plain in Daqing City, Heilongjiang Province, which is a petrochemical industry gathering place based on petroleum refining, chemical industry, chemical fiber and fertilizer. In recent years, the quantity demand of petroleum and petrochemical production for groundwater in Daqing Oilfield is growing, and it’s of great significance to analyze and study the quality and pollution degree of groundwater for groundwater exploitation, utilization and protection. In this paper, groundwater quality of Daqing Oilfield evaluated by Nemerow Index is poor, and most points are Class IV groundwater; When evaluating groundwater pollution by hierarchical ladder method, the results show that the severe and extremely severe pollution points account for 34.48% in shallow phreatic water and 20% in deep confined water, showing that shallow groundwater is more seriously polluted than the deep. The main components influencing the quality of groundwater in the study area are total hardness, total dissolved solids, Cl-, SO42- and so on, which are affected by both the native environment and human activities; The main pollution components in groundwater are nitrite and nitrate nitrogen which are affected by human activities. Daqing Oilfield groundwater pollution is characterized by inorganic pollution, while organic components related to human activities contribute less to the groundwater pollution currently.  相似文献   

19.
River water (Water of Luce, Scotland) is used in laboratory experiments designed to investigate physical and chemical properties of Fe. Mn, Cu, Ni, Co, Cd and humic acids in riverine and estuarine systems. Using NaCl, MgCl2 and CaCl2 as coagulating agents, coagulation of dissolved (0.4 μm filtered) Fe, Cu, Ni, Cd and humic acids increases in a similar matter with increasing salt molarily: Ca2+ is the most dominant coagulating agent. Removal by coagulation with Ca2+ at seawater concentrations ranges from large (Fe-80%. HA-60%, Cu-40%) to small (Ni, Cd-15%) to essentially nothing (Cd, Mn-3%). Destabilization of colloids is the indicated mechanism. Solubility-pH measurements show that between a pH of 3 and 9, Fe, Cu, Ni, Mn, Co and Cd are being held in the dissolved phase by naturally occurring organic substances. Between pH of 2.2 and 1.2 a large proportion of dissolved Fe, Cu. Ni and Cd (72, 35,44 and 36% respectively) is precipitated along with the humic acids; in contrast, Mn and Co show little precipitation (3%). Adsorption-pH experiments, using unfiltered river water spiked with Cu, indicate that adsorption of Cu onto suspended particles is inhibited to a large extent by the formation of dissolved Cu-organic complexes.The experimental results demonstrate that solubilities and adsorption properties of certain trace metals in freshwaters can be opposite to those observed with artificial solutions or predicted with chemical models. Interaction with organic substances is a critical factor.  相似文献   

20.
The results obtained by measuring the sulfate content and its O18O16 ratios through time in some volcanic, tectonic and dam Italian lakes are reported here. The variations with time of the oxygen isotopic composition of the lake waters are also reported. The measurements refer mainly to surface water; however, a few deep samples were also studied.In the case of all the lakes examined, the variations with time of the oxygen isotopic composition and of the concentration of the dissolved sulfate cannot be explained in terms of the addition and of seasonal variations of the O18 content of rainwater sulfate. Biological redox processes involving bacterial reduction of sulfate and sulfide oxidation can reasonably account for the results obtained.According to Lloyd (1967), when sulfate is formed by bacterial sulfide oxidation, 68 per cent of the sulfate oxygen is water oxygen, while 32 per cent is dissolved molecular oxygen. The isotopic enrichment of the dissolved molecular oxygen in the lake waters relative to the isotope content of the atmospheric oxygen is mainly related to the biological activity in the waters.Assuming that a stagnation period takes place during summer and fall while a period of strong bio-respiratory activity takes place during winter and spring, it follows that a small isotope fractionation effect on molecular dissolved oxygen can be expected during stagnation while a high isotope fractionation can be expected during winter and spring. The O18 content of the sulfate dissolved in volcanic and tectonic lakes varies according to this hypothesis. The fact that similar O18 contents of the dissolved sulfate are or are not found in the same period of different years is probably related to similarities or differences in the climatic conditions.The bio-physical behaviour of the Corbara dam lake is different from that of other lakes. However, because of the continuous feeding by the Tiber River, variations of the sulfate concentration and its oxygen isotopic composition can be caused by the contribution of polluted water.  相似文献   

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