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1.
The concentrations of 45 elements, and the content of organic substances, amorphous inorganic substances and minerals were determined in 26 samples of Elbe River bottom sediments to determine the correlation between the element composition and the grain size in the ￡ \le 4, 4--8, 8--16, 16--32, 32--63 7m and bulk samples ￡ \le 63 7m fractions. The purpose of this study was to obtain information about the role of particle size and their mineral composition as a control of element concentrations in sediments, the potential remobilization of elements under changing environmental conditions, and the chemical speciation of the large excess concentrations of elements in this system.¶About 22--56% of the estimated element yield was associated with sediments with a grain size of less than 4 7m and 82--97% of the element yield was found in the fraction smaller than 32 7m. Sequential extraction carried out for 20 potentially reactive elements in the ￡ \le 63 7m bulk samples and the ￡ \le 4 7m fraction showed the increased importance of exchangeable ions in the order Mn = Ni < Mg < Sr < Cu < Zn < Ca < K < Cd < Na < Mo, reducible fractions Zn < Sr < Mo < Co < Cu < Ni < Pb < Mn < Cr < Be < V = Fe < As < Ag, oxidizable chemical phases As = Ca < Cd < K < Sr < Fe = Mn < Zn = Mg < Mo < Co = Ag < Pb < Li < Cu = V < Ni < Cr = Na < Be with small concentrations from lithogenic phases Mn < As < Pb < Sr < Zn = Cu = Na < Be < V < Ni < Cr < Fe < K < Mg < Li. The major accumulative phases were identified for the individual elements.  相似文献   

2.
Multivariate analysis methods have been applied to studying variations in the concentrations of Ag, Al, As, B, Ba, Br, Ca, Cd, Co, Cr, Cs, Cu, Fe, K, Li, Mg, Mn, Mo, Na, Ni, P, Pb, Rb, S, Sb, Si, Sn, Sr, Th, Tl, U, V, Zn, Cl?, NO 3 ? , SO 4 2? as components of precipitation at 11 rural stations under project “Ecogeochemistry of Barents Region”. Hierarchic factor analysis revealed the structure and space-time distribution of seven first-order factors and two second-order factors. The combinations of ingredients that determine the composition of first-order factors characterize the sources of precipitation composition, which have been found to be specific and volatile products of fuel oil and coal combustion, marine and earth aerosols, and biogenic processes. Second-order factors showed two independent sets of components, which are typical of the chemistry of precipitation at the examined stations in winter and summer. Step-by-step discriminant and cluster analysis made it possible to classify the observational stations by precipitation chemistry and demonstrate the extent of difference between them.  相似文献   

3.
Temporal variation of runoff chemistry and its seasonal controls relating to chemical weathering processes and drainage system evolution were examined at Urumqi Glacier No.1 in Xinjiang, China, over a full melt season. The dominant ions in meltwater runoff are HCO3?, Ca2+, and SO42?; and Fe, Sr, and Al are dominant elements. Concentrations of major ions and some elements show periodic variations with seasons and negatively correlate with discharge, whereas other elements (e.g., Al, Ni, Cu, Zn, Cd, and Pb) show a random change, providing insights into the hydrological and physicochemical controls. HCO3? and Ca2+ are primarily derived from calcite, SO42? and Fe mainly come from pyrite, and Sr and Al principally originate from silicate. Hydrochemical fluxes of solutes exhibit strong seasonality but are positively related to discharge, suggesting an increasing release of solutes during higher flow conditions. Solute yields, cation denudation rate, and chemical weathering intensity observed at Urumqi Glacier No.1 are higher than those at most basins worldwide. This suggests that chemical weathering in central Asia may be stronger than at other glacial basins with similar specific discharge. Concentrations of some elements (e.g., Fe, Al, As, Pb, and Zn) are close to or exceed the guidelines for drinking water standards in meltwater‐fed rivers. These rivers may face future challenges of water quality degradation, and relationships between changing flow and water quality conditions should be established soon, given that development of channelized flow is expected to be earlier over a melt season in a warming climate.  相似文献   

4.
The analysis of physicochemical variables and selected dissolved elements was performed on the Apure River waters for 15 months. The variables pH, alkalinity, dissolved O2, conductivity and Na, Ca, Mg and Cd concentrations showed maximum values during low water, whereas K, Si, Fe, Al, Mn, Zn, Cu, Cr and dissolved organic carbon (DOC) showed maximum concentrations during rising and high water. Five important factors were found to control the amount and temporal variability of the dissolved elements: lithology, hydrology, vegetation–floodplain processes, redox conditions and organic complexation. Weathering of silicates, carbonates and evaporites in the Andes provides most of the proportion of Na, Ca, Mg and HCO3? to waters. The temporal variability of these ions is controlled by a dilution process. Although Si can be taken up by the biomass, Si and K can be leached from the floodplain by weathering of clays. Microbial decay of the submerged plants in the floodplain during the inundation periods provides DOC and K to river waters and changes the redox conditions in water. The changing redox conditions control the solubility of Mn, Zn and Fe. Dissolved Mn is a function of pH‐dependent redox process, whereas Zn solubility is controlled by scavenging of Zn during the oxidation of Mn2+ to MnO2. Positive relationships between Al, Fe, Cu, Cr and DOC suggest that these elements are complexed by organic colloids generated in the floodplain. Moreover, the binding capacity of Fe with DOC increases under reducing conditions. Although Cd seems to be provided by weathering in the Andes, several processes can affect the mobility of Cd during transport. Copyright © 2010 John Wiley & Sons, Ltd.  相似文献   

5.
The enrichment of some metals (Al, Mg, Na, K, Cu, Zn, Cd) in volcanic gases is measured by an emanation coefficient εx relating the amount of the element x in lavas and in aerosols.εx is determined in the volcanic emissions of Mount Etna (Sicily), with regard to that of210Pb. The accuracy of the results is limited by the geochemical behavior of common lead compared to that of210Pb. Concerning the most volatile species, it appears that practically all the volcanic aerosols are produced by evaporation followed by gas-to-particle conversion and the spattered fraction appears to be negligible.  相似文献   

6.
The status report on metal pollution in tropical estuaries and coastal waters is important to understand potential environmental health hazards. Detailed baseline measurements were made on physicochemical parameters (pH, temperature, redox potential, electrical conductivity, salinity, dissolved oxygen, total dissolved solid), major ions (Na, Ca, Mg, K, HCO3, Cl, SO4 and NO3) and metals concentrations (27Al, 75As, 138Ba, 9Be, 111Cd, 59Co, 63Cu, 52Cr, 57Fe, 55Mn, 60Ni, 208Pb, 80Se, 66Zn) at estuaries and coastal waters along the Straits of Malacca. Principal component analysis (PCA) was employed to reveal potential pollution sources. Seven principal components were extracted with relation to pollution contribution from minerals-related parameters, natural and anthropogenic sources. The output from this study will generate a profound understanding on the metal pollution status and pollution risk of the estuaries and coastal system.  相似文献   

7.
Materials of expedition studies in 2013 in the Prielbrus’e National Park were used to analyze the concentrations of a wide range of pollutants (SO42-, Cl?, Na+, K+, F?, Mn, Cu, Zn, Pb, Cr, Ni, NO3-, NH4+) in the water of mountain rivers forming the main artery of the region, the Baksan R. The analyzed data characterize seasonal variations in pollutant concentrations at seven sampling sections and their dynamics along the river down to the 35th km from the source in different seasons.  相似文献   

8.
The hydrochemical analyses of twenty-three springs were used to determine the properties and types of groundwater of the Tertiary-Quaternary Aquifer of northern Jordan. The result shows that the geological formation influences the quality of the investigated groundwater more than the anthropogenic factors. The water of the Quaternary-Tertiary aquifer is enriched in Ca++ due to the dissolution of the nearby carbonate rocks. The investigated water has a low EC values with Ca(Na)-HCO3 water type. Most springs belong to this hydrochemical facies except Malka. Groundwater in the Malka wells has high salinity with NaCl waters and a strong Ca(Mg)-HCO3 facies (900 to 1000 mg/l TDS). The area long-term hydrochemical data have been also evaluated; general trend of increase of the analyzed ion was observed. Bicarbonate represents the most abundant anion in the studied water, which exceeds the permissible limits. Nitrates (NO 3 ? ) also exceed the permissible limit and are the most common contaminant in the investigated water. Data on dissolved major and trace elements (K+, Na+, Mg2+, Ca2+, Cl?, SO 4 2? , Fe, Zn, Cu and Pb) in the investigated water revealed that the concentrations lie within the natural background range. The positive correlation values between various ions indicate that most of ions come from same lithological sources. According to the residual sodium carbonate, and EC values, the studied springs are suitable for agricultural purposes.  相似文献   

9.
Chemical studies have been carried out on a number of water wells from the Dibdiba Formation northeast of Kuwait. Water salinity of this formation ranges between 3,300 mg/l to 7,000 mg/l, increasing with depth. The water entrapped in Dibdiba Formation is mainly sodium chloride type which can be differentiated into three different groups according to the ranges of concentration of the main cations and anions. These groups are: (3331113) sodium chloride water type in which Cl > Na, group (3333113) sodium chloride water type in which Na > Cl. In both groups the sequence of dominant cations is Na > Ca > Mg. Group (3333111) sodium chloride water type has Na > Cl and the sequence of dominant cations is Na > Mg > Ca. Chemical ratios of Ca/Mg, Na/Cl, and C1/HCO3 were worked out for Dibdiba ground water. The ratio of Ca/Mg Dibdiba Formation ranges from 0.4 to 8.58, the ratio of Na/Cl ranges between 0.98 to 1.33, and the ratio of C1/HCO3 is 232. A plot of chemical analysis on a trilinear diagram shows that Dibdiba Formation ground-water chemical properties are dominated by alkalies (Na > Ca) and strong acid (Cl > SO4). Water chemistry may reflect the history of the flow path, indicating regional flow as shown by increasing Na+, Cl-, SO–4 and where Ca+, Mg+ achieve equilibrium.  相似文献   

10.
The extent of the effect of technogenic sources in the Baikal Natural Territory on Lake Baikal water area and coastal zone is assessed. Regional pollution from sources remote from the lake migrates over tens of kilometers in accordance with wind rose and transforms into local in the water protection zone of Lake Baikal. Snow pollution in lake water area has been recorded near the coastal populated localities Listvyanka, Kultuk, Baikal’sk, Slyudyanka, Ust’-Barguzin, Severobaikal’sk, Nizhneangarsk, and at Selenga R. mouth and found to have a local character. The southern depression ranks first in terms of the input of NO2, NO3, NH4, PO4, F, Al, Na, Ba, Mo, Mn, Pb, Cu, Zn, Sr, Hg, and oil products onto lake water area through the atmosphere. However, larger amounts of SO4, H2CO3, Cl, Ca, Mg, and K falls onto the northern depression, and more Be, V, Cr, and Co falls onto the middle part, because of the operation of coastal enterprises, boiler-houses, TPPs, stove heating, motor-car emissions, and natural transport of dust in low-snow areas. Data on the past 15 years show the pollution to drop by half in the late 1990s and early 2000s because of industrial decline. However, a small increase in regional pollution by individual components could be seen in the recent 5 years.  相似文献   

11.
泥炭沼泽不同植物群落中地表糙度变化及其影响机制   总被引：3，自引：0，他引：3  
对藏南沉错CCl孔216个沉积物样品进行了15种金属元素含量的测试,研究金属元素含量的分布特征,以及与粒度参数的变化关系．结果显示：金属元素的分布特征可分为三组,K、Na、Mg、Al、Ti、Ba、Cu、Zn、Fe、Pb、Cr、V等12种元素具有较为相似的变化趋势;Ca和Sr变化趋势相同;而Mn与其他任何一种元素都不相似．元素分布与粒度参数的相关分析结果表明,Ca、Ti、Pb的变化与沉积物粒度没有明显的关系;K、Na、Al、Ba、Cu、Fe、Cr、V等8种元素与沉积物粘土含量（〈4um）呈正相关关系;Mg、Zn、Mn与粉砂含量（4—63μm）呈正相关关系;而Sr与砂含量（〉63gm）呈正相关关系本研究中大部分元素的粒度效应与其他湖泊、海洋等水体沉积物中元素的粒度效应具有一致的结果．与本岩芯已有的过去1400年来的环境重建资料对比可以发现,在不同的环境变化阶段,元素组合特征都与湖区环境状况具有较好的对应性．其中大部分元素的含量变化受物源条件即流域风化侵蚀程度的影响,而Ca含量不受沉积物粒度变化影响,且与沉积物中碳酸盐含量、Sr／Ba具有很好的相关性,说明其变化受物源条件影响小,而主要与湖水理化性质、蒸发强度以及湖泊沉积过程有关．  相似文献   

12.
Abstract

The deposition of chemical elements in a catchment occurs through three different processes: wet, dry and cloud deposition. Total deposition cannot be inferred from measurements made with open-field raingauges, and still constitutes a challenge to scientific method. The chemical composition of samples from an open-field raingauge (bulk precipitation) was analysed over a period of several years in a small Mediterranean catchment in the Maures Massif, France. The input of chloride measured in this way was two times lower than the output, despite the fact that this element is reputed to be conservative, which means input and output should roughly balance. This implies that input has previously been underestimated. Analysis of the bulk precipitation data was carried out taking into account both the history of rain events and of sampling. This study allowed the relative parts of the different deposition processes to be quantified. Dry deposition can provide from 20% to more than 80% of the anthropogenic and terrigenic elements (Ca2+, Mg2+, K+, NO3 ?, SO4 2-, SiO2) to the rain samples. The occult deposition of marine elements on the catchment area (50% of total deposition) was found to be mostly due to cloud deposition during wet periods.  相似文献   

13.
The crater lake water from Maly Semiachik volcano in Kamchatka was used for the international analytical laboratory comparison of major and minor elements, and hydrogen, sulfur, and oxygen isotope data. Eight institutions participated in this program, giving analytical results of 9 major and 20 minor elements mainly by using ICP-AES for cations and IC for anions. Among the major elements, Na, Mg and Si showed coefficients of variation (CV) of 10% or more, whereas B, Al, Fe, Mn had coefficients less than 7%. The CV% of the minor elements Co, Cu, P, Cr, Pb was much greater (>30%) while the V analyses agreed well (<10%). Ti, Sr, Zn, and F were intermediate (between 10 and 20 CV%). The errors observed for these constituents are inherent to the methods applied: large dilutions and spectrometric interferences. Even the major anions such as Cl (>2000 ppm) and SO4 (>5000 ppm) gave considerable ranges (5.1 and 8.8 CV%, respectively) as did the obtained pH values (22 CV%). The measured δ18O of the water samples and δ34S of sulfate are in excellent agreement but the δD values had CV% of 8. Technical recommendations are presented to improve the analytical results for these elements with significant deviations from the mean values.  相似文献   

14.
Dew samples were collected between October 2007 and February 2008 from a suburban site in Agra. pH, conductivity, major inorganic ions (F?, Cl?, NO 3 ? , SO 4 2? , Na+, K+, Ca2+, Mg2+, and NH 4 + ), and some trace metals (Cr, Sn, Zn, Pb, Cd, Ni, Mn, Fe, Si, Al, V, and Cu) were determined to study the chemistry of dew water. The mean pH was 7.3, and the samples exhibited high ionic concentrations. Dew chemistry suggested both natural and anthropogenic influences, with acidity being neutralized by atmospheric ammonia and soil constituents. Ion deposition flux varied from 0.25 to 3.0?neq?m?2?s?1, with maximum values for Ca2+ followed by NH 4 + , Mg2+, SO 4 2? , Cl?, NO 3 ? , Na+, K+, and F?. Concentrations of trace metals varied from 0.13 to 48?μg?l?1 with maximum concentrations of Si and minimum concentration of Cd. Correlation analysis suggested their contributions from both crustal and anthropogenic sources.  相似文献   

15.
Surface sediment samples collected from the inner shelf region of the Bay of Bengal, were analysed for the major elements and total and acetic acid available trace elements (Al, Ca, Cd, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, Pb, Si, Zn) to evaluate geochemical processes influencing their distribution. Major elemental analysis showed that the sediments had high concentrations of Si and relatively low concentrations of Al and Fe. Both major elemental and trace metal concentrations indicated that the sediments represent weathered products of granite and charnockite. Normalization of metals to Al indicated relatively high enrichment factors for Pb, Cd, Zn and Cr. The higher proportions of nondetrital Pb (66%), Cd (41%) and Co (28%) reveal metal contamination due to anthropogenic inputs. Factor analysis (FA) identified six possible types of sedimentological and geochemical associations. The dominant factor accounting for 26.9% of the total variance identifies an anthropogenic input and accumulation of nondetrital Cd, Co, Cr, Ni and Pb. Association of these metals with CaCO3 reveals that shell fragments in the surface sediments are likely act as a carrier phase for nondetrital metals. The results are discussed in the context of the sources and pathways of elements in the Bay of Bengal.  相似文献   

16.
Epiphyton chemistry was studied in the Ivankovo Reservoir; a large number of micro- and macroelements (Ag, Al, As, Ba, Ca, Cd, Ce, Co, Cr, Cu, Fe, K, La, Li, Mg, Mn, Mo, Na, Nd, Ni, P, Pb, S, Sc, Sr, Ti, V, Y, Yb, Zn, W) were determined with the use of up-to-date analytical methods. Comparative characteristics of the geochemistry of macrophyte epiphyton of different ecological groups is given for the Ivankovo Reservoir. The potential of epiphyton as a biogeochemical indicator of anthropogenic impact on the water body is examined.  相似文献   

17.
Source apportionment of particulate matter <10 µm in diameter (PM10), having considerable impacts on human health and the environment, is of high priority in air quality management. The present study, therefore, aimed at identifying the potential sources of PM10 in an arid area of Ahvaz located in southwest of Iran. For this purpose, we collected 24‐h PM10 samples by a high volume air sampler. The samples were then analyzed for their elemental (Al, As, B, Ba, Be, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, Pb, Se, Si, Sn, Sr, Li, Ti, V, Zn, Mo, and Sb) and ionic (NH, Cl?, NO, and SO) components using inductively coupled plasma optical emission spectrometry and ion chromatography instruments, respectively. Eight factors were identified by positive matrix factorization: crustal dust (41.5%), road dust (5.5%), motor vehicles (11.5%), marine aerosol (8.0%), secondary aerosol (9.5%), metallurgical plants (6.0%), petrochemical industries and fossil fuel combustion (13.0%), and vegetative burning (5.0%). Result of this study suggested that the natural sources contribute most to PM10 particles in the area, followed closely by the anthropogenic sources.  相似文献   

18.
Volcanic gases from Showashinzan are qualitatively the same as those liberated from igneous rocks when they are heated in vacuum. Their main components are H2O, CO2, and H2. Then follow HCl, HF, N2, SO2, H2S, S, CH4, CO, Ar, Si, B, Mg, Na, K, Ca, Al, Fe, P, Br, NH3, As, Zn, Sr, Ba, Cu, Pb, Sn, Sb, Bi, Ge, Ag, Cr, Ni, Mo, Rn, Ra, etc. They come through fumaroles of high temperature (～750°C.). Metallic compounds deposit as sublimates around the outlet of fumaroles. They are fractionated there according to their thermodynamic properties. When the temperature of gases falls, heavy metal elements deposit before reaching the surface of the earth. Ra is among them. Owing to the contribution of Ra thus depositted, Rn content of vapor is larger in low temperature fumaroles than in high temperature ones. Chemical compounds of H, C, N, O, and S vary their composition according to the condition of temperature and pressure. Sulfur exists as SO2 more than H2S. As the temperature of gases falls, SO2 and H2 decrease and H2S increases. Mutual relation among them is ruled by the chemical equilibrium: SO2+3H2=H2S+2H2O. The structure of Showashinzan is not simple. Some deviations from the general rule are explained in connection with ground water.  相似文献   

19.
High-magnesium andesites associated with basalts erupted after the opening of the Sea of Japan are present at Saga–Futagoyama in northwest Kyushu, southwest Japan. High Mg/(Mg + Fe) [=0.84] of orthopyroxene phenocrysts and bulk rock Mg–Fe–Ni compositions suggest that these high-magnesium andesites were originally primitive melts insignificantly modified in crustal magma chambers. KDCa–Na [= (Ca/Na)pl/(Ca/Na)bulk rock] ranges from 1.21 to 0.97 and suggests that the high-magnesium andesite magmas would originally have contained H2O less than 1.8 wt.%. Nb/La does not show a negative correlation with respect to SiO2. These lines of evidence indicate that hydrous components derived from the subducting slab would not have played a significant role in the genesis of the high-magnesium andesite magmas. Instead, the normative olivine − quartz − [CaTs + Jd] compositions and a negative correlation between Sr/Nd and SiO2 indicate that the basalt-high-magnesium andesite association would have been formed by multi-stage partial melting of relatively anhydrous source at pressure ranging from 1.5 to 0.5 GPa.  相似文献   

20.
We present concentrations of environmentally available (unfiltered acidified 2% v/v HNO3) As, Cu, Cd, Pb, V, Sr, and major ions including Ca2+, Cl?, and SO42? in a July 2005 and a March 2006 shallow snow profile from the lower Eliot Glacier, Mount Hood, Oregon, and its proglacial stream, Eliot Creek. Low enrichment factors (EF) with respect to crustal averages suggests that in fresh March 2006 snow environmentally available elements are derived primarily from lithogenic sources. Soluble salts occurred in lower and less variable concentrations in July 2005 snow than March 2006. Conversely, environmentally available trace elements occurred in greater and more variable concentrations in July 2005 than March 2006 snow. Unlike major solutes, particulate‐associated trace elements are not readily eluted during the melt season. Additionally, elevated surface concentrations suggest that they are likely added throughout the year via dry deposition. In a 1‐h stream sampling, ratios of dissolved (<0·45 µm) V:Cl?, Sr:Cl?, and Cu:Cl? are enriched in the Eliot Stream with respect to their environmentally available trace element to Cl? ratios in Eliot Glacier snow, suggesting chemical weathering additions in the stream waters. Dissolved Pb:Cl? is depleted in the Eliot Stream with respect to the ratio of environmentally available Pb to Cl? in snow, corresponding to greater adsorption onto particles at greater pH values. Copyright © 2009 John Wiley & Sons, Ltd.  相似文献   

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