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1.
Dongping Lake area, located in the lower reaches of Yellow River, is an ideal place to study the changes of modern river and lake sedimentary environment. The sediment samples of Dawen River, Yellow River, and Dongping Lake were collected, and the major elements, trace elements and organic matter geochemical composition of the samples were analyzed. Cluster analysis, characteristic element ratio method and graphic method were used to explore the geochemical characteristics of sediments and their environmental implication. The results show that the contents of SiO_2, Na_2O, TiO_2 and Zr in sediments of Dawen River and Yellow River are relatively high, and the contents of iron and manganese oxides, organic matter, CaO, P_2O_5 and Sr in lake sediments are relatively high. That reveals the differences of sedimentary environments between the rivers and the lake. The contents of Sr and Zr in Dawen River are affected by the rapid migration of clastic materials in the upstream carbonate source area during the flood season; the δCe,ΣREE and REE's ratios in the sediments of the Yellow River reflect the influence of the Loess source; and the distribution of elements changes along the flow direction during the flood season. The characteristics of p H, element composition and LREE HREE fractionation of the lake sediments indicate that the sediment source is complex, and the lake environment is affected by the flood season. The study shows that the geochemical content and its variation characteristics of sediments effectively reveal the sedimentary environment, material composition and characteristics of flood season of rivers and the lake in the study area.  相似文献   

2.
The Ponnaiyar River is one of the largest rivers of the Tamil Nadu state (India), flowing a distance of 430 km from its point of origin to the sea. This work contributes with new data of magnetic and elemental composition of river sediments, and improves the knowledge obtained by preliminary and previous studies of rivers from Southeastern India. Magnetic susceptibility, anhysteretic and isothermal remanent magnetization and chemical determinations (major and trace metals) were measured. Magnetic results reveal the predominance of magnetite-like mineral with magnetic grain size variations along the river and in depth. Most of the uppermost samples have the major presence of trace metals and higher values of magnetic concentration. Magnetic and chemical variables were also analysed as potential pollution indicators using multivariate statistical techniques: canonical correlation and fuzzy c-means clustering analyses, which confirmed the existence of relationships, but not in a simple way, between magnetic and chemical variables. Furthermore, fuzzy analysis allows classifying the data in different well-differentiated groups regarding the trace metal load, concentration and feature-dependent parameters. The most polluted samples show high concentration of trace elements and magnetic carriers, softer and coarser magnetic minerals; on the contrary, the unpolluted samples (from the deepest sediments) have the opposite characteristics.  相似文献   

3.
We present multi-element concentrations in the surface sediments from the offshore of Cauvery delta of southeast India to evaluate the impact of coastal pollution on the geochemical behaviour of surface deposits. For this study, 16 surface sediment samples were collected from the offshore of Cauvery delta of southeast India and were analysed using traditional XRF for various major (SiO2, Al2O3, MgO, Fe2O3, MnO, Na2O, K2O, CaO, P2O5, TiO2) and trace elements (Rb, Sr, Ba, Y, Zr, Nb, V, Cr, Co, Ni, Cu, Zn, Th, Pb) after powdering it to ASTM 230 (<63 μm). The main objectives of this study were to understand the geochemical behaviour of the coastal surface sediments and its performance and relation with the pollution indices and statistical analysis. To meet out the objective, pollution indices such as enrichment factor (EF), contamination factor (CF) and Geoaccumulation Index (I geo) were calculated and statistical analyses were performed to understand the relationship between the geochemical parameters. Both EF and I geo show the enrichment of Cu, Cr and Zr, whereas CF shows enrichment of Cu and Cr. Statistical analyses exhibit poor correlation between these elements and fine fraction indicating the insignificant role played by both grain size and organic matter. Strong positive association between Cu and Zn with CaCO3 exhibits the role of carbonates in precipitating these metals from the overlying water column possibly related to agricultural pollution. Distribution and association of other elements suggest the influence of mineralogy in geochemical composition of surface sediments. Based on this study, we suggest that environmental indices alone should not be considered for evaluating environmental conditions and a prior geogenic characterisation of the sediments is necessary.  相似文献   

4.
Geochemical analysis by means of XRF and ICP-AES was carried out on 35 selected saples,Major and trace elements were determined.They were:CaCO3,P2O5,Fe2Oe,TiO2,SiO2,Al2O3,CaO,K2O,MnO,Rb,Cs,Ga,Zr,Ta,Nb,Sr,Ba,Cr,Ni,Zn,Pb,Cu,V and B.The country rocks studied were of sandy-muddy lithofacies.belonging to a typical tide marine transgressive heterolithic succession of Middle Miocee age.They are called the Ituzatingo Formation.The formation outcrops in northeastern Argentina on the left of the Parana River Valley.The depositional setting largely depends on the outstanding internal structures and textures(i.e.,herringbone cross stratification,tidal bindles,reactivation surfaces).In the study area.loessial friable sediment was used as geochemical background because it overlies shallow marine sediments.The results show significant differences.Boron is absent in loessial sediments.On the other hand .several trace elements such as vanadium and chromium are concentrated in the shallow marine sediments.These results may be useful to discernuncertain beds in the area studied.  相似文献   

5.
In this paper we present sedimentological, geochemical, mineralogical and 14C Accelerator Mass Spectrometry (AMS) dating data of a 21.0‐m core obtained from Alikes Lagoon, Zakynthos Island. It is the first time that sedimentological and geochemical data are presented, up to 21‐m depth, from an Holocene coastal lagoon environment of the Ionia Sea, western Greece. The sedimentological properties and the geochemical composition of sediments were studied for the time period between 8540 years bp to present. Samples were analysed for their particle size, calcium carbonate and total organic carbon (TOC) content. Moreover, bulk sample chemical analyses for major and trace elements were carried out, as well as bulk, oriented mineralogical analyses for the clay fraction (<2 µm) were determined by powder X‐Ray diffraction. The grain size characteristics, statistical parameters and TOC, for the Holocene analysed samples, suggest a coastal environment (restricted‐shallow) with reduced salinity such as a tidal flat and/or particularly marsh in a lagoon margin. Sediment characteristics as well as trace element records may contain additional new palaeoclimate information that provide important new constraint on sediment depositional environment and Holocene climate. Stratigraphic variation of geochemical indices, such as Rb/Ti, Cs/Ti, Eu/Eu*, Th/Ti, La/Ti, Ta/Ti, Yb/Ti and Y/Ti, for the sediments with ages from 8540 to 7210 years bp , remain relatively constant indicating that the provenance of the Alikes Lagoon remained similar throughout the mid Holocene. However, geochemical indices in sediments with ages from 7110 years bp to present, indicate the transition from a warm and wet climate in the middle Holocene to a relatively cold climatic conditions in modern times. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

6.
The bed and suspended (slime) sediment phases associated with effluent water that are produced from phosphate-ore-upgrading process at Al-Abyad mine in the southern part of Jordan were analyzed chemically and mineralogically. The results show that the effluent water is highly oxic and mildly alkaline in nature. The geochemical behavior of each phase was controlled by the effluent water physicochemical parameters, sediment particle size, mineralogical constituents of the studied phases, and the prevailing climatic nature of the area. Bed sediments have higher concentrations of many elements than slime. Accordingly, the bed sediments can be considered as a sink rather than a pool for many elements. The geochemical dissociation of major oxides and trace elements between bed and slime sediments was evident using t test, particularly between P2O5, SiO2, CaO, K2O, Mn, Sr, Y, and Co, and to lesser extent, V, U, Zn, and Cr. This might be attributed to effluent water characteristics, mineralogy, and the presence of fine-grained materials. The spatial distribution of major oxide and trace element concentrations along the stream drainage exhibited a slight increase with distance either in bed or slime sediment phases. However, they increased suddenly at the last three sampling sites, which might be due to the abundance of fine-grained materials that are mainly composed of clay minerals (montmorillonite) that would enhance the adsorption process. Moreover, the XRD results confirmed the existence of elemental geochemical dissociation as a function of mineral control.  相似文献   

7.
Underground developments such as subways and shopping facilities have been increasing in number and magnitude in the relatively shallow subsurface of many urban areas where the earth materials commonly are composed of marine sediments. Marine sediments can contain significant amounts of toxic trace elements such as arsenic, boron, and lead. Changes in the subsurface environment caused by excavation and construction in underground developments could potentially cause these toxic elements to be dissolved into pore water of the sediments, which might lead to groundwater pollution. The purpose of this study is to investigate correlations among chemical properties of marine sediments, such as pH and electrical conductivity (EC), concentrations of toxic trace elements, and stratigraphic characteristics of the sediments. We selected three sites with different stratigraphic settings in the southern Kanto Plain around the Tokyo Metropolis. We collected core samples from shallow strata at a site in the Arakawa Lowland, southern Saitama, and at two sites in the Musashino Upland, Middle Tokyo. All sites have both marine and non-marine sediments up to 50–60 m in thickness. We determined trace element concentrations in the pore water, pH, EC, and loss on ignition. The results show that (1) the marine sediments tend to have low pH, high EC, and high sulfur concentration compared to the non-marine sediments (2) the concentration of most of the soluble heavy metals vary depending on the concentration of sulfate, the pH, and the formation processes of the strata, (3) the arsenic concentration is not related to sulfur concentration but apparently to Fe and Al concentrations, (4) the boron concentration is not related to any other properties implying that the boron level is independent of and cannot be predicted by common chemical properties, and (5) for all three sites, concentrations of most of the trace elements, EC, pH, and sulfate concentration were correlated with each other. This study shows that the concentration and potential mobilization of many toxic trace elements in marine sediments could be predicted by easily measurable pore water chemical properties such as pH and EC. This could be useful for predicting and avoiding the risk of groundwater pollution during underground development projects.  相似文献   

8.
In all, 53 elements were analyzed in 1406 coastal sea sediment samples collected from an area off Hokkaido and the Tohoku region of Japan during a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define natural geochemical background variation and mass transport processes. The terrestrial area is covered by mafic volcanic rocks and accretionary complexes associated with ophiolite, which has small amounts of felsic volcanic rocks and granite. The spatial distribution patterns of elements enriched in mafic lithologies such as Fe (Total Fe2O3) and Sc in marine environments are influenced by adjoining terrestrial materials. The spatial distribution patterns of Cr and Ni concentrations, which are highly abundant in ultramafic rocks on land, are used to evaluate the mass transport from land to the sea and the dispersive processes caused by oceanic currents. The scale of mass transport by oceanic currents occurs up to a distance of 100–200 km from the coast along the coastal areas. The regional differences of elements rich in felsic lithologies such as K (K2O), Nb and La in marine sediments are determined mainly by the relative proportion of minerals and lithic fragments enriching felsic materials to those associated with mafic materials. The spatial distribution of elemental concentration is not always continuous between the land areas and coastal sea areas. That difference is interpreted as resulting from (1) transportation of marine sediments by oceanic currents and storm waves, (2) contribution of volcanic materials such as tephra, (3) occurrence of shell fragments and foraminifera tests and (4) distribution of relict sediments of the last glacial age and early transgression age. Contamination with Cu, Zn, Cd, As, Mo, Sn, Sb, Hg, Pb and Bi was not observed in marine environments because the study area has little anthropogenic activity. Terrestrial materials are the dominant source for these metals. The Mo, Cd, Sn, Sb, Hg, Pb and Bi are abundant in silty and clayey sediments locally because of early diagenetic processes, authigenic precipitation and organic substances associated with these elements. The spatial distribution of As concentration shows exceptions: it is concentrated in some coarse and fine sands on the shelf. The enrichment is explained by adsorption of As, sourced from a coal field, to Fe hydroxide.  相似文献   

9.
The present study investigates the distribution of trace metals (Zn, Hg, Cd, Cu, and Pb), as indicators of pollution, in the surficial offshore shelf sediments along the northern coast of Heraklion Prefecture (Crete, Mediterranean Sea). The concentrations and the spatial distribution of the different trace metals, in relation to the sedimentological characteristics and the water circulation pattern of the entire continental shelf, are associated with human inshore sources of pollutants located along the coastline of the study area. Although the trace metal concentrations measured are higher than the background values, they are not considered to be dangerous to human health, as they are lower than the standard values given by the World Health Organisation, with only a few localised exceptions. Furthermore, results reveal the important role of local hydrodynamism that moves fine-grained material and associated trace metals offshore (seawards to wave breaking zone) and then transports them eastwards by entrapping them in the prevailing offshore shelf-water circulation.  相似文献   

10.
In China, soil pollution is very serious, which has jeopardized the ecology, food safety, the people's health, and even the sustainable development of agriculture. In order to investigate the soil pollution situation, a total of 874 agricultural and non-agricultural topsoil samples were collected from Dexing area, northeast of Jiangxi Province, China. The total elemental concentrations of 17 elements (As, Hg, Mo, Cd, Cr, Zn, Cu, Mn, Ti, Pb, Fe, Ca, K, Si, Al, Mg, and Na) were determined. The geochemical background and threshold was predicted with the method of the median ± median absolute deviation (MAD). The agricultural soil median concentration of trace elements was similar to that of the non-agricultural soil. In contrast to Jiangxi soil background of trace elements, the geochemical background of the study area was obviously higher. The maps of the pollution indices for As, Cd, Cr, Cu, Hg, Mn, Mo, Pb, Ti and Zn of non-agricultural soil and agricultural soils in the study area, showed that the highest level of pollution is distributed near and along the Lean River, especially in the neighboring and surrounding Dexing and Leping mining area.  相似文献   

11.
The tsunami of 11th March 2011 was originated at the east coast of Japan and deposited ca.1 cm thick sediment layer along the coast of southwestern Mexico up to a maximum distance of 320 m from the beach. The sedimentological, mineralogical and geochemical characteristics of the sediments deposited during the tsunami (JT) are compared with the pre-tsunami sediments (PRT). JT sediments consist of dominant coarser fractions (>54% of medium to coarse sand), whereas PRT deposits comprise abundant finer fractions (>58% of fine sand). Assemblage of mafic and heavy minerals suggests similar provenance for both. The higher abundance and variation of heavy minerals along with higher concentrations of bromine (Br) and sodium (Na) in the JT deposits reveal the influence of high energy sea waves in transportation of heavy mineral rich coarse sediments onto the coastal lowlands.  相似文献   

12.
The Mesoproterozoic Srisailam Formation, exposed along the northern part of the Cuddapah basin, India, comprises mainly medium- to fine-grained siliciclastics, and is devoid of any carbonate sediment. Preliminary sedimentological studies helped in recognizing fifteen distinct facies (five facies associations) in Chitrial outlier of the Srisailam Formation deposited in continental half-graben basin(s). Black shales (sensu lato) are minor components of the Srisailam Formation, and inferred to have deposited in deep lacustrine and prodelta facies of the half-graben(s). The black shales show restricted thickness (up to 29.0 m), and are characterized by overall high ‘black shale' to ‘total shale' ratio (>0.51). Their geochemical characteristics were studied to constrain provenance, palaeoclimate, and tectonic setting of deposition of the Srisailam Formation. Further, an attempt has been made to use the Srisailam black shales as proxy for constraining the timing of breakup of the supercontinent Columbia.The Srisailam black shales are geochemically quite distinct. At similar SiO2 contents they are considerably different from PAAS. They are characterized by considerably lower ΣREE (Av. 136.0 ± 50.4 ppm) but a more conspicuous negative Eu-anomaly (Av. 0.34 ± 0.09) than PAAS. Al2O3/TiO2 and TiO2/Zr ratios coupled with Eu/Eu*, GdCN/YbCN, La/Sc, Th/Sc, and Th/Cr ratios suggest their derivation from granite and granodiorite. The CIA values (65–90, Av. 72 ± 9) as a whole indicate moderate chemical weathering under semiarid climate. Discriminating geochemical parameters indicate passive margin depositional setting. The combined sedimentological and geochemical characteristics reveal deposition of the Srisailam sediments in continental rift basin(s).Thick succession of black shales (with high CIA values) that deposited with shelf carbonates proxy for mantle superplume and supercontinent breakup events. The sedimentological characteristics and geochemical data of the Srisailam black shales plausibly exclude any large-scale breakup of Columbia during the interval (1400–1327 Ma) of deposition of the Srisailam Formation.  相似文献   

13.
Groundwater samples from 33 locations within the Coastal Plain Sands aquifer of Calabar (Nigeria) were collected and analysed for 43 trace elements by means of ICP-MS. The aim of this study is to determine the natural background levels of trace elements as a guide for future pollution monitoring of the aquifer. Secondly, this article focuses on the pollution vulnerability of the coastal plain sand aquifer. Statistical methods have been used to determine the source(s) of these elements. Results show that the area is characterised by four types of groundwater, including: Na-HCO3, Na-HCO3-Cl, Na-Cl and Ca-Na-HCO3-Cl. Secondly, all the elements considered are below normal averages. In addition, the Spearman correlation shows significant correlation especially among the lanthanide group of elements (p<0.0001). Factors analyses indicate mainly two groups of elements. The first group being due to the natural geochemical process (weathering/leaching of the basement lithology; characteristics of the elements) and the second is due to tidal flushing of the estuary. This indicates that the source of the trace element in the aquifer is due to a geogenic process and not anthropogenic. Thus, the present data set will serve as a reference source for pollution monitoring in the area.  相似文献   

14.
Algal species which are ubiquitous along the coastlines of many countries reflect the environmental conditions of the coastal seawater and may serve as useful biomonitors of anthropogenic pollution. Heavy metal concentrations of ten elements (As, Cd, Co, Cr, Cu, Fe, Mn, Ni, Pb and Zn) of potential environmental concern were determined in seawater, sediments and twelve species of benthic marine macroalgae from four locations (Glenelg, Port Adelaide, Port Broughton and Port Pirie) along the South Australian coastline. The four sites chosen represented varying degrees of metal contamination, where the capacity for benthic macroalgae to accumulate heavy metals from the environment was evaluated. Spatial differences in heavy metal concentration in both seawaters and sediments were observed at all sites with the highest concentrations of heavy metals including Cd (125 μg g?1), Pb (2,425 μg g?1) and Zn (7,974 μg g?1) found in the finer sediment fractions (<250 μm) of Port Pirie. While all algal species studied (Acrosorium polyneurum, Anotrichium tenue, Cystophora Cephalornithos Cystophora monillifera, Cystophora monilliformis, Dictyopteris australis, Gelidium micropterum, Gracilaria, Hormophysa Cuneiformis, Sargassum cinctum, Scaberia agardhii and Ulva lactuca) accumulated metals to varying degrees, Blindigia marginata was a good biomonitor species for a number of metals including Cd, Co, Cr, Fe, Pb and Zn, exhibiting both relatively high total metal concentrations and significant concentration factors.  相似文献   

15.
The present study was conducted on the Manasbal Lake (34°14′N: 74°40′E) to assess the geochemical characteristics of the lake bottom sediments, its environmental implications and its response in the local catchment area. This study tracks the spatial distribution of grain size, geochemical analysis, C/N ratio, calcium carbonate (CaCO3) and organic matter (OM) of the lake bottom sediments. It is observed that the clay fraction (49.79%) is predominant in the lake bottom sediments, followed by silt (35.88%) and sand (14.33%) and its spatial distribution is controlled by water depth. Geochemistry and normalized diagrams for the major oxides and trace elements reveal enrichment of CaO, K2O, P2O5, S, Cl, Ni, Zn and Sr. Chemical index of alteration (CIA) reflects low to moderate weathering intensity and near compositional similarity with the bedrock exposed in the catchment area around the lake. Environmental indices (EF, Igeo) suggest that the sediments are enriched in Cu, Ni, Zn, Cr, Co, Pb followed by Mn content. Pollution load index (PLI) reveal that all the sampling sites reflect low to moderately polluted category except for few stations that are towards the southern and southeastern side of the lake. OM (16.85%), CaCO3 (14.04%) and C/N ratio (15.5) of the lake bottom sediments is attributed to high organic activity within the lake, shell fragments, contributions from the lake flora and fauna adhering to the clayey silty sediments. The C/N ratio of 15.5 suggests a mixed source of organic matter both terrestrially and in situ formation within the lake. Sulphur and chlorine are high amongst the trace elements suggesting anthropogenic detritus input into the lake and this is due to the chemical fertilizers from the agricultural runoff and organic load into the lake. Thus, the present study suggests that in order to preserve the pristine lake ecology and the environment; continued monitoring and restoration efforts need to be undertaken.  相似文献   

16.
The levels and depth distributions of As, Cd, Cu, Zn, Pb, Hg, Fe and Mn in two sediment cores DY2 and DY4 collected from the ＂Cattle Pond＂ of Dongdao Island, South China Sea, were determined and analyzed with the main objective to identify the sources of these elements and evaluate the corresponding sedimentological and geochemical processes. Lithological characters and sedimentary parameters such as LOI950℃, CaO, LOI550℃ and TOC indicate that the depth of 96 cm and 87 cm are the critical points for DY2 and DY4 cores, respectively. As, Cd, Cu, Zn, Hg and P are remarkably enriched in the ornithogenic sediments above the critical depth points; their concentration-versus-depth profiles are similar to those of TOC and LOI550℃; the ratios of As, Cd, Cu, Zn, Hg over Ca are significantly correlated with P/Ca. Statistical and comparative analyses of these elements＇ levels in the ornithogenic sediments of DY2 and DY4 strongly suggest that seabird droppings are the main source of these elements. Additionally, for the upper sediment layers of DY2 and DY4 cores, Fe oxide sorption mechanism, like organic matter, may also play an important role in the abundances of heavy metals. Heavy metal Pb has geochemical characteristics distinctly different from those of As, Cd, Cu, Zn, Hg and P, and its isotope composition indicates an origin of anthropogenic emissions from the surrounding countries. These geochemical characteristics in the orinithogenic sediments of Xisha Islands are compared with the studies in the remote Antarctic and Arctic regions.  相似文献   

17.
《Applied Geochemistry》2001,16(3):387-396
The concentration variations of 16 trace elements were determined along the main stem of a medium-sized stream (catchment area=107 km2), which drains areas covered with acid sulphate soils developed on sulphide-bearing marine sediments. During high flows in autumn, there was a strong downstream increase in the concentrations of Al, Cd, Co, Cu, Mn, Ni, Se, U and Zn and a moderate increase in those of Cr and Tl, related to extensive leaching of the acid sulphate soils, which increase in abundance from the headwater towards the basin outlet. During high flow in early summer, the downstream increase in the concentrations of these elements was not as strong as in autumn, due to decreased amounts of available mobile element fractions in the acid sulphate soils. Under baseflow conditions, the runoff from areas with acid sulphate soils is low in comparison to that in areas covered with other soils/sediments, resulting in relatively small loads of trace elements throughout the stream. The concentration variations of As, Pb, Sb, Ti and V were unrelated to catchment cover and did not vary along the stream in a regular manner. These 5 elements are, therefore, in contrast to the others, not leached more abundantly from the acid sulphate soils than from other soils/sediments. Based on the identified hydrogeochemical features and controls, it is suggested that water-quality improvement measures should include methods that primarily aim at reducing the leaching of hazardous chemical elements in the source areas (acid sulphate soils).  相似文献   

18.
Pollution from mining activities is a significant problem in several parts of the Republic of Macedonia. A geochemical study of the surficial sediments of Lake Kalimanci in the eastern part of the Republic of Macedonia was carried out to determine their elemental compositions and to evaluate the pollution status of lake sediments by employing an enrichment factor (EF). The major and trace element contamination in surficial lake sediments was studied to assess the effects of metalliferous mining activities. The mean concentrations of major elements (wt%) Si 23.5, Al 7.9, Fe 6.6, Mg 1.3, Ca 3.8, Na 1.1, K 2.3, Ti 0.4, P 0.2, Mn 0.6 and trace elements ranged within Mo 1.0–4.6 mg kg?1, Cu 144.4–1,162 mg kg?1, Pb 1,874–16,300 mg kg?1, Zn 2,944–20,900 mg kg?1, Ni 21.7–79.3 mg kg?1, Cd 16.5–136 mg kg?1, Sb 0.6–3.6 mg kg?1, Bi 3.0–24,3 mg kg?1 and Ag 1.4–17.3 mg kg?1. The EF ranged within 0.12–590.3. Among which, Cd, Pb, Zn and As have extremely severe enrichment. The data indicate that trace elements had extremely high concentrations in Lake Kalimanci surficial sediments owing to the anthropogenic addition of contaminants.  相似文献   

19.
贵州主要城市地表松散沉积物中微量元素与土壤环境   总被引：2，自引：0，他引：2  
通过贵阳等九个城市地表土壤和水系沉积物中的微量元素地球化学分析表明,城市环境不同程度地遭受有微量元素污染.在自然作用和人为作用过程中,微量元素造成城市的大气污染、水土污染、元素异常、环境灾变等环境问题,笔者认为,贵州城市地表土壤和沉积物中的生命有害元素污染,可能对长江和珠江流域造成不良影响,应尽快开展多目标生态环境地球化学调查,科学准确的划分地表环境的安全、隐患及污染区,并对已遭受微量元素污染的地区制定出有效的修复方案和治理措施.  相似文献   

20.
海相沉积物中自生沉积碳酸盐相的微量元素携带极为丰富的原始地质信息,然而海相沉积物中碳酸盐相的测定还没有建立统一的标准方法.本文以修正的Tessier七步提取流程为基础,以电感耦合等离子体质谱法(ICP-MS)为检测手段,针对海相沉积物碳酸盐相组分中V、Cr、Co、Ni、Sr五种微量元素建立了分级提取方法.实验以海相沉积物样品和标准物质作为参考样品,对比了NaAc和EDTA提取碳酸盐相的效果.结果表明,NaAc不能完全提取出沉积物碳酸盐相中的微量元素;EDTA可以较好地提取自生海相沉积物碳酸盐相中的微量元素,但是由于其络合能力太强还会提取有机物结合态的金属元素.本研究确定的分级提取方法是:首先用中性盐NaC1去除离子交换态,然后用提取专一性较强的焦磷酸钠(pH =10)去除有机态,再用EDTA提取仅自生海相沉积物的碳酸盐相.方法精密度(RSD)均＜5％,各元素的检出限在0.5～ 4.3 ng/g之间,回收率在88.0％ ～ 101.6％之间,方法的选择性和稳定性能够满足地球化学样品形态分析的要求.  相似文献   

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