泾河上游全新世黄土-古土壤序列微量元素分布特征及环境变化

在野外考察的基础上,对泾河上游赵家村全新世黄土-古土壤剖面进行系统采样,利用X-Ray荧光光谱仪测定了Ba、Zn、Cu、Pb、Cr、Rb、Sr、Co、Th、Zr等10个微量元素的含量及其变化,并与磁化率、粒度进行了相关性分析,研究表明大部分微量元素如Ba、Zn、Cu、Rb、Co、Th、Zr在古土壤层(S0)中富集,而在马兰黄土层(L1)中含量较低; 而Pb、Cr、Sr在古土壤层中含量低于马兰黄土层.同时,微量元素Ba、Zn、Cu、Rb、Co、Th、Zr与磁化率、黏粒(<0.005 mm)含量呈正相关,与粗粉沙(0.01～0.05 mm)含量呈负相关; 而元素Pb、Cr、Sr与黏粒、磁化率呈负相关,与粗粉沙呈正相关关系.在古土壤成壤改造过程中,由于有机质含量显著增加,络合-螯合作用增大,加之黏粒胶体的吸附作用,导致大多数微量元素在古土壤层的相对富集; 而元素Cr性质稳定,在整个剖面的波动较小; Sr含量在全新世黄土层(L0)和表土层(TS)中逐渐升高,主要是由于气候暖干化日趋严重,表土层碱性增强,CaCO3淋溶作用明显减弱; Pb元素在表土层含量较高的主要原因是工业"三废"排放、金属采矿和冶炼、煤炭和石油的燃烧以及汽车尾气排放等人类活动的干扰.     

某些富铁铝土壤形成中微量元素的含量变化与剖面分布

用一米平面光栅摄谱仪对某些富铁铝土壤,母质及母岩中B,Ba,Co,Cr,Cu,Mn,Mo,Ni,Pb,Sn,Sr,Ti,V,Zn,Zr15种微量元素含量作了测定。     

厩肥对粉煤灰微量元素释放规律影响的研究

该文对粉煤灰在降雨淋洗条件下微量元素的释放规律进行了室内模拟试验。试验处理分别为粉煤灰、粉煤灰+石灰、粉煤灰+石灰+厩肥及其混合物的堆肥腐熟4种情况。实验结果显示淋出液中B、Sr、Ba和Li的最大浓度大于1 mg/L，而其它元素均小于此值。石灰的应用增大了淋出液中B和Ba的浓度而降低了Li、Mo和Cr的浓度；厩肥的应用及其堆肥腐熟处理增大了B、Mo、Zn、V以及Cu、Ni、Cd、As、Mn、Ti、Co、Sn和Se的浓度，而降低了Sr、Ba、Li和Cr的浓度。除V外，淋出液中所有微量元素的浓度随淋出液体积的增加而减小。Cr、Zn以及Cd、Cu和As可能是粉煤灰对环境产生潜在危害的主要元素。     

关中东部全新世黄土——古土壤序列微量元素分布特征及意义

X-荧光光谱仪、磁化率仪和激光粒度仪对尧禾村(YHC)全新世黄土-古土壤序列的微量元素、磁化率、粘粒(<5μm)含量进行了测量。将磁化率曲线、粘粒曲线、Rb/Sr变化曲线和Ba/Sr变化曲线进行了对比分析发现:YHC剖面的磁化率曲线、粘粒曲线、Rb/Sr曲线和Ba/Sr曲线具有高度的同步同向变化趋势,可很好的指示研究区域内全新世的气候变化。而元素的含量变化是该区域气候变化的结果,其中Pb元素在黄土中的含量明显高于古土壤层,属于淋失性元素。Mn、Cr、Cu、Zn、Co、Ti元素在古土壤含量高于黄土层,属于富集性元素。     

新乡市大棚菜田土壤重金属积累特征及污染评价

采用微波消解-ICP-AES技术,测定不同种植年限大棚菜田土壤样品中As、Pb、Zn、Cd、Cr、Mn、Ni、Cu等重金属的含量,研究不同种植年限与大棚菜田土壤重金属累积的相关性以及大棚菜田土壤重金属累积特征,并利用地积累指数法进行污染评价。结果表明:大棚菜田土壤重金属Zn、Pb、Ni、Mn和Cu的含量与种植年限具有极显著相关性;大棚菜田土壤中重金属Cd和Cr的含量与种植年限不相关。重金属元素间相关性分析表明,Zn与Pb、Cd、Ni、Mn、Cr、Cu,Pb与Cd、Ni、Mn、Cr、Cu,Cd与Ni、Mn、Cr,Ni与Mn、Cr、Cu,Mn与Cr、Cu具有污染同源性,Cu与Cd、Cr不具有污染同源性。地积累指数法污染评价结果显示Cd的污染等级达到了6级,已构成了极严重污染;Zn和Cu的污染等级达到2级,已构成了中度污染;Pb、Mn的污染等级达到1级,已经构成了轻~中度污染;As、Ni、Cr均未构成污染。     

表面活性剂与EDTA对紫色土镉的化学行为影响

Elemental composition and geochemical characteristics of iron-manganese nodules from nine main soils in China were studied by chemical and multivariate statistical analyses to better understand the reactions and functions of ironmanganese nodules in soils and sediment. Compared to the corresponding soils, Mn, Ba, Cd, Co and Pb had strong accumulation, Ni had moderate accumulation, while Ca, Cu, Fe, Na, P, Sr and Zn accumulated to a minor degree in the iron-manganese nodules. In contrast, Si, Al, K, Mg and Ti were reduced in the iron-manganese nodules. The contents of Ba, Cd, Co, Cu, Ni, Pb and Zn were positively and significantly correlated with that of MnO2 in the iron-manganese nodules, while the contents of Cr, Cu, Ni, Pb and Zn were positively and significantly correlated with that of Fe2O3 in soils. Based on a principle component analysis, the elements of iron-manganese nodules were divided into four groups： 1） Mn, Ba, Cd, Co, Cu, Li, Ni, Pb and Zn that were associated with Mn oxides, 2） Fe, Cr and P that were associated with Fe oxides, 3） Si, K, and Mg that were included in the elemental composition of phyllosilicate, and 4） Ca, Na, Al and Ti that existed in todorokite, birnessite, lithiophorite and phyllosilicate. It was suggested that accumulation, mineralization and specific adsorption were involved in the formation processes of soil iron-manganese nodules.     

泾河泾阳段高河漫滩沉积元素与化合物指示的洪水事件

根据泾阳泾河高漫滩沉积剖面中128个样品的元素、化合物含量与粒度分析,研究了泾阳泾河高漫滩剖面沉积特征与洪水变化.结果表明,元素Ma,Ni,Cu,Zn,Ga,Pb,Ba,Rb,V和化合物Al2O3,Fe2O3,K2O含量在剖面各层中变化明显,分辨率高,能够清晰地指示洪水以及降水量的变化.JYa剖面分为18个沉积层,指示了18次大小不同的洪水和18个降水较多的年份.沉积物粒度细,元素Mn,Ni,Cu,Zn,Ga,Pb,Rb,V和化合物Al2O3Fe2O2,K2O含量高,元素Ba含量低,指示沉积时洪水强度小,洪水水位低,降雨量少.沉积物粒度粗,元素Mn,Ni,Cu,Zn,Ga,Pb,Rb,V和化合物Al2O3,Fe2O3,K2O含量低;元素Ba含量高,指示沉积时洪水强度大,洪水水位高,降雨量多.在这18次洪水事件中,在同一次洪水沉积层内形成了两个以上薄层的元素和化合物含量、粒度成分的微小变化,指示多数期次的洪水发生时期常有两个以上洪峰出现.泾阳泾河高漫滩第14,12,13,8,5,1层洪水沉积反映了泾河泾阳段全流域性的年降水量增加,且年降水量至少达到约800 mm.     

洛川苹果林地重金属分布特征和污染评价

通过取样调查和试验分析,选用As、Cr、Cu、Ni、Pb,Zn、Mn、Co.V等9种重金属元素研究了洛川苹果林地典型剖面(LC剖面)的重金属分布特征,并利用地累积指数法、重金属富集指数法、重金属潜在生态危害指数法,对洛川苹果林地重金属的污染状况和金属元素富集规律进行了初步研究.结果表明:As、Cr,Ni、Mn、V含量变化走势基本相同,总体上由表层向下波动递增,Cu、Pb、Zn、Co4元素含量垂向变化特征基本相似,由表层向下总体呈先减少后增多趋势;除Pb和Zn外,As、Cr、Cu、Ni、Mn,Co和V均有一定程度的富集.As的生态危害指数(Eri)较高,在9种重金属元素中最大,潜在生态危害指数(RJ)为39.9,但小于轻微生态危害的阈值150,表明该区苹果林地重金属尚未构成污染危害.     

Ratios of Closely Related Elements in Soil and Their Implications

This paper has investigated the ratios of closely related elements such as Mn, Cr, V, Ni, Co, Cu, Pb, Cd, Ba, Sr, La and Ce in the major soils of China, and the factors affecting them, and explored their use as indicators in soil formation, material transport and environmental pollution. Results show that the effect of soil-forming processes on the ratios of closely related elements varied with different elements, and became greater in the sequence of Ce/La <V/Cr=Ni/Co<Zn/Cu=Zn/Pb<Zn/Cd <Mn/Cr <Ba/Sr. The magnitude of the variation in the ratios of closely related elements depended on the chemical properties of the elements themselves, on the one hand, and the parent material and climatic conditions on the other.     

当归药材与产地土壤中无机元素的相关分析研究

采用ICP-MS和AAS测定了95批当归药材及其产地土壤中8种重金属元素和7种其他无机元素含量,研究药材与产地土壤中无机元素的相关性。结果表明,当归药材中的特征性无机元素是Fe、Mn、Mg、As、Cr及Ni,土壤中的特征性无机元素是Zn、Mn、Pb、Cr及Ni;当归药材中,无机元素Mn与Zn、Cr、Fe、Cu,Ni与Fe、Cd、Sb、Zn,As与Sb、Pb、Cr、Mn,Cu与Mg、Pb、Zn,Cr与Fe、Pb,Mg与Sb、Zn,以及Ca与Na呈显著正相关,而K与Na、Pb、Cd呈显著负相关;当归对土壤中的Na有富集作用;无机元素Sb、Ca和Na在当归药材与土壤中呈显著正相关。研究发现,中药当归含有丰富的有益无机元素,有害重金属元素含量极低,符合相关标准,在国际贸易及GAP种植方面具有明显的优势和广阔的发展前景。     

Trace elements in surface soils from the mineralized area of Madison County, Missouri, U.S.A.

Duplicate, bulked surface soil samples, from sites 10m apart, were collected at 97 locations 1000 m apart on a regular grid measuring 8x11 km. Data were obtained for Ag, Ba, Be, Cd, Co, Cr, Cu, Li, Mn, Ni, Pb, V and Zn. One field sample was a good predictor of its nearby duplicate for Co, Cu, Ni and Pb, satisfactory for Ba, Be, Cr, Mn and Zn, but poorer for Cr, Li and V. Maps of the variation in precision of the field samples did not reveal any association between abandoned mine sites and high variability. The median coefficient of variation for trace elements in the field duplicates was between 8 and 19.5%. The duplicated field data were averaged to yield a mean soil metal concentration at each sample location. Concentrations of Ba, Be, Cr, Li, Sr and V were comparable with other published values for similar soils in Missouri. Concentrations of Co, Cu, Mn, Ni, Pb and Zn were higher which was explained by pollution from mining activities. A graphical technique was used to calculate background levels for metals in the second group. Samples of forest litter were collected at 12 locations: Ag, Ba, Cd, Mn, Sr and Zn concentrations were higher in the litter whereas Li and V concentrations were higher in the subjacent mineral soil. Computer isoline maps of the distribution of elements revealed an association between areas of high soil Cu, Co, Ni, Pb and Zn and abandoned mines or mineralized rocks.     

Distribution of 32 Elements in Organic Surface Soils: Contributions from Atmospheric Transport of Pollutants and Natural Sources

Data are presented for 32 elements (Li, Be, B, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ge, As, Rb, Sr, Y, Zr, Mo, Ag, Cd, Sb, Cs, Ba, La, Ce, Pr, Nd, Sm, Hf, Tl, Pb, Bi) in organic-rich surface soils in Norway, based on samples from 464 sites. By considering geographical distributions based on isopleths, results from factor analysis, and ANOVA of median values from 12 different geographical regions, the contributions from natural and anthropogenic sources are estimated for each element. Long-range atmospheric transport of pollutants from areas out of Norway is a dominant source for Cd, Sb, Pb, and Bi and also a strongly contributing factor for Zn, As, Mo, and Tl. Also V, Ni, Cu, and Ge are somewhat affected, but other factors dominate for these elements. Local point sources of pollution provide significant contributions to soil concentrations of Ni, Cu, Zn, As, Mo, and Cd. The local bedrock is the overriding source of Li, Be, Ti, V, Cr, Mn, Rb, Zr, Cs, Ba, REE, Hf, and probably of Ge and Ag. Surface enrichment by root uptake in plants and return to the soil surface by decaying plant material is particularly evident for Mn, Zn, Rb, Cs, and Ba. These elements show no clear difference between south and north in the country, indicating that their plant uptake does not depend on latitude. In the case of B and Sr, atmospheric deposition of marine aerosols is an important source. Rb and Ag, and to a less extent Mn, Ga, and Ba, appear to be depleted in soils near the coast presumably due to cation exchange with airborne marine cations.     

我国几种土壤中铁锰结核的元素组成和地球化学特点

The objective of this research was to isolate a dichlorvos （2,2-dichlorovinyl dimethyl phosphate）-degrading strain of Ochrobactrum sp., and determine its effectiveness in remediation of a dichlorvos-contaminated soil. A dichlorvos-degrading bacterium （strain DDV-1） was successfully isolated and identified as an Ochrobactrum sp. based on its 16S rDNA sequence analysis. Strain DDV-1 was able to utilize dichlorvos as a sole carbon source, and the optimal pH and temperature for its cell growth and degradation were 7.0 and 30 ℃, respectively. Also, the growth and degradation of strain DDV-1 showed the same response to dissolved oxygen. In addition, the soil degradation test indicated that in soil spiked with 100 mg L^-1 or 500 mg L^-1 dichlorvos and inoculated with 0.5% or 1.0% （v/v） strain DDV-1, complete degradation of dichlorvos could be achieved in 24 h. The present study showed that strain DDV-1 was a fast dichlorvos-degrading bacterium in soil. However, further research will be needed to clarify the degradation pathway and the properties of the key enzymes involved in its biodegradation.     

东北及内蒙古东部的土壤微量元素

土壤中的微量元素在动植物生活中所起的重要作用日益被人们所重视.了解土壤中的这一部分资源对指导微量元素肥料的施用,从而达到农业增产以及对消除由土壤微量元素缺乏或过剩引起的某些动植物病害均具有重要的意义.探讨土壤微量元素在土壤剖面中的累积和迁移及其地理分布规律,则可进一步阐明土壤发生过程与生物地球化学特性的关系.     

海南岛土壤中若干元素的因子分析

本文用因子分析方法对海南岛土壤中若干元素的分布规律进行初步探讨.通过Q型分析表明,该地区土壤样品主要分成两大类.一类为富含铁族元素,另一类为铁族元素含量相对较低的.由R型分析结果表明,除铁族元素为一类外,易淋溶元素锶、抗风化元素锆分别各成一种类型.说明土壤中元素分布与成土母质类型和元素地球化学性质有关.     

华中黄棕壤和黄褐土粘粒胶膜的微量元素地球化学特征

The relationships between the basic properties and trace elementsin soil argillans and corresponding matrix soils were studied by sampling from the B horizons of 26 Alfisols in croplands of the subtropical area in Central China. The soil elements (K, Na, Ca, Mg, Mn, Co, Cu, Cr, Cd, Li, Mo, Ni, Pb, Ti, V, and Zn) were extracted by acid digestion and their contents were measured using inductively coupled plasma optical emission spectrometry (ICP-OES). The mean contents of clay and organic matter in the argillans were approximately 1.1 and 1.3 times greater than those in the matrix soils, respectively. The pH values and the contents of P₂O₅ and bases (K₂O, Na₂O, CaO, and MgO) in the argillans were higher than those in the corresponding matrix soils. Cu, Cd, Ti, and V were enriched in the argillans. Correlation coefficients and factor analyses showed that Co, Cu, Li, and Zn were bound with phyllosilicates and manganese oxides (Mn-oxides) in the argillans. Cr and Pb were mainly associated with iron oxides (Fe-oxides), while Ni was bound with Mn-oxides. Cd, Ti, and V were chiefly associated with phyllosilicates, but Cr and Mo were rarely enriched in the argillans. In contrast, in the matrix soils, Co and Zn were associated with organic matter and Fe-oxides, Cr existed in phyllosilicates, and Mo was bound to Fe-oxides. Cd, Ti, and V were associated with organic matter. The results of this study suggest that clays, organic matter, and minerals in the argillans dominate the illuviation of trace elements in Alfisols. Argillans might be the active interfaces of elemental exchange and nutrient supply in cropland soils in Central China.     

Metal Pools, Fluxes, and Budgets in an Acidified Forested Catchment on the Precambrian Shield, Central Ontario, Canada

Atmospheric emissions of metals have decreased in North America; yet, metals remain an environmental concern due to their environmental persistence and toxicity to biota. In this study, pools and mass budgets were calculated for 15 metals in an acidified forested catchment in Central Ontario. Metals that were enriched in bulk deposition over background average values (As, Cd, Pb, Zn) were generally enriched in the forest floor and upper lake sediment. While the metal pool in vegetation is small compared with the soil pool, internal cycling of metals via litterfall is comparable to atmospheric deposition, soil water, and stream fluxes. Partitioning coefficients calculated from metal concentrations in soil water and bulk soil suggest that Cd, Mn, Ni, and Zn are the most mobile. The mineral soil and lake sediments were sinks for most metals, while the wetland was a source of metals during the study year, which was a drought year. Overall, lithogenic metals (Al, Ba, Co, Fe, Mn, Rb, Sr, Zn) primarily from a weathering source generally exhibited net export from the catchment, while metals contained in atmospheric pollution (As, Cd, Cr, Cu, Ni, Pb, V) exhibited net retention. Despite the acidified nature of the catchment, it functions to retain many pollutant metals.     

Inductively coupled plasma optical emission spectrometric determination of minerals in thyme honeys and their contribution to geographical discrimination

Twenty-four Spanish thyme honey samples were analyzed using inductively coupled plasma optical emission spectrometry (ICP-OES). Twenty-four minerals were quantified for each honey. The elements Al, As, Ba, Ca, Cr, Cu, Fe, K, Li, Mg, Mn, Na, P, Pb, S, Se, Si, Sr, and Zn were detected in all samples; seven elements are very abundant (Ca, K, Mg, Na, P, S, and Si), and six are not abundant (Al, Cu, Fe, Li, Mn, and Zn). Eleven of them are trace elements (As, Ba, Cd, Co, Cr, Ni, Mo, Pb, Se, Sr, and V) at <1 mg kg(-)(1). Classification of thyme honeys according to their origin (coast, mountains) was achieved by pattern recognition techniques on the mineral data. By means of principal component analysis, a good separation by geographical origin is obtained when scores for the two first principal components are plotted. Classification functions of 11 metals (Al, As, Cr, Cu, K, Li, Mg, Na, P, S, and V) were obtained using stepwise discriminant analysis and applied to classify correctly approximately 100% of the honey samples.     

Geochemical investigations on atmospheric precipitation in a medium-sized city (Göttingen,F.R.G.)

The concentration of 27 elements was investigated in 10 samples of precipitation from Göttingen, collected during May and September 1972. Göttingen is a non-industrial town of 130000 inhabitants, situated in a rural area, and essentially all the dissolved and undissolved material in rainwater is locally derived. Elemental concentrations in freshwater and shale are used for comparison with the dissolved elements in precipitation and the undissolved residue. The two phases have been separated after evaporation (concentration factors: 15 to 25-times). Phosphorous, Zn, Mn, and Pb are enriched in rainwater, while Si, Mg, Na, Ca, Cl, Fe, Hg, K, Li, and Al are depleted relative to average freshwater. Sulfate, Cd, and Cu have similar concentrations in rain and freshwater. The factors of accumulation between elements in residue and average shale are calculated after normalization to the Al-value. They are: ? 100 for Ag, Hg, Pb; between 10 and 20 for Zn, Cd, P, Cu, Mo; > 2 for Cr, Bi, Ni, Ba, Ti, V ; between 0.9 and 2.0 for Rb, K, Na, Li, Mg, Mn, Fe, Si, Ca; and 0.5 for Tl. The trace element accumulation is due to different anthropogenic sources: combustion of liquid petroleum fuels contributes to Ph, V, Ni, Mo, Hg, and sulfate, combustion of coal to Ba, sulfate, and chloride, and to the. readily volatile elements such as Hg, Cd, Tl, Bi, and Ag, combustion of refuse to Ag, Bi, Pb, Cd, Hg, Zn, Cr, Cu, Ba, and Mo in highly variable amounts. Fertilizers and road salts change the chemistry of soils and indirectly supply P, alkali and alkaline-earth metals to the fly dust. Modest industrial activity is responsible for high Cu and Cr concentrations. Despite the appreciable accumulation of some toxic elements, the precipitation in Göttingen is relatively pure compared to other areas. Favorable geologic conditions around Göttingen decrease the negative influences of potentially harmful airborne elements. The high carbonate content in the dust neutralizes the anthropogenic acids in the rainwater. Furthermore, the toxic trace elements are diluted, especially in the center of Göttingen, by a large amount of airborne dust.