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1.
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. 相似文献
2.
3.
Gonzálvez A Armenta S Pastor A de la Guardia M 《Journal of agricultural and food chemistry》2008,56(13):4943-4954
Different sample preparation methods were evaluated for the simultaneous multielement analysis of wine samples by inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS). Microwave-assisted digestion in closed vessel, thermal digestion in open reactor, and direct sample dilution were considered for the determination of Li, Be, Na, Mg, Al, K, Ca, Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Sr, Y, Mo, Cd, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Tl, Pb, and Bi in 12 samples of red wine from Valencia and Utiel-Requena protected designation of origin. ICP-MS allows the determination of 17 elements in most of the samples, and using ICP-OES, a maximum of 15 elements were determined. On comparing the sample pretreatment methodology, it can be concluded that the three assayed procedures provide comparable results for the concentration of Li, Na, Mg, Al, K, Ca, Mn, Fe, Zn, and Sr by ICP-OES. Furthermore, ICP-MS data found for Cu, Pb, and Ba were comparable. Digestion treatment provides comparable values using both total decomposition in open system and microwave-assisted treatment for Cu by ICP-OES and for Cr, Ni, and Zn by ICP-MS. Open vessel total digestion provides excess values for Cr, Mn, Fe, and Zn by ICP-OES and defect values for Se. However, direct measurement of diluted wine samples provided uncomparable results with the digestion treatment for Mn, Cu, Pb, Zn, Ba, and Bi by ICP-OES and for Mg, Cr, Fe, Ni, and Zn by ICP-MS. Therefore, it can be concluded that microwave-assisted digestion is the pretreatment procedure of choice for elemental analysis of wine by ICP-based techniques. 相似文献
4.
关中盆地全新世黄土-土壤剖面微量元素的地球化学特征及其古气候意义 总被引：2，自引：0，他引：2
通过对老官台全新世黄土剖面12种微量元素的测定分析,结合本剖面已测定的粒度、磁化率、光释光(OSL)年龄,研究和揭示了它们在表生环境下的地球化学特征和古气候意义。微量元素在风化成壤过程中,其活动性由强至弱顺序为BaSrCdPbLiZnCuCrMnCoRbNi。其中Rb、Li、Cr、Co、Zn、Cu、Mn、Ni八种元素在土壤形成过程中相对富集,含量较高;Sr、Ba、Cd三种元素在土壤中相对淋失,含量较低;但Zn、Cu、Mn、Ni、Pb五种元素对黄土层和土壤层的区别不是很明显。因此,Rb、Li、Cr、Co的高含量反映了较温湿的成壤环境,低含量反映了较冷干的粉尘加积环境;而Sr、Ba、Cd低含量反映了较温湿的成壤环境,高含量反映了较冷干的粉尘加积环境。Pb、Zn、Cu、Mn、Ni、Cd元素含量在表土层中的富集主要与现代耕作活动或工业污染有关,反映了人类活动强度的不断增强。LGT剖面主要微量元素的变化清楚地记录了关中盆地自末次冰消期以来气候环境经历的显著波动变化。 相似文献
5.
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. 相似文献
6.
Water, Air, &; Soil Pollution - Concentrations of Al, Cd, Co, Cr, Cu, Mn, Ni, Pb, Sr, V, Zn,N, P, K, Ca, Mg, Fe and S were measured in water, river bottomsediments and in Elodea canadensis... 相似文献
7.
我国几种土壤中铁锰结核的元素组成和地球化学特点 总被引：7，自引：0，他引：7
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. 相似文献
8.
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. 相似文献
9.
Barium, Be, Co, Cr, Cu, Li, Mn, Ni, Pb, Sr, and V concentrations were determined in 97 surface soil samples collected 1000 m apart on a regular grid in Madison county, Missouri, U.S.A. The data were normalized by a log10 transformation and a matrix of correlation coefficients computed. Strong correlations were observed between several metals and statistically significant correlations were found between others. The data were then analyzed by R-mode factor analysis. Three factors satisfactorily explained the data variance and were interpreted as follows. Factor 1 (55% variance) comprised a group of elements which contaminated local soils as a consequence of operations connected with non-ferrous metal mining. Factor 2 (33 % variance) contained elements which accumulate in soils during weathering. The remaining elements were grouped together in factor 3 (12% variance) and here soil contents appeared to be controlled by rock composition. 相似文献
10.
Aguilar EG Cantarelli MA Marchevsky EJ Escudero NL Camiña JM 《Journal of agricultural and food chemistry》2011,59(17):9059-9064
The characterization of amaranth seeds (Amaranthus spp.) was developed for Amaranthus hypochondriacus, Amaranthus cruentus, and Amaranthus dubius. The elemental concentrations were determined by inductively coupled plasma optic atomic spectroscopy. Pattern recognition methods were used for the characterization of seed samples: nonsupervised methods included principal components analysis and cluster analysis; supervised methods were linear discriminant analysis and partial least squares discriminant analysis (PLS-DA). Informed are the concentrations of the following elements: Ag, Al, Ba, Ca, Co, Cr, Cu, Fe, K, La, Li, Mg, Mn, Mo, Na, Ni, P, S, Sr, V, Zn, and Zr. The lowest mineral content was found in A. hypochondriacus, and the highest one was found in A. dubius. For the classification, selected variables for all multivariate methods were Ba, Cr, Li, Mn, Ni, S, and Sr. Nonsupervised methods allowed us to distinguish between the three species of amaranth; however, PLS-DA supervised methods showed the best prediction ability. 相似文献
11.
Larry P. Gough Larry L. Jackson John A. Sacklin 《Water, air, and soil pollution》1988,38(1-2):157-167
Element-concentration baselines are given for Parmelia sulcata and associated soils. Parmelia chlorochroa was found sporadically and therefore only representative concentration ranges are reported for this species. Element data include (1) for lichens; Al, As, Ba, B, Ca, Cr, Cu, Fe, Hg, Mn, Ni, P, Sr, S, Ti, V, Y, and Zn; and (2) for soils: Al, Ba, Be, Ca, Cs, Cr, Cu, Fe, Hg, Mg, Mn, Ni, Nb, P, Pb, Sr, S, Ti, V, Y, and Zn. Very little (usually < 10 %) of the variability in the element data for lichen material occurs regionally (> 7.2 km); thus, P sukata is, in general, chemically similar throughout the park. This same uniformity was found for soil geochemistry. Numerous samples collected at close intervals would be required, therefore, to produce detailed element-concentration maps for P. sulcata and soils. No instances of elemental phytotoxic conditions were found; however, P. sulcata apparently possesses large concentrations of Ba, Cu, Fe, Pb, S, V, and possibly Zn. 相似文献
12.
Multielement analysis of Canadian wines by inductively coupled plasma mass spectrometry (ICP-MS) and multivariate statistics 总被引：1，自引：0，他引：1
Trace element fingerprints were deciphered for wines from Canada's two major wine-producing regions, the Okanagan Valley and the Niagara Peninsula, for the purpose of examining differences in wine element composition with region of origin and identifying elements important to determining provenance. Analysis by ICP-MS allowed simultaneous determination of 34 trace elements in wine (Li, Be, Mg, Al, P, Cl, Ca, Ti, V, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Br, Rb, Sr, Mo, Ag, Cd, Sb, I, Cs, Ba, La, Ce, Tl, Pb, Bi, Th, and U) at low levels of detection, and patterns in trace element concentrations were deciphered by multivariate statistical analysis. The two regions were discriminated with 100% accuracy using 10 of these elements. Differences in soil chemistry between the Niagara and Okanagan vineyards were evident, without a good correlation between soil and wine composition. The element Sr was found to be a good indicator of provenance and has been reported in fingerprinting studies of other regions. 相似文献
13.
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. 相似文献
14.
Opekunova M. G. Opekunov A. Yu. Kukushkin S. Yu. Ganul A. G. 《Eurasian Soil Science》2019,52(4):380-395
Eurasian Soil Science - Background concentrations of heavy metals (Cu, Zn, Ni, Co, Fe, Mn, Cr, Pb, Hg, Cd, Ba, Sr, and Sc) in soils and bottom sediments were determined for the background and... 相似文献
15.
To determine “normal” levels of trace elements in soils, soil samples taken all over Belgium were analysed. The selection of the sampling places was based on the geological substrata, from which the soils originate and on the texture class to which they belong. The elements As, B, Be, Cd, Co, Cr, Cu, Hg, Mn, Ni, Pb, Sb, Se, Ti, V and Zn were determined using an extraction method with strong acids. The found concentrations were called “total acid extraction concentrations”, although this extraction does not extract all the elements which are incorporated into the minerals. This has been done, however, by arc emission spectrography which was applied to determine the elements Ag, B, Co, Cr, Ga, Mo, Ni, Sn, Sr and V. The greatest difference between the “overall total” concentrations and the “total extractable concentrations” were found for chromium. Based on the obtained results, an upper limit for normal levels of trace elements was fixed. For Ag, Cd, Hg, Pb and Sb, this upper limit value is almost the same for all the investigated soils irrelevant of their texture. The same conclusion could not be made for the other elements. For these elements, the soil texture and also the geological parent material, on which the soil was formed, have an influence on the upper limit value. 相似文献
16.
通过野外采样和实验室分析,在分析土壤基本理化性质的基础上,重点研究宝鸡长青镇铅锌冶炼厂周边土壤中重金属元素的含量和形态特征,并进行了污染评价。结果表明,宝鸡长青镇铅锌冶炼厂周边土壤中Cu、Pb、Zn、Mn、Co、Ni、Cr的平均含量分别为31.8、41.3、102.6、704.6、14.4、37.4、83.2mg·kg-1,均高于陕西省和全国土壤元素背景值,尤其是Cu、Pb和Zn。土壤中Cu、Zn、Ni和Cr主要以残余态的形式存在,Pb、Mn和Co主要以可还原态和残余态的形式存在,重金属的迁移顺序为Mn（63.91%）〉Pb（60.08%）〉Co（51.70%）〉N（i37.12%）〉Zn（32.09%）〉C（r30.58%）〉Cu（19.95%）,其中,Mn、Pb和Co有50%~65%可以发生迁移,易被生物体利用,危害较大。评价结果表明,宝鸡长青镇铅锌冶炼厂周边土壤主要受到了Pb的轻度污染。 相似文献
17.
Amanda L. Landre Shaun A. Watmough Peter J. Dillon 《Water, air, and soil pollution》2010,209(1-4):209-228
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. 相似文献
18.
Isela Lavilla A. V. Filgueiras F. Valverde J. Millos A. Palanca C. Bendicho 《Water, air, and soil pollution》2006,172(1-4):273-293
Depth concentration profiles of 26 elements, i.e. trace elements (As, Ba, Cd, Co, Cr, Cu, Hg, Ni, Pb, Rb, Sr, V and Zn), lithophiles (Si, Al, Fe, Mn, Na, K, Mg, Ca and Ti) and nutrients (C, P, N, S) have been established in a sediment core collected at the Respomuso Lake (Pyrenees, Spain). This high altitude lake of glacier origin was transformed into reservoir in the fifties of last century. Correlations among the depth profiles of the above elements were established. HCl-extractable elements, which are better related to bioavailability, followed the profiles of total contents. Principal component analysis was applied to establish the binding behaviour of trace elements in the sediment matrix and, in turn, to search for their anthropogenic or natural sources. It was seen that Cu, Ni, Pb, Sr and Zn clustered together, and with exception of Sr, they were not clearly associated with any major component of the sediment. Their depth profiles correlate well with each other, hence indicating their presence as a result of atmospheric pollution. Redox-sensitive elements such as Fe and Mn follow a similar trend along the vertical profile. Depth profiles of As an Co correlate well with those of Fe and Mn. Principal component analysis showed that As, Co, Fe and Mn clustered together, which confirms the close association of As and Co with Fe-Mn oxyhydroxides. As concentrations in many strata exceed the ERM value, and therefore, significant biological effects are expected. Dissolution of minerals such as pyrite, chalcopyrite and galena taking part in the mineralogy of this area accounts for the As concentration found. Ba, Cr, Rb and V were associated with the sediment matrix (aluminosilicates), hence showing low mobility. 相似文献
19.
Local variability in the heavy metal concentrations of precipitation and seepage water from forest sites in the Solling Concentrations of Cr, Mn, Fe, Co, Ni, Cu, Zn, Cd and Pb in precipitation and seepage water have been measured continuously with local replicates during a 6-months period at a beech and a spruce forest site. Variation coefficients of the avarage concentrations were, in most cases, well below 30 %, being mainly caused by local differences. Comparison of means showed a significant increase of heavy metal concentration in the canopy drip of beech (Mn, Fe, Pb) and spruce (Cr, Mn, Fe, Ni, Zn, Pb) compared to bulk precipitation measured in the open field. Concentration of Mn, Co, Ni, Zn and Cd in the seepage water is significantly higher under spruce compared to beech. These results point at higher filter efficiency of the spruce canopy, compared with beech, for air pollutants, but a smaller retention capacity of the soil under spruce for heavy metals. 相似文献
20.
洛川苹果林地重金属分布特征和污染评价 总被引：2，自引：0，他引：2
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. 相似文献