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1.
The concentrations of 13 trace elements were determined in soils and Sangiovese grapes collected in vineyard zones of Tuscany (Italy). The purpose was to establish a correspondence among the chemical composition of grape, the geochemistry of vineyard soil and the geolithological features of cultivation zone, and determine the provenance of the grapes by means of their chemical fingerprints. Statistical analysis of Ba, Rb and Sr concentrations distinguished three classes of grapes according to the geochemical and geopedological characteristics of the soils. Grapes with the highest Sr levels grew on high‐Sr soils derived from calcareous, calcareous‐marly and marly‐clayey rocks, whereas the most elevated Rb concentrations characterized the berries cultivated on soils formed from clayey‐marly and sandy‐marly lithologies. Grapes with the highest Ba concentrations grew on soil derived from arenaceous rocks and carbonate lithologies of evaporitic origin. These findings suggested that Ba, Rb and Sr could be used as fingerprints for the chemical traceability of Sangiovese grapes. 相似文献
3.
Croffie Maame E. T. Williams Paul N. Fenton Owen Fenelon Anna Daly Karen 《Journal of Soils and Sediments》2022,22(3):818-830
Purpose
Information about particle size distribution (PSD) and soil texture is essential for understanding soil drainage, porosity, nutrient availability, and trafficability. The sieve-pipette/gravimetric method traditionally used for particle size analysis is labour-intensive and resource-intensive. X-ray fluorescence (XRF) spectrometry may provide a rapid alternative. The study’s aim was to examine the use of XRF for rapid determination of PSD in Irish soils.
MethodsSoils (n?=?355) from existing archives in Ireland were analysed with a benchtop energy-dispersive XRF (EDXRF). Correlation and regression analyses were determined to compare Rb, Fe, Al, and Si concentrations to % clay, % silt, and % sand. Also, linear regression models were developed to compare % clay, % sand, and % silt measured by the gravimetric method to values predicted by EDXRF.
ResultsThe relationship between element concentration and PSD was dependent on parent material. Rb, Al, and Fe showed a significant (p?<?0.05) correlation (r?>?0.50) with % clay and % sand in soils derived from limestone and siliceous stone parent materials. Rb was the best predictor for % clay (R2?=?0.49, RMSE?=?10.20) in soils derived from limestone and siliceous stone-derived soils.
ConclusionGeochemistry and clay mineralogy of the soils’ parent material strongly influenced the EDXRF’s ability to predict particle size. The EDXRF could predict % clay in soils from parent materials which weather easily, but the opposite was true for soils with parent material recalcitrant to weathering. In conclusion, this study has shown that the EDXRF can screen % clay in soils derived from limestone and siliceous stone parent materials.
相似文献4.
Shin-ichi Yamasaki Akira Takeda Masami Nanzyo Ichiro Taniyama Makoto Nakai 《Soil Science and Plant Nutrition》2013,59(4):755-765
Five hundred and fourteen soil samples collected from 78 sites in Japan were analyzed for their contents of trace and ultra-trace elements. We estimated the background levels (natural abundance) of 57 elements in soils. The concentration ranges were so wide that the ratios of the highest values to the lowest values were more than 100 for all the elements, with the exception of Be, Ga, Mo, Ag, In, Sn, and Ba. While the concentrations of the first transition elements (21Sc to 30Zn in atomic numbers) were higher than the concentration of the other elements, those of lighter (3Li and 4Be) and heavier elements tended to decrease, with an increase or decrease of atomic numbers, with the apparent exception of Pb, Th, and U. Concentrations of elements with even atomic numbers were, in most of the cases, higher than the concentrations of both adjacent elements with odd atomic numbers. Frequency distribution of most of the elements was strongly positively skewed. Markedly positive correlation coefficients (r>0.9) were observed among the elements within the same group in the Periodic Table in many combinations. The dendrogram obtained by cluster analysis showed that the occurrence and distribution of the elements in soils were mostly controlled by the chemical properties of each element, rather than by the nature and properties of individual soil samples. The total contents of the elements in soils were strongly dependent on the chemical composition of the parent rocks from which respective soils were derived. 相似文献
5.
湖南张家界典型植烟土壤地球化学特征研究 总被引：1，自引：0，他引：1
为了研究张家界山地植烟区域土壤的成土环境及地球化学元素的丰缺状况和迁移富集规律,为烟区优质特色烟叶的生产和布局提供科学依据,本文采集23个长期耕种的典型植烟土壤剖面样品,测定分析了25种地球化学元素(氧化物)的含量,并对土壤的风化发育状况和元素(氧化物)的迁移富集特征进行了研究。结果表明,张家界烟区主要成土母质如石灰岩、板页岩、紫色砂页岩风化物均受到了较强的风化作用,化学风化指数(CIA)介于73.19～88.03之间,总体上土壤具有Ca、Na贫乏而Fe、Al相对富集的化学组成特征。其中紫色砂页岩风化物发育形成的紫色土的风化作用较强,土壤的淋溶作用较强;石灰岩风化物发育形成的土壤富铝化程度较低。黄壤、水稻土、紫色土中地球化学元素多数表现出一定的富集特征,大量有益营养元素的富集对于提高烟叶产量具有重要作用。土壤剖面淋溶层中元素(氧化物)P、B、Se、Mn、Zn、Cu、Ni、Y、Sc、La、Fe2O3、SiO2的含量均高于中国或世界土壤元素(氧化物)中值(均值),而N、S、Cl、Mo、Co、Sr、Br、I、CaO、MgO、K2O、Na2O、Al2O3的含量偏低,其中元素(氧化物)N、P、S、Mo、Se、Mn、Zn、Br、I、CaO、MgO在土壤剖面中的含量变化较大。通过对元素(氧化物)富集系数的聚类分析,将元素(氧化物)分为3类:呈较强富集特征的元素N、P、S、Se;呈较强迁移特征的元素(氧化物)Br、I、Mn、CaO;变化较稳定的其他元素。微量元素B、Zn、Cu和稀土元素Y、Sc、La含量较丰富且变化相对稳定,表明除了常量元素N、P、S以外,微量元素Se、B、Zn、Cu和稀土元素Y、Sc、La可能是影响张家界烟区烤烟品质的重要特征元素。 相似文献
6.
Georgios Papastergios Anestis Filippidis Jose-Luis Fernandez-Turiel Domingo Gimeno Constantinos Sikalidis 《Water, air, and soil pollution》2011,216(1-4):141-152
The aim of the present study was to estimate the geochemical background and anomaly threshold values of the surface soils in Kavala, northern Greece. In order to reach this goal, a simple and practical procedure was applied. This procedure included the extraction of 42 major and trace elements by analytical grade HNO3 from 65 surface soil samples, analysis by inductively coupled plasma?Coptical emission spectrometry and inductively coupled plasma?Cmass spectrometry, the distribution of the elemental data displayed on probability graphs (Q-Q plots), and the visualization of the results spatially by GIS software. The results indicated that natural factors mostly influence the elevated concentrations of Al, Ca, Fe, K, Mg, Si, B, Ba, Ce, Ga, Ge, La, Li, Mn Rb, Sb, Se, Sn, Sr, Y, and Zr, while anthropogenic activities mostly influence the elevated concentrations of Ag, As, Cd, Co, Cr, Cs, Cu, Hg, Mo, Ni, Pb, Th, Ti, U, V, W, and Zn. Nevertheless, almost all the elements determined showed their elevated concentrations inside the industrial part of Kavala area, which implies that the anthropogenic activities taking place in the study area, influence importantly the spatial distribution of the elements. The methodology followed in this research seems to be an adequate alternative for soil environmental studies. 相似文献
7.
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. 相似文献
8.
9.
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
10.
Yanchong Huangfu Michael E. Essington Shawn A. Hawkins Forbes R. Walker John S. Schwartz Alice C. Layton 《Communications in Soil Science and Plant Analysis》2019,50(11):1358-1369
Determining the total elemental concentrations of soils requires a total dissolution method, in which hydrofluoric acid (HF) is commonly used. However, this method is tedious and risky due to the dangerous reagent HF. This study compared a single acid extraction technique using a nitric acid (HNO3) extraction method to total dissolution (HF + microwave assisted aqua regia) for evaluating the total elemental concentrations in soils and sediments. The two methods were used to analyze the elemental content of soils and sediments from the Oostanaula Creek and Pond Creek watersheds in East Tennessee. Twenty-one elements (Al, Ba, Ca, Co, Cr, Cu, Fe, K, La, Li, Mg, Mn, Nd, P, S, Si, Sr, Ti, V, Zn, and Zr) were subsequently measured using inductively coupled plasma optical emission spectrometry (ICP-OES). The extraction efficiency for HNO3 relative to the total was compared and discussed. In general, HNO3 can extract the elements in absorbed phases and those residing in non-silicate minerals. Six elements (Ba, Co, Fe, Ca, Mn, and P) generated significant correlations between total and HNO3 in both OC and PC watersheds. Finally, the elements were grouped according to the interrelationships of their total elemental concentrations based on the dendrogram plots, suggesting their geochemical association in soils and sediment forming minerals. 相似文献
11.
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
12.
The concentrations of 21 elements were determined in 1 yr old needles of Norway spruce (Picea abies) at 39 different sites: The following soil parameters were measured at 3 different depths: pH, loss on ignition, total and EDTA-extractable concentrations of 28 elements. Needle concentrations were tested for correlations with soil parameters. The following significant correlations were found with pH: Al, Co, Cs, Mn, and Rb in needles increased with decreasing soil pH, whereas Ba and Sr decreased. Needle concentrations of As, Ca, Cu, Fe, K, La, Mg, P, Sb, Sc, V, and Zn had no significant correlations with soil pH. AI and Ba in needles correlated also with A1 and Ba extracted from the soil. Needle concentrations of the pairs Co and Mn, Cs and Rb, and Ba and Sr showed significant positive interelement correlations, whereas concentrations of P and K had negative interelement correlations with Mn. 相似文献
13.
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
14.
柴达木盆地中西部极度干旱,气候冷温,盐生植物黑果枸杞占有一定生态位。采集0 ~ 40 cm土样,用超细粉末压片－X射线荧光光谱法,测定部分元素含量,研究了柴达木黑果枸杞原生地土壤元素分布特征。结果表明:原生地土壤中人体必需微量元素Se、Sr含量较高,Co、Ni、V、Zn等含量相对低;Cl、S含量、富集程度（Kc > 3.0）俱高,稀土类元素富集程度普遍偏低,Ag、Pb、Br、W有局部聚集现象（C.V > 50%）,但未有含量超过《土壤环境质量农用地土壤污染风险管控标准》土壤污染风险筛选值控制限值的元素。柴达木黑果枸杞原生地土壤能够较高程度富集Cl（Kc > 40.0）、S（Kc > 7.5）、Se（Kc > 4.0）及Sr（Kc > 1.0）等元素是母质与气候双重因素造就的结果。 相似文献
15.
海南岛北部玄武岩上土壤发生研究Ⅲ.元素地球化学特征 总被引：10，自引：0，他引：10
对海南岛北部玄武岩上不同风化成土年代的土壤研究发现，随风化成土年龄增加，土壤具有Sr、Ba含量减少，Sr/Be比值降低，而Ni、Cr、Co、V、Sc以及Fe/Ni和Fe/Co比值有增加的趋势。Ba/Nb与风化成土年龄相关性极好，可作为反映土壤风化程度的良好指标。运用质量平衡原理，以Ti为非移动元素探讨元素的迁移，发现元素淋溶作用在土壤发育初期最强烈。90％以上的Ca、Mg、K、Na在新成土阶段淋失，P的淋失也基本发生在此阶段：约60％Si至雏形土阶段时已遭淋溶。 相似文献
16.
Little is known about solubility and soil solution concentrations of most elements occurring in the solid phase of soils. This study reports changes in solution concentrations of 60 mineral elements following CaCO3 addition to a moderately acid semi‐natural soil, and possible mechanisms accounting for the differing solubility patterns as related to soil acidity are discussed. Soil solutions were obtained by high‐speed centrifuging and ultrafiltration (0.2 μm) of samples at 60% water‐holding capacity of the A horizon of a Cambisol developed from a shale–gneiss moraine and supplied with CaCO3 at 20 rates to yield a soil solution pH range of 5.2–7.8. Concentrations of elements were determined in the solutions by ICP‐AES or (for most elements) ICP‐MS. Several distinct patterns of soil solution concentrations as a function of soil solution pH were demonstrated. Positively related to pH and CaCO3 supply were soil solution concentrations of As, Br, Mo, S, Sb, Se, U, and W, and to a lesser degree, Co, Cr, Hg, Mg, and Sr. Inversely related to pH were concentrations of Al, B, Ba, Bi, Cs, Ce, Eu, Ga, Ge, Fe, Li, K, Rb, Na, Th, and Ti; less distinctly inversely rated were Dy, Er, Gd, Hf, La, Lu, Mn, Nd, Pr, Sm, Sc, Si, Tl, Tm, and Yb. ‘U‐shaped’ relationships to pH were demonstrated for the concentrations of Ag, Cd, Nb, Ni, P, V, and Zr. There were no or irregular relations between pH and concentrations of Be, Cu, Ho, Pb, Ta, and Tb. Differences between elements in their soil solution concentrations as related to total (HNO3‐digestible) concentrations and the solubility of organic C were also treated. Increasing the pH of a soil by adding CaCO3 changes the solubility of most mineral elements substantially, the several distinct patterns observed being governed by, for example, ionic properties and charge, affinity for organic compounds, and pH‐dependent formation and solubility of complexes. 相似文献
17.
Shin-ichi Yamasaki Akira Takeda Kazuhiko Kimura Noriyoshi Tsuchiya 《Soil Science and Plant Nutrition》2016,62(2):121-126
The concentrations of chromium (Cr) and zirconium (Zr) in 503 soil samples collected from 78 site in Japan were determined by using two utterly different methods. The first was the relatively widely used inductively coupled plasma-mass spectrometry (ICP-MS) combined with digestion with hydrofluoric acid (HF) and perchloric acid (HClO4). The second was a non-destructive polarizing energy dispersive X-ray fluorescence spectrometric method (EDXRF) using pressed powder pellets. The Cr concentrations obtained by EDXRF were higher than those obtained by ICP-MS in ~75% of the samples. The EDXRF/ICP-MS ratios ranged from 0.48 to 9.65, and the geometric mean was 1.23. A typical example having big a difference in Cr content between the two methods was found in seven samples taken from a podzolic soil developed on sand dunes in northern Hokkaido. This sampling site is around 20 km from the northern edge of a serpentinite area that extends from north to south, forming the backbone mountain range of Hokkaido. The Cr concentrations obtained by ICP-MS for the seven samples were 27.9–52.2 mg kg?1, similar to the average for all the samples, whereas those obtained by EDXRF were 101–460 mg kg?1, falling within the range between the third quartile and the maximum for all the samples. It would be difficult to predict these results from the analytical data of other elements because the samples were high in silica (SiO2) and low in magnesia (MgO), and did not show any characteristics typical of soils derived from serpentinite. X-ray adsorption near-edge structure (XANES) showed that Zr occurred as zircon (ZrSiO4) in soils. The differences between the two methods were greater for Zr than for Cr. Zirconium concentrations obtained by EDXRF were higher than those by ICP-MS for all samples except three. The difference between the two methods was more pronounced in soils derived from granite that is widespread in western Japan. The EDXRF/ICP-MS ratios for seven soil samples from different horizons at a single sampling site ranged from 4.82 to 6.94 and were generally higher at the A horizon (Apg and Ag) and decreased with depth. Our results indicate that there is a high possibility of underestimation of Cr and Zr contents in soils for a considerable number of samples if determined with ICP-MS, and it could also overlook some important chemical characteristics of soils. 相似文献
18.
Trace element (TE) and rare earth element (REE) contents in red soils from the Dongting Lake area of China were determined to understanding the provenance and weathering characteristics of the red soils. The results showed similar REE distribution patterns among red soils from the Dongting Lake area, Xiashu loess from Zhenjiang, loess and the Pliocene red soil from the Loess Plateau. These patterns implied a similar provenance from dust-storms, except for red soil R5 which formed by bedrock weathering and had significant light REE (LREE) enrichment and heavy REE (HREE) depletion due to longer weathering periods and higher intensity of weathering. Trace element, especially the Rb/Sr and Li/Ba ratios, and REE, especially the LREE/HREE ratio and δEu could trace weathering intensity. Higher Rb/Sr, Li/Ba, and LREE/ HREE ratios and negative Eu anomalies were present in the red soil from the Dongting Lake area. The weathering intensity was in the decreasing order of R5 in the Dongting Lake area > red soil from the Dongting Lake area (including reticulate red soil, weak reticulate red soil, and homogeneous red soil formed by dust storms) > Xiashu loess from Zhenjiang > Loess-paleosol and Pliocene red soil from the Loess Plateau. Variations in the TE and REE contents of soil could be effectively used to study the provenance and the weathering intensity. 相似文献
19.
Baseline element concentrations are given for dune grass (Ammophilia arenaria), willow (Salix repens), moss (Hylocomium splendens) and associated surface soils. Baseline and variability data for pH, ash, Al, As, Ba, C, Ca, Cd, Ce, Co, Cr, Cu, Fe, Hg, K, La, Li, Mg, Mn, Na, Nb, Nd, Ni, P, Pb, S, Sc, Se, Sr, Th, Ti, V, Y, Yb, and Zn are reported; however, not all variables are reported for all media because, in some media, certain elements were below the analytical detection limit. Spatial variation in element concentration between five Frisian Islands are given for each of the sample media. In general, only a few elements in each media showed statistically significant differences between the islands sampled. The measured concentrations in all sample media exhibited ranges that cannot be attributed to anthropogenic additions of trace elements, with the possible exception of Hg and Pb in surface soils. 相似文献
20.
Soil solutions expelled by high‐speed centrifugation (13900 g) of intact soil sample cores at field moisture from 30 forest topsoils (A horizons of mainly Dystric and Eutric Cambisols, according to the FAO‐Unesco system) low in clay were subjected to analysis of 60 elements, using ICP‐MS and ICP‐AES. Concentrations measured were related to soil and soil solution properties assumed to be important for the solubility of elements, using stepwise regression analysis. On an average two thirds of the variability in soil solution concentration of elements were accounted for by, in particular, organic C concentrations, pH and/or nitrate concentrations of the solutions, varying among elements from 19 to 90 %. Concentrations of elements strongly positively related to soil solution acidity were Al, Be, Ge, Li, Ni, Pb, and Zn, strongly negatively related to acidity were Ca, Mo, and W. Most positively related to nitrate concentrations in soil solutions were B, Ba, Cd, Mg, Mn, and Sr; negatively were Nb, Ta, and Ti. Concentrations of organic C in the soil solutions correlated positively, often quite closely, with most of the other elements studied, including La, all the lanthanides, and with Ag, Br, Cr, Fe, Ga, Hf, Hg, In, P, Th, U, Y, and Zr. Soluble organic compounds were apparently ’︁carriers’ of these elements in the soil solution. The concentrations of elements in HNO3 digests of the soils usually accounted for just little or no statistical variability of their soil solution concentrations. 相似文献