Searching the most appropriate sample pretreatment for the elemental analysis of wines by inductively coupled plasma-based techniques

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.     

Metal content of Sphagnum mosses from two Northern Canadian bog ecosystems

Samples of Sphagnum moss were collected from Kinoje Lake, northern Ontario, and Porter Lake, Northwest Territories (N.W.T.), Canada. The samples were analyzed for the elements Cd, Ca, Cr, Cu, Fe, Pb, Mg, Mn, Hg and Zn. On a dry-weight basis, Ca was highest in concentration followed by Mg, Fe and Mn. The other elements were an order of magnitude or more lower in concentration. In general, concentrations were similar to those reported in the literature from Scandinavia. The two Canadian sites were similar in elemental composition except that the Ontario site was higher in Cd and Pb, while the N.W.T. site was higher in Mg and Hg. These differences could be due to a combination of regional geochemical and human activity differences.     

Determining baselines and variability of elements in plants and soils near the Kenai National Wildlife Refuge,Alaska

Recent investigations on the Kenai Peninsula had two major objectives: (1) to establish elemental baseline concentrations ranges for native vegetation and soils; and, (2) to determine the sampling density required for preparing stable regional geochemical maps for various elements in native plants and soils. These objectives were accomplished using an unbalanced, nested analysis-of-variance (ANOVA) barbell sampling design. Hylocomium splendens (Hedw.) BSG (feather moss, whole plant), Picea glauca (Moench) Voss (white spruce, twigs and needles), and soil horizons (02 and C) were collected and analyzed for major and trace total element concentrations. Using geometric means and geometric deviations, expected baseline ranges for elements were calculated. Results of the ANOVA show that intensive soil or plant sampling is needed to reliably map the geochemistry of the area, due to large local variability. For example, producing reliable element maps of feather moss using a 50 km cell (at 95% probability) would require sampling densities of from 4 samples per cell for Al, Co, Fe, La, Li, and V, to more than 15 samples per cell for Cu, Pb, Se, and Zn.     

Baseline element concentrations in soils and plants,Bull Island,Cape Romain National Wildlife Refuge,South Carolina,U.S.A.

Baseline element concentrations are given for Spanish moss (Tillandsia usneoides), loblolly pine (Pinus taeda), and associated soils. Baseline and variability data for ash, Al, Ba, C, Ca, Cd, Ce, Co, Cr, Cu, Fe, K, La, Li, Mg, Mn, Na, Nb, Nd, Ni, P, Pb, S, Sc, Sr, Th, Ti, V, Y, 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 among and within 0.5 km grid cells are given for each of the media. In general, only a few elements in Spanish moss showed statistically significant landscape patterns, whereas several elements in loblolly pine and in soils exhibited differences among sampling grids. Significant differences in the concentration of three elements in Spanish moss and eight elements (including total S) in loblolly pine were observed between two sampling dates (November and June); however, the absolute amount of these differences was small. Except for perhaps Ni and Pb concentrations in Spanish moss, element levels in all sample media exhibited ranges that indicate natural rather than anthropogenic additions of trace elements.     

Determination of Thallium and Other Elements (As,Cd, Cu,Mn, Pb,Se, Sb,and Zn) in Water and Sediment Samples from the Vicinity of the Zinc-Lead Smelter in Poland (3 pp)

Background, Goal and Scope   The aim of this study was to check the concentration of some elements in water samples collected near Pb-Zn mining and smelting works and comparison of the obtained data with results achieved for sediment samples originated from the same reservoirs. Objective   Here, 8 water samples and 3 bottom sediments collected from water reservoirs in the vicinity of 3 big Polish Pb-Zn smelters were analysed.Methods   Water analysis was performed after filtration through a 0.45 µm filter and pH adjustment to 2. For decomposition of dried sediment samples, microwave assisted digestion with total dissolution of silicate matrix was applied. The elements studied were determined using ICP-MS and ICP-OES methods. Results and Discussion   The concentrations of most studied elements in water samples were on the 0.X µg/L level, while only the contents of Tl, As, Mn, Cd, Pb and Sb in two water reservoirs were above the limits established for drinking water. The content of studied metals in sediments was in a wide range from X mg/kg (Se and Sb) to X000 mg/kg (Pb and Zn).Conclusions  and Recommendation. The study indicates that the impact of Tl, As, Cd, Cu, Mn, Pb, Zn, Se and Sb on bottom sediments is much more extensive than on the water in ponds located in the vicinity of a post-flotation waste heap. Monitoring of surface and underground waters, if limited only to the dissolved elements, can lead to faulty conclusions about environmental pollution. The bottom sediments mainly contain easily mobilised phases, and water-sediment equilibrium could be changed easily.     

Evaluation of Nitric Acid Extraction of Elements from Soils and Sediments in Two watersheds in East Tennessee

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.     

comparison of sulphur and heavy metal contents and their regional distribution in humus and moss samples from the vicinity of Nikel and Zapoljarnij,Kola Peninsula,Russia

Terrestrial moss and humus (the O-horizon) are often used separately for determining and monitoring airborne heavy metal pollution. Here, we directly compare the results of analyses of moss and humus samples taken at a density of one site per 300 km² in a 12 000 km² area (45 samples) around the nickel smelter in Nikel, the nickel ore roasting plant in Zapoljarnij, both in Russia, and the iron ore mine and mill near Kirkenes in Norway. The samples were air dried, digested in conc. HNO₃ and analysed for more than 30 elements by ICP-MS and ICP-AES at the laboratory of the Geological Survey of Finland (GTK). For most elements, observed levels and variations are considerably greater in soil than in moss. The main contaminants, Ni and Cu, reach equally high median levels in the moss and soil, but maximum values are far higher in soil. Both media show comparable regional distribution patterns for the heavy metals, but not for sulphur. Cu and Ni can be used to delineate the limits of contamination in the survey area. Both media show the same picture, with a generally very steep gradient from east to west and background levels being reached 30–50 km from the nickel smelter. When moss is used, Cu/Ni, Cu/S and Ni/S ratios can be used to separate input from the smelting and roasting proccesses in Russia. Both media are well suited to use separately to detect airborne pollution in this heavily contaminated area. The moss data are generally easier to interpret, but moss is not available at the most polluted sites. Levels for many elements other than Cu and Ni are close to the detection levels in moss samples, but not in humus samples. Information gathered from both media thus complement each other in a regional multi-element survey.     

Uptake Kinetics of As, Hg, Sb, and Se in the Aquatic Moss Fontinalis antipyretica Hedw

Laboratory experiments were carried out to study the uptake kinetics of selected metals and metalloids in the aquatic moss Fontinalis antipyretica. For this purpose, moss specimens from a clean site were exposed to concentrations of As, Hg, Sb, and Se ranging from 0.1 to 10,000???g?l^?1, for incubation times of between 1 and 22?days, and the tissue concentrations of the metals in the moss specimens were then measured. Uptake kinetics followed different patterns in relation to exposure time, although the most common was Michaelis?CMenten kinetics. On the contrary, the contamination factors followed very similar patterns in relation to the exposure concentrations in all cases, with a good fit to logarithmic equations. The bioconcentration factors tended to decrease as exposure concentration increased. The bioconcentration factors for Hg were extremely high, even at the lowest concentration in water and for the shortest incubation time, which implies that F. antipyretica has a high capacity to magnify Hg levels in water, which is an important characteristic in a good biomonitor. According to the time to reach equilibrium, the minimum exposure time recommended for use in active biomonitoring by means of transplants is very variable, although high levels of the elements, except Sb, were found in the moss tissues within a few days. We do not recommend the use of this moss species to biomonitor low concentrations of Sb in water. The differences in maximum contamination factors and lowest bioconcentration factors suggest that As and Se were the most toxic of the elements under study.     

Accumulation Capacities of Particulate Matter in an Acrocarpous and a Pleurocarpous Moss Exposed at Three Differently Polluted Sites (Industrial, Urban and Rural)

The aim of this study was to compare the capacity of two morphologically different moss species to accumulate elements when exposed to three different types of air pollution (rural, urban and industrial). Transplants of Pseudoscleropodium purum and Ceratodon purpureus were exposed for 6 months, and the concentrations of 18 elements (Al, Ti, V, Cr, Mn, Fe, Co, Cu, Zn, As, Mo, Cd, Sn, Sb, Ba, La, Pb and Bi) in the mosses samples were analysed by inductively coupled plasma–mass spectrometry. On the whole, the metals were accumulated by mosses, and this accumulation was correlated with concentrations in the atmospheric particles. Whereas P. purum is to be preferred for Al, Cu, Zn and Fe monitoring, C. purpureus was most efficient at accumulating Mo, Ti, V, As, Sn, La and Pb. In both species, a phenomenon of saturation was observed during the exposure at the most contaminated site (industrial).     

Baseline element concentrations in soils and plants,Wattenmeer National Park,North and East Frisian Islands,Federal Republic of Germany

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.     

Background levels of trace and ultra-trace elements in soils of Japan

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.     

Fluctuations of element concentrations during the growing season of Polytrichum formosum (Hedw.)

Fourteen elements (Al, Ba, Ca, Cd, Cr, Cu, Fe, K, Mg, Ni, Pb, Sr, Ti, and Zn) were quantitatively determined by AES/ICP in aboveground parts of the endohydric moss Polytrichum formosum (Hedw.) after sampling over regular intervals from 1985 to 1987. With the exception of K, Mg, and Zn all elements showed a large continuous fluctuation (> 30%) during the growing season. Four different patterns of seasonal variation were found: (1) large seasonal variations of element concentrations (～80%) with maximum concentrations in winter and lowest concentrations in the summer months (Al, Fe, Cr, Mg, Pb, and Ti), (2) smaller seasonal variations (～50%) with maximum concentrations in winter and lowest concentrations in summer (Ba, Ca, Cd, Cu, Sr), (3) slight seasonal variations (～30%) with maximum concentrations in the summer (K), and (4) slight seasonal changes (～30%) with maximum concentrations in the winter (Mg and Zn). The relative biological variance of element concentrations between 9 different stands of Polytrichum formosum decreases in the following sequence: Ti, Al, Pb, Fe, Cr, Ni, Ba, Ca, Cu, Cd, K, Mg, Sr, Zn. The relative biological variance of individual elements is generally lower than the variance in element concentrations caused by seasonal changes. Because of its high biological variance for most elements investigated (seasonal as well as between different stands of Polytrichum formosum) this moss should only be used as a passive bioindicator, if all other environmental parameters are standardized.     

湘中地区发育于黑色页岩上的土壤重金属污染特征

对湘中地区的安化、桃江、宁乡系统采集了黑色页岩土壤及其相应的黑色页岩样品,并运用ICP-MS对样品进行微量元素和重金属分析。结果表明:在黑色页岩及其风化形成的土壤样品中,Cr、Cu、U、Mo、Sn、Sb、Tl、Ba等重金属元素都呈明显的富集状态;同时,土壤与母岩的稀土元素在陨石粒径标准化后均表现为相同的右倾型分配模式。运用富集指数法对该区黑色页岩土壤进行评价,发现湘中地区黑色页岩发育的土壤都不同程度地受到了重金属的复合污染,且以桃江的污染最为严重;地质累积指数分析结果进一步表明,黑色页岩土壤中普遍受污染的元素主要有Cr、U、Mo、Sb、Ba等。土壤中重金属元素的污染程度排序为:安化:Sb>Ba>Mo>Co=Cu=U;桃江:Sb>Pb>V=Mn=Co=Cu=U=Mo=Ba>Cr=Cd;宁乡:Mo=U=Sb=Ba>Th。     

Red soils derived from limestone contain higher amounts of trace elements than those derived from various other parent materials

The concentrations of 48 trace elements (Li, Be, Sc, V, Cr, Co, Ni, Cu, Zn, Ga, As, Br, Rb, Sr, Y, Zr, Nb, Mo, Ag, In, Cd, Sn, Sb, I, Cs, Ba, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu, Hf, Ta, W, Tl, Pb, Bi, Th and U) in 14 soils derived from limestone, sampled at three sites, are compared with the concentrations in 500 soil samples derived from a variety of other parent materials. The 500 samples were collected from 75 sites nationwide in order to include the wide range of common soil types in Japan. Most analytical results were obtained by inductively coupled plasma mass spectrometry (ICP-MS), but Cr, As, Br, Zr, Sn, and I concentrations were determined by energy dispersive X-ray fluorescence spectrometry (EDXRF), because the acid dissolution techniques employed in this study were found to be incapable of recovering these elements completely. In order to examine the reliability of analyses, the concentrations of many elements were also determined by EDXRF, inductively coupled plasma-atomic emission spectrometry (ICP-AES), and atomic absorption spectrometry (AAS). Box and whisker diagrams (Tukey plots), constructed using log-transformed values of each element, show clearly that geometric means of nearly all the trace elements in soils derived from limestone are higher than those in soils derived from other parent materials. The only exceptions are Sr, Ag and Eu, though statistical analysis (Student’s t-test) shows that the differences for these three elements were not significant at p < 0.05. Similarly, the observed differences of geometric means for Sc, Br and Ba between limestone soils and other types of soils were also not significant at p < 0.05. It can be concluded, therefore, that the concentrations of the above-mentioned 48 trace elements in soils derived from limestone are significantly higher than those in other types of soils, with the exception of Sc, Br, Sr, Ag, and Ba, though it was necessary to exclude 81 soil samples, developed on scoriaceous (basaltic) volcanic ash from Mt. Fuji, as an exceptional group for comparisons of V and Cu, as these soils contain higher levels of these two elements. The above results can be attributed to the gradual accumulation of trace elements in the limestone soils due to the intense weathering processes.     

Levels of Arsenic and Antimony in Water and Sediment from Prestea, A Gold Mining Town in Ghana and its Environs

Arsenic and antimony concentrations in water and sediment samples collected from Prestea, a gold mining town in the Western Region of Ghana and its environs were studied. The concentrations of these elements were measured using instrumental neutron activation analysis (INAA). INAA was preferred to other modern analytical techniques because of its relatively higher selectivity, sensitivity and high precision. Beside its multi-elemental nature, INAA is very fast and thus presents a very good analytical tool for the determination of elemental concentrations in various samples including water and sediment. The samples were irradiated using a 30 kW tank-in-pool Ghana Research Reactor-1 (GHARR-1) operating at a thermal neutron flux of 5 × 10¹¹ n s^?1 cm^?2. The samples were irradiated and counted without any chemical treatment. Elevated levels of As and Sb were found in both water and sediment. Generally, As and Sb concentrations in the water samples ranged from 0.90–8.25 ppm and 0.09–0.75 ppm respectively. These values far exceed the WHO recommended values for As and Sb in water, 0.01 ppm and 0.005 ppm respectively. The levels of As in sediment ranged from 942–10,200 ppm, and that of Sb was 8.5–90.4 ppm. Arsenic concentrations in both water and sediment were generally higher than Sb concentrations. This is, however, not surprising as arsenopyrites (FeAsS₂) are among the major pathfinder minerals associated with gold mined from Ghana. Our results show that the study area is polluted as far as the levels of As and Sb in water and sediment are concerned.     

Uptake of macro nutrients,barium, and strontium by vegetation from mineral soils on carbonatite and pyroxenite bedrock at the Lillebukt Alkaline Complex on Stjernøy,Northern Norway

Carbonatite originating from the Lillebukt Alkaline Complex at Stjernøy in Northern Norway possesses favorable lime and potassium (K) fertilizer characteristics. However, enrichments of barium (Ba) and strontium (Sr) in carbonatite may cause an undesired uptake by plants when applied to agroecosystems. A field survey was carried out to compare concentrations of Ba, Sr, and macronutrients in indigenous plants growing in mineral soil developed on a bedrock of apatite–biotite–carbonatite (high in Ba and Sr) and of apatite–hornblende–pyroxenite (low in Ba and Sr) at Stjernøy. Samples of soil and vegetation were collected from three sites, two on carbonatite bedrock and one on pyroxenite bedrock. Ammonium lactate (AL)‐extracted soil samples and nitric acid microwave‐digested samples of soil, grasses, dwarf shrubs, and herbs were analyzed for element concentration using ICP‐MS and ICP‐OES. Concentrations of magnesium (Mg) and calcium (Ca) in both soil (AL) and plants were equal to or higher compared to values commonly reported. A high transfer of phosphorus (P) from soil to plants indicates that the apatite‐P is available to plants, particularly in pyroxenite soil. The non‐exchangeable K reservoir in the soil made a significant contribution to the elevated K transfer from soil to plant. Total concentrations of Ba and Sr in surface soil exhibited a high spatial variation ranging from 490 to 5,300 mg Ba kg^?1 and from 320 to 1,300 mg Sr kg^?1. The transfer of AL‐extractable elements from soil to plants increased in the order Ba < Sr < Ca < Mg < K, hence reflecting the chemical binding strength of these elements. Concentrations of Ba and Sr were low in grasses (≈ 20 mg kg^?1), intermediate in dwarf shrubs and highest in herbs. Plant species and their affinity for Ca seemed more important in explaining the uptake of Ba and Sr than the soil concentration of these elements. The leguminous plant species Vicia cracca acted as an accumulator of both Ba (1.800 mg kg^?1) and Sr (2.300 mg kg^?1).     

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.     

Statistical models for the accumulation of PAH,chlorinated hydrocarbons and trace metals in epiphytic Hypnum cupressiforme

Concentrations of PAH (1.12-benzoperylene, 3.4-benzopyrene, fluoranthene), chlorinated hydrocarbons (α-BHC, lindane, PCB) and trace metals (Zn, Pb, Cu) in bulk precipitation, as well as PAH and trace metal concentrations in atmospheric dust samples from 14 sites in Bavaria, F.R.G. are presented for two vegetation periods (1979 and 1980). The same substances were also analyzed in epiphytic moss (Hypnum cupressiforme var. filiforme) sampled from tree trunks in October 1979 and 1980. Using mean immission values and the amount of precipitation as predictors and concentrations of pollutants in moss samples as criteria, a number of multiple regression models were computed in order to quantify the relationships between absolute air pollution data and accumulated trace substance values. Beta values of all variables help to determine whether bulk precipitation or atmospheric particulate matter has dominant influence on the uptake of trace substances by mosses. The study shows that epiphytic mosses can be used to monitor both heavy-metal, PAH and chlorinated hydrocarbons.     

Instrumental Determination of Trace Metals in Fly Ash by INAA and AAS Techniques and its Statistical Analysis

For low-level detection of elements in an environmental sample, a number of techniques is available. However, satisfactory evaluation of the results by comparing the techniques is difficult. An attempt has been made in this study to analyse fly ash samples collected from a major coal fired power plant by two different techniques, viz. INAA and AAS, to determine elemental concentrations. A statistical approach was formulated and the experimental data was subjected to Wilcoxon sign rank test, paired ‘t’-test and linear regression analysis. The results confirm the hypothesis that ‘no significant difference exists between the two techniques’.     

基于矿物元素指纹的羊肉产地溯源技术

为探讨矿物元素指纹对羊肉产地溯源的有效性,找寻表征地域特性的元素指标,利用电感耦合等离子体质谱仪分析中国内蒙古自治区阿拉善盟、锡林郭勒盟和呼伦贝尔市3个牧区,及重庆市和山东省菏泽市2个农区脱脂羊肉和土壤样品中4种常量元素(K、Ca、Na、Mg)和13种微量元素(V、Mn、Fe、Cr、Ni、Cu、As、Be、Sb、Zn、Se、Ba、Tl)的含量,对其进行方差分析、相关分析和判别分析。结果表明,羊肉中矿物元素含量组成在地域间有明显差异,农区元素含量普遍高于牧区。脱脂羊肉中Ca、Zn、Be、Ni、Fe、Ba、Sb、Mn和Se9种元素含量的地域差异与土壤相关,它们对农牧区的正确判别率达90%以上,对5个地域的正确判别率在70%～100%之间。利用羊肉中矿物元素指纹分析技术可鉴别和追溯羊肉的产地来源,为羊肉及其他食品的产地溯源研究提供方法参考。