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。     

珠江三角洲典型肝癌发病区土壤重金属富集特征分析及生态风险测度

测定了珠江三角洲经济区顺德典型肝癌发病区的29个表层土壤样品重金属含量,并用平均富集因子(AEFs)分析了研究区重金属元素污染程度,结果表明表层土壤重金属按富集程度可分为3类,严重富集(AEFs>5),主要有Cd、Hg;中度富集(AEFs=2~5),包括Zn、Cu、Ni、As、Co、Mn;轻微富集(AEFs<2),包括Fe、Cr、Pb、Se;Mo的富集程度最低,29个样点的EF值均小于0.2。进一步通过因子分析和聚类分析研究表层土壤中重金属的类别和来源,发现表层土壤中的17种重金属主要有5种不同组合,反映了5种不同的来源或迁移特性:因子1包括Ni、Li、V、Co、Cr、Fe和Al,因子2包括OM、Se和Ce,因子3主要包括Pb和Zn,因子4包括Cd、As和Mn,因子5由pH、Mo和Hg组成,其中因子1、2、4代表3种不同特性的自然源因子,因子3为交通及工业污染源因子,因子5为燃煤污染源因子。以广东省土壤背景值为参比标准进行的潜在生态危害评价结果表明,研究区表层土壤重金属潜在生态危害指数较高,总体以强度为主(RI>300),其中单项生态危害系数较高的是Hg和Cd,其余6种金属元素Pb、Cu、Ni、As、Cr属于轻微生态危害性。     

太原市污灌区土壤重金属污染现状评价

对太原市污灌区土壤重金属分布特征进行了分析评价,结果表明重金属Pb、Zn、Cu、Ni、Mn、Cr、As、Hg、Cd含量均值均未超过土壤环境质量标准（GB15618—1995）,但其平均值均显著高于太原市土壤背景值。各重金属间的相关分析表明,Pb、Zn、Cu、Ni、Mn、Cr、As、Cd之间呈极显著相关,说明这8种元素污染源可能相同。Hg是本区表层土壤重金属污染的主要因子,重金属元素的污染程度依次为Hg〉Cd〉Pb〉As〉Cu〉Zn〉Cr〉Mn〉Ni。土壤重金属单项污染指数均值均大于1,综合污染指数为2.81,总体上,污染水平为中度及其以上。各种重金属单因子污染指数和综合指数在研究区有相似的空间分布格局,总体分布趋势为东南部小店地区和中南部晋源区相对较高,南部清徐县相对较小;通过因子分析并结合污灌区污染源调查,表明Hg除受污水灌溉的影响外,燃煤释放的Hg可能是重要来源之一,Cd、Zn、Pb和Cu可能来自污水灌溉和大气沉降,以污水灌溉的贡献为主,Ni、Mn、As、Cr来自污水灌溉。Hg、Cd是太原市污灌区土壤中需要优先控制的重金属。     

唐海县农田土壤重金属元素来源解析

利用因子分析对唐海县191个浅层土壤的53种元素进行分析,提取了7个主因子。根据主因子组合中的标识元素判别当地8种重金属(Cu、Zn、Ni、Cr、Pb、Cd、As和Hg)来源。结果显示Pb、Zn、Ni的主要来源是土壤成土母质。Cr和Cu一部分源于土壤本底,另一部分来源于外界污染造成的元素叠加。Cd具有独立的外源成因。Hg的来源较为复杂,煤烟尘也许是当地Hg的来源之一。     

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。     

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.     

博斯腾湖湿地边缘带农田土壤重金属的污染风险评价

对新疆博斯腾湖湿地边缘带农田土壤中8种重金属元素(As、Cd、Cr、Cu、Mn、Ni、Pb和Zn)地球化学特征进行分析。采用污染负荷指数(PLI)、潜在生态风险指数(RI)和生态风险预警指数(IER)对农田土壤重金属污染与环境风险进行评价。结果表明:(1)湿地边缘带农田土壤Pb和Zn呈现重度污染,As、Cd、Cr和Ni轻度污染,Cu轻微污染,Mn无污染。土壤As、Cd、Cr、Cu、Ni、Pb和Zn平均含量处于轻微风险水平。Cd是污染程度与生态风险等级最高的重金属元素;(2)湿地边缘带农田土壤PLI平均值为1.43,呈现轻度污染,RI平均值为20.62,呈现轻微生态风险状态,IER的平均值为–4.53,呈现无警态势。湿地边缘带PLI、RI与IER空间分布格局基本一致;(3)湿地边缘带农田土壤Pb与Zn来源主要受到人类活动的影响,Cr、Cu、Mn与Ni来源主要受到土壤地球化学作用的控制,As与Cd受自然因素和人为因素共同影响。     

浙江省永康城市土壤重金属元素富集特征

永康169个城市土壤X荧光光谱测试分析表明:Cu、Mn、Co、Fe、Cr、Pb、Ni、Ti八种重金属元素的平均含量超过金衢盆地土壤背景值,且以工业用地类样品的富集程度最高。永康城市土壤重金属污染水平呈整体较轻,局部严重态势;各重金属元素的离散程度均较大,Cu为强变异元素,变异系数为152.93%,其他元素也为中强变异,表明永康城市土壤重金属元素含量在研究区内有较大差异。多元统计分析表明,Cr、Ni、Cu、Pb、Mn等重金属元素主要来源于当地的五金制造等工业和交通运输的影响;Fe、Ti、Co来源主要与成土过程中元素的积累有关,其中Fe有部分来源于五金生产。     

广州市流花湖沉积物重金属污染特征及潜在生态风险评估

近年来重金属污染日益加重,对人类及水生态系统健康产生较大危害。本研究选择广州市典型城市湖泊——流花湖,利用地累积指数(Igeo)、潜在生态风险指数(RI)对沉积物中12种重金属的污染水平、垂向分布特征及其潜在生态风险进行评价,并通过多元统计分析对金属元素的来源进行解析。结果表明:①湖泊沉积物重金属含量(Mn、V除外)均显著高于区域土壤背景值,自下而上呈现先增加后减少的趋势;②地累积指数评价结果显示Cd、Zn、Sb、Cu、Pb和As这6种重金属污染较严重,其中Cd偏重度污染的状态(Igeo=3.89);③不同重金属元素污染水平有较大差异,Cd、Cu、Zn、Sb、Pb、As、Ni、Cr、Tl、Co的单个重金属污染指数(Cif)均为中等污染水平以上,而生态风险系数(Eif)表现为Cd(Eif=818.6)极严重等级,Sb(Eif=82.64)重度风险等级,其他10种重金属Eif均为轻度风险等级;④该湖RI指数变化幅度剧烈(105.85相似文献   

湘中下寒武统黑色页岩土壤的地球化学特征

以湘中发育于下寒武统黑色页岩之上的土壤为研究对象,选择安化东坪、烟溪,桃江,宁乡等地的典型土壤及相应成土母岩,利用等离子质谱(ICP-MS)、X射线荧光光谱(XRF)等分析技术,对土壤、成土母岩(黑色页岩)的主量元素和微量元素(包括重金属元素、稀土元素等)进行了较系统的分析测定。结果表明,湘中下寒武统黑色页岩土壤风化作用强烈,风化指数CIA均在73以上。强烈的风化使得土壤具有明显贫CaO、Na2O,而富Al2O3、Fe2O3的化学组成特征。土壤因继承成土母岩(黑色页岩)的特征而富集Mo、Cd、Sn、Sb、U、V、Cr、Co、Ni、Cu、Zn、Tl、Pb、Th等多种重金属元素,其综合富集指数(EI值)平均在3以上,最高达17。地质累计指数(Igeo)评价结果显示,土壤重金属的富集已达到污染程度,土壤存在Cd、Mo、Sb、U、Sn、V、Cu、Tl、Ba等重金属的污染,并以Cd、Mo、Sb等重金属污染最强,达中度至极强污染程度。重金属与主量元素的相关性分析显示,土壤中的重金属主要赋存于黏土矿物和铁氧化物(针铁矿)等矿物相中,其中Ba、Sn、Th、Cu、Sc等主要赋存黏土矿物中;Zn、Ni、Mn、Co、Cd、Tl、Pb等则主要赋存于铁氧化物矿物(针铁矿)中;而Cr、V、Mo、Sb、U等则不受黏土矿物和铁氧化物矿物的控制。此外,不同地区土壤的Zr/Hf、Ta/Nb、Nd/Sm等元素比值相对稳定,依次为36.20、0.085、5.30(n=73),并与相应的成土母岩(黑色页岩)相应值基本一致。土壤与成土母岩具有相同的稀土配分型式,且成土过程中稀土元素不发生明显的分异。微量元素比值和稀土元素特征指示土壤中的重金属来自成土母岩(黑色页岩)本身,为自然污染源。     

Assessment of the Contamination of Cultivated Soils by Eighteen Trace Elements Around Smelters in the North of France

Ag, As, Bi, Cd, Co, Cr, Cu, Hg, In, Ni, Pb, Sb, Se, Sn,Tl, Th, U and Zn contamination of cultivated surfacehorizons has been assessed around two lead and zincsmelters in the North of France. The verticaldistribution of Ag, As, Bi, Cu, Hg, Se, Sb and Tl inthe soils has also been examined. The soils around thelead and zinc smelter at Noyelles-Godault arecontaminated by Ag, As, Bi, Cd, Cu, Hg, In, Ni, Pb, Sb,Se, Sn, Tl and Zn. The original concentration in themost contaminated soils may be multiplied by a factorof around 2 to 100, according to the element. Cadmium,Pb and Zn are the most abundant contaminants. The Pband Zn concentrations are correlated to those of theother contaminants, with the exception of Se. Aroundthe Auby zinc smelter, there is a contamination by thesame elements, but in different proportions, inaddition to Cr contamination. Contamination by Se canreach a depth of around 1 m, whereas contamination byAg, As, Bi, Cu, Hg, Sb and Tl is confined to the top 30cm. Although the contaminant content in most soilsdepends on the distance from the plant, Secontamination would appear to vary to a greater extentaccording to the physico-chemical soil conditions.     

Contamination of Urban Soils in an Area of Northern France Polluted by Dust Emissions of Two Smelters

The contamination of 27 urban topsoils has been assessed around two lead and zinc smelters (Metaleurop Nord and Umicore) in the North of France. Eighteen trace elements have been analysed (Ag, As, Bi, Cd, Co, Cr, Cu, Hg, In, Ni, Pb, Sb, Se, Sn, Tl, Th, U and Zn). The investigation included the study of the vertical distribution of Cd, Pb and Zn as indicators of pollution. It was shown that Cd, In, Pb, Sb and Zn were major pollutants followed in lesser quantities by Ag, Bi, Cu and Hg. In addition, As, Ni, Se, Sn and Tl were present at levels slightly higher than regional agricultural values. The other elements (Co, Cr, Th and U) were at endogenous levels. The observations have highlighted the strong heterogeneity of the physico-chemical parameters of urban soils and the existence of heavy contamination of the under layers by Cd, Pb and Zn. A potential transfer of metals from the topsoil to the deeper layers and especially Cd and Zn, is not excluded. Indeed the soil rework is not the only factor explaining contamination level of the deeper layers of the studied soils. The comparison of the studied element concentrations in urban soils with nearby local agricultural values shows that the dust emission originating from the Metaleurop and Umicore smelters were not the only source of contamination. Thus a large contamination of the studied urban soils by Sb and In could be explained by domestic combustion of coal for heating.     

The distribution of heavy metals in sediments of Sörfjord,West Norway

The bottom sediments of Sörfjord, West Norway, contain unusually high concentrations of Ag, Ba, Bi, Cd, Cu, In, Pb, Sb, Sn, and Zn. The concentrations of Zn and Pb reach ～ 10% by weight in some sediments. The concentrations of most of the elements are positively correlated, those of Pb, Cd, and Cu with Zn being particularly well developed; correlations also exist between Sb and Zn, and Ag and Cu. The concentrations of the metals in the bottom sediments decrease southwards and northwards from a locality close to a source of industrial waste.     

Effect of bentonite characteristics on the elemental composition of wine

Physical, chemical, and mineralogical characteristics of six bentonites were assessed and related to their elemental release to wine. Extraction essays of bentonites in wine at three pH levels were carried out. The multielemental analysis of bentonites and wines was performed by atomic absorption spectrometry (AAS) and inductively coupled plasma mass spectrometry (ICP-MS). Bentonite addition resulted in significantly higher concentrations of Li, Be, Na, Mg, Al, Ca, Sc, V, Mn, Fe, Co, Ni, Ga, Ge, As, Sr, Y, Zr, Nb, Mo, Cd, Sn, Sb, Ba, W, Tl, Bi, and W. In contrast, the concentrations of B, K, Cu, Zn, and Rb significantly decreased. A strong correlation between Na concentrations of treated wines and its content in bentonite exchange complex was observed. Al and Fe contents reflected bentonite extractable aluminous and ferruginous constituents, while Be, Mg, Ca, V, Mn, Ni, Ge, Zr, Nb, Mo, Sn, Sb, Tl, Pb, and U concentrations reflected the elemental composition of bentonites. Several nonconformances with OIV specifications demonstrated the need for an effective control.     

Background Contents of Heavy Metals in Soils and Bottom Sediments in the North of Western Siberia

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...     

Application of ICP sector field MS and principal component analysis for studying interdependences among 23 trace elements in Polish beers.

Twenty-three metallic elements, including almost all essential and toxic metals such as lead, cadmium, mercury, arsenic, silver, and thallium, have been quantified in 35 types of bottled and canned Polish beer by using double-focusing sector field inductively coupled plasma mass spectrometry (ICP-MS) with ultrasonic nebulization. The samples were digested using concentrated HNO3 in closed PTFE vessels and applying microwave energy under pressure. The means and medians of the concentrations of Rb, Mn, and Fe were on the order of 200 ng/mL; Cu, Zn, V, Cr, Sn, As, Pb, and Ni were detected at 1-5 ng/mL; Ag, Ga, Cd, Co, Cs, Hg, U, and Sb were found at < 1 ng/mL; and In, Tl, Bi, and Th were present at < 0.1 ng/mL. The concentrations of Hg, Cd, As, Pb, and Zn were 1-3 orders of magnitude lower than proposed tolerance limits. The interdependences among determined trace elements were examined using the principal component analysis (PCA) method. The PCA model explained 74% of the total variance. The metals tend to cluster together (As, Tl, Cs, Sn, Th, Bi, and Hg; Cd and Co; Cs and Cr; Fe and Zn; Mn and V).     

Evaluating the Contribution of Long-Range Transport of Heavy Metals from the Asian Continent to Their Concentrations in Sediment Cores from Lake Shinji,Western Japan

The historical trend of heavy metal pollution recorded in sediment cores from Lake Shinji, western Japan, was investigated to evaluate the contribution of increasing long-range transport of heavy metals from the Asian continent in recent years. The concentrations of Cd, Co, Cr, Cu, Ni, Pb, Sb, and Zn and lead isotope ratios were determined for sediment cores collected at two sites in the lake. Among the metals, Cd, Sb, and Zn showed markedly high concentrations since the 1970s. Moreover, a high Pb concentration and less radiogenic lead isotope ratios have been observed since the 1980s in the core from a site close to the mouth of a major river. Air masses from the Asian continent, including China, Russia, and South Korea, have less radiogenic lead isotope ratios than those from Japan. This suggests that the recent increase in Pb concentration in the sediment core is primarily due to the long-range transport of heavy metals from the Asian continent, followed by their deposition in the catchment area of the river. The concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of the sediment around 2000 were calculated on the basis of the metal concentrations in excess of those before 1940. They were then compared with the volume-weighted annual average concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of rain samples collected on the shore of the lake for 1999–2001. The result showed that the ratios of the former to the latter are 1.0 for Cd, 0.69 for Sb, and 0.31 for Zn. Thus, it is likely that the long-range transport of Cd and Sb from the Asian continent also contributes significantly to the recent increase in the concentrations of these metals in the sediment core from Lake Shinji. For Zn, however, the contribution from the Asian continent was evaluated to be small, suggesting the importance of local sources such as effluent discharges.     

Modelling trace metal extractability and solubility in French forest soils by using soil properties

Soil/solution partitioning of trace metals (TM: Cd, Co, Cr, Cu, Ni, Sb, Pb and Zn) has been investigated in six French forest sites that have been subjected to TM atmospheric inputs. Soil profiles have been sampled and analysed for major soil properties, and CaCl₂‐extractable and total metal content. Metal concentrations (expressed on a molar basis) in soil (total), in CaCl₂ extracts and soil solution collected monthly from fresh soil by centrifugation, were in the order: Cr > Zn > Ni > Cu > Pb > Co > Sb > Cd , Zn > Cu > Pb = Ni > Co > Cd > Cr and Zn > Ni > Cu > Pb > Co > Cr > Cd > Sb , respectively. Metal extractability and solubility were predicted by using soil properties. Soil pH was the most significant property in predicting metal partitioning, but TM behaviour differed between acid and non‐acid soils. TM extractability was predicted significantly by soil pH for pH < 6, and by soil pH and Fe content for all soil conditions. Total metal concentration in soil solution was predicted well by soil pH and organic carbon content for Cd, Co, Cr, Ni and Zn, by Fe content for Cu, Cr, Ni, Pb and Sb and total soil metal content for Cu, Cr, Ni, Pb and Sb, with a better prediction for acidic conditions (pH < 6). At more alkaline pH conditions, solute concentrations of Cu, Cr, Sb and Pb were larger than predicted by the pH relationship, as a consequence of association with Fe colloids and complexing with dissolved organic carbon. Metal speciation in soil solutions determined by WHAM‐VI indicated that free metal ion (FMI) concentration was significantly related to soil pH for all pH conditions. The FMI concentrations of Cu and Zn were well predicted by pH alone, Pb by pH and Fe content and Cd, Co and Ni by soil pH and organic carbon content. Differences between soluble total metal and FMI concentrations were particularly large for pH < 6. This should be taken into account for risk and critical load assessment in the case of terrestrial ecosystems.     

Heavy metal contamination of soils in Northern Slovakia

Environmental damages like forest decline in Northern Slovakia could be a result of long-distance transport of pollutants with the dominating north-west winds. On 10 sites, primarily in the northbound upper slopes of west-east oriented mountain ranges in Northern Slovakia, the extent of the heavy metal contamination in soils along a north-south transect was examined. Oi, Oe, Oa, A, and B horizons were sampled and the total concentrations of Al, Cd, Cr, Cu, Fe, Mn, Ni, Pb, and Zn were determined. The ranges of heavy metal concentrations in the forest floor were higher than reported for comparable samples from Bavarian soils except for Zn (Cd: 0.65–1.77; Cr: 12–40; Cu: 19–41; Ni: 8–24; Pb: 70–187; Zn: 31–92 mg kg^?1), in the mineral soil the concentrations were lower. The depth distribution of the metal concentrations indicated a contamination with Cd, Cr, Cu, Ni, Pb, and Zn. The concentration differences between forest floor and mineral soil tended to be higher at the northern than at the southern sites for Cu, Ni, Pb, and Zn, indicating a long-distance transport from the north. Correlation and principal component analyses of the total metal concentrations revealed three groups: Cu, Pb, and Zn inputs mainly seemed to result from long-distance transport from the north, Cr and Ni inputs additionally from local sources. Cd probably had its origin mainly in local sources. This result was further confirmed by the grouping of the sites when clustered.