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。     

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

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。     

农业生态与土壤中化学元素关系的研究

研究农业生态与土壤环境中化学元素的关系结果表明，农业生态与土壤的N、P、K、Na、Ca、Mg、S、Fe、Mn、Cu、Zn、B、Mo、V、Co、Ni、Cr、Pb、Cd、Hg、Se、F、Tl、Ba、Te、Ta、Sr、Ti、Si及稀土元素密切有关。     

河北省集约化养殖场畜禽粪便中重金属含量及变化特征

通过对河北省全省区域典型集约化养殖场的主要畜禽粪便采样,分析测定畜禽粪便中Cu、Zn、Cd、Pb、Cr、As、Hg、Ni 8种重金属含量并进行数据分析,结果表明河北省集约化养殖场畜禽粪便中8种重金属的含量(中位值)均符合德国腐熟堆肥标准和中国有机肥料标准,但数据离散且呈偏态分布。按德国腐熟堆肥标准和中国有机肥(NY 525—2012)的标准,河北省畜禽粪便的Cu、Zn、Cr、Cd、Pb、Ni、Hg和As超标率分别为41.73%、50.39%、31.50%、5.51%、0.79%、7.87%、4.63%和12.60%。鸡粪重金属超标率顺序为ZnCrCuNiAsCdPbHg,其中,Cu、Zn、Cr超标率分别为22.22%、40.74%和33.33%。猪粪重金属超标率顺序为CuZnCrAsNi和Cd,其中,Cu、Zn、Cr和As超标率分别为80.43%、78.26%、30.43%和21.74%,Pb和Hg不超标。牛粪重金属超标率顺序为CrHgZn,其他重金属均不超标。按施用量15 t·hm~(-2)推算出猪粪、鸡粪和牛粪的最严格土壤安全施用年限分别为26、79年和207年。因此,施用集约化畜禽粪便有机肥带来的环境风险需要引起足够的重视。     

大庆龙凤湿地土壤重金属空间分布特征

对大庆龙凤湿地土壤Cu,Cr,Cd,Zn,Pb和As六种重金属元素的空间分布特征进行了研究.结果表明:湿地土壤表土层(0-10 cm)Cu,Cr,Cd,Zn,Pb和As在水平分布上的变化较大,除Cr和Zn外,Cu,Cd,Pb和As含量均低于松嫩平原土壤重金属含量平均值;在土壤剖面中,Cu,Cr,Cd和As都随着土层深度的增加逐渐减少,而Pb和Zn则是先增加后减少,这与区域内土壤的理化性质、成母土质、岩石风化及淋溶作用有极大的关系.Cu,Cd,Zn,Pb,As五种重金属元素之间,除Cu和As间相关关系不显著外,其余各重金属元素之间均呈极显著的正相关关系,而Cr只与Cu呈显著正相关,与其他各重金属元素之间均未表现出显著的相关性,由此推测Cu,Cd,Zn,Pb,As元素的来源可能相同,且具有一定的共生组合性,而Cr则受湿地周边复杂环境及人为随机因素的影响较大.     

几种重金属钝化剂及其不同添加比例对猪粪堆肥重金属(As,Cu,Zn)形态转化的影响

采用连续提取法研究了猪粪堆肥处理中重金属浓度和形态的变化以及不同添加比例的重金属钝化剂对其浓度和形态的影响.结果表明:经过堆肥处理后,重金属As,Cu和Zn的浓度普遍升高;堆肥处理能促进重金属As,Cu和Zn的形态向活性降低的方向转化,因此堆肥处理可以降低重金属的生物有效性.在3种重金属钝化剂及不同添加比例处理中,猪粪堆肥重金属As的最佳钝化剂及其添加比例为7.5%的粉煤灰,对可交换态As的钝化效果为51.4%;重金属Cu的最佳钝化剂及其添加比例为2.5%的粉煤灰,对可交换态Cu的钝化效果为29.7%;重金属Zn的最佳钝化剂及其添加比例为5.0%的钙镁磷肥,对可交换态Zn的钝化效果为50.0%.因此,堆肥处理中添加重金属钝化剂可以降低猪粪堆肥中重金属的有效性,有利于降低猪粪堆肥土地利用中重金属污染的风险.     

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.     

降雨和微肥在油菜环境下对重金属淋失的影响

通过室外油菜盆栽试验研究2种微肥(硅肥与硒肥)在不同自然降雨条件下对土壤重金属淋失的影响。从油菜苗期至角果发育成熟期,连续收集了6次自然降雨事件的淋溶液,监测了淋失液中溶解态Pb、Zn、Cu、Cd、As 5种重金属的浓度,并计算其迁移总量。结果表明,在油菜常规种植密度下,淋溶水样体积与降雨量成正比;在典型自然酸雨(pH为4.56～4.73)淋洗下,土壤中各种重金属呈现出不同的淋溶趋势:淋溶液中Zn、Cd的最高浓度出现在第1次降雨,随着降雨次数的增加,浓度都呈整体下降趋势;与之相反,淋溶液中Pb的最高浓度出现在最后1次降雨,且随着降雨次数的增加,浓度呈逐渐上升趋势;Cu的最高浓度出现在雨强最大的暴雨(110.1mm)期间,其余降雨情况下,Cu的溶出浓度基本趋于稳定;而As的淋失浓度较低,且随降雨次数的增加,有一个缓慢的下降趋势。相比CK和Si处理,基施硒肥的措施能显著降低土壤淋溶液中5种重金属的淋失总量,而基施硅肥能使淋溶液中Cd、As的淋失总量有一定程度的降低;在油菜环境下,5种重金属的淋失水溶性大小为Zn>Cd>Cu>As>Pb。     

黑水虻生物转化猪粪过程中重金属的迁移变化

利用黑水虻处理猪粪为一种高效的环境友好型的技术，但猪粪中重金属的含量对黑水虻的转化产生影响。该研究在30 ℃环境下猪粪中接种7日龄的黑水虻幼虫，研究黑水虻的生长和对猪粪的转化效率，以及猪粪中的重金属（Cu、Zn、Cr、Cd、As）在黑水虻虫体和虫粪中的变化情况。结果表明：在8 d的生长过程中，0~2 d时，生长速率最慢，4~6 d时生长速率最快，在第8天时虫体干质量最高。黑水虻对猪粪的转化率随着时间的延长而增加，在第6天时达到了最大11.5%，而到第8天时下降。在转化过程中虫体中Cu、Cr、As的浓度随着黑水虻幼虫生长降低，在第8天时，虫体Cu、Cr、As浓度较第2天分别降低了24.5%、21.7%、33.1%。Cd含量随着黑水虻幼虫生长增加，在第8天时，虫体Cd浓度较第2天增加了75.3%。Cu、Cr、As、Cd在虫粪中浓度的变化同虫体变化相反。Zn在虫体和虫粪中含量没有发生显著变化。在第8天时虫粪中的Cd含量显著低于猪粪，而Cu、Cr、As、Zn含量与猪粪比没有显著差异。黑水虻幼虫对猪粪中Cd的富集系数最高，达到了3.8，其余都小于1，各重金属的富集顺序为Cd>Zn>Cu>Cr>As。转化后Cu、Cr、As、Zn有83.6%～92.7%分布于虫粪，而Cd有49.8%～69.7%分布于虫粪，30.3%～50.2%分布于虫体。转化后Cu、As的生物活性提高，Cr、Cd的生物活性降低，Zn的生物活性没有明显的变化。研究结果为畜禽粪便的黑水虻生物转化提供参考。     

广东红壤微量元素含量及分布特征

2004年对广东部分红壤9种微量元素含量调查结果表明,9种微量元素平均含量为B 41.38 mg kg-1,Mo21.71 mg kg-1,Cu 77.37 mg kg-1,Pb 33.94 mg kg-1,Zn 265.52 mg kg-1,As 19.018 mg kg-1,Hg 0.056 mg kg-1,Cr 248.95mg kg-1,Cd 0.324 mg kg-1。同族微量元素相比,原子量小的元素的含量大于原子量大的元素的含量。母岩、成土风化作用影响这些微量元素在土壤中的含量。     

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.     

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.     

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...     

The dynamic state of the ionome in roots,nodules, and shoots of soybean under different nitrogen status and at different growth stages

The relative distribution of 22 mineral elements in the roots, nodules and shoots of the soybean (Glycine max L. Merr. cv. Tsurumusume) at R1 (beginning of the flowering stage) and R7 (beginning of the mature stage) was investigated in response to ammonium and manure N treatment. Plants receiving only atmospheric nitrogen served as the negative control. The addition of ammonium sulfate to the soil caused soil acidification, induced Al and Mn toxicities, and significantly reduced the biomass production in roots and nodules. Ca, Mg, Fe, Mn, Cu, and Zn concentrations were significantly higher in shoots, and those of Mo and Co higher in nodules. The addition of manure to the soil significantly enhanced the levels of Sr, Ba, Cr, and Cd in shoots, whereas the concentration of Cs was decreased at R7. Moreover, when the soybean developed from R1 to R7, the levels of essential elements in nodules decreased, whereas those of nonessential elements increased, irrespective of the nitrogen source. Furthermore, the variation in the concentrations of many elements was not consistent for nodules and roots when soybean developed from R1 to R7. The variation of Mn, Zn, B, and Al concentrations was independent of N treatments. However, Ca, Fe, Cu, Mo, and Se levels were affected strongly by N treatments. This study is the first to document the dynamic variation of the soybean ionome in nodules, roots, and shoots from vegetative to reproductive stage of soybean.     

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.     

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.     

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.     

Multielemental analysis and classification of amaranth seeds according to their botanical origin

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.     

Presence of war related elements in dandelion (Taraxacum officinale) as a possible consequence of military activities in east Croatia

This is the first study on concentrations of war related elements in dandelion from war effected areas of Croatia. Previous research done on human subjects, soil and water has shown abnormalities in distribution of war associated metals and metalloids in war affected areas compared with peacetime locations. Dandelion, as wide spread perennial herb, is considered as very useful plant in determination of trace elements pollution in various ecosystems. Aim of the research was to try to determine whether concentrations of war related elements (Al, As, B, Ba, Cd, Co, Cr, Cu, Fe, Hg, Li, Mg, Ni, P, Pb, Sb, Si, Sr, U, V and Zn) concentrations in dandelion (Taraxacum officinalle) samples in areas of high intensity of combat activities differ from areas of low intensity of combat activities, and to clarify possible contamination in dandelion as an indicator (and edible) plant with it's role in food chain. Leaves of the dandelion were taken at locations (28 locations at 11 settlements) were divided into two major subgroups: high and low intensity of combat activities, at the locations of major explosions, former minefields, army trenches?…?Analysis was done using ICP-MS and data was interpreted using Mann Whitney test and PCA. Results have shown that there is difference in concentration of war related elements among different locations, with generally, higher concentrations of war elements in war areas compared with control group. Maximum concentrations of As, B, Ba, Cd, Co, Cr, Cu, Li, Mg, Ni, P, Pb, Sb, Si, Sr, U, V and Zn were higher in areas of high intensity of combat activities. When results are compared with similar researches, overall presence of metals and metalloids is legally acceptable, however, there are differences in concentrations between war and peacetime locations.     

Effects of fertilization, crop year, variety, and provenance factors on mineral concentrations in onions

Mineral concentrations of onions (Allium cepa L.) grown under various conditions, including factors (fertilization, crop year, variety, and provenance), were investigated to clarify how much each factor contributes to the variation of their concentrations. This was because the mineral concentrations might be affected by various factors. The ultimate goal of this study was to develop a technique to determine the geographic origins of onions by mineral composition. Samples were onions grown under various conditions at 52 fields in 18 farms in Hokkaido, Japan. Twenty-six elements (Li, Na, Mg, Al, P, K, Ca, Mn, Fe, Co, Ni, Cu, Zn, Rb, Sr, Y, Mo, Cd, Cs, Ba, La, Ce, Nd, Gd, W, and Tl) in these samples were determined by inductively coupled plasma atomic emission spectrometry and inductively coupled plasma mass spectrometry. Fertilization conditions and crop years of onions caused variations of P, Ni, Cu, Rb, Sr, Mo, Cs, and Tl concentrations in onions; different onion varieties also showed variations in numerous element concentrations. However, the variations of mineral compositions of onions by these factors were smaller than the differences between production places with a few exceptions. Furthermore, Na, Rb, and Cs in group IA of the periodic table, Ca, Sr, and Ba in group IIA, and Zn and Cd in group IIB showed similar concentration patterns by group; this result demonstrated that elements in the same periodic groups behaved similarly in terms of their absorption in onions.