海伦市土壤主要微量元素空间分布特征

以海伦市研究区1 175件表层(0~20 cm)土壤样品主要微量元素(B、Cu、Mn、Mo、Zn)的实测含量为研究对象,采用地统计学与GIS相结合的方法,对土壤微量元素的含量及空间分布特征进行分析。结果表明:研究区表层土壤中B和Mo含量较缺乏;Mn和Mo的块金效应大于75%,空间自相关性弱,B、Cu和Zn块金效应在25%~75%之间,属于中等空间相关,空间变异主要受到自然因素影响;B和Cu的空间分布相似,由中心向四周逐渐减少,Mn和Mo含量呈明显带状分布,Zn含量北部高于南部。微量元素之间既存在着共生关系,也可能存在拮抗关系。土壤有机质含量、成土母质、土壤类型和土地利用对微量元素均有不同程度的影响。     

中国煤中有害微量元素含量的空间分布

煤中有害微量元素对生态环境和人体健康的潜在影响是地球化学和能源环境领域研究的热点之一,地球化学制图对深刻理解地球化学过程及其变化规律具有重要作用。目前,尚缺乏中国煤中有害微量元素含量的空间分布图。通过对中国煤炭样品中1 167个Be、1 315个Co、1 406个Cu、1 191个Mo、1 247个Th 和1 390个Zn含量数据进行统计分析,测算中国煤中Be、Co、Cu、Mo、Th 和 Zn 的平均含量,并利用ArcGIS技术绘制中国煤中Be、Co、Cu、Mo、Th、Zn的含量地球化学空间分布地图。结果表明:中国煤中有害微量元素含量跨度大,数据分布呈正偏性,不符合正态分布特征;中国煤中Be、Co、Cu、Mo、Th和Zn 的平均含量分别为2.10、5.53、21.36、2.19、7.35和30.02 mg/kg;各元素含量的空间分布极不均匀;煤中有害微量元素含量空间分布格局是多种因素综合作用的结果,如物源区母岩、热液作用、水运移作用等,其中热液作用是煤中有害微量元素异常富集的典型特征。研究成果可为煤中微量元素研究和环境管理提供直观有效的参考。      

Sediment-water interactions in the metal-contaminated floodplain of the Clark Fork River,Montana, USA

The distribution and concentration of metals and metalloids in the floodplain of the Clark Fork River of western Montana, USA, are mainly controlled by post-depositional diagenetic mechanisms of metal fractionation. Due to the influx of wastes into the river's headwaters from mining processes around the turn of the century, extensive amounts of contaminated material were deposited onto the floodplain. Tailings were deposited as widespread overbank deposits and point bars adjacent to abandoned channels, and are characterized by orange and gray mottled sediment, which is devoid of vegetation and covered by a blue metal sulfate precipitate during dry periods. Examination of stratigraphic profiles of floodplain sediment indicates three periods of deposition: 1) pre-mining, represented by coarse sand and organic overbank deposits under reducing conditions; 2) syn-mining, characterized by transition sediments and tailings deposits under oxidizing conditions; and, 3) post-mining, distinguished by grass-bound topsoil.Sites were established where sediments and water throughout the stratigraphic section were collected and analyzed. Chemical analyses indicate enriched concentrations of cadmium, copper, manganese, and zinc in sediments and porewater, and arsenic in groundwater, in areas contaminated by tailings deposits. Vertical trends in concentrations of metals show that they are distributed based on apportionment of metal phases between reducing-oxidizing environments and pH fluctuations.     

Temporal transport of major and trace elements in the upper reaches of the Xijiang River,SW China

This study investigated the temporal variations of major and trace element contents and controlling factors in the upper reaches of the Xijiang River, SW China. The results showed the major ions principally derived from the weathering of carbonate and silicate rocks, with a seasonal variation impacted by the monsoonal climate. The contents of dissolved trace elements also varied seasonally in the two main tributaries: the Nanpan and Beipan rivers. Most dissolved trace elements such as Mn, Zn and Pb being affected by anthropogenic contributions displayed a large seasonal variability, from onefold to hundred-fold, while V, Rb and U show a relative stable trend uncorrelated with the different seasons, suggesting a natural origin by rock weathering. Suspended particle matter in the Nanpan and Beipan rivers was depleted in Ca, Mg, Na, K and Sr, but enriched in Al, Fe and Sb compared to the upper crust (UC) values. A binary mixture of silicate-rich and carbonate-rich sources dominates the behavior of elements such as Ca and Sr in riverine sediments, while a third end-member with an anthropogenic signature influenced the content of trace elements like Mn, Sb, Pb, Zn, Cd, Cr and Cu. The enrichments of Sb relative to the UC would be related to the mining activity in the studied area. The study highlights the importance of investigating temporal variations of major and trace element contents of rivers controlled by the monsoon climate and impacted by human activity.     

珠江三角洲经济区河水中微量元素的空间分布

在珠江三角洲经济区采集了29个河水样品,利用高分辨率仪器ICP MS测量了河水中微量元素的含量。结果表明,河水中稀土元素的平均含量按西江、北江、珠三角河、深圳河、东江的顺序呈增加趋势;珠三角河及深圳河具有较高重金属含量,西江和北江中重金属含量相对较低,东江居中。经分析发现,珠江三角洲经济区河水中微量元素的空间分布特征是自然条件和人类活动共同作用的结果;自然环境对稀土元素的空间分布起主要作用;人类活动是影响重金属分布特征不可忽视的重要因素。     

Effects of forest slash and burn on the distribution of trace elements in floodplain sediments and mountain soils of the Subandean Amazon,Peru

Forest clearing through slash and burn to open up agricultural land is an ongoing process in large parts of the Amazon Basin. This activity severely affects the structure and balance of the natural ecosystem, and also has the potential to cause substantial changes in landscape geochemistry. The latter is the topic of this study, with special attention on translocation of potentially toxic trace elements from deforested areas to downstream aquatic and terrestrial systems. Sampling of floodplain sediments and mountain soils (Inceptisols on redbed lithologies) was carried out in two adjacent Subandean river basins, with deforestation extents of ca. 1/3 and 2/3 of the basin areas. Several toxic and potentially toxic metals (e.g., Hg, Cd, Pb, Cu and Ni) and other major and minor elements showed concentration peaks at certain depths in the alluvial deposits of both basins. These peaks were associated with organic matter, and occurred just below layers of combustion residues originating from burning of in situ biomass. Downward migration of particles originating in the combustion residues is suggested to be the direct mechanisms of the metal enrichments. Further evidence of an in situ origin of the metal peaks in the sediments was provided by the geochemical composition of soils located upstream of the floodplains. Disturbed soils (i.e. soils of pasture, coffee plantations, secondary forest and recently swidden fields) were found to be similar to soils under natural forest. Moreover, trace element concentrations in floodplain deposits were similar in the two drainage basins despite the large difference in exploitation degree. Thus, no evidence was found of large scale (basin-wide) increases in trace-metal leaching or translocation as a result of the extensive deforestation and agricultural land-use that has been practiced in the Amazonian highland jungle over more than 100 a.     

青藏高原典型山地冰川中痕量元素的空间分布和来源分析

为了探究青藏高原雪冰中痕量元素的空间分布与主要来源,对2019年7—9月在青藏高原七一冰川、八一冰川、岗什卡雪峰、煤矿冰川、玉珠峰冰川、古仁河口冰川以及玉龙雪山白水河1号冰川采集的表雪样酸化后,利用电感耦合等离子体质谱仪（ICP-MS）测试了常量元素Al、Fe与痕量元素As、Ba、Co、Cr、Cu、Li、Mn、Mo、Pb、Sr、Tl、Zn、Cd共15种元素的含量,通过Jonckheere-Terpstra非参数检验分析痕量元素空间分布趋势。结果表明：中部煤矿冰川和玉珠峰冰川浓度最高,南部古仁河口冰川和玉龙雪山最低,东北部3条冰川居中;本研究与其他研究区关于冰川As、Cu、Pb、Zn、Cd浓度对比的结果显示,青藏高原冰川中元素含量的空间分布总体趋势为：中部>北部>南部。富集因子分析表明,Co、Cr、Cu、Tl、Fe、Li、Mn、Mo、Sr元素主要受粉尘输入影响,Pb、Cd、Zn元素受人为源影响较大（例如有色金属冶炼、交通排放、化石燃料燃烧等）。后向轨迹结果表明,东北部3条冰川主要受东北和西北部地区影响;中部冰川元素来源复杂,以青藏高原西部和北部的粉尘输入为主,且受西部临近煤矿...     

我国新疆北部积雪中痕量元素的时空分布及污染评估

积雪中记录的痕量元素含量,能很好地评估当地大气污染状况。利用电感耦合等离子体质谱仪（ICP-MS）,对2018年1月和3月采自新疆北部的天山北坡、伊犁河谷、塔城地区和阿勒泰地区的积雪样品进行了16种痕量元素测试。结果表明：北疆地区积雪中痕量元素含量的平均值在0.06 ng·g^-1（Cd）～1 481.1 ng·g^-1（Al）之间。时间分布上,消融期多数痕量元素浓度低于积累期、稳定期;Pb、Cr等元素消融期含量高于其他时期,可能与外源输入有关。空间分布上,塔城地区和天山北坡的多数痕量元素含量高出伊犁河谷和阿勒泰地区1~3倍。与其他地区雪冰中痕量元素含量对比,发现新疆北部高出青藏高原北部1~3倍,与受人类活动影响较大的天山乌鲁木齐河源1号冰川相应痕量元素浓度接近,揭示了新疆北部积雪中痕量元素较高的浓度特征。元素富集系数表明,Fe、Be等元素主要来自地壳粉尘,Pb、Cd、Zn、As等元素呈显著富集（EFc>10）,受人类排放活动主导。结合后向气团轨迹分析,塔城地区的痕量元素可能受到哈萨克斯坦的影响,阿勒泰地区的痕量元素可能受到中亚、阿尔泰山南缘等地的影响,天山北坡与伊犁河谷主要受新疆本地气团的影响。     

Spatial distribution and geochemical baselines of major/trace elements in soils of Medak district,Andhra Pradesh,India

Regional-scale variations in soil geochemistry were investigated with special reference to differences among soil groups and lithology in an area of 9,699 km² in Medak district, Andhra Pradesh, India. The concentrations of 29 elements (major: Si, Al, Fe, Mn, Mg, Ca, Na, K, Ti, P and trace: As, Ba, Cd, Co, Cr, Cu, F, Mo, Ni, Pb, Rb, Se, Sr, Th, U, V, Y, Zn, Zr) in 878 soil samples collected (557-topsoil, 321-subsoil) at a sampling density of 1 site/17 km² from 557 sites representative of all the soil types present in studied area were determined, and their elemental composition are discussed. The baseline levels of these elements in soils are determined over different lithological units for the identification of anomalous values relative to these. For the first time, geochemical maps for Medak district are prepared on 1:50,000 scale and the lithogeochemical database generated provides information on the lateral and vertical distribution of elements in soil. The spatial variations in the distribution of elements reflect underlying geologic characteristics. Box-plots reveal that the concentration of most of the elements in soils were not strongly dependent on the soil group but the soil-geochemistry abruptly changes with the change in the soil parent materials indicating that the distribution of elements is mostly influenced by the bedrock lithology and other natural processes acting on them. For instance, the concentrations of Co, Cu, Fe, Mn, Ti, V and Zn are high in soils developed on basaltic terrain while the soils developed on granitic and gneissic terrain exhibit high elemental concentrations of K, Pb, Rb, Si, Th and Y. Alfisols had relatively high contents of elements while entisols had lower concentrations of most of the elements. The database can be used in the chemical characterisation of different geological units as well as applications in various environmental and agricultural fields. The results indicate that regional geology is an important determinant of soil geochemical baselines for soil pollution assessment and further emphasizes the importance of determining background levels locally. The defined baselines can be used to establish background values for future soil surveys.     

The distribution of trace elements in carbonaceous chondrites

12 carbonaceous chondrites, amongst them representatives of nearly all known petrologic types were analyzed for twenty trace elements by spark source mass spectrography combined with the isotope dilution method. Data on different element groups (refractory, moderately volatile and volatile) show that the distribution of the trace elements in the carbonaceous chondrites, with the exception of Renazzo, can be well explained by Anders' two-component model. This is also valid for the highly metamorphosed CV5 chondrite Karoonda.Furthermore, it is observed that the $\text{Zr}\text{Hf}$-ratios in the carbonaceous chondrites increase with increasing petrologic type which is interpreted as the result of mixing two components with different $\text{Zr}\text{Hf}$-ratios     

Spatial distribution of major and trace elements in shallow reservoir sediments: an example from Lake Waco, Texas

 Sediment geochemistry of a shallow (6-m average) reservoir (Lake Waco) was evaluated for the spatial distribution of major and trace elements. Sixty bottom and core samples along a 21-km transect within the reservoir, 18 overbank sediment samples, and 8 rock types in the drainage area were collected and analyzed for major (Al, Ca, Fe) and trace elements (As, Ba, Cr, Cu, Hg, Mn, Ni, Pb, Sr, V, Zn). Elemental concentrations in the reservoir sediments closely correspond to concentrations in the regional rocks and represent a mixture of overbank sediment composition of the tributaries. Elemental concentrations were statistically regressed against Al concentrations in order to establish regional baseline levels and thereby distinguish natural from anthropogenic sources. Spatial geochemical trends, considered in terms of element-to-Al ratio versus V-to-Al ratio, relate to the natural and anthropogenic sources contributing to the elemental concentrations. The spatial elemental distribution in the reservoir, which receive sediments from two mineralogically contrasting basins, reflect textural and mineralogical transition within the reservoir and suggest a progressive mixing of sediment from the tributaries. The spatial elemental distribution and sediment texture suggest that the sediment-source, which determines the sediment-type, has a greater influence on the major- and trace-element distributions in shallow reservoir sediments than bathymetry. Received: 25 September 1997 · Accepted: 3 February 1998     

The biogeochemical distribution of trace elements in the Indian Ocean

The present review deals with the distributions of dissolved trace metals in the Indian Ocean in relation with biological, chemical and hydrographic processes. The literature data-base is extremely limited and almost no information is available on particle processes and input and output processes of trace metals in the Indian Ocean basin and therefore much research is needed to expand our understanding of the marine chemistries of most trace metals. An area of special interest for future research is the Arabian Sea. The local conditions (upwelling induced productivity, restricted bottom water circulation and suboxic intermediate waters) create a natural laboratory for studying trace metal chemistry.     

Dissolved trace elements in the Mississippi River: Seasonal,interannual, and decadal variability

A monthly trace element sampling of the lower Mississippi River, utilizing ultra-clean methods, was conducted from October 1991 to December 1993. Dissolved concentrations were determined for Fe, Mn, Zn, Ph, V, Mo, U, Cu, Ni, Cd, Rb, and Ba. The results show significant seasonal dissolved concentration changes for a number of elements. Specifically, dissolved Mn and Fe are found to increase rapidly in the fall and then decrease in the spring. Zn and Pb follow a similar seasonal trend, though with lower percentage concentration changes. V, Mo, and U follow an opposite seasonal trend to Mn and Fe. The data do not allow a complete determination of the causes of this variability. However, changes in the adsorption process do not appear to play an important role. Hydrologic factors are also of minimal importance for most elements, with the probable exception of Ba and U. I suggest here that redox processes, occurring both in-stream and in source regions, play an important role in determining seasonal variations in dissolved trace elements.No evidence was found of significant dissolved trace element concentration changes over the past decade and interannual variability in mean concentrations was generally small. The time series also encompassed a period of extreme flooding in the U.S. Midwest. However, the flooding did not significantly influence dissolved trace element concentrations in the lower Mississippi River.     

Spatial variability of topsoil contamination with trace elements in preschools in Vilnius,Lithuania

An investigation of the spatial variability of topsoil contamination level was performed in 49 preschool playgrounds located in Vilnius city and correlated with urban (height and age of the preschools and height of surrounding buildings) and natural (altitude) factors. Composite samples, consisting of 20–30 sub-samples, were collected from 10 cm topsoil layer with a 3–5 m distance from each other. Sieved fraction (< 0.63 mm) was ashed at 400 °C, ground to < 1.0 μm and analysed for the real total concentrations of 22 trace elements (Ag, B, Ba, Co, Cr, Cu, Ga, Li, Mn, Mo, Nb, Ni, Pb, Sc, Sn, Sr, Ti, V, Y, Yb, Zn and Zr) using optical atomic emission spectrophotometry. Information on construction year and height (number of building stories) of preschool and surrounding buildings was acquired from the Centre of Registers of Lithuania. Out of 22 analysed elements, 13 to a greater extent exceeded the background values in several areas and were used to calculate the total contamination index (Z_s13). Out of 49 analysed areas, 21 had moderately hazardous to hazardous levels of contamination as indicated by Z_s13. The main contaminating elements, exceeding the permissible concentrations were Ag, Cu, Mo, Pb, Sn and Zn, the origins of which coincide with city industry and traffic. Topsoil around the newer preschool buildings, despite their location, contained lower concentrations of contaminants, while areas at higher altitudes were more contaminated than those located at lower altitudes. The latter causality is biased, as the city industry, and hence the highest contamination, is in districts located higher above sea level than the remaining studied sites.     

Avulsions, channel evolution and floodplain sedimentation rates of the anastomosing upper Columbia River, British Columbia, Canada

Ages of channels of the anastomosing upper Columbia River, south‐eastern British Columbia, Canada, were investigated in a cross‐valley transect by ¹⁴C dating of subsurface floodplain organic material from beneath levees. The avulsion history within the transect was deduced from these data, and morphological stages in channel development were recognized. Additionally, floodplain sedimentation rates were established. The new data demonstrate that the upper Columbia River is a long‐lived, dynamic anastomosing system. Results show that anastomosis at the study location has persisted since at least 2700 cal. years BP, with avulsions occurring frequently. At least nine channels have formed in the studied cross‐valley transect within the past 3000 years. Channel lifetimes from formation to abandonment appear to be highly variable, ranging from approximately 800 to 3000 years. Log jams provoking avulsions and/or silting up of old channels are proposed as reasons for this variability. Long‐term average floodplain sedimentation rates appear to be significantly lower than previously proposed by Smith (1983, Int. Assoc. Sedimentol. Spec. Publ., 6, 155–168). A long‐term (4550 years) average of 1·75 mm year^?1 (after compaction) was based on ¹⁴C dates, while a short‐term sedimentation rate of 0·8 mm was determined for a single, relatively small, seasonal flood in 1994 using sediment traps. However, short‐term sedimentation rates vary considerably over the floodplain, with levees aggrading up to four times faster than floodbasins. Channels of the upper Columbia River anastomosed reach follow a consistent pattern in their development, with each stage being characterized by different morphology and processes. Channel evolution comprises the following succession: (1) avulsion stage, in which a crevasse splay channel deepens by scour and levee sedimentation; (2) widening and deepening stage, in which bank slumping and bed scouring dominates; (3) infilling stage, in which either channel narrowing (bank accretion) or channel shallowing (bed accretion) takes place; and (4) abandonment stage, in which the residual (remnant) channel is filled exclusively by silt, clay and organic material. Vertical stacking (super‐ imposition) of active channels on recent channel‐fill sand bodies is a notable feature of the upper Columbia River, which suggests that reoccupation of residual channels is a common process.     

Variations of trace elements under hydrological conditions in the Min River,Eastern Tibetan Plateau

In order to better understand the relative importance of hydrologic variation and anthropogenic disturbance and their complex interactions within the trace elemental geochemical cycle, water samples were collected monthly over 1 year in the Min River, eastern Tibetan Plateau, and analyzed for trace element composition. The dissolved trace elements exhibited different relationships with increasing discharge compared with major elements. The elements analyzed can be divided into three groups according to their behavior in response to changing discharge: (1) elements that showed weak positive correlation with discharge, e.g. Cu, V, and Ba; (2) elements that exhibited weak negative correlation with discharge, including Rb, Sr, Pb, Sb, Zn, Cr, Cd, and U; and (3) elements that displayed no significant correlation with variation in discharge, e.g. Ti, Fe, Co, Ni, and As. Cu was strongly affected by anthropogenic activities and flushed into the river with increasing discharge. Ba has a strong solubility in the terrestrial environment, dissolved quickly, and was released into the river. The positive relationship between V concentration and discharge may be attributed to secondary reactions, such as precipitation and adsorption on oxides and aluminosilicate clays. Conservative behavior had an impact on the geochemical behavior of Sr and Rb across hydrologic variation. Pb, Zn, Sb, Cd, and Cr underwent a mild dilution effect connected with anthropogenic activities. The chemostatic behavior of U was regulated by carbonate dissolution and biological uptake. In addition, higher temperatures enhanced biotic activities, affecting the concentrations of Fe and Ni. The relationship between power law slopes and coefficient of variation for discharge and solute concentration suggests that concentrations of trace elements vary significantly with increasing discharge compared with major elements. Silicate mineral weathering had less effect on the fluvial solutes with increasing discharge. Mining activity may exert an additional control on concentration–discharge dynamics of anthropogenic trace elements.     

Grain size partitioning of metals in contaminated,coarse-grained river floodplain sediment: Clark Fork River,Montana, U.S.A.

The traditional concept of the relationship between metal content and grain size assumes that the fine fraction carries most of the metals in natural sediments. This concept is supported in many cases by strong, significant linear relationships between total-sediment metal concentrations and percentages of various fine-size fractions. Such observations have led to development of methods to correct for the effects of grain size in order to accurately document geographical and temporal variations and identify trends in metal concentrations away from a particular source. Samples from the floodplain sediment of a large, coarse-grained river system indicates that these concepts do not hold for sediments contaminated by mining and milling wastes. In this particular system, the application of methods to correct for grain-size effects would lead to erroneous conclusions about trends of metals in the drainage. This indicates that the a priori application of grain-size correction factors limits interpretation of actual metal distributions and should not be used unless data indicate that correlations exist between metals and particular size fractions.     

Geochemistry of trace elements in surface waters of the Arno River Basin,northern Tuscany,Italy

Trace element geochemistry of the Arno River and its main tributaries was investigated on the basis of two sampling campaigns carried out in November 1996 and June 1997. By analyzing filtered and unfiltered water samples, Fe and Al are found in solution mainly as colloidal particles of size lower than 0.45 μm. In June (lower flow rate), Fe and Al are enriched in the filtered waters from the main river, and this feature was interpreted in terms of higher water temperature promoting the formation of smaller particles, thus reducing their aggregation properties. Iron and Al show perfectly synchronous downstream profiles along the Arno River, correlate quite well each to other, and display abrupt concentration increases near to Florence, where the lithology of the catchment changes from siliciclastic dominated to clay-sand (lacustrine-marine)-dominated. The same behaviour is shown by most of the other trace elements in the river, thus supporting a general lithological control. Trace elements in the final part of the Arno River are influenced by flocculation processes in addition to mixing. Adsorption phenomena on oxy-hydroxides are denoted by good elemental correlations with Fe (and Al). Sporadic anomalous concentration values, possibly related to anthropogenic contributions, may prevent such correlations. Referring to the quality of waters for potable use and fish life, toxic elements are below the acceptable limits of current European regulations, with few exceptions for Hg exceeding guideline values. Multivariate analysis groups trace elements according to geochemical affinities and natural or anthropogenic sources, thus distinguishing contaminated from uncontaminated samples. The results achieved in this work will help regional and national Authorities for compliance with the EU water policy, especially in assessing the water quality at the river basin scale and its vulnerability to human activities.