ICP-AES在新疆哈拉奇地区水系沉积物样品分析中的应用研究

本文采用四酸溶样ICP6300电感耦合等离子体发射光谱法测试了新疆哈拉奇地区水系沉积物样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La Pb B W Sn Cd 21种微量元素,明确了该方法测试样品中的Li P Ti V Cr Mn Co Ni Cu Zn Sr Y Nb Mo Ba La 16个元素的检出限、准确度、精密度满足规范（DZ/T0130.2006-2006）要求,而Pb B Cd Sn W5个元素测试质量不能满足规范要求,并对新疆哈拉奇地区水系沉积物采样粒度样品进行了分析测试,验证了该区化探扫面选择10-80目粒度是合适的,但在异常查证工作中要选择10-60目采样粒度更合理。     

Statistical assessment of geochemical pattern in overbank sediments of the river Sava,Croatia

Four overbank profiles from the three terraces of different age were sampled in 10 to 20 cm intervals for the bulk content of major and minor (Ca, Mg, Fe, Ti, Al, Na, K and P) and trace (Mo, Cu, Pb, Zn, Ni, Co, Mn, As, U, Th, Sr, Cd, Sb, V, La, Cr, Ba, W, Zr, Ce, Sn, Y, Nb, Ta, Sc, Li, Rb and Hf) elements in the minus 0.125 mm fraction. Univariate statistics together with analysis of variance discriminated between the lower-lying carbonate (CA) population dominantly composed of carbonates and the overlying silicate (SI) population being dominantly of silicate mineralogy. This stratified pattern resulted from the intensive erosive action of melting glaciers exerted on limestones and dolomites in the alpine region, followed by local inputs mainly of silicate composition. Elements exhibiting the greatest between-population variability are Ca and Mg being enriched in the CA population and Fe, Mn, P, Sr, Al, Na, K, Li, Rb, Y, Zr, Ni, Cr and Ti being enriched in the SI population. Anomalously high Hg, Pb and Ba concentrations (maximum values: 6,500±2,860 ppb, 225±13 ppm and 1,519±91 ppm, respectively) in the lowermost part of the profile S7, which is nearest to the Croatian-Slovenian border, derive from the mineralized Slovenian catchment area. This profile also contains trimodal frequency distributions of Fe, Mn and P whose highest concentrations coincide with increased values of Zn and Cu which are bimodally distributed. Geochemical patterns of majority of elements in all four profiles consistently reflect the average compositions of the upstream drainage basins.     

甘肃北山金、铜矿床红沙的植物地球化学特征及其找矿意义

北山地区植被属戈壁荒漠植被类型，主要植物群落为红沙，红沙中多数元素特别是成矿元素及其伴生元素的含量和变化系数矿区大于背景区，元素含量背景区呈对数正态分布，矿区呈偏对数正态或多峰分布，红沙中的元素组合分类背景区为Au,Cu,Pb,Zn,As,Sb,Mo,V,Mn和Ag,Sn,Sr,Ba及Ti,Cr,Co,Ni,金矿区为Au,Ag,As,Sb,Mo,Mn,Sr和Cu,Pb,Zn,Sn,Ba及Co,Ni,Ti,V,Cr,铜矿区为Cu,Pb,Zn,Mo,Au,Ag,Ba和As,Sb,Sn,Mn及Ti,V,Cr,Co,Ni,Sr，矿区红沙中浓集系数较大的元素多数在矿区岩石中的浓集系统亦较大，金，铜矿床红沙和岩石中的特征元素分别都有Au,Ag,Ag,Sb,Mo,(Mn)和Cu,Pb,(Ba,Ti,Cr)。在金，铜矿床（体上方分别发育有良好的Au和Cu的生物地球化学异常和元素组合及分带，根据红沙的地球化学特征能，判断金或铜矿种类型，并能对掩埋，隐伏金，铜矿床（体）进行定位预测。     

庐江沙溪斑岩型铜金矿床绿泥石的地球化学特征及找矿指示

文章在前人对岛弧环境斑岩型矿床绿泥石主微量元素找矿指示研究的基础上,以陆内环境的长江中下游成矿带中的沙溪斑岩型铜金矿床为对象,利用LA-ICP-MS技术对沙溪斑岩型铜金矿床中绿泥石进行了主微量元素研究。结果显示,绿泥石中Ti、Ba、Co、K、Pb、Sr、Fe、V/Ni靠近矿化中心的位置含量高,Mn、Mg元素远离矿化中心的位置含量高。沙溪斑岩型铜金矿床中绿泥石元素含量分布主要受温度、被交代矿物、流体pH值和氧化还原环境、围岩性质影响。受交代矿物的影响,绿泥石中的有些元素(Si、Na、Mg、K、Al)的含量高低不能直接对矿化中心进行指示,但沙溪斑岩型铜金矿床绿泥石部分元素(Ti、Ba、Co、Pb、Sr、Fe)和元素比值(V/Ni)具有指示矿化中心的作用。     

Trace element geochemistry in topsoil from East China

The concentrations of 23 trace elements in 50 topsoil samples collected from sites ranging between 18°19′N and 49°13′N in East China were analyzed. Sc, Ti, V, Cr, Mn, Co, Ni, Cu, Zn, Ga, and Ta have mean contents more than two times higher than in the continental upper crust. Three elements, Rb, Sr, and Ba, are present at lower concentrations than in the continental upper crust. Finally, a group of elements consisting of Ge, Y, Zr, Nb, Sc, Hf, Pb, Th, and U are present at concentrations 1–2 times higher than in the continental upper crust. However, concentrations of trace elements are mainly affected by parent rock. The contents of Sc, Ti, V, Cr, Mn, Co, and Cu for 29 soils from basalt were found to increase from north to south, whereas Rb, Sr, and Ba contents were found to decrease. In addition, element concentration shows a close relationship with annual average temperature (AAT) as well as annual average precipitation (AAP). Since the 29 soils are all from basalt, the trends of the elemental contents should reflect the influence of climate, which determines the intensity of weathering. These elemental trends suggest that the content of certain elements may indicate the intensity of basalt weathering. Ba/Nb and Sr/Nb ratios were both found to have good correlations with AAT and AAP in this study, which means that these ratios can also indicate the intensity of chemical weathering of basalt.     

Geochemistry and Behavior of Trace Elements During the Complete Evaporation of the Merouane Chott Ephemeral Lake: Southeast Algeria

The Merouane Chott, located in arid southeastern Algeria, experiences annual cycles of filling from September through February followed by its complete evaporation from February through June. The concentration of 15 trace elements (Li, B, Ti; V, Cr, Mn, Co, Cu, Ni, Zn, As, Sr, Ba, Pb, Bi, and U) were measured in chott water samples collected from January through June 2003 during the complete evaporation of the lake. The corresponding concentrations of these trace elements in the major external inputs to this closed basin chott were also obtained. The trace metals show two distinct behaviors. Li, B, Cr, Co, and U tend to be conserved in the chott waters throughout its evaporation. Much of Cr, Co, and U originated from external sources. It is likely, therefore, that the concentration of these elements will increase in the chott waters in future years. In contrast, Ti, Sr, Ba, Zn, Ni, and Pb precipitate continuously during chott evaporation. Of these elements, most of the Sr, Ba, and Zn originated from outside the chott, and thus it is likely these elements will become increasingly concentrated in the chott bottom salts with time. V, As, and Cu exhibit intermediate behaviors. These contrasting behaviors are confirmed by analysis of chott bottom solids.     

太平洋北部铁锰结核富集区沉积物的元素地球化学特征

本文对太平洋北部铁锰结核富集区沉积物的元素地球化学作了较为详细的研究。因子分析提供的信息表明,元素的分布主要受三个因子控制:（1）粘土及Fe、Mn氧化物水化物胶体的吸附作用;（2）生物化学作用过程有关的自生沉积作用;（3）海底页岩风化及附近海区的火山喷发作用。元素的来源:（1）Fe、Mn、Cu、Co、Ni、Zn、Cr、Cr、Mg、Al、Ti、K共生,主要来自粘土吸附;（2）C_有机、N、Sr、Na及Si、Ca、Sr主要来自生物化学过程沉积;（3）Pb主要来源于岩石碎屑（火山喷发碎屑）。     

岩石中低量稀土和其他痕量元素的X-荧光光谱测定

用X-荧光光谱测定岩石中低量稀土元素的仪器参数和测定条件,文[1]已作过讨论。本文介绍样品分析所采用的基本校正,谱线重叠校正和背景处理方法,并将这些方法应用于其他少量和痕量元素的测定。基体的吸收校正岩石样品中最重的主元素是铁,镧系元素La～Er的La线和Ti,Sc,Cr,Mn,Fe,     

Mineral and inorganic chemical composition of the Pernik coal, Bulgaria

The mineral and inorganic chemical composition of five types of samples from the Pernik subbituminous coals and their products generated from the Pernik preparation plant were studied. They include feed coal, low-grade coal, high-grade coal, coal slime, and host rock. The mineral matter of the coals contains 44 species that belong mainly to silicates, carbonates, sulphates, sulphides, and oxides/hydroxides, and to a lesser extent, chlorides, biogenic minerals, and organic minerals. The detrital minerals are quartz, kaolinite, micas, feldspars, magnetite, cristobalite, spessartine, and amphibole. The authigenic minerals include various sulphides, silicates, oxihydroxides, sulphates, and carbonates. Several stages and substages of formation were identified during the syngenetic and epigenetic mineral precipitations of these coals. The authigenic minerals show the greatest diversity of mineral species as the epigenetic mineralization (mostly sulphides, carbonates, and sulphates) dominates qualitatively and quantitatively. The epigenetic mineralization was a result of complex processes occurring mostly during the late development of the Pernik basin. These processes indicate intensive tectonic, hydrothermal and volcanic activities accompanied by a change from fresh to marine sedimentation environment. Thermally altered organic matter due to some of the above processes was also identified in the basin. Most of the trace elements in the Pernik coals (Mo, Be, S, Zr, Y, Cl, Ba, Sc, Ga, Ag, V, P, Br, Ni, Co, Pb, Ca, and Ti) show an affinity to OM and phases intimately associated with OM. Some of the trace elements (Sr, Ti, Mn, Ba, Pb, Cu, Zn, Co, Cr, Ni, As, Ag, Yb, Sn, Ga, Ge, etc.) are impurities in authigenic and accessory minerals, while other trace elements (La, Ba, Cu, Ce, Sb, Bi, Zn, Pb, Cd, Nd, etc.) occur as discrete phases. Elements such as Sc, Be, Y, Ba, V, Zr, S, Mo, Ti, and Ga exceed Clarke concentrations in all of the coal types studied. It was also found that a number of elements in the Pernik coals (F, V, As, Pb, Mo, Li, Sr, Ti, Ga, Ni, Ge, Cr, Mn, etc.) reveal mobility in water and could have some environmental concerns.     

A statistical approach to the study of the distribution of trace elements and their organic/ inorganic affinity in lower Gondwana coals of India

Trace-element analyses of seventy six coal samples representing all the major Lower Gondwana coal basins of India were carried out. Eighteen trace elements, viz., B, Ba, Co, Cr, Cu, Ga, Ge, La, Mn, Mo, Nb, Ni, Pb, Sn, Sr, V, Y and Zr were determined quantitatively in coal ash. An attempt was made to correlate the coals of different coalfields on the basis of multivariate analysis. In addition, the organic/inorganic affinities between the trace elements were established by the coefficients of correlation between the trace elements and ash present. A synthesis of the data reveals that there is similarity in the concentration ranges of trace elements among the coal seams of different coalfields, but the possibility of environmental differences exists due to the statistically different multivariate means of the trace-element concentrations.It is inferred that Ge, Cr, Y and La occur in these coals as organo-metallic complexes and chelates. The elements Ni, Co, Ga, V and Cu show both organic and inorganic association, whereas Mn and Ba are exclusively incorporated in the inorganic fractions.     

Distribution,fractionation, and contamination assessment of heavy metals in offshore surface sediments from western Xiamen Bay,China

Surface sediment samples were collected at 21 offshore sites in western Xiamen Bay, Southeast China. Total concentrations of Li, V, Cr, Co, Ni, Cu, Zn, Sr, Mn, Pb, Ba, Fe, and Ti were determined by inductively coupled plasma-optical emission spectrometry; Hg was determined by atomic fluorescence spectrometry. A modified BCR sequential extraction procedure was used to extract fractions of the above elements. Concentrations of Pb, Cr, and Hg at most sites met the primary standard criteria of Marine Sediment Quality except site S12 for Pb and S7 for Cr, while concentrations of Zn at 17 sites and Cu at seven sites exceeded the criteria. The mean concentration of Hg was three times higher than the background, with a possible source being the Jiulong River. Fe, Ti, Ba, Co, V, and Li dominated the residual phase, mainly from terrestrial input. Ni, Cr, Pb, and Hg in the non-residual phase varied largely between sites. Sr, Mn, Cu, and Zn were mainly in the non-residual fraction. Most sites showed considerable ecological risk; exceptions were site S7 (very high) and sites S10, S11, and S14 (moderate). Cu showed moderate-to-high pollution and Pb exhibited no-to-low pollution, while other metals had a non-pollution status according to their ratios of secondary phase to primary phase (RSP). Results of two assessment methods showed moderate pollution and a very high ecological risk for Cu, Zn, Ni, and Cr at site S7, which might be due to the local sewage treatment plant.     

Comparison of sequential extraction and principal component analysis for determination of heavy metal partitioning in sediments: the case of protected Lagoon El Kelbia (Tunisia)

A sequential extraction procedure applied to surface sediments from El Kelbia Lagoon determined the partitioning of Ba, Co, Cr, Cu, Ni, Sr, V and Zn among evaporites, carbonates, Fe–Mn oxides, organic matter and silicates. To validate the procedure, the sequential extraction results (SER) were compared to principal components analysis (PCA) using major and trace element concentrations and mineralogical quantitative data of surface sediments. SER showed that a part of Sr was highly mobile; Cu, Sr, and Zn and a part of Co and Ni were mobile depending on pH conditions; Cr and V were strongly bound to silicate phases; Co and Ni were partitioned between carbonates, oxides and silicates, and a great part of Ba and Sr were bound to organic matter or sulfides. An agreement was found with PCA in terms of partitioning among minerals for most trace elements. Moreover, the absence of correlation between Ca concentrations and the abundances of calcite, gypsum or dolomite could be explained by an important fraction of Ca bound to organic matter. Also, unexpected negative correlations between abundances of smectite and illite could be explained by a transformation of illite into smectite. Thus, SER and PCA were mostly convergent, which enabled: (1) validation of the extraction procedure used, and (2) refinement of interpretations of the origin and relations between minerals.     

Atmospheric pollution indicated by trace elements in snow from the northern slope of Cho Oyu range,Himalayas

Samples collected from a 0.87 m snow pit at a high altitude site in the Cho Oyu range, Himalayas were measured for V, Cr, Mn, Co, Ni, Cu, Zn, As, Rb, Sr, Cd, Sn, Sb, Ba, Tl, Pb, Bi, Th, and U using inductively coupled plasma mass spectrometry. In addition, major ions, oxygen stable isotopes, and microparticles were also measured to assist the interpretation of seasonal variation of trace elements. The trace elements show a distinct seasonality, i.e., higher concentrations during the non-monsoon season than those during the monsoon season. Significant correlation is observed between Ba and the other trace elements. Crustal enrichment factor (EF_c) analysis indicates that V, Mn, Co, Ni, Rb, Sr, and Th originate mainly from crustal dust, while anthropogenic inputs make an important contribution to the other trace elements (i.e., Cu, Zn, As, Cd, Sn, Sb, Ti, Pb, Bi, and U). Evidence from air mass back trajectories suggests that atmospheric trace element pollution reaching the studied area is transported dominantly by Indian summer monsoon during the monsoon season, while it is transported mainly by the westerlies during the non-monsoon season.     

Taxonomical and Biogeochemical Investigation of Elements in Holocene Mollusk Shells in the South and Southwestern Marmara Basin, Turkey

Concentrations of some heavy metals and trace elements such as Cr,Ga,Ni,Zn,Mo,Cu, Pb,Yb,Y,Nb,Ti,Sr,Ba,Mn,Sc,Co,V,Zr,Fe,Al,W,Se,Bi,Sb,As,Cd in recent mollusk shells and factors affecting their distribution and deposits collected from various depths in the southern and southwestern parts of the Marmara Sea are investigated.The distribution of the elements in the shells is categorized into four groups.Of these,concentrations of 12 elements(As,Bi,Cd,Co,Ga,Mo,Nb, Sb,Se,Sc,W and Yb)are below zero [(0.053-0.79)×10~(-6)];concentrations of seven elements(Cr,Ni, Pb,V,Y,Zr and Cu)are(1.0-6.0)×10~(-6);concentrations of four elements(Ti,Mn,Ba and Zn)are 10- 20×10~(-6);and concentrations of five elements(Si,Al,Fe,Mg and Sr)are(47.44-268.11)×10~(-6).The taxonomic characteristics of the 29 elements were studied separately in mollusk shells such as Chamalea gallina(Linné),Pitar-rudis(Poll),Nassarius reticulatus(Linné),Venerupis senescens (Coocconi),Mytilus galloprovincialis(Lamarck),Mytilaster lineatus(Gemelin in Linné)and Chlamys glabra.It was found that,in mollusk taxonomy,the elements have unique values.In other words, element concentrations in various mollusk shells depend mainly on the taxonomic characteristics of mollusks.In various bionomic environments different element distributions of the same species are attributed to the different geochemical characters of the each environment.Data obtained in this study indicate that the organisms are the most active and deterministic factors of the environment.     

山东招远前孙家金矿床地质和元素地球化学研究

对矿区地表和井下四个中段共采集地层、岩体、蚀变岩、石英脉和矿体样品503件,测试了Au、Ag、As、Sb、Cu、Pb、Zn、Sn、Bi、Mo、Co、Ni、Mn、Cr、V、Ti、Ba、Rb和Sr等19种元素的含量,运用Suffer软件编制了19种元素的矿脉地球化学纵剖面图,根据格里戈良分带指数法计算了元素的地球化学分带,建立了原生晕地球化学立体分带模式。综合地质地球化学资料分析得出以下认识：由花岗岩→钾长石化花岗岩→绢英岩化花岗岩→绢英岩→石英脉或硅化带→金矿石,随着蚀变作用增强,成矿元素Au、Ag、As、Cu、Pb、Bi、Mo、Sb增加,然而成矿作用主要发生在绢英岩化后的硅化阶段。矿区成矿元素Au、Ag、As、Cu、Pb、Sn、Bi、Mo、Co．Ni含量呈多峰分布,分布范围大,离散度大,其中Au、Ag高含量峰值区峰型突出,成矿富集趋势强烈。矿区成矿阶段可分为：石英-金-黄铁矿阶段、石英-金-多金属硫化物阶段和石英-碳酸盐阶段。F1因子（Au、Ag、As、Co、Ni、Sn、Bi）为主成矿阶段的元素组合,F3因子（Mo、Sb）和F5因子（Cu、Zn）反映了成矿热液活动的多期叠加。F4因子Rb、Sr、Ba组合在本区最具典型意义,Rb与Sr、Ba为对抗性元素,Sr、Ba、Ca低值带,Rb、K高值带恰好与Au、矩高值带吻合,显示花岗岩长石类矿物的钾长石化和绢云母化与成矿关系密切。与矿体的侧伏方向一致,总体上矿脉纵剖面地球化学高值带均向SW侧伏。其中Au、Ag高值带宽且比较连续,上下均未封闭,结合金矿体虽已出露地表但规模不大和原生晕分带特征,推测为一浅剥蚀矿床,向SW深部仍有一定延深。矿区原生晕分带序列自上而下为（Hg2、Sr、Ba、Rb）→（矩、Au、Sn、Mo、Cu→（Zn、Pb）→（Sb、Mn）→（Ni、V、Co、As、Hg1、Bi）。As、Sb、Hg高值带偏于中下部,可能指示下部隐伏矿体的存在。     

Distribution of major and trace elements in La Luna Formation, Southwestern Venezuelan Basin

The La Luna Formation (Maraca section), Maracaibo Basin, was studied by means of V and Ni analysis of the bitumen, total organic carbon (TOC), total sulfur (St), major elements (Si, Al, Fe, Mg, Mn, Ca, Ti, Na, K, P), trace elements (V, Ni, Co, Cr, Cu, and Zn), and electron microprobe analysis (EPMA) of the whole rock, and St, major elements (Si, Al, Fe, Mg, Mn, Ca, Ti, Na, K, P), trace elements (V, Ni, Co, Cr, Cu, Zn, Mo, Ba, U, Th) and rare earth elements (La, Ce, Nd, Sn, Eu, Th, Yb, Lu) of the carbonate-free fraction. The results are discussed based on the organic and inorganic association of trace elements and their use as paleoenvironmental indicators of sedimentation. An association between V and organic matter is suggested by means of correlation between V and Ni vs. TOC, the use of EPMA (whole rock) and V and Ni concentrations (carbonate-free fraction), whereas Ni is found in the organic matter and the sulfide phase. Fe is present as massive and framboidal pyrite, whereas Zn precipitates into a separate phase (sphalerite), and Ni, Cu and, in some cases, Zn, can be found as sulfides associated with pyrite. Concentrations of V and Ni (bitumen), TOC, St, V, Ni, Cr, Cu and Zn (whole rock), U, Th, Mo (carbonate-free fraction) are indicative of changes in the dysoxic sedimentation conditions in the chert layers (TOC, St, V, Ni, Cu and low Zn and V/Cr <4) to euxinic anoxic conditions in the argillaceous limestone (TOC, St, V, Ni, Cu and high Zn and V/Cr >4). In the sequence corresponding to the argillaceous limestone, variations in the concentrations of TOC, St, V, Ni, Zn, Cu and Cr (whole rock) can be observed, also suggesting variable sedimentation conditions. The following is proposed: (i) sedimentation intervals under euxinic conditions associated with high contribution and/or preservation of organic matter, allowing a high concentration level of V and Ni in the organic phase and the accumulation of Cu, Zn and Ni (in a smaller proportion) in the sulfide phase; (ii) sedimentation intervals under anoxic conditions and in the presence of relatively lower H₂S, which allowed lower concentrations of V and Ni in the organic phase and higher concentrations of Cu, Zn, and Ni in the sulfide phase. Rare earth elements (REE) concentrations exhibit a marked increase in Ce, Nd, Sm, Eu, Y and Lu for the QM-3 interval, relative to Post-Archean Average Shale (PAAS). REE enrichment in shales has been related to the presence of phosphate minerals such as monazite or apatite. However, these minerals were not detected through XRD or EPMA in the whole rock or in the carbonate-free fraction. The association of REE with organic matter is suggested due to the absence of phosphate minerals, although assessment of these elements require further analysis.     

X射线荧光光谱法测定多目标地球化学调查样品中主次痕量组分

采用低压聚乙烯镶边垫底的粉末样品压片制样,用PW2440X射线荧光光谱仪对多目标地球化学调查样品中Na2O、MgO、Al2O3、SiO2、P、K2O、CaO、Ti、Mn、Fe2O3、Co、Nb、Zr、Y、Sr、Rb、Pb、Th、Zn、Cu、Ni、V、Cr、Ba、La等组分进行测定。重点讨论了微量元素的背景选择和谱线重叠校正问题。使用经验系数法和康普顿散射线作内标校正基体效应,经标准物质分析检验,结果与标准值吻合,用GBW07308和GBW07310水系沉积物国家一级标准物质作精密度试验,统计结果RSD(n=12)除La、Cr、Co和Th<14.00%以外,其余各组分均小于6.00%。     

用X射线荧光光谱法测定Cl、S等31个元素

采用硼酸镶边垫底的粉末样品压片制样,用ARL ADVANT′XP＋型X射线荧光光谱仪对土壤和水系沉积物样品中Na、Mg、Al、Si、P、S、Cl等31个组分进行测定。重点研究了Cl和S等元素的测定条件、痕量元素的背景选择和谱线重叠校正问题。使用经验系数法和康普敦散射作内标校正基体效应。经标准物质校验,结果与标准值吻合。方法的检出限、精密度和准确度能满足多目标地球化学调查样品的分析要求。     

泉州城市表层土壤中金属元素来源分析

采集了泉州市47个城市表层土壤样,用ICP-MS检测技术,研究了土壤中26种重金属元素的富集特征、环境风险及污染来源。富集因子结果显示,与泉州市土壤背景值相比,Li、Ni、Co、Cu、Zn、Sr、Cd、Sn、Sb、Pb、Ta在城市表层土壤中的富集因子大于1,而Ti、V、Cr、Fe、Mn、Ga、Ge、As、Rb、Y、Nb、Cs、Bi、Th、U的富集因子小于1。从功能区上看,工业区污染最为严重,其次依次为农业区、商住区、城市绿地、交通区。环境风险指数表明,泉州市城市表层土壤中重金属污染具有极高的环境风险,达到极高风险级别的样品占48.9%。采用多元统计分析方法对土壤样品中各金属元素来源进行解析,结果表明,研究区城市表层土壤中金属元素总体可分成5类：①交通运输类（Sn、Pb、Sb、Bi）;②工业因子类（Cr、Co、Ni、Fe、Mn）;③自然因子类别（Ga、Ge、Ti、V、Cu）;④混合因子类别（Zn、Cd、Sr、Th、U、Y、As、Cs、Nb、Ta、Rb）;⑤生活垃圾因子类别（Li）。     

Taxonomical and Biogeochemical Investigation of Elements in Holocene Mollusk Shells in the South and Southwestern Marmara Basin,Turkey

Concentrations of some heavy metals and trace elements such as Cr, Ga, Ni, Zn, Mo, Cu, Pb, Yb, Y, Nb, Ti, Sr, Ba, Mn, Sc, Co, V, Zr, Fe, Al, W, Se, Bi, Sb, As, Cd in recent mollusk shells and factors affecting their distribution and deposits collected from various depths in the southern and southwestern parts of the Marmara Sea are investigated. The distribution of the elements in the shells is categorized into four groups. Of these, concentrations of 12 elements （As, Bi, Cd, Co, Ga, Mo, Nb, Sb, Se, Sc, W and Yb） are below zero [（0.053-0.79）×10^-6]; concentrations of seven elements （Cr, Ni, Pb, V, Y, Zr and Cu） are （1.0-6.0）×10^-6; concentrations of four elements （Ti, Mn, Ba and Zn） are 10- 20×10^-6; and concentrations of five elements （Si, Al, Fe, Mg and Sr） are （47.44-268.11）×10^-6. The taxonomic characteristics of the 29 elements were studied separately in mollusk shells such as Chamalea gallina （Linn6）, Pitar rudis （Poli）, Nassarius reticulatus （Linn6）, Venerupis senescens （Coocconi）, Mytilus galloprovincialis （Lamarck）, Mytilaster lineatus （Gemelin in Linne） and Chlamys glabra. It was found that, in mollusk taxonomy, the elements have unique values. In other words, element concentrations in various mollusk shells depend mainly on the taxonomic characteristics of mollusks. In various bionomic environments different element distributions of the same species are attributed to the different geochemical characters of the each environment. Data obtained in this study indicate that the organisms are the most active and deterministic factors of the environment.