共查询到20条相似文献，搜索用时 750 毫秒
1.
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。 相似文献
2.
沉积物的元素地球化学特征是对沉积盆地水体环境以及古气候条件变化的响应。本文根据元素（Al、Fe、Mg、Ca、K、Na、P、V、Ni、Co、Cr、Cu、Zn、Sr、Ba、Cd、Li、Mn、Pb、Ti）的含量及其比值（Al/Ti、Fe/Mn、Sr/Ba、Mg/Ca、Sr/Ca、Na/Ca、V/Cr、Ni/Co、Ni/V）的变化，对三水盆地古近系心组红岗段生油层的沉积条件进行了系统分析。心组红岗段下部（亚段A）表现为较稳定的地球化学特征。各元素丰度及其比值指示这一时期陆源输入持续较高、且物源组成变化不大。由于海水入侵的影响，湖盆水体盐度相对较高，底部水体以弱氧化条件为主，O2-H2S界面位于水/沉积物界面附近。红岗段中上部（亚段B、C）的元素地球化学特征变化较为频繁且幅度很大，反映古气候和湖盆沉积条件的迅速变迁。在潮湿气候条件下，沉积物的地球化学特征表现为以Al、Ti为代表的外源元素含量及其比值较高，而Mg、Ca等盆内化学沉积元素含量较低。古氧气指标指示底部水体为还原环境，有利于有机质保存。因而，相应于较高的有机碳含量。在间歇性干旱时期，陆源输入减少，外源元素含量及其比值显著降低。随着蒸发作用的加强，水体盐度加大，内源元素丰度以及Mg/Ca、Sr/Ba、Sr/Ca和Na/Ca比值大幅度上升。底部水体为氧化环境，O2-H2S界面多位于水/沉积物界面或沉积物中。上述两种气候条件在红岗段中上部沉积时期交替出现。红岗段沉积后期由于淡水的长期输入，湖水出现逐渐淡化趋势。 相似文献
3.
青藏高原南部枪勇冰川雪冰中痕量元素的组成特征及其环境意义 总被引：2，自引：0，他引：2
为了认识青藏高原南部雪冰中痕量元素的组成特征、背景含量水平以及人为污染的可能影响,利用高分辨电感耦合等离子体质谱仪首次对2009年4月19日采自枪勇冰川一个40 cm 雪坑中 Al、 Fe、 Ba、 Cd、Co、Cr、Cu、Li、Ni、Zn、Pb、Sb、Sr、U 和 V 共15个痕量元素的浓度进行了测试和研究.分析表明,不同痕量元素之间浓度变化很大,从 Cd 的0.004 ng/g 变化到 Fe 的8628 ng/g;同一痕量元素的浓度变化范围也较大,最大值/最小值从13(Cd)变化到94(Sr).研究表明,不同痕量元素记录反映了人类活动与自然活动的不同影响.对痕量元素地壳富集系数分析表明,岩石和土壤粉尘是 Ba、Fe、Sr、Co、Cr、V 和 U 的主要来源;而人为污染是枪勇冰川中 Pb、Zn、Cu、Li、Ni、Cd 和 Sb 的一个重要来源.对比研究表明,无论是以粉尘源为主要来源的痕量元素,还是以人为源为主要来源的痕量元素,它们的浓度明显高于中亚有关地区冰川中痕量元素的浓度,更远远地高于格陵兰和南极雪冰中的相应浓度,揭示了该地区大气中痕量元素受到粉尘和人为源污染物带来的显著影响 相似文献
4.
5.
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, 相似文献
6.
Yaping Liu Shugui Hou Sungmin Hong Soon-Do Hur Khanghyun Lee Yetang Wang 《Environmental Earth Sciences》2011,63(2):311-320
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 (EFc) 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. 相似文献
7.
泥页岩中微量元素特征对反演泥页岩形成时的沉积和古地理气候条件具有重要意义。采集淮南煤田山西组泥页岩样品,利用ICP-MS对泥页岩中微量元素进行了测试分析,探讨了研究区山西组泥页岩中微量元素的地球化学特征及其意义。结果表明,B、Cr、U、Ga、Li、Sn、Pb、Mo、Th、W等元素富集,Cd、Co、Cu、Ti、Zn、Sc、Ba、Mn、Ni、Sr等元素亏损;揭示淮南煤田山西组形成于温暖湿润和半咸水-高咸水的沉积环境中,沉积体系为开放型,体系内为弱氧化-还原环境,其中以弱还原-还原环境为主,且表现出从早期弱氧化到中后期的还原环境的演化特征;依据U/Th、Ni/Co、Sr/Cu、B/Ga、Sr/Ba、TOC等地球化学参数结果推测,盐度和氧化还原条件受到多种因素的影响,有机质的原始堆积量是影响山西组泥页岩中有机质含量的主要因素,而盐度和氧化还原条件影响有机质中各显微组分含量。研究区温暖湿润的气候和较为还原的环境为有机质的堆积和保存提供了有利条件,为页岩气的成藏提供了物质基础。 相似文献
8.
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。 相似文献
9.
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. 相似文献
10.
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. 相似文献
11.
Riad A. Higazy 《Geochimica et cosmochimica acta》1952,2(3):170-184
The epidioritc and quartzite of the Malin Head district, (Ireland) are considered by Holmes and Reynolds [7] to be metasomatically transformed into skarn-rocks and mica-schist respectively. The trace element contents of these rocks were investigated using semi-quantitative methods in order to study the behaviour of the different trace elements during the metasomatic changes which have taken place. The elements which have been determined are Rb, Ba, Ag and Pb; Sr, Y and La; Li, Cr, Ni, Co, V, Cu, Sc, Sn and Mo; Ga; Zr, Be, Tl, Ge and In. The trace elements follow the major elements for which they can substitute in favourable crystal lattices, the substitution being in accord with Goldschmidts rules. Rb, Ba and probably Pb and Ag follow and substitute for K; Sr and Y for Ca and probably K; Li, Cr, Ni, Co, V, Cu, Sc, Sn and Mo for Mg, Fe2 and Fe3; and Ga for Al. 相似文献
12.
采用经验和数法校正基体效应,X荧光光谱测定样品中的主、次痕量元素是一种简便而快速的方法,但由于经验系数的求取很大程度上取决于标准样品的类型、含量范围和计算方法,往往使用范围有一定的局限性,本文提出的标准分类法计算经验系数, 相似文献
13.
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. 相似文献
14.
Major and trace element composition of the Ordovician Obolus phosphorites and associated Dictyonema shales were determined by ICP-MS and chemical and microchemical elemental analyses. Relative to the phosphorites, the Dictyonema shales are substantially enriched in a variety of trace elements, except for As, Be, Co, Y, REE, Sr, and Pb. The Obolus phosphorites show enrichment of As, Bi, Hg, Mo, La, Y, Pb, and Sr and depletion of Ag, Ba, Be, Cd, Cr, Cu, Hf, Ni, Sc, Sn, U, V, Zn, and Zr relative to the world average phosphorite composition. The average trace element composition of the Dictyonema shales is close to the mean shale composition, except for higher contents of Mo, Hg, Pb, Se, Ta, Te, Th, V, and U and lower contents of Ba, Bi, Cd, Co, Re, Sr, and Zn. The results suggest that the change from phosphate sedimentation in aerated environments to anoxic carbonaceous sedimentation was accompanied by changes in the composition and concentration of trace elements in the sediment. Both facies show similar trends of trace element distribution indicative of the stability of the composition of seawater and terrigenous sediment input. 相似文献
15.
Doklady Earth Sciences - Published data and research results from the authors on the concentrations of dissolved trace elements (P, Si, Li, Rb, Cs, Sr, Ba, Mn, Fe, Co, Ni, Cu, Zn, Cd, Tl, Pb, Al,... 相似文献
16.
M. M. Bazova 《Geochemistry International》2017,55(1):131-143
The paper presents data on the specifics of the distributions of chemical elements in natural waters of the Kola North depending on the landscape–geochemical characteristics of the water catchment areas and aerotechnogenic pollution. The territory is subdivided into seven zones with different dominant rock types and typical landscapes. Lakes in the Kola region generally contain elevated concentrations of Cu, Ni, Co, Cr, V, Mo, U, Sb, Bi, Al, Fe, Mn, Sr, Li, Rb, Pb, Zn, Cd, La, and Ce. The waters of lakes in the influence zones of Cu–Ni mines are enriched in La, Ce, Sm, Gd, Pr, and Nd. In waterlogged landscapes, waters are enriched in certain trace elements because of their migration with humic acids. Technogenic acidic precipitation is proved to result in leaching of several elements, first of all Cd, Zn, and As (as well as other elements contained in rocks composing the water catchment areas) and their transfer into the waters. 相似文献
17.
The geochemistry of trace elements in the underground and open-pit mine of the Goze Delchev subbituminous coal deposit have been studied. The coals in both mines are highly enriched in W, Ge and Be, and at less extent in As, Mn and Y as compared with the world-wide Clarkes for subbituminous coals. Ni and Ti are also enhanced in the underground coals, and Zr, Cr and Mo in the open-pit mine coals.Characteristic for the trace element contents in the deposit is a regular variation with depth. The following patterns were distinguished for profile I: a — the element content decreases from the bottom to the top of the bed paralleling ash distribution (Fe, Co, As, Sb, V, Y, Mo, Cs, REE, Hf, Ta, Th, P and Au); b — Ge and W are enriched in the near-bottom and near-top coals; c — in the middle part of the bed the content of K and Rb is maximal, while that of U is slightly enriched; d — Ba content decreases from the top to the bottom of the bed. In profile II, W and Be contents decrease from the bottom to the top. The near-bottom, and especially the near-roof samples of profile IV are highly enriched in Ge, while for W the highest is the content of the near-bottom sample.Ge, Be, As, Mn, Cl and Br are mainly organically associated. The organic affiliation is still strong for Co, B, Sr, Ba, Sb, U, Th, Mo, La, Ce, Sm, Tb and Yb in the underground coals, and Fe, Co, Na, W, Sr, Y and Ag in the coals from the open-pit mine. K, Rb, Ti, Zr, Hf and Ta are of dominant inorganic affinity. The chalcophile and siderophile elements correlate positively with Fe and each other and may be bound partly with pyrite or other sulphides and iron containing minerals.Compared statistically by the t-criteria, the elements Na, Li, Cu, Zn, Pb, Cr, Ni, Co, Mo, Fe and Be are of higher content in the open-pit mine. Tungsten is the only element of higher concentration in the underground mine. The contents of Ge, As, Sr, V, Mn, Y, Zr and P are not statistically different in both mines.It was supposed that there were multiple sources of the trace elements in the deposit. The source of the highly enriched elements (W, Ge, Be, and As) most probably were the thermal waters in the source area. The contemporary mineral springs are of high content of these elements. Another source were the hosting Mesta volcanic rocks, which are enriched in Sb, Mo, Hf, U, Th, As, Li and Rb. Some of the volcanics were hydrothermally altered and enriched or depleted of many elements. Thus, the hydrothermal solutions were also suppliers of elements for the coals. It is obvious that the contents, distribution and paragenesis, of the trace elements in both Goze Delchev coals reflect the geochemical specialization of the source area, including rocks, paleo- and contemporary thermal waters. 相似文献
18.
长江口外海域表层沉积物微量元素地球化学特征 总被引：1，自引：1，他引：0
对采自长江口外海域187个表层沉积物的25个微量元素含量进行了标准差系数、相关分析及R型因子分析,探讨了微量元素的来源和分布特征。长江口外海域沉积物微量元素Li、V、Cr、Co、Ni、Ga、Cu、Zn、Th和Rb分布基本相似;Sr分布与Li、Cu、Pb、Zn、Th和Rb相反;研究区东南部Sr分布与生物作用有明显关系;Cd和Mo分布与粒度之间的相关性较差,主要受氧化还原环境的控制;Zr分布反映了长江物源的影响。相关分析和R型因子分析结果表明,沉积作用、粒度控制效应、海洋生物作用、氧化还原环境和源区地质背景等对长江口外海域表层沉积物中微量元素分布起着主要控制作用。 相似文献
19.
The chemical status of major and trace elements (TE) in various boreal small rivers and watershed has been investigated along a 1500-km transect of NW Russia. Samples were filtered in the field through a progressively decreasing pore size (5, 0.8 and 0.22 μm; 100, 10, and 1 kD) using a frontal filtration technique. All major and trace elements and organic carbon (OC) were measured in filtrates and ultrafiltrates. Most rivers exhibit high concentration of dissolved iron (0.2–4 mg/l), OC (10–30 mg/l) and significant amounts of trace elements usually considered as immobile in weathering processes (Ti, Zr, Th, Al, Ga, Y, REE, V, Pb). In (ultra)filtrates, Fe and OC are poorly correlated: iron concentration gradually decreases upon filtration from 5 μm to 1 kD whereas the major part of OC is concentrated in the <1–10 kD fraction. This reveals the presence of two pools of colloids composed of organic-rich and Fe-rich particles. According to their behavior during filtration and association with these two types of colloids, three groups of elements can be distinguished: (i) species that are not affected by ultrafiltration and are present in the form of true dissolved inorganic species (Ca, Mg, Li, Na, K, Sr, Ba, Rb, Cs, Si, B, As, Sb, Mo) or weak organic complexes (Ca, Mg, Sr, Ba), (ii) elements present in the fraction smaller than 1–10 kD prone to form inorganic or organic complexes (Mn, Co, Ni, Zn, Cu, Cd, and, for some rivers, Pb, Cr, Y, HREE, U), and (iii) elements strongly associated with colloidal iron in all ultrafiltrates (P, Al, Ga, REE, Pb, V, Cr, W, Ti, Ge, Zr, Th, U). Based on size fractionation results and taking into account the nominal pore size for membranes, an estimation of the effective surface area of Fe colloids was performed. Although the total amount of available surface sites on iron colloids (i.e., 1–10 μM) is enough to accommodate the nanomolar concentrations of dissolved trace elements, very poor correlation between TE and surface sites concentrations was observed in filtrates and ultrafiltrates. This strongly suggests a preferential transport of TE as coprecipitates with iron oxy(hydr)oxides. These colloids can be formed on redox boundaries by precipitation of Fe(III) from inflowing Fe(II)/TE-rich anoxic ground waters when they meet well-oxygenated surface waters. Dissolved organic matter stabilizes these colloids and prevents their aggregation and coagulation. Estuarine behavior of several trace elements was studied for two small iron- and organic-rich rivers. While Si, Sr, Ba, Rb, and Cs show a clear conservative behavior during mixing of freshwaters with the White sea, Al, Pb and REE are scavenged with iron during coagulation of Fe hydroxide colloids. 相似文献
20.
山东招远前孙家金矿床地质和元素地球化学研究 总被引：6，自引：1，他引：5
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。 相似文献