Rock, till, and stream-sediment geochemistry in the search for porphyry-type Mo---Cu---Au deposits in the proterozoic rautio batholith, Western Finland

About 170 bedrock, 550 till, and 180 organic-rich stream-sediment samples were collected at a regional scale over the Rautio batholith, and 490 rock and 1050 till samples at a local scale from around the Susineva Mo---Cu---Au occurrence which is located in the middle of the batholith. The rock samples from the regional study and selected rock samples from the Susineva area were analyzed for 32 elements. The rest of the rock samples from Susineva and all other sample types were analyzed for Mo and Cu only.     

Carbonation processes in municipal solid waste incinerator bottom ash and their effect on the leaching of copper and molybdenum

The interaction of CO₂ with municipal solid waste incinerator (MSWI) bottom ash was studied in order to investigate the resulting changes in pH and bottom ash mineralogy and the impact that these changes have on the mobility of Cu and Mo. Carefully controlled carbonation experiments were performed on bottom ash suspensions and on filtered bottom ash leachates. Changes in leachate composition were interpreted with the geochemical model MINTEQA2, and neoformed minerals were investigated by means of chemical and spectroscopic analysis. The leaching of Cu and Mo during artificial carbonation is compared to the leachability of Cu and Mo from a sample of naturally carbonated bottom ash from the same incinerator. During carbonation in the laboratory, a precipitate was formed that consisted mainly of Al-rich amorphous material, calcite, and possibly gibbsite. Carbonation to pH ≈8.3 resulted in a reduction of more than 50% in Cu leaching, and a reduction of less than 3% in Mo leaching. The reduction in Cu leaching is attributed to sorption to the neoformed amorphous Al-minerals. During natural weathering/carbonation of bottom ash, additional sorption sites are formed which further reduce the leaching of Cu and Mo on a time scale of months to years.     

Experimental Modeling of Cyanobacterial Bloom in a Thermokarst Lake: Fate of Organic Carbon,Trace Metal,and Carbon Sequestration Potential

Thermokarst lakes, formed during permafrost thaw in Western Siberia Plain over past tens to hundreds years, cover overall territory close to million km² and may represent significant source of CO₂ and CH₄ to the atmosphere. These acidic (3 < pH < 6) and humic [10 < dissolved organic carbon (DOC) < 50 mg/L] lakes are essentially inhabited by heterotrophic bacterioplankton with rare phytoplankton bloom occurring during warm periods. In order to understand possible effects of phytoplankton bloom on thermokarst lake hydrochemistry under climate warming scenario, we cultured pure cyanobacterium (Gloeocapsa sp.) and native cyanobacterial associate separated from the natural lake water. As substrates, sterilized thermokarst lake water and peat leachate from western Siberia were used. In these laboratory microcosm experiments which lasted 10 days, we monitored daily pH, biomass, DOC, and 40 major and trace elements. Despite significant variation of pH (4 to ~10.5) and biomass (a factor of 3–5), very few dissolved elements responded to massive cyanobacterial growth. The DOC varied within a factor of 1.2–1.5, exhibiting slow increase due to exometabolite production in thermokarst lake water and an initial decrease due to photodegradation in peat leachate. Elements appreciably affected by photosynthesis in both lake water and peat leachate substrates were P, Zn, Mn, and, in a lesser degree, Cd, K, Rb, Sr, Ba, Cr, Al, and U. While P, K (Rb), Mn, and Zn removal from solution during cell growth could be linked to biological demand by cyanobacteria, the adsorption of Cd, Sr, Ba, Al, Cr, U on the cell surface in response to the pH rise is most likely. Many other trace elements did not exhibit any significant evolution of the concentration during 10-day experiment either due to their strong complexation with allochthonous organic matter and essentially organic/organo-mineral colloidal status (Fe, Ni, Co, Cu, Pb, REEs, Ti, Zr, Hf, Th) or due to the lack of element interaction with cyanobacterial cells, via both adsorption and intracellular uptake (B, Si, V, Mo, As, Sb, Cs). Therefore, possible intensification of cyanobacterial bloom in thermokarst lakes caused by leaching of thawing peat will likely affect only few macronutrients and micronutrients such as P, K, Mn, and Zn, while the majority of trace elements bound to allochthonous DOC in the form of organic and organo-mineral colloids will not be affected by cyanobacterial biomass production and pH rise due to photosynthesis. Cyanobacterial bloom in organic-rich (20 mg DOC/L) thermokarst lakes exhibited significant potential of carbon sequestration from the atmosphere, which is more than an order of magnitude higher than the CO₂ evasion due to heterotrophic plankton respiration of allochthonous DOC.     

The leaching of trace elements from municipal solid waste incinerator bottom ash at different stages of weathering

For a proper assessment of the environmental impact of the utilisation and disposal of Municipal Solid Waste Incinerator (MSWI) bottom ash it is necessary to understand weathering processes and their effects on (trace) element leaching. The authors have investigated the processes that control the leaching of Cd, Pb, Zn, Cu, and Mo from 3 categories of bottom ash: (A) unweathered bottom ash (grate siftings and unquenched samples), (B) quenched/non-carbonated bottom ash (freshly quenched and 6-week-old samples), and (C) weathered bottom ash (1.5- and 12-year-old samples). Leaching experiments were performed in a pH-stat at a large range of pH values. The speciation code MINTEQA2 was used for subsequent modelling of precipitation/dissolution processes. The speciation of trace elements in weathered bottom ash was also investigated by microanalytical techniques. In A- and B-type bottom ash the general controlling processes are thought to be precipitation/dissolution of relatively soluble minerals or, in the case of Cu in particular, extensive complexation with dissolved organic C. At the “natural” pH of the samples, the leaching of Cd, Pb, Cu, Zn and Mo is generally significantly lower from C-type bottom ash than from less weathered types of bottom ash. This reduction in leaching is due to the neutralisation of bottom ash pH and the formation of less soluble species of these elements as weathering continues. In the more weathered (C-type) bottom ash trace element leaching does not seem to be solubility-controlled; although slow precipitation reactions cannot be totally excluded, it is hypothesised that the controlling mechanism in those samples is sorption to neoformed minerals.     

黑龙江省讷河市土壤某些微量元素地球化学特征

根据东北黑土地1：250000土地质量地球化学调查数据，对黑龙江省讷河市土壤中微量元素B、Cu、Mo、Fe、Mn、Zn元素全量和有效态含量分布特征进行了分析研究.结果显示：①土壤表层Mn元素含量丰富，Fe、Mo元素含量较丰富，B、Cu、Zn元素含量较缺乏；②土壤表层微量元素Cu、Fe、Mn、Zn有效态含量丰富，B有效态含量中等，Mo有效态含量缺乏；③黑土剖面中微量元素淋溶淀积程度明显，表现为以淋溶层较低，表层和淀积层较高，而草甸土淋溶淀积不明显.依据土壤中微量元素全量和有效态含量分布特点，应选择施用微量元素肥料，促进农业可持续发展.     

黑龙江省讷河市土壤某些微量元素地球化学特征

根据东北黑土地1：250000土地质量地球化学调查数据,对黑龙江省讷河市土壤中微量元素B、Cu、Mo、Fe、Mn、Zn元素全量和有效态含量分布特征进行了分析研究.结果显示：①土壤表层Mn元素含量丰富,Fe、Mo元素含量较丰富,B、Cu、Zn元素含量较缺乏;②土壤表层微量元素Cu、Fe、Mn、Zn有效态含量丰富,B有效态含量中等,Mo有效态含量缺乏;③黑土剖面中微量元素淋溶淀积程度明显,表现为以淋溶层较低,表层和淀积层较高,而草甸土淋溶淀积不明显.依据土壤中微量元素全量和有效态含量分布特点,应选择施用微量元素肥料,促进农业可持续发展.     

Influence of parent sediments on the concentration of heavy metals in urban and suburban soils in Turku,Finland

The purpose of this study was to examine the influence of parent sediment material on soil geochemistry and to locate possible pollution sources in the area of Turku town in southwestern Finland. The study area is glaciated terrain and subsurface samples were chosen to represent five different parent sediment materials: glacial till, glaciofluvial or littoral sand, clay, peat and marine mud. Elemental concentrations of surface (100 samples) and background soil (50 samples) were analysed by ICP-AES (Al, Ba, Ca, Co, Cr, Cu, Fe, K, Mg, Mn, Na, Ni, P, S, Sr, Ti, V) and by graphite furnace AAS (As, Cd, Mo, Se). Loss-on-ignition was determined as an indicator of organic matter. Analytical results were examined using multivariate statistical methods. The results indicate that the studied soils are not heavily contaminated; there were only few sample sites with elevated heavy metal concentrations. High Pb concentrations were observed along main traffic routes, and also in places where there has been small-scale use of antifouling paints. However, concentrations of heavy metals in topsoil were in general significantly lower than those measured in large cities elsewhere. The parent material strongly affects the geochemical character of the soils. Clays naturally have a significantly higher concentration of heavy metals than sands or till material. This is also reflected in concentrations in organic topsoil. When assessing target levels for polluted soil, the primary sediment appears to be a more important factor than the amount of organic matter.     

REE Geochemistry of Moderate－and High－Sulfur Coals from North Shanxi,China

Contents of the rare-earth elements(REE) in two coal seams from North Shanxi Province,China,were determined using the instrumental neutron activation method.Based on the REE distribution tpatterns,and correlation analysis and cluster analysis,the main conclusions were drawn as follows.The REE contents are controlled mainly by the coal-forming environments,but might be affected by acidic solution Jeaching after peat sedimentation.The REE distribution patterns should be nearly the same in the sublayers of the same coal seam,and the occurrence of abnormal patterns might indicate the geological effect during post-sedimentation.The REE in coals are present mainly in the inorganic phase,and might be derived mainly from terrigenous detrital minerals.Some harmful elements,such as V,P,Mo,Cr,Cu,Mo,Th and Cd,might have cleaning potential during processing and dressing by washing because they are associated with REE.     

Geological factors influencing the concentration of trace elements in the Philippi peatland, eastern Macedonia, Greece

Six peat samples obtained from the Holocene and the Weichselian of the Philippi peat deposit, eastern Macedonia, Greece, were analyzed for 48 trace elements by Inductively Coupled Plasma–Mass Spectrometry (ICP–MS). The ash contents of these samples were also determined. Most of the trace elements are associated with the minerals in the peat, while Ge, Mo, Pb, Se, Ta, Tl, U, and W display a greater affinity with the organic matter. Compared with crustal averages (Clarke concentrations), the Philippi peat is enriched in some elements (Ag, As, Au, Cd, Mo, Se, Te, U, and W) because of the respective mineralizations in the area. The Philippi peat is also enriched in Cr, Cu, Mo, Pb, Sc, Sn, T, V, Y, and Zn in comparison with typical fen peats, as well as in As, Cr, Mo, Se, and U in comparison with typical coals. Climatic and hydrogeological conditions strongly influenced the peat-forming environment resulting in a differentiation between Holocene and Weichselian peat. Generally, the Holocene peat contains lower concentrations of trace elements in the northern and southern part of the fen, than the Weichselian one. The opposite trend is observed in the fen area close to the western basin margins.     

四川盆地典型农业区土壤中铜、钴、钼和锌的空间分异及其影响因素

为定量化分析地理因子对土壤中铜（Cu）、钴（Co）、钼（Mo）和锌（Zn）空间分异的影响,作者采集和测定了四川盆地长寿之乡江津区156件表土样品,综合运用数理统计、地统计和地理探测器等方法,分析表土中Cu、Co、Mo和Zn含量的空间分异特征及其驱动因子。表土中Cu、Co、Mo和Zn均值分别为27.0×10^-6、18.5×10^-6、0.4×10^-6和216.8×10^-6,分别是中国土壤背景值的1.19倍、1.45倍、0.20倍和2.17倍。研究区表层土壤中Cu（36.6%）、Co（16.9%）、Mo（51.7%）和Zn（89.4%）变异系数都呈中等变异,但Zn和Mo的空间分布不均匀性更加显著。总体上,江津区表土中Cu、Co、Mo和Zn含量在北部相对较高,而南部地区相对较低。土壤中Fe和Mn及成土母岩和土壤类型分别是影响江津区表土中Cu、Co、Mo和Zn空间分异的主控驱动因子,但影响程度不一。总体上,Fe和Mn的独立及交互作用最高,对江津区表土中Cu、Co、Mo和Zn含量的空间分异起到重要作用。     

Lithogeochemistry of hypogene, supergene and leached cap samples, berg porphyry copper deposit, British Columbia

In this paper we examine the influence of the development of supergene oxide and sulphide zones on the original hypogene geochemical patterns at the Berg deposit, British Columbia.The deposit, in the alpine zone of the Tahtsa Range, was logged (GEOLOG) and sampled in fourteen diamond drill holes along a N—S section and from outcrop where possible. Anomalous populations of major and trace elements were defined using log probability graphs and a sequential extraction (10% hydrochloric acid— ammonium oxalate — potassium chlorate/hydrochloric acid — nitric/perchloric acids) was used to study the distribution of elements between carbonate, oxide, sulphide and silicate phases.Core logs and assays show that primary ore minerals (chalcopyrite—molybdenite) extend from the outer part of the porphyry intrusion into the surrounding hornfels where the best grades of copper are found close to the intrusive contact. Maximum copper grades, however, result from development of a supergene enrichment blanket. Within the hypogene zone, principal lithogeochemical patterns reflect the differences in composition of the hornfels, originally intermediate to basic volcanics, and the intrusion, as well as the introduction of F and trace metals (Cu, Mo, Pb, Zn and Ag). Distribution of Ag is broadly comparable to that of Cu and Mo whereas anomalous Pb and Zn are present as peripheral haloes around the potential ore zones.Emergence of strongly acidic ground water and precipitation of iron oxides, indicate that leaching processes are active. Furthermore, although primary sulphides, associated with both their oxidation products and secondary sulphides, can still be found in surface samples, sequential extractions on drill core clearly indicate vertical redistribution of copper between oxide, carbonate and sulphide phases. Using ratios of metal concentrations to TiO₂, the surface concentrations of trace metals can be compared with those at depth and the relative amount of enrichment or depletion can be quantified. In highly leached sites the absolute concentrations of Cu, Mn and Zn are low which is reflected in TiO₂ ratios of <1. However, Mo, Pb and Ag are enriched at the same sites (TiO₂ ratios >1). In areas where physical erosion exceeds leaching (topographic lows) primary sulphides co-exist with secondary sulphide and oxide minerals. Here Cu, Mo, Pb, Zn, Mn and Ag are enriched. Fluorine is relatively unaffected by the leaching process. It would appear signature for a cale alkaline Cu and Mo porphyry deposit in an area where outcrop was intensely leached.     

Younger Dryas glacial advance in the southern Gulf of St. Lawrence,Canada: analogue for ice inception?

In the summer of 1999, the Maritimes and Northeast Pipeline Company excavated a 3-m-deep trench across northern Nova Scotia exposing a continuous transect of surficial deposits along a 237-km corridor. A Lateglacial palaeosol with preserved A horizon (peat and wood) buried under 2-10 m of surface till consisted mainly of herbaceous plant material with few large wood fragments. Large pieces of wood from two sites yielded conventional radiocarbon ages of 10.9 ¹⁴C kyr BP (GSC-6435) and 10.8 ¹⁴C kyr BP (GSC-6419). Previous to these finds, only a few localities were known to reveal till overlying peat, so the extent of Younger Dryas (YD) glaciers could not be clearly established. Glacial flow lines indicated by fabric and fluting of the YD surface till sheet in northern Nova Scotia and ice-marginal deposits imply an ice cap centred over eastern P.E.I. and the southern Gulf of St. Lawrence. This glacier also dammed a series of glacial lakes against the highland-rimmed west coast of Cape Breton Island. Glaciers developed and advanced during the YD in the uplands and offshore shelf areas from small remnants of Late Wisconsinan ice. Renewed ice growth was enabled by increased precipitation and local cooling in the Gulf of St. Lawrence due to deflection of the jet stream and expanded sea-ice cover in the North Atlantic. The YD may provide an analogy to glacier development in Maritime Canada during the interglacial/glacial transition.     

鄂西地区上二叠乐平统大隆组硅质岩成因及有机质富集机理

晚二叠世是古生代环境、生物演化的关键时期,发育广泛的富有机质沉积,并成为南方重要的烃源岩层位。为了解该时期的富有机质堆积机理,我们选择了鄂西台内盆地晚二叠世大隆组富有机质硅质岩(TOC平均值为5.8%,峰值为18%)作为研究对象。硅质岩中常量元素Al/Fe均值为0.79,Mn/Ti均值为0.21,显示为大陆边缘环境下的生物成因,即非热水成因。∑REE值与Al2O3含量有着良好的正相关关系,表明当时陆源物质的输入对硅质岩的形成有很大影响。微量元素U/Th、V/(V+Ni)均说明硅质岩沉积环境为缺氧水体环境。通过对草莓状黄铁矿粒径的统计表明,大多数(64%～89%)的草莓状黄铁矿粒径小于5μm,反映缺氧甚至硫化的环境。而且,U、V、Mo的富集以及Ni、Cu元素的亏损说明水体的缺氧主要是由于海水分层,水体循环受阻造成的。TOC与氧化还原参数的变化步调基本一致,两者有着较好的正相关关系,而与生产力指标Ba/Al相关性很差,说明有机质富集主要是由水体的缺氧而不是初级生产力控制的。     

An experimental study of heavy metal attenuation and mobility in sandy loam soils

Column flow-through experiments reacting wastewater solutions with sandy loam soil samples were performed to study heavy metal attenuation by two soils with different physical and chemical properties. Reacted soil columns were leached with synthetic acid rain to study the mobility of attenuated heavy metals under leaching conditions. This study demonstrates that cation exchange, surface adsorption, chelation with solid organic material, and precipitation were the important attenuation mechanisms for the heavy metals (Cd, Cr, Cu, Mo, Ph, and Zn). Adsorption on soil hydrous oxide surfaces was the primary attenuation mechanism for Cd and Zn in both soils, and for Cu in a soil with low organic matter content. Wastewater solution pH is also an important factor that influences the retention of heavy metals. Cadmium, Cu, Cr, and Zn became mobile after prolonged application of spiked wastewater solution, either through saturation of soil adsorption sites or due to decreasing pH. Only Cr, Pb, and Mo, which are attenuated primarily through precipitation, show significant net retention by soil. Acid rain water removed heavy metals left in the column residual pore solution and weakly sorbed heavy metals in the soils, and has the ability to mobilize some strongly attenuated heavy metals, especially when the soil organic matter content is high. The results have important applications in predicting heavy metal mobility in contaminated soil, the disposal of acid mine drainage, and assessing the risks of landfall leachate leakage.     

Early Jurassic anoxic conditions and organic accumulation in the eastern Tethys

The Bilong Co oil shale, located in the South Qiangtang depression, northern Tibet Plateau, may record the Early Jurassic anoxic event in the eastern Tethys. New geochemical data from the Bilong Co oil shale section are presented in order to determine the mechanism of organic accumulation and to evaluate Early Jurassic anoxia in the eastern Tethys. In organic-rich oil shales, many redox proxies including the relationship of Mo to total organic carbon (TOC), Re/Mo ratios, and pyrite framboid size distribution suggest deposition under euxinic conditions. However, the correlation between TOC and P and Mo contents indicates that organic matter accumulation was controlled mainly by primary productivity. The Sr/Al ratios and clastic influx proxies such as Si, Ti, Th, Zr, and Al concentrations suggest a continuous supply of fresh water from a nearby continent during oil shale deposition. This supply could have initiated stratification of the water so that the upper zone became favourable for marine life. Increased primary productivity could have led to formation of anoxic/sulphidic bottom waters, which enhanced the preservation of organic matter. Deposition of organic-rich oil shales terminated when primary productivity decreased, leading to more oxic bottom water conditions.     

Molybdenum and tungsten in volcanic rocks and in surface and <100 °C ground waters in Iceland

The concentrations of Mo and W in tholeiite series basaltic to silicic volcanics in Iceland increase with the concentrations of incompatible magmatic elements. In normal Mid Ocean Ridge Basalt (MORB), Mo and W levels are as low as 0.03 and 0.01 ppm but in rhyolites they are up to 4 and 1.3 ppm, respectively. In the slightly evolved Tertiary tholeiites of the main study area of Skagafjördur, northern Iceland, Mo and W concentrations are 1.01 and 0.32 ppm, respectively, on average. Surface waters in this area typically contain <0.5 ppb Mo and <0.1 ppb W. Concentrations are higher in ground waters and, on the whole, they increase with increasing temperature and increasing age of these waters, being as high as ∼100 ppb for Mo and ∼10 ppb for W in the hottest (∼90 °C) and oldest (>10,000 years) waters. In river and ground waters, the average Mo/W ratio is the same as that of the basalt host rock. On the other hand, in peat soil waters, the average Mo/W ratio is higher due to adsorption processes involving W. In river and ground waters, both Mo and W display conservative behavior. Progressive water-rock interaction leads to successively lower aquatic B/Mo and B/W ratios. However, the B/Mo and B/W ratios of the most reacted waters are considerably higher than those of the basalt due to non-stoichiometric rock dissolution: B is dissolved preferentially to both Mo and W because B is largely present in a soluble form, but Mo and W are concentrated in the Fe-Ti-oxides. These minerals are stable, under both surface and sub-surface conditions, i.e. the waters are over-saturated with respect to these minerals. The main supply of Mo and W to surface waters is from dissolution of plagioclase and pyroxene, as well as volcanic glass. Olivine is not an important source due to its scarcity in the basalts. In <30 °C ground waters, the dominant supply of Mo and W is plagioclase. At higher temperatures pyroxene also contributes, with its contribution increasing with increasing temperature, as deduced from its decreasing stability at higher temperature. Dissolution of basaltic glass produces lower B/Mo and B/W aqueous ratios than dissolution of crystalline basalt.     

秭归地区闪长岩岩体风化壳微量元素地球化学特征

通过对秭归地区闪长岩岩体风化壳中微量元素的分布规律研究,将该风化剖面中的微量元素划分为3类。第一类包括Sc、V、Cr、Co、Ni、Cu、Zn、Zr、Hf、Nb、Ta、U、Th、Mo、W,基本属于非活动性元素,在风化过程中得以有效保留,其中U、Cr、Cu等受氧化还原条件的影响,有时呈局部富集现象,规律性不明显。第二类以Ca、Rb、Cs、Sr、Ba、Pb、Ga、Gd、Tl为代表,随着风化作用的进行而逐步从风化壳中淋失,属活动性元素。第三类以稀土元素为代表,在风化壳内部发生局部的再分配,从剖面上层随风化溶液向下淋滤亏损,到剖面中下部沉淀富集,其中重稀土元素的淋失程度大于轻稀土元素。由于母岩中斜长石的风化淋滤,Eu在氧化环境下逐渐从正异常变为负异常。Ce在地表氧化条件下很容易生成四价氧化物（方铈石）,并在表层明显富集,剖面介质中氧化还原条件的变化导致Ce的波动变化。     

Pb isotopic ratios and elemental abundances for selective leachates from near-surface till: implications for mineral exploration

Pb isotope ratios obtained from fine-grained fractions ( < 63 and < 2 gmm from near-surface ( < 1 m depth) till surrounding ore deposits show isotopic overprinting from the underlying sulfide mineralization, and provide a new approach to mineral exploration for massive sulfide deposits (VMS) in glaciated terrains.In this study, Pb isotopic measurements, and selective leaching of 6 near-surface till samples down-ice from the Chisel Lake (Manitoba) and Manitouwadge (Ontario) VMS deposits were carried out in order to determine the location and nature of the Pb within till. Elemental abundances from selective leachates for all 6 samples display similar patterns and show that chalcophile elements (Cu, Ni, Pb and Zn), derived predominantly from the underlying VMS deposits, occur as (i) adsorbed/exchangeable metals; (ii) associated with oxyhydrous Fe and Mn; (iii) crystalline Fe oxides, and/or (iv) silicate. Despite the relative proximity of some of the till samples to the VMS deposits, only a very small component of the chalcophile elements is present as sulfide. This result is consistent with those from studies of weathered (oxidized) tills, which show that labile minerals such as sulfides have been completely destroyed and their chemical constituents reprecipitated or scavenged locally by clay-sized phyllosilicates and secondary oxides/hydroxides.Pb isotopic ratios for selective leachates from till samples with VMS-like (anomalous) signatures are similar to those from ore (galena) within the proximal VMS deposits. This indicates that the Pb is of a secondary nature and was probably scavenged and deposited after destruction of original sulfide minerals during till formation. The lack of a predominant sulfide-held Pb component within the selective leachates supports this interpretation. In contrast, Pb isotopic ratios for the same selective leachates from “background” samples are significantly higher and show that the Pb is not derived from proximal VMS deposits but from a more radiogenic source.Till samples were also leached using 2.5 M HCl (ldconventional” leaching). The Pb isotope ratios from the conventional leachates are similar to those obtained from the selective leachates, and show a large difference in Pb isotopic ratios between anomalous and background samples. We propose, therefore, that the conventional leaching rather than selective leaching or complete dissolution of a particular grain-size fraction be adopted for mineral exploration purposes using glacial sediments.The results from this study support the effective use of Pb isotope ratios from near-surface till as an exploration tool despite the weathered nature of the latter. We feel that this represents a more cost-effective technique over traditional geochemical prospecting methods, if used in conjunction with Pb abundance data.     

晋北中高硫煤中稀土元素的地球化学特征

应用中子活化分析方法，测定了晋北两层中高硫煤中稀土元素的含量。通过对稀土元素的分布模式，相关分析和聚类分析的研究，得出如下认识；成煤环境对稀土元素的含量具有控制作用。但中高硫煤中稀土元素总量会受到沉积期后酸性溶液下渗淋滤作用的影响；同一煤层中各分层的稀土元素应具有基本相同的分布模式，异常的稀土元素分布模式指示了沉积期后地质作用的影响；煤中稀土元素的主要赋存状态为无机相，主要来源为陆源碎屑矿物；煤中与稀土伴生的有害元素有V，P，Mo,Cr,Cu,Mo,Th和Cd等，在加工洗选过程中有洁净潜势。