青海阿尔茨托山地区地球化学（异常）场的多重分形研究

以研究区成矿地质背景为基础，将其划分为4个地球化学区，从多重分形理论出发，应用“元素含量—面积”模型方法，对各区主要成矿元素的地球化学(异常)场进行分析研究。结果表明，由于地质构造背景和化探元素富集的成因机理不同，各区元素地球化学(异常)场具有两种不同的多重分形特征模式：只有两个无标度区的简单多重分形模式和有两个以上无标度区的高丛集多重分形模式，具有相同成因的元素组合具有相似的多重分形特征。在此基础上．探讨了各区元素的成矿富集规律和空间分布特征，进而划分了地球化学背景和异常，经检验对比，证明了该方法的有效性和实用性。     

Geochemical investigation of oils and source rocks from Qianjiang depression of Jianghan basin, a terrigenous saline basin, China

Six oils and seven suspected source rocks from the Jianghan saline basin, in the central eastern part of China, have been examined using a variety of geochemical techniques. The results from this study show that oils from the third and fourth sections of the Qianjiang Formation (Eocene) are derived from similar source materials but have a different source from the oils of Xingouzui Formation (Eocene) in the same basin. The oils of the Xingouzui Formation (Eocene) are more mature, and probably have a greater input of terrigenous source material and in all probability have migrated greater distances than the Qianjiang oils. Oils from these sections are derived from an environment characterized as being extremely anoxic, strongly reducing and highly saline. The suspected source rocks examined in the study were from the Qianjiang Formation and were generally mature, except for the shallowest sample. The biomarker distributions in the suspected source rocks examined from the Qianjiang Formation were very different from those of the oils present in the same sections. It is proposed that oils from the Qianjiang Formation have sources in addition to, or exclusive of, the suspected source rocks examined in this study.     

Source of salinity in the groundwater of Lenjanat Plain,Isfahan, Iran

The present study aimed at identifying the salinity source in the groundwater of Lenjanat Plain. To do so, non-isotopic geochemical methods were employed: groundwater samples were collected seasonally from 33 wells widespread in the area, and physicochemical parameters as well as major and minor elements were measured in the 132 samples. The data collected from the field and laboratory measurements were interpreted through statistical and hydrogeochemical graphs, mass ratios and saturation indexes obtained from modeling. The results revealed that hydrogeochemical properties of the study aquifer were controlled by rock/water interactions including ion exchange, dissolution of evaporation deposits (halite and gypsum) and precipitation/dissolution of carbonates. Based on the values of Cl/Br ratio in Lenjanat groundwater (329–4,492), dissolution of evaporation deposits in aquifer was the main cause for groundwater salinity. Considering the Lenjanat groundwater geochemical properties, the data confirm the reported Cl/Br ratios for groundwater affected by the dissolution of evaporation deposits (Cl/Br > 300) and overlaps with the range of Cl/Br ratios for domestic sewage effluent groundwater. Selecting the best chemical components and their ratios in non-isotopic geochemical methods provides an accurate distinction between sources of groundwater salinity.     

Natural uranium in Forsmark,Sweden: The solid phase

U-bearing solid phases from Forsmark, Sweden, a proposed host for radioactive waste repositories, have been identified and characterized. Elevated dissolved U was found in some groundwater samples during the site investigations, prompting a need to study the local U geochemistry. Previous hydrochemical and whole-rock geochemical studies indicated that U was derived from local pegmatites, and mobilized and re-deposited during several geological events. In this study, down-hole gamma logs guided sampling of local pegmatites, cataclasites, and fracture fillings. Back-scattered electron-imaging, petrographic microscopy, and electron microprobe analyses were used to find and analyze U phases in thin sections. The results show that the principal U sources at Forsmark include pegmatitic uraninite (PbO up to ∼22 wt%) and metamict uranothorite. These primary minerals show variable degrees of alteration such as enrichment in Ca and Al and/or replacement by secondary Ca–U(VI)-silicates, haiweeite and uranophane. The haiweeite contains up to ∼5 wt% Al₂O₃, a chemical signature reflecting early (Proterozoic) events of hydrothermal fluid migration. Coffinitized, secondary uraninite is found in association with FeAl-silicates or Palaeozoic sulfide/sulfate minerals, indicating remobilization-precipitation and/or a secondary, sedimentary source of U. It is inferred that U was oxidized during geologically early periods. Later, U(IV) phases formed in fractures open to fluid circulation during the Palaeozoic. This study establishes the phases available as local U sources and/or sinks, and which will be considered in future isotopic and hydrochemical studies aimed to constrain the mechanisms and timing of water–U phase interaction.     

Element chemostratigraphy of the Devonian/Carboniferous boundary – A compositional approach

The Devonian/Carboniferous (D/C) boundary is a critical interval in the Phanerozoic history, which is associated with vigorous climatic perturbations, continental glaciation, global sea-level fall and rapidly increased extinction rates in marine realms. In many sections world-wide, these global changes left a marked lithological signature, in particular the Hangenberg black shale (products of deep-shelf anoxia) and the overlying Hangenberg sandstone (sudden siliciclastic influx into predominantly carbonate depositional environments). Both layers bear a distinct geochemical signature. Even though either or both of these two lithologies are absent at many sections, their correlative counterparts can be indicated by subtle geochemical markers. We studied elemental geochemistry of fourteen D/C boundary sections in six key areas across Europe with the aim to select globally correlatable elemental proxy for the D/C boundary. Analysis of raw/log-transformed geochemical data (EDXRF, c.p.s. units), presenting the standard approach here, indicates that concentrations of terrigenous elements (Al, K, Rb, Ti and Zr) are mainly controlled by diluted Ca (carried by marine calcium carbonate) in limestone facies and, accordingly, their variations can be related to carbonate production in the sea rather than to terrigenous input from continent. Nevertheless, due to the relative nature of geochemical observations, reliance solely on statistical processing of raw data might lead to incomplete picture of multivariate data structure and/or biased interpretations. For this reason, the aim of this contribution is to discuss the logratio alternatives of the standard statistical methods, which may better reflect the relative nature of the data. For this purpose, principal component analysis was employed to reveal main geochemical patterns and while the geochemical signature of the D/C boundary was further analysed using Q-mode clustering that leads to predicative orthonormal logratio coordinates – balances. The comprehensive picture of the multivariate data structure provided by these statistical tools makes them a primary choice for exploratory compositional data analysis. At the same time, it turns out that the standard and compositional approaches have synergic effects. This fact can be extensively used in further geochemical studies.     

Evolution of coastal sandy aquifer system in Kalpitiya peninsula,Sri Lanka: sedimentological and geochemical approach

The study on the evolution of groundwater sources has arisen because of growing concern about deterioration of groundwater resources due to overexploitation. The chemical nature of a coastal aquifer depends on the initial composition of aquifer media, internal geochemical processes and external chemical inputs. Therefore, geochemical characteristics of an aquifer can be used as indicative components on elaborating the origin of aquifer media and its evolutionary processes. This study was aimed at understanding the evolution of Quaternary coastal aquifers of the Kalpitya area, Sri Lanka, by studying groundwater quality and aquifer media. The textural, mineralogical and chemical characteristics of aquifer media and chemical nature of groundwater of the area imply that the aquifer media may not have been derived from marine processes and paleo coastal formations of the western coast but are indicative of a fluvial origin due to past strong fluvial processes. Fluviatile sand depositions had taken place initially and with the gradual sea level rise, deposits were transported, sorted and then re-deposited to form barrier islands parallel to the coast. These have evolved to the present state during the Quaternary period. Intermittent climatic changes caused several changes in the depositional pattern of the aquifer material and the chemical nature of the aquifer. Present day groundwater geochemistry indicates an evolution of a fresh water aquifer with relics of ionic constituents showing paleo geochemical processes that were active during the evolution. In addition, anthropogenic activities have also significantly altered the geochemical nature of groundwater in the present aquifer system.     

安徽马头地区斑岩型钼铜矿异常结构研究

利用元素质量平衡计算方法,将元素含量转换成迁移量,直观展现出由元素迁移量构成的原生异常,根据异常的空间分布规律,总结出了由成矿地球化学环境指示元素(Na2O、Ba、Sr)负异常、矿化剂元素(S)正异常、成矿元素(Mo、Cu)及其伴生元素(Ag、As、Sb、W等)正异常构成的马头斑岩型钼铜矿原生异常结构,利用原生异常结构可以对深部成矿前景进行判断和评价;地表岩石(屑)测量结果表明研究区地表同样存在异常结构,且对原生异常结构有很好的继承性,利用地表异常结构可以指明找矿方向、成矿有利地段和矿床产出位置。上述研究成果的取得,不仅丰富和充实了地球化学勘查方法技术,为其他同类型矿床的地球化学勘查提供了参考案例,同时对勘查地球化学应用基础理论而言也是有益的尝试。     

断裂带地球化学深穿透理论与方法在钾盐找矿中的应用

文中介绍了断裂带地球化学深穿透理论与技术方法,并结合钾盐找矿实践,对相关技术方法的应用进行了探讨。断裂带地球化学深穿透技术包括地表测线、稀有气体同位素示踪和钾盐深度预测模型,笔者的主要思路是通过地表元素异常来捕捉可能来自深部的物源信息,预测大概的找钾靶区和深度,降低找矿成本。沿垂直于构造断裂带的方向采集地表沉积物、水样,分析其化学元素含量或比值,可以有效识别地球化学异常点;通过分析沿断裂带上升的卤水中逸出的稀有气体(氦、氩、氖等)同位素组成,可以判别气体的来源和断裂的深度,从而辅助判别卤水来源和深度;通过文章给出的一系列地球化学指标和方法,可以识别异常、综合判别卤水或盐类物质来源和深度,灰色模型和异常判别程序的编制可以大大缩短运算和判别时间。上述方法在实际工作中取得了较好的效果,在今后研究和实践中可以进一步提高和完善。     

中国东部新生代玄武岩记录古太平洋俯冲带壳幔相互作用

大陆玄武岩通常具有与洋岛玄武岩相似的地球化学成分,其中含有显著的壳源组分.对于洋岛玄武岩来说,虽然其中的壳源组分归咎于深俯冲大洋板片的再循环,但是对板片俯冲过程中的壳幔相互作用缺乏研究.对于大陆玄武岩来说,由于其形成与特定大洋板片在大陆边缘之下的俯冲有关,可以用来确定古大洋板片俯冲的地壳物质再循环.本文总结了我们对中国东部新生代玄武岩所进行的一系列地球化学研究,结果记录了古太平洋板片俯冲析出流体对地幔楔的化学交代作用.这些大陆玄武岩普遍具有与洋岛玄武岩类似的地球化学成分,在微量元素组成上表现为富集LILE和LREE、亏损HREE,但是不亏损HFSE的分布特点,在放射成因同位素组成上表现为亏损至弱富集的Sr-Nd同位素组成.在排除地壳混染效应之后,这些玄武岩的地球化学特征可以由其地幔源区中壳源组分的性质来解释.俯冲大洋地壳部分熔融产生的熔体提供了地幔源区中的壳源组分,其中包括洋壳镁铁质火成岩、海底沉积物和大陆下地壳三种组分.华北和华南新生代大陆玄武岩在Pb同位素组成上存在显著差异,反映它们地幔源区中的壳源组分有所区别.中国东部新生代玄武岩的地幔源区是古太平洋板片于中生代俯冲至亚欧大陆东部之下时,在>200 km的俯冲带深度发生壳幔相互作用的产物.在新生代期间,随着俯冲太平洋板片的回卷引起的中国东部大陆岩石圈拉张和软流圈地幔上涌,那些交代成因的地幔源区发生部分熔融,形成了现今所见的新生代玄武岩.      

Paleoenvironments and geochemistry across a continuous Permian–Triassic boundary section at B?kk Mountains,Hungary

The Bálvány North Permian-Triassic boundary sediments were deposited on a carbonate platform in the tropical part of the western Paleo Tethys ocean.The overall elemental geochemistry of the detailed two-metre-thick section across the boundary that we studied shows that the clastic content of the sediments came from dominantly silica-rich continental sources though with some more silica-poor inputs in the uppermost Permian and lowest Triassic limestones as shown by Ni/Al and Nb/Ta ratios.These inputs bracket, but do not coincide with, the main extinctions and associated C, O and S changes.Increased aridity at the Permian-Triassic boundary with increased wind abrasion of suitable Ti-bearing heavy minerals accounts for both the high Ti/Al and Ti/Zr ratios.Various geochemical redox proxies suggest mainly oxic depositional conditions, with episodes of anoxia, but with little systematic variation across the Permian–Triassic extinction boundary.The lack of consistent element geochemical changes across the Permian-Triassic boundary occur not only in adjacent shallower-water marine sections, and in other marine sections along the SW Tethys margin such as the Salt Range sections in Pakistan, but also in deeper shelf and oceanic sections, and in non-marine African and European continental sediments.In the absence of significant changes in physical environments, chemical changes in the atmosphere and oceans,reflected in various isotopic changes, drove the Permian–Triassic extinctions.     

Petrographic and geochemical source-modeling of volcanic lithics from archaeological contexts: A case study from British Camp,San Juan Island,Washington

Classification and sourcing of vulcanic lithics is simplified through petrographic and geochemical analyses. In examining volcanic lithics, major element geochemistry is required for classification, trace element geochemistry is necessary for discrimination of materials from different sources, and rare earth elements are used in source-modeling. Materials such as those found in the debitage at the British Camp shell midden, San Juan Island (45SJ24), are ubiquitous in the Gulf of Georgia region of the Pacific Northwest. Previous archaeological reports over the past 100 years have classified this volcanic debitage as basalt and predicted a local source. Petrographic analyses of thin sections and geochemical analyses using ICP emission spectrometry have shown that these artifacts are formed of dacite rather than basalt. The analysis also shows that the major lithic material used for stone chipping during the entire temporal sequence at the British Camp site is invariably from the same distant source in the High Cascades, possibly as far as 200 km from the site. © 1996 John Wiley & Sons, Inc.     

Magnetostratigraphic correlations of Permian–Triassic marine-to-terrestrial sections from China

We have studied three Permian–Triassic (PT) localities from China as part of a combined magnetostratigraphic, ⁴⁰Ar/³⁹Ar and U–Pb radioisotopic, and biostratigraphic study aimed at resolving the temporal relations between terrestrial and marine records across the Permo-Triassic boundary, as well as the rate of the biotic recovery in the Early Triassic. The studied sections from Shangsi (Sichuan Province), Langdai (Guihzou Province), and the Junggar basin (Xinjiang Province), span marine, paralic, and terrestrial PT environments, respectively. Each of these sections was logged in detail in order to place geochronologic, paleomagnetic, geochemical, conodont and palynologic samples within a common stratigraphic context. Here we present rock-magnetic, paleomagnetic and magnetostratigraphic results from the three localities.At Shangsi, northern Sichuan Province, we sampled three sections spanning Permo-Triassic marine carbonates. Magnetostratigraphic results from the three sections indicate that the composite section contains at least eight polarity chrons and that the PT boundary occurs within a normal polarity chron a short distance above the mass extinction level and a reversed-to-normal (R-N) polarity reversal. Furthermore, the onset of the Illawarra mixed interval lies below the sampled section indicating that the uppermost Permian Changhsingian and at least part of the Wuchiapingian stages postdate the end of the Kiaman Permo-Carboniferous Reversed Superchron.At Langdai, Guizhou Province, we studied magnetostratigraphy of PT paralic mudstone and carbonate sediments in two sections. The composite section spans an R-N polarity sequence. Section-mean directions pass a fold test at the 95% confidence level, and the section-mean poles are close to the mean PT pole for the South China block. Based on biostratigraphic constraints, the R-N transition recorded at Langdai is consistent with that at Shangsi and demonstrates that the PT boundary occurred within a normal polarity chron a short distance above the mass extinction level.In the southern Junggar basin, Xinjiang Province, in northwest China, we determined the magnetostratigraphy of three sections of a terrestrial sequence. Normal and reversed polarity directions are roughly antipodal, and magnetostratigraphies from the three sections are highly consistent. Combined bio- and magneto-stratigraphy used to correlate this sequence to other PT sequences suggests that the previously-proposed biostratigraphic PT boundary in the Junggar sections was most likely misplaced by earlier workers suggesting that further work is necessary to confidently place the PT boundary there.     

Application of Optically Stimulated Luminescence Technique in Exploring a Concealed Sandstone-type Uranium Deposit

Identifying ore-induced geochemical anomalies at the surface that indicate concealed deposits in buried areas remains a significant challenge in geochemical exploration. In this study, in order to trace the source of the geochemical anomalies, systematic luminescence intensity analyses were conducted on quartz grains from the Quaternary regolith at the Hadatu sandstone-type uranium deposit in the Erenhot Basin. The optically stimulated luminescence (OSL) ages were much older than the depositional ages of the Quaternary regolith. Moreover, quartz OSL ages were closely related to both borehole grades and sampling depths. Thus, the abnormal mineral OSL ages from near-surface sediments were ultimately controlled by the sandstone-type uranium deposits. This is identical to the rapid changes of quartz OSL ages (0.063 ka/cm) and equivalent doses (0.19 Gy/cm) with depths in a given sampling site. The instantaneous soil radon concentration was positively correlated with the quartz OSL apparent age, indicating their ore-induced origin and, as a result, their effectiveness in the exploration of concealed uranium deposits. Other parameters, including mobile-state uranium and 210Po contents, were poorly correlated with quartz OSL ages and therefore should only be used with caution for geochemical exploration. This is the first time an attempt has been made to discriminate the ore-induced sources for different surface anomaly parameters, including instantaneous soil radon, mobile-state uranium and 210Po contents for concealed sandstone-type uranium deposits.     

基于多目标区域地球化学调查的中国土壤碳储量计算方法研究

土壤碳储量问题在碳循环和全球变化领域具有重要意义,长期以来这一基本参数的计算受到数据来源的制约。全国多目标区域地球化学调查采用双层网格化采样和分析,取得了大量高密度和高精度土壤地球化学数据,为土壤碳库的高精度计算提供了数据基础。文中重点探讨利用这些数据计算土壤碳储量的方法。首先提出针对多目标区域地球化学调查数据的"单位土壤碳量(USCA)"概念,用以代表调查数据基本面积单元(4km2)的碳储量,并作为区域和全国尺度土壤碳储量计算的基本单位。在收集分析14个省市414条的土壤剖面数据的基础上,发现土壤有机碳(TOC)的垂直分布与无机碳和其他元素不同,存在指数分布规律,运用面积积分运算方法发现利用直线模型计算土壤有机碳库的误差(+20%～+100%)远大于指数模型的误差(-10%～+20%)。因此,文中建议"有机碳单位土壤碳量(USCATOC)"需使用指数模型拟合后积分求算,而"无机碳单位土壤碳量(USCATIC)"则使用直线模型,"全碳单位土壤碳量(USCATC)"采用两者加和计算。文中还分析了其他元素的垂直分布特征,并提出氮储量计算需采用与有机碳类似的方法,其他51种元素(氧化物)储量采用与无机碳类似的方案,按照直线模型计算单位土壤元素量和单位土壤氧化物量(USEA)。     

Separating anthropogenic from natural anomalies in environmental geochemistry

Environmental geochemistry has attracted increasing interest during the last decade. In Sweden, geochemical mapping is carried out with methods that allow the data to be used in environmental research, including sampling plant roots and mosses from streams, soils and bedrock. These three sample types form an integrated strategy in environmental research, as well as in geochemical exploration. However, one problem that becomes prominent in geochemical mapping is to distinguish the signals derived from natural sources from those derived from anthropogenic sources. So far, this has mostly been done by using different types of samples, for example, different soil horizons. This is both expensive and time-consuming.We are currently developing alternative statistical solutions to this problem. The method used here is PLSR (partial least squares regression analysis). In this paper, we present an initial discussion on the applicability of PLSR in differentiating anthropogenic anomalies from natural contents.PLSR performs a simultaneous, interdependent principal component analysis decomposition in both X- and Y-matrices, in such a way that the information in the Y-matrix is used directly as a guide for optimal decomposition of the X-matrix. PLSR thus performs a generalized multivariate regression of Y on X overcoming the multicollinearity problem of correlated X-variables. The advantage of PLSR is that it gives optimal prediction ability in a strict statistical sense.Bedrock geochemistry from different lithologies in the mapping area in southern Sweden (Y-matrix) is analyzed together with stream or soil data (X-matrix). By modelling the PLS-regression between these two data sets, separate multivariate geochemical models based on the different bedrock types were developed. This step is called the training or modelling stage of the multivariate calibration. These calibrated models are subsequently used for predicting new (X) geochemical samples and estimating the corresponding Y-variable values. Information is obtained on how much of the metal contents in each new geochemical sample correlate with the different modelled bedrock types.By computing the appropriate X-residuals, we obtain information on the anthropogenic impact that is also carried by these new samples. In this way, it is possible from one single geochemical survey to derive both conventional geochemical background data and anthropogenic data, both of which can be readily displayed as maps.The present study concerns development of data analysis methods. Examples of the applications of the methodology are presented using Pb and U. The results show the share of these contents in different sampling media that is derived from bedrock on the one hand, and from anthropogenic sources, on the other.     

热带雨林景观土壤测量采样深度与样品粒级试验研究——以加纳国雅卡锰金矿为例

加纳国雅卡锰金矿床位于著名的阿散蒂金矿带上。在该成矿带进行土壤测量采样深度、样品粒级试验以及方法技术的适应性和有效性研究,可为下一步开展大面积土壤地球化学测量提供技术依据,从而圈定可靠土壤地球化学异常。本文采用的工作方法为土壤垂向剖面法,选择有代表性的地段进行试验研究,结果显示在已知矿上方获得了明显的土壤地球化学异常。通过实验研究,选取土壤测量采样深度60～80 cm,截取样品粒级-4～+20目,获得了可靠、明显的土壤地球化学异常。研究证明该方法具有显著的地球化学找矿效果。     

西藏玉龙斑岩铜(钼)矿床物质来源研究

本文运用多种地球化学方法,分析所掌握的有关数据,以玉龙斑岩铜(钼)矿床的主要矿体—斑岩型和矽卡岩-次生富集型矿体为主要研究对象,追索玉龙矿床成矿物质的来源。最终判定玉龙矿床成矿物质主要来源于下地壳或上地幔,有少量上地壳围岩物质加入。但在不同类型的矿体中,不同来源的物质所占比例存在差异。     

长江中下游地区1∶20万金元素不同尺度数据的地球化学特征响应

通过对长江中下游地区1∶20万金元素不同尺度数据的地球化学特征响应的研究,认为长江中下游存在地球化学巨省,这个地球化学巨省为长江中下游地区提供源源不断的矿源。同时,讨论了低密度地球化学方法能够用于全国或全球地球化学填图的可行性。     

Astronomical and terrestrial causes of physical, chemical and biological changes at geological boundaries

The boundary horizons of the Cretaceous-Tertiary (Um Sohryngkew River section, Meghalaya and Anjar section, Kutch), the Permo-Triassic (Guling, Lalung, Ganmachidam and Attargoo sections, Spiti valley) and the Eocene-Oligocene (Tapti River section, Gujarat) have been identified in the sedimentary records of the Indian subcontinent. These sections have been studied for geochemical anomalies. The results are discussed in the framework of extra-terrestrial and terrestrial causes proposed to explain the physical, chemical and mineralogical observations at these boundaries. A critical analysis suggests that although the astronomical causes, particularly the bolide impacts, can easily explain the geochemical and physical changes, the terrestrial causes (volcanism) may have played a significant role in creating the biological stress observed in fossil records (mass extinction) at or near some of these boundaries.     

老万场红土型金矿成矿过程的地球化学作用

根据地质地球化学研究所揭示的与成矿地球化学作用有关的宏观和微观特征,对老万场金矿的物质来源和成矿过程的地球化学作用进行了讨论,阐述了成矿（成土）过程中Ａｕ和相关元素的地球化学行为以及本类红土型放形成的地球化学机理。指出了喀斯特红土化作用在原始卡林型金矿风化成土过程中对红土型金矿形成的影响。