内蒙古拜仁达坝及维拉斯托银多金属矿床的硫和铅同位素研究

拜仁达坝和维拉斯托是近年来在内蒙古东部地区发现的2个大型银多金属矿床,文章对其开展了硫和铅同位素研究。结果表明,拜仁达坝矿床矿石中硫化物的δ34S值为-4.0‰～+1.6‰,维拉斯托矿床矿石中硫化物的δ34S值为-0.8‰～+2.0‰,与岩浆热液型矿床的硫同位素值接近,表明这2个矿床中的硫主要来自岩浆。拜仁达坝矿区43件金属硫化物的206Pb/204Pb值为18.333～18.515,207Pb/204Pb值为15.532～15.656,208Pb/204Pb值为38.057～38.610;维拉斯托矿区20件金属硫化物的206Pb/204Pb值为18.304～18.377,207Pb/204Pb值为15.520～15.610,208Pb/204Pb值为38.112～38.435。拜仁达坝东矿区矿石中的铅同位素组成与维拉斯托矿区相似,变化范围小,相对贫放射性铅同位素,并且均为混合铅。矿石中的铅可能来自围岩地层及深源岩浆。     

The construction and development of SHRIMP I: An historical outline

In 1973 Bill Compston advocated the building of an ion microprobe at the Research School of Earth Sciences (RSES) at the Australian National University (ANU). The commercial ion probes available at this time were too small to have sufficient sensitivity for trace element analysis and too low in mass resolution to avoid molecular interferences. The project commenced in 1974 with the appointment of a former ANU PhD student Steve Clement who had expertise in beam transport theory. To achieve high sensitivity and high mass resolution, beam transport theory indicated that a much larger magnet than in any commercially available mass spectrometer would be required. Clement chose an ion optical design, by Professor Matsuda of Osaka University in 1974, which had the required combination of high mass resolution and high transmission. Clement's job was to produce the detailed scientific designs and machine drawings for the new instrument as well as testing the completed instrument. Clement coined the term SHRIMP-Sensitive High Resolution Ion MicroProbe. By the end of 1977 nearly all the components had been manufactured and the big electromagnet had been successfully tested. In the following year the secondary mass analyzer was assembled and tested using a thermal ionization source and showed great promise with flat-topped peaks at 5000 resolution and 50% transmission with 50 V energy spread. At this stage the machine had far exceeded the specifications for the available commercial ion probes. Continued development during 1981 to the point where the original design specifications were fully realized was time consuming since learning how to use the entirely novel instrument was no simple task; no one else had an instrument like SHRIMP. The application of the instrument to zircon U–Pb geochronology established the necessary operating conditions for measuring Pb isotopic compositions and the elemental ratios Pb/U and U/Zr from 20 μm diameter spots on single zircon grains. Application of this in the early 1980s started a revolution in Precambrian geology by the ability to produce rapidly accurate and precise age determinations on structurally complex zircon samples.     

Clay mineral,geochemical and Sr–Nd isotopic fingerprinting of sediments in the Murray–Darling fluvial system,southeast Australia

The Willyama Supergroup of the Broken Hill region in southern Australia consists of supracrustal sedimentary and magmatic rocks, formed between 1810 and 1600 Ma. A statistical analysis of nearly 2000 SHRIMP U–Pb zircon spot ages, compiled from published and unpublished sources, provides evidence for three distinct tectonostratigraphic successions and four magmatic events during this interval. Succession 1 includes Redan Geophysical Zone gneisses and the lower part of the Thackaringa Group (Cues Formation). These rocks were deposited after 1810 Ma and host granite sills of the first magmatic event (1710–1700 Ma). Succession 2 includes the upper Thackaringa Group (Himalaya Formation), the Broken Hill Group and the Sundown Group and was deposited between 1710 and 1660 Ma. These rocks all contain detrital zircons from the first magmatic event (1710–1700 Ma) and in some cases from the second magmatic event (1690–1680 Ma). The second magmatic event (1690–1680 Ma) was bimodal, resulted from crustal extension, and was coeval with deposition of the Broken Hill Group and deepening of the basin. With this event a mafic sill swarm focused in the Broken Hill Domain. Mafic sills lack any trace of inheritance, unlike the granitoids that commonly contain inherited zircons typical of the supracrustal sediments. Succession 3, the Paragon Group and equivalents were deposited after 1660 Ma, but before a regional metamorphic event at 1600 Ma. Metamorphism was closely followed by inversion of the succession into a fold‐and‐thrust belt, accompanied by a fourth late to post‐orogenic magmatic event (ca 1580 Ma) characterised by granite intrusion and regional acid volcanism (the local equivalents of the Gawler Range Volcanics in South Australia).     

Mineralogy of metal contaminated estuarine sediments,Derwent estuary,Hobart, Australia: implications for metal mobility

The mobility, bioaccessibility and transfer pathways of metals and metalloids in estuarine sediments have been the focus of much detailed research. However, to date, few studies have examined the mineralogical siting of metals and metalloids in such sediments. This is despite the fact the mineralogy of sediments is an important factor that controls which and how much of a particular metal is released to pore waters and overlying water columns. This study reports on the mineralogical siting of metals in contaminated estuarine sediments, Hobart, Australia, and aims to evaluate the mobility of metals in the contaminated substrates. Mineralogical, mineral chemical and bulk chemical analyses demonstrate that the sediments contain very high levels of several metals and metalloids. The contaminated sediments have concentrations of zinc (Zn), lead (Pb), copper (Cu) and cadmium (Cd) ranging from 0.55 to 4.23 wt%, 0.16 to 0.70 wt%, 415 to 951 mg/kg and 23 to 300 mg/kg, respectively. Franklinite and lesser sphalerite are the main repositories of Zn, whereas much of the Pb and Cu is hosted by sulfides, organic matter and undetermined iron (Fe) oxides. While the release of contaminant loads from franklinite through dissolution is likely to be insignificant, even small releases of metals from the highly contaminated sediments can still cause the deterioration of local water quality. The contaminated sediments represent long-term sources of metal pollutants, particularly Zn, to local waters. This study demonstrates that mineralogical analyses are a vital tool to recognise the potential mobility of trace metals in estuarine environments.     

Geochemical evidence (C,N and Pb isotopes) of recent anthropogenic impact in south‐central Chile from two environmentally distinct lake sediment records

In this paper, we compare the elemental and isotopic (C, N, Pb) geochemistry of lake sediments from two contrasted environments in south‐central Chile. The first lake, Laguna Chica de San Pedro (LCSP), is situated in the urbanised area of the Biobio Region (36°S). The second lake, Lago Puyehue (40° S), is located 400 km to the southeast of LCSP and within an Andean national park. Our aim is to identify environmental impacts associated with increasing industrial activities and land degradation during the last 150 a. In LCSP, shifts in C/N atomic ratios, δ¹³C and δ¹⁵N from 1915–1937 to the late 1980s are attributed to successive land degradation episodes in the lake watershed. Based on a Pb isotopic mixing model, we estimate that up to 20% of lead in LCSP sediments is supplied from urban atmospheric pollution. By contrast, human impact in the watershed of Lago Puyehue is very limited. We observe no change in organic geochemistry during the last 150 a and lead contamination remains lower than 5%, even during the last decades. Although contamination levels are much higher in LCSP than in Lago Puyehue, a peak in anthropogenic Pb is recorded during the same period (1974–1976) at both sites. This maximum contamination level is consistent with increased industrial activity in the vicinity of Concepción. Copyright © 2010 John Wiley & Sons, Ltd.     

●●以下文章网络预出版（在线出版）于2022年12月20日，预计刊于《地质论评》2023年第69卷第1期(2023年1月15日发行纸质版）或2023年第69卷第2期（2023年3月15日发行纸质版）

元素富集机制的研究是重现成矿过程和查明成矿机制的基础,有助于深化对矿床的认识,为找矿提供理论依据。本文总结了近年来关于铅锌元素的迁移与沉淀机制的研究及其应用,包括3种铅锌迁移沉淀模式,4种含铅锌流体驱动模式,铅锌的迁移形式及其沉淀机制;同时简述了我国高温高压实验的发展历程以及4种高温高压模拟实验方法。重点介绍了4种高温高压实验模拟方法及其研究现状：① 高压釜实验;② 热液金刚石压腔—激光拉曼实验;③ 熔融毛细硅管—激光拉曼实验;④ 计算机模拟实验。从封闭—平衡—静止到（半）开放—非平衡—流动、淬火分析到原位观察,应是今后高温高压实验的发展方向。以地质特征为基础,采用高温高压成岩成矿模拟实验结合计算机模拟,精细刻画成矿过程并揭示元素富集机制不仅是解决实际地质问题的有效手段,更是很长一段时间内要为之努力的方向。     

酸溶-电感耦合等离子发射光谱法测定密西西比型铅锌矿床矿石中的铅

密西西比型(MVT)铅锌矿床的主要矿物有方铅石、闪锌矿,常伴生有重晶石、萤石等矿物,使得MVT型矿石在酸处理过程中易生成不溶于水和酸的硫酸铅钡复盐,故而检测矿样中铅的含量偏低。本文建立了采用盐酸-硝酸-氢氟酸体系酸溶分解MVT型矿石,电感耦合等离子体发射光谱法(ICP-OES)测定铅含量的分析方法。实验比较了盐酸-硝酸-氢氟酸、盐酸-硝酸-氢氟酸-高氯酸、盐酸-硝酸-硫酸三种酸溶体系的溶样效果,并通过X射线衍射论证了方法的可行性。结果表明,盐酸-硝酸-氢氟酸体系克服了复盐硫酸铅钡和硫酸铅沉淀的生成,适量的氢氟酸促进了Pb SO4的溶解,X射线衍射表征也表明此种酸溶体系的沉淀中不含有Pb SO4,可更彻底地分解MVT型矿石。本方法精密度(RSD)为0.3%~0.6%,实际样品的加标回收率为96.0%~99.2%,铅的最佳检测范围为0.01%~20.0%。     

Characterization of Galena and Vein Paragenesis in the Penjom Gold Mine, Malaysia: Trace Elements, Lead Isotope Study and Relationship to Gold Mineralization Episodes

The Penjom Gold Mine is located 30 km from the Bentong-Raub Suture at the western boundary of the Central Belt in Peninsular Malaysia. Gold mineralization hosted within the vein system is associated with pyrite, arsenopyrite, and minor base metals including galena. Trace element and lead isotope analysis was undertaken on nine samples that represent two stages of galena formed during two tectonic events. Both the Pb isotopes and the trace elements show that the first stage galena within the mineralized areas at the footwall has different geochemical characteristics compared with galena in non mineralized areas in the hanging wall, suggesting that galena crystallized from two different ore fluids and probably at two different times. Higher Te, Se and Bi in the galena from the mineralized area may indicate hydrothermal fluids that migrate through the structural conduit and leached out the metal along the pathway that consist of dominant carbonaceous unit. The Pb isotopic ratio composition are transitional between the bulk crustal growth and an upper crustal growth curve, indicating that derivation was from arc rocks associated with continental crust or a crustal source that includes arc volcanic and old continental sedimentary rocks.     

Mired in the past — looking to the future: Geochemistry of peat and the analysis of past environmental changes

Peat cores from ombrotrophic bogs have been used as a valuable archive to study environmental change for over a century. Much of this focus on the peat record has been on biological proxies of environmental change, such as pollen and peat-forming macrofossils, but there is growing interest in the geochemical record to study environmental changes. Several studies of long-term peat records in Europe have reconstructed past changes in atmospheric lead pollution, for example, and the general cohesiveness of the results and their agreement with known historical trends in metal production exemplify the best potential of peat geochemistry as an environmental archive. Based on the success with lead, a current emphasis in peat reconstructions is to assess the record of past mercury deposition and results thus far show generally consistent trends, e.g., a pre-anthropogenic mercury accumulation rate of about 0.5–1.5 μg Hg m^− 2 year^− 1. Despite this general consistency there is increasing concern that there may be diagenetic effects on the quantitative record of some metals, which can be inferred based on a strong relationship between mercury and other organically bound elements and proxies for peat decomposition (C/N ratio). However, it is possible that changes in decomposition and the alteration of some metal records could provide climatic information. A few recent studies show that closer examination of the geochemical matrix, in some cases along with biological proxies, can provide valuable information on landscape changes and climate; for example, partitioning metals into different weight fractions and source regions can be applied to climate studies. The best interpretations of the peat geochemical record in the context of environmental and climate change will likely come when geochemical and biological records are considered simultaneously.     

Physico-chemical Speciation of Lead in South San Francisco Bay

The speciation of lead at a site in the South San Francisco Bay was determined using a combination of physical size fractionation and electrochemical analyses. The ‘ total dissolvable ’ Pb was 8·1 nM from analysis of an acidified unfiltered sample. The ‘ dissolved ’ Pb was equal to 0·20 nM (41 ng l⁻¹), only 2·5% of the ‘ total dissolvable ’ Pb. The difference yielded the ‘ particulate ’ Pb equal to 7·9 nM (1·6 μg l⁻¹). Results from crossflow ultrafiltration indicated that almost all (0·19 nM) of the dissolved Pb was ‘ in solution ’ [<10K nominal molecular weight (MW)] and that colloidal Pb (10K MW to 0·2 μm)accounted for onlyc. 1% of the dissolved Pb at this station. This small concentration (0·01 nM) of colloidal Pb may be attributed to the low amount of organic carbon associated with colloid size fraction as determined by dissolved organic carbon analyses.The chemical speciation of lead was determined in the dissolved sample and ultrafiltered sub-sample. Differential pulse anodic stripping voltammetry (DPASV) on a thin mercury film (TMF) rotating glassy carbon disk electrode (RGCDE) was used to distinguish the kinetically labile inorganic species (Pb′) from the Pb-chelated by organic ligands (PbL_i). Lead titration results were similar for both samples revealing that Pb′, PbL_iand excess unbound ligands were present primarily in the ultrafiltrate, rather than in the colloidal phase. The titration data can be interpreted as dissolved Pb being influenced by two classes of Pb-binding ligands. In the dissolved sample, the concentration of the stronger class of ligands was [L₁]=0·89±0·35 nM, with a conditional stability constant ofK^cond_L1,Pb′=3±1×10¹⁰M⁻¹. The weaker class was [L₂]=12·8±1·9 nM, withK^cond_L1,Pb′=4±1×10⁸ M⁻¹. The presence of these ligands, in excess of the dissolved Pb, resulted in [Pb′]=7±2 pM and [Pb²⁺]=0·3 pM (62 pg l⁻¹). While less than 2·4% of the ambient Pb was ‘ in solution ’, it existed chiefly in the form of organic complexes with [PbL₁]=0·15 nM and [PbL₂]=0·03 nM. More significantly, there were large concentrations of unchelated Pb-binding ligands, (L_i′), available to buffer the free Pb²⁺concentration in the event of perturbations in dissolved Pb.