湘东北燕山期陆内碰撞造山带金多金属成矿地球化学

文章采用微量元素(包括稀土元素)地球化学示踪方法，着重讨论了金大规模成矿的物质来源、含矿流体来源及含矿流体运移的能量问题。认为湘东北地区金多金属矿床成矿物质和含矿流体具多来源，大规模花岗质岩浆活动能为成矿元素的活化和成矿流体运移提供巨量能源；成矿物质一部分源于深部含矿热液，可能与富铅、富氯、中高温(320℃左右)、相对还原的酸性环境下的气成热液有关，而冷家溪群及相关地层金多金属成矿物质在热液活动和动力变质作用下的活化迁移有利于金多金属的大规模成矿。侏罗纪以来，岩石圈地球动力学转折及伴随的热液作用和动力变质作用对区内金多金属成矿起重要的作用，而岩浆作用、动力作用和/或热液活动影响程度的可能差异，导致了金多金属矿床具有不同的成矿特点。     

Mudstones of the Tanqua Basin, South Africa: an analysis of lateral and stratigraphic variations within mudstones, and a comparison of mudstones within and between turbidite fans

Permian deep‐water mudstones in the Tanqua Basin, South Africa, have been studied using geochemical and spectral gamma ray techniques. The mudstones occur as thick sequences between sand‐rich submarine fans, but also occur as thinner mud‐rich units within each fan. The interfan mudstones are interpreted to have accumulated during transgression and the consequent period of relatively high sea‐level, while the submarine fans and their intrafan mudstones were deposited during regression and relatively low sea‐level. Geochemical analyses revealed systematic differences between interfan and intrafan mudstones because the two types of mudstones have slightly different source lithologies. Differences between the two types of mudstone suggest that changes in relative sea‐level played a role in controlling exposure of sediment source areas. There are geochemical signals that display systematic stratigraphic trends within both interfan and intrafan mudstones. These are best explained by gradual denudation, exposure and weathering of different lithologies within a single sediment source area. Both interfan and intrafan mudstones have uniform geochemical signals along the flow direction except for the relative amount of uranium. It is most likely that the basinward increase in uranium in the mudstones is the result of reduced clastic dilution of uranium‐bearing pelagic fallout.     

An automated salt‐tracing gauge for flow‐velocity measurement

This article introduces the SVG (salt‐velocity gauge), a novel automated technique for measuring flow velocity by means of salt tracing. SVG allows a high measuring rate (up to one every 2 seconds), short control section length (down to 10 cm), high accuracy (+[sol ]?1·5 cm s^?1), and unbiased calculation of the mean velocity in experimental conditions with turbulent, supercritical flow. A few cubic centimetres of saturated salt solution (NaCl) are injected into the flow at regular time intervals using a programmable solenoid valve. The tracer successively passes two conductivity probes placed a short distance downstream. The transformation of the signal between the two probes is modelled as a one‐dimensional diffusion wave equation. Model calibration gives an estimation of the mean velocity and the diffusion for each salt plume. Two implementations of the SVG technique are described. The first was an outdoors simulated rainfall experiment in Senegal (conductivity probes at 40 cm apart, 8 Hz measurement rate, salt injections at 10 second intervals). Mean velocity was estimated to range between 0·1 and 0·3 m s^?1. The second was a laboratory‐based flume experiment (conductivity probes at 10 cm apart, 32 Hz, salt injections at 2 second intervals). Another SVG with probes at 34 cm apart was used for comparison. An acoustic Doppler velocimeter (ADV) was also used to give an independent assessment of velocity. Using the 10 cm salt gauge, estimated mean velocity ranged from 0·6 to 0·9 m s^?1 with a standard deviation of 1·5 cm s^?1. Comparisons between ADV, 10 cm SVG and 34 cm SVG were consistent and demonstrated that the salt‐tracing results were unbiased and independent of distance between probes. Most peaks were modelled with r² > 90 per cent. The SVG technology offers an alternative to the dye‐tracing technique, which has been severely criticized in the literature because of the wide interval of recommended values for the correction factor α to be applied to the timings. This article demonstrates that a fixed value of α is inappropriate, since the correction factor varies with velocity, diffusion and the length of the control section. Copyright © 2005 John Wiley & Sons, Ltd.     

区域生态地球化学评价核心与对策

生态地球化学是地学与土壤学、农业、环境学和生态学等多学科交叉融合产生的新学科,是地球化学领域新的发展方向。区域生态地球化学评价是在区域地球化学调查基础上,针对影响流域/区带生态系统安全性的元素异常而开展的一项评价和研究工作。多目标区域地球化学调查获得的海量高精度地球化学数据,可为环境质量评价提供背景值、为土地的质量和生态管护提供地球化学依据;调查还发现了一系列影响流域生态安全性的元素异常,针对异常元素分布特征,区域生态地球化学评价将开展异常元素追踪和成因甄别、生态效应评价和生态系统安全性的预警预测等项评价和研究工作。文章论述了区域地球化学调查成果,介绍了区域地球化学评价的思路,阐述了区域生态地球化学评价的主要问题与对策。