长江口氧化还原敏感元素的早期成岩过程

通过测试长江口沉积物及间隙水中Fe、Mn、U及Mo的含量,结合早期成岩模型及地球化学热力学分析,探讨了在河口环境中影响间隙水氧化还原敏感元素(Fe、Mn、U及Mo)分布的主要因素.根据Fick第一定律,估算了Fe、Mn、U及Mo在沉积物-水界面的扩散通量.结果表明,间隙水Fe、Mn、U及Mo的含量分别介于0.8~106μmol/L、14.8~258μmol/L、1.9~14.4nmol/L及60~546nmol/L之间.在垂直剖面上,间隙水Fe、Mn峰值分别出现在约5cm或10cm的深度.早期成岩过程是影响长江口沉积物间隙水Fe、Mn分布的主要因素.吸附系数对间隙水Fe、Mn的分布也有重要的影响.吸附系数越高,间隙水Fe、Mn浓度越低.影响间隙水U分布的主要因素为Fe,而Mo与Fe、Mn之间不存在相关性.通量计算结果显示Fe、Mn、U及Mo的扩散通量分别介于3.0~10.5μmol·(m2·d)-1、35.7~439.5μmol·(m2·d)-1、-2.3~0.2nmol·(m2·d)-1及-36.0~94.6nmol·(m2·d)-1之间.沉积物中自生铀组分约占总铀的6%~67%.      

铁元素对海相沉积物早期成岩作用的影响

铁元素是地壳中丰度最高的元素之一,在海相沉积物成岩过程中起着非常重要的作用.铁元素作为海洋初级生产力的微营养元素,影响海相沉积物中有机质的输入,其在早期成岩阶段与硫化物和磷元素的耦合关系,可以促进或者降低有机质的保存;铁元素在海相沉积物早期成岩过程中可以改变孔隙水的化学性质,影响亚稳定碳酸盐矿物的保存,导致碳酸盐沉积物...     

重元素的生物地球化学循环

根据有关资料,本文介绍铅,等１０种重元素在地球不同圈层的分布和它们在这些圈层间运动,迁移,转化的生物地球化学循环。     

豆荚状铬铁矿铂族元素地球化学研究进展

豆荚状铬铁矿是蛇绿岩中特有的一类矿产，按其化学成分可分为高Cr型和高Al型两种。其中的PGE主要以RuS2和Os、Ir、Ru合金等包体形式存在，或以类质同像形式进入铬铁矿晶格。两种类型的铬铁矿均表现出负倾斜型PGE配分模式，其Pt、Pd含量相近；与高Al型铬铁矿相比，高Cr型铬铁矿有更高的Os、Ir、Ru含量，部分豆荚状铬铁矿表现出Pt、Pd相对富集的平坦到正倾斜型PGE配分模式。目前对豆荚状铬铁矿PGE含量及配分模式还缺少一个统一的解释，但其PGE地球化学可为豆荚状铬铁矿的成因及构造背景解释提供更多的信息。     

水库汞生物地球化学循环研究进展

对近年来国内外有关水库汞生物地球化学循环的研究现状进行了综述,主要从基质释汞行为、汞释放对水体的影响、汞在水库水生食物链中的迁移富集和水库对河流汞输送的影响等四个方面进行了探讨,并指出该领域研究工作的薄弱环节及发展方向.     

生物硅早期成岩作用研究进展

硅质浮游生物是海洋初级生产力的主要提供者,其死亡后所产生的硅质残骸(生物硅)向海底的传输,是保持海洋硅循环动态平衡的重要环节。由于海洋沉积物中的硅质微体生物化石记录了古海洋初级生产力的变化及其时空分布,因而生物硅也成为古环境重建的重要替代指标。本文对生物硅在水柱沉降和表层沉积物埋藏过程中所发生的早期成岩转变及其主要影响因素进行了综述,为全面了解最近几十年来该领域的研究进展提供参考。     

分散元素硒的地球化学循环及其富集作用

本文概述了硒的物理,化学性质,形态和存在形式以及硒的地球化学循环和富集作用。硒呈四种主要的无机形态存在于自然界中：硒化物（－２价）,元素硒（０价）,亚硒酸盐（＋４价）和硒酸盐（＋６价）。不同硒形态的存在,很大程度上取决于ｐＨ和Ｅｈ条件,硒的天然的,总的地球化学循环主要涉及壳岩源和海洋沉积物,次一级的循环强烈受到生物化学反应的影响,这些反应使硒在有机组分中固定或迁移。人类活动向环境中排放的硒极大地改     

硅的生物地球化学循环研究进展

生命元素硅在陆地生态系统和水生生态系统中都扮演着重要的角色。它的生物地球化学循环与全球碳循环和全球气候交化密切相关。因此,近年来逐渐成为研究的热点。本文概述了近年来国内外有关硅的生物地球化学循环的研究进展,包括陆地和海洋中硅的生物地球化学循环过程及人类活动对硅循环的影响等方面,指出日前研究中存在的问题,展望了研究的重点。     

Remobilization of Iodine in Marine Sediments During Early Diagenesis

Based on the sedimentary geochemical studies of the Antarctic Ocean and the various geochemical parameters available,this paper deals with the process of emobilization of iodine in marine sediments during early diagenesis.The results showed that the process is not always controlled completely by organic matter as was expected previously.On average the adsorption and oxide phases of iodine account respectively for 23% and 32% of the total in continental-shelf and hemipelagic surficial sediments.Chemical analysis has revealed that the upward diffusion flux and redox conditions would play an important role in the concentration of iodine in the surface sediments.And the species of iodine in the surfial sediments characteristic of high I/Corg ratios would bepredominated by the oxide and adsorption phases.As experimentally evidenced,it is the early diagenetic remoibilization of iodine associated with the oxide and adsorption phases that led to the decrease of I/Corg with increasing depth.Calculations suggested that the diffusion flux of iodine from the deep parts of te sedimentary columum upwards is on the same order of magnitude as the deposition flux of it from sea water.This may be one of the important factors leading to the depletion of iodine in sedimentary rocks.On the basis of the above discussion and calculations the author has proposed a model for the remobilization of iodine in marine sediments during early diagenesis.     

Rock-magnetic characterization of early, redoxomorphic diagenesis in turbiditic sediments from the Madeira Abyssal Plain

Rock‐magnetic measurements of two sediment cores from the Madeira Abyssal Plain (MAP), north Atlantic, are used to investigate post‐depositional changes in the concentration, grain size and composition of magnetic minerals in the sediments that have occurred within organic‐rich turbidite horizons. The changes are associated with an initial stage of suboxic (reductive) diagenesis, following depletion of porewater O₂, and a later stage of oxidative diagenesis associated with the slow descent of an oxidation front through the sediment, as a result of diffusion of O₂ from the overlying sea water. The turbidites are of late Quaternary age (δ¹⁸O stages 1–3) and derive both from different sites on the NW African continental margin, and from the flanks of the Canary Islands. Thus, the turbidites are variable compositionally, especially in terms of carbonate, detrital magnetic mineral and organic carbon content. Diagenetic changes in these sediments have been identified using solid‐phase geochemical data (U, Mn, C_org and CaCO₃) reported previously in more than one study. Rock‐magnetic parameters of the sediments, when expressed on a carbonate‐free basis, reveal that significant depletion of detrital ferrimagnetic iron (Fe²⁺/Fe³⁺) oxide grains has occurred within organic‐rich turbidites during redoxomorphic diagenesis. Normalized quotients of magnetic parameters also show that reductive diagenesis is a ferrimagnetic grain size‐selective process, but it has a minimal effect on the canted‐antiferromagnetic Fe³⁺ oxides in the sediment. Such components, if present, therefore become relatively enriched in magnetic assemblages as the ferrimagnetic grains are dissolved progressively, and bulk magnetic concentration is thus depleted. There is clear evidence in both cores for the existence of ultrafine ferrimagnetic grains at depth within the suboxic zone of the organic‐rich turbidites, beneath both active and fossil oxidation fronts. These grains are most probably associated with populations of live magnetotactic bacteria, which commonly inhabit such organic‐rich horizons and play a part in the chain of bacterially mediated reactions normally associated with suboxic diagenesis. These results show that simple and rapid rock‐magnetic techniques can be used to characterize early diagenetic processes involving iron phases in deep‐sea sediments, at least as effectively as more laborious, time‐consuming and sample‐destructive geochemical measurements.     

Exploring the impact of diagenesis on (isotope) geochemical and microstructural alteration features in biogenic aragonite

For the Quaternary and Neogene, aragonitic biogenic and abiogenic carbonates are frequently exploited as archives of their environment. Conversely, pre‐Neogene aragonite is often diagenetically altered and calcite archives are studied instead. Nevertheless, the exact sequence of diagenetic processes and products is difficult to disclose from naturally altered material. Here, experiments were performed to understand biogenic aragonite alteration processes and products. Shell subsamples of the bivalve Arctica islandica were exposed to hydrothermal alteration. Thermal boundary conditions were set at 100°C, 175°C and 200°C. These comparably high temperatures were chosen to shorten experimental durations. Subsamples were exposed to different ¹⁸O‐depleted fluids for durations between two and twenty weeks. Alteration was documented using X‐ray diffraction, cathodoluminescence, fluorescence and scanning electron microscopy, as well as conventional and clumped isotope analyses. Experiments performed at 100°C show redistribution and darkening of organic matter, but lack evidence for diagenetic alteration, except in Δ₄₇ which show the effects of annealing processes. At 175°C, valves undergo significant aragonite to calcite transformation and neomorphism. The δ¹⁸O signature supports transformation via dissolution and reprecipitation, but isotopic exchange is limited by fluid migration through the subsamples. Individual growth increments in these subsamples exhibit bright orange luminescence. At 200°C, valves are fully transformed to calcite and exhibit purple‐blue luminescence with orange bands. The δ¹⁸O and Δ₄₇ signatures reveal exchange with the aqueous fluid, whereas δ¹³C remains unaltered in all experiments, indicating a carbonate‐buffered system. Clumped isotope temperatures in high‐temperature experiments show compositions in broad agreement with the measured temperature. Experimentally induced alteration patterns are comparable with individual features present in Pleistocene shells. This study represents a significant step towards sequential analysis of diagenetic features in biogenic aragonites and sheds light on reaction times and threshold limits. The limitations of a study restricted to a single test organism are acknowledged and call for refined follow‐up experiments.     

Rare earth element geochemistry of scleractinian coral skeleton during meteoric diagenesis: a sequence through neomorphism of aragonite to calcite

Rare earth element geochemistry in carbonate rocks is utilized increasingly for studying both modern oceans and palaeoceanography, with additional applications for investigating water–rock interactions in groundwater and carbonate diagenesis. However, the study of rare earth element geochemistry in ancient rocks requires the preservation of their distribution patterns through subsequent diagenesis. The subjects of this study, Pleistocene scleractinian coral skeletons from Windley Key, Florida, have undergone partial to complete neomorphism from aragonite to calcite in a meteoric setting; they allow direct comparison of rare earth element distributions in original coral skeleton and in neomorphic calcite. Neomorphism occurred in a vadose setting along a thin film, with degradation of organic matter playing an initial role in controlling the morphology of the diagenetic front. As expected, minor element concentrations vary significantly between skeletal aragonite and neomorphic calcite, with Sr, Ba and U decreasing in concentration and Mn increasing in concentration in the calcite, suggesting that neomorphism took place in an open system. However, rare earth elements were largely retained during neomorphism, with precipitating cements taking up excess rare earth elements released from dissolved carbonates from higher in the karst system. Preserved rare earth element patterns in the stabilized calcite closely reflect the original rare earth element patterns of the corals and associated reef carbonates. However, minor increases in light rare earth element depletion and negative Ce anomalies may reflect shallow oxidized groundwater processes, whereas decreasing light rare earth element depletion may reflect mixing of rare earth elements from associated microbialites or contamination from insoluble residues. Regardless of these minor disturbances, the results indicate that rare earth elements, unlike many minor elements, behave very conservatively during meteoric diagenesis. As the meteoric transformation of aragonite to calcite is a near worst case scenario for survival of original marine trace element distributions, this study suggests that original rare earth element patterns may commonly be preserved in ancient limestones, thus providing support for the use of ancient marine limestones as proxies for marine rare earth element geochemistry.     

新疆雅满苏铁矿区碳酸盐岩地质地球化学特征及其对矿床成因的制约

新疆雅满苏铁矿床赋存于下石炭统雅满苏组中,矿区发育火山岩、碳酸盐岩及矽卡岩,因此,研究碳酸盐岩与矽卡岩及成矿的关系对厘定矿床成因类型和指导找矿勘查具有重要的理论和实际意义。文章在野外地质剖面测制和调查研究的基础上,对矿区及外围碳酸盐岩进行了岩相学、主量元素、稀土元素及微量元素分析,探讨了矿区碳酸盐岩的地质、地球化学特征。研究结果表明,雅满苏铁矿区的碳酸盐岩含有浅海相生物化石、鲕粒结构及内碎屑构造,与火山岩互层产出,指示沉积作用及火山喷发活动发生于浅海环境;矿区碳酸盐岩岩石类型包括微晶灰岩、细晶灰岩、大理岩、含凝灰质大理岩、糜棱岩化碳酸盐岩和方解石构造片岩,它们的主量元素含量差别不大,说明在变质变形和成矿作用过程中没有主量元素组分的明显带入带出;稀土、微量元素含量除方解石构造片岩稍有降低外,其余岩性均变化不大,也表明变质变形和成矿作用过程中没有外来物质的明显加入,包括成矿物质;与矿体毗邻的碳酸盐岩为方解石构造片岩,没有发生矽卡岩化,表明该碳酸盐岩在构造及成矿作用过程中只发生了构造片理化和热液重结晶,没有发生接触交代。因此,雅满苏铁矿床不是狭义的矽卡岩(接触交代)型铁矿床,而是海相火山岩型铁矿床。研究区的矽卡岩并非是接触交代的产物,而应是火山热液交代含碳酸盐的火山岩而成。是否有下部地层中的碳酸盐岩提供成岩成矿物质还需要进一步研究。     

日本海南部48ka以来的环境磁学记录及其反映的千年尺度环境变化

本文系统分析了日本海郁陵海盆南部陆坡KCES钻孔48ka以来的古地磁、岩石磁学和沉积学性质。在已经报道的以 AMS 14C 测年、火山灰地层和特征深色层年龄模型上,以磁化率、非磁滞剩磁和饱和等温剩磁为归一参数的"地磁场强度"特征低值可以与北大西洋ODP 983钻孔对比,方向可以与日本海和太平洋其他钻孔进行对比,强度年龄与之前年龄一致且更详细。48ka以来末次冰期(36~15kaB.P.)的磁性矿物输入最多,颗粒最细,软磁组分最高,末次冰期其他时段和冰消期、冰后期的磁性矿物输入降低,颗粒变粗,高矫顽力磁组分增加。岩石磁学的系统变化揭示早期成岩作用在7kaB.P.以来程度稍强,48~7kaB.P.作用较弱,不足以影响岩石磁学参数的环境记录。由于样品的不连续,末次冰期岩石磁学与千年冷暖事件的对应不明显,而在冰消期(15~11kaB.P.)海面急剧上升、全球温度变化剧烈的时期,岩石磁学参数表现为非常均匀的粗颗粒快速堆积,但是磁性矿物含量减少,软磁性组分也减少。此时陆源输入中的稳定元素Ti的相应变化暗示物质源区的变化和/或强劲水动力条件的筛选作用。与此同时,底流强劲并且方向多变,沉积物中砂和粉砂含量剧增都说明海底处于动荡和充氧的条件,与末次盛冰期时的分层海洋明显不同。因此,KCES钻孔的岩石磁学变化记录了陆源物质输入、底流演变和沉积后变化,这些都可能与著名的千年事件具有成因关系。     

成都市多目标地球化学调查和双层采样的效果

成都平原多目标地球化学调查在研究元素基准值及分布特征，构造、农业、环境污染的研究，天然气的预测，pH值的计算等方面取得了进展。并且判定深层样对研究深部元素分布、构造研究、根深作物发育、天然气预测、浅层样对浅层元素分布、农业地质、环境污染等研究有着特殊的作用。多目标地球化学调查及其双层采样方法可以推广。     

古流体研究的无机地球化学方法综述

研究与成藏过程相关的古流体活动有助于深入认识油气成藏过程,从经济目的出发预测储层质量,精确分析不同阶段古流体活动对油气成藏的影响具有重要意义。目前国内外石油地质学家主要利用同位素地球化学、元素地球化学、流体包裹体分析等无机地球化学方法分析古流体活动特征及其对油气成藏的影响。在归纳前人研究成果的基础上,总结了各种无机地球化学方法的最新研究进展,认为同位素地球化学方法有助于分析古流体来源与成因,元素地球化学方法可示踪烃类流体的运移,流体包裹体分析技术结合岩相学研究可分析油气运移的时间、期次、相态、通道和油气藏的富集规律,并指出油气运移和聚集的有利方向。在运用无机地球化学方法研究古流体活动时不应局限于单一方法,综合利用多种无机地球化学方法更有利于全面分析古流体活动特征。     

大姚铜矿白垩系马头山组砂岩类的地球化学特征及成岩成矿背景分析

分析大姚铜矿砂岩类的常量元素，反映其成岩成矿的构造背景，砂岩铜矿中碎屑岩的常量元素特征主要受物源区控制。大姚砂岩铜矿成矿受氧化-还原环境控制，分析大姚六苴矿床岩石和矿石样品的Fe^2＋／Fe^3＋值与铜元素含量之间的关系，探讨砂岩铜矿的氧化-还原环境特征，从而建立大姚砂岩铜矿的地球化学相。     

安徽庐枞盆地泥河玢岩型铁矿床地质-原生晕地球化学找矿模型

开展长江中下游地区玢岩型铁矿床轴向原生晕地球化学分析及建模,可弥补地球物理勘探结果的多解性及探测精度的局限性,对定位和评价深部盲矿体具有至关重要的作用。文章在以往研究的基础上,开展庐枞盆地泥河玢岩型铁矿床钻孔原生晕的研究工作,采用多元统计分析方法,查明了主要成矿指示元素在不同地质体中的富集和亏损,确定了磁铁矿、硫铁矿和硬石膏矿体的矿中、近矿及远矿指示元素组合,结合矿床成因模型,建立了泥河玢岩型铁矿床地质-原生晕地球化学找矿模型,通过罗河和小包庄玢岩型铁矿床的佐证,认为该模型可以应用于长江中下游成矿带玢岩型铁矿床的勘探工作中。