土壤矿物学特征在华南赤红壤有机质稳定中的调控作用研究

以广州市从化的赤红壤剖面为研究对象,系统测定了土壤的pH值和机械组成,土壤剖面中有机质含量、氧化铁矿物和粘土矿物的含量及分布特征,并进行了相关性分析。研究结果表明,赤红壤剖面的总有机质、稳定有机质含量、矿物稳定有机质含量和生化稳定有机质含量的变化趋势在整体上是一致的,均随深度的增加而降低。其中,矿物稳定有机质主要存在于土壤剖面的中间层,氧化铁矿物则大都集中在土壤剖面的中上层;赤红壤剖面各层位中高岭石含量都占绝对优势,为58.7%~84%,蒙脱石的含量次之,为8.5%~16.8%,除此之外,还含有较多的三水铝石。蒙脱石的含量随深度增加而降低,高岭石和三水铝石的含量随深度增加而升高。土壤有机质与氧化铁矿物的相关性较之与粘土矿物、三水铝石要大得多,有机质含量与无定形铁含量的相关系数均高于0.90,与蒙脱石、高岭石、三水铝石的相关系数分别为0.697 1、-0.681 2、-0.049 8,可见无定形铁在土壤有机质稳定中起着重要作用,提醒应更加关注土壤中有机质碳库稳定锁定中的矿物学机制及其影响因素。     

青海湖底沉积物的矿物物相及有机质保存研究

盐湖沉积环境是烃源岩发育的重要地质环境。本文以青海湖湖底沉积物为例，根据有机质与粘土矿物含最及矿物表面积的关系，分析了矿物学因素对盐湖相富有机质沉积物中有机质保存的影响。研究发现：湖底沉积物中有机质丰富，为上层水中的浮游生物和南河流携带束的陆地高等植物两种来源。矿物物相分析发现沉积物中粘土矿物含量达到32．4％，以伊利石为主。沉积物经密度分离后测试发现，有机碳含量与粘土矿物含量及矿物表面积之间具有很好的正相关性，说明粘土矿物吸附是青海湖底沉积物中有机质的主要赋存形式。     

高砷含水层沉积物矿物学特征及砷的活化

利用X射线衍射和X射线荧光分析、沉积物序列提取试验及矿物饱和度的计算,对采自江汉平原中部沙湖地区典型高砷含水层钻孔沉积物样品矿物学进行了分析,并讨论了控制含水层中砷释放和迁移的地球化学机制.对矿物在沉积物与土壤中的分布及组成的对比分析,在一定程度上指示了矿物赋存环境和/或高砷水形成的环境背景:土壤与沉积物中高岭石以低于其他3种粘土矿物的含量普遍存在,指示了含水层沉积物形成过程江汉平原存在一定的湿热古气候环境;沉积物绿泥石含量低于土壤中绿泥石,恰恰反映了土壤比沉积物略强的碱性环境;沉积物中黄铁矿的存在,显示了含水层局部的强还原性环境,指示地下水中广泛存在的Fe2+容易与二价硫发生沉淀并结合砷.砷主要以无定形铁锰氧化物结合态(平均在31％以上)形式存在,其次以碳酸盐和有机质结合态存在.无定形铁锰氧化物的还原溶解可能是控制砷迁移到地下水中主要的地球化学机制.相对高含量的绿泥石容易在含水层中发生风化,其溶解过程可以将铁释放到地下水中,从而成为影响地下水中砷活化的潜在因素.     

天然有机质与矿物间的吸附及其环境效应的研究进展

本文综述了天然有机质与矿物间吸附行为的研究进展.具体介绍了天然有机质与矿物间的吸附机理,包括配位交换、范德华力、静电引力、疏水作用、离子交换及阳离子桥;阐述了不同分子大小及亲疏水性组分的天然有机质在矿物上的吸附行为;讨论了影响吸附行为的环境条件（pH,离子强度）及天然有机-矿物体系对全球碳循环、重金属和有机污染物产生的环境效应,并提出了研究展望.     

天然富有机质含铵伊利石高温高压稳定性研究

含铵伊利石等含铵黏土矿物是地壳中重要的储氮矿物,研究其高温高压稳定性对地球壳–幔圈层间氮循环具有重要意义。本研究通过高温高压(HTHP)模拟实验,初步探索了天然富有机质(具类石墨结构)的含铵伊利石矿物结构及其携带的C、N元素的稳定性。结果表明,在高温(600℃)常压环境下,含铵伊利石层状结构发生塌陷,结构羟基脱失,层间NH4+脱失,其表面类石墨的结构有序度下降,部分含C、N官能团脱失,但仍有近一半得以保存。伊利石层间NH4+的热稳定性受矿物层状结构的制约,当伊利石因高温发生层间塌陷时,NH4+失去伊利石片层保护后受热发生分解。而不同形态有机氮的热稳定性主要与其在类石墨有机质芳香结构中的位置有关。含铵伊利石结构在高温高压(600℃、2 GPa)下保持稳定,类石墨的有序度以及石墨化程度均增强,表明压力在一定程度上补偿了温度的影响。此外,伊利石表面具网状片层结构的类石墨有机质对矿物结构有物理保护作用。同时,有机质中的部分C、N元素在高温高压下与伊利石结构中的Al和O等元素形成稳定的化合键,亦可增强有机质的稳定性。含铵伊利石在高温高压下的稳定性表明,含铵黏土矿物很有可能是携带地壳中的氮经俯冲进...     

环境矿物界面反应动力学

环境矿物界面反应动力学主要探讨地表中各种有毒、有害离子或分子与矿物表面之间的反应速率与反应机制。矿物表面存在一组化学活性很强的表面功能基，当它们与环境中毒害物质发生作用时，会因其极性、荷电性和Lewis酸碱性不同而表现出不同的作用力和反应速率，进而控制有毒、有害物质在大气、水体和沉积物中的赋存形态，稳定性及迁移转化速率。本文简要介绍了环境矿物界面反应动力学理论，并给出几个应用实例。     

土壤矿物学研究综述

土壤矿物是土壤物质组成的主体 ,是土壤微量元素的主要来源。土壤矿物的研究是土壤学研究的前沿基础领域。通过对土壤矿物尤其是粘土矿物的研究 ,可以揭示土壤的发生学特性、母质特征、成土过程及环境 ,揭示土壤的发育程度和肥力水平 ,为环境保护、优质生产和土壤改良提供基础依据。本文指出了土壤矿物学的研究意义 ,综述了土壤矿物学的研究进展 ,总结了不同类型土壤矿物的组成特征及其与成土作用、风化程度和生物气候条件间的变化规律     

土壤重金属环境质量矿物学评价方法

利用环境矿物学理论和方法阐明了土壤矿物控制重金属活动状态，具体分析了重金属在矿物表面、层间域和孔道内可能的赋存位置。实验研究结果表明，矿物吸附重金属的作用受到介质pH值、介质离子强度等因素的影响。采用系统聚类分析方法，能定量地分析稳定的硫化物结合态微量有毒有害重金属元素的数量。利用粉晶X射线衍射分析方法，能定量地测定土壤矿物组成和含量。新提出土壤环境质量矿物学方法评价流程。该方法是在利用生态地球化学方法所完成的元素总量调查成果的基础上，开展单元性与剖面性土壤矿物组成与含量测定，查明表层土壤和深层土壤的矿物组成和分布，评价土壤中重金属的赋存状态及其对食物链的影响。旨在为农业地质环境评价提供新方法，切实提高农业地质环境调查质量与服务水平。     

长沙地区地表红壤铁氧化物矿物胶膜的矿物学

<正>在干旱—半干旱环境中的岩石表面常有黑色薄膜状岩石漆发育,在内陆沙漠、海滨沙漠、南北极地、高山、洞穴、岩石裂隙等陆生风化环境中皆有分布,其主要包含黏土矿物、铁锰氧化物、有机质等成分。无独有偶,在亚热带地区的表层红壤中也存在着类似的"薄膜",其中的铁锰氧化物矿物晶粒小至纳米级,这些矿物"薄膜"多附着于土壤基质表面,亦被称为矿物胶膜。本研究采用同步辐射微区X射线衍射和透射电子显微镜技术对表层红壤铁氧化物矿物胶膜中铁氧化物矿物的成分与结构进行了矿物学表征。     

沉积矿物学在古环境恢复中的应用进展

沉积矿物学是界于沉积学与矿物学之间的边缘交叉学科,它通过沉积物（岩）中矿物的组成、含量、组合特征、成因和单矿物化学成分、晶体结构、形态、性质的分析,研究沉积物在搬运、风化剥蚀、沉积过程和成岩过程中矿物的物理、化学行为特征．进而研究它们在时间、空间上的分布特征与规律,从而探讨物质来源、成因、形成演化历史与环境变迁等。近些年来沉积矿物学在研究古气候、物质来源、沉积环境、油气勘探以及构造演化中发挥着重要作用,成为古环境恢复与重建的重要研究手段之一。在阐述粘土矿物、重矿物、碳酸盐类矿物等的古环境意义的基础上,对其近20a来在湖泊、黄土、海洋古环境恢复当中的应用进展进行了回顾和评述。随着新的沉积矿物研究方法的不断出现和应用,结合沉积物的物理指标、化学指标以及古生物学等其他指标,沉积矿物学将在古环境重建中发挥越来越重要的作用,具有广阔的应用前景。     

Mineralogical and geochemical patterns of urban surface soils, the example of Pforzheim, Germany

This study presents a combined geochemical and mineralogical survey of urban surface soils. Many studies on urban soils are restricted to purely chemical surveys in order to investigate soil pollution caused by anthropogenic activities such as traffic, heating, industrial processing, waste disposal and many more. In environmental studies, chemical elements are often distinguished as lithogenic and anthropogenic elements. As a novel contribution to those studies, the authors combined the analysis of a broad set of chemical elements with the analysis of the main mineralogical phases. The semi-quantification of mineralogical phases supported the assignment of groups of chemical elements to lithogenic or anthropogenic origin. Minerals are important sinks for toxic elements. Thus, knowledge about their distribution in soils is crucial for the assessment of the environmental hazards due to pollution of urban soils. In Pforzheim, surface soils (0–5 cm depth) from various land use types (forest, agriculture, urban green space, settlement areas of various site densities) overlying different geological units (clastic and chemical sediments) were investigated. Urban surface soils of Pforzheim reflect to a considerable degree the mineral and chemical composition of parent rocks. Irrespective of the parent rocks, elevated concentrations of heavy metals (Zn, Cu, Pb, Sn, Ag) were found in soils throughout the whole inner urban settlement area of Pforzheim indicating pollution. These pollutants will tend to accumulate in inner urban surface soils according to the available adsorption capacity, which is normally higher in soils overlying limestone than in soils overlying sandstone. However, inner urban surface soils overlying sandstone show elevated concentrations of carbonates, phyllo-silicates and Fe and elevated pH values compared with forest soils overlying sandstone. Thus, in comparison to forest soils overlying sandstones, inner urban soils overlying sandstone affected by pollution concurrently possess elevated concentrations of mineral phases typically providing relatively high adsorption capacities for heavy metals.     

成都市中心城区地表沉积物中重金属分布及矿物学特征

城市地表沉积物已成为城市环境污染的重要组成部分,是城市环境中各种污染物的"源"和"汇",通过研究城市地表沉积物的物化及矿物学特征对城市环境质量的监测具有良好的指示作用。本文在成都市中心城区不同区域采集40件地表沉积物样品,利用激光粒度分析仪、扫描电镜能谱和X射线衍射等技术分析研究了地表沉积物的粒径分布特征、重金属分布特征、矿物组成特征及微区形貌特征。结果表明:地表沉积物粒径的质量和体积分布特征具有较高一致性,均以中细颗粒物为主,其中小于0. 3mm的地表沉积物占总质量或体积的70%以上,小于0. 125mm的地表沉积物占总质量或体积的40%左右; Cu、Pb、Zn、As、Hg、Cr、Cd、Ni等重金属随着沉积物粒径的减小而呈明显增加的趋势,主要存在于小于0. 125mm粒径的沉积物中,同时在成都市中心城区各方位区域和各环路区域的分布上存在一定的差异; Si、Ca、K、Na等造岩元素在不同粒径级别沉积物中都大量存在;地表沉积物矿物组成主要是石英、长石类、方解石等,且各类矿物在不同粒径级别沉积物中所占含量大致相当,但细粒径矿物表现出胶体行为,极易吸附各种微量重金属。研究认为,城市地表沉积物的粒径分布特征和矿物组成特征是影响重金属在沉积物中分布的内在因素,而人类活动是决定地表沉积物重金属污染程度的关键因素。     

Environmental impact and geochemistry of old tailing pile from the Sanggok mine creek, Republic of Korea

This study evaluates the pollution load on a creek based on the physicochemical and mineralogical properties of old tailings. The Sanggok mine is one of the largest lead–zinc producers in the Hwanggangri mining district, Republic of Korea. The vertical profile of the old tailings in the mine area can be divided into three units based on color change, and mineralogical and textural variations, as well as physical and chemical properties. Unit I (surface accumulation and oxidized heterogeneous tailing soil) has lower pH and higher Eh than unit II (originally unoxidized dumped tailing soil) and unit III (pebble-bearing bottom soil). The conductivity data indicates that unit I and II have very high values compared to unit III and basement. The mine area consists mainly of carbonate rocks; however, mineral constituents of tailing soil and sediments near the mine were mainly composed of quartz, mica, feldspar, amphibole, calcite, dolomite, magnesite, and clay minerals. Units I and II are characterized by high abundances of siderite, locally pyrite, and dolomite. Precipitates in the mining drainage mainly included: smectite, illite, berthierine, quartz, siderite, hexahydrite, and Ca-ferrate. Among the separated metallic minerals, tailing soils and sediments of highly concentrated toxic metals are found: some pyrite, arsenopyrite, chalcopyrite, sphalerite, galena, malachite, goethite, various hydroxide, and uncertain secondary minerals. Units I and II are characterized by relatively high concentrations of Ca, Fe, Mn and low contents of Al, Mg, K, Na, Ti, rare earth elements (REEs) that correlated with the proportion of secondary minerals. Potentially toxic elements such as Ag, As, Cd, Cu, Pb, Sb, and Zn are highly enriched in the upper two units. This metal concentration can be influenced by changes in the depth because of oxic and suboxic zonal distribution. The removal zone (unit I) has probably migrated below the elevation of the maximum enrichment layer due to deepening of the oxic/suboxic boundary. In most of the materials, the enrichment index is higher than 3.62. The highest value of 42.55 is found in the oxidation surface soils of the tailing pile. An average enrichment index of the profiles and precipitates are 27.62 and 22.62, respectively. Rocky basement soils have an average enrichment index of 6.63, which is influenced by overlying the tailing pile. The water quality and habitat of the Sanggok creek are severely polluted. Polluted surface water may also negatively impact the agricultural soil and groundwater.     

云南泸沽湖矿物学沉积记录及其环境辨识意义

通过对泸沽湖矿物学沉积记录的精细剖析发现，泸沽湖的物质沉积过程相对稳定，沉积物粒度分布、矿物组成与组合沉积记录在纵向上的变化均具明显的韵律性，矿物结构与化学沉积记录也表现出规律性的变化特点。在泸沽湖上述矿物学沉积记录的典型特征基础上，通过对这些记录的环境标志性特征、环境辨识可适性等的探索性研究，在200，100和50a短时间尺度上，比较准确地重建了泸沽湖区域气候与环境演化的历史谱系，探讨了全球性气候因子对泸沽湖区域气候与环境变迁的控制     

Sorption of Trace Elements on Mineral Surfaces: Modern Perspectives from Spectroscopic Studies,and Comments on Sorption in the Marine Environment

The partitioning (or sorption) of trace elements from aqueous solutions onto mineral surfaces and natural organic matter (NOM) has played a major role in determining the trace element content of natural waters. This review examines sorption processes on mineral surfaces for nine trace elements (Cr, Co, Ni, Cu, Zn, Sr, Cd, Hg, Pb), focusing on the results of modern x-ray spectroscopic studies. Such studies provide unique information on the structure and composition of sorption products, including their mode of attachment to mineral surfaces or functional groups in NOM under in situ conditions (i.e., with aqueous solution present at 25°C). The types of chemical reactions (acid-base, ligand exchange, redox, dissolution/reprecipitation) that can occur at mineral-aqueous solution interfaces are also reviewed, and some of the factors that affect the reactivity of mineral surfaces are discussed, including changes in the geometric and electronic structures of mineral surfaces when they first react with aqueous solutions and constraints on the bonding of adions to surface functional groups imposed by Pauling bond valence sums. A summary of electrical double layer (EDL) theory is presented, including the results of several recent x-ray spectroscopic and parameter regression studies of the EDL for metal-(oxyhydr) oxide-aqueous solution interfaces. The effects of common inorganic and organic complexants on the sorption of trace metal cations at mineral-solution interfaces are considered, in the context of spectroscopic studies where possible. The results of sorption studies of trace metal cations on NOM, common bacteria, and marine biomass are reviewed, and the effects of coatings of NOM and microbial biofilms on cation uptake on mineral surfaces are discussed, based on macroscopic and spectroscopic data. The objective here is to assess the relative importance of inorganic versus organic sorption processes in aquatic systems. The paper concludes with a discussion of the effects of water composition on trace element removal mechanisms, with the aim of providing an understanding of the effects of the high salinity of seawater on trace element sorption processes. The information presented in this review indicates that sorption processes on mineral, NOM, and microbial and algal surfaces, including true adsorption and precipitation, are highly effective at removing trace elements from natural waters and generally supports Krauskopf's (1956) conclusion that such processes are likely responsible for the present trace element concentrations in seawater.     

Sedimentological characteristics, heavy metal distribution and magnetic properties in subtidal sediments, Ria de Pontevedra, NW Spain

The rias of NW Spain are coastal ecosystems of high biological productivity and great economic importance. They are intensively exploited by man for fish and shellfish. There are a number of important centres of population and industrial activity along their margins, which serve as sources of contamination. In this context, it is desirable to achieve the best possible understanding of the physico‐chemical processes that control spatial and temporal variations in the geochemical, mineralogical and sedimentological characteristics of near‐surface sediments in the Ria de Pontevedra and, in particular, the distribution and mobility of heavy metal contaminants. Thus, adequate environmental planning can be achieved for this site and understanding gained for comparable contexts. Core samples were examined from the inner, middle and outer parts of the ria. Grain‐size distributions reflect the presence of two main populations, one dominated by silt and clay, derived mainly from terrestrial sources, and the other by fine sand to coarse silt, which is derived mainly from continental shelf and ria mouth sources. Mineralogical analysis shows an abundance of terrestrial intensive‐weathering products near the ria head, a dominance of shelf‐derived sediment towards the mouth and the presence of several diagenetic minerals whose nature varies with location within the ria. In the inner ria, the near‐surface sediments are slightly enriched in Pb, Cu and Zn from anthropogenic sources. These sediments are fine grained and have a high organic content; hence, they have a higher potential to sorb contaminants than the coarser grained, less organic‐rich sediments of the mid and outer ria. The estimated sedimentation rates for the fine‐grained organic‐rich sediments from the inner part of the ria are about 1 mm year^–1. The dominant authigenic minerals in the inner ria are iron sulphides, whereas in the mid and outer ria, iron silicates and oxyhydroxides are more important. These differences in authigenic iron mineralogy are clearly reflected by the magnetic properties of the sediments.