沉积物磷原位钝化技术研究进展

水体磷含量是湖泊富营养化最主要的限制因子之一.伴随着湖泊流域工农业发展,外源污染物的长期输入致使沉积物中蓄积了大量的磷及其他污染物.湖泊沉积物一方面是水体磷重要的汇,但另一方面还是水体磷重要的源.在单纯控制湖泊外源污染条件下,沉积物磷的释放仍可导致水体持续富营养化,湖水水质得到明显改善通常需要数十年,因此控制湖泊沉积物内源污染释放是快速恢复湖泊水质必不可少的措施.沉积物内源污染控制技术包括生物修复、环保疏浚以及原位钝化技术.受水深等环境条件限制,生物修复技术和环保疏浚在深水、亚深水型湖泊难以实施.沉积物磷原位钝化技术具有生态、经济、快速和效果稳定等特点,在控制湖泊底泥内源污染中可望发挥重要作用,尤其适合于深水、亚深水型湖泊内源污染控制.系统阐述了不同沉积物原位钝化剂的钝化原理,对比分析了铝盐、铁盐、钙盐和粘度矿物作为磷钝化剂的优缺点和应用条件,概述了国内外沉积物原位钝化技术的应用现状,在此基础上提出了沉积物原位钝化技术未来的重点研究方向:一是研究发展新型钝化剂;二是因地制宜,探索适合不同类型湖泊的底泥原位钝化技术体系;三是加强底泥原位钝化技术与其他技术的联合应用研究与示范;四是加强钝化剂负面影响评价,建立科学的应用技术方案.     

沉积物污染和环境沉积学

环境沉积学着重研究人类活动与沉积循环（包括风化作用、侵蚀作用、沉积作用和早期成岩作用）相互间的影响,寻求人类与自然协调发展的更佳方式。现在,全球河流、湖泊和海洋中沉积物污染严重,沉积学家应予以关注并为解决由此所产生的环境问题做出贡献。实际上,为了对沉积物环境质量进行评估和治理被污染的环境,需要沉积学家去研究污染物的时空分布与岩相、沉积相和沉积体系之间的相互关系,研究污染物在沉积作用和早期成岩作用中的行为,研究沉积物中污染物的存在形式等重要课题。     

矿山水土污染与防治对策研究

矿山水土环境污染是采矿活动引发的主要环境地质问题之一。我国矿山数量众多,水土污染比较普遍,尤以金属矿山最为严重,矿山水土污染防治是今后开展国土空间生态保护修复的重要内容。基于全国矿山地质环境摸底调查成果资料,对矿业活动不同阶段的水土污染风险以及不同矿山的水土污染类型、特征和污染物迁移演化规律等进行了研究。分析指出:矿业活动过程包括勘探、建矿、开采、洗选、冶炼等多个阶段,而水土污染风险贯穿于矿业活动全过程,不同阶段的污染风险不同;矿产资源开发造成的水土污染物类型、特征因开采的矿产类型不同而不同,呈现出特征污染物与矿体母岩的高度相关性;矿山及其周边污染物的迁移作用受污染物自身的物理化学性质和外界环境条件的影响,在矿山长期持续开采条件下矿山水土污染物存在累积效应,而矿产资源集中开采区的污染物扩散表现出叠加效应。通过对某典型水土环境污染案例的分析研究,初步证实了上述推断。根据我国矿山水土环境污染多发性和复杂性的特点,建议今后开展矿山水土污染防治工作应区分不同类型矿山、不同地质环境条件、不同污染物特征、不同污染程度,采取分类施策、系统修复、标本兼治的对策,以实现矿山环境明显改善。     

沉积物中PCBs分析测定与迁移转化研究进展

多氯联苯(PCBs)是一种具有亲脂性、低水溶性、高稳定性和高生物富集性等特性的持久性有机污染物(POPs),而沉积物作为疏水性有机污染物(HOCs)的重要地质宿体,PCBs在POPs中发生的环境过程是研究的热点。本文综述国内外近几年来沉积物中PCBs分析测定以及迁移转化的研究动态,并对今后PCBs污染的生物修复研究提出了自己的见解。     

中国农田土壤重金属污染防治现状与问题思考

土壤是农业可持续发展的基础。经过近40年的经济快速发展与农业高度集约化生产后,我国农田土壤污染与土壤环境质量下降问题逐渐凸显。当前,中国农田土壤重金属污染形势不容乐观,对农产品的安全生产和食品安全构成威胁。文章首先对我国农田土壤重金属污染现状与污染特点、农田重金属污染来源及修复技术研究现状等进行了总结。结果显示：(1)我国农田土壤重金属污染点位超标率相对较高,但以轻度污染为主;(2)污染土壤中主要以Cd、As、Hg、Pb和Cr这5种健康风险重金属元素为主,尤其以Cd风险最高,而以生态风险为主的Ni、Cu和Zn 3种重金属环境风险相对较小;(3)农田土壤污染分布总体表现为南方重于北方,东部重于西部;(4)农田土壤污染逐渐呈现由工业源向农业源、城郊向农村、土壤向食物链转移的发展趋势。基于文献计量方法对我国近30年来农田土壤污染防治研究的热点与趋势进行了分析。结果表明,我国农田土壤污染防治研究主要始于2000年前后,2009年后进入快速发展阶段,研究热点主要包括重金属污染监测、土壤环境环境质量评价、重金属污染土壤修复技术等,近10年来污染土壤修复技术表现为从单一修复技术向联合修复技术发展态势。此外,文章对我国农田重金属污染修复的一般程序、不同污染程度农田土壤的安全利用技术与高风险污染土壤的管控技术进行了评价,最后,对我国当前农田重金属污染防治过程中出现的问题进行了思考,同时针对我国今后农田重金属污染防治研究进行展望,提出了基于源头控制与风险管控措施相结合的农田重金属污染防治体系,以期为未来我国农田土壤重金属污染防治研究规划以及土壤重金属污染防治技术的创新提供参考与借鉴。     

中国淡水湖泊沉积物地球化学背景与环境质量基准建立的思考

利用中国150余个淡水湖泊表层沉积物和深层沉积物的地球化学数据,采用中位数绝对中位差的方法统计获得了中国主要淡水湖泊沉积物的As、Cd、Cr、Cu、Hg、Ni、Pb、Zn、TN、TP、TOC及pH的地球化学背景值,为我国湖泊沉积物环境质量基准的建立和湖泊生态环境质量监管提供了重要依据。统计结果表明,我国表层湖泊沉积物中的As、Cd、Hg等重金属元素以及TP、TOC等发生了显著富集,显示出强烈的人类活动对湖泊沉积物环境质量的改变。在探讨国外环境质量基准值对我国淡水湖泊沉积物环境质量评价适应性的基础上,提出直接采用国外相关标准还不能客观评价我国湖泊沉积物的污染程度和生态风险,应充分考虑我国湖泊沉积物的地球化学背景,建立适应我国情况的沉积物环境质量基准。     

特约主编致读者

特约主编致读者  陈世宝 土壤是人类赖以生存的最基本和最重要的自然资源。土壤环境质量与生态安全是支撑我国生态文明建设的重要基础,也是我国经济和社会可持续发展的重大民生问题。随着我国社会和经济高速发展,土壤不断遭到各种“有害”物质的污染。土壤污染的发生特征与土壤的特殊地位和功能是分不开的。土壤污染具有多来源、迁移多途径、过程多因素及时空分异的环境演化特征。首先,土壤是人类生存环境基本要素之一,大气或水体中的污染物质通过迁移、转化后进入土壤,使土壤遭受污染;其次,在农业生产中,为了提高农产品的产量和品质,人们大量施用化肥和农药,过量的化肥和农药造成土壤污染;此外,土壤历来就作为工业与生活废物（废渣、污水和垃圾等）的处理场所,大量有机和无机污染物随之进入土壤。万物土中生,土壤污染是农产品质量不安全的源头。当今,由土壤污染引起的农产品质量与安全问题越来越引起社会的广泛关注,也给我们的生活带来了诸多不利影响。土壤污染主要包括重金属污染、农药和持久性有机物污染、过量化肥施用引起的氮和磷污染等多方面。土壤调查结果显示,目前我国有近3亿亩耕地受到不同程度污染,约占耕地总面积的1/6,每年仅因土壤重金属污染带来的直接经济损失超过数百亿元,因土壤污染引起的人体健康与环境群发事件已引起社会各界高度关注。近年来,尽管我国各级政府对土壤污染的关注不断提升,由于土壤污染具有隐蔽性、不可逆性和长期性,与水体和大气污染相比,土壤污染的趋势还远未得到有效遏制。 农田土壤环境质量的不断恶化,将直接影响我国农田生态系统的食品安全、人体健康和经济的可持续发展,同样会给我们生存环境带来危害。土壤既是环境污染物的“汇”,也是其他环境要素污染的“源”。土壤受到污染后,土壤中的污染物将通过多种方式溶在水中或以粉尘形式飘在空中,导致水环境和大气环境质量下降,致使天不再蓝,水不再碧;而对于农产品的质量安全而言,“净土”是“洁食”的前提和基本保障,唯有净土才能洁食,才能保证人体的健康,最终才能保障整个社会的稳定与发展。 土壤污染与人为不合理的污染物排放或生产活动密切相关。最近30多年来,工业化、城市化、农业集约化的快速发展以及人们对土壤资源高强度的开发利用,使大量未经处理的固体废弃物向土壤转移,过量的化肥与农药在土壤中残留,含重金属超标的污水灌溉等造成我国大面积农田土壤发生显性或隐性的重金属污染。由此,针对我国土壤污染的特征与防治现状,全局性、前瞻性地开展我国土壤污染防治科技发展战略研究,全面提升我国土壤污染防治科技创新能力,是新时期我国生态文明建设的重要内容之一,也是落实《土壤污染防治行动计划》和《土壤污染防治法》工作的重要科技保障。 近10多年来,美国、欧洲、日本等发达国家针对土壤污染的成因与过程、污染物毒性评价及污染土壤治理技术等方面开展了系统的基础理论与技术研发,在土壤污染物源解析、多介质与多界面传输过程及不同尺度预测模型等方面取得突破性进展,构建了基于不同土壤污染物的毒性数据库和土壤污染风险识别方法与风险评估体系,并形成和发展了较完整的土壤环境监测方法、技术及污染土壤修复技术体系。相比而言,我国在土壤污染研究的基础数据信息、多尺度下土壤环境污染物的界面过程、污染物的环境迁移转化与生态健康效应及土壤污染监测与预警体系等相关领域的研究相对滞后,相关基础研究难以满足当前我国土壤污染防治工作的需求。基于此,本专辑共收录论文22篇,汇集了土壤污染监测与土壤环境质量评价、土壤与地下水污染风险评估及污染土壤修复研究的若干最新研究成果。其中,5篇论文是针对土壤中新型污染物抗生素环境监测方法、全国土地质量地球化学调查及土壤中重金属等元素分布模式的驱动机制与互动过程等研究的,4篇论文有关土壤中不同污染物健康风险评估及污染土壤等级划分,不同类型污染土壤修复技术研究有7篇论文,土壤污染与地下水化学特征及其成因相关研究的文章有5篇,农田土壤污染防治相关研究进展的文章有1篇。值得一提的是,本专辑有幸收录了成杭新等和李括等的2篇关于我国土地质量地球化学调查20年相关成果及表生地球化学动力学与土壤中化学元素分布模式的驱动机制相关的力作,论文对我国近20年来耕地地球化学状况、省会城市土壤环境质量状况、主要淡水湖泊沉积物环境质量状况及主要农耕区土壤碳库变化等方面的调查成果做了较全面的总结,相关研究结果揭示了时空大尺度中国土壤环境质量变化趋势并为今后我国土地管理与土壤污染防治工作提供了很好的借鉴。通过本专辑相关论文的发表,以期为我国土壤污染防治的环境污染监测技术、污染物健康风险评价、污染土壤修复、土壤污染风险评估及管控技术等方面的研究提供参考。土壤污染与防治,除了开展上述基础研究外,还要大力开展土壤与环境质量保护的宣传与科普工作,让全社会认识到唯有“净土”才能“洁食”,“净土”与“蓝天、碧水”是同等重要的国家生态与环境安全发展的长远战略问题。 感谢所有作者、审稿专家及编辑部全部工作人员在本专辑出版过程中的辛苦付出！     

水体沉积物环境质量基准建立方法研究进展

近20年来，不同的研究机构和研究者先后提出了多种水体沉积物环境质量基准建立方法，这些方法大多产生于北美地区，都是以底栖动物为保护目标，直接或间接地以污染物的生物效应为依据，可划分为2类：即基于沉积物毒性试验、现场生物效应观察和效应发生频率统计的方法;基于平衡分配理论，污染物在沉积物固相—间隙水相间的分配关系的方法。各种方法都有其适用范围和局限性。目前研究中存在的主要问题是：无法明确污染物—生物效应间的因果关系，难以确定影响污染物生物有效性的因素及其影响程度。因此，至今还没有提出一种可广泛应用的沉积物环境质量基准建立方法。建立统一的沉积物毒性试验、测定标准，提高数据的可靠性，重视不同基准建立方法的结合，将是今后研究的重点和发展方向。     

湖泊沉积物中重金属的环境地球化学

概要地回顾了近年来国内外湖泊沉积物中重金属环境污染方面的研究成果,介绍了湖相沉积物重金属研究的主要内容、方法和可能的发展方向.认为就重金属成因方面应加强区分其主要来源是岩石和矿物风化的碎屑产物、大气降尘、人类活动等的研究;重金属污染方面更应重视污染物质的生物有效性、迁移转化机理和重金属“二次污染“的研究;研究手段上,注重运用同位素示踪与定年技术来研究重金属的来源和污染历史,应用高分辨率沉积物钻心研究环境的变迁.最后提出加强多学科的综合研究,建立中国湖泊基准数据库,为探讨湖泊湿地的可持续发展提供依据.     

受污染湖泊沉积物中氮素转化对有机污染物降解的促进效应与机制

目前有关硝化反应动力学及其共代谢降解有机污染物的研究多为实验室微生物纯培养体系,来源于野外环境样品的很少.以受污染湖泊严家湖1号塘沉积物为研究对象,野外钻探采样,并选取不同深度沉积物进行室内外加氮源的硝化实验.结果表明:表层土和钻井一处50～100 cm沉积物发生明显的硝化反应,同时有机污染物中六氯苯含量降低最多,分别...     

Hydrogen and carbon in solid solution in oxides and silicates

The dissolution of H₂O and CO₂ in structurally dense, nominally anhydrous and non-carbonate oxide matrices such as MgO and CaO is reviewed. H₂O and CO₂ are treated as gaseous oxide components which enter into solid solution with the refractory oxide hosts. They form anion complexes associated with cation vacancy sites. Evidence is presented that OH^? pairs which derive from the dissolution of H₂O are subject to a charge transfer (CT) conversion into peroxy moieties and molecular hydrogen, O ₂ ^2? ... H₂. Because the O ₂ ^2? moiety is small (O^?-O^? distance ≈ 1.5 Å) high pressure probably favors the CT conversion. Mass spectroscopic studies show that molecular H₂ may be lost from the solid which retains excess oxygen in the form of O ₂ ^2? , leading to the release of atomic O. The dissociation of O ₂ ^2? moieties into a vacancy-bound O^? state and an unbound O^? state can be followed by measuring the internal redox reactions involving transition metal impurities, the transient paramagnetism of the O^? and their effect on the d.c. conductivity. Evidence is presented that CO₂ molecules dissolve dissociatively in the structurally dense oxide matrix, as if they were first to dissociate into CO+O and then to form separate solute moieties CO ₂ ^2? and O ₂ ^2? , both associated with cation vacancy sites. In the CO ₂ ^2? moiety (C-O^? distance 1.2–1.3 Å, OCO angle ≈ 130°) the C atom probably sits off center. The transition of the C atom into interstitial sites is accompanied by dissociation of the CO ₂ ^2? moiety into CO^? and O^?. This transition can be followed by infrared spectroscopy, using OH^? as local probes. Further support derives from magnetic susceptibility, thermal expansion, low frequency dielectric loss and low temperature deformation measurements. The recently observed emission of O and Mg atoms besides a variety of molecules such as CO, CO₂, CH₄, HCN and other hydrocarbons during impact fracture of MgO single crystals is presented and discussed in the light of the other experimental data.     

Comparative urbanization in Ghana and Kenya in time and space

There are few inter-African country urban analyses because of the continent’s enormous size and socioeconomic diversity, language barriers, and wide variations in national and regional urban research capacity. Nevertheless, comparative urban studies are critical in understanding contemporary African urbanization. In this comparative spatial and temporal analysis of Ghana and Kenya’s urbanization, we find that both countries are urbanizing rapidly and are faced with many common urban problems. Moreover, Ghana is more urbanized than Kenya and has a larger indigenous urban imprint and a more widely dispersed urban pattern. Besides their physiographic and population conditions, we trace these countries’ convergent and divergent urban trends to their shared but unique experiences of colonialism, nationalism and globalization.     

煤中气孔和镶嵌结构及其在煤变质研究中的意义

河南省禹县、新密和荥巩煤田山西组Ⅱ₁煤的贫煤和无烟煤中,气孔发育。气孔形态有椭圆状（图版1）、圆状及不规则状（图版2）,有的几个气孔连在一起呈大的朵状气孔(图版3)。此外,在荥巩煤田西部无烟煤中还发育有镀嵌结构(图版4)。      

岩溶地区现代土壤与洞穴石笋中单甲基支链烷烃与烷基环己烷对比研究

利用GC-MS（气相色谱—质谱仪）,对采自湖北清江流域和尚洞洞顶的土壤样品与洞内石笋样品进行分析,发现土壤中存在的七个系列单甲基支链烷烃在所有的石笋样品中均可以找到,呈现相似的分布模式,石笋中七个系列支链烷烃有可能来自洞穴滴水携带的土壤中的支链烷烃,但是也不能排除石笋原地生长的微生物的贡献。烷基环己烷的分布在土壤与石笋中呈现了相似的分布模式,但是主峰碳数有所变化,高碳数部分与低碳数部分的相对含量也发生了变化。主要原因可能是微生物选择性降解的结果,也有可能是土壤与石笋中微生物种类分布差异所造成的。本次研究初步显示了相对封闭稳定的洞穴沉积物与上覆土壤层中生物标志化合物的异同。      

Re-Os and Pd-Ag systematics in Group IIIAB irons and in pallasites

Using improved analytical techniques, which reduce the Re blanks by factors of 8 to 10, we report new Re-Os data on low Re and low PGE pallasites (PAL-anom) and IIIAB irons. The new pallasite samples nearly double the observed range in Re/Os for pallasites and allow the determination of an isochron of slope 0.0775 ± 0.0008 (T = 4.50 ± 0.04 Ga, using the adjusted λ¹⁸⁷Re = 1.66 × 10⁻¹¹ a⁻¹) and initial (¹⁸⁷Os/¹⁸⁸Os)₀ = 0.09599 ± 0.00046. If the data on different groups of pallasites (including the “anomalous” pallasites) are considered to define a whole-rock isochron, their formation would appear to be distinctly younger than for the iron meteorites by ∼60 Ma. Five IIIAB irons (Acuna, Bella Roca, Chupaderos, Grant, and Bear Creek), with Re contents ranging from 0.9 to 2.8 ppb, show limited Re/Os fractionation and plot within errors on the IIAB iron meteorite isochron of slope 0.07848 ± 0.00018 (T = 4.56 ± 0.01 Ga) and initial (¹⁸⁷Os/¹⁸⁸Os)₀ = 0.09563 ± 0.00011. Many of the meteorites were analyzed also for Pd-Ag and show ¹⁰⁷Ag enrichments correlated with Pd/Ag, requiring early formation and fractionation of the FeNi metal, in a narrow time interval, after injection of live ¹⁰⁷Pd (t_1/2 = 6.5 Ma) into the solar nebula. Based on Pd-Ag, the typical range in relative ages of these meteorites is ≤10 Ma. The Pd-Ag results suggest early formation and preservation of the ¹⁰⁷Pd-¹⁰⁷Ag systematics, both for IIIAB irons and for pallasites, while the younger Re-Os apparent age for pallasites suggests that the Re-Os system in pallasites was subject to re-equilibration. The low Re and low PGE pallasites show significant Re/Os fractionation (higher Re/Os) as the Re and PGE contents decrease. By contrast, the IIIAB irons show a restricted range in Re/Os, even for samples with extremely low Re and PGE contents. There is a good correlation of Re and Ir contents. The correlation of Re and Os contents for IIIAB irons shows a similar complex pattern as observed for IIAB irons (Morgan et al., 1995), and neither can be ascribed to a continuous fractional crystallization process with uniform solid-metal/liquid-metal distribution coefficients.     

Geogenic and anthropogenic zinc in epiphytic and terricolous lichens in Finland

At 31 sites in Finland the Zn content was determined of the epiphytic lichen Hypogymnia physodes (L.) Nyl. growing on pine and birch, the terricolous lichen Cladina spp. in pine bark, and the inner part of birch bark. The anomalous contents of Zn in H. physodes on pine and Cladina spp. in soil appeared to be strongly related to sulphide ore deposits. Anthropogenic Zn correlated closely with S and Fe in H. physodes on pine and with Fe in Cladina spp. The binding of geogenic Zn was related to iron hydroxides, and was attributed to the different uptake mechanism of S in these lichens. Elevated values of Zn in H. physodes on birch were due to both geogenic and anthropogenic sources. Zinc in pine bark increased with the Zn content in H. physodes and reached a limiting value.     

Water-extractable and exchangeable phosphate in Martian and carbonaceous chondrite meteorites and in planetary soil analogs

Aqueous extraction contributes to the formation and weathering of planetary materials and renders electrolytes such as phosphate available for biology. In this context, the solubility of phosphate is measured in planetary materials, represented by the Mars meteorites Nakhla, Dar al Gani 476 (DaG 476), Elephant Morraine 79001 (EETA 79001), and terrestrial analogs, and in the Murchison CM2 and Allende CV3 carbonaceous chondrites. The Mars meteorites contain high levels of phosphate that is readily extracted by water, up to 15 mg kg⁻¹ in Nakhla and DaG 476 and 38 mg kg⁻¹ in EETA 79001, while the terrestrial analogs and the carbonaceous chondrites contain 0.5 to 6 mg kg⁻¹. Correspondingly, high phosphate concentrations of 4 to >28 mg L⁻¹ are obtained in extracts of the Mars meteorites at high solid/solution ratios, exceeding the concentrations of 0.4 to 2.0 mg L⁻¹ in the extracts of the terrestrial analogs. A wide range of planetary conditions, including N₂ and CO₂ atmospheres, solid/solution ratios of 0.01 to 1.0 kg L⁻¹, extraction times of 1 to 21 d, and temperatures of 20 to 121°C affect the amounts of extractable phosphate by factors of only 2 to 5 in most materials. Phosphate-fixing capacity and exchangeable phosphate are assessed by the isotopic exchange kinetics (IEK) method, which quantifies the amount of P isotopically exchangeable within 1 min (E_1min) and between 1 min and 3 months (E_1min-3m) and the amount of P that cannot be exchanged within 3 months (E_>3m). The IEK results show that the DaG 476 Mars meteorite and terrestrial analogs have low P-fixing capacities, while the carbonaceous chondrites have high P-fixing capacities. Aqueous processing under early planetary CO₂ atmospheres has large effects on the available phosphate. For example, the fraction of total P that is exchangeable in 3 months increases from 1.6 to 11%, 13 to 51.6%, and 43.9 to 90.4% in the DaG 476 Mars meteorite, Allende, and Murchison, respectively. The results show that solutions with high phosphate concentrations can form in the pores of planetary lava ash and basalts and in carbonaceous asteroids and meteorites. These solutions can help prebiotic synthesis and early microbial nutrition. The Martian and carbonaceous chondrite materials contain sufficient phosphate for space-based agriculture.     

Amphibole and chlorite in mafic and ultramafic rocks in the lower crust and upper mantle

Stabilities of amphibole and chlorite in mafic and ultramafic compositions have been considered in the model system CaO+MgO+Al₂O₃+SiO₂+H₂O. From topological arguments two petrogenetic grids have been constructed. Although available experimental data in CMASH are compatible with the grid in which amphibole reacts out before chlorite in model ultramafic compositions for the pressure range 6 to 15 kbar, naturally observed mineral assemblages and some experimental data in more complex systems favour the other grid in which chlorite reacts out before amphibole at all pressures. This discrepancy between natural and model systems is due to differential movement of the dehydration equilibria of the two hydrates reflecting the variation of activity of H₂O or of components other than CMASH.     

Orogenesis in time and space in Mexico

The evolution of the border region of part or all of a craton, on the basis of geological data gathered from Mexico, may best be described in terms of geotectonic cycles. These consist, in chronological order, of (1) an orthogeosynclinal phase (eu- and miogeosynclines) with or without initial magmatic activity, (2) an anatexitic phase consisting of batholith emplacement with attendant regional metamorphism in the eugeosyncline and deposition of a clastic or flysch wedge over the miogeosyncline, (3) an orogenic phase consisting principally of the folding and thrusting of the sediments of the miogeosyncline together with the clastic or flysch wedge against the foreland, and (4) a taphrogenic or block-faulting phase accompanied by (a) accumulation of post-orogenic debris or molasse, (b) subsequent magmatic activity consisting largely of igneous extrusions with fewer intrusions, and (c) final magmatic activity consisting of igneous extrusions. A region that has gone through the above phases of a geotectonic cycle may be termed a structural belt. In the post-Precambrian geologic history of Mexico, three geotectonic cycles are recognized: one occurred along the Pacific border of Mexico between Cambrian and middle Jurassic (?) time (Jaliscoan geotectonic cycle), the second occurred along the present Gulf of Mexico border of the country at the same time (Huastecan geotectonic cycle), and the third occurred over the entire country from the United States border to the Guatemalan border between Late Jurassic and Pliocene time (Mexican geotectonic cycle). The early Mesozoic clastic rocks in northwestern Mexico may signify a fourth geotectonic cycle in that region. In the three recognized geotectonic cycles, however, the geologic record shows only two orogenic phases, one of which occurred in late Paleozoic time in an arcuate belt along the eastern side of Mexico (Coahuilan orogeny), and the other in early Tertiary time in a belt traversing central Mexico from the United States border to the Guatemalan border (Hidalgoan orogeny).     

银川平原地下水资源开发与植被变化

植被状况的变化是反映区域性生态环境状况的重要指标。地下水是影响植被变化的主要因素。宁夏地处干旱半干旱地带,是全国生态系统最脆弱的省区之一。2000年后,随着宁夏黄河引水量的减小,水资源的不合理应用使银川平原的生态植被出现了退化的趋势。本文利用MODIS-NDVI遥感数据,对银川平原2000~2004年间的植被变化趋势进行了研究。在此基础上,对引用黄河水量及多年地下水位的变化对植被的影响进行了分析,并对适宜于植被发育的地下水位埋深进行了探讨。