大沽河地下咸淡水过渡带的水-岩作用模拟

大沽河是青岛市最大的地下水源地,过量开采导致严重的地下咸水入侵,研究地下咸-淡水的地球化学作用对于地下咸水的治理具有重要的指导作用。本文选取大沽河地下咸淡水过渡带作为研究区,在地下水动态监测的基础上,通过地下水水质和含水介质矿物分析,借助当前成熟的水文地球化学模拟软件—PHREEQC 2.0,计算地下水中主要离子和络合离子的含量,定量确定矿物的饱和指数和地下水流向上矿物相与水之间的物质交换量。研究结果表明:(1)地下水中钠、钾、镁、钙主要以单一离子形态存在,硫、碳主要以络阴离子形态存在,而硅和铝主要以络合物形态存在;(2)在地下水流动路径上,方解石、白云石、伊利石、高岭土处于过饱和状态;而石膏、CO2、氯化钠、萤石、玉髓处于不饱和状态;(3)咸淡水过渡带地下水化学类型由HCO3-Ca·Na型水向Cl-Na型水转变的趋势。     

东昆仑造山带低山头花岗岩体岩石地球化学特征及其地质意义

低山头一带花岗岩体归属东昆仑弧盆系北昆仑岩浆弧带,位于东昆仑成矿带伯喀里克—香日德成矿亚带东昆仑造山带中段,岩石类型主要为石英闪长岩、正长花岗岩及二长花岗岩。为了加强该地区花岗岩体岩石地球化学与成岩成矿背景探讨,对花岗岩体开展了主量元素、微量元素及矿质元素研究。主量元素组成上,石英闪长岩具中硅（57.64%和58.47%）、富钠（Na₂O/K₂O均为2.57）特点,正长花岗岩具高硅（75.45%~75.99%）、富钾（Na₂O/K₂O为0.74~0.94）特点,二长花岗岩具高硅（66.80%~73.45%）、富钠（Na₂O/K₂O为1.50~2.13）特点;花岗岩体铝饱和指数A/CNK<1,为准铝质岩浆岩;碱饱和指数NK/A集中在0.26~0.69之间,属钙碱性岩石;里特曼组合指数σ₄₃在1.18~2.31之间,属钙碱性类型。花岗岩体轻稀土元素相对重稀土元素富集,岩浆分异特征明显,大离子亲石元素（LILE）富集Rb、K、Ba、Th、Sr、Nd,仅正长花岗岩Sr亏损,高场强元素（HFSE）富集Zr、Hf、Ce,而Nb、P、Ti明显亏损,源区物质为壳幔混合物质,属挤压应力环境中同碰撞I型花岗岩。在岩体实测剖面中获得11种元素分析数据,与青海全省、东昆仑成矿带及其亚成矿带平均元素丰度值进行对比,初步划分不同岩性、不同类型、不同时代花岗岩,以及富集的含矿元素为Au、Zn、Y、Pb等。与区域有成矿事实且为I型花岗岩成因进行对比,认为研究区有较好的找矿前景。     

利用测井资料分析成岩作用对储集层的影响

应用测井资料进行压实作用、孔隙演化、裂缝、矿物成分详尽分析基础上 ,结合成岩作用各个阶段对储集层性能影响的研究 ,讨论了应用测井资料分析成岩作用对储集层影响的物理基础 ,进而指出应用测井资料分析成岩作用不同阶段对储集层影响的可行性。方法为 :(1 )成岩作用早期 :应用孔隙度测井和岩性测井资料 ,通过压实曲线分析压实作用区间 ;(2 )成岩作用中期 :首先根据孔隙度测井资料分析声波孔隙度、密度 -中子测井孔隙度 ,分析次生孔隙 ,并应用交会图技术 ,确定矿物成分 ,分析胶结、交代作用形式和强度 ,然后根据泥质指示测井确定泥质含量 ,进一步利用自然伽玛能谱测井 ,尤其是Th、K含量分析粘土矿物 ;(3)成岩作用晚期 :进行次生孔隙、裂缝、颗粒成分与含量、粘土矿物分布规律研究。以上分析方法经吐哈盆地实际资料验证 ,效果良好     

Strontium and neodymium isotopic compositions of detrital sediment of NS90-103 from South China Sea: Variations and their paleoclimate implication

Strontium, neodymium isotopic compositions and trace elements of the detrital sediments of Core NS90-103 from South China Sea were analyzed. The results show that the⁸⁷Sr/⁸⁶Sr ratios of the detritus during the last glacial range from 0.722 4 to 0.723 0. They are significantly higher than those during the Holocene and the maximum of the last interglacial, which range from 0.721 0 to 0.721 7. This indicates stronger continental weathering during the last glacial. On the other hand, the¹⁴³Nd/¹⁴⁴Nd ratios of these detritus are higher during the last glacial too, similar to the variation of the⁸⁷Sr/⁸⁶Sr ratios. The trace element geochemistry of these detritus indicates that more authigenic sediments, such as ferromanganese, during the last glacial may partly contribute to the increase of¹⁴³Nd/¹⁴⁴Nd ratios. Furthermore, much more detritus from continent of South China to the north of the South China Sea may probably contribute to¹⁴³Nd/¹⁴⁴Nd ratios increase during the last glacial, which was the result of the enhancement of northeast monsoon.     

Cyclicity in the Main and Upper Zones of the Bushveld Complex, South Africa: Crystallization from a Zoned Magma Sheet

The major element composition of plagioclase, pyroxene, olivine,and magnetite, and whole-rock ⁸⁷Sr/⁸⁶Sr data are presented forthe uppermost 2·1 km of the layered mafic rocks (upperMain Zone and Upper Zone) at Bierkraal in the western BushveldComplex. Initial ⁸⁷Sr/⁸⁶Sr ratios are near-constant (0·7073± 0·0001) for 24 samples and imply crystallizationfrom a homogeneous magma sheet without major magma rechargeor assimilation. The 2125 m thick section investigated in drillcore comprises 26 magnetitite and six nelsonite (magnetite–ilmenite–apatite)layers and changes up-section from gabbronorite (An₇₂ plagioclase;Mg# 74 clinopyroxene) to magnetite–ilmenite–apatite–fayaliteferrodiorite (An₄₃; Mg# 5 clinopyroxene; Fo₁ olivine). The overallfractionation trend is, however, interrupted by reversals characterizedby higher An% of plagioclase, higher Mg# of pyroxene and olivine,and higher V₂O₅ of magnetite. In the upper half of the successionthere is also the intermittent presence of cumulus olivine andapatite. These reversals in normal fractionation trends definethe bases of at least nine major cycles. We have calculateda plausible composition for the magma from which this entiresuccession formed. Forward fractional crystallization modelingof this composition predicts an initial increase in total iron,near-constant SiO₂ and an increasing density of the residualmagma before magnetite crystallizes. After magnetite beginsto crystallize the residual magma shows a near-constant totaliron, an increase in SiO₂ and decrease in density. We explainthe observed cyclicity by bottom crystallization. Initiallymagma stratification developed during crystallization of thebasal gabbronorites. Once magnetite began to crystallize, periodicdensity inversion led to mixing with the overlying magma layer,producing mineralogical breaks between fractionation cycles.The magnetitite and nelsonite layers mainly occur within fractionationcycles, not at their bases. In at least two cases, crystallizationof thick magnetitite layers may have lowered the density ofthe basal layer of melt dramatically, and triggered the proposeddensity inversion, resulting in close, but not perfect, coincidenceof mineralogical breaks and packages of magnetitite layers. KEY WORDS: layered intrusion; mineral chemistry; isotopes; magma; convection; differentiation     

基于GIS的个旧花岗岩凹陷带空间信息成矿预测模型

基于GIS技术,对云南个旧花岗岩凹陷带进行数字矿床空间信息成矿预测模型的研究。在了解个旧矿田地质的基础上,通过工作区信息统计单元的划分、预测区地质信息(包括地层、构造、岩浆岩、矿化蚀变以及物、化、遥异常等)变量的确定以及编码和赋值,采用特征分析法确定空间网格单元成矿异常有利度模型,从成矿预测单元中最终圈定了找矿优选靶区。结果表明了信息统计单元结合特征分析数学方法是可行的。     

Evaporites,brines and base metals: Low‐temperature ore emplacement controlled by evaporite diagenesis

Salt beds and salt allochthons are transient features in most sedimentary basins, which through their dissolution can carry, focus and fix base metals. The mineralisation can be subsalt, intrasalt or suprasalt, and the salt body or its breccia can be bedded or halokinetic. In all these evaporite‐associated low‐temperature diagenetic ore deposits there are four common factors that can be used to recognise suitably prepared ground for mineralisation: (i) a dissolving evaporite bed acts either as a supplier of chloride‐rich basinal brines capable of leaching metals, or as a supplier of sulfur and organics that can fix metals; (ii) where the dissolving bed is acting as a supplier of chloride‐rich brines, there is a suitable nearby source of metals that can be leached by these basinal brines (redbeds, thick shales, volcaniclastics, basalts); (iii) there is a stable redox interface where these metalliferous chloride‐rich waters mix with anoxic waters within a pore‐fluid environment that is rich in organics and sulfate/sulfide/H₂S; and (iv) there is a salt‐induced focusing mechanism that allows for a stable, long‐term maintenance of the redox front, e.g. the underbelly of the salt bed or allochthon (subsalt deposits), dissolution or halokinetically maintained fault activity in the overburden (suprasalt deposits), or a stratabound intrabed evaporite dissolution front (intrasalt deposits). The diagenetic evaporite ‐ base‐metal association includes world‐class Cu deposits, such as the Kupferschiefer‐style Lubin deposits of Poland and the large accumulations in the Dzhezkazgan region of Kazakhstan. The Lubin deposits are subsalt and occur where long‐term dissolution of salt, in conjunction with upwelling metalliferous basin brines, created a stable redox front, now indicated by the facies of the Rote Faule. The Dzhezkazgan deposits (as well as smaller scale Lisbon Valley style deposits) are suprasalt halokinetic features and formed where a dissolving halite‐dominated salt dome maintained a structural focus to a regional redox interface. Halokinesis and dissolution of the salt bed also drove the subsalt circulation system whereby metalliferous saline brines convectively leached underlying sediments. In both scenarios, the resulting redox‐precipitated sulfides are zoned and arranged in the order Cu, Pb, Zn as one moves away from the zone of salt‐solution supplied brines. This redox zonation can be used as a regional pointer to both mineralisation and, more academically, to the position of a former salt bed. In the fault‐fed suprasalt accumulations the feeder faults were typically created and maintained by the jiggling of brittle overburden blocks atop a moving and dissolving salt unit. A similar mechanism localises many of the caprock replacement haloes seen in the diapiric provinces of the Gulf of Mexico and Northern Africa. Evaporite‐associated Pb–Zn deposits, like Cu deposits, are focused by brine flows associated with both bedded and halokinetic salt units or their residues. Stratabound deposits, such as Gays River and Cadjebut, have formed immediately adjacent to or within the bedded salt body, with the bedded sulfate acting as a sulfur source. In allochthon/diapir deposits the Pb–Zn mineralisation can occur both within a caprock or adjacent to the salt structure as replacements of peridiapiric organic‐rich pyritic sediments. In the latter case the conditions of bottom anoxia that allowed the preservation of pyrite were created by the presence of brine springs and seeps fed from the dissolution of nearby salt sheets and diapirs. The deposits in the peridiapiric group tend to be widespread, but individual deposits tend to be relatively small and many are subeconomic. However, their occurrence indicates an active metal‐cycling mechanism in the basin. Given the right association of salt allochthon, tectonics, source substrate and brine ponding, the system can form much less common but world‐class deposits where base‐metal sulfides replaced pyritic laminites at burial depths ranging from centimetres to kilometres. This set of diagenetic brine‐focusing mechanisms are active today beneath the floor of the Atlantis II Deep and are thought to have their ancient counterparts in some Proterozoic sedex deposits. The position of the allochthon, its lateral continuity, and the type of sediment it overlies controls the size of the accumulation and whether it is Cu or Pb–Zn dominated.     

GIS软件在油气长输管道项目矿（产）权确认中的应用

通过在西气东输三线西段（二标段）管道工程项目运用,很好的解决了对矿（产）区、集体用地的矿（产）权确认,为管道经过矿（产）权区确定合理的补偿金额提供科学谈判依据;有效减少了补偿损失;为今后在长输管道穿越矿（产）区、集体用地的补偿提供了测算手段和方法,形成的补偿协议对管道运营单位确定管道权益和维护使用也具有现实意义。     

南海西南海域表层沉积物中微量元素Ba的地球化学特征

分析南海西南海域表层沉积物中微量元素Ba的地球化学特征,并探讨生物成因Ba的分布及其与表层海水生产力的关系。南海西南海域表层沉积物Ba总量的变化范围为398~1 270 μg/g,平均值为851 μg/g,从上陆坡到下陆坡,沉积物中的Ba含量逐渐增加;微量元素Ba主要赋存于陆源碎屑相和生物成因相中,且明显受到沉积环境水深和陆源物质输入的影响。生物成因Ba含量的变化范围为30.6~938 μg/g,陆坡区和深海区平均值分别为495 μg/g、349 μg/g,占沉积物Ba总量的54％和51％,总体上,与沉积物Ba总量具有相对一致的分布特征。尽管研究区表层沉积物中Al、Ti成分为典型的陆源碎屑组分,但是,利用大陆上地壳Ba/Al比值和陆坡区沉积物回归分析获得的Ba/Al比值进行生物成因Ba的计算,过高地估算了沉积物中陆源Ba的含量;而采用页岩Ba/Ti比值来估算陆坡区表层沉积物中的生物成因Ba含量显得相对可靠。在深海区,利用经验的Ba/Al或Ba/Ti比值均不能获得有效的生物成因Ba值。因此,在获取沉积物中生物成因钡含量时,需结合各海区的特点选取合适的参数来扣除陆源Ba的含量。     

综合找矿方法在鄂东南危机矿山接替资源勘查中的应用——以铜绿山、鸡冠咀、大冶铁矿等矿山为例

以鄂东南地区铜绿山矿田内的铜绿山铜铁矿、鸡冠嘴铜金矿、铁山矿田内的大冶铁矿近几年接替资源勘查方法及成果为例,阐述综合找矿方法在不同矿山深部找矿中的应用效果.