贵州梵净山前寒武系甚低级变质作用研究

本文运用伊利石结晶度、绿泥石结晶度、云母b0值和绿泥石地质温度计研究了梵净山前寒武系甚低级变质作用。结果表明经Kisch伊利石结晶度标样校正的伊利石结晶度Kübler指数为0.20~0.99°Δ2θ,绿泥石结晶度árkai指数为0.22~0.63°Δ2θ。由此阐明梵净山前寒武系经历了成岩作用到浅变质作用的影响,迄今依然保留了成岩带、近变质带和浅变质带的岩石记录。成岩岩石具有伊蒙混层特征成岩指示矿物,浅变质带具有钠云母特征变质指示矿物。钾云母(伊利石)b0值范围为:0.9000~0.9045nm;平均0.9018nm,b0值累积频率曲线分布介于典型中压—中低压系列之间,估算的压力为366MPa。峰期变质温度为293~364℃,平均342℃,古变质温压梯度为27℃/km。近变质带界线穿越地层和梵净山背斜轴线,表明甚低级变质作用为成岩-构造运动同期或后期构造增厚引起下部和底部岩石随温压的升高而产生的。     

An Overview of Dissolved and Suspended Matter Fluxes in the Loire River Basin: Natural and Anthropogenic Inputs

The spatial and temporal distributions of major elements were investigated in the surface waters and in associated suspended matter at two sites of the upper Loire basin (Orleans and Brehemont) between 1995 and 1998.According to geochemical and isotopic patterns, the dissolved load appears to result from a process of mixing rainwater inputs, weathering processes of carbonate and silicate bedrock, and agricultural and urban inputs. Natural inputs influence 60% of water chemical composition at both sites. Annual dissolved fluxes were estimated to be 1300 10³ t/y at Orleans and 1620 10³ t/y at Brehemont. Major elements are transported mainly in the dissolved fraction. After correcting for atmospheric and anthropogenic inputs, the silicate specific export rate was calculated to be 11 t/y/km² throughout the basin and the carbonate specific export rate to be from 47 t/y/km² at Orleans to 23 t/y/km² at Brehemont.The suspended load appears to result from at least two particle reservoirs: a silicate reservoir and a carbonate reservoir. The silicate reservoir has a detrital origin, mainly during periods of high flow, while the carbonate reservoir has a detrital origin during periods of high flow and an authigenic origin during periods of low flow. Of the total annual flow of suspended matter, this authigenic material represents 16% at Orleans, 25% at Brehemont and 37% in the fluvial part of the estuary. After correcting authigenic inputs, the specific export rate due to mechanical weathering was estimated to be 8 t/y/km² throughout the Loire basin.     

鄂尔多斯盆地渭北地区上三叠统延长组长7油层组碳酸盐结核中自生碳酸盐矿物的特征

早期形成的碳酸盐结核在埋藏期间会经历多种碳酸盐矿物相沉淀的复杂胶结作用,岩石学研究是探究结核成因的关键。通过野外剖面观察、岩石学观察和阴极发光技术,分析了鄂尔多斯盆地渭北地区上三叠统延长组长7油层组泥页岩中各种形状的方解石和白云石结核中自生碳酸盐矿物的特征。这些结核为成岩早期的产物,构成结核的自生碳酸盐矿物特征显著:(1)球粒方解石结核中,方解石呈纤维状或刃片状,球粒间充填晶粒方解石或因压实呈贴面结合,纤维状方解石发桔红色和暗红色2种光,刃片状方解石发暗红色光;(2)粉晶方解石结核中,方解石呈他形粒状,含有机质包裹体或纤维状晶形残余,晶间含沥青和纤维状方解石残余,主要发暗红色光;(3)白云石结核有泥晶和粉晶2种晶体类型,粉晶白云石结核含较多泥质,泥质条带或有机质条带处常见纤柱状白云石;(4)沿裂缝充填的方解石和白云石常呈纤维状或纤柱状结构,发暗红色光或不发光。研究区长7油层组碳酸盐结核中的方解石和白云石具有不同的成因类型和复杂的胶结作用:球粒方解石和泥晶白云石代表了结核开始形成时的胶结作用,可以准确地反映结核的成因;粉晶方解石、粉晶白云石反映了交代成因;裂缝中纤维状、纤柱状方解石和白云石集合体则为结核经历了较强压实作用之后充填裂缝而成。     

合肥盆地钻井地层的同位素测年与地层划分

合肥盆地内部中、新界地层大面积被第四系覆盖，其地层的时代与划分主要依赖已有的6口深井地层资料。由于缺乏可靠的化石记录，这6口深井地层时代与划分一直存在着很大的分歧，制约了对该盆地的油气勘探与远景评价。本文利用这6口深井泥岩类岩屑中自生伊利石，在其结晶度分析基础上，进行了K-Ar同位素测年，成功地获得了不同深度上的地层形成时代。据此地层年龄，文中对这6口深井所钻遇的地层进行了重新的划分。     

鄂尔多斯盆地纳岭沟铀矿床绿泥石特征及地质意义

纳岭沟铀矿床位于鄂尔多斯盆地北部,具有明显的后期热液作用的特征,矿体空间展布主要受控于绿色-灰色砂岩的过渡界面,与绿泥石化的蚀变砂岩关系密切。通过对纳岭沟铀矿床不同颜色砂岩中的绿泥石进行详细的岩相学研究和电子探针化学成分分析,依据绿泥石的成因与共生矿物的关系,识别出绿泥石主要的3种类型:填隙物型绿泥石,片状与黄铁矿共生型绿泥石以及黑云母蚀变型绿泥石;同时通过绿泥石的Fe-Si图解确定了纳岭沟铀矿床不同颜色砂岩中的绿泥石主要为铁镁绿泥石和密绿泥石。根据Al/(Fe+Mg+Al)-Mg/(Fe+Mg)的关系图解确定出不同颜色砂岩中的绿泥石具有铁镁质流体和泥质两种来源,通过绿泥石中主要阳离子与镁的关系图解和计算得出的绿泥石形成温度共同确定出绿泥石是多期次的中低温热液流体作用的产物。综合研究表明,纳岭沟铀矿床的绿泥石形成至少经历了温度稍高的还原性流体和温度稍低的氧化性流体等两个期次的流体作用,稍高温的还原性流体与成矿关系更为重要。与绿泥石形成有关的热液流体作用不仅带入了部分铀,还促进了铀的活化和运移。     

甘肃龙首山碱交代型铀矿床绿泥石特征及意义

绿泥石化是龙首山铀矿床重要的蚀变类型之一。通过对龙首山碱交代型铀矿床的绿泥石等蚀变矿物进行的岩相学和电子探针成分分析研究,确定了龙首山地区绿泥石的化学类型主要为铁镁绿泥石,少数为蠕绿泥石。依据绿泥石成因或与共生矿物的关系,绿泥石可被划分为黑云母蚀变型、长石蚀变型、沥青铀矿共生型和副矿物共生型等4种类型。泥质岩是本区绿泥石的主要原岩类型,是多期次地质作用形成的产物。研究认为,龙首山地区碱交代型铀矿床的成矿过程可表述为矿前期在相对较高温度的热液流体作用下,黑云母发生绿泥石化蚀变,随后热液继续交代长石,形成长石蚀变型绿泥石,进而在成矿期热液温度相对较低的条件下形成与沥青铀矿紧密共生的绿泥石。绿泥石在铀成矿过程中不但活化了花岗岩里的铀,而且还给铀矿化供应了相对良好的积淀环境。     

粤东新寮岽铜多金属矿床绿泥石特征及其地质意义

新寮岽铜多金属矿是近年来在粤东地区新发现的一个铜矿床,在该矿区绿泥石化十分强烈,并与铜矿化关系密切。按照矿物共生组合关系,矿区绿泥石可分为与硫化物共(伴)生及未与硫化物共(伴)生呈单独产出两类,两类绿泥石主要呈叶片状、纤维状、蠕虫集合体状等形态产出。本文在岩矿鉴定的基础上,以矿区绿泥石为研究对象,利用电子探针技术,对其微区化学成分进行了研究。结果表明：随着孔深的增加,与矿化有关绿泥石的Si和Mg元素含量逐渐升高,Al、Fe、Mn元素含量逐渐降低,而与矿化无关的绿泥石成分变化规律不明显。两类绿泥石主要为富铁种属的蠕绿泥石、铁镁绿泥石;绿泥石为泥质岩或者铁镁质岩受热液交代蚀变的产物,绿泥石结构的离子置换主要体现为Fe对Mg的置换,反映其可能形成于富铁及相对酸性环境;由绿泥石地质温度计估算得出两类绿泥石形成温度为166.32～245.62℃,平均为219.15℃,且与硫化物共(伴)生的绿泥石的形成温度相对较高,但两者均属中-低温范围。绿泥石的形成机制主要表现为溶蚀-结晶和溶蚀-迁移-沉淀结晶2种。     

低温绿泥石成分温度计Fe/(Fe+Mg)校正的必要性问题

绿泥石是沉积岩、低级变质岩和水热蚀变岩中的常见矿物,基于四次配位Al含量的绿泥石成分温度计是确定古成岩或变质温度的最主要的手段之一。介绍了四种应用最为广泛的绿泥石成分温度计的原理,并从离子替代规律和比较研究的角度着重讨论了近年来关于绿泥石成分温度计校正的必要性。研究表明,在铝饱和的条件下,根据绿泥石中的Fe/(Fe Mg)值对绿泥石温度计进行校正并不能使计算值与实际值更为接近,而且从晶体化学的角度看,全岩的Fe/(Fe Mg)主要影响的是绿泥石中六次配位Fe与Mg的占位,而且偶合置换(Si4 )Ⅳ(Mg2 )Ⅵ—(Al3 )Ⅳ(Al3 )Ⅵ和(Si4 )Ⅳ(Fe2 )Ⅵ—(Al3 )Ⅳ(Al3 )Ⅵ共同控制着四次配位Al的占位。所以在铝饱和的岩石体系中可不必进行Fe/(Fe Mg)值的校正。     

绿泥石片岩各向异性特性研究

为研究十堰地区片岩的各向异性特性,开展了武当群绿泥石片岩长方体试样的单轴压缩和圆盘试样的间接拉伸试验,探讨了试样各向异性的力学特性和在不同受力状态下的变形破裂特性,揭示了不同变形破裂的力学机制。研究表明,武当群绿泥石片岩具有明显的各向异性性质,平行片理方向强度高,垂直片理方向强度低。该片岩特殊的定向排列片束状构造和片理间的弱胶结作用,致使不同方向上的破坏特征具有明显差异,其力学机制也不相同。在压应力作用下,泊松效应容易引起平行片理面的张拉劈裂和压杆失稳,垂直片理方向容易发生片理面间的剪切破坏。在同一方向上强度具有一致性,即平行片理面抗压和抗拉强度均较垂直片理面强度大。由于片理面间的抗拉承载力极低,在小角度劈裂荷载下,容易发生张拉劈裂和拉剪破坏,因此,实际工程中应尽可能避免片理面间的受拉破坏和沿片理的拉剪破坏。研究结果可以为隧道、边坡支护加固和防水处理提供参考。     

Petrographic and mineralogical study of hydrothermal alteration of the Rokko Granite at Hakusui-kyo and Horai-kyo along the Arima-Takatsuki Tectonic Line in western Japan

Field, hand specimen, and microscopic investigations alongside X-ray diffraction analyses revealed four types of hydrothermal alteration (Type-A, -B, -C, and -D) based on the mode of occurrence of altered rocks and alteration mineral assemblage at Hakusui-kyo and Horai-kyo along the Arima-Takatsuki Tectonic Line (ATTL) in western Japan. Type-A alteration locally occurred as gray alteration halos with sulfide minerals. Type-B and -C alterations were confined to fault gouge veins and occurred as greenish-gray veins and brown veins, respectively. Type-C alteration crosscut Type-B alteration. These alterations were associated with a number of granitic fragments including cohesive breccia and micrographic facies. Type-D alteration occurred locally in brown sediments. Different mineralogical features in the four alterations are summarized as (Type-A) illite; (Type-B) chlorite; (Type-C) limonite (Fe³⁺ hydroxides and goethite) and calcite; and (Type-D) limonite. We propose that the alterations can be broadly divided into Paleocene hydrothermal alteration (Type-A) and post-Late Miocene hydrothermal alteration (Type-B, -C, and -D): Type-A alteration occurred at approximately 200 °C during hydrothermal activity after a granitic intrusion in Late Cretaceous; Type-B, -C and -D alterations occurred under hydrothermal activity accompanying deep fluids with repeated ascents invoked by the seismicity of the ATTL after the Late Miocene. The fluids may have been the “Arima-type thermal waters” (i.e., mixtures of convective groundwater and Na-Ca-Cl-HCO₃-type fluids). Type-B alteration occurred in fractures at depths where the temperature was ≥150 °C. Type-C alteration overprinted Type-B alteration as a result of mixing of new deep fluids and descending oxidized meteoric water near the surface. Fe³⁺ hydroxides and calcite precipitated from the fluids due to the oxidation of Fe²⁺ and the degassing of CO₂, respectively, at ambient to near-boiling temperatures. When the ascending fluids gushed out from the fractures, they generated Type-D alteration at the surface under similar temperature conditions due to the oxidation of Fe²⁺.