蓟县中、新元古界的成岩作用——源于矿物学的数据

本文运用系列黏土矿物学和碳酸盐结构占位的方法研究了蓟县中、新元古界剖面出露的碎屑岩和碳酸盐岩。这些方法包括了伊利石结晶度、绿泥石结晶度、黏土矿物组合、粒度分布、多型、有序度、Mg/Ca离子占位以及地质温压计。结果表明:伊利石结晶度Kübler指数范围为0.37°～1.37°Δ2θ,绿泥石结晶度árkai指数范围为0.31°～2.40°Δ2θ,以及1M_d的多型,一致指示本区处于晚期成岩作用影响范围,仅非常有限局部达到了初始变质的状态;黏土矿物组合主要是伊利石、伊蒙混层、绿蒙混层和高岭石;粒度分布范围为8～24 nm,其上界(23～24 nm)达到了NEWMOD计算的理论成岩带/近变质带界限,与结晶度数据一致,也表明了本区处于晚期成岩阶段。白云石有序度的数据表明,本区碳酸盐岩白云石的有序度值范围为0.19～0.99,可分为4个带:甚低级有序带、低级有序带、中级有序带、高级有序带。与川东石炭-二叠系碳酸盐岩相比,中低级有序带有一定的油气前景。本区由西向东,由甚低级有序带变化到高级有序带,白云石有序度升高。估计的成岩作用温度为183～200±20℃,压力为330 MPa,...     

碎屑岩自生粘土矿物的沉淀作用及其对储层的影响——以川西坳陷上三叠统须家河组砂岩为例

粘土矿物是影响碎屑岩储层物性的重要因素.本文以川西坳陷孝泉-新场-合兴场地区上三叠统须家河组砂岩为例,应用铸体薄片、普通薄片、X射线衍射分析和扫描电镜分析,研究了在成岩过程中自生粘土矿物的沉淀作用及其对储层的影响.结果表明自生绿泥石对储层原生孔隙的保存和次生孔隙的发育有利,自生高岭石的含量反映了次生孔隙的发育程度,而伊利石对储层的影响是负面的.     

琉球群岛以东海区沉积物重矿物分布及来源

琉球群岛东部海区沉积物中富含大量火山碎屑矿物、岛屿岩石遭受风化蚀变形成的普通角闪石以及水生的铁锰微结核,其重矿物种类、特征、组合分区等与火山作用、沉积环境、地形、物质来源等内外生因素密切相关。通过对本区重矿物的种类、特征及组合分区的研究,初步判断位于研究区北部、菲律宾板块向欧亚大陆俯冲而导致的正在活动的的琉球岛弧区为火山碎屑的主要源区,重矿物成分主要为水携成因来源,受同期火山作用控制;少量紫苏辉石来自先期形成的海岭或海底高原(如冲大东海岭、奄美海岭及九州海岭等)上的火山岩系,是经过剥蚀、搬运再沉积的产物;琉球群岛、九州等火山活动产物受海底高地等阻隔而在本区表现为向南或东南影响力逐渐减小;本区地质历史上的及正在进行的岩浆活动主要以基性及中性岩浆为主。此外,流经本区的黑潮对自生铁锰微结核的富集具有重要影响。     

粤北青嶂山岩体江头矿区铀矿微区矿物学、年代学特征及其成矿动力背景制约

粤北诸广和贵东是华南最重要的两个花岗型铀矿密集区,青嶂山(龙源坝)岩体位于两者之间,是华南花岗岩型铀矿研究薄弱地区。江头铀矿区地处青嶂山岩体北部与南雄断陷盆地的结合部位,该矿区的铀成矿年代学研究几为空白。本文通过电子探针方法研究了青嶂山岩体、及与该岩体密切相关的江头矿区中的铀矿物微区矿物学特征,获得岩浆成因的晶质铀矿与热液成因的沥青铀矿的U-Th-Pb化学年龄,探讨了华南铀成矿作用动力学背景及成矿地质体。研究表明:青嶂山岩体粗粒斑状黑云母花岗岩和中粒斑状黑云母花岗岩中的铀矿物主要有晶质铀矿、铀石,部分晶质铀矿存在明显铀释放的特征,其晶质铀矿化学年龄分别为246.8±8.8Ma、161.5±8.0Ma,与前人获得的锆石U-Pb年龄结果在误差范围内一致,分别代表了区内印支期与燕山期花岗岩体的成岩年龄,表明在南雄断陷盆地形成之前,青嶂山岩体与诸广岩体可能为一有机整体,有着相同的成岩、成矿环境。江头矿区矿石中铀矿物主要为沥青铀矿,伴有少量钛铀矿、铀石等,沥青铀矿化学年龄分别为121.3±9.8Ma、98.8±8.0Ma、73.2±8.8Ma,分别代表区内3期铀成矿作用的时代,结合华南中生代以来...     

Mineralogy and Isotope Geochemistry of Active Submarine Hydrothermal Field at Suiyo Seamount, Izu–Bonin Arc, West Pacific Ocean

This report presents mineralogical, geochemical and isotopic data on samples obtained using the Benthic Multi‐coring System (BMS) to drill a submarine hydrothermal deposit developed in a caldera on the summit of the Suiyo Seamount in the Izu–Bonin Island Arc, south of Japan. This deposit is regarded as the first example of Kuroko‐type sulfide mineralization on a volcano at the volcanic front of an island arc. The mineralization and hydrothermal alteration below the 300 × 150‐m area of active venting was investigated to depths of 2–9 m below the sea floor. Drilling beneath the area of active venting recovered a sequence of altered volcanic rocks (dacite lavas, pyroclastic rocks of dacite–rhyolite compositions and pumice) associated with sulfide veining and patches/veins of anhydrite. No massive sulfide was found, however, and the subsea‐floor mineralization to 10 m depth is dominated by anhydrite and clay minerals with some sulfides. Sulfide‐bearing samples contained high Au (up to 42 ppm), Ag (up to 263 ppm), As (up to 1550 ppm), Hg (up to 55 ppm), Sb (up to 772 ppm), and Se (up to 24 ppm). Electron probe microanalyzer indicated that realgar, orpiment, and mimetite were major As‐bearing minerals. The sulfides were also characterized by high Zn (>10%) compared to Cu (<6.3%) and Pb (<0.6%). The δ²⁰²Hg/¹⁹⁸Hg, δ²⁰²Hg/¹⁹⁹Hg and δ²⁰²Hg/²⁰⁰Hg of the sulfide‐bearing dacite samples and a sulfide chimney decreased with increasing Hg/Zn concentration ratio. The variation of the δ²⁰²Hg/¹⁹⁸Hg ranged from ?2.8 to +0.5‰ to relative to S‐HG02027. The large range of these δ²⁰²Hg/¹⁹⁸Hg was greater than might be expected for such a heavy element and may be due to a predominance of kinetic effects. The variation of δ²⁰²Hg/¹⁹⁸Hg of sulfide‐bearing dacite samples suggested that light Hg isotope in the vapor mixed with oxygenated seawater near sea floor during mineralization. Lead isotope ratios of the sulfide were very similar to those of the dacite lava, suggesting that lead is of magmatic origin. The ⁸⁷Sr/⁸⁶Sr ratio (0.70872) of anhydrite was different from that of the dacite lava, and suggests an Sr derivation predominantly from seawater. Hydrothermal alteration of the dacite in the Suiyo hydrothermal field was characterized by Fe‐sulfides, anhydrite, barite, montmorillonite, chlorite/montmorillonite mixed‐layer minerals, mica, and chlorite with little or no feldspar or cristobalite. Hydrothermal clay minerals changed with depth from montmorillonite to chlorite/montmorillonite mixed‐layer minerals to chlorite and mica. Hydrogen isotope ratios of chlorite/montmorillonite and mixed‐layer, mica‐chlorite composites obtained below the active venting sites ranged from ?49 to ?24‰, suggesting seawater as the dominant fluid causing alteration. Oxygen isotope ratios of anhydrite ranged from 9.2 to 10.4‰ and anhydrite formation temperatures were calculated to be 188–207°C. Oxygen isotope ratios ranged from +5.2 to +9.2‰ for montmorillonite, +3.2 to +4.5‰ for chlorite/montmorillonite mixed‐layer minerals, and +2.8 to +3.8‰ in mixtures of chlorite and mica. The formation temperatures of montmorillonite and of the chlorite–mica mixture were 160–250°C and 230–270°C, respectively. The isotope temperatures for clay minerals (220–270°C) and anhydrite (188°C) were significantly lower than the borehole temperature (308.3°C) measured just after the drilling, suggesting that temperature at this site is now higher than when clay minerals and anhydrite were formed.     

Environmental effect and genetic influence: a regional cancer predisposition survey in the Zonguldak region of Northwest Turkey

The Cretaceous-Eocene volcano-sedimentary units of the Zonguldak region of the western Black Sea consist of subalkaline andesite and tuff, and sandstone dominated by smectite, kaolinite, accessory chlorite, illite, mordenite, and analcime associated with feldspar, quartz, opal-CT, amphibole, and calcite. Kaolinization, chloritization, sericitization, albitization, Fe–Ti-oxidation, and the presence of zeolite, epidote, and illite in andesitic rocks and tuffaceous materials developed as a result of the degradation of a glass shards matrix, enclosed feldspar, and clinopyroxene-type phenocrysts, due to alteration processes. The association of feldspar and glass with smectite and kaolinite, and the suborientation of feldspar-edged, subparallel kaolinite plates to fracture axes may exhibit an authigenic smectite or kaolinite. Increased alteration degree upward in which Al, Fe, and Ti are gained, and Si, Na, K, and Ca are depleted, is due to the alteration following possible diagenesis and hydrothermal activities. Micromorphologically, fibrous mordenite in the altered units and the presence of needle-type chrysotile in the residential buildings in which cancer cases lived were detected. In addition, the segregation pattern of cancer susceptibility in the region strongly suggested an environmental effect and a genetic influence on the increased cancer incidence in the region. The most likely diagnosis was Li-Fraumeni syndrome, which is one of the hereditary cancer predisposition syndromes; however, no mutations were observed in the p53 gene, which is the major cause of Li-Fraumeni syndrome. The micromorphology observed in the altered units in which cancer cases were detected may have a role in the expression of an unidentified gene, but does not explain alone the occurrence of cancer as a primary cause in the region.     

Oxidized and reduced mineral assemblages in greenstone belt rocks of the St. Ives gold camp, Western Australia: vectors to high-grade ore bodies in Archaean gold deposits?

Hydrothermal sulfide–oxide–gold mineral assemblages in gold deposits in the Archaean St. Ives gold camp in Western Australia indicate extremely variable redox conditions during hydrothermal alteration and gold mineralization in space and time. Reduced alteration assemblages (pyrrhotite–pyrite) occur in deposits in the southwest of the camp (e.g., Argo, Junction deposits) and moderately to strongly oxidized assemblages (magnetite–pyrite, hematite–pyrite) occur in deposits in the Central Corridor in the northeast (e.g., North Orchin, Revenge deposits). Reduced mineral assemblages flank the Central Corridor of oxidized deposits and, locally, cut across it along E–W trending faults. Oxidized mineral assemblages in the Central Corridor are focused on gravity lows which are interpreted to reflect abundant felsic porphyritic intrusions at about 1,000 m below present surface. Hydrothermal magnetite predates and is synchronous with early phases of gold-associated albite–carbonate–pyrite–biotite–chlorite hydrothermal alteration. Later-stage, gold-associated pyrite is in equilibrium with hematite. The spatial distribution and temporal sequence of iron sulfides and oxides with gold indicate the presence of at least two spatially restricted but broadly synchronous hydrothermal fluids with contrasting redox states. Sulfur isotope constraints support the argument that the different mineral assemblages reflect differences in redox conditions. The δ ³⁴S values for pyrite for the St. Ives gold camp range between −8.4‰ and +5.1‰ with the negative values occurring in oxidized magnetite-rich domains and slightly negative or positive values occurring in reduced, pyrrhotitic domains. Preliminary spatial and paragenetic analysis of the distribution of iron sulfides and oxides in the St. Ives camp suggests that gold grades are highest where the redox state of the hydrothermal alteration assemblages switches from relatively reduced pyrrhotite–pyrite to relatively oxidized magnetite–pyrite and hematite–pyrite both in space and time. Gold deposition is inferred to have occurred where fluids of contrasting redox state mixed.     

Platinum-group minerals from the Jinbaoshan Pd–Pt deposit,SW China: evidence for magmatic origin and hydrothermal alteration

The Jinbaoshan Pt–Pd deposit in Yunnan, SW China, is hosted in a wehrlite body, which is a member of the Permian (∼260 Ma) Emeishan Large Igneous Province (ELIP). The deposit is reported to contain one million tonnes of Pt–Pd ore grading 0.21% Ni and 0.16% Cu with 3.0 g/t (Pd + Pt). Platinum-group minerals (PGM) mostly are ∼10 μm in diameter, and are commonly Te-, Sn- and As-bearing, including moncheite (PtTe₂), atokite (Pd₃Sn), kotulskite (PdTe), sperrylite (PtAs₂), irarsite (IrAsS), cooperite (PtS), sudburyite (PdSb), and Pt–Fe alloy. Primary rock-forming minerals are olivine and clinopyroxene, with clinopyroxene forming anhedral poikilitic crystals surrounding olivine. Primary chromite occurs either as euhedral grains enclosed within olivine or as an interstitial phase to the olivine. However, the intrusion has undergone extensive hydrothermal alteration. Most olivine grains have been altered to serpentine, and interstitial clinopyroxene is often altered to actinolite/tremolite and locally biotite. Interstitial chromite grains are either partially or totally replaced by secondary magnetite. Base-metal sulfides (BMS), such as pentlandite and chalcopyrite, are usually interstitial to the altered olivine. PGM are located with the BMS and are therefore also interstitial to the serpentinized olivine grains, occurring within altered interstitial clinopyroxene and chromite, or along the edges of these minerals, which predominantly altered to actinolite/tremolite, serpentine and magnetite. Hydrothermal fluids were responsible for the release of the platinum-group elements (PGE) from the BMS to precipitate the PGM at low temperature during pervasive alteration. A sequence of alteration of the PGM has been recognized. Initially moncheite and atokite have been corroded and recrystallized during the formation of actinolite/tremolite, and then, cooperite and moncheite were altered to Pt–Fe alloy where they are in contact with serpentine. Sudburyite occurs in veins indicating late Pd mobility. However, textural evidence shows that the PGM are still in close proximity to the BMS. They occur in PGE-rich layers located at specific igneous horizons in the intrusion, suggesting that PGE were originally magmatic concentrations that, within a PGE-rich horizon, crystallized with BMS late in the olivine/clinopyroxene crystallization sequence and have not been significantly transported during serpentinization and alteration.     

Typomorpic Characteristics of the Major Minerals in the Puziwan Gold Deposit, Datong, Shanxi, China

Utilizing theories of minerageny and prospecting mineralogy, the authors studied the attitude, morphotype and chemical composition of metallic minerals of pyrite, gold, chalcopyrite, galena and sphalerite, non-metallic minerals of quartz, carbonate, dolomite and rutile in the Puziwan gold deposit. The study shows the following results. （1） The mineral assemblage is complex and the species of sulfide are abundant with occurrences of sulfosalt minerals. （2） The composition in the minerals is complex and there rich micro elements, including As, Sb, Bi, Se, Te, Au, Ag, Cu, Pb, Zn, and Cr, Ni, V. The typomorphic characteristics of the association of the elements and their specific value suggest that gold mineralization is associated with shallow magmatic hydrothermal activity, the oreforming fluid is the mixture of abundant rising alkali magmatic water originating from the mantle or the lower crust and the descending acid atmospheric water. （3） Ankerite, Fe-rich sphalerite, granular Ti-rich rutile are widely distributed, which indicate great denudation depths, high mineralization temperature. The deposit is found in the middle and shallow positions of the porphyry series. The deep layers are not favorable for gold mineralization. （4） Copper minerals are rich in the ores and sulfides have high content of copper, suggesting possible porphyry-type Cu （Au） mineralization in deep positions and the surrounding areas.