山东车镇凹陷东部古近系沙河街组成岩作用   总被引：6，自引：4，他引：6       下载免费PDF全文

李潇丽  田成 《古地理学报》2002,4(4):70-80

车镇凹陷沙河街组的沉积体系受控于盆地内的构造、物源供给以及沉积时的气候环境。以岩石学特征为基础，描述了成岩过程中压实与压溶作用、胶结作用、溶解作用与次生孔隙的特征，以及次生孔隙带在本区的分布。论述了碳酸盐胶结物与粘土矿物胶结作用的特点。粘土矿物蒙脱石-伊利石转变具有明显的渐变与突变交替的演化程式，其演化经历了蒙脱石带、渐变带、迅速转化带和伊利石带以及蒙脱石向伊利石的转变带。沙河街组的成岩作用划分为早期成岩阶段（A期、B期）和晚期成岩阶段（A期、B期、C期），并提出了成岩阶段的划分标志。  相似文献   

泌阳凹陷安棚油田深层系成岩作用研究及其在成岩圈闭预测中的应用   总被引：14，自引：2，他引：14  

金振奎  陈祥  明海慧  周新科  邹元荣  张响响 《沉积学报》2002,20(4):614-620

深层系一般指沉积盆地中埋藏深度在2 500～2 700 m以下的地层,其储集物性普遍很差,但在一定条件下,深部溶蚀作用可产生优质储层,形成成岩圈闭.然而这种成岩圈闭的预测一直是一个难题.安棚油田位于河南泌阳凹陷东南部,勘探成果表明,在该油田深层系下第三系核桃园组核三段下部(简称(核三下)席状的扇三角洲砂体中存在成岩圈闭.本次通过定量的成岩作用研究和成岩阶段划分,对成岩圈闭的形成机理和分布进行了探讨.研究表明,该区核三下的砂体经历了压实、胶结、溶蚀等多种成岩作用,不同的成岩作用发生于不同的埋藏深度.2 700～3 100 m之间以胶结强烈为特征,属于胶结带.3 100～3 900 m之间以次生溶蚀孔隙发育为特征,尤其是3 200～3 600 m之间, 属于深部溶蚀带.本区核三下砂体自南而北埋藏深度逐渐变浅,其上倾方向处于胶结带的部分由于强烈胶结而变成致密层,可封堵油气,而下倾方向处于溶蚀带的部分由于次生溶蚀孔隙发育而成为良好储层,从而形成成岩圈闭.根据不同埋藏深度、不同成岩阶段孔隙发育和保存的特征,可预测成岩圈闭分布。  相似文献   

一种新的储层孔隙成因类型--石英溶解型次生孔隙   总被引：26，自引：2，他引：26  

邱隆伟  姜在兴  陈文学  李晓红  熊志东 《沉积学报》2002,20(4):621-627

石英作为碎屑岩储层中的一种难溶组分,普遍认为它和次生孔隙的形成关系不十分密切。研究认为泌阳凹陷核桃园组储层中的碎屑石英颗粒存在明显的溶解现象,并形成以石英直接溶解型孔隙为主的储集空间特征。石英颗粒被溶解的部分在薄片中所占的范围为 2 %～ 7%者常见,高者达 8%以上,在总孔隙中所占的相对含量也多数在10 %～ 35 %之间,早成岩B期是其最主要形成期。石英溶解型次生孔隙的大量存在为碎屑岩储层中SiO₂ 胶结物及次生孔隙成因等问题的解释以及储层预测和评价提供了新的可能性。  相似文献   

黄河三角洲地区浅层沉积序列及构造沉降特征   总被引：3，自引：0，他引：3  

陈清华  刘池阳  鹿洪友  王冠民  李广雪 《大地构造与成矿学》2002,26(4):386-389

在整个黄河三角洲地区和莱洲湾南岸晚更新世以来经历了海陆相沉积的频繁交替,本文通过古地磁和14C测年资料对不同钻孔的晚更新世地层进行了精确的年代对比,揭示了不同时期的沉积序列。并通过27口钻井的联合对比剖面,揭示出本区晚更新世以来的新构造运动表现为二凹夹一隆的构造特征,对黄河三角洲发育位置和沉降特征有强烈的控制作用。  相似文献   

渤海湾盆地埕岛东斜坡地区东三段油气成岩成藏模式     

操应长  姜在兴 《矿物岩石》2002,22(2):64-68

通过分析埕岛东斜坡地区东三段砂岩成岩作用特征 ,以及对该地区油气成藏系统的研究 ,总结出东三段砂岩体的成岩成藏模式。东三段上部砂体成藏于馆陶组沉积期 ,对应于早成岩 B期阶段 ,油气过早进入砂岩体 ,充填了孔隙 ,抑制了成岩作用的进行 ,使原生孔隙得以良好的保存。目前该砂体位于晚成岩 A期阶段 ,伴随形成了次生孔隙 ,并正处于第二次成藏期  相似文献   

塔里木盆地北部白垩系卡普沙良群储层特征     

余谦  朱忠发  黄慧琼  付清平 《矿物岩石》2002,22(2):74-80

白垩系卡普沙良群是塔里木盆地北部重要的油气储集层位之一，包括亚格列木组层、舒善河组和巴西盖组储集层（有称为卡普沙良群中上部储集层）。从储层岩石学、储层物性、储层孔隙结构及储集性控制因素等方面对储层特征进行了系统分析，总结储层的储集特征。研究结果表明，该储层为砂岩储集岩，储层物性及孔隙结构较好，储集性纵横向上分别受沉积韵律与沉积相带展布的控制，同时还受压实作用、溶蚀作用和胶结作用等成岩作用的控制；并认为亚格列木组储集性较好，横向上以跨越阿克库勒－沙雅西的储集砂体为最好，它具有多套砂体叠置发育的特点。  相似文献   

Facies analysis of the Trypali carbonate unit (Upper Triassic) in central-western Crete (Greece): an evaporite formation transformed into solution-collapse breccias   总被引：1，自引：0，他引：1  

F. Pomoni-Papaioannou  V. Karakitsios 《Sedimentology》2002,49(5):1113-1132

The Trypali carbonate unit (Upper Triassic), which crops out mainly in central‐western Crete, occurs between the parautochthonous series (Plattenkalk or Talea Ori‐Ida series, e.g. metamorphic Ionian series) and the Tripolis nappe (comprising the Tripolis carbonate series and including a basal Phyllite–Quartzite unit). It consists of interbedded dolomitic layers, represented principally by algally laminated peloidal mudstones, foraminiferal, peloidal and ooidal grainstones, as well as by fine‐grained detrital carbonate layers, in which coarse baroque dolomite crystals and dolomite nodules are dispersed. Baroque dolomite is present as pseudomorphs after evaporite crystals (nodules and rosettes), which grew penecontemporaneously by displacement and/or replacement of the host sediments (sabkha diagenesis). However, portions of the evaporites show evidence of resedimentation. Pre‐existing evaporites predominantly consisted of skeletal halite crystals that formed from fragmentation of pyramidal‐shaped hoppers, as well as of anhydrite nodules and rosettes (salt crusts). All microfacies are characteristic of peritidal depositional environments, such as sabkhas, tidal flats, shallow hypersaline lagoons, tidal bars and/or tidal channels. Along most horizons, the Trypali unit is strongly brecciated. These breccias are of solution‐collapse origin, forming after the removal of evaporite beds. Evaporite‐related diagenetic fabrics show that there was extensive dissolution and replacement of pre‐existing evaporites, which resulted in solution‐collapse of the carbonate beds. Evaporite replacement fabrics, including calcitized and silicified evaporite crystals, are present in cements in the carbonate breccias. Brecciation was a multistage process; it started in the Triassic, but was most active in the Tertiary, in association with uplift and ground‐water flow (telogenetic alteration). During late diagenesis, in zones of intense evaporite leaching and brecciation, solution‐collapse breccias were transformed to rauhwackes. The Trypali carbonate breccias (Trypali unit) are lithologically and texturally similar to the Triassic solution‐collapse breccias of the Ionian zone (continental Greece). The evaporites probably represent a major diapiric injection along the base of the parautochthonous series (metamorphic Ionian series) and also along the overthrust surface separating the parautochthonous series from the Tripolis nappe (Phyllite–Quartzite and Tripolis series). The injected evaporites were subsequently transformed into solution‐collapse breccias.  相似文献   

Timanian orogenic deformation along the northeastern margin of Baltica, Northwest Russia and Northeast Norway, and Avalonian–Cadomian connections     

D. Roberts  A. Siedlecka 《Tectonophysics》2002,352(1-2)

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Isothermal annealing of partially metamict zircon: evidence for a three-stage recovery process     

T. Geisler 《Physics and Chemistry of Minerals》2002,29(6):420-429

 Raman spectroscopy and the powder diffraction technique have been used to monitor the recovery process of two partially metamict zircons (2.6 and 4.8 × 10¹⁸ α-decays g⁻¹) from Sri Lanka during a series of isothermal annealing experiments in the temperature range from 870 to 1622 K. These experiments show for the first time that structural recovery in partially metamict zircon proceeds via three distinct recovery stages, each of which occurs within a distinct time-temperature regime. Whereas the first two stages have previously been recognized (recovery of damaged crystalline remnants and epitaxial recrystallization), the third stage has not yet been identified as a single activated process. It is suggested that anisotropic defect annealing during the first stage at low temperatures, where the structure recovers preferentially along the a(b) plane, produces a geometrical situation where large structural rearrangements are necessary to remove the remaining defects inside the crystalline material. This situation is approximately reached when the amorphous domains start to recrystallize. The reason for anisotropic annealing can be found in a different connectivity between polyhedral linkages in both directions of the zircon lattice. High apparent activation energies, in the range of 6.4 to 7.9 eV, were determined for the third recovery stage from the Raman data, which are interpreted to reflect large structural rearrangements (i.e. polyhedral tilting) associated with the final recovery of the c axis. This explains the occurrence of a distinct recrystallization stage without defect annealing. Finally, it should be mentioned that the first recovery stage is not necessarily expected to occur in less damaged zircon crystals (<∼2 × 10¹⁸ α-decays g⁻¹), since less stable defects along the basal plane might have already been self-annealed during radiation damage accumulation under ambient temperatures. Received: 6 September 2001 / Accepted: 25 February 2002  相似文献   

Celestite formation, bacterial sulphate reduction and carbonate cementation of Eocene reefs and basinal sediments (Igualada, NE Spain)   总被引：5，自引：0，他引：5  

Conxita Taberner  James D. Marshall†  James P. Hendry‡  Catherine Pierre§  & M. F. Thirlwall¶ 《Sedimentology》2002,49(1):171-190

Petrographic and geochemical studies of an Upper Eocene reef and associated basinal sediments from the mixed carbonate–siliciclastic fill of the south‐eastern Pyrenean foreland basin near Igualada (NE Spain) provide new insights into the evolution of subsurface hydrology during the restriction of a marine basin. The reef deposits are located on delta‐lobe sandstones and prodelta marls, which are overlain by hypersaline carbonates and Upper Eocene evaporites. Authigenic celestite (SrSO₄) is an important component in the observed diagenetic sequences. Celestite is a significant palaeohydrological indicator because its low solubility constrains transportation of Sr²⁺ and SO₄^2? in the same diagenetic fluid. Stable isotopic analyses of carbonates in the reef indicate that meteoric recharge was responsible for aragonite stabilization and calcite cementation. Sulphur and oxygen isotope geochemistry of the celestite demonstrates that it formed from residual sulphate after bacterial sulphate reduction, but also requires that there was a prior episode of sulphate recycling. Meteoric water reaching the reef and basinal areas was most probably charged with SO₄^2? from the dissolution of younger Upper Eocene marine evaporites. This sulphate, combined with organic matter present in the sediments, fuelled bacterial sulphate reduction in the meteoric palaeoaquifer. Strontium for celestite precipitation was partly derived in situ from dissolution of aragonite corals in the reef and basinal counterparts. However, ⁸⁷Sr/⁸⁶Sr data also suggest that Sr²⁺ was partly derived from dissolution of overlying evaporites. Mixing of these two fluids promoted celestite formation. The carbonate stable isotopic data suggest that the local meteoric water was enriched in ¹⁸O compared with that responsible for stabilization of other reefs along the basin margin. Furthermore, meteoric recharge at Igualada post‐dated evaporite deposition in the basin, whereas other parts of the same reef complex were stabilized before evaporite formation. This discrepancy resulted from the spatial distribution of continental siliciclastic units that acted as groundwater conduits.  相似文献