显式自由表面模型时间分裂格式的一个积分方案

讨论了有关显式自由表面模型的时间分裂格式中的分裂误差。在传统的积分方案中，由于采用蛙跳格式，斜压动量方程具有三层的时间离散结构，但是，正压动量方程在相应的时间层上只有二层的离散结构。因此，正压方程与斜压方程的时间离散结构是不相容的。分析结果表明，这是导致分裂误差的原因。本提出一种能保持时间离散结构相容的正压和斜压方程的时间积分方案。该积分方案的分裂误差很小因此特别适合于需要长期积分的气候研究。该方案在北太平洋的一个自由表面模型中得到了应用。     

Electrical aerosol spectrometer of Tartu University

The electrical aerosol spectrometer (EAS) of the parallel measuring principle at Tartu University is an efficient instrument for rapid measurement of the unstable size spectrum of aerosol particles. The measuring range from 10 nm to 10 μm is achieved by simultaneously using a pair of differential mobility analyzers with two different particle chargers. The particle spectrum is calculated and measurement errors are estimated in real time by using a least-squares method. Experimental calibration ensures reliability of measurement. The instrument is well suited for continuous monitoring of atmospheric aerosol.     

山东车镇凹陷东部古近系沙河街组成岩作用

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。     

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

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。     

一种新的储层孔隙成因类型--石英溶解型次生孔隙

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。     

Study on effects of damping in laminated rubber bearings on seismic responses for a ⅛ scale isolated test structure

The effects of damping in various laminated rubber bearings (LRB) on the seismic response of a ?‐scale isolated test structure are investigated by shaking table tests and seismic response analyses. A series of shaking table tests of the structure were performed for a fixed base design and for a base isolation design. Two different types of LRB were used: natural rubber bearings (NRB) and lead rubber bearings (LLRB). Three different designs for the LLRB were tested; each design had a different diameter of lead plug, and thus, different damping values. Artificial time histories of peak ground acceleration 0.4g were used in both the tests and the analyses. In both shaking table tests and analyses, as expected, the acceleration responses of the seismically isolated test structure were considerably reduced. However, the shear displacement at the isolators was increased. To reduce the shear displacement in the isolators, the diameter of the lead plug in the LLRB had to be enlarged to increase isolator damping by more than 24%. This caused the isolator stiffness to increase, and resulted in amplifying the floor acceleration response spectra of the isolated test structure in the higher frequency ranges with a monotonic reduction of isolator shear displacement. Copyright © 2002 John Wiley & Sons, Ltd.     

渤海湾盆地埕岛东斜坡地区东三段油气成岩成藏模式

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     

Facies analysis of the Trypali carbonate unit (Upper Triassic) in central-western Crete (Greece): an evaporite formation transformed into solution-collapse breccias

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.     

Numerical Analysis of Space–Time Finite Element Formulations for Miscible Displacements

A finite element formulation is proposed to approximate a nonlinear system of partial differential equations, composed by an elliptic subsystem for the pressure–velocity and a transport equation (convection–diffusion) for the concentration, which models the incompressible miscible displacement of one fluid by another in a rigid porous media. The pressure is approximated by the classical Galerkin method and the velocity is calculated by a post-processing technique. Then, the concentration is obtained by a Galerkin/least-squares space–time (GLS/ST) finite element method. A numerical analysis is developed for the concentration approximation. Then, stability, convergence and numerical results are presented confirming the a priori error estimates.     

Celestite formation, bacterial sulphate reduction and carbonate cementation of Eocene reefs and basinal sediments (Igualada, NE Spain)

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.