银额盆地哈日凹陷油气成藏条件及成藏模式

近年来,银额盆地哈日凹陷的油气勘探呈现出良好的态势,但对于哈日凹陷油气成藏条件相关研究甚少,已不能满足目前油气勘探开发的需求。本研究基于钻录井、地球物理、分析化验等资料,系统分析哈日凹陷油气成藏的烃源岩、储层、圈闭等条件,总结油气成藏条件配置关系,以期为哈日凹陷的后续油气勘探及地质研究提供依据。哈日凹陷主要发育三套烃源岩,其中银根组烃源岩有机质丰度极高,成熟度较低,有机质类型为Ⅰ-Ⅱ1型;巴二段烃源岩有机质丰度较高,成熟-高成熟,有机质类型为Ⅱ1-Ⅱ2型;巴一段烃源岩有机质丰度中等,成熟-高成熟,有机质类型为Ⅱ1-Ⅱ2型。储层类型为砂（砾）岩常规储层、碳酸质泥岩非常规储层和火山岩储层,且均属于特低孔超低渗储层,其中砂、砾岩储层和灰质泥岩储层物性最好,白云岩储层和火成岩储层次之,目前主力油藏主要集中在砂、砾岩储层和灰质泥岩储层这两种类型中。哈日凹陷主要发育两套岩性圈闭,即巴一段砂岩岩性圈闭和巴二段泥岩岩性圈闭,形成了源内（准）连续成藏模式和近源不连续成藏模式。     

伏牛山构造带变质流体脉变形特征及构造意义

伏牛山构造带由多条近平行的断裂带和夹持其间的变形岩片组成,洛南-栾川断裂带和瓦穴子-乔端断裂带为其中的两条主要断裂带。这两条断裂带虽遭受多期强烈构造活动的影响,但主造山期的构造特征至今仍然保存完好,并以中深层次的韧性剪切变形为主,形成了典型的糜棱岩和同构造期石英脉。本文从宏观、微观、超微观变形特征及年龄等方面对这些变质流体脉进行了研究,以探讨与其形成密切相关的构造活动特征、年代及其在秦岭造山带和华北板块南缘强变形带中的作用。石英脉中石英颗粒动态重结晶特征总体显示远离剪切带只有少量的膨凸式,靠近断裂带为亚颗粒式,形成核-幔结构,位错特征显示远离剪切带位错密度较小,靠近断裂带较大,位错形态显示瓦乔断裂带以挤压为主,洛南-栾川断裂带以剪切为主。两条断裂带石英脉的变形特征说明它们的糜棱岩化过程均为塑性变形中的晶质塑性变形,形成过程均为挤压在先,剪切在后。所测糜棱岩中石英脉的ESR年龄分别为372.9±30.0 Ma、275.0±20.0 Ma和218.0±20.0 Ma,真实地记录了晚加里东至中-晚海西期北秦岭的构造活动及所受影响。其中372.9±30.0 Ma是宽坪岩块向华北板块下的斜向俯冲汇聚和走滑的年代, 275.0±20.0 Ma是瓦乔断裂带的形成年龄。218.0±20.0 Ma的年龄则反映了华南、华北两大板块印支晚期全面闭合作用在秦岭造山带内部的影响。从以上3个年龄可以看出:北秦岭各构造带自北向南演化,时代上自北向南变新。     

Andesite and dacite genesis via contrasting processes: the geology and geochemistry of El Valle Volcano,Panama

The easternmost stratovolcano along the Central American arc is El Valle volcano, Panama. Several andesitic and dacitic lava flows, which range in age 5–10 Ma, are termed the old group. After a long period of quiescence (approximately 3.4 Ma), volcanic activity resumed approximately 1.55 Ma with the emplacement of dacitic domes and the deposition of dacitic pyroclastic flows 0.9–0.2 Ma. These are referred to as the young group. All of the samples analyzed are calc-alkaline andesites and dacites. The mineralogy of the two groups is distinct; two pyroxenes occur in the old-group rocks but are commonly absent in the young group. In contrast, amphibole has been found only in the young-group samples. Several disequilibrium features have been observed in the minerals (e.g., oscillatory zoning within clinopyroxenes). These disequilibrium textures appear to be more prevalent among the old- as compared with the young-group samples and are most likely the result of magma-mixing, assimilation, and/or polybaric crystallization. Mass-balance fractionation models for major and trace elements were successful in relating samples from the old group but failed to show a relationship among the young-group rocks or between the old- and young-group volcanics. We believe that the old-group volcanics were derived through differentiation processes from basaltic magmas generated within the mantlewedge. The young group, however, does not appear to be related to more primitive magmas by differentiation. The young-group samples cannot be related by fractionation including realistic amounts of amphibole. Distinctive geochemical features of the young group, including La/Yb ratios〉15, Yb〈1, Sr/Y〉150, and Y〈6, suggest that these rocks were derived from the partial melting of the subducted lithosphere. These characteristics can be explained by the partial melting of a source with residual garnet and amphibole. Dacitic material with the geochemical characteristics of subducted-lithosphere melting is generated apparently only where relatively hot crust is subducted, based on recent work. The young dacite-genesis at El Valle volcano is related to the subduction of relatively hot lithosphere.     

Cognate clinopyroxene from Paleogene mantle xenolith-bearing basanite lavas (East Serbia, SE Europe): the role of dissolution of mantle orthopyroxene

The study focuses on clinopyroxene from mantle xenolith-bearing East Serbian basanites and suggests that dissolution of mantle orthopyroxene played an important role in at least some stages of the crystallization of these alkaline magmas. Five compositional types of clinopyroxene are distinguished, some of them having different textural forms: megacrysts (Type-A), green/colourless-cored phenocrysts (Type-B), overgrowths and sieve-textured cores (Type-C), rims and matrix clinopyroxene (Type-D), and clinopyroxene from the reaction rims around orthopyroxene xenocrysts (Type-E). Type-A is high-Al diopside that probably crystallized at near-liquidus conditions either directly from the host basanite or from compositionally similar magmas in previous magmatic episodes. Type-B cores show high ^VIAl/^IVAl≥1 and low Mg# of mostly <75 and are interpreted as typical xenocrysts. Type-C, D and E are interpreted as typical cognate clinopyroxene. Type-D has Mg#<78, Al₂O₃?=?6–13?wt.%, TiO₂?=?1.5–4.5?wt.%, and Na₂O?=?0.4–0.8?wt.% and compositionally similar clinopyroxene is calculated by MELTS as a phase in equilibrium with the last 30?% of melt starting from the average host lava composition. Type-C has Mg#?=?72–89, Al₂O₃?=?4.5–9.5?wt.%, TiO₂?=?1–2.5?wt.%, Na₂O?=?0.35–1?wt.% and Cr₂O₃?=?0.1–1.5?wt.%. This clinopyroxene has some compositional similarities to Type-E occurring exclusively around mantle orthopyroxene. Cr/Al vs Al/Ti and Cr/Al vs Na/Ti plots revealed that Type-C clinopyroxene can crystallize from a mixture of the host basanite magma and 2–20?wt.% mantle orthopyroxene. Sieve-textured Type-C crystals show characteristics of experimentally produced skeletal clinopyroxene formed by orthopyroxene dissolution suggesting that crystallization of Type-C was both texturally and compositionally controlled by orthopyroxene breakdown. According to FeO/MgO^cpx/melt modelling the first clinopyroxene precipitating from the host basanite was Type-A (T?~?1250?°C, p?~?1.5?GPa). Dissolution of orthopyroxene produced decreasing FeO/MgO^melt and crystallization of Type-E and sieve-textured Type-C clinopyroxene (0.3–0.8?GPa and 1200–1050?°C). The melt composition gradually shifted towards higher FeO/MgO^melt ratios precipitating more evolved Type-C and Type-D approaching near-solidus conditions (<0.3?GPa; ~950?°C).     

Dauphiné twinning and texture memory in polycrystalline quartz. Part 3: texture memory during phase transformation

Samples of quartz-bearing rocks were heated above the α (trigonal)–β (hexagonal) phase transformation of quartz (625–950°C) to explore changes in preferred orientation patterns. Textures were measured both in situ and ex situ with neutron, synchrotron X-ray and electron backscatter diffraction. The trigonal–hexagonal phase transformation does not change the orientation of c- and a-axes, but positive and negative rhombs become equal in the hexagonal β-phase. In naturally deformed quartzites measured by neutron diffraction a perfect texture memory was observed, i.e. crystals returned to the same trigonal orientation they started from, with no evidence of twin boundaries. Samples measured by electron back-scattered diffraction on surfaces show considerable twinning and memory loss after the phase transformation. In experimentally deformed quartz rocks, where twinning was induced mechanically before heating, the orientation memory is lost. A mechanical model can explain the memory loss but so far it does not account for the persistence of the memory in quartzites. Stresses imposed by neighboring grains remain a likely cause of texture memory in this mineral with a very high elastic anisotropy. If stresses are imposed experimentally the internal stresses are released during the phase transformation and the material returns to its original state prior to deformation. Similarly, on surfaces there are no tractions and thus texture memory is partially lost.     

A subsidiary fast-diffusing substitution mechanism of Al in forsterite investigated using diffusion experiments under controlled thermodynamic conditions

Diffusion of Al in synthetic forsterite was studied at atmospheric pressure from 1100 to 1500 °C in air along [100] with activities of SiO₂, MgO and Al₂O₃ (a_SiO2, a_MgO and a_Al2O3) buffered. At low a_SiO2, the buffer was forsterite + spinel + periclase (fo + sp + per) at all temperatures, while at high a_SiO2 and subsolidus conditions a variety of three-phase assemblages containing forsterite and two other phases from spinel, cordierite, protoenstatite or sapphirine were used at 1100–1350 °C. Experiments at high a_SiO2 and 1400 °C used forsterite + protoenstatite + melt (fo + en + melt), and at 1500 °C, fo + melt. The resulting diffusion profiles were analysed by LA–ICP–MS in scanning mode. Diffusion profiles in the high a_SiO2 experiments were generally several hundred microns in length, but diffusion at low a_SiO2 was three orders of magnitude slower than in high a_SiO2 experiments carried out at the same temperature, producing short profiles only a few microns in length and close to the spatial resolution of the analytical method. Interface concentrations of Al in the forsterite, obtained by extrapolating the diffusion profiles to the crystal/buffer interface, were only a fraction of those expected at equilibrium, and varied among the differing buffer assemblages according to (a_Al2O3)^1/2 and (a_SiO2)^3/4, pointing to the substitution of Al in forsterite by an octahedral-site, vacancy-coupled (OSVC) component with the stoichiometry Al _4/3 ³⁺ vac_2/3SiO₄, whereas the main substitution expected from previous equilibrium studies would be the coupled substitution of 2 Al for Mg + Si, giving the stoichiometry MgAl₂O₄. It is proposed that this latter substitution is not seen on the length scales of the present experiments because it requires replacement of Si by Al on tetrahedral sites, and is accordingly rate-limited by the slow diffusivity of Si. Instead, diffusion of Al by the OSVC mechanism is relatively fast, and at high a_SiO2, even faster than Fe–Mg interdiffusion.     

基于模糊数学综合评判的库岸稳定性分段——以新疆某水电站近坝库岸为例

从影响库岸稳定性的诸因素中筛选出六个主要因素：坡度、坡体形态、坡体完整性程度、库水面宽度、主风向与库岸夹角及坡体结构,根据其影响程度确定了它们的权重,将库岸稳定性分为良好、较好、较差和差四级。按照各个影响因素对斜坡和各级稳定性的影响不同,对各单因素进行离散化处理,得到各影响因素的隶属度矩阵。通过对各单因素矩阵与影响因素权重运算,得到各个单元分区的稳定性评价结果。运用该方法对新疆某水电站近坝库岸段20km的稳定性进行了评价,认为稳定性较差库岸段总长约4.1km,占20.3%,主要为地质灾害分布处及工程地质条件较差的地段。该综合评判成果与现场勘察及遥感解译结果较为一致。     

有色示踪剂模拟槽实验图像分析法

图像分析法是处理有色示踪剂模拟槽实验结果的常用方法之一。本文以食用亮蓝为示踪剂,从污染物的检测精度和污染羽描绘的准确度两个方面将图像分析法与传统取样法进行对比,并利用Matlab编程对模拟槽内的污染物贮存质量进行定量计算。结果表明,与传统取样法结果相比：图像分析法的检测精度可提高1个数量级;污染羽的描绘准确度至少可提高3%左右,在实验所设置的非均质条件下可提高17%左右。利用自行编制的Matlab程序对本实验模拟槽内贮存亮蓝质量进行计算可得,当剖分格数为3 700²（1 369万）时,亮蓝贮存质量的计算值最接近实测值,最小误差仅为0.5%。综合来讲,图像分析法是一种准确度高、空间分辨率高的信息采集和处理手段,可实现对非均质地层中有色示踪剂运移过程更为精细的描述。     

Geochemical characteristics of tin-bearing magnetite-skarns

Geological and geochemical characteristics of tin-bearing magnetite-skarns are reviewed in this paper, together with the author’s opinion with respect to the mechanism of transport of tin in this environment. In addition to cassiterite, the most common form of occurrence of tin in nature, three other forms of occurrence are also of interest in tin-bearing magnetite-skarns: (1) tin present in the form of fine exsolution colloidal grains of cassiterite; (2) tin found as independent tin-bearing minerals, such as malayaite, stokesite, nordenskiöldine, Sn-paigeite, Sn-ludwigite and hulsite in a variety of skarns; (3) tin occurring in the lattice of some skarn minerals, such as garnet, pyroxene, spinel, amphibole, epidote, wollastonite and axinite in the manner of ionic replacement. When Mg²⁺ and Fe²⁺ bearing minerals, in some cases even Sulfides or other mineralizer-containing minerals, replace tin-bearing Fe³⁺ and Ti⁴⁺ skarn minerals during the late stage of skarn alteration, tin in the pre-existing silicates maybe extracted and remobilized, thus contributing to the formation of associated tin deposits.