方解石矿物包裹体中水的氢同位素组成在线测试方法

水是矿物流体包裹体的重要组成,承载着流体性质和演化信息。提取矿物包裹体中水的方法主要有真空破碎法及爆裂法。为了减少真空破碎法表面积增大引起水的吸附以及爆裂法在高温下发生同位素交换反应,本文自制了一个在线提取装置,以高纯He作为载气,与高温裂解装置—稳定同位素质谱仪(EA/HT-IRMS)相连,进行一系列的条件实验,确认了方解石矿物包裹体中水的氢同位素组成在线测试的关键技术参数。实验证实,当爆裂温度为420℃、爆裂时间为5 min、含水量为0.1～0.3μL时,利用在线提取装置—EA/HT-IRMS对方解石矿物包裹体中水的δD进行测试的精密度优于±1.5‰(1σ)。相对于传统离线分析方法,本方法实现方解石矿物包裹体中水的在线提取及氢同位素组成的在线测试,简化了操作流程,并提高实验测试效率。     

斑节对虾甲壳病理性白斑形成机制的初步研究

利用电子探针、Ｘ射线能谱、红外光谱和Ｘ射线衍射。初步研究了健康的斑节对虾Ｐｅｎａｅｕｓｍｏｎｏｄｏｎ甲壳和患病对虾甲壳白斑的形貌、无机组成以及所含的钙化矿物。实验结果表明，健康对虾甲壳的内外表面的钙磷原子比分别为１．２—１．４和１．５６—１．６８；在透射光偏光显微镜下，可见到不均匀分布的大小不等的毛发状、树枝状和十字消光放射球纤状雏晶，有些鲕粒中心可包含石英微粒；红外光谱表明，健康对虾甲壳所包含的沉淀矿物主要是胶磷石。患病对虾甲壳表面白斑区的钙磷原子比可达３１．８３—４３．５６，其剖面中间层鲕粒除合少量硫以外，全部都是钙，偏光显微镜和扫描电镜照片清楚地显示泥晶状、放射纤维状、放射花瓣状微晶集合体逐步交代并覆盖胶磷石，红外光谱和Ｘ射线衍射谱都清楚地证实该矿物是方解石。     

Mass transfer and preferred orientation development during extensional microcracking in slate-belt folds, Elura Mine, Australia

Microstructures in slate belt rocks at the Elura Mine, near Cobar, south-eastern Australia, indicate that volume loss by syntectonic dissolution is coupled with mass accretion by reprecipitation of the dissolved material in dilational sites. The mass accretion is sustained primarily by repetitive tensile microfracturing at high pore-fluid pressures. Oriented growth in the inter- and intragranular microcracks is locally host-controlled, creating lattice- and shape-preferred orientations. The grain-scale crack-seal features throughout the rock reflect rhythmic fluid pressure fluctuations; a balance is achieved between the fracture-induced permeability (and consequent flushing rates), and the rate of fluid build-up in a relatively sealed environment.
Instability in the balancing factors can lead to localization and intensification of tensile failure (and hence, tension vein formation) in the grain aggregate. Growth of veins by crack-seal also reflects a steady state, but with more localized fluctuations of fluid flow on the aggregate scale. Still larger imbalances between flushing and fluid accumulation (i.e. pressure variations) induce breccia veining. The larger pressure gradients over greater distances, associated with dilation localization (from pervasive microfracturing to spaced breccia domains), allow fluid channelling with an increased potential for chemical fluid/rock disequilibrium. Therefore, large breccia vein systems tend to be sites of extensive fluid/rock interaction and replacement, as spectacularly illustrated by the syntectonic sulphide orebodies at Elura. The huge amounts of silicate, carbonate and sulphide accumulated during folding at Elura illustrate the large scale of source and sink couples possible in solute mass transfer.     

贵州锦丰(烂泥沟)金矿床含砷黄铁矿和脉石英及其包裹体的稀土元素特征

贵州锦丰(烂泥沟)金矿是滇黔桂“金三角“目前已探明的最大的卡林型金矿床.含砷黄铁矿是该矿床最主要的载金矿物,脉石英是最显著的热液蚀变作用产物.含砷黄铁矿、脉石英及其包裹体具有相同的稀土元素特征,表现为轻重稀土分馏明显(LREE/HREE:7.95～31.77,(La/Yb)N:8.97～40.49);轻稀土有一定的分异((La/Sm)n:3.20～5.29),曲线右倾程度大;重稀土分异不明显((Gd/Yb)n:1.41～3.35),曲线平坦;负铕异常明显(δEu 0.59～0.71);微弱的铈负异常(δCe 0.97～0.98).代表成矿流体特征的脉石英包裹体稀土配分型式及特征值与区域上不同时代的幔源基性-超基性岩差别较大,而与矿床围岩、矿石、含砷黄铁矿及其包裹体稀土配分型式及特征值十分相似,具上部地壳普通沉积岩的特点,反映成矿流体主要不是来源于地幔,而是以壳源为主.Eu负异常反映了偏酸性(富CO2)、还原性的成矿环境;微弱的Ce负异常表明成矿流体来源于以沉积水和热脱水为主的盆地流体.     

云南白秧坪东矿区控矿断裂带构造岩的方解石组构

断裂带构造岩的方解石组构综合分析,可以推断构造活动的应力场方位,利用e双晶的C—T(C—压应力轴,T—张应力轴)图解推断古应力的方位,已为众多的地质学家在实践中引用。云南白秧坪东矿区推覆构造的华昌山断裂带和水磨房断裂带,是矿区的主要控矿构造,其构造岩的方解石及e双晶极点组构均显示点极密加环带的型式,大部分发育近岩组坐标c轴的光轴极密,代表光轴方向的压力导致沿岩组坐标ab面滑动;在C—T应力系统中,显示华昌山、水磨房断裂带晚期较强烈活动的应力场方位,主压应力方向为SE-NW向,主张应力方向为NE-SW向,断层以左旋运动为主;华昌山断裂带SE盘往NW方向逆冲,水磨房断裂带则由NW往SE方向反冲,与野外宏观构造分析吻合。     

Mn content of reservoir calcite cement: A novel inorganic geotracer of secondary petroleum migration in the tectonically complex Junggar Basin (NW China)

Electronic probe microanalysis(EPMA) results of reservoir calcite cement from fourteen core samples in the Junggar Basin show that Mn-content varies largely between different samples from below the detect limitation to 4.14%,while it displays a generally good correlation with oil-gas shows.This,therefore,likely indicates that concentration of the Mn-content of the calcite cement has a close rela-tion to the intensity of petroleum fluid charging during hydrocarbon secondary migration.In order to assess this hypothesis,oxygen and strontium isotopic measurements on sixteen calcite veins host in source sequences were carried out to investigate the feature of the oil-source petroleum fluid.Analytical results imply that during hydrocarbon generation and migration,deep hot fluid has dissolved volcanic minerals interlined between mudstone source rocks.As Mn is a kind of typical trace element enriched in volcanic rocks,it is reasonable to conclude that the petroleum fluid formed in the source sequences would be Mn-rich.Consequently,calcite cements precipitated from such Mn-rich petroleum fluid would be Mn-rich accordingly.Due to the geologic chromatographic effect during migration along reservoir rocks,the decreasing of the Mn-content of the reservoir calcite cements indicates the migration direction.Then,this novel geotracer was further successfully applied in the study of hydrocarbon migration in the Junggar Basin in combination with organic geochemical analyses during the hydrocarbon migration.The Mn content of the reservoir calcite cement appears promising as a novel inorganic geotracer for the petroleum migration.This paper represents a search for novel indicators of secondary petroleum migration in tectonically complex basins based on fundamentals of the reservoir fluid-rock interactions.     

Fluid flow record from fracture-fill calcite in the Eocene limestones from the South-Pyrenean Basin (NE Spain) and its relationship to oil shows

The presence of oil shows associated with fractures provides a significant opportunity to a) unravel the type, origin and evolution of fluids involved in fracture-fills, and b) examine how they relate to oil migration. Two stages of calcite cement (C1 and C2) were distinguished in the fractures of the Eocene Armàncies platform carbonates; C1 is characterised by fence-like crystals, exhibits dull red luminescence and contains abundant twin planes, inclusions and δ¹⁸O values that range from − 6.2‰ to − 4.8‰ VPDB. C2 consists of blocky clean crystals, is characterized by dark brown-red luminescence that alternates with yellow bands, and contains hydrocarbon fluid inclusions with homogenisation temperatures of approximately 120 °C. δ¹⁸O values range from − 9.6‰ to − 8.9‰ VPDB. The remaining porosity after C2 precipitation is filled with liquid oil that reached 115 °C. This would seem to indicate that free oil and fluid inclusions oil probably come from the same migration pulse. Oil migration timing was coeval with C2 and continued after calcite cementation was completed.     

Diamond-bearing and diamond-free metacarbonate rocks from Kumdy–Kol in the Kokchetav Massif, northern Kazakhstan

Abstract Dolomite marble from the Kumdy–Kol area of the Kokchetav Massif contains abundant microdiamond, mainly in garnet and a few in diopside. The mineral assemblage at peak metamorphic condition consists of dolomite + diopside + garnet (+ aragonite) ± diamond. Inclusions of very low MgCO₃ calcite and almost pure calcite occur in diopside and are interpreted as aragonite and/or aragonite + dolomite. Single-phase Mg–calcite in diopside with a very high MgCO₃ component (up to 21.7 mol%) was also found in diamond-free dolomitic marble, and is interpreted as a retrograde product from aragonite + dolomite to Mg–calcite. The dolomite stability constrains the maximum pressure (P) at < 7 GPa using previous experimental data, whereas the occurrence of diamond yields the minimum peak pressure–temperature (P–T) condition at 4.2 GPa and 980 °C at X co ₂ = 0.1. The highest MgCO₃ in Mg–calcite constrains the minimum P–T condition higher than 2.5 GPa and 800 °C for the exhumation stage. As these marbles were subjected to nearly identical P–T metamorphic conditions, the appearance of diamond in some carbonate rocks was explained by high X co ₂. A low X co ₂ condition refers to high oxidized conditions and diamond (and/or graphite) becomes unstable. Difference in X co ₂ for marble from the same area suggests local heterogeneity of fluid compositions during ultrahigh-pressure metamorphism.     

In-situ Growth of Calcite at Devils Hole, Nevada: Comparison of Field and Laboratory Rates to a 500,000 Year Record of Near-Equilibrium Calcite Growth

Calcite grew continuously for 500,000 years on the submerged walls of an open fault plane (Devils Hole) in southern Nevada, U.S.A. at rates of 0.3 to 1.3 mm/ka, but ceased growing approximately 60,000 years ago, even though the fault plane remained open and was continuously submerged. The maximum initial in-situ growth rate on pre-weighed crystals of Iceland spar placed in Devils Hole (calcite saturation index, SI, is 0.16 to 0.21 at 33.7 °C) for growth periods of 0.75 to 4.5 years was 0.22 mm/ka. Calcite growth on seed crystals slowed or ceased following initial contact with Devils Hole groundwater. Growth rates measured in synthetic Ca-HCO₃ solutions at 34 °C, CO₂ partial pressures of 0.101, 0.0156 (similar to Devils Hole groundwater) and 0.00102 atm, and SI values of 0.2 to 1.9 were nearly independent of P_{CO 2}, decreased with decreasing saturation state, and extrapolated through the historical Devils Hole rate. The results show that calcite growth rate is highly sensitive to saturation state near equilibrium. A calcite crystal retrieved from Devils Hole, and used without further treatment of its surface, grew in synthetic Devils Hole groundwater when the saturation index was raised nearly 10-fold that of Devils Hole water, but the rate was only 1/4 that of fresh laboratory crystals that had not contacted Devils Hole water. Apparently, inhibiting processes that halted calcite growth in Devils Hole 60,000 years ago continue today.