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1.
New insights into geochemical behaviour in ancient marine carbonates (Upper Jurassic Ammonitico Rosso): Novel proxies for interpreting sea‐level dynamics and palaeoceanography 
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下载免费PDF全文 Rute Coimbra Adrian Immenhauser Federico Olóriz Víctor Rodríguez‐Galiano Mario Chica‐Olmo 《Sedimentology》2015,62(1):266-302
Elemental concentrations in Phanerozoic sea water are known to fluctuate both in time and space. With regard to carbonates precipitated from marine fluids, elemental concentrations in the carbonate crystal lattice are affected by a complex array of equilibrium and non‐equilibrium as well as post‐depositional alteration processes. To assess the potential of carbonate elemental chemostratigraphy, seven Upper Jurassic sections were investigated along a proximal to distal transect across the south‐east Iberian palaeomargin. The aim was to explore stratigraphic and spatial variations in calcium, strontium, magnesium, iron and manganese elemental abundances. The epicontinental geochemical record is influenced by the combination of continental runoff and a significant diagenetic overprint. In contrast, the epioceanic geochemical record agrees with reconstructed open marine sea water values, reflecting a moderate degree of syn‐depositional to early marine pore water diagenesis. Establishing a fair degree of preservation of matrix micrite, a thorough statistical approach was applied and elemental associations tested for their environmental significance. Principal component and hierarchical cluster analyses revealed a persistent relation between carbonate magnesium, iron and strontium abundances. Processes related to early diagenetic nodulation in Ammonitico Rosso facies most probably account for the incorporation of these elements in the calcium carbonate lattice. The clear decoupling of carbonate manganese abundance with respect to the remaining elements is documented and related to high sea floor spreading rates and hydrothermal activity during the Late Jurassic. The investigation of potential time‐fluctuation of geochemical patterns was approached through variogram computation. The observed temporal behaviour is most likely to be forced by relative sea‐level dynamics, reflecting Late Jurassic palaeoceanographic conditions and potential planetary interactions. The data obtained in this study highlight the utility of elemental data from carbonate matrix micrites as geochemical proxies for studying the influence of remote trigger factors. 相似文献
2.
Dissolved (<1 kDa) and colloidal (1 kDa-0.45 μm) size fractions of sulfate, organic carbon (OC), phosphate and 17 metals/metalloids were investigated in the acidic Vörå River and its estuary in Western Finland. In addition, geochemical modelling was used to predict the formation of free ions and complexes in these waters. The sampling was carried out during high-water flow in autumn and in spring when the abundantly occurring acid sulfate (AS) soils in the catchment area are extensively flushed. Based on the high concentrations of sulfate, acidity and several metals, it is clear that the Vörå River and its estuary is strongly affected by AS soils. The high dissolved form of metals limits also the existence of fish and other organisms in this estuary, and certainly also in other similar shallow brackish estuaries elsewhere in the Gulf of Bothnia. However, generally already <20% saline sea water reduces the concentration for OC and several elements (Al, Cu, Cr, Fe, Pb, PO4 and U) by half and c. 20–30% saline sea water is needed to halve concentrations of Cd, Co, Mn, Ni and Zn. Consequently, these elements as well as organic matters were rapidly precipitated in the estuary, even after mixing with fairly small amounts of the alkaline brackish sea water. Aluminium, Cu, Fe and U most likely precipitate together with organic matter closest to the river mouth. Manganese is relatively persistent in solution and, thus, precipitates further down the estuary as Mn oxides, which concomitantly capture Ba, Cd, Co, Cu, Ni and Zn. In the inner estuary, the high contents of Al is as important than Fe in removing PO4 and, thus, also reducing the risk of algae blooms in near coastal areas influenced by AS soils in the Gulf of Bothnia. Moreover, the dispersion of metals far out in the estuary is dependent on hydrological conditions, i.e. with high flows the plume of metal-rich water will spread further out in the estuary. Furthermore, the extensive drainage of the catchment and subsequent artificial enlargement of the river channel during recent decades has not only enabled oxidation of sulfidic sediments, but strongly increased flow peaks that reach further out in the estuary. 相似文献
3.
Atsuyuki Ohta Noboru Imai Shigeru Terashima Yoshiko Tachibana Ken Ikehara Takashi Okai Masumi Ujiie-Mikoshiba Ran Kubota 《Applied Geochemistry》2007,22(12):2872
A total of 49 elements have been identified in 338 coastal sea sediment samples collected from an area situated off the Ise-Tokai region of Japan for a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define the natural geochemical background variation, mass transport, and contamination processes. The elemental concentrations of coastal sea sediments are determined primarily by particle size and regional differences. Most elemental concentrations increase with a decrease in particle size. Some elements such as Ca, Mn, and Yb are found to exist in large quantities in coarse particles containing calcareous shells, Fe–Mn oxides, and felsic volcanic sediments. Regional differences reflect the mass transfer process from terrestrial areas to coastal seas and the influence of the local marine geology. An analysis of variance (ANOVA) reveals that for many elements, the particle size effect is predominant over regional difference. The mean chemical compositions of coastal sea sediments are similar to those of stream sediments in adjacent terrestrial areas and in the upper crust of Japan. This observation supports the fact that coastal sea sediments have certainly originated from terrestrial materials. However, the spatial distributions of elemental concentrations are not always continuous between the land and coastal seas. The scale of mass movement observed in marine geochemical maps occurs at a distance of 20 km from the river mouth. A detailed examination of the spatial distribution patterns of K (K2O) and Cr concentrations suggests that terrestrial materials supplied through rivers are deposited near the shore initially, and then gravity-driven processes shift the sediments deeper into the basin. Contamination with heavy metals such as Zn, Cd and Pb was observed in coastal bays surrounded by urban and industrial areas. It is noteworthy that the areas with the highest concentration of these elements usually do not occur near the shore (not near the contamination source) but at the center of the bay. Unexpected low concentrations of Zn, Cd and Pb near shore may either be due to a decreased anthropogenic load in the most recent sediments or to dilution by unpolluted flood sediments. 相似文献
4.
对珠江口和南黄海近海海域10个站位的表层沉积物中67种元素进行分析,试图揭示两海域近海表层沉积物中主要元素的地球化学特征,包括分布特征及其控制因素,并通过两海域元素地球化学特征,初步探讨近海沉积环境特征。通过总结两海域表层沉积物中元素含量及分布特征,可以发现,近海海域总体上以陆源沉积为主,除Ca和Sr之外,大多数元素表现出明显的亲陆性。珠江口海域和南黄海海域沉积物元素含量的对比研究显示,前者相对富集As、Cd、Hg、Sb、Sr、Ca、Rb、C,后者相对富集Al2O3、Zr、Hf、Sc、Rb、Ga、Cs、V、Co、Cr、Cu、Mn、Ni、K2O、Na2O、B、Ba、I等。与上地壳相比,Ag、As、Bi、Hg、Li、N、Pb、Sb、Se、Cl、Br、I在两海域表层沉积物中均发生明显富集;Mo、Sn均呈现分散趋势;Sr、CaO在南黄海海域明显贫化,K2O、Na2O、Ba则在珠江口海域表现出贫化;其他元素与上地壳元素丰度相近。 相似文献
5.
P. Li S. L. Yang J. D. Milliman K. H. Xu W. H. Qin C. S. Wu Y. P. Chen B. W. Shi 《Estuaries and Coasts》2012,35(5):1316-1327
To delineate temporal and spatial variations in suspended sediment concentration (SSC) in the Yangtze (Changjiang) Estuary and adjacent coastal waters, surface-water samples were taken twice daily from 10 stations over periods ranging from 2 to 12?years (total number of samples >28,000). Synoptic measurements in 2009 showed an increase in surface SSC from 0.058?g/l in the upper sections of the estuary to ??0.6?g/l at the Yangtze River turbidity maximum at the river mouth, decreasing seaward to 0.057?g/l. Annual periodicities reflect variations in the Yangtze discharge, which affect the horizontal distribution and transport of SSC, and seasonal winds, which result in vertical resuspension and mixing. Over the past 10?C20?years, annual surface SSC in the lower Yangtze River and the upper estuary has decreased by 55%, due mainly to dam construction in the upper and middle reaches of the river. The 20?C30% decrease in mean surface SSC in the lower estuary and adjacent coastal waters over the same period presumably reflects sediment resuspension, in part due to erosion of the subaqueous Yangtze Delta. SSCs in the estuary and adjacent coastal waters are expected to continue to decline as new dams are constructed in the Yangtze basin and as erosion of the subaqueous delta slows in coming decades. 相似文献
6.
古城地区是塔东探区的重点勘探区块,下奥陶统鹰三段是塔东探区首要的勘探层系。探寻多期热液作用改造后的优质白云岩储层是扩大研究区勘探成果的关键。本文在储层岩石学特征判识的基础上,应用U-Pb同位素定年技术,结合碳氧锶镁同位素和稀土元素分析测试,分析了热液性质,明确了热液作用发生的确切时期及期次,探讨了热液作用对白云岩储层的影响。研究结果表明,古城地区鹰三段白云岩储层发育准同生-浅埋藏海水成因的粉晶-中晶白云岩及热液作用产物。热液作用可划分为二期:第一期为中-晚奥陶世贫镁热液,表现为鞍状白云石充填缝洞及重结晶次生加大的粗晶白云石,U-Pb测定年龄为464±12Ma到473.9±9.1Ma,氧同位素值比早奥陶世正常海相白云石明显偏负,锶同位素比值明显高于早奥陶世海水值,稀土元素Eu正异常,锶、铁、镁元素含量低;第二期为晚奥陶世-早志留世钙质热液,表现为方解石充填缝洞及对先存白云石的溶蚀,U-Pb测定年龄为448±15Ma到457.4±6.6Ma,氧锶同位素组成严重偏离同时期正常海相白云石范围,轻稀土元素明显富集,Eu正异常,锶、钙元素含量高,锰元素含量低。第二期热液作用是白云岩储层溶蚀的关键,同期NNE向断裂带作为其输导系统,是优质储层发育的有利部位,为有利区带预测提供依据。 相似文献
7.
Major ions in typical subterranean rivers and their anthropogenic impacts in southwest karst areas,China 总被引：5，自引：0，他引：5
Subterranean rivers contain much of the groundwater in karst and supply many local people in southwest China. The quality
of groundwater in subterranean rivers is of concern because of its sensitivity to anthropogenic activity. Groundwater samples
in a rural catchment were collected at the discharge point, and the concentrations of major ions including potassium, sodium,
calcium, magnesium, chloride, sulfate, nitrate and bicarbonate were analyzed in this study. Rainfall and discharge were also
observed at the same time. It could be concluded from the data that the concentrations of sulfate and nitrate had a peak in
the rainy season when the concentrations of sodium, calcium, magnesium and bicarbonate were low. The concentrations of potassium
and chloride changed randomly throughout the year. The concentration of major ions in flood process was not completely controlled
by discharge. Only the concentrations of nitrate and sulfate had obviously increased during the past two decades. It was believed
that dilution, eluviation, karst erosion and anthropogenic activity can explain the ion variations and hence this study helps
to understand environmental problem in karst. 相似文献
8.
系统探讨了黔中小流域水体悬浮物和沉积物中微量及稀土元素地球化学特征。结果表明,元素含量在河流与湖泊、悬浮物与沉积物之间均存在明显差异。稀土元素北美页岩标准化分布模式大致为轻稀土相对富集的平坦模式,δEu为0.82～1.25,δCe为0.79～1.25,整体变化不大,均表现为弱异常。麦翁河稀土总量与分布模式均发生异常,主要受上游盘龙煤矿影响。悬浮物的∑REE与pH呈反相关关系,而沉积物的∑REE却与pH表现出正相关关系,表明悬浮物与沉积物中稀土元素行为的控制因素不同。元素相关分析、因子分析及微量元素图解均表明悬浮物与沉积物中的元素具有同源性,主要来源于流域岩石化学风化和土壤物理侵蚀的产物,而某些金属元素Zn、Co、Cu、Cr、Ni则来源于周边工矿企业、农业生产等人为排放。本研究丰富和发展了喀斯特地区水体元素地球化学,揭示了小流域化学风化与物理侵蚀过程中的元素特征和物质输送状况,并为该流域的生态环境现状、治理及管理提供了科学依据和基础资料。 相似文献
9.
碳酸盐成岩作用是沉积学最为活跃的领域之一,与之有关的研究成果会直接影响人们对碳酸盐油气储层形成机制和层控矿床形成机制的理解。近年来,碳酸盐成岩作用在多个领域取得了令人瞩目的研究成果,主要包括以下几个方面:(1)实验室沉淀白云石获得成功:人们模拟海水(泻湖)条件下的细菌硫酸盐还原环境,在常温下沉淀出具有序反射的白云石。(2)热液白云化作为新的主流模式成为关注的热点:人们已认识到热液白云岩储层、沉积-喷流型铅锌矿床和Mississippi河谷型铅锌矿床具有共同的形成机制,它们均受构造(伸展、走滑构造)和热流体流动的强烈控制。(3)深埋藏条件下封闭系统的白云化作用受到关注:一些对油气储集空间和层控矿床有较大意义的白云化作用主要是在相对封闭条件下发生的,在对岩石储集空间的变化的贡献上以及在相应的地球化学指标上不同于开放条件下的白云化作用。(4)混合水白云化模式受到质疑:人们重新研究了作为混合水白云化典型地点的美国威斯康星弧碳酸盐的成岩作用,根据流体包裹体分析、阴极发光分析、偏光显微镜观察及稳定同位素分析等方法并结合有机物成熟度的数据,得出威斯康星弧与白云化有关的水-岩相互作用是由与温度升高有关的浓卤水导致的,白云化作用是热水成岩作用的结果。(5)淡水环境的成岩机制受到挑战:新近研究证明,大范围的低位体系域中可以没有具化学活性的淡水透镜体,海水环境同样可以产生成熟的石灰岩,细菌硫酸盐还原作用可以引起海水对碳酸盐的不饱和。(6)锶同位素在海相碳酸盐研究中的广泛应用:由于锶同位素不像氧、碳同位素那样因温度、压力和微生物作用而分馏,矿物可直接反映流体的同位素组成,地质历史中海水锶同位素组成也具有独特的长期变化趋势,这使得海相碳酸盐的锶同位素组成在沉积期后流体示踪中得到广泛应用。(7)硫酸盐还原作用对碳酸盐成岩作用的影响受到重视:如BSR和TSR可减小SO42-对白云石沉淀(或白云化)的动力学屏障,其产物H2S和CO2可在不同条件下对碳酸盐储层产生影响,BSR和TSR可提高成岩流体锶含量,甚至在形成天青石矿床中也具极大的潜在价值。 相似文献
10.
The objective of this study is to locate as closely as possible the sites of strontium, magnesium, sodium, and potassium in modern aragonitic corals, specifically whether these cations are adsorbed, or are substituted in the carbonate lattice or are incorporated in organic components. In addition to locating the sites of each of these four elements we wanted to find out quantitatively how much of each element occurs at each site. The experiments in this study are based on the dissolution rate of aragonite in distilled water and on the substitution of strontium and magnesium by calcium and sodium. Special attention has been given to the occurrence of strontium, magnesium, sodium, and potassium in the organic components of the corals. The main site for strontium in the corals is in the aragonite lattice. Twenty-five per cent of the total magnesium occurs in adsorbed sites and in organic compounds. The rest of the magnesium may be located in the aragonite lattice, but it is easily removed by repeated leaching or by replacement with calcium ions. Another possibility is that magnesium may occur in a dispersed mineral phase more soluble than aragonite because magnesium was released at a higher Mg to Ca ratio than is found in the solid coral; also because no local concentration of magnesium could be detected with an electron microprobe. About 12% of the total sodium is in adsorbed sites and is included in the organic compounds. The rest of the sodium might be in the lattice replacing calcium, but the low total exchange capacity is not enough to provide the needed charge balance. Another possibility is that sodium is located in a proposed mineral phase. Potassium is in adsorbed sites and incorporated in the organic compounds to an extent greater than all the other elements studied (30% of the total potassium), but again the evidence suggests that the remaining potassium is in a proposed mineral phase. Calcite is detected on the surfaces of aragonite corals after 5 months in the substitution experiment. The change of argonite to calcite took place after the inhibitor magnesium was exchanged from the surface sites and replaced by calcium. The organic compounds in corals contain small amounts of strontium, magnesium, sodium and potassium. Strontium is preferentially enriched in the organic compounds over magnesium. 相似文献
11.
为了查明曹妃甸浅层地下水水化学及咸化成因,采集研究区河水、地下淡水、微咸水、咸水、卤水、雨水和海水等不同类型水样,对其水化学组成、离子比、Piper三线图、吉布斯图、氢氧同位素组成及14C测年结果进行了分析。结果表明：(1)曹妃甸浅层地下水包括全新世沉积层潜水和晚更新世沉积层微承压水,且非原始封存在地层中而是形成于全新世中晚期。(2)地下潜水向海方向分布有淡水、微咸水、咸水水质类型,微承压水以咸水和卤水为主要水质类型;近冲洪积扇前缘水化学特征主要受岩石风化作用控制,围填海区及河口处水化学特征受海水混合作用控制,滨海平原区水化学特征主要受蒸发/结晶作用控制。(3)曹妃甸浅层地下水咸化过程主要是晚更新世以来海侵海退时期形成海洋蒸发盐经大气降水和河水多期溶滤所致,其盐分来源于海水蒸发盐,河口及围填海区地下潜水盐分主要来源于现代海水入侵。 相似文献
12.
The monthly geochemical study of Bizerte lagoon principal affluent water consists in characterizing the water geochemical facies and their inorganic pollution degree by nutrients. The major elements analysis shows calcium sulfate to chloride calcium balanced facies. The geochemical analysis of water nutritive salts shows generally a good to excellent quality. Wadi Guenniche is considered more polluted as we recorded the highest nutrients contents. The principal component analysis of the connections between the physicochemical and geochemical parameters of Bizerte lagoon affluent water show that the low salinities, the turbidity, and the low contents of major sodium, chloride ions, and nutritive elements are the major factors of the environment controlling the good quality of this fresh water. 相似文献
13.
Atsuyuki Ohta Noboru ImaiShigeru Terashima Yoshiko TachibanaKen Ikehara Hajime KatayamaAtsushi Noda 《Applied Geochemistry》2010
In all, 53 elements were analyzed in 1406 coastal sea sediment samples collected from an area off Hokkaido and the Tohoku region of Japan during a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define natural geochemical background variation and mass transport processes. The terrestrial area is covered by mafic volcanic rocks and accretionary complexes associated with ophiolite, which has small amounts of felsic volcanic rocks and granite. The spatial distribution patterns of elements enriched in mafic lithologies such as Fe (Total Fe2O3) and Sc in marine environments are influenced by adjoining terrestrial materials. The spatial distribution patterns of Cr and Ni concentrations, which are highly abundant in ultramafic rocks on land, are used to evaluate the mass transport from land to the sea and the dispersive processes caused by oceanic currents. The scale of mass transport by oceanic currents occurs up to a distance of 100–200 km from the coast along the coastal areas. The regional differences of elements rich in felsic lithologies such as K (K2O), Nb and La in marine sediments are determined mainly by the relative proportion of minerals and lithic fragments enriching felsic materials to those associated with mafic materials. The spatial distribution of elemental concentration is not always continuous between the land areas and coastal sea areas. That difference is interpreted as resulting from (1) transportation of marine sediments by oceanic currents and storm waves, (2) contribution of volcanic materials such as tephra, (3) occurrence of shell fragments and foraminifera tests and (4) distribution of relict sediments of the last glacial age and early transgression age. Contamination with Cu, Zn, Cd, As, Mo, Sn, Sb, Hg, Pb and Bi was not observed in marine environments because the study area has little anthropogenic activity. Terrestrial materials are the dominant source for these metals. The Mo, Cd, Sn, Sb, Hg, Pb and Bi are abundant in silty and clayey sediments locally because of early diagenetic processes, authigenic precipitation and organic substances associated with these elements. The spatial distribution of As concentration shows exceptions: it is concentrated in some coarse and fine sands on the shelf. The enrichment is explained by adsorption of As, sourced from a coal field, to Fe hydroxide. 相似文献
14.
广西钦州石炭-二叠纪深海硅质岩的锶同位素组成及其地质意义 总被引：6，自引：0，他引：6
报道了广西钦州海槽早石炭世-早二叠世深水硅质岩的锶同位素测定结果和经年代校正后的87Sr/86Sr初始值,建立了锶同位素演化曲线;通过与同时代上扬子地区台地相碳酸盐岩87Sr/86Sr比值和演化曲线的对比,研究了二者的异同和造成差异的原因。深水硅质岩和同期台地相碳酸盐岩的锶同位素演化曲线在总体特征上具有一定的相似性,反映海平面变化对其影响的一致性。玄武岩喷发等局部事件和硅质岩中无法回避的陆源碎屑的影响是造成87Sr/86Sr比值和演化曲线差异的主要原因。硅质岩锶同位素演化曲线显示,海平面上升发生于早石炭世,在晚石炭世早期达到最大值,晚石炭世晚期,海平面有所下降,在其后的早二叠世,海平面再次上升。 相似文献
15.
四川江油石炭纪锶同位素曲线—年代地层对比和海平面变化 总被引：4，自引：0，他引：4
据从采自四川江油马角坝石炭系剖面中的未蚀变海相岩石样品中获得的22个锶同位素测试数据，建立了剖面的石炭纪锶同位素演化曲线。马角坝剖面的锶同位素曲线与我们在贵州惠水、Denison等在北美建立的同时代锶同位素曲线总体上是一致的，表明了锶同位素曲线对海相地层进行年代地层划分对比的重要性，根据对比结果，讨论了马角坝石炭系剖面的年代地层划分和海平面变化。 相似文献
16.
A total of 402 coastal sea-sediment samples were collected from the continental shelf, slope, and basin off Tsushima Island in the western Sea of Japan, and were analyzed for 51 elements as part of a nationwide marine geochemical mapping project. The samples were compared to potentially related sample sets, and the results were considered from the viewpoint of the origin of marine surface sediments in the western Sea of Japan. The spatial distribution of elemental concentrations in the coastal sea sediments correspond to texture, grain size, the presence of shells and foraminifera, and the mud content of surface marine sediments. Most elemental concentrations increased with increasing mud content. Some samples located in littoral areas included sediment particles apparently supplied from nearby rivers, but their contribution was limited. Overall, the mean chemical compositions of clastic material in coastal sea sediments appear to differ from those of stream sediments in adjacent terrestrial areas. In addition, the geochemistry of the coastal sea sediments cannot be fully explained by the mixing of the material supplied from Korean and Chinese stream sediments, which are the most feasible sources. Coastal sea sediments in the study area are well mixed by transportation processes; therefore, elemental abundances in these marine sediments may be homogenized to such an extent that it is not possible to determine their origin. Alternatively, most of the clastics in the sediment may actually represent relict reworked material, originally formed in the Yellow Sea and Tsushima Strait during the last glacial stage and subsequent transgression. 相似文献
17.
扬子地区中-晚奥陶世转折期的碳同位素漂移事件及其成因探讨 总被引：1，自引：1，他引：0
中-晚奥陶世转折期的两次全球性碳同位素正漂--Middle Darriwilian Inorganic Carbon Excursion（MDICE）和Guttenberg Inorganic Carbon Excursion（GICE）--在发生时间上与生物辐射、全球大规模海侵和地球磁极的倒转等重大地质事件,以及海水锶、氧、硫同位素的显著变化相吻合,说明它们可能受相同形成机制的控制。在报道了扬子地区陈家河剖面中-晚奥陶世界线附近的这两次碳同位素正漂事件,并与塔里木盆地进行对比之后发现,扬子地区和塔里木盆地的MDICE和GICE与海水锶同位素比值的快速剧烈下降出现在同一层位,指示这两次碳同位素的正漂的形成可能和当时洋中脊热液活动的加剧有关。海底热液系统能够通过向海水中注入铁等生命必需元素,刺激海洋生物的繁盛,提高海洋的生产力和有机碳的埋藏,进一步引起了MDICE和GICE这两次碳同位素正漂。 相似文献
18.
《Journal of Asian Earth Sciences》2011,40(6):713-723
Bleaching related to seepage of petroleum fluids and subsurface migration of crude oil and natural gas can alter the chemical and mineralogical properties of rocks, while concurrently depleting hydrocarbon reservoirs. Mud volcanoes constitute one type of petroleum seepage present in several areas on the southern margin of the Junggar Basin in the Xinjiang Uygur Autonomous Region, NW China. The results of XRD, XRF, XANES, and Mössbauer spectroscopy on rock samples collected from areas affected by these mud volcanoes revealed an enrichment of certain minerals and elements, as well changes in mineralogical, molecular, or ionic carrier (“species”). After bleaching, reddish sedimentary rocks showed depletion in silica and enrichment of calcium, magnesium, manganese, and iron. Other elements, including aluminum, potassium, sodium, and titanium, were largely unchanged. Reduced iron and sulfur compounds predominated in the bleached rocks, producing changes in color from the original reddish into green, deep gray, and black. Iron and calcium were associated with carbonates, indicating carbonation of these elements during the bleaching processes. Manganese also appeared to be associated with carbonate, though not with sulfate even though sulfate was present in the bleached rocks. Alkaline conditions were apparently the dominant because reduced manganese would have been absent under acidic condition. The alteration of certain minerals, clay minerals in particular, was also observed in bleached rocks, the alteration of smectite-group minerals to chlorite and muscovite, for example. Mineralogical and geochemical changes in rocks bleached by hydrocarbon fluids could provide a better overall understanding of bleaching processes, and may have applications in surface geochemical exploitation and remote imaging. 相似文献
19.
对洞穴次生碳酸盐沉积87Sr/86Sr比值的研究进行了回顾,对其潜在的应用前景作了展望。87Sr/86Sr是进行沉积物来源示踪的重要地球化学指标之一。在以往的研究中,根据洞穴次生碳酸盐沉积87Sr/86Sr的变化对一些可能的Sr来源的相对贡献进行了研究,并进一步对其蕴涵的气候环境演化意义进行了探讨。在未来的研究中,示踪物源仍然将是洞穴沉积87Sr/86Sr研究的主要功能。这一指标可能在对地表土壤的化学风化强度及其变化、东亚地区的大气粉尘活动和冬季风演化、岩溶地下水古水文演化研究等方面发挥重要作用。 相似文献
20.
The Tarim basin, which is located in the Xin-jiang Autonomous Region in western China , is alarge-scale superi mposed basin situated between theTianshan Mountains to the north and the KunlunMountains to the south, with an area of 560 000km2. The Tazhong uplift ,locatedin the central partof the basin, has an area of 30 000 km2.It is sur-rounded by the Manjiaer depressionin the north,theTangguzibasi depressionin the south,the Bachu up-lift inthe west andthe Tadong saginthe east .It hasbeco… 相似文献