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1.
Detrital glaucony in the Palaeogene glauconitic sandstones in Siri Canyon, Danish North Sea, has been analysed from 15 exploration wells by X‐ray diffraction, electron microprobe and scanning electron microscopy. These sandstones consist of mixed‐layer illite/smectite and have a large variability in chemical composition and structure. In the most shallow wells (ca 1700 m), the glaucony is rich in Fe and consists of mixed‐layer illite/smectite with random‐interstratification (R = 0). In the depth interval from 1700 to 2000 m, the composition changes as Si is incorporated. The structure changes to ordered R = 1. Further increase in burial leads to the loss of Fe. Ordered R = 3 mixed‐layer illite/smectite is recognized from burial depths of 2200 m. The proportion of illite in illite/smectite mixed layers increases only slightly with depth and temperature. Although the structural changes generally are associated with chemical changes, they can also take place isochemically when the detrital glaucony is tightly embedded in earlier cement, which prevented chemical exchange. The glaucony transformation in the Siri Canyon sandstones partly reflects a supply of Si and partly significant loss of Fe. Thus, the glaucony transformation relates to the general diagenesis of the host sandstone. These sandstones are cemented by microquartz at an early stage, followed by precipitation of Fe‐rich grain‐coating berthierine or chlorite.  相似文献   

2.
Iheya‐North‐Knoll is one of the small knolls covered with thick sediments in the Okinawa Trough back‐arc basin. At the east slope of Iheya‐North‐Knoll, nine hydrothermal vents with sulfide mounds are present. The Integrated Ocean Drilling Program (IODP) Expedition 331 studied Iheya‐North‐Knoll in September 2010. The expedition provided us with the opportunity to study clay minerals in deep sediments in Iheya‐North‐Knoll. To reveal characteristics of clay minerals in the deep sediments, samples from the drilling cores at three sites close to the most active hydrothermal vent were analyzed by X‐ray diffraction, scanning electron microscope and transmission electron microscope. The sediments are classified into Layer 0 (shallow), Layer 1 (deep), Layer 2 (deeper) and Layer 3 (deepest) on the basis of the assemblage of clay minerals. Layer 0 contains no clay minerals. Layer 1 contains smectite, kaolinite and illite/smectite mixed‐layer mineral. Layer 2 contains chlorite, corrensite and chlorite/smectite mixed‐layer mineral. Layer 3 is grouped into three sub‐layers, 3A, 3B and 3C; Sub‐layer 3A contains chlorite and illite/smectite mixed‐layer mineral, sub‐layer 3B contains chlorite/smectite and illite/smectite mixed‐layer minerals, and sub‐layer 3C contains chlorite and illite. Large amounts of di‐octahedral clay minerals such as smectite, kaolinite, illite and illite/smectite mixed‐layer mineral are found in Iheya‐North‐Knoll, which is rarely observed in hydrothermal fields in mid‐ocean ridges. Tri‐octahedral clay minerals such as chlorite, corrensite and chlorite/smectite mixed‐layer mineral in Iheya‐North‐Knoll have low Fe/(Fe + Mg) ratios compared with those in mid‐ocean ridges. In conclusion, the characteristics of clay minerals in Iheya‐North‐Knoll differ from those in mid‐ocean ridges; di‐octahedral clay minerals and Fe‐poor tri‐octahedral clay minerals occur in Iheya‐North‐Knoll but not in mid‐ocean ridges.  相似文献   

3.
Iron silicate minerals are a significant component of sedimentary systems but their modes of formation remain controversial. Our analysis of published data identifies end‐member compositions and mixtures and allows us to recognize controls of formation of different mineral species. The compositional fields of glaucony, Fe‐illite, Fe–Al smectites are determined in the M+/4Si vs. Fe/Sum of octahedral cations (M+ = interlayer charge). Solid solutions could exist between these phases. The Fe–Al and Fe‐rich clay minerals form two distinct solid solutions. The earliest phases to be formed are Fe–Al smectites or berthierine depending on the sedimentation rate. Reductive microsystems appear in the vicinity of organic debris in unconsolidated sediments. The Fe is incorporated first in pyrite and then in silicates after oxidation. Potassium ions diffuse from the sea‐water–sediment interface. If not interrupted, the diffusion process is active until reaction completion is reached, i.e. formation of Fe‐illite or glauconite or a mineral assemblage (berthierine–nontronite) according to the available Al ion amounts in the microsystem. Mixed‐layer minerals are formed when the diffusion process is interrupted because of sedimentation, compaction or cementation. Despite the common belief of their value as palaeoenvironment indicators, these minerals can form in a variety of environments and over a period of millions of years during sediment burial.  相似文献   

4.
Abstract. This paper presents a measurement and study of Kübler Indexes (KI) of illite, "crystallinities" of chlorite (ChC), and apparent mean crystallite sizes and lattice strain of both illite and chlorite of the Jinshan ductile shear zone in the Jinshan gold deposit of East China. It is found that the KI values and apparent mean crystallite sizes of illite decrease and the lattice strain of chlorite apparently increase, whereas the apparent mean crystallite sizes of chlorite and the lattice strain of illite remain constant, from altered mylonite to altered and higher-strained ultramylonite in the shear zone. Only slight decrease of ChC is observed.
An obvious negative correlation exists between KI and apparent mean crystallite sizes in altered mylonite with lower strain, whereas a positive correlation is found between ChC and apparent mean crystallite sizes in altered ultramylonite with higher strain. No any correlations between KI and lattice strain exist, whereas a negative correlation and a positive correlation between ChC and lattice strain occur separately in the altered mylonite and ultramylonite. It is suggested that illite Kiibler Indexes and chlorite "crystallinities" most likely reflect deformation behaviors and mechanisms of altered rocks although other factors involving water/rock ratio may apply as well.  相似文献   

5.
Chlorite is a common sheet silicate that occurs in various lithologies over a wide grade range involving diagenesis and low‐grade metamorphism. Thus, the reaction progress of chlorite offers a unique opportunity for direct correlation of zonal classification of metasedimentary rocks based on illite crystallinity with metabasite mineral facies. To provide such correlation, chlorite crystallinity indices, apparent mean crystallite sizes and lattice strains, crystallite size distributions and compositions of chlorite from coexisting metapelites and metabasites were determined by X‐ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), analytical electron microscopy (AEM) and electron microprobe (EMP) methods. Samples were from Palaeozoic and Mesozoic formations of the Bükkium (innermost Western Carpathians, Hungary) that underwent Alpine (Cretaceous) orogenic metamorphism. Metapelites range in grade from late diagenesis to epizone, whereas metabasites vary from prehnite–pumpellyite through pumpellyite–actinolite to greenschist facies. Despite significant differences in composition, mineral assemblages and textures, reaction progress, as measured in part by chlorite crystallinity, in metapelites paralleled that in metabasites. Chlorite crystallinity and mean crystallite size increase and the proportion of mixed layers in chlorite decreases, whereas the calculated lattice strain does not change significantly with increasing metamorphic grade. Similar trends, but (especially at higher grades) significant differences, were found in mean crystallite size values using various methods for XRD line profile analyses. The increase in crystallite size with increasing grade was demonstrated also by direct TEM measurements on ion‐milled whole‐rock samples, but with a larger scatter of data at higher grades. In spite of the different kinds of mixed layering in chlorite (Mg‐rich smectitic, mostly random, local corrensite‐like units in metabasites, and Fe‐rich berthierine and dioctahedral smectite in metapelites), XRD‐calculated and TEM‐measured parameters were found to be reliable tools for measuring reaction progress and metamorphic grade of the same degree in both lithotypes.  相似文献   

6.
The spatial distribution of clay minerals in sandstones, which may both enhance or degrade reservoir quality, is poorly understood. To address this, clay mineral distribution patterns and host‐sediment properties (grain size, sorting, clay fraction abundance and bioturbation intensity) have, for the first time, been determined and mapped at an unprecedentedly high‐resolution in a modern estuarine setting (Ravenglass Estuary, UK). Results show that the estuary sediment is dominated by illite with subordinate chlorite and kaolinite, although the rivers supply sediment with less illite and significantly more chlorite than found in the estuary. Fluvial‐supplied sediment has been locally diluted by sediment derived from glaciogenic drift deposits on the margins of the estuary. Detailed clay mineral maps and statistical analyses reveal that the estuary has a heterogeneous distribution of illite, chlorite and kaolinite. Chlorite is relatively most abundant on the northern foreshore and backshore and is concentrated in coarse‐grained inner estuary dunes and tidal bars. Illite is relatively most abundant (as well as being most crystalline and most Fe–Mg‐rich) in fine‐grained inner estuary and central basin mud and mixed flats. Kaolinite has the highest abundance in fluvial sediment and is relatively homogenous in tidally‐influenced environments. Clay mineral distribution patterns in the Ravenglass Estuary have been strongly influenced by sediment supply (residence time) and subsequently modified by hydrodynamic processes. There is no relationship between macro‐faunal bioturbation intensity and the abundance of chlorite, illite or kaolinite. Based on this modern‐analogue study, outer estuarine sediments are likely to be heavily quartz cemented in deeply‐buried (burial temperatures exceeding 80 to 100°C) sandstone reservoirs due to a paucity of clay grade material (<0·5%) to form complete grain coats. In contrast, chlorite‐enriched tidal bars and dunes in the inner estuary, with their well‐developed detrital clay coats, are likely to have quartz cement inhibiting authigenic clay coats in deeply‐buried sandstones.  相似文献   

7.
Hydrothermal alteration, involving chiefly chlorite and illite, is extensively distributed within host rocks of the Pleistocene Hishikari Lower Andesites (HLA) and the Cretaceous Shimanto Supergroup (SSG) in the underground mining area of the Hishikari epithermal gold deposit, Kagoshima, Japan. Approximately 60% of the mineable auriferous quartz‐adularia veins in the Honko vein system occur in sedimentary rocks of the SSG, whereas all the veins of the Yamada vein system occur in volcanic rocks of the HLA. Variations in the abundance and chemical composition of hydrothermal minerals and magnetic susceptibility of the hydrothermally altered rocks of the HLA and SSG were analyzed. In volcanic rocks of the HLA, hydrothermal minerals such as quartz, chlorite, adularia, illite, and pyrite replaced primary minerals. The amount of hydrothermal minerals in the volcanic rocks including chlorite, adularia, illite, and pyrite as well as the altered and/or replaced pyroxenes and plagioclase phenocrysts increases toward the veins in the Honko vein system. The vein‐centered variation in mineral assemblage is pronounced within up to 25 m from the veins in the peripheral area of the Honko vein system, whereas it is not as apparent in the Yamada vein system. The hydrothermal minerals in sandstone of the SSG occur mainly as seams less than a few millimeters thick and are sporadically observed in halos along the veins and/or the seams. The alteration halos in sandstone of the SSG are restricted to within 1 m of the veins. In the peripheral area of the Honko vein system, chlorite in volcanic rocks is characterized by increasing in Al in its tetrahedral layer and the Fe/Fe + Mg ratio toward the veins, while illite in volcanic rocks has relatively low K and a restricted range of Fe/Fe + Mg ratios. Temperature estimates derived from chlorite geothermometry rise toward the veins within the volcanic rocks. The magnetic susceptibility of tuff breccia of the HLA varies from 21 to less than 0.01 × 10?3 SI within a span of 40 m from the veins and has significant variation relative to that of andesite (27–0.06 × 10?3 SI). The variation peripheral to the Honko vein system correlates with an increase in the abundance of hematite pseudomorphs after magnetite, the percentage of adularia and chlorite with high Fe/Fe + Mg ratios, and the degree of plagioclase alteration with decreasing distance to the veins. In contrast, sedimentary rocks of the SSG maintain a consistent magnetic susceptibility across the alteration zone, within a narrow range from 0.3 to 0.2 × 10?3 SI. Magnetic susceptibility of volcanic rocks of the HLA, especially tuff breccia, could serve as an effective exploration tool for identifying altered volcanic rocks.  相似文献   

8.
The Neoproterozoic and Lower Paleozoic along the profile of Yuanguping in western Hunan Province, China underwent anchimetamorphism. The illite crystallinity (IC) of the <2 μm fractions ranges from 0.23-0.34°△2θfor the Neoproterozoic to 0.23-0.35°△A2θ for the Lower Paleozoic (calibrated with the Kisch IC set, Kisch, 1991). This indicates that the metamorphic grade of the Neoproterozoic and Lower Paleozoic is the anchizone. The peak metamorphic temperature is estimated to be 290-210℃. This result does not agree with the greenschist or subgreenschist facies of the Banxi Group, nor with the lower-greenschist facies or sedimentary cover of the Sinian to Lower Paleozoic, as most previous researchers thought. The illite (K-mica) b0 values range from 0.9074 to 0.8963 (nm) for the Neoproterozoic and the Lower Paleozoic. Based on cumulative frequency curves of the illite (K-mica) b0, the peak metamorphic pressure of the Banxi Group was derived to be of a type that is slightly higher than that of the N. Ne  相似文献   

9.
An inverse Monte Carlo (MC) method was developed to determine the distribution of octahedral cations (Al3+, Fe3+, and Mg2+) in bentonite illite–smectite (I–S) samples (dioctahedral 2:1 phyllosilicates) using FT–IR and 27Al MAS NMR spectroscopies. FT–IR allows determination of the nature and proportion of different cation pairs bound to OH groups measuring the intensities of OH-bending bands. 27Al MAS NMR data provide information about cation configuration because 27Al MAS NMR intensity depends on Fe distribution. MC calculations based on FT–IR data alone show Fe segregation by short-range ordering (Fe clusters within 9 to 15?Å from a given Fe atom). Fe segregation increases with illite proportion. MC calculations based on IR and 27Al NMR simultaneously yield similar configurations in which Fe clusters are smaller. The latter calculations fail to build appropriate cation distributions for those samples with higher number of illite layers and significant Fe content, which is indicative of long-range Fe ordering that cannot be detected by FT–IR and 27Al MAS NMR. The proportion of Mg–Mg pairs is negligible in all samples, and calculations, in which the number of Mg atoms, as second neighbours, is minimised, create appropriate configurations.  相似文献   

10.
The rare earth element (REE) contents of sixteen surficial calcareous sediments from the southwestern Carlsberg Ridge, Indian Ocean, have been determined. The total REE vary from 35 ppm to 126 ppm and are inversely related to the calcium carbonate content. REEs show a strong positive correlation with Al + Fe + K + Mg + Na (r 2= 0.98) and Mn + Fe + Cu + Ni (r 2= 0.86) suggesting that the REE is associated with a combined phase of clays (mainly illite) and Mn-Fe oxyhydroxides. The aeolian input into these sediments is suggested from the weak positive Eu/Eu* anomaly. Shale-normalized (NASC) pattern along with La(n)/Yb(n) ratio suggest enrichment of heavy REE (HREE) relative to the light REE (LREE) with a negative Ce/Ce* anomaly implying retention of a bottom water REE pattern. An erratum to this article is available at .  相似文献   

11.
To obtain a better understanding of climate change in south China in the Quaternary, a clay mineralogical study was undertaken on the red earth profile at Jiujiang, using X‐ray diffraction (XRD) and particle‐size distribution analysis methods. The XRD results showed that the clay minerals of the Jiujiang red earth were mainly mixed‐layer illite–smectite (I/S), illite, kaolinite and vermiculite, with trace amounts of mixed‐layer kaolinite–smectite (K/S). Changes in clay mineral composition displayed a trend of three‐stage evolution. The higher mixed‐layer I/S clays and kaolinite contents in the lower portion suggest extremely warm and humid climates over the period c. 700 to c. 350 ka ago. A gradual decrease in I/S clays and kaolinite reveals a gradual climate change from warm/humid to cool/dry during the period c. 350 to c. 130 ka ago. The higher illite and vermiculite contents indicate a relatively cool and dry climate during the period since c. 130 ka ago. The particle‐size distribution pattern of the upper section was similar to that of the Xiashu loess, while that of the middle to lower section was similar to those of fluvially reworked red earth. A rapid increase in the abundance of large grain‐size components at 2.6 m depth indicates an intensification of the winter monsoon and a cool and dry climate during the period, in good agreement with results from the clay mineral composition and homogeneous structure. The red earth sequences in south China could probably be used to test the response of tropical to subtropical regions to global climate changes.  相似文献   

12.
Hydrothermal alteration mapping with spaceborne hyperspectral data was simulated in the Comstock mining district, Nevada in order to evaluate the mineral mapping capabilities of the proposed Australian Resource Information and Environment Satellite (ARIES‐1). As a result, a suite of hydrothermal alteration minerals, including kaolinite, dickite, illite, chlorite, alunite and carbonate was identified from the simulated data in the 0.4–2.5 μm wavelength region and their areal abundance variations mapped accordingly. The recognised alteration zoning shows a major change in alteration assemblages across the Comstock and Silver City Faults, and a gradual variation from north to south along the faults. In the bleached Miocene volcanic rocks, dickite, kaolinite, illite and alunite were recognised. Coexistence of dickite of relatively high temperature, high‐crystallinity kaolinite of medium temperature and low‐crystallinity kaolinite of low temperature suggests supergene processes overprinting earlier hypogene alteration. The bleached rocks probably represent hydrothermal alteration in the fluid up‐flow zones in the central and shallower parts of the hydrothermal system. Illite in the bleached zones is characterised by relatively short AI–OH band wavelengths (2190–2200 nm), indicating no or very low Fe and/or Mg contents. Fault‐controlled propylitic alteration is mapped in the central part of the district mainly in the footwall of the Comstock Fault. The associated illite is characterised mainly by medium AI–OH band wavelengths (2200–2208 nm). This propylitic alteration may be contemporaneous with Au–Ag mineralisation. Additional and more extensive propylitic zones, containing illite with long AI–OH band wavelengths (2204–2216 nm), were mapped in the southern part of the district. These zones resulted from either a pre‐mineralisation propylitic alteration, or the peripheral hydrothermal alteration in the fluid down‐flow zones of the Miocene hydrothermal system.  相似文献   

13.
The metamorphic conditions of the Upper Permian Yangjiagou Formation in eastern Changchun, China, were evaluated based on the mineral assemblage, illite crystallinity, illite polytypism,the b dimension of illite, and the chemical composition of chlorite. The pelitic rocks in the Yangjiagou Formation are characterized by illite + kaolinite + chlorite ± mixed-layer chlorite/smectite and detrital quartz + plagioclase. Illite in the formation has a crystallinity of 0.38-0.55 and comprises mixed 2 M_1 and1 M_d polytypes, indicating a metamorphic temperature of 200℃. Based on the chemical composition of chlorite and the chlorite geothermometer, we estimated diagenetic to very low-grade metamorphic conditions with temperatures of 185℃～204℃. The b dimension of illite varies from 8.992 A to 9.005 A.We used a mathematical algorithm to extend Guidotti and Sassi's(1986) diagram relating illite b dimension with temperature and pressure, and used this diagram, together with illite crystallinity and chlorite chemical composition, to semi-quantitatively estimate the formation pressure at1.2 kbar. These reveal that the Yangjiagou Formation has experienced very low-grade metamorphism.  相似文献   

14.
伊利石是一种重要的矿产资源,准确获得矿石中矿物组成和含量具有重要的理论和实际意义.Rietveld全图拟合法采用整个衍射图进行分析,具有较高的准确度.然而由于缺少纯的伊利石样品,目前对于该方法在分析伊利石矿样的精确度和误差来源尚不清楚.本文采用Rietveld全图拟合法对人工配制和天然的伊利石典型矿样进行了分析和计算,...  相似文献   

15.
《地学前缘(英文版)》2020,11(4):1353-1367
Chronologically well-constrained loess-palaeosols(recorded glacial and inter-glacial climate) revealed pedogenesis induced ionic substitutions,caused end-member compositional deviations in illite and chlorite,linked to widespread climatic changes occurred during Late Pleistocene.Further,micro-level climatic resolution is yet to be resolved.Thus,layer-wise X-ray diffraction analyses of clay separates,followed by Rietveld refinement revealed varied cell parameters and interatomic distances.Obtained values for detrital and pedogenic illite and chlorite when plotted against stratigraphic succession show notable changes in the crystallographic axes.The illite lattices associated with inadequately pedogenized palaeosols have been altered into illite/smectite mixed layers,but,the chlorite lattices represent expansion of a-,b-and contraction of c-axes with much greater amount of distortions,suggestive of warm-humid and acidic environment.The detrital 48,44 and 83,74 bonded illite and chlorite with2 sub-types each,when pedogenized retained 48,44 and 34;and 83 and 74 bonds(in their neo-formed 3 and 2 sub-types),respectively.The Al-O bond shows expansion,but,unchanged Si-O and decreased Si-K and K-O bonds show loss of Al and retention of Si and K ions in the illite lattices.The illite with 32 atoms and 48 bonds represent contraction of K-O,Si-K,Al-O and Si-O bonds caused bond reinforcement;however,loss of Al~(3+)reflects all-out illite alteration.Owing to Al-O and K-O bond expansion,major K~+ and Al~(3+) ionic loss occurred during the LGM,however,further ionic loss depends upon the magnitude of the loess-palaeosol weathering that they have suffered.The clilate sensitive Fe,Mg and Al ionic losses for Fe-O,Mg-O and Al_(11)-O_9 bond length expansions were recognized in the chlorite lattices.Such ionic losses are common,but,complete distortion is attributed to Al,Si,Fe and Mg ionic losses,followed by weakening of Al-O,Si-O,Fe-O and Mg-O bonds.Though,Si-O_4 and Fe_1-O_4 bonds,and Si and Fe_(1 st) ions remain intact.Thus,three major glacial episodes of ～5 ka each occurred under alkaline environment,but,intervened by two successive cycles of 55 ka each,encompassing three alternate warm and cold climatic sub-cycles of 12-15 ka.But,the coldness increases with each warm-cold sub-cycle that attained the glacial maxima.Further,these events correlate well with the deep-sea records of the North Atlantic(MIS-1 to MIS-5 e) and CLP loess-palaeosols(～127 ka).  相似文献   

16.
This study collected the early Oligocene to middle Miocene sediments from the Gerze Basin of Tibet, and used X-Ray diffraction （XRD） and Scanning Electron Microscope （SEM） to discuss their clay mineralolgy, clay indices, better understand the clay mineralogy and its paleoclimatic significance. The results show that clay minerals of the Gerze Basin sediments are mainly composed of iilite and chlorite, with minor amounts of smectite and kaolinite, and their relative content varies along the section. Variations of relative contents and clay indices suggest that the Gerze Basin has experienced three-stage evolution of paleoclimate： I ） high ilUte and chlorite contents, with fluctuant smectite and low （I＋Ch）/（K＋S） ratio, indicative of a dominant seasonal arid climate from the early Oligoeene to late Oligocene; Ⅱ） higher illite and chlorite contents and larger （I＋Ch）/（K＋S） ratio but absence of kaolinite, indicating a colder and drier climate from the late Oligocene to early Miocene; Ⅲ） high iilite and chlorite contents with fluctuant （I＋Ch）/（K＋S） ratios and occasional occurrence of kaolinite, suggesting that the climate became warmer and more humid compared with that of stage Ⅱ in the mid-Miocene. These conclusions were also reinforced by the clay morphology, which suggests that physical weathering dominated in stage Ⅱ, while relatively strong chemical weathering was dominant in stages Ⅰ and Ⅲ Clay minerals of the sediments mainly consist of illite and chlorite, indicating that the source rock played a significant role in clay origin. It is inferred that global cooling and the enhancement of denudation and obstruction of northward moisture due to the uplift of the Qinghai-Tibet Plateau were responsible for the provenance of iUite and chlorite under weak chemical weathering. Though the Qinghai-Tibet Plateau reached a certain elevation by the mid-Miocene, yet the mid-Miocene widespread warming might have largely impacted the Gerze climate.  相似文献   

17.
作为流体作用过程中水—岩反应的产物，粘土矿物可以帮助人们认识水—岩反应的机制和流体活动的特征。本文以江西金山金矿为例，通过对热液蚀变粘土矿物伊利石和绿泥石结晶度、平均结晶大小和晶格应变的测定，讨论了岩石变形对伊利石和绿泥石结晶生长差异的影响。在岩石应变较弱、水／岩比较小的糜棱岩带，伊利石的平均结晶大小与结晶度成负相关，而在岩石应变较强、水／岩比较大的超糜棱岩带，绿泥石的平均结晶大小与结晶度成正相关。由应变较弱的蚀变糜棱岩带到应变较强的蚀变超糜棱岩带，伊利石的结晶度有变小的趋势，而绿泥石的结晶度则基本保持不变。认为在成矿流体作用过程中，粘土矿物的形成和特点不仅受水／岩比的影响，而且在岩石变形过程中，岩石的应变和恢复速率也影响粘土矿物的结晶大小；伊利石和绿泥石平均结晶大小与其结晶度之间的关系可以反映岩石变形的机制和行为。  相似文献   

18.
云南小湾断层泥矿物特征及其构造意义   总被引：2，自引：0，他引：2       下载免费PDF全文
通过显微镜观察、X射线衍射、红外光谱和化学分析等方法研究云南小湾断层泥中伊利石矿物特征,结果显示:(1)断层泥中的伊利石发育定向排列,其集合体呈扭折褶皱变形,有时呈流状构造充填在碎屑之间;(2)伊利石的X射线衍射特征为△[(002)-(001)]>8°,Ir>1,BB1<4°,属ISII有序混层,膨胀层约占15%,晶胞参数b0=8.993Å,1M多型结构;(3)层间阳离子2Ca+Na+K≈1,MgO含量变化1.05%-2.89%,结晶水(H2O+)含量变化4.43%-5.23%。综合上述特征认为,断层泥伊利石不同于其它成因的伊利石,它是断层活动的直接产物,因此,根据它的特征可以推测断层活动机制。  相似文献   

19.
Detailed b lattice parameter and illite crystallinity (IC) studies of K-white micas in slates from the Stawell and Ballarat-Bendigo Zones (SZ, BBZ) in the western Lachlan Fold Belt of Victoria, Australia, reveal a metamorphic pattern characterized by regional metamorphism associated with crustal thickening and younger contact metamorphism accompanied by deformation. The IC data indicate that rocks regionally metamorphosed prior to the intrusion of the Early and Late Devonian granitoids, vary in grade from epizonal (greenschist facies) to diagenetic (zeolite facies) and that most are of epizonal to anchizonal (prehnite–pumpellyite facies) grade. In the BBZ, a decrease in grade from west to east occurs. Across fault zones, IC values show little change, indicating that limited vertical displacement has occurred. This is in accord with the thin skinned deformation model proposed for the western Lachlan Fold Belt. The b lattice parameters (x=9.022 Å; n=137; σn=0.009) indicate baric conditions intermediate between those of New Hampshire (P=Al2SiO5 triple point) and Otago (intermediate P ). Thus, a moderately low geothermal gradient existed 450–430 Ma ago, when these rocks were deformed. KD Fe/Mg (actinolite)/Fe/Mg (chlorite) values (0.52–0.70) obtained from coexisting actinolite and chlorite in metabasites from fault zones support the moderately high-P (c. 4 kbar) metamorphism suggested by the b cell parameter values. The metamorphic conditions indicated by these data are contrary to the low-P/high-T conditions proposed by previous authors, who inferred an intimate association between deformation, granitoid intrusion and gold mineralization. The b lattice parameter of white micas in slates adjacent to Early Devonian (c. 400 Ma) granitoids with schist bearing aureoles in the north-eastern part of the BBZ (x=9.002 Å; n=27; σn=0.007), indicate pressures in the order of c. 2.5 kbar which are in accord with those obtained from andalusite–cordierite and zoisite–garnet bearing assemblages observed in the higher grade metapelitic and calcareous rocks. This contrasts with the higher pressure (c. 4 kbar) existing during regional metamorphism and implies that c. 6.5–8 km of metasedimentary rocks in the BBZ were removed before the emplacement of the Early Devonian granitoids. Metamorphic assemblages in hornfelses associated with Late Devonian granitoids indicate a further 5–6 km of metasediment were removed in the next 40 Ma prior to their emplacement. This study shows the value of white mica studies in elucidating the tectonothermal history of a low-grade metamorphic terrane dominated by metapelitic rocks.  相似文献   

20.
The dissolution rate of illite, a common clay mineral in Australian soils, was studied in saline-acidic solutions under far from equilibrium conditions. The clay fraction of Na-saturated Silver Hill illite (K1.38Na0.05)(Al2.87Mg0.46Fe3+0.39Fe2+0.28Ti0.07)[Si7.02Al0.98]O20(OH)4 was used for this study. The dissolution rates were measured using flow-through reactors at 25 ± 1 °C, solution pH range of 1.0-4.25 (H2SO4) and at two ionic strengths (0.01 and 0.25 M) maintained using NaCl solution. Illite dissolution rates were calculated from the steady state release rates of Al and Si. The dissolution stoichiometry was determined from Al/Si, K/Si, Mg/Si and Fe/Si ratios. The release rates of cations were highly incongruent during the initial stage of experiments, with a preferential release of Al and K over Si in majority of the experiments. An Al/Si ratio >1 was observed at pH 2 and 3 while a ratio close to the stoichiometric composition was observed at pH 1 and 4 at the higher ionic strength. A relatively higher K+ release rate was observed at I = 0.25 in 2-4 pH range than at I = 0.01, possibly due to ion exchange reaction between Na+ from the solution and K+ from interlayer sites of illite. The steady state release rates of K, Fe and Mg were higher than Si over the entire pH range investigated in the study. From the point of view of the dominant structural cations (Si and Al), stoichiometric dissolution of illite occurred at pH 1-4 in the higher ionic strength experiments and at pH ?3 for the lower ionic strength experiments. The experiment at pH 4.25 and at the lower ionic strength exhibited lower RAl (dissolution rate calculated from steady state Al release) than RSi (dissolution rate calculated from steady state Si release), possibly due to the adsorption of dissolved Al as the output solutions were undersaturated with respect to gibbsite. The dissolution of illite appears to proceed with the removal of interlayer K followed by the dissolution of octahedral cations (Fe, Mg and Al), the dissolution of Si is the limiting step in the illite dissolution process. A dissolution rate law showing the dependence of illite dissolution rate on proton concentration in the acid-sulfate solutions was derived from the steady state dissolution rates and can be used in predicting the impact of illite dissolution in saline acid-sulfate environments. The fractional reaction orders of 0.32 (I = 0.25) and 0.36 (I = 0.01) obtained in the study for illite dissolution are similar to the values reported for smectite. The dissolution rate of illite is mainly controlled by solution pH and no effect of ionic strength was observed on the dissolution rates.  相似文献   

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