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1.
Clay mineral found in rivers, estuaries, and marine sedimentary environments is an important group of minerals which is the by-product of chemical weathering. The main constituents of this fine-grained sediment include mudstones, clay stones, and shales. This is probably the first report of a Fourier transform infrared spectroscopy (FTIR) and scanning electron microscope (SEM) investigation on the clay minerals to characterize them in the Sundarban mangrove core sediments of Moipith Matla and Belamati Island. This study was carried out in the selected stretch for FTIR and SEM analyses. The study reveals the dominant association of kaolinite with subordinate amount of quartz, illite, and chlorite. The abundance of kaolinite, illite, chlorite, and clay with quartz helps in increasing the sediment in the island region. The geochemical and mineralogical evolution of mangrove sediment results in the interaction of biotic and abiotic parameters, whose balance is conditioned by the climate that governs the hydrologic regime, the sedimentation dynamics, and of the organic matter. This study on the characterization of clay provides substantial impact in the water-holding capacity, productivity, and mineralogical and chemical transformation in order to establish much more and intermediate equilibrium between marine influence and continental contribution, as a part of the estuarine environment.  相似文献   

2.
Clay minerals, byproducts of chemical weathering, are important group of minerals found in rivers, estuaries, and marine sedimentary environments, which include mudstones, clay stones, and shales. In the present study, FTIR and SEM investigation on the clay minerals in Sundarban mangrove core sediments collected from Moipith Matla and Belamati Island are carried out. The study indicated the dominant association of kaolinite with subordinate amount of quartz, illite and chlorite. The abundance of kaolinite, illite chlorite and clay with quartz helps in increasing sediment in the islands region. The geochemical and mineralogical evolution of mangrove sediments are results of the interaction of biotic and abiotic parameters, whose balance is conditioned by the climate that governs the hydrologic regime, the sedimentation dynamics and the organic matter. This study on the charaterstation of clay provides us with substantial impact in the water holding capacity, productivity and mineralogical and chemical transformation in order to establish much more and intermediate equilibrium between marine influence and continental contribution, as part of the estuarine environment, than to the tropical climate conditions.  相似文献   

3.
The influence of hydrodynamics on the chemical composition of sediments is based on the uneven distribution of element abundances in different size fractions. In this study, 72 size‐fractional sediments from the Huanghe (Yellow River) and Changjiang (Yangtze River) riverbeds were measured with XRD, SEM, ICP‐AES and ICP‐MS. The analysis results show that the mineral and chemical characteristics change with grain size in the Huanghe and Changjiang sediments. According to the principal components analysis, three independent geochemical factors were found. The first factor elements, Zr, Hf, Th, U, Y, La and TiO2 are influenced by the existence of heavy minerals. The second factor elements, Al2O3, alkalis, alkaline earth (excluding Ca and Sr) and most of the transitional metals are dominated by clay minerals. The third factor group includes Ca and Sr, which were controlled by calcium‐bearing mineral contents and chemical weathering intensities. The various grain size distributions greatly affect the mineralogical and chemical compositions of bulk sediments. Compared to other size fractions, the 5–6PHI size fractions of the Huanghe and Changjiang sediments have special mineralogical and chemical compositions, and intermediate volume percentages. Weight or volume percentage of each size fraction may be more suitable than mean grain‐size of the bulk sediment to elucidate the grain size effects. Chemical Index of Alteration (CIA) values increase steeply with decreasing grain size, while Weathering Index of Parker (WIP) values are relatively stable. Because of the big influence of the abundance of clay minerals on CIA values, it is questionable to use CIA as a proxy of weathering intensity. Considering the clay mineral effects, stability in values and heterogeneous material properties, WIP has the potential to indicate the chemical weathering intensity of sediments. Copyright © 2014 John Wiley & Sons, Ltd.  相似文献   

4.
Iron (III) oxides are ubiquitous in near-surface soils and sediments and interact strongly with dissolved phosphates via sorption, co-precipitation, mineral transformation and redox-cycling reactions. Iron oxide phases are thus, an important reservoir for dissolved phosphate, and phosphate bound to iron oxides may reflect dissolved phosphate sources as well as carry a history of the biogeochemical cycling of phosphorus (P). It has recently been demonstrated that dissolved inorganic phosphate (DIP) in rivers, lakes, estuaries and the open ocean can be used to distinguish different P sources and biological reaction pathways in the ratio of 18O/16O (δ18OP) in PO43−. Here we present results of experimental studies aimed at determining whether non-biological interactions between dissolved inorganic phosphate and solid iron oxides involve fractionation of oxygen isotopes in PO4. Determination of such fractionations is critical to any interpretation of δ18OP values of modern (e.g., hydrothermal iron oxide deposits, marine sediments, soils, groundwater systems) to ancient and extraterrestrial samples (e.g., BIF’s, Martian soils). Batch sorption experiments were performed using varied concentrations of synthetic ferrihydrite and isotopically-labeled dissolved ortho-phosphate at temperatures ranging from 4 to 95 °C. Mineral transformations and morphological changes were determined by X-Ray, Mössbauer spectroscopy and SEM image analyses.Our results show that isotopic fractionation between sorbed and aqueous phosphate occurs during the early phase of sorption with isotopically-light phosphate (P16O4) preferentially incorporated into sorbed/solid phases. This fractionation showed negligible temperature-dependence and gradually decreased as a result of O-isotope exchange between sorbed and aqueous-phase phosphate, to become insignificant at greater than ∼100 h of reaction. In high-temperature experiments, this exchange was very rapid resulting in negligible fractionation between sorbed and aqueous-phase phosphate at much shorter reaction times. Mineral transformation resulted in initial preferential desorption/loss of light phosphate (P16O4) to solution. However, the continual exchange between sorbed and aqueous PO4, concomitant with this mineralogical transformation resulted again in negligible fractionation between aqueous and sorbed PO4 at long reaction times (>2000 h). This finding is consistent with results obtained from natural marine samples. Therefore, 18O values of dissolved phosphate (DIP) in sea water may be preserved during its sorption to iron-oxide minerals such as hydrothermal plume particles, making marine iron oxides a potential new proxy for dissolved phosphate in the oceans.  相似文献   

5.
    
Almost the entire suspended load of Yamuna River is transported during the monsoon period; quartz and illite are the dominant minerals of these suspended sediments. Basin lithology, tributary contributions, and sediment grain size seem to control mineral distribution in the sediments. Trace metal concentrations of Yamuna core sediments reflect their mineralogical composition. Illite is the chief clay mineral of the Himalayan river sediments. The mineralogical characteristics of the Himalayan river sediments differ significantly from the Peninsular Indian rivers, which chiefly carry montmorillonite.  相似文献   

6.
Anaerobic oxidation of methane (AOM) occurring in the marine sediment is an important process for methane cycle and methane sequestration. In this work, a one-dimensional numerical model was developed to study the distribution of advective methane flux with the AOM process. The model has been applied to investigate the gas hydrates bearing sediments of Shenhu areas located in the northern South China Sea, where advective methane transport was detected. The modeling results suggest that methane flux will be consumed in the sediment column via dissolution, sorption, and AOM reaction. Only when the methane flux was one order of magnitude higher than current level, then a portion of methane will enter water column and possibly escape to the atmosphere. The numerical simulation also revealed that, due to the lower permeability of the silt–clay sediments, a much thicker sulfate-methane transition zone exists in the Shenhu area, where AOM is able to consume more.  相似文献   

7.
The bed and suspended (slime) sediment phases associated with effluent water that are produced from phosphate-ore-upgrading process at Al-Abyad mine in the southern part of Jordan were analyzed chemically and mineralogically. The results show that the effluent water is highly oxic and mildly alkaline in nature. The geochemical behavior of each phase was controlled by the effluent water physicochemical parameters, sediment particle size, mineralogical constituents of the studied phases, and the prevailing climatic nature of the area. Bed sediments have higher concentrations of many elements than slime. Accordingly, the bed sediments can be considered as a sink rather than a pool for many elements. The geochemical dissociation of major oxides and trace elements between bed and slime sediments was evident using t test, particularly between P2O5, SiO2, CaO, K2O, Mn, Sr, Y, and Co, and to lesser extent, V, U, Zn, and Cr. This might be attributed to effluent water characteristics, mineralogy, and the presence of fine-grained materials. The spatial distribution of major oxide and trace element concentrations along the stream drainage exhibited a slight increase with distance either in bed or slime sediment phases. However, they increased suddenly at the last three sampling sites, which might be due to the abundance of fine-grained materials that are mainly composed of clay minerals (montmorillonite) that would enhance the adsorption process. Moreover, the XRD results confirmed the existence of elemental geochemical dissociation as a function of mineral control.  相似文献   

8.
Pore water chemistry and 234U/238U activity ratios from fine-grained sediment cored by the Ocean Drilling Project at Site 984 in the North Atlantic were used as constraints in modeling in situ rates of plagioclase dissolution with the multicomponent reactive transport code Crunch. The reactive transport model includes a solid-solution formulation to enable the use of the 234U/238U activity ratios in the solid and fluid as a tracer of mineral dissolution. The isotopic profiles are combined with profiles of the major element chemistry (especially alkalinity and calcium) to determine whether the apparent discrepancy between laboratory and field dissolution rates still exists when a mechanistic reactive transport model is used to interpret rates in a natural system. A suite of reactions, including sulfate reduction and methane production, anaerobic methane oxidation, CaCO3 precipitation, dissolution of plagioclase, and precipitation of secondary clay minerals, along with diffusive transport and fluid and solid burial, control the pore fluid chemistry in Site 984 sediments. The surface area of plagioclase in intimate contact with the pore fluid is estimated to be 6.9 m2/g based on both grain geometry and on the depletion of 234U/238U in the sediment via α-recoil loss. Various rate laws for plagioclase dissolution are considered in the modeling, including those based on (1) a linear transition state theory (TST) model, (2) a nonlinear dependence on the undersaturation of the pore water with respect to plagioclase, and (3) the effect of inhibition by dissolved aluminum. The major element and isotopic methods predict similar dissolution rate constants if additional lowering of the pore water 234U/238U activity ratio is attributed to isotopic exchange via recrystallization of marine calcite, which makes up about 10-20% of the Site 984 sediment. The calculated dissolution rate for plagioclase corresponds to a rate constant that is about 102 to 105 times smaller than the laboratory-measured value, with the value depending primarily on the deviation from equilibrium. The reactive transport simulations demonstrate that the degree of undersaturation of the pore fluid with respect to plagioclase depends strongly on the rate of authigenic clay precipitation and the solubility of the clay minerals. The observed discrepancy is greatest for the linear TST model (105), less substantial with the Al-inhibition formulation (103), and decreases further if the clay minerals precipitate more slowly or as highly soluble precursor minerals (102). However, even several orders of magnitude variation in either the clay solubility or clay precipitation rates cannot completely account for the entire discrepancy while still matching pore water aluminum and silica data, indicating that the mineral dissolution rate conundrum must be attributed in large part to the gradual loss of reactive sites on silicate surfaces with time. The results imply that methods of mineral surface characterization that provide direct measurements of the bulk surface reactivity are necessary to accurately predict natural dissolution rates.  相似文献   

9.
In the geochemical study of sedimentation, hydrogen and oxygen isotope data are useful for a discussionon formation conditions and material sources of sediments. Hydrogen and oxygen isotope analyses were madeon clays separated from the sea-floor surface sediments at 9 stations in the western sea region of the AntarcticPeninsula. On the basis of these isotopic data and the clay mineral components and by use of statistical dia-grams, it may be concluded that the clay fraction in this sea region is composed mainly of terrigenous detritus:i.e. it was formed by surface weathering or supergene alteration of the rocks from the terrigenous region in thepeninsular in the presence of meteoric water. However, at least a part of montmorillonite is a marine authigenicmineral formed by alteration of submarine eruptive materials or terrigenous pyroclasts in the presence of seawater. The above result is consistent with the idea derived from the study of clay mineralogy.  相似文献   

10.
The December 2004 Indian Ocean Tsunami (IOT) had a major impact on the geomorphology and sedimentology of the east coast of India. Estimation of the magnitude of the tsunami from its deposits is a challenging topic to be developed in studies on tsunami hazard assessment. Two core sediments (C1 and C2) from Nagapattinam, southeast coast of India were subjected to textural, mineral, geochemical and rock-magnetic measurements. In both cores, three zones (zone I, II and III) have been distinguished based on mineralogical, geochemical and magnetic data. Zone II is featured by peculiar rock-magnetic, textural, mineralogical and geochemical signatures in both sediment cores that we interpret to correspond to the 2004 IOT deposit. Textural, mineralogical, geochemical and rock-magnetic investigations showed that the tsunami deposit is featured by relative enrichment in sand, quartz, feldspar, carbonate, SiO 2, TiO 2, K 2O and CaO and by a depletion in clay and iron oxides. These results point to a dilution of reworked ferromagnetic particles into a huge volume of paramagnetic materials, similar to what has been described in other nearshore tsunami deposits (Font et al. 2010). Correlation analysis elucidated the relationships among the textural, mineral, geochemical and magnetic parameters, and suggests that most of the quartz-rich coarse sediments have been transported offshore by the tsunami wave. These results agreed well with the previously published numerical model of tsunami induced sediment transport off southeast coast of India and can be used for future comparative studies on tsunami deposits.  相似文献   

11.
The sorption of226Ra from oil-production brine by soils and sediments was investigated. Sorption was rapid, and the percentage sorbed increased with brine dilution. Greatest removals of226Ra from sediments in the laboratory occurred with alkaline DTPA, HCl, and BaCl2, with lesser removals using CaCl2 and NaCl solutions. Digestion of sediments with NaOCl indicates that most of the native and sorbed226Ra is associated with the mineral rather than organic fraction of the sediments. Correlation analysis based on 14 soils indicates that the retention of226Ra may involve precipitation reactions associated with sulfate-bearing minerals, as well as ion-exchange reactions with the clay mineral fractions of surficial earth materials. Oceanographer, Naval Ocean Research and Development Activity, Code 334; NSTL Station, Mississippi 39529 NORDA Contribution #83:334:01.  相似文献   

12.
Gas associated with Carboniferous coal seams and younger Miocene sediments in the SW Upper Silesian Basin in Czech Republic shows wide compositional variation. Coal-related gas extracted from cross-measure degassing boreholes, as well as gas released during canister desorption of coal samples from three different mines was analyzed to evaluate the genetic origin and the influence of sorption/desorption processes on the gas composition. Analyses comprised the compositional and stable carbon and isotope composition of coal-related gases. The isotopic composition of gas from cross-measure boreholes indicates thermogenic origin in the southern part of the basin and microbial CO2 reduction and mixed type origin in the northern part. Gas from canister desorption shows similar origins, but larger compositional and isotopic variation. No consistent isotopic fractionation due to desorption could be observed. Differences in geochemical composition of thermogenic gases could indicate a contribution of gas migrated from deeper formations below the Carpathian overthrust.  相似文献   

13.
鄂尔多斯盆地东北缘保德地区煤层气成因   总被引：3，自引：0，他引：3  
       鄂尔多斯盆地东北缘保德地区煤层气井组试采取得较好效果,但煤层气成因尚未形成统一认识,影响到对区域煤层 气勘探开发潜力的进一步认识。本文基于各类煤层气样品组分和稳定同位素的分析,对其成因进行了探讨。结果表明,煤 层气组分以甲烷为主,重烃浓度极低;δ13CCH4明显偏轻,部分δ13CCH4和δDCH4分布在热成因与二氧化碳还原型生物成因气过 渡区间;δ13CCO2相对较重,且与δ13CCH4之间存在负相关关系。分析认为,该区煤层气具有混合成因,以热成因气为主,兼 具生物成因气的特征,生物甲烷形成于二氧化碳还原途径,煤层水的化学和动力条件以及煤岩孔渗条件有利于产甲烷菌的 大量繁殖。  相似文献   

14.
This paper presents new major and trace-element data and Lu-Hf and Sm-Nd isotopic compositions for representative suites of marine sediment samples from 14 drill sites outboard of the world’s major subduction zones. These suites and samples were chosen to represent the global range in lithology, Lu/Hf ratios, and sediment flux in subducting sediments worldwide. The data reported here represent the most comprehensive data set on subducting sediments and define the Hf-Nd isotopic variations that occur in oceanic sediments and constrain the processes that caused them.Using new marine sediment data presented here, in conjunction with published data, we derive a new Terrestrial Array given by the equation, εHf = 1.55 × εNd + 1.21. This array was calculated using >3400 present-day Hf and Nd isotope values. The steeper slope and smaller y-intercept of this array, compared to the original expression (εHf = 1.36 × εNd + 2.89; Vervoort et al., 1999) reflects the use of present day values and the unradiogenic Hf of old continental samples included in the array.In order to examine the Hf-Nd isotopic variations in marine sediments, we have classified our samples into 5 groups based on lithology and major and trace-element geochemical compositions: turbidites, terrigenous clays, and volcaniclastic, hydrothermal and hydrogenetic sediments. Compositions along the Terrestrial Array are largely controlled by terrigenous material derived from the continents and delivered to the ocean basins via turbidites, volcaniclastic sediments, and volcanic inputs from magmatic arcs. Compositions below the Terrestrial Array derive from unradiogenic Hf in zircon-rich turbidites. The anomalous compositions above the Terrestrial Array largely reflect the decoupled behavior of Hf and Nd during continental weathering and delivery to the ocean. Both terrigenous and hydrogenetic clays possess anomalously radiogenic Hf, reflecting terrestrial sedimentary and weathering processes on the one hand and marine inheritance on the other. This probably occurs during complementary processes involving preferential retention of unradiogenic Hf on the continents in the form of zircon and release of radiogenic Hf from the breakdown of easily weathered, high Lu-Hf phases such as apatite.  相似文献   

15.
The effect of organic matter on the sorption of dissolved organic matter (DOM) on lake sediments is critical to understanding the fate and transport of contaminants at the sediment–water interface in lake ecosystems. Results indicate that DOM sorption on sediment is largely due to ligand exchange between the DOM and hydroxyl groups, and the amount of DOC sorbed is a linear function of added DOC. With increasing organic matter content the sediment has lower binding strength, higher releasing ability for DOM, and the higher amount of DOM sorbed by sediment naturally. There was no clear difference before and after the sediment was treated with H2O2, but the constant b implied that after the sediments were treated DOC release was promoted. Organic matter in the sediment tends to impede the sorption of DOC and results in a remarkable decrease in DOC sorption rates.  相似文献   

16.
Boom Clay is currently viewed as a reference host formation for studies on deep geological disposal of radioactive waste in Belgium. The interactions between bulk rock Boom Clay and 0.1 M KOH, 0.1 M NaOH, 0.1 M Ca(OH)2, young cement water and evolved cement water solutions, ranging in pH from 12.5 to 13.2, were examined as static batch experiments at 60 °C to simulate alkaline plume perturbations, which are expected to occur in the repository due to the presence of concrete. Both liquids and solids were investigated at specific times between 90 and 510 days in order to control the elemental budget and to search for potential mineralogical alterations. Also, the clay fraction was separated from the whole-rock Boom Clay at the end of each run and characterized for its mineralogical composition. Thereby, the importance of the mineral matrix to buffer the alkaline attack and the role of organic matter to protect clay minerals were also addressed. The results indicate that the degree of geochemical perturbation in Boom Clay is dependent on the initial pH of the applied solution together with the nature of the major cation in the reactant fluids. The higher the initial pH of the media, the stronger its interaction with Boom Clay. No major non-clay mineralogical alteration of the Boom Clay was detected, but dissolution of kaolinite, smectite and illite occurred within the studied experimental conditions. The dissolution of clays is accompanied by the decrease in the layer charge, followed by a decrease in the cation-exchange capacity. The highest TOC values coincide with the highest total elemental concentrations in the leachates, and correspondingly, the highest dissolution degree. However, no quantitative link could be established between the degree of organic matter decomposition and clay dissolution.  相似文献   

17.
《Applied Geochemistry》2005,20(1):193-205
Sorption and precipitation of Co(II) in simplified model systems related to the Hanford site high-level nuclear waste tank leakage were investigated through solution studies, geochemical modeling, and X-ray absorption fine structure (XAFS) spectroscopy. Studies of Co(II) sorption to pristine Hanford sediments (ERDF and Sub), which consist predominantly of quartz, plagioclase, and alkali feldspar, show an adsorption edge centered at pH ≈ 8.0 for both sediments studied, with sorption >99% above pH ≈ 9.0. Aqueous SiO2 resulting from dissolution of the sediments increased in concentration with increasing pH, though the systems remained undersaturated with respect to quartz. XAFS studies of Co(II) sorption to both sediment samples reveal the oxidation of Co(II) to Co(III), likely by dissolved O2, although this oxidation was incomplete in the Sub sediment samples. The authors propose that Fe(II) species, either in aqueous solution or at mineral surfaces, partially inhibited Co(II) oxidation in the Sub sediment samples, as these sediments contain significantly higher quantities of Fe(II)-bearing minerals which likely partially dissolved under the high-pH solution conditions. In alkaline solutions, Al precipitated as bayerite, gibbsite, or a mixture of the two at pH > 7; an amorphous gel formed at pH values less than 7. Aqueous Co concentrations were well below the solubility of known Co-bearing phases at low pH, suggesting that Co was removed from solution through an adsorption mechanism. At higher pH values, Co concentrations closely matched the solubility of a Co-bearing hydrotalcite-like solid. XAFS spectra of Co(II) sorbed to Al-hydroxide precipitates are similar to previously reported spectra for such hydrotalcite-like phases. The precipitation processes observed in this study can significantly reduce the environmental hazard posed by 60Co in the environment.  相似文献   

18.
Clay mineralogy of Triassic sediments in southern Israel and Sinai   总被引：1，自引：0，他引：1  
The clay mineral composition of Triassic sediments in the Negev and Sinai depends upon the environment of deposition. Kaolinite predominates in continental and epicontinental sediments. The mineralogical composition of the marine clays resembles that of corresponding samples from North Africa and Europe, which comprise various mixtures and interstratifications of illite, montmorillonite, vermiculite and chlorite. Evaporitic sediments are poor in clay minerals and those present are largely detrital. The results presented suggest that chlorite was formed diagenetically by prolonged percolation of seawater through pervious layers overlying impervious ones (hard beds).  相似文献   

19.
Forty-two substrate sediment samples and three cores procured from the shelf region between Chennai and Cuddalore were analyzed to understand the spatial and vertical sediment distribution. Samples subjected to grain size, bulk and clay mineralogical analyses, REE and trace element geochemistry yielded interesting results about the sediment characteristics with respect to the modern day environment. The present study revealed that the study area is characterized by high energy environment marked by predominant composition of medium sand. Results confirmed the evidence of more illite than kaolinite, smectite, and chlorite in the clay mineral assemblage indicating a terrigenous source. Geochemical data also revealed that the enrichment of light rare earth elements (LREE) in the sediments is due to continental source of Precambrian times. High feldspar content in the sediments which is emphasized by bulk mineralogical data displayed positive Eu anomaly. By using the paleoredox index, the area of interest is considered to have undergone no major changes in its depositional settings.  相似文献   

20.
Sediments of the western part of the Valjevo-Mionica basin(Serbia)were examined both geochemically and mineralogically to explain,on the basis of their sedimentologicai characteristics,the causes of changes in their qualitative and quantitative composition.A total of 62 samples obtained from the drilihole at depths up to 400 m was investigated.Using correlation of the obtained data,six geochemical zones were defined,two of which being specially distinguished by their mineralogical, geochemical and sedimentological characteristics.The first one,upper zone A,consists of banded marlstones interbedded with clay and oil shales and is characterized by presence of analcite and searlesite.These minerals and very high contents of Na_2O indicate sedimentation in alkaline conditions with increased salinity in arid climate.That provided pronounced water stratification,as well as higher bioproductivity in the basin and sedimentary organic matter preservation.Therefore,the zone A sediments are characterized by high organic matter contents of the type which provides good potential for production of liquid hydrocarbons.Another specific zone,zone F,contains sediments with very high MgO,K_2O and Li concentrations.Their geochemical correlation,as well as almost complete absence of illite in this zone,indicates the presence of interstratified clay mineral type illite-saponite (lithium-bearing Mg-smectite).  相似文献   

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