Effect of illite particle shape on cesium sorption

USGS Publications Warehouse

Rajec, Pavol; Šucha, Vladimír; Eberl, Dennis D.; Środoń, Jan; Elsass, Françoise E.

1999-01-01

Samples containing illite and illite-smectite, having different crystal shapes (plates, “barrels”, and filaments), were selected for sorption experiments with cesium. There is a positive correlation between total surface area and Cs-sorption capacity, but no correlation between total surface area and the distribution coefficient, Kd. Generally Kd increases with the edge surface area, although “hairy” (filamentous) illite does not fit this pattern, possibly because elongation of crystals along one axis reduces the number of specific sorption sites.

Microbial Reduction of Structural Fe3+ in Nontronite by a Thermophilic Bacterium and its Role in Promoting the Smectite to Illite Reaction

DTIC Science & Technology

2007-01-01

role in promoting the smectite to Hike reaction GENGXIN ZHANG,’ HAIUANG DONG, 1 * JINWOOK KIM,2 AND D.D. EBERL3 ’Department of Geology, Miami...Geological Survey, Boulder, Colorado 80303, USA. ABSTRACT The illitization process of Fe-rich smectite (nontronite NAu-2) promoted by microbial reduction of...layers of illite/ smectite or highly charged smectite were detected under other conditions. The morphology of biogenic illite evolved from lath and flake

Synthesis of illite-smectite from smectite at earth surface temperatures and high pH

USGS Publications Warehouse

Eberl, D.D.; Velde, Bruce; McCormick, T.C.

1993-01-01

It is well known that illite-smectite can form from smectite at elevated temperatures in natural and experimental systems. However, the conversion of smectite to illite-smectite is also found in some natural systems that have never been heated. The present experiments show that illite layers can form from smectite by chemical reaction at 35° and 60°C at high solution pH. The rate of this reaction is accelerated by wetting and drying.

Mineralogy and provenance of clays in miarolitic cavities of the Pikes Peak Batholith, Colorado

USGS Publications Warehouse

Kile, D.E.

2005-01-01

Clay samples from 105 cavities within miarolitic granitic pegmatites throughout the Pikes Peak batholith, in Colorado, were analyzed by powder X-ray diffraction (XRD). Smectite (beidellite), illite, and kaolinite were found within the cavities. Calculation of crystallite-thickness distribution (CTD), mean thickness of the crystallites, and variance in crystallite thickness, as deduced from XRD patterns, allowed a determination of provenance and mode of formation for illite and smectite. Authigenic miarolitic-cavity illite and smectite show lognormal CTDs and larger mean thicknesses of crystallites than do their soil-derived counterparts; non-lognormal illite in a cavity results from mixing of cavity and soil illite. Analysis of mean thickness and thickness variance shows that crystal growth of illite is initiated by a nucleation event of short duration, followed by surface-controlled kinetics. Crystallization of the miarolitic cavity clays is presumed to occur by neoformation from hydrothermal fluids. The assessment of provenance allows a determination of regional and local distributions of clay minerals in miarolitic cavities within the Pikes Peak batholith.

A closer look at 40Ar/39Ar systematics of illite, recoil, retention ages, total gas ages, and a new correction method

NASA Astrophysics Data System (ADS)

Fitz-Diaz, E.; Hall, C. M.; van der Pluijm, B.

2013-12-01

One of the fundamentals of 40Ar-39Ar systematics of illite considers the effects of 39Ar recoil (ejection of 39Ar from tiny illite crystallites during the nuclear reaction 39K(n,p)39Ar), for which sample vacuum encapsulation prior to irradiation has been used since the 1990's. This technique separately measures the fraction of recoiled 39Ar and the Ar (39Ar and 40Ar) retained within illite crystals as they degas during step heating in vacuum. Total-gas ages (TGA) are calculated by using both recoiled and retained argon, while retention ages (RA) only involve retained Ar. Observations in numerous natural examples have shown that TGA fit stratigraphic constraints of geological processes when the average illite crystallite thickness (ICT) is smaller than 10nm, and that RA better matches these constrains for larger ICTs. Illite crystals with ICT >50nm show total gas and retention ages within a few My and they are identical, within analytical error, when ICT exceeds 150nm. We propose a new age correction that takes into account the average ICT and corresponding recoil for a sample , with such corrected ages (XCA) lying between the TGA and RA end-member ages. We apply this correction to samples containing one generation of illite and it particularly affects illite populations formed in the anchizone, with typical ICT values between 10-40nm. We analyzed bentonitic samples (S1, S2 and S3) from sites in Cretaceous carbonates in the front of the Monterrey salient in northern Mexico. Four size fractions (<0.05, 0.05-0.2, 0.2-1 & 1-2 μm) were separated, analyzed with XRD and dated by Ar-Ar. XRD analysis provides mineralogic characterization, illite polytype quantification, and illite crystallite thickness (ICT) determination using half-height peak width (illite crystallinity) and the Scherrer equation. All samples contain illite as the main mineral phase, ICT values between 8-27nm, from fine to coarser grain size fractions. Ages show a range in TGA among the different size fractions of S1, S2 and S3, respectively: 46-49, 36-43 and 40-52 My) and RA (54-64, 47-52 and 53-54 My. XCA calculations produce tighter constrained ranges (53-57, 45.5-48.5 and 49-52 My) with an overall average 51.1Ma×3.9 My. In the ICT vs. apparent age plot, authigenic illite grains show a greater slope that is in general slightly positive for TGA, slightly negative for RA, but close to zero for XCA. In the ICT vs. XCA plot thinner crystallites shows more dispersion than thicker ones. In order to test if such dispersion in the age of the finer/thinner illite is due to a different formation history in each site or the result of retention capability, degassing spectra were modeled for site XCA averages and overall XCA average. The modeling shows that local site ages best match the measured spectra, instead of a single age for the combined sites. The closeness between experimental and artificial degassing patterns also supports the hypothesis that each sample preserves a single age population. All illite grains in these samples grew progressively during folding in a time window that is constrained by the three sites. Small and large grains represent the same population in each sample, representing progressive degrees of grain growth (Ostwald ripening).

Illitization and paleothermal regimes in the Middle Ordovician St. Peter Sandstone, Central Michigan Basin: K-Ar, Oxygen Isotope, and fluid inclusion data

DOE Office of Scientific and Technical Information (OSTI.GOV)

Girard, J.P.; Barnes, D.A.

1995-01-01

Hydrocarbon reservoirs occur in the Middle Ordovician St. Peter Sandstone in the central Michigan basin at depths of 1.5-3.5 km and are diagenetically altered. Latest diagenetic cements include saddle dolomite, pervasive microcrystalline illite and chlorite, and quartz. A K-Ar and {sup 18}O/{sup 16}O study of the fine-grained authigenic illite in 25 samples from 16 wells covering a large area within the basin yields K-Ar ages ranging from 367 to 322 Ma and {delta}{sup 18}O values between 12.7 and 16.9% SMOW. The {delta}{sup 18}O values of diagenetic quartz overgrowths range from 15.2 to 18.9%. Fluid inclusion temperatures in the quartz cementmore » range from 70 to 170{degrees}C, reflecting multiple generations of diagenetic quartz and/or precipitation over most of the diagenetic history. Reequilibrated fluid inclusions in the saddle dolomite cement yield temperatures ranging from 90 to 150{degrees}C. A regionally significant episode of illitization occurred during the Late Devonian-Mississipian. Temperatures of illite formation are indirectly estimated to be in the range of 125-170{degrees}C and most paleodepths of illitization are between 2.8 and 3.2 km. These results imply that (1) illite formed from {sup 18}O-rich fluids, and (2) elevated geothermal gradients, i.e., greater than 34% C/km, existed in the Michigan basin in the late Paleozoic. The K-Ar ages and the {delta}{sup 18}O values are not correlated to present depths of the samples or paleodepths of illitization. Illites with young ages and low {delta}{sup 18}O values tend to be geographically distributed along the north-south branch of the buried Precambrian rift. The {delta}{sup 18}O values of the diagenetic quartz follow a similar trend. The spread of illite K-Ar ages and {delta}{sup 19}O values, and their geographic distribution, are best explained as reflecting abnormally high thermal regimes in the part of the basin located above the presumably highly fractured basement along the rift.« less

K-Ar dating and delta O-18-delta D characterization of nanometric illite from Ordovician K-bentonites of the Appalachians: illitization and the Acadian-Alleghenian tectonic activity

USGS Publications Warehouse

Clauer, Norbert; Fallick, Anthony E.; Eberl, Dennis D.; Honty, Miroslav; Huff, Warren D.; Auberti, Amelie

2013-01-01

Nanometric (2 diagram that illitization occurred in all fractions by simultaneous nucleation and crystal growth, except for one sample. In that sample, a period of growth without nucleation was detected on top of the nucleation and growth episode. The K-Ar ages organize into two isochrons, the first at 319.9 ± 2.0 Ma with an initial 40Ar/36Ar ratio of 271 ± 66 Ma, and the second at 284.9 ± 1.2 Ma with an initial 40Ar/36Ar ratio of 310 ± 44. One data point above the older isochron and three between the two isochrons suggest a detrital contamination for the former separate and a possible further generation of nanoparticles for the three others. The samples with the older crystallization age consist of illite and illite-rich mixed-layers, and those with the younger age contain smectite-rich mixed-layers without illite, or illite-enriched illite-smectite mixed-layers. The K-Ar ages fit the age trends published previously for similar K-bentonites with regional age patterns between 240 and 270 Ma in the southwestern region, between 270 and 300 Ma in the central zone and the southern Appalachians, and between 315 and 370 Ma in the northernmost. Each of the two generations of illite crystals yields very consistent δ18O (V-SMOW) values at 17 ± 1‰ for the older and at 21 ± 1‰ for the younger. If crystallization temperatures of the nanometric illite were between 100 and 200 °C, as suggested by microthermometric determinations, the hydrothermal fluids had δ18O values of 4 ± 1‰ in the Dalton district and of 8 ± 1‰ in the Lafayette, Trenton, and Dirtseller districts at 100 °C, and of 11 ± 1 and 15 ± 1‰ in the same locations at 200 °C, probably because the water-rock isotope exchanges at elevated temperature occurred in rock-dominated systems. The δ18O of the fluids remained unchanged during local crystal growth, but varied depending on the geographic location of the samples and timing of illitization. The δD (V-SMOW) values of the different size fractions do not provide consistent information; they range from −70 to −45‰ for most nanometric and micrometric fractions (V-SMOW), but with no apparent coherent pattern. Nanometric illite-rich crystals from K-bentonite that underwent tectono-thermal alteration yield constant ages, constant clay mineralogy, constant crystallite size distributions for all of the nucleating and growing illite-type crystals of each sample, as well as constant δ18O values implying constant fluid chemistry, all pointing to geologically sudden crystallization.

Illite equilibria in solutions: III. A re-interpretation of the data of Sass et al. (1987)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Aja, S.U.

1991-11-01

In a recent solubility study of Goose Lake and Beavers Bend illite, SASS et al. (1987) inferred the existence of three components of natural illites (K{sub 0.24}/O{sub 10}(OH){sub 2}), (K{sub 0.67}/O{sub 10}(OH){sub 2}), and (K{sub 0.90}/O{sub 10}(OH){sub 2}) which were interpreted to be smectite, illite, and K-mica, respectively. They also speculated that illite-smectite equilibrium is metastable under diagenetic conditions except between 90 and 110C where it is stabilized by an ordering transition. A re-interpretation of the data of SASS et al. (1987) indicates that the solubility-controlling phases have the following K atoms per half cell: 0.29, 0.52, 0.69, 0.084, andmore » 1.0. Furthermore, solution equilibration investigations of kaolinite-microcline mixtures have shown that these two minerals do not coexist stably. Thus, the question of an ordering transition whose main effect is to stabilize illite-smectite equilibria relative to kaolinite-microcline assemblage does not arise.« less

Changes in particle morphology during illitization: An experimental study

USGS Publications Warehouse

Whitney, Gene; Velde, Bruce

1993-01-01

Smectite was reacted at several temperatures between 200°C and 500°C to produce interstratified illite/smectite (I/S) with different proportions of expandable layers. Dispersed and sedimented products were examined using a transmission electron microscope. Particle size and aspect ratio showed no systematic change as a function of reaction extent during R0 illitization. However, particles exhibited rounded edges during the early stages of the reaction, suggesting some dissolution of primary smectite. Additionally, increasing particle contrast in the electron beam suggests thickening of particles with increasing reaction extent. The thickening of particles is thought to be produced by the nucleation and precipitation of secondary illite layers on primary smectite layers. In the most extensively reacted I/S, particles have become aggregated into clumps or quasicrystals by lateral growth of illite layers. Internal uniformity of crystallographic alignment of individual growing crystals within each aggregate was reflected in the increasing frequency of 60° and 120° interfacial angles within each aggregate. In highly illitic I/S, these aggregates took on an overall euhedral form and became crystallographically contiguous, producing single crystal electron diffraction patterns.

Interpretation of K-Ar dates of illitic clays from sedimentary rocks aided by modeling

USGS Publications Warehouse

Srodon, J.; Clauer, Norbert; Eberl, D.D.D.

2002-01-01

K-Ar dates of illitic clays from sedimentary rocks may contain "mixed ages," i.e., may have ages that are intermediate between the ages of end-member events. Two phenomena that may cause mixed ages are: (1) long-lasting reaction during the burial illitization of smectite: and (2) physical mixing of detrital and diagenetic components. The first phenomenon was investigated by simulation of illitization reactions using a nucleation and growth mechanism. These calculations indicate that values for mixed ages are related to burial history: for an equivalent length of reaction time, fast burial followed by slow burial produces much older mixed ages than slow burial followed by fast. The type of reaction that occured in a rock can be determined from the distribution of ages with respect to the thickness of illite crystals. Dating of artificial mixtures confirms a non-linear relation between mixed ages and the proportions of the components. Vertical variation of K-Ar age dates from Gulf Coast shales can be modeled by assuming diagenetic illitization that overprints a subtle vertical trend (presumably of sedimentary origin) in detrital mineral content.

Experimental study and modelling of selenite sorption onto illite and smectite clays.

PubMed

Missana, T; Alonso, U; García-Gutiérrez, M

2009-06-15

This study provides a large set of experimental selenite sorption data for pure smectite and illite. Similar sorption behavior existed in both clays: linear within a large range of the Se concentrations investigated (from 1x10(-10) to 1x10(-3) M); and independent of ionic strength. Selenite sorption was also analysed in the illite/smectite system with the clays mixed in two different proportions, as follows: (a) 30% illite-70% smectite and (b) 43% illite-57% smectite. The objective of the study was to provide the simplest model possible to fit the experimental data, a model also capable of describing selenite sorption in binary illite/smectite clay systems. Selenite sorption data, separately obtained in the single mineral systems, were modeled using both a one- and a two-site non-electrostatic model that took into account the formation of two complexes at the edge sites of the clay. Although the use of a two-site model slightly improved the fit of data at a pH below 4, the simpler one-site model reproduced satisfactorily all the sorption data from pH 3 to 8. The complexation constants obtained by fitting sorption data of the individual minerals were incorporated into a model to predict the adsorption of selenium in the illite/smectite mixtures; the model's predictions were consistent with the experimental adsorption data.

Anatomy of a metabentonite: nucleation and growth of illite crystals and their colescence into mixed-layer illite/smectite

USGS Publications Warehouse

Eberl, D.D.; Blum, A.E.; Serravezza, M.

2011-01-01

The illite layer content of mixed-layer illite/smectite (I/S) in a 2.5 m thick, zoned, metabentonite bed from Montana decreases regularly from the edges to the center of the bed. Traditional X-ray diffraction (XRD) pattern modeling using Markovian statistics indicated that this zonation results from a mixing in different proportions of smectite-rich R0 I/S and illite-rich R1 I/S, with each phase having a relatively constant illite layer content. However, a new method for modeling XRD patterns of I/S indicates that R0 and R1 I/S in these samples are not separate phases (in the mineralogical sense of the word), but that the samples are composed of illite crystals that have continuous distributions of crystal thicknesses, and of 1 nm thick smectite crystals. The shapes of these distributions indicate that the crystals were formed by simultaneous nucleation and growth. XRD patterns for R0 and R1 I/S arise by interparticle diffraction from a random stacking of the crystals, with swelling interlayers formed at interfaces between crystals from water or glycol that is sorbed on crystal surfaces. It is the thickness distributions of smectite and illite crystals (also termed fundamental particles, or Nadeau particles), rather than XRD patterns for mixed-layer I/S, that are the more reliable indicators of geologic history, because such distributions are composed of well-defined crystals that are not affected by differences in surface sorption and particle arrangements, and because their thickness distribution shapes conform to the predictions of crystal growth theory, which describes their genesis.

Timing of Hydrocarbon Fluid Emplacement in Sandstone Reservoirs in Neogene in Huizhou Sag, Southern China Sea, by Authigenic Illite 40Ar- 39Ar Laser Stepwise Heating

NASA Astrophysics Data System (ADS)

Hesheng, Shi; Junzhang, Zhu; Huaning, Qiu; yu, Shu; Jianyao, Wu; Zulie, Long

Timing of oil or gas emplacements is a new subject in isotopic geochronology and petroleum geology. Hamilton et al. expounded the principle of the illite K-Ar age: Illite is often the last or one of the latest mineral cements to form prior to hydrocarbon accumulation. Since the displacement of formation water by hydrocarbons will cause silicate diagenesis to cease, K-Ar ages for illite will constrain the timing of this event, and also constrain the maximum age of formation of the trap structure. In this study, the possibility of authigenic illites 40Ar- 39Ar dating has been investigated. The illite samples were separated from the Tertiary sandstones in three rich oil reservoir belts within the Huizhou sag by cleaning, fracturing by cycled cooling-heating, soxhlet-extraction with solvents of benzene and methanol and separating with centrifugal machine. If oil is present in the separated samples, ionized organic fragments with m/e ratios of 36 to 40 covering the argon isotopes will be yielded by the ion source of a mass spectrometer, resulting in wrong argon isotopic analyses and wrong 40Ar- 39Ar ages. The preliminary experiments of illite by heating did show the presence of ionized organic fragments with m/e ratios of 36 to 44. In order to clean up the organic gases completely and obtain reliable analysis results, a special purification apparatus has been established by Qiu et al. and proved valid by the sequent illite analyses. All the illite samples by 40Ar- 39Ar IR-laser stepwise heating yield stair-up age spectra in lower laser steps and plateaux in higher laser steps. The youngest apparent ages corresponding to the beginning steps are reasonable to be interpreted for the hydrocarbon accumulation ages. The weighted mean ages of the illites from the Zhuhai and Zhujiang Formations are (12.1 ± 1.1) Ma and (9.9 ± 1.2) Ma, respectively. Therefore, the critical emplacement of petroleum accumulation in Zhujiang Formation in Huizhou sag took place in ca 10 Ma. Late fault activity strengthened the entrance of hydrocarbon fluids into the oil systems based on the data of the studies of the fault evolvement history, petroleum system combinations, and homogeneous temperatures of fluid inclusions.

Reconstructing fluid-flow events in Lower-Triassic sandstones of the eastern Paris Basin by elemental tracing and isotopic dating of nanometric illite crystals

NASA Astrophysics Data System (ADS)

Blaise, Thomas; Clauer, Norbert; Cathelineau, Michel; Boiron, Marie-Christine; Techer, Isabelle; Boulvais, Philippe

2016-03-01

Lower- to Middle-Triassic sandstones from eastern Paris Basin were buried to a maximum depth of 2500 m at a paleo-temperature of about 100 °C. They contain extensive amounts of authigenic platy and filamentous illite particles similar to those reported in reservoirs generally buried at 3000 to -5000 m and subjected to temperatures of 120 to -150 °C. To evaluate this unexpected occurrence, such sandstones were collected from drill cores between 1825 and 2000 m depth, and nanometric-sized sub-fractions were separated. The illite crystals were identified by XRD, observed by SEM and TEM, analyzed for their major, trace, rare-earth elements and oxygen isotope compositions, and dated by K-Ar and Rb-Sr. Illite particles display varied growth features in the rock pore-space and on authigenic quartz and adularia that they postdate. TEM-EDS crystal-chemical in situ data show that the illite lath/fiber and platelet morphologies correspond at least to two populations with varied interlayer charges: between 0.7 and 0.9 for the former and between 0.8 and 1.0 for the latter, the Fe/Fe + Mg ratio being higher in the platelets. Except for the deeper conglomerate, the PAAS-normalized REE patterns of the illite crystals are bell-shaped, enriched in middle REEs. Ca-carbonates and Ca-phosphates were detected together with illite in the separates. These soluble components yield 87Sr/86Sr ratios that are not strictly in chemical equilibrium with the illite crystals, suggesting successive fluids flows with different chemical compositions. The K-Ar data of finer <0.05 μm illite separates confirm two crystallization events at 179.4 ± 4.5 and 149.4 ± 2.5 Ma during the Early and Late Jurassic. The slightly coarser fractions contain also earlier crystallized or detrital K-bearing minerals characterized by lower δ18O values. The δ18O of the finest authigenic illite separates tends to decrease slightly with depth, from 18.2 (±0.2) to 16.3 (±0.2)‰, suggesting different but contemporaneous crystallization conditions deeper in the section. The illite platelets and filaments crystallized in changing physical-chemical crystallization conditions induced by fluids flows through the host-rock pore system. These flow events were probably driven by repetitive rifting episodes of the North Atlantic Ocean, although located several hundreds kilometers away from eastern Paris Basin, and/or by fracturing events in the nearby basement of the Vosges Massif. Complex relationships between geodynamical events, thermal anomalies, and advective fluids confirm that remote tectonic activities can impact quiescent basins, even if located far from tectono-thermal activities, by discrete and long-distance fluid flows.

Very low-grade metamorphic rocks in some representative districts in Tibet

NASA Astrophysics Data System (ADS)

Bi, X.; Mo, X.

2011-12-01

*Response author: Bi,Xianmei,bixm10@sina.com Very low grade metamorphic rocks are widely distributed in Tibet, providing an insight into deformation and metamorphism during the evolution of the Tibetan Plateau. Eighty five Samples of clay mineral-bearing rocks has been collected from various strata including D, P1, T1, T2, T3, J1, J3, K1, K2 and N strata in the Qiangtang terrane, the Gangdese, the Yarlung Zangbo suture and the Tethyan Himalaya. Analyses and refining of clay minerals in samples have been conducted in the Laboratory of X-ray Diffraction, Institute of Petroleum Exploration. Index of illite crystallinity (Ic) along with average thickness of crystal layers of illite, reflectivity of vitrinite and of clay mineral association have been employed as indicators of degree of very low-grade metamorphism. The scheme of classification[1,2] of very-low grade metamorphism based on clay mineral indexes ( mainly index of illite crystallinity) has been used in the present work, that is, low metamorphism (Ic<0.25), higher very-low grade metamorphism (Ic = 0.25-0.30), lower very-low grade metamorphism (Ic = 0.30-0.42) and diagenesis (Ic>0.42). The analytical results show interesting information. In the Qiangtang terrane, clay minerals in the Jurassic strata have indexes of illite crystalinity (Ic) 0.47-0.70, indicating higher diagenesis and in favor of petroleum-generation. However, index of illite crystalinity (Ic) for the Devonian is 0.23, indicating low metamorphism. Indexes of illite crystalinity (Ic) for the J-K strata in middle Gangdese are mostly 0.37-0.25 (very-low grade metamorphism) and a few 0.78-0.48 (diagenesis). Indexes of illite crystalinity (Ic) for the C-P strata in eastern Gangdese are mostly 0.25-0.42 (very-low grade metamorphism) and a few 0.20-0.25 (low metamorphism). The Mesozoic and Cenozoic magmatism and related mineralization are very strong in the Gangdese, which may affect in some extent on indexes of illite crystalinity. In Tethyan Himalaya, clay mineral-bearing rocks from P1, T1, T2, T3, J1 and J3 strata underwent low-very low grade metamorphism, having indexes of illite crystalinity (Ic) 0.12 for P1 stratum, 0.21 for T1 stratum and 0.22-0.33 for the strata from T2 to J3, whereas K1 and N strata underwent diagenesis, having Ic = 0.52 and 1.61, respectively. Metamorphic degree generally reduced from older strata to younger strata according to clay mineral indexes. The rocks affected by magmatism or by major faulting, however, were out of the general trend and increased their metamorphic degree by 0.1-0.3 units reduction of index of illite crystallinity. Rocks within Yarlung Zangbo suture show higher metamorphic degree than those in Tethyan Himalaya. For instance, while the late Triassic has 0.19 of index of illite crystallinity in the former (the Yarlung Zangbo suture), 0.27-0.33 of indexes of illite crystallinity in the latter. The early Cretaceous has 0.28 of index of illite crystallinity in the former, whereas 0.52 in the latter. However, the late Cretaceous Xigaze Group formed in a fore-arc environment was weakly metamorphosed, having Ic 0.7-1.6 and all falling into diagenesis field.

Spectroscopic study on variations in illite surface properties after acid-base titration.

PubMed

Liu, Wen-xin; Coveney, R M; Tang, Hong-xiao

2003-07-01

FT-IR, Raman microscopy, XRD, 29Si and 27Al MAS NMR, were used to investigate changes in surface properties of a natural illite sample after acid-base potentiometric titration. The characteristic XRD lines indicated the presence of surface Al-Si complexes, preferable to Al(OH)3 precipitates. In the microscopic Raman spectra, the vibration peaks of Si-O and Al-O bonds diminished as a result of treatment with acid, then increased after hydroxide back titration. The varied ratio of signal intensity between (IV)Al and (VI)Al species in 27Al MAS NMR spectra, together with the stable BET surface area after acidimetric titration, suggested that edge faces and basal planes in the layer structure of illite participated in dissolution of structural components. The combined spectroscopic evidence demonstrated that the reactions between illite surfaces and acid-leaching silicic acid and aluminum ions should be considered in the model description of surface acid-base properties of the aqueous illite.

Discrimination of hydrothermal alteration mineral assemblages at Virginia City, Nevada, using the airborne imaging spectrometer

NASA Technical Reports Server (NTRS)

Hutsinpiller, Amy

1988-01-01

The purpose of this study is to use airborne imaging spectrometer data to discriminate hydrothermal alteration mineral assemblages associated with silver and gold mineralization at Virginia City, NV. The data is corrected for vertical striping and sample gradients, and converted to flat-field logarithmic residuals. Log residual spectra from areas known to be altered are compared to field spectra for kaolinitic, illitic, sericitic, and propylitic alteration types. The areal distributions of these alteration types are estimated using a spectral matching technique. Both visual examination of spectra and the matching techniques are effective in distinguishing kaolinitic, illitic, and propylitic alteration types from each other. However, illitic and sericitic alteration cannot be separated using these techniques because the spectra of illite and sericite are very similar. A principal components analysis of 14 channels in the 2.14-2.38 micron wavelength region is also successful in discriminating and mapping illitic, kaolinitic, and propylitic alteration types.

A structural coarse-grained model for clays using simple iterative Boltzmann inversion

NASA Astrophysics Data System (ADS)

Schaettle, Karl; Ruiz Pestana, Luis; Head-Gordon, Teresa; Lammers, Laura Nielsen

2018-06-01

Cesium-137 is a major byproduct of nuclear energy generation and is environmentally threatening due to its long half-life and affinity for naturally occurring micaceous clays. Recent experimental observations of illite and phlogopite mica indicate that Cs+ is capable of exchanging with K+ bound in the anhydrous interlayers of layered silicates, forming sharp exchange fronts, leading to interstratification of Cs- and K-illite. We present here a coarse-grained (CG) model of the anhydrous illite interlayer developed using iterative Boltzmann inversion that qualitatively and quantitatively reproduces features of a previously proposed feedback mechanism of ion exchange. The CG model represents a 70-fold speedup over all-atom models of clay systems and predicts interlayer expansion for K-illite near ion exchange fronts. Contrary to the longstanding theory that ion exchange in a neighboring layer increases the binding of K in lattice counterion sites leading to interstratification, we find that the presence of neighboring exchanged layers leads to short-range structural relaxations that increase basal spacing and decrease cohesion of the neighboring K-illite layers. We also provide evidence that the formation of alternating Cs- and K-illite interlayers (i.e., ordered interstratification) is both thermodynamically and mechanically favorable compared to exchange in adjacent interlayers.

In situ immobilisation of toxic metals in soil using Maifan stone and illite/smectite clay.

PubMed

Ou, Jieyong; Li, Hong; Yan, Zengguang; Zhou, Youya; Bai, Liping; Zhang, Chaoyan; Wang, Xuedong; Chen, Guikui

2018-03-15

Clay minerals have been proposed as amendments for remediating metal-contaminated soils owing to their abundant reserves, high performance, simplicity of use and low cost. Two novel clay minerals, Maifan stone and illite/smectite clay, were examined in the in situ immobilisation of soil metals. The application of 0.5% Maifan stone or illite/smectite clay to field soils significantly decreased the fractions of diethylenetriaminepentaacetic acid (DTPA)-extractable Cd, Ni, Cr, Zn, Cu and Pb. Furthermore, reductions of 35.4% and 7.0% in the DTPA-extractable fraction of Cd were obtained with the Maifan stone and illite/smectite clay treatments, respectively, which also significantly reduced the uptake of Cd, Ni, Cr, Zn, Cu and Pb in the edible parts of Brassica rapa subspecies pekinensis, Brassica campestris and Spinacia oleracea. Quantitatively, the Maifan stone treatment reduced the metal uptake in B. rapa ssp. Pekinensis, B. campestris and S. oleracea from 11.6% to 62.2%, 4.6% to 41.8% and 11.3% to 58.2%, respectively, whereas illite/smectite clay produced reductions of 8.5% to 62.8% and 4.2% to 37.6% in the metal uptake in B. rapa ssp. Pekinensis and B. campestris, respectively. Therefore, both Maifan stone and illite/smectite clay are promising amendments for contaminated soil remediation.

Biogeochemical modification of Nontronite by Shewanella oneidensis MR-1: Evidence of Microbially induced Smectite-to-Illite reaction

NASA Astrophysics Data System (ADS)

Koo, T. H.; Kogure, T.; Kim, J. W.

2017-12-01

The biogeochemical modification of chemistry/structure of smectite associated with microbial Fe(III) respiration is a major process of promoting smectite-to-illite reaction (S-I reaction). Direct evidence of illitization including K-fixation and changes in Al/Si, formation of K-nontronite/illite-like structure has not been suggested systematically. Nontronite (NAu-1) was inoculated with Fe-reducing bacteria (FeRB), Shewanella oneidensis MR-1 at 30 ° with pH buffered (7.0 and 8.0) M1 medium in the anaerobic chamber, and the evidence of illitization was suggested by microscopic/spectroscopic measurements as well as aqueous chemistry in the supernatant with various incubation time. A progressive morphological change in bio-reduced notnronite (altered nontronite → K-nontronite → illite) corresponded to chemical modification in solid phase (Al/Si 0.16 to 0.28). Fe and Al contents in the supernatant increased continuously up to 70 days of incubation (3.4 to 20 and 1.7 to 13 20 mmol/mg of NAu-1, respectively) then decreased in 120 days of incubation (20 to 8 and 13 to 3 mmol/mg of NAu-1, respectively) indicating new mineral phase precipitated. Si contents showed slightly decreased in 7 days (133 to 100 mmol/mg of NAu-1) then showed fluctuated pattern (increased to 183 mmol/mg of NAu-1 in 70 days, then decreased to 102 mmol/mg of NAu-1 in 120 days of incubation). Formation of biotic silica globule within 120-day incubation supported the dissolution of bio-reduced notnronite. Indeed, modification in structure (appearance of 10-Å shoulder in X-ray diffraction profile) and formation of discrete illite-like packet (d001=1.0 nm) in the wavy bio-reduced nontronite matrix (d001=1.2-1.3 nm) strongly suggest that bio-reduced nontronite underwent the reductive dissolution and precipitated the newly formed illite

Characterization and modeling of illite crystal particles and growth mechanisms in a zoned hydrothermal deposit, Lake City, Colorado

USGS Publications Warehouse

Bove, D.J.; Eberl, D.D.; McCarty, D.K.; Meeker, G.P.

2002-01-01

Mean thickness measurements and crystal-thickness distributions (CTDs) of illite particles vary systematically with changes in hydrothermal alteration type, fracture density, and attendant mineralization in a large acid-sulfate/Mo-porphyry hydrothermal system at Red Mountain, near Lake City, Colorado. The hydrothermal illites characterize an extensive zone of quartz-sericite-pyrite alteration beneath two deeply rooted bodies of magmatic-related, quartz-alunite altered rock. Nineteen illites from a 3000 ft vertical drill hole were analyzed by XRD using the PVP-10 intercalation method and the computer program MudMaster (Bertaut-Warren-Averbach technique). Mean crystallite thicknesses, as determined from 001 reflections, range from 5-7 nanometers (nm) at depths from 0-1700 ft, then sharply increase to 10-16 nm at depths between 1800-2100 ft, and decrease again to 4-5 nm below this level. The interval of largest particle thickness correlates strongly with the zone of most intense quartz-sericite-pyrite alteration (QSP) and attendant high-density stockwork fracturing, and with the highest concentrations of Mo within the drill core. CTD shapes for the illite particles fall into two main categories: asymptotic and lognormal. The shapes of the CTDs are dependent on conditions of illite formation. The asymptotic CTDs correspond to a nucleation and growth mechanism, whereas surface-controlled growth was the dominant mechanism for the lognormal CTDs. Lognormal CTDs coincide with major through-going fractures or stockwork zones, whereas asymptotic CTDs are present in wallrock distal to these intense fracture zones. The increase in illite particle size and the associated zone of intense QSP alteration and stockwork veining was related by proximity to the dacitic magma(s), which supplied both reactants and heat to the hydrothermal system. However, no changes in illite polytype, which in other studies reflect temperature transitions, were observed within this interval.

Restore the change process of Longmaxi shale pore structure during the diagenesis by the potassium and the magnesium

NASA Astrophysics Data System (ADS)

Zhou, W.

2016-12-01

The pore structure of Longmaxi shale was changing during the diagenetic process, mainly caused by the illitization and serpentinzation. The evolution of shale pore structure mainly relates to the element migration. Based on the result of electron microprobe analyser (EMPA), it is possible to find the distribution of element in shale directly and to distinguish the destroyed primary pore structure as element will remain in the migration way. The migration of potassium in Longmaxi shale mainly happened during early diagenesis phase to middle diagenesis phase (Geothermal temperature: 60°-140°). During the illitization, potassium mainly came from potassium feldspar, migrated though the connected pore structure and reacted with smectite. Illite and illite/smectite in Longmaxi shale distribute continuously in 10micron-level flocculent formation, which means that primary connective pore structure in Longmaxi shale has a same scale. The concentration of potassium has an obvious gradient that potassium content in middle of flocculation of Illite/smectite is about 6.8% and 4.8% in the boundary parts (Fig.). In addition, as SiO2 was generated during the illitization, which makes Longmaxi shale very compacted. The migration of magnesium in Longmaxi shale happened during low temperature serpentinization (Geothermal temperature: 140°-350°). Magnesium mainly came from dolomite and migrated in primary pores. According to the result of EMPA, it can be recognized that the migration path of magnesium is much simpler than potassium, which is caused as serpentinization do not have much reaction with clay minerals around (Fig.). Serpentine jams the primary pores of Longmaxi shale too. As reaction temperature of serpentinization is higher than illitization and serpentine is inserts in illite/smectite, the formation process of Longmaxi shale pore structure can be mainly divided into two phases: geothermal temperature˜140° and˜140°.

Acid-base properties of aqueous illite surfaces

DOE Office of Scientific and Technical Information (OSTI.GOV)

Du, Q.; Sun, Z.; Forsling, W.

In this paper, the acid-base properties of illite/water suspensions are examined using the constant capacitance surface complexation model. On the basis of results of potentiometric titrations and solubility experiments, the authors conclude that the proton reactions in the supernatants of illite suspensions can be successfully represented by proton reactions of Al(H{sub 2}O){sub 6}{sup 3+} and Si(OH){sub 4} in water solutions. For illustrating the acidic characteristics of aqueous illite surfaces, two surface protonation models are proposed: (1) one site-one pK{sub a} model, {triple_bond}SOH {r_reversible} {triple_bond}SO{sup {minus}} + H{sup +}, pK{sub a}{sup int} = 4.12-4.23; (2) two sites-two pK{sub a}s model, {triple_bond}S{submore » 1}OH {r_reversible} {triple_bond}S{sup 1}O{sup {minus}} + H{sup +}, pK{sub a{sub I}} = 4.17-4.44, and {triple_bond}S{sub II}OH {r_reversible} {triple_bond}S{sub II}O{sup {minus}} + H{sup +}, pK{sub a{sub II}}{sup int} = 6.35-7.74. Evaluation of these two models indicates that both of them can give good descriptions of the experimental data of systems with different illite concentrations and ionic strengths and that the one site-one pK{sub a} model can be considered as a simplification of the two sites-two pK{sub a}s model. Since both models assume only deprotonation reactions at the illite surfaces, they suggest that the surface behavior of the illite is similar to that of amorphous SiO{sub 2}. Model assumptions, experimental procedures, and evaluative criteria are detailed in the paper.« less

Empirical test of an illite/muscovite 40Ar/39Ar thermochronometer

NASA Astrophysics Data System (ADS)

Verdel, C.; van der Pluijm, B. A.; Niemi, N. A.; Hall, C. M.

2010-12-01

Minerals which both preserve age information and indicate metamorphic conditions are particularly useful in thermochronology. Variations in sub-greenschist facies metamorphism have traditionally been quantified in terms of the illite to muscovite transition, a transformation which involves the growth of crystallites of increasing thickness at higher metamorphic temperatures. Thickness variations may influence Ar retention within these K-rich minerals, both in nature and during neutron irradiation. Along a transect in the southwestern US from the Grand Canyon to Death Valley, metamorphic conditions of a stratigraphic interval (the Middle Cambrian Bright Angel Shale and laterally equivalent Carrara Fm.) range from zeolite facies in the east to greenschist facies in the west, as determined by estimating illite crystallite thickness with X-ray diffraction. 40Ar/39Ar step-heating experiments were conducted on illite/muscovite-rich, micron to submicron grain sizes of these shales that were encapsulated in quartz tubes prior to irradiation. The proportion of 39Ar expelled during irradiation decreases in these samples as both crystallite thickness and grain size increases. Spectra from the least metamorphosed samples (diagenetic zone) are staircase-shaped and reach maximum ages that appear to reflect the age of detrital muscovite. Spectra from the highest grade samples (epizone) display partial plateaus and yield much younger maximum ages. Based on these findings we conclude that Ar can escape from illite via two processes: loss from low retention sites on crystallite edges and c-axis perpendicular volume diffusion. Based on our empirical data, the closure temperature of illite appears to lie at or near the anchizone-epizone bounday, or roughly 200-300 °C. Illite/muscovite thickness and 40Ar/39Ar data may therefore be useful for studies of detrital muscovite geochronology in very low grade shales and as a thermochronometer for higher grade pelites.

XRD measurement of mean thickness, thickness distribution and strain for illite and illite-smectite crystallites by the Bertaut-Warren-Averbach technique

USGS Publications Warehouse

Drits, Victor A.; Eberl, Dennis D.; Środoń, Jan

1998-01-01

A modified version of the Bertaut-Warren-Averbach (BWA) technique (Bertaut 1949, 1950; Warren and Averbach 1950) has been developed to measure coherent scattering domain (CSD) sizes and strains in minerals by analysis of X-ray diffraction (XRD) data. This method is used to measure CSD thickness distributions for calculated and experimental XRD patterns of illites and illite-smectites (I-S). The method almost exactly recovers CSD thickness distributions for calculated illite XRD patterns. Natural I-S samples contain swelling layers that lead to nonperiodic structures in the c* direction and to XRD peaks that are broadened and made asymmetric by mixed layering. Therefore, these peaks cannot be analyzed by the BWA method. These difficulties are overcome by K-saturation and heating prior to X-ray analysis in order to form 10-Å periodic structures. BWA analysis yields the thickness distribution of mixed-layer crystals (coherently diffracting stacks of fundamental illite particles). For most I-S samples, CSD thickness distributions can be approximated by lognormal functions. Mixed-layer crystal mean thickness and expandability then can be used to calculate fundamental illite particle mean thickness. Analyses of the dehydrated, K-saturated samples indicate that basal XRD reflections are broadened by symmetrical strain that may be related to local variations in smectite interlayers caused by dehydration, and that the standard deviation of the strain increases regularly with expandability. The 001 and 002 reflections are affected only slightly by this strain and therefore are suited for CSD thickness analysis. Mean mixed-layer crystal thicknesses for dehydrated I-S measured by the BWA method are very close to those measured by an integral peak width method.

Clay mineralogy and its palaeoclimatic significance in the Luochuan loess-palaeosols over ˜1.3 Ma, Shaanxi, northwestern China

NASA Astrophysics Data System (ADS)

Won, Changdok; Hong, Hanlie; Cheng, Feng; Fang, Qian; Wang, Chaowen; Zhao, Lulu; Churchman, Gordon Jock

2018-03-01

To understand climate changes recorded in the Luochuan loess-palaeosols, Shaanxi province, northwestern China, clay mineralogy was studied using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), and scanning electron microscopy (SEM) methods. XRD results show that clay mineral compositions in the Luochuan loess-palaeosols are dominantly illite, with minor chlorite, kaolinite, smectite, and illite-smectite mixed-layer clays (I/S). Illite is the most abundant species in the sediments, with a content of 61%-83%. The content of chlorite ranges from 5%-22%, and the content of kaolinite ranges from 5%-19%. Smectite (or I/S) occurs discontinuously along the loess profile, with a content of 0-8%. The Kübler index of illite (IC) ranges from 0.255°-0.491°, and the illite chemical index (ICI) ranges from 0.294-0.394. The CIA values of the loesspalaeosols are 61.9-69.02, and the R3+/(R3+ + R2+ + M+) values are 0.508-0.589. HRTEM observations show that transformation of illite to illite-smectite has occurred in both the loess and palaeosol, suggesting that the Luochuan loess-palaeosols have experienced a certain degree of chemical weathering. The Luochuan loess-palaeosols have the same clay mineral assemblage along the profile. However, the relative contents of clay mineral species, CIA, ICI, and IC values fluctuate frequently along the profile, and all these parameters display a similar trend. Moreover, climate changes suggested by the clay index are consistent with variations in the deep-sea δ18O records and the magnetic susceptibility value, and thus, climate changes in the Luochuan region have been controlled by global climate change.

Near-surface clay authigenesis in exhumed fault rock of the Alpine Fault Zone (New Zealand); O-H-Ar isotopic, XRD and chemical analysis of illite and chlorite

NASA Astrophysics Data System (ADS)

Boles, Austin; Mulch, Andreas; van der Pluijm, Ben

2018-06-01

Exhumed fault rock of the central Alpine Fault Zone (South Island, New Zealand) shows extensive clay mineralization, and it has been the focus of recent research that aims to describe the evolution and frictional behavior of the fault. Using Quantitative X-ray powder diffraction, 40Ar/39Ar geochronology, hydrogen isotope (δD) geochemistry, and electron microbeam analysis, we constrain the thermal and fluid conditions of deformation that produced two predominant clay phases ubiquitous to the exposed fault damage zone, illite and chlorite. Illite polytype analysis indicates that most end-member illite and chlorite material formed in equilibrium with meteoric fluid (δD = -55 to -75‰), but two locations preserve a metamorphic origin of chlorite (δD = -36 to -45‰). Chlorite chemical geothermometry constrains crystal growth to T = 210-296 °C. Isotopic analysis also constrains illite growth to T < 100 °C, consistent with the mineralogy, with Ar ages <0.5 Ma. High geothermal gradients in the study area promoted widespread, near-surface mineralization, and limited the window of clay authigenesis in the Alpine Fault Zone to <5 km for chlorite and <2 km for illite. This implies a significant contrast between fault rock exposed at the surface and that at depth, and informs discussions about fault strength, clays and frictional behavior.

Variation of illite/muscovite 40Ar/39Ar age spectra during progressive low-grade metamorphism: an example from the US Cordillera

NASA Astrophysics Data System (ADS)

Verdel, Charles; van der Pluijm, Ben A.; Niemi, Nathan

2012-09-01

40Ar/39Ar step-heating data were collected from micron to submicron grain-sizes of correlative illite- and muscovite-rich Cambrian pelitic rocks from the western United States that range in metamorphic grade from the shallow diagenetic zone (zeolite facies) to the epizone (greenschist facies). With increasing metamorphic grade, maximum ages from 40Ar/39Ar release spectra decrease, as do total gas ages and retention ages. Previous studies have explained similar results as arising dominantly or entirely from the dissolution of detrital muscovite and precipitation/recrystallization of neo-formed illite. While recognizing the importance of these processes in evaluating our results, we suggest that the inverse correlation between apparent age and metamorphic grade is controlled, primarily, by thermally activated volume diffusion, analogous to the decrease in apparent ages with depth observed for many thermochronometers in borehole experiments. Our results suggest that complete resetting of the illite/muscovite Ar thermochronometer occurs between the high anchizone and epizone, or at roughly 300 °C. This empirical result is in agreement with previous calculations based on muscovite diffusion parameters, which indicate that muscovite grains with radii of 0.05-2 μm should have closure temperatures between 250 and 350 °C. At high anchizone conditions, we observe a reversal in the age/grain-size relationship (the finest grain-size produces the oldest apparent age), which may mark the stage in prograde subgreenschist facies metamorphism of pelitic rocks at which neo-formed illite/muscovite crystallites typically surpass the size of detrital muscovite grains. It is also approximately the stage at which neo-formed illite/muscovite crystallites develop sufficient Ar retentivity to produce geologically meaningful 40Ar/39Ar ages. Results from our sampling transect of Cambrian strata establish a framework for interpreting illite/muscovite 40Ar/39Ar age spectra at different stages of low-grade metamorphism and also illuminate the transformation of illite to muscovite. At Frenchman Mtn., NV, where the Cambrian Bright Angel Formation is at zeolite facies conditions, illite/muscovite 40Ar/39Ar data suggest a detrital muscovite component with an apparent age ≥967 Ma. The correlative Carrara Fm. is at anchizone conditions in the Panamint and Resting Spring Ranges of eastern California, and in these locations, illite/muscovite 40Ar/39Ar data suggest an early Permian episode of subgreenschist facies metamorphism. The same type of data from equivalent strata at epizone conditions (greenschist facies) in the footwall of the Bullfrog/Fluorspar Canyon detachment in southern Nevada reveals a period of slow-to-moderate Late Cretaceous cooling.

Thallium (Tl) sorption onto illite and smectite: Implications for Tl mobility in the environment

NASA Astrophysics Data System (ADS)

Martin, Loïc A.; Wissocq, Aubéry; Benedetti, M. F.; Latrille, Christelle

2018-06-01

Clay minerals play a relevant role in the transport and fate of trace elements in the environment. Though illite has been referred as an important Thallium (Tl) bearing phase in soils, mechanisms and affinity of thallium for clay minerals remain poorly known. This study investigated the sorption behavior of thallium as Tl(I) onto illite and smectite, two clay minerals occurring mainly in soils and sediments. Different sorption experiments were carried out under various pH conditions and Tl concentrations, in competition with sodium and calcium at a constant ionic strength of 0.01 mol L-1. Our results showed that illite displayed more affinity than smectite for thallium. With illite, the distribution coefficients (Kd in L kg-1) varied between 102.75 ± 0.17 and 104.0 ± 0.17 in Na solutions versus between 102.25 ± 0.17 and 103.0 ± 0.17 in Ca solutions, depending on pH. With smectite, Kd (in L kg-1) ranged between 102.50 ± 0.16 and 103.20 ± 0.16 and between 101.25 ± 0.16 and 101.95 ± 0.16 in Na and Ca solutions, respectively. Sorption behavior was described with the Multi-Site Ion Exchanger model and selectivity coefficients with respect to protons were calculated for the first time. In all cases, independently of clay mineral and background electrolyte, low capacity but highly reactive sites were dominant in thallium uptake, highlighting Tl affinity for those sites. Moreover, the exchangeable and reversible interactions between Tl+ and clays reactive sites suggested that in changing conditions, thallium could be released in solution. The role of clay minerals in thallium environmental cycle is evident and confirmed illite to be a dominant Tl bearing phase, in some environment competing with manganese oxides. Compared to others Tl bearing mineral phases, clays are ranked as follows: MnO2 > illite > smectite ∼ ferrihydrite ≥ Al2O3 ∼ goethite > SiO2. Finally, over the three monovalent cations (Tl, Rb, Cs) Tl is the one less sorbed on illite independently of the background cations.

Microbial reduction of structural iron in interstratified illite-smectite minerals by a sulfate-reducing bacterium

USGS Publications Warehouse

Liu, D.; Dong, H.; Bishop, M.E.; Zhang, Jiahua; Wang, Hongfang; Xie, S.; Wang, Shaoming; Huang, L.; Eberl, D.D.

2012-01-01

Clay minerals are ubiquitous in soils, sediments, and sedimentary rocks and could coexist with sulfate-reducing bacteria (SRB) in anoxic environments, however, the interactions of clay minerals and SRB are not well understood. The objective of this study was to understand the reduction rate and capacity of structural Fe(III) in dioctahedral clay minerals by a mesophilic SRB, Desulfovibrio vulgaris and the potential role in catalyzing smectite illitization. Bioreduction experiments were performed in batch systems, where four different clay minerals (nontronite NAu-2, mixed-layer illite-smectite RAr-1 and ISCz-1, and illite IMt-1) were exposed to D. vulgaris in a non-growth medium with and without anthraquinone-2,6-disulfonate (AQDS) and sulfate. Our results demonstrated that D. vulgaris was able to reduce structural Fe(III) in these clay minerals, and AQDS enhanced the reduction rate and extent. In the presence of AQDS, sulfate had little effect on Fe(III) bioreduction. In the absence of AQDS, sulfate increased the reduction rate and capacity, suggesting that sulfide produced during sulfate reduction reacted with the phyllosilicate Fe(III). The extent of bioreduction of structural Fe(III) in the clay minerals was positively correlated with the percentage of smectite and mineral surface area of these minerals. X-ray diffraction, and scanning and transmission electron microscopy results confirmed formation of illite after bioreduction. These data collectively showed that D. vulgaris could promote smectite illitization through reduction of structural Fe(III) in clay minerals. ?? 2011 Blackwell Publishing Ltd.

XRD-based 40Ar/39Ar age correction for fine-grained illite, with application to folded carbonates in the Monterrey Salient (northern Mexico)

NASA Astrophysics Data System (ADS)

Fitz-Díaz, Elisa; Hall, Chris M.; van der Pluijm, Ben A.

2016-05-01

Due to their minute size, 40Ar/39Ar analysis of illite faces significant analytical challenges, including mineral characterization and, especially, effects of grain size and crystallography on 39Ar recoil. Quantifying the effects of 39Ar recoil requires the use of sample vacuum encapsulation during irradiation, which permits the measurement of the fraction of recoiled 39Ar as well as the 39Ar and 40Ar∗ retained within illite crystals that are released during step heating. Total-Gas Ages (TGA) are calculated by using both recoiled and retained argon, which is functionally equivalent to K-Ar ages, while Retention Ages (RA) only involve retained Ar in the crystal. Natural applications have shown that TGA fits stratigraphic constraints of geological processes when the average illite crystallite thickness (ICT) is smaller than 10 nm, and that RA matches these constraints for ICTs larger than 50 nm. We propose a new age correction method that takes into account the average ICT and corresponding recoiled 39Ar for a sample, with X-ray Corrected Ages (XCA) lying between Total-Gas and Retention Ages depending on ICT. This correction is particularly useful in samples containing authigenic illite formed in the anchizone, with typical ICT values between 10 and 50 nm. In three samples containing authigenic illite from Cretaceous carbonates in the Monterrey Salient in northern Mexico, there is a range in TGAs among the different size-fractions of 46-49, 36-43 and 40-52 Ma, while RAs range from 54-64, 47-52 and 53-54 Ma, respectively. XCA calculations produce tighter age ranges for these samples of 52.5-56, 45.5-48.5 and 49-52.5 Ma, respectively. In an apparent age vs ICT or %2M 1illite plot, authigenic illite grains show a slope that is in general slightly positive for TGA, slightly negative for RA, but close to zero for XCA, with thinner crystallites showing more dispersion than thicker ones. In order to test if dispersion is due to a different formation history or the result of retention capability, degassing spectra were modeled for site XCA averages and overall XCA average. Modeling shows that local site age average best match the measured spectra, instead of a global average age, indicating that illite growth reflects local deformation, and is not the result of regional metamorphism. Modeling also shows that Ar-degassing spectra are very sensitive to grain size, such that age interpretation based on Ar-plateaus is meaningless for most fine-grained clays.

Molecular dynamics simulations of cesium adsorption on illite nanoparticles.

PubMed

Lammers, Laura N; Bourg, Ian C; Okumura, Masahiko; Kolluri, Kedarnath; Sposito, Garrison; Machida, Masahiko

2017-03-15

The charged surfaces of micaceous minerals, especially illite, regulate the mobility of the major radioisotopes of Cs ( 134 Cs, 135 Cs, 137 Cs) in the geosphere. Despite the long history of Cs adsorption studies, the nature of the illite surface sites remains incompletely understood. To address this problem, we present atomistic simulations of Cs competition with Na for three candidate illite adsorption sites - edge, basal plane, and interlayer. Our simulation results are broadly consistent with affinities and selectivities that have been inferred from surface complexation models. Cation exchange on the basal planes is thermodynamically ideal, but exchange on edge surfaces and within interlayers shows complex, thermodynamically non-ideal behavior. The basal planes are weakly Cs-selective, while edges and interlayers have much higher affinity for Cs. The dynamics of NaCs exchange are rapid for both cations on the basal planes, but considerably slower for Cs localized on edge surfaces. In addition to new insights into Cs adsorption and exchange with Na on illite, we report the development of a methodology capable of simulating fully-flexible clay mineral nanoparticles with stable edge surfaces using a well-tested interatomic potential model. Copyright © 2016 Elsevier Inc. All rights reserved.

Clay Mineralogy, Authigenic Smectite Concentration, and Fault Weakening of the San Gregorio Fault; Moss Beach, California

NASA Astrophysics Data System (ADS)

Mazzoni, S.; Moore, J.; Bish, D. L.

2002-12-01

The apparently weak nature of the San Andreas fault system poses a fundamental geophysical question. The San Gregorio fault at Moss Beach, CA is an active splay of the right-lateral San Andreas fault zone and has a total offset of about 150 km. At Moss Beach, the San Gregorio fault offsets Pliocene sedimentary rocks and consists of a clay-rich gouge zone, eastern sandstone block, and western mudstone block. In the presence of fluids, smectite clays can swell and become very weak to shearing. We studied a profile of samples across the fault zone and wall rocks to determine if there is a concentration of smectite in the gouge zone and propose a possible formation mechanism. Samples were analyzed using standard quantitative X-ray diffraction methods and software recently developed at Los Alamos National Lab. XRD results show a high smectite/illite (weak clay/strong clay) ratio in the gouge (S/I ratio=2-4), lower in the mudstone (S/I ratio=2), and very low in the sandstone (S/I ratio=1). The variability of smectite/illite ratio in the gouge zone may be evidence of preferential alteration where developed shear planes undergo progressive smectite enrichment. The amount of illite layers in illite/smectites is 5-30%, indicating little illitization; therefore, these fault rocks have not undergone significant diagenesis above 100 degrees C and illite present must be largely detrital. Bulk mineralogy shows significant anti-correlation of smectite with feldspar, especially in the gouge, suggesting authigenic smectite generation from feldspar. Under scanning-electron microscope inspection, smectites have fibrous, grain coating growth fabrics, also suggesting smectite authigenesis. If in situ production of smectite via chemical alteration is possible in active faults, it could have significant implications for self-generated weakening of faults above the smectite-to-illite transition (<150 degrees C, or 5-7km).

Cesium sorption reversibility and kinetics on illite, montmorillonite, and kaolinite

DOE PAGES

Durrant, Chad B.; Begg, James D.; Kersting, Annie B.; ...

2017-08-17

Understanding sorption and desorption processes is essential to predicting the mobility of radionuclides in the environment. In this study, we investigate adsorption/desorption of cesium in both binary (Cs + one mineral) and ternary (Cs + two minerals) experiments to study component additivity and sorption reversibility over long time periods (500 days). Binary Cs sorption experiments were performed with illite, montmorillonite, and kaolinite in a 5 mM NaCl/0.7 mM NaHCO3 solution (pH 8) and Cs concentration range of 10 –3 to 10 –11 M. The binary sorption experiments were followed by batch desorption experiments. The sorption behavior was modeled with themore » FIT4FD code and the results used to predict desorption behavior. Sorption to montmorillonite and kaolinite was linear over the entire concentration range but sorption to illite was non-linear, indicating the presence of multiple sorption sites. Based on the 14 day batch desorption data, cesium sorption appeared irreversible at high surface loadings in the case of illite but reversible at all concentrations for montmorillonite and kaolinite. Additionally, a novel experimental approach, using a dialysis membrane, was adopted in the ternary experiments, allowing investigation of the effect of a second mineral on Cs desorption from the original mineral. Cs was first sorbed to illite, montmorillonite or kaolinite, then a 3.5–5 kDalton Float-A-Lyzer® dialysis bag with 0.3 g of illite was introduced to each experiment inducing desorption. Nearly complete Cs desorption from kaolinite and montmorillonite was observed over the experiment, consistent with our equilibrium model, indicating complete Cs desorption from these minerals. Results from the long-term ternary experiments show significantly greater Cs desorption compared to the binary desorption experiments. Approximately ~ 45% of Cs desorbed from illite. However, our equilibrium model predicted ~ 65% desorption. Importantly, the data imply that in some cases, slow desorption kinetics rather than permanent fixation may play an important role in apparent irreversible Cs sorption.« less

Ostwald ripening and interparticle-diffraction effects for illite crystals

USGS Publications Warehouse

Eberl, D.D.; Srodon, J.

1988-01-01

The Warren-Averbach method, an X-ray diffraction (XRD) method used to measure mean particle thickness and particle-thickness distribution, is used to restudy sericite from the Silverton caldera. Apparent particle-thickness distributions indicate that the clays may have undergone Ostwald ripening and that this process has modified the K-Ar ages of the samples. The mechanism of Ostwald ripening can account for many of the features found for the hydrothermal alteration of illite. Expandabilities measured by the XRD peak-position method for illite/smectites (I/S) from various locations are smaller than expandabilities measured by transmission electron microscopy (TEM) and by the Warren-Averbach (W-A) method. This disparity is interpreted as being related to the presence of nonswelling basal surfaces that form the ends of stacks of illite particles (short-stack effect), stacks that, according to the theory of interparticle diffraction, diffract as coherent X-ray scattering domains. -from Authors

Microbial reduction of structural iron in interstratified illite-smectite minerals by a sulfate-reducing bacterium.

PubMed

Liu, D; Dong, H; Bishop, M E; Zhang, J; Wang, H; Xie, S; Wang, S; Huang, L; Eberl, D D

2012-03-01

Clay minerals are ubiquitous in soils, sediments, and sedimentary rocks and could coexist with sulfate-reducing bacteria (SRB) in anoxic environments, however, the interactions of clay minerals and SRB are not well understood. The objective of this study was to understand the reduction rate and capacity of structural Fe(III) in dioctahedral clay minerals by a mesophilic SRB, Desulfovibrio vulgaris and the potential role in catalyzing smectite illitization. Bioreduction experiments were performed in batch systems, where four different clay minerals (nontronite NAu-2, mixed-layer illite-smectite RAr-1 and ISCz-1, and illite IMt-1) were exposed to D. vulgaris in a non-growth medium with and without anthraquinone-2,6-disulfonate (AQDS) and sulfate. Our results demonstrated that D. vulgaris was able to reduce structural Fe(III) in these clay minerals, and AQDS enhanced the reduction rate and extent. In the presence of AQDS, sulfate had little effect on Fe(III) bioreduction. In the absence of AQDS, sulfate increased the reduction rate and capacity, suggesting that sulfide produced during sulfate reduction reacted with the phyllosilicate Fe(III). The extent of bioreduction of structural Fe(III) in the clay minerals was positively correlated with the percentage of smectite and mineral surface area of these minerals. X-ray diffraction, and scanning and transmission electron microscopy results confirmed formation of illite after bioreduction. These data collectively showed that D. vulgaris could promote smectite illitization through reduction of structural Fe(III) in clay minerals. © 2011 Blackwell Publishing Ltd.

Correlative microscopy of the constituents of a dinosaur rib fossil and hosting mudstone: Implications on diagenesis and fossil preservation.

PubMed

Kim, Jung-Kyun; Kwon, Yong-Eun; Lee, Sang-Gil; Kim, Chang-Yeon; Kim, Jin-Gyu; Huh, Min; Lee, Eunji; Kim, Youn-Joong

2017-01-01

We have applied correlative microscopy to identify the key constituents of a dorsal rib fossil from Koreanosaurus boseongensis and its hosting mudstone discovered at the rich fossil site in Boseong, South Korea, to investigate the factors that likely contributed to diagenesis and the preservation of fossil bone. Calcite and illite were the commonly occurring phases in the rib bone, hosting mudstone, and the boundary region in-between. The boundary region may have contributed to bone preservation once it fully formed by acting as a protective shell. Fluorapatite crystals in the rib bone matrix signified diagenetic alteration of the original bioapatite crystals. While calcite predominantly occupied vascular channels and cracks, platy illite crystals widely occupied miniscule pores throughout the bone matrix. Thorough transmission electron microscopy (TEM) study of illite within the bone matrix indicated the solid-state transformation of 1M to 2M without composition change, which was more evident from the lateral variation of 1M to 2M within the same layer. The high level of lattice disordering of 2M illite suggested an early stage of 1M to 2M transformation. Thus, the diagenetic alteration of both apatite and illite crystals within the bone matrix may have increased its overall density, as the preferred orientation of apatite crystals from moderate to strong degrees was evident despite the poor preservation of osteohistological features. The combined effects of rapid burial, formation of a boundary region, and diagenesis of illite and apatite within the bone matrix may have contributed to the rib bone preservation.

Illite authigenesis during faulting and fluid flow - a microstructural study of fault rocks

NASA Astrophysics Data System (ADS)

Scheiber, Thomas; Viola, Giulio; van der Lelij, Roelant; Margreth, Annina

2017-04-01

Authigenic illite can form synkinematically during slip events along brittle faults. In addition it can also crystallize as a result of fluid flow and associated mineral alteration processes in hydrothermal environments. K-Ar dating of illite-bearing fault rocks has recently become a common tool to constrain the timing of fault activity. However, to fully interpret the derived age spectra in terms of deformation ages, a careful investigation of the fault deformation history and architecture at the outcrop-scale, ideally followed by a detailed mineralogical analysis of the illite-forming processes at the micro-scale, are indispensable. Here we integrate this methodological approach by presenting microstructural observations from the host rock immediately adjacent to dated fault gouges from two sites located in the Rolvsnes granodiorite (Bømlo, western Norway). This granodiorite experienced multiple episodes of brittle faulting and fluid-induced alteration, starting in the Mid Ordovician (Scheiber et al., 2016). Fault gouges are predominantly associated with normal faults accommodating mainly E-W extension. K-Ar dating of illites separated from representative fault gouges constrains deformation and alteration due to fluid ingress from the Permian to the Cretaceous, with a cluster of ages for the finest (<0.1 µm) fraction in the early to middle Jurassic. At site one, high-resolution thin section structural mapping reveals a complex deformation history characterized by several coexisting types of calcite veins and seven different generations of cataclasite, two of which contain a significant amount of authigenic and undoubtedly deformation-related illite. At site two, fluid ingress along and adjoining the fault core induced pervasive alteration of the host granodiorite. Quartz is crosscut by calcite veinlets whereas plagioclase, K-feldspar and biotite are almost completely replaced by the main alteration products kaolin, quartz and illite. Illite-bearing micro-domains were physically separated by means of microsawing and drilling devices. K-Ar and XRD data from these separates are compared with bulk K-Ar and XRD data from the adjacent fault gouges, which may help to further unravel complex histories archived in multiply activated brittle fault zones. Scheiber, T., Viola, G., Wilkinson, C.M., Ganerød, M., Skår, Ø., and D. Gasser (2016): Direct 40Ar/39Ar dating of Late-Ordovician and Silurian brittle faulting in the southwestern Norwegian Caledonides. Terra Nova 28, 374-382.

Reversibility of radiocaesium sorption on illite

NASA Astrophysics Data System (ADS)

de Koning, Arjan; Comans, Rob N. J.

2004-07-01

Adsorption of trace amounts of radiocaesium on NH 4-, K-, and Na-saturated Fithian illite and subsequent desorption by 1 M NH 4 showed that a substantial amount of radiocaesium (44%, 46%, and 91% for NH 4-, K-, and Na-illite, respectively) cannot be desorbed after only 5 min of adsorption. Our results suggest that this instantaneous fixation is caused by the collapse of the frayed edges of the clay mineral and the relatively high concentration of radiocaesium building up in solution in the batch desorption experiments. Consequently, commonly applied high-NH 4 extractions underestimate truly exchangeable amounts of radiocaesium in soils and sediments containing illitic clay minerals. The rate of desorption of trace amounts of radiocaesium from the solids using high NH 4 or Cs concentrations has a half-life of about 2 yr, reflecting radiocaesium desorption from (partially) collapsed interlayers. Extraction of radiocaesium from illite after 5 min of contact time with a Cs-selective adsorbent or a 1 × 10 -6 M CsCl solution shows that 100% of the bound radiocaesium is readily available. The desorption rate in the presence of a Cs-selective adsorbent has a half-life of about 0.2 yr. Desorption of radiocaesium from illite using different ammonium concentrations shows that radiocaesium partitioning follows reversible ion-exchange theory if the NH 4 concentration is below 1 × 10 -4 M, and sufficient time (weeks) is allowed for the reaction to proceed. Thus, radiocaesium sorption reversibility in the natural environment is much higher than generally assumed, and equilibrium solid/liquid partitioning may be assumed for the long-term modelling of radiocaesium mobility in the natural environment. In the particular case of anoxic freshwater sediments with very high NH 4 concentrations in the pore waters (up to several mmol.L -1), collapse of the frayed edges of illite may occur, influencing radiocaesium partitioning. If collapse occurs before radiocaesium adsorbs to illite, high caesium sorption reversibility as measured by high-NH 4 extraction can be expected because further collapse of the frayed edges during the extraction procedure will be limited. This effect has indeed been observed earlier in the extraction of radiocaesium from anoxic freshwater sediments with high-NH 4 solutions and was as yet unexplained.

Measurement of illite particle thickness using a direct Fourier transform of small-angle X-ray scattering data

USGS Publications Warehouse

Shang, Chao; Rice, James A.; Eberl, Dennis D.; Lin, Jar-Shyong

2003-01-01

It has been suggested that interstratified illite-smectite (I-S) minerals are composed of aggregates of fundamental particles. Many attempts have been made to measure the thickness of such fundamental particles, but each of the methods used suffers from its own limitations and uncertainties. Small-angle X-ray scattering (SAXS) can be used to measure the thickness of particles that scatter X-rays coherently. We used SAXS to study suspensions of Na-rectorite and other illites with varying proportions of smectite. The scattering intensity (I) was recorded as a function of the scattering vector, q = (4 /) sin(/2), where  is the X-ray wavelength and  is the scattering angle. The experimental data were treated with a direct Fourier transform to obtain the pair distance distribution function (PDDF) that was then used to determine the thickness of illite particles. The Guinier and Porod extrapolations were used to obtain the scattering intensity beyond the experimental q, and the effects of such extrapolations on the PDDF were examined. The thickness of independent rectorite particles (used as a reference mineral) is 18.3 Å. The SAXS results are compared with those obtained by X-ray diffraction peak broadening methods. It was found that the power-law exponent (α) obtained by fitting the data in the region of q = 0.1-0.6 nm-1 to the power law (I = I0q-α) is a linear function of illite particle thickness. Therefore, illite particle thickness could be predicted by the linear relationship as long as the thickness is within the limit where α <4.0.

Clay mineralogy of the ocean sediments from the Wilkes Land margin, east Antarctica: implications on the paleoclimate, provenance and sediment dispersal pattern

NASA Astrophysics Data System (ADS)

Verma, Kamlesh; Bhattacharya, Sanjeeb; Biswas, P.; Shrivastava, Prakash K.; Pandey, Mayuri; Pant, N. C.

2014-11-01

Core U1359 collected from the continental rise off Wilkes Land, east Antarctica, is analyzed for the clay mineralogy and carbon content. The temporal variation of the clay mineralogical data shows a dominance of illite with chlorite, smectite and kaolinite in decreasing concentration. Clay mineral illite is negatively correlated with smectite which shows enrichment during 6.2-6.8, 5.5-5.8, 4.5 and 2.5 Ma. The mineralogical analyses on the silt size fraction (2-53 μm) of some selected samples were also carried out. The combined result of both the size fractions shows the presence of chlorite and illite in both size fractions, smectite and kaolinite only in clay size fraction (<2 μm) and similarity in the crystallinity and chemistry of illite in both fractions. Similar nature of illite in both fractions suggests negligible role of sorting probably due to the deposition from the waxing ice sheet. During times of ice growth, nearby cratonic east Antarctica shield provided biotite-rich sediments to the depositional site. On the other hand, the presence of smectite, only in the clay size fraction, suggests the effective role of sorting probably due to the deposition from distal source in ice retreat condition. During times of ice retreat, smectite-rich sediment derived from Ross Orogen is transported to the core site through surface or bottom water currents. Poor crystallinity of illite due to degradation further corroborates the ice retreat condition. The ice sheet proximal sediments of U1359 show that in the eastern part of Wilkes Land, the `warming' was initiated during late Miocene.

Thermal expansion of ceramic samples containing natural zeolite

NASA Astrophysics Data System (ADS)

Sunitrová, Ivana; Trník, Anton

2017-07-01

In this study the thermal expansion of ceramic samples made from natural zeolite is investigated. Samples are prepared from the two most commonly used materials in ceramic industry (kaolin and illite). The first material is Sedlec kaolin from Czech Republic, which contains more than 90 mass% of mineral kaolinite. The second one is an illitic clay from Tokaj area in Hungary, which contains about 80 mass% of mineral illite. Varying amount of the clay (0 % - 50 %) by a natural zeolite from Nižný Hrabovec (Slovak Republic), containing clinoptilolite as major mineral phase is replaced. The measurements are performed on cylindrical samples with a diameter 14 mm and a length about 35 mm by a horizontal push - rod dilatometer. Samples made from pure kaolin, illite and zeolite are also subjected to this analysis. The temperature regime consists from linear heating rate of 5 °C/min from 30 °C to 1100 °C. The results show that the relative shrinkage of ceramic samples increases with amount of zeolite in samples.

Illitization within bentonite engineered barrier system in clay repositories for nuclear waste and its effect on the swelling stress: a coupled THMC modeling study

NASA Astrophysics Data System (ADS)

Zheng, L.; Rutqvist, J.; Birkholzer, J. T.; Liu, H. H.

2014-12-01

Geological repositories for disposal of high-level nuclear waste generally rely on a multi-barrier system to isolate radioactive waste from the biosphere. An engineered barrier system (EBS), which comprises in many design concepts a bentonite backfill, is widely used. Clay formations have been considered as a host rock throughout the world. Illitization, the transformation of smectite to illite, could compromise some beneficiary features of EBS bentonite and clay host rock such as sorption and swelling capacity. It is the major determining factor to establish the maximum design temperature of the repositories because it is believed that illitization could be greatly enhanced at temperatures higher than 100 oC. However, existing experimental and modeling studies on the occurrence of illitization and related performance impacts are not conclusive, in part because the relevant couplings between the thermal, hydrological, chemical, and mechanical (THMC) processes have not been fully represented in the models. Here we present a fully coupled THMC simulation study of a generic nuclear waste repository in a clay formation with a bentonite-backfilled EBS. Two scenarios were simulated for comparison: a case in which the temperature in the bentonite near the waste canister can reach about 200 oC and a case in which the temperature in the bentonite near the waste canister peaks at about 100 oC. The model simulations demonstrate that illitization is in general more significant under higher temperature. However, the quantity of illitization is affected by many chemical factors and therefore varies a great deal. The most important chemical factors are the concentration of K in the pore water as well as the abundance and dissolution rate of K-feldspar. For the particular case and bentonite properties studied, the reduction in swelling stress as a result of chemical changes vary from 2% up to 70% depending on chemical and temperature conditions, and key mechanical parameters. The modeling work is illustrative in light of the relative importance of different processes occurring in EBS bentonite and clay host rock at higher than 100 oC conditions, and could be of greater use when site specific data are available.

Selected elements in major minerals from bituminous coal as determined by INAA: Implications for removing environmentally sensitive elements from coal

USGS Publications Warehouse

Palmer, C.A.; Lyons, P.C.

1996-01-01

The four most abundant minerals generally found in Euramerican bituminous coals are quartz, kaolinite, illite and pyrite. These four minerals were isolated by density separation and handpicking from bituminous coal samples collected in the Ruhr Basin, Germany and the Appalachian basin, U.S.A. Trace-element concentrations of relatively pure (??? 99+%) separates of major minerals from these coals were determined directly by using instrumental neutron activation analysis (INAA). As expected, quartz contributes little to the trace-element mass balance. Illite generally has higher trace-element concentrations than kaolinite, but, for the concentrates analyzed in this study, Hf, Ta, W, Th and U are in lower concentrations in illite than in kaolinite. Pyrite has higher concentrations of chalcophile elements (e.g., As and Se) and is considerably lower in lithophile elements as compared to kaolinite and illite. Our study provides a direct and sensitive method of determining trace-element relationships with minerals in coal. Mass-balance calculations suggest that the trace-element content of coal can be explained mainly by three major minerals: pyrite, kaolinite and illite. This conclusion indicates that the size and textural relationships of these major coal minerals may be a more important consideration as to whether coal cleaning can effectively remove the most environmentally sensitive trace elements in coal than what trace minerals are present.

BORON RELEASE FROM WEATHERING ILLITES, SERPENTINE, SHALES, AND ILLITIC/PALYGORSKITIC SOILS

EPA Science Inventory

Despite extensive research on B adsorption and release from soils, mineral sources of B within natively high B soils remain poorly under- stood. The objectives of this study were to identify source minerals contributing to the continued B release after extraction of soluble B and...

K-Ar age constrains on chemically weathered granitic basement rocks (saprolites) in Scandinavia

NASA Astrophysics Data System (ADS)

Margreth, Annina; Fredin, Ola; Viola, Giulio; Knies, Jochen; Sørlie, Ronald; Lie, Jan-Erik; Margrethe Grandal, Else; Zwingmann, Horst; Vogt, Christoph

2017-04-01

Remnants of in-situ weathered bedrock, saprolite, are found in several locations in Scandinavia. Saprolites contain important information about past climate conditions and landscape evolution, although their age and genesis are commonly difficult to constrain. It is generally thought that clay-poor, coarse-grained (arêne) saprolites, mostly occurring as thin regolith blankets or in larger outcrops, formed in temperate climate during the Cenozoic, whereas clay-rich (argillic) saprolites, commonly restricted to small, fracture-bounded outcrops, formed in (sub-)tropical climate during the Mesozoic. Recent methodological and conceptual advances in K-Ar dating of illite-bearing fault rocks have been applied to date clay-rich saprolites. To test the K-Ar dating technique for saprolites, we first selected an offshore site in the Viking Graben of the North Sea, where weathered and fractured granitic basement highs have been drilled during petroleum exploration, and an abandoned kaolin mine in Southern Sweden. Both targets provide independent age control through the presence of overlying Mesozoic sedimentary rocks. Clay-rich saprolites occurring in fractured basement rocks were additionally sampled in a joint valley landscape on the southwestern coast of Norway, which can be regarded as the possible onland correlative to the offshore basement high. In order to offer a sound interpretation of the obtained K-Ar ages, the mineralogical and chemical composition of the saprolites requires a thorough characterization. Scanning electron microscopy of thin sections, integrated by XRD and XRF analysis, reveals the progressive transformation of primary granitic rock minerals into secondary clay minerals. The authigenesis of illite is particularly important to understand, since it is the only K-bearing clay mineral that can be dated by the K-Ar method. K-feldspars and mica are the common primary K-bearing minerals, from which illite can be formed. While progressive leaching of interlayer potassium is observed in micas without significant modification of the mineral structure, K-feldspars are gradually dissolved with concomitant precipitation of illite, smectite and kaolinite. Individual illite minerals are difficult to identify, but low-K contents in smectite point to small amounts of illite-interlayers. This finding is supported by XRD patterns (powder analyses on clay size fractions) that lack a clear 10 Å peak indicating the presence of illite/mica, but show a prominent and slight asymmetric 14 Å peak representing smectite with potential low (<10 %) illite-interlayer content. In agreement with previous models of diminishing contamination of protolithic K-bearing phases in the finest grain size fractions, K-Ar ages invariably decrease with grain size suggesting that the finest grain-size is predominantly composed of authigenic, syn-weathering illite, whose age can thus be used to constrain the timing of saprolitization. The obtained Late Permian to Late Triassic ages i) are in accordance with independent age constraints supporting previous hypotheses of intense chemical weathering during the Mesozoic and ii) correlate with similar K-Ar ages obtained from nearby brittle faults suggesting a genetic relationship between weathering and brittle deformation. The combined investigation and K-Ar dating of illite-bearing fractured and weathered bedrock provides new insights into the tectonic and climatic evolution of the Scandinavian landscape prior to the major, and often obliterating, Quaternary glaciations.

The role of minerals in the thermal alteration of organic matter. III - Generation of bitumen in laboratory experiments

NASA Technical Reports Server (NTRS)

Huizinga, Bradley J.; Tannenbaum, Eli; Kaplan, I. R.

1987-01-01

A series of pyrolysis experiments, utilizing two different immature kerogens (from the Monterey and Green River Formations) mixed with common sedimentary minerals (calcite, illite, or Na-montmorillonite), was conducted to study the impact of the mineral matrix on the bitumen that was generated. Calcite has no significant influence on the thermal evolution of bitumen and also shows virtually no adsorption capacity for any of the pyrolysate. In contrast, montmorillonite (M) and illite, to a lesser extent, alter bitumen during dry pyrolysis. M and illite also display strong adsorption capacities for the polar constituents of bitumen. By this process, hydrocarbons are substantially concentrated within the pyrolysate that is not strongly adsorbed on the clay matrices. The effects of the clay minerals are significantly reduced during hydrous pyrolysis. The strong adsorption capacities of M and illite, as well as their thermocatalytic properties, may in part explain why light oils and gases are generated from certain argillaceous source-rock assemblages, whereas heavy immature oils are often derived from carbonate source rocks.

Estimation of landslide-triggering factors using clay minerals, ASTER satellite image and GIS in the Busan area, southeastern Korea

NASA Astrophysics Data System (ADS)

Jeong, G. C.; Kim, M. G.; Choi, J. J.; Ryu, J. O.; Nho, J. G.; Choo, C. O.

2016-12-01

This study aims at estimating landslide-inducing factors such as extreme rainfall, slope, and geological factors in Busan city, southeastern Korea, using clay mineralogy, DM analysis and DB construction in order to develop the landslide evaluation standards suitable for the country. GIS-based data collected from the study area include geological maps, topological maps, soil maps, forest maps and others in the DB construction. Data extraction and processing for landslide-induced factors consist of expandable clay minerals identified using XRD, along with XRF and weathering sensitivity analysis and fundamental soil analysis on 38 bulk samples composed of weathered rocks and soils. Finally landslide sensibility maps were constructed using ArcGIS, together with ASTER satellite images for identifying clay minerals on regional areas helpful for saving time and money. In Mt. Cheonma, 16 samples are composed of quartz, albite, illite, vermiculite, and kaolinite, with little difference in mineralogy. In Mt. Hwangryeong and Mt. Geumryeun, 12 samples consist of quartz, albite, illite, vermiculite, kaolinite and hornblende, with little difference in mineralogy. In Mt. Songhak, 10 samples are composed of quartz, illite, vermiculite, and kaolinite. Quartz, albite and illite are abundant in most samples, regardless of sites studied. IDW interpolation method was applied to the Busan area. The resolution of space grids consists of 5 m x 5 m. Especially, illite was used as the most effective factor that induces landslide using IDW interpolation and ASTER satellite images. In conclusion, sensibility maps constructed using 16 layers including illite content, weathered sensibility are well in accordance with the real sites where landslides took place, showing that areas with high sensibility are closely related to the high frequencies of landslide. This research was supported by the Public Welfare & Safety Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT & Future Planning (grant number 2012M3A2A1050976)

Hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

NASA Astrophysics Data System (ADS)

Ylagan, Robert F.; Altaner, Stephen P.; Pozzuoli, Antonio

1996-12-01

A rhyolitic hyaloclastite from Ponza island, Italy, has been hydrothermally altered producing four distinct alteration zones based on XRD and field textures: (1) non-pervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is a volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the non pervasive argillic zone, characterized by smectite and disordered opal-CT. Obsidian clasts, some pumice lapilli, and pyrogenic plagioclase and biotite are unaltered. Smectite has an irregular flakey morphology, although euhedral particles are occasionally observed. The propylitic zone is characterized by mixed-layer illite/smectite (I/S) with 10 to 85% illite (I), mordenite, opal-C and authigenic K-feldspar (akspar). The matrix of the hyaloclastite is completely altered and obsidian clasts are silicified; however, plagioclase and biotite phenocrysts remain unaltered. Flakey I/S replaces pumice, and mordenite, akspar and silica line and fill pores. I/S particles are composed predominantly of subequant plates and euhedral laths. The silicic zone is characterized by highly illitic I/S with ≥ 90% I, quartz, akspar and occasional albite. In this zone the matrix and clasts are completely altered, and pyrogenic plagioclase shows significant alteration. Illitic I/S has a euhedral lath-like morphology. In the sericitic zone the hyaloclastite altered primarily to illitic I/S with ≥ 66% I, quartz, and minor akspar and pyrite. Clay minerals completely replace pyrogenic feldspars and little evidence remains of the original hyaloclastite texture. Unlike other zones, illitic I/S is fibrous and pure illite samples are composed of euhedral laths and hexagonal plates. The temperatures of hydrothermal alteration likely ranged from 30 to 90 °C for the argillic zone, from 110 to 160 °C for the propylitic zone, from 160 to 270 °C for the silicic zone, and were possibly as high as 300 °C for the sericitic zone. The four zones occur as linear bands that increase in intensity north of the bentonite mine at Cala dell'Acqua. The alteration zones have two orientations and may be structurally controlled by E-W- and NE-SW-trending faulting which is consistent with the dominant structural trends of the Pontine archipelago. Finally, hydrothermal alteration most likely involved seawater based on the geologic evolution of Ponza.

Mineralogy and geochemistry of the Lower Cretaceous siliciclastic rocks of the Morita Formation, Sierra San José section, Sonora, Mexico

NASA Astrophysics Data System (ADS)

Madhavaraju, J.; Pacheco-Olivas, S. A.; González-León, Carlos M.; Espinoza-Maldonado, Inocente G.; Sanchez-Medrano, P. A.; Villanueva-Amadoz, U.; Monreal, Rogelio; Pi-Puig, T.; Ramírez-Montoya, Erik; Grijalva-Noriega, Francisco J.

2017-07-01

Clay mineralogy and geochemical studies were carried out on sandstone and shale samples collected from the Sierra San José section of the Morita Formation to infer the paleoclimate and paleoweathering conditions that prevailed in the source region during the deposition of these sediments. The clay mineral assemblages (fraction < 2 μm) of the Sierra San José section are composed of chlorite and illite. The abundance of illite and chlorite in the studied samples suggest that the physical weathering conditions were dominant over chemical weathering. Additionally, the illite and chlorite assemblages reflect arid or semi-arid climatic conditions in the source regions. K2O/Al2O3 ratio of shales vary between 0.15 and 0.26, which lie in the range of values for clay minerals, particularly illite composition. Likewise, sandstones vary between 0.06 and 0.13, suggesting that the clay minerals are mostly kaolinte and illite types. On the chondrite-normalized diagrams, sandstone and shale samples show enriched light rare earth elements (LREE), flat heavy rare earth elements (HREE) patterns and negative Eu anomalies. The CIA and PIA values and A-CN-K plot of shales indicate low to moderate degree of weathering in the source regions. However, the sandstones have moderate to high values of CIA and PIA suggesting a moderate to intense weathering in the source regions. The SiO2/Al2O3 ratios, bivariate and ternary plots, discriminant function diagram and elemental ratios indicate the felsic source rocks for sandstone and shale of the Morita Formation.

Coupled THMC models for bentonite in clay repository for nuclear waste

NASA Astrophysics Data System (ADS)

Zheng, L.; Rutqvist, J.; Birkholzer, J. T.; Li, Y.; Anguiano, H. H.

2015-12-01

Illitization, the transformation of smectite to illite, could compromise some beneficiary features of an engineered barrier system (EBS) that is composed primarily of bentonite and clay host rock. It is a major determining factor to establish the maximum design temperature of the repositories because it is believed that illitization could be greatly enhanced at temperatures higher than 100 oC and thus significantly lower the sorption and swelling capacity of bentonite and clay rock. However, existing experimental and modeling studies on the occurrence of illitization and related performance impacts are not conclusive, in part because the relevant couplings between the thermal, hydrological, chemical, and mechanical (THMC) processes have not been fully represented in the models. Here we present fully coupled THMC simulations of a generic nuclear waste repository in a clay formation with bentonite-backfilled EBS. Two scenarios were simulated for comparison: a case in which the temperature in the bentonite near the waste canister can reach about 200 oC and a case in which the temperature in the bentonite near the waste canister peaks at about 100 oC. The model simulations demonstrate that illitization is in general more significant at higher temperatures. We also compared the chemical changes and the resulting swelling stress change for two types of bentonite: Kunigel-VI and FEBEX bentonite. Higher temperatures also lead to much higher stress in the near field, caused by thermal pressurization and vapor pressure buildup in the EBS bentonite and clay host rock. Chemical changes lead to a reduction in swelling stress, which is more pronounced for Kunigel-VI bentonite than for FEBEX bentonite.

Zeta Potential Measurements on Three Clays from Turkey and Effects of Clays on Coal Flotation

PubMed

Hussain; Dem&idot;rc&idot;; özbayoğlu

1996-12-25

There is a growing trend of characterizing coal and coal wastes in order to study the effect of clays present in them during coal washing. Coarse wastes from the Zonguldak Coal Washery, Turkey, were characterized and found to contain kaolinite, illite, and chlorite. These three clays, obtained in almost pure form from various locations in Turkey, have been subjected to X-ray diffraction (XRD) analysis to assess their purity and zeta potential measurements in order to evaluate their properties in terms of their surface charge and point of zero charge (pzc) values. It was found from XRD data that these clays were almost pure and their electrokinetic potential should therefore be representative of their colloidal behavior. All three clay minerals were negatively charged over the range from pH 2.5 to 11. Chlorite and illite have pzc at pH 3 and pH 2.5, respectively, whereas kaolinite has no pzc. The effect of these clays in Zonguldak coal, wastes, and black waters on coal flotation was studied by floating artificial mixtures of Zonguldak clean coal (4.5% ash) and individual clay. The flotation tests on coal/individual clay revealed that each clay influences coal flotation differently according to its type and amount. Illite had the worst effect on coal floated, followed by chlorite and kaolinite. The loss of yield in coal was found to be 18% for kaolinite, 20% for chlorite, and 28% for illite, indicating the worst effect of illite and least for kaolinite during coal flotation.

The Crystal Structure of Illite/Smectite.

DTIC Science & Technology

1988-04-04

summarized from Tellier and Reynolds (1987). Figure 3 shows a comparison between experimental and calculated diffraction patterns for the ethylene glycol...PUBLICATIONS Tellier . K. and Reynolds, R. C. (1987) Calculation of one-dimensional X-ray diffraction profiles of interstratified illite/smectite as...Abst.) 24th Annual fMeet Clay Min. Soc., Socorro, N. M., p. 115 PARTICIPATING SCIENTIFIC PERSONNEL Kathleen Tellier : Dept. of Earth Sciences

Polymerization on the rocks: negatively-charged alpha-amino acids

NASA Technical Reports Server (NTRS)

Hill, A. R. Jr; Bohler, C.; Orgel, L. E.; Bada, J. L. (Principal Investigator)

1998-01-01

Oligomers of the negatively-charged amino acids, glutamic acid, aspartic acid, and O-phospho-L-serine are adsorbed by hydroxylapatite and illite with affinities that increase with oligomer length. In the case of oligo-glutamic acids adsorbed on hydroxylapatite, addition of an extra residue results in an approximately four-fold increase in the strength of adsorption. Oligomers much longer than the 7-mer are retained tenaciously by the mineral. Repeated incubation of short oligo-glutamic acids adsorbed on hydroxylapatite or illite with activated monomer leads to the accumulation of oligomers at least 45 units long. The corresponding reactions of aspartic acid and O-phospho-L-serine on hydroxylapatite are less effective in generating long oligomers, while illite fails to accumulate substantial amounts of long oligomers of aspartic acid or of O-phospho-L-serine.

Mineralogy of parent rock and peaty-podzolic soil of Iremel Ridge, Southern Urals

NASA Astrophysics Data System (ADS)

Khalitov, R. M.; Perova, E. N.; Abakumov, E. V.; Suleimanov, R. R.

2017-08-01

The mineralogy of soils and parent rocks of the Iremel Ridge has been studied by the methods of micromorphology, laser diffraction, computed X-ray microtomography, and X-ray fluorescence analysis. In hard rock and soil, the major minerals have been identified: quartz, illite, and a chlorite-group mineral (Fe analogue of sudoite), as well as accessory minerals: monazite, xenotime, rutile, zircon, and florencite. It has been found that chlorite, illite, and quartz are present in all horizons of the studied peaty-podzolic soil. Insignificant amounts of mixed-layered mineral and kaolinite could be suggested in the T and EL horizons of peaty-podzolic soil. The mixed-layered mineral is most probably of soil origin, which is related to the transformation of illites inherited from the parent rock under acidic conditions.

Effects of chemical surface modification on the ice nucleation ability of feldspar and illite

NASA Astrophysics Data System (ADS)

Augustin, Stefanie; Wex, Heike; Kanter, Sandra; Ebert, Martin; Niedermeier, Dennis; Stratmann, Frank

2014-05-01

Mineral dust is the most abundant ice nuclei (IN) in the atmosphere and thus it is thought to be important for ice nucleation in clouds (Murray et al. [2012]). The clay minerals contribute approximately two thirds of the mineral dust mass (Atkinson et al. [2013]), and illite is the most abundant clay mineral found in the atmosphere [Broadley et al., 2012]. In the past years a lot of the ice nucleation research focused on proxies for clay minerals like Arizona Test Dust (ATD), kaolinite and illite (see reviews by Murray et al. [2012] and Hoose and Möhler. [2012]). In most experiments, these substances acted as IN only at relatively low temperatures (lower than -25°C). Very recently Atkinson et al. (2013) showed that K-feldspar, which is a common crustal material, is the most active mineral dust with freezing temperatures above -20°C. In the present study we compared the immersion freezing behavior of size segregated illite and feldspar particles. We used illite-NX (Arginotec) and a feldspar sample from Minas Gerais, Brazil (consisting to roughly 80% of a K-feldspar with the remainder being a Na-feldspar). Both substances were examined in the framework of the INUIT research project. For the illite-NX particles freezing onset was observed at temperatures around -34°C. The feldspar sample already induced freezing at -23°C. The data obtained was in agreement to those reported in Broadley el al. [2012] and Atkinson et al. [2013]. To simulate chemical aging of the particle surface we coated the particles with sulfuric acid and repeated the measurements. The illite-NX showed a rather small change in the ice nucleation ability, whereas the freezing ability of the feldspar was strongly reduced and became similar to that of illite-NX. It seems that the sulfuric acid destroyed those sites on the particle surface which are responsible for the initiation of freezing. We continue our work in trying to better understand what exactly it is that gives K-feldspar its good IN ability. Acknowledgement: Part of this work was done within the framework of the DFG funded Ice Nucleation research UnIT (INUIT, FOR 1525) under WE 4722/1-1. Murray, B. J., O'Sullivan, D., Atkinson, J. D. and Webb, M. E., Chem. Soc. Rev., 41, 6519-6554, 2012. Atkinson J. D. , B. J. Murray, M. T. Woodhouse, T. F. Whale, K. J. Baustian, K. S. Carslaw, S. Dobbie, D. O'Sullivan and T. L. Malkin, Nature, 498, 355-358, 2013. Broadley S. L., B. J. Murray, R. J. Herbert, J. D. Atkinson, S. Dobbie, T. L. Malkin, E. Condlie, and L. Neve, Atmos. Chem. Phys., 12, 287-307, 2012. Hoose, C. and O. Möhler, Atmos. Chem. Phys., 12, 9817-9854, 2012.

2.9-1.9 Ga paleoalterations of Archean granitic basement of the Franceville basin (Gabon)

NASA Astrophysics Data System (ADS)

Mouélé, Idalina Moubiya; Dudoignon, Patrick; El Albani, Abderrazak; Meunier, Alain; Boulvais, Philippe; Gauthier-Lafaye, François; Paquette, Jean-Louis; Martin, Hervé; Cuney, Michel

2014-09-01

The Archean granitoids in the Kiéné area, Gabon, are overlained by the Paleoproterozoic sediments of the Franceville basin (2.1 Ga). The basin is known for its high-grade uranium deposits among which some have been forming natural nuclear fission reactors. Most of the studies were dedicated to the FA-FB Paleoproterozoic sediments hosting these uranium deposits. Little is known on the Archean basement itself and specifically on the hydrous alteration events it experienced before and after the sediment deposition. The present work is focused on their petrographical, mineralogical and geochemical characterization. Dating the successive alteration events has been attempted on altered monazite crystals. Rocks in different alteration states have been sampled from eight drill cores crosscutting the Archean - Paleoproterozoic unconformity. The Archean granitoids observed in the deepest levels exhibit typical petrographical features of a propylitic alteration while they are intensely illitized up to the unconformity. The propylitic alteration is mainly pervasive but the original texture of the granitoïds is conserved in spite of the formation of new minerals: Mg-chlorite, allanite and epidote forming a typical paragenesis. The illitic alteration is much more invasive near the unconformity. The illitization process leads to the replacement of feldspars and the corrosion of quartz crysals by an illitic matrix while the ferromagnesian minerals are pseudomorphosed by a Fe-chlorite + phengite + hematite assemblage. The final fluid-rock interaction step is marked by fissural deposits of calcite and anhydrite. The δ13C isotopic data show that the fissural carbonates precipitated from diagenetic fluids enriched carbon products deriving from the maturation of organic matter. The U-Pb isotopic analyzes performed on monazite crystals have dated three distinct events: 3.0-2.9 Ga (magmatic), 2.6 Ga (propylitic alteration) and 1.9 Ga (diagenetic illitization). The calculation of geochemical mass balances suggests that the water-rock ratio during the propylitic alteration event was weak. On the contrary, it was much higher during the overprinted illitization which is characterized by an intense leaching of Na, Ca, Mg, Sr, REE and an enrichment in K, Rb,Cs. Neither the petrographic features nor the geochemical data militate for an Archean weathering event (paleosol). In the present case, diagenetic fluids have percolated from the unconformity into the basement where they overprinted the illitization processes upon the previously propylitized rocks. These fluids were probably oxidant as they are also responsible of the U mobilization which led to the formation of the ore deposits close to the FA-FB interface.

Decoupling of paramagnetic and ferrimagnetic AMS development during the experimental chemical compaction of illite shale powder

NASA Astrophysics Data System (ADS)

Bruijn, Rolf H. C.; Almqvist, Bjarne S. G.; Hirt, Ann M.; Benson, Philip M.

2013-03-01

Inclination shallowing of detrital remanent magnetization in sedimentary strata has solely been constrained for the mechanical processes associated with mud deposition and shallow compaction of clay-rich sediment, even though a significant part of mud diagenesis involves chemical compaction. Here we report, for the first time, on the laboratory simulation of magnetic assemblage development in a chemically compacting illite shale powder of natural origin. The experimental procedure comprised three compaction stages that, when combined, simulate the diagenesis and low-grade metamorphism of illite mud. First, the full extent of load-sensitive mechanical compaction is simulated by room temperature dry axial compression. Subsequently, temperature controlled chemical compaction is initiated by exposing the sample in two stages to amphibolite or granulite facies conditions (temperature is 490 to 750°C and confining pressure is 170 or 300 MPa) both in the absence (confining pressure only) and presence of a deformation stress field (axial compression or confined torsion). Thermodynamic equilibrium in the last two compaction stages was not reached, but illite and mica dehydroxylation initiated, thus providing a wet environment. Magnetic properties were characterized by magnetic susceptibility and its anisotropy (AMS) in both high- and low-applied field. Acquisition of isothermal remanent magnetization (IRM), stepwise three-component thermal de-magnetization of IRM and first-order reversal curves were used to characterize the remanence-bearing minerals. During the chemical compaction experiments ferrimagnetic iron-sulphides formed after reduction of magnetite and detrital pyrite in a low sulphur fugacity environment. The degree of low-field AMS is unaffected by porosity reduction from 15 to ˜1 per cent, regardless of operating conditions and compaction history. High-field paramagnetic AMS increases with compaction for all employed stress regimes and conditions, and is attributed to illite transformation to iron-bearing mica. AMS of authigenic iron-sulphide minerals remained constant during compaction indicating an independence of ferrimagnetic fabric development to chemical compaction in illite shale powder. The decoupling of paramagnetic and ferrimagnetic AMS development during chemical compaction of pelite contrasts with findings from mechanical compaction studies.

Effect of Pseudomonas fluorescens and pyoverdine on the phytoextraction of cesium by red clover in soil pots and hydroponics.

PubMed

Hazotte, Alice; Péron, Olivier; Gaudin, Pierre; Abdelouas, Abdesselam; Lebeau, Thierry

2018-05-12

With the aim of improving the phytoextraction rate of cesium (Cs), the effect of Pseudomonas fluorescens ATCC 17400 and its siderophore pyoverdine (PVD) on the uptake of Cs by red clover was studied in soil pots. This work also provides a mechanistic understanding of the Cs-bacteria (or PVD)-illite-plant interactions by using a simplified experimental design, i.e., hydroponics with either Cs in solution or Cs-spiked illite in suspension. For soil spiked with 11.2 mmol kg -1 (1480 mg kg -1 ) of Cs, 0.43% of total Cs was taken up by red clover in 12 days (119 μmol g -1 (16 mg g -1 ) of Cs dry matter in roots and 40 μmol g -1 (5 mg g -1 ) in shoots). In hydroponics with Cs in solution (0.1 mmol L -1 or 13 mg L -1 ), 75% of Cs was taken up vs. only 0.86% with Cs-spiked illite suspension. P. fluorescens and PVD did not increase Cs concentrations in aboveground parts and roots of red clover and even decreased them. The damaging effect of PVD on red clover growth was demonstrated with the biomass yielding 66% of the control in soil pots (and 100% mortality after 12 days of exposition) and only 56% in hydroponics (78% with illite in suspension). Nonetheless, PVD and, to a lesser extent, P. fluorescens increased the translocation factor up to a factor of 2.8. This study clearly showed a direct damaging effect of PVD and to a lower extent the retention of Cs by biofilm covering both the roots and illite, both resulting in the lower phytoextraction efficiency.

Role of water in the smectite-to-illite reaction

USGS Publications Warehouse

Whitney, Gene

1990-01-01

A series of hydrothermal experiments was performed to determine the effect of fluid abundance on the reaction of smectite to illite. Experiments were conducted on K-saturated montmorillonite (<0.1-µm fraction) in a closed system at 250° to 400°C using run times of 1, 7, 14, 30, and 60 days at 100 MPa (1 kbar) pressure. In fluid-deficient systems (pore spaces not saturated), the rate and extent of illitization was significantly inhibited. A rock:water ratio of 20:1 (mass:mass) produced an R0 illite/smectite (I/S) having 82% smectite layers after 60 days at 250°C, whereas a rock:water ratio of 1:1 produced an I/S having 57% smectite layers under the same conditions. The effect became less pronounced at higher temperatures, with the 20:1 and the 1:1 experimental products differing by only 11% expandability at 400°C after 60 days. In addition, the low-fluid experiments produced fewer crystalline byproducts (quartz, cristobalite, chlorite) than did the fluid-rich runs, and the I/S was more difficult to disperse and orient in the fluid-deficient samples, suggesting enhanced cementation at grain contacts or the production of particle morphologies that did not lend themselves to orientation. The difference in reactivity of the smectite and I/S as a function of water content appears to be attributable to the reduced capacity for low volumes of water to mediate the dissolution, solute transport, and precipitation reactions that make up the series of reactions collectively termed illitization. Of these variables, solute transport is likely to be affected most by reduction of fluid.

Ad-/desorption behavior of Sulfadiazine on soil and soil components

NASA Astrophysics Data System (ADS)

Meng, N.; Lewandowski, H.; Kasteel, R.; Narres, H.-D.; Klumpp, E.; Vereecken, H.

2009-04-01

Sulfadiazine [4-amino-N-(2-pyrimidinyl)benzene sulfonamide, SDZ] belongs to the widely used antibacterial veterinary pharmaceuticals which reach the environment by the application of manure. Therefore the adsorption and desorption behavior of 14C labeled sulfadiazine was investigated with different inorganic soil components including Al2O3, goethite, illite and compared with air-dried topsoil. The batch sorption experiments with Al2O3and soil were performed in natural pH-values (8.2 and 7.5, negatively charged SDZ). Experiments with illite and goethite were done with pH-values of 4.2 and 6.8 (natural pH of illite and goethite, neutral and partly negatively charged SDZ) and also done in buffer solution about pH 8 for comparing the adsorption on all adsorbents in same pH range. The adsorption isotherms on all sorbents are strongly nonlinear and can be fitted well by the Freundlich equation. From the initial slope of the isotherm the partition coefficient Kd could be determined. The adsorption of SDZ on illite at pH 4.2 and on goethite at pH 6.8 has higher Kd-values than at pH 8, which demonstrates that the negative charge of SDZ obstructs the adsorption. The desorption isotherms show hysteresis effects for all adsorbents. The strong hysteresis was found for goethite and soil indicates strongly physical or chemical binding. On the other hand, the low hysteresis effect for Al2O3 and illite indicates the weak binding of the adsorbed SDZ. The properties of the inorganic matrix and especially the charges of the inorganic compounds in relation to the charge of SDZ are important parameters for the sorption process. The data could be described by modeling with different sorption rates and sites.

Research of CO2 and N2 Adsorption Behavior in K-Illite Slit Pores by GCMC Method

PubMed Central

Chen, Guohui; Lu, Shuangfang; Zhang, Junfang; Xue, Qingzhong; Han, Tongcheng; Xue, Haitao; Tian, Shansi; Li, Jinbu; Xu, Chenxi; Pervukhina, Marina; Clennell, Ben

2016-01-01

Understanding the adsorption mechanisms of CO2 and N2 in illite, one of the main components of clay in shale, is important to improve the precision of the shale gas exploration and development. We investigated the adsorption mechanisms of CO2 and N2 in K-illite with varying pore sizes at the temperature of 333, 363 and 393 K over a broad range of pressures up to 30 MPa using the grand canonical Monte Carlo (GCMC) simulation method. The simulation system is proved to be reasonable and suitable through the discussion of the impact of cation dynamics and pore wall thickness. The simulation results of the excess adsorption amount, expressed per unit surface area of illite, is in general consistency with published experimental results. It is found that the sorption potential overlaps in micropores, leading to a decreasing excess adsorption amount with the increase of pore size at low pressure, and a reverse trend at high pressure. The excess adsorption amount increases with increasing pressure to a maximum and then decreases with further increase in the pressure, and the decreasing amount is found to increase with the increasing pore size. For pores with size greater larger than 2 nm, the overlap effect disappears. PMID:27897232

Investigation of Cyclodextrin-Enhanced Electrokinetic Soil Remediation. Fate and Transport of Nitroaromatic Contaminants and Cyclodextrin Amendments in Expansive Clays

DTIC Science & Technology

2004-09-01

report increasing adsorption capacity depending on the specific clay type, in the order kaolinite < illite < montmorillonite (11). This finding suggests... kaolinite , illite, and montmorillonite . Finally, there is a wide varia- tion in adsorption constants among the different nitroaromatic compounds...common to micas, chlorites, pyrophyllite, talc, kaolinite , and gibbsite . As is now known, clays typically consist of layered crystalline structures

Rock Deformation at High Confining Pressure and Temperature.

DTIC Science & Technology

debugged, delivered and installed to the contracting agency. Clay specimens of illite, kaolinite and montmorillonite were deformed in tri-axial compression...at 25 and 3000C at a constant confining pressure of 2 kb and a constant strain rate of .0001 sec. The illite and kaolinite are stronger under these...conditions than montmorillonite . Cores from dolomite single crystals were deformed at a confining pressure of 7 kb and temperatures of 300 and 500C

Microbial Effects in Promoting the Smectite to Illite Reaction: Role of Organic Matter Intercalated in the Interlayer

DTIC Science & Technology

2007-01-01

organic matter in the smectite to illite reaction. For example, Small etal. (1994) demonstrated that potassium oxalate and potassium acetate in...potassium oxalate and potassium acetate on this reaction (Small 1994). This study supplements our previous study in that microbes play an...Keeling, J.L., Raven, M.D., and Gates, W.P, (2000) Geology and characterization of two hydrothermal nontronites from weathered metamorphic rocks at

Effects of substrate mineralogy on the biodegradability of fuel components

DOE Office of Scientific and Technical Information (OSTI.GOV)

Apitz, S.E.; Meyers-Schulte, K.J.

1996-11-01

Experiments were carried out to determine the effects of mineralogy on the biodegradability of components of a whole fuel by a soil microbial consortium. Samples of quartz sand (Fischer Sea Sand) and illite clay (API 35) were spiked with marine diesel fuel, aged, slurried, and inoculated, and concentrations of fuel components were monitored over time. To help distinguish biotic from abiotic processes, identical samples were poisoned with mercuric chloride and were run in parallel. While there was a chromatographic and biomarker evidence of n-alkane biodegradation in the sand samples, illite samples showed no evidence of biogenic loss of aliphatic components.more » Polycyclic aromatic hydrocarbons, on the other hand, were lost equivalently on both minerals and in both cases were lost to a much greater extent than were total petroleum hydrocarbons (TPHs). These results suggest that under experimental conditions, illite inhibited the bioavailability of some TPH components to the soil microbial consortium.« less

Origin and time-space distribution of hydrothermal systems in east-central Australian sedimentary basins: Constraints from illite geochronology and isotope geochemistry.

NASA Astrophysics Data System (ADS)

Uysal, I. Tonguç

2016-04-01

Some well-known precious mineral deposits and hydrocarbon resources occur extensively in east-central Australian sedimentary Basins. The metal occurrences are abundant in northwestern and eastern part of Queensland, whereas no significant deposits are known in large areas further south, which may, however, be hidden beneath the Jurassic-Cretaceous sedimentary basins. Important hydrocarbon resources exist within the Jurassic-Cretaceous sedimentary rocks at relatively shallow depths, of which the distribution represent zones of high paleo-geothermal gradients. This study examines the time-space distribution in relation to the regional tectonic history of concealed metal deposits and areas of high paleo-geothermal gradient leading to hydrocarbon maturation. To this end, authigenic illitic clay minerals representing various locations and stratigraphic depths in east-central Australia were investigated, of which the Rb-Sr and Ar-Ar geochronology and stable isotope geochemistry assist in delineating zones of hydrothermal systems responsible for hydro-carbon maturation/migration and potentially ore deposition. The Late Carboniferous - Early Permian crustal extension that affected large areas of eastern Australia and led to the epithermal mineralisations (e.g., the Drummond Basin) is also recorded in northern South Australia and southwest Queensland. A Late Triassic - Early Jurassic tectonic event being responsible for coal maturation and gas generation in the Bowen Basin and the epithermal mineralisation in the North Arm goldfield in SE Queensland likewise affected the areas much further west in Queensland. Some illites from the basement in outback Queensland and fault gouges from the Demon Fault in NE New South Wales yield younger Rb-Sr and Ar-Ar ages indicating the effect of hydrothermal processes as a result of a Middle-Upper Jurassic tectonic event. The majority of illite samples from the crystalline basement rocks, Permian Cooper Basin, and Jurassic-Cretaceous Eromanga Basin from all over east-central Australia give Cretaceous ages (~130 to ~60 Ma) reflecting episodic hydrothermal events restricted to certain tectonic zones. The Cretaceous events were responsible for the hydro-carbon generation/maturation in the Cooper, Eromanga, and Gunnedah Basins and deposition of some Au and basemetal resources in the eastern part of Queensland. The stable isotope composition of the Late Triassic - Early Jurassic illites in eastern Queensland and all mid-late Cretaceous illites from outback and eastern Australia is distinctively different with low 18O and D values indicating meteoric-hydrothermal systems due to extensional tectonics. Results of this study suggest that illite geochronology and geochemistry is a powerful tool in delineation of concealed hydrothermal systems that were responsible for ore generation and hydrocarbon/maturation and migration.

Roles of Nano- and Micro-Scale Subsurface Geochemical Reactions on Environmentally Sustainable Geologic Carbon Dioxide Sequestration

NASA Astrophysics Data System (ADS)

Hu, Yandi

Geologic CO2 sequestration (GCS) is a promising approach to reduce anthropogenic CO2 emissions into the atmosphere. At GCS sites, injected CO2 is kept in formation rock by an overlying low permeability caprock. During and after CO2 injection, geochemical reactions can affect the porosity, permeability, and pollutant transport in aquifers. Despite their importance, nano- and micro-scale subsurface geochemical reactions are far from well-understood. Clay mobilization has been reported to decrease aquifer permeability during water flooding, and clay minerals are abundant in caprock. Thus, we studied CO2-brine-clay interactions under varied conditions relevant to different GCS sites (at 35-95°C and under 35-120 atm CO2, in water, NaCl, MgCl2, or CaCl2 solutions). Biotite, Fe-bearing mica, was used as a model clay mineral. We observed numerous fibrous illite precipitates on mica after reaction for only 3 h, which had not been previously reported. A few hours later, the mica surface cracked and fibrous illite detached. The mobilization of fibrous illite can decrease the aquifer's permeability greatly and affect the safety and efficiency of GCS. Mechanisms related to ion exchange, mica swelling, and CO2 intercalation were explored. Oriented aggregation of illite nanoparticles forming the fibrous illite was directly observed, suggesting a new mechanism for fibrous illite formation. Interestingly, besides the pH effect, aqueous CO2 enhances mica cracking over N2. These findings can help to achieve safer subsurface operations. At GCS field sites, Fe concentration increased near the injection sites and originally adsorbed pollutants were released. As the brine flows, Fe re-precipitated because of pH increase. To better predict the fate and transport of aqueous pollutants, the nucleation and growth of Fe(III) (hydr)oxides were studied. New information about sizes and volumes of the Fe(III) (hydr)oxide nanoparticles precipitated in solution and on quartz, mica, and sapphire were provided using small angle X-ray scattering, in the presence of different ions (Al 3+, Cl-, NO3-, and SO 42-). Using complementary techniques, the controlling mechanisms related to surface charge, bond formation, and interfacial energies were explored. These new findings can help better predict pollutant transport in aquifers not only at GCS sites, but also in managed aquifer recharge and acid mine drainage sites.

Microbial mobilization of cesium from illite: Role of organic acids and siderophores

NASA Astrophysics Data System (ADS)

Hazotte, Alice; Peron, Olivier; Abdelouas, Abdesselam; Lebeau, Thierry

2015-04-01

Understanding the behavior of cesium (Cs) in soils and geological formations is interesting in the context of nuclear accidents and nuclear waste disposals. Indeed, this radionuclide with a 30-years half-life can contaminate crops and more generally the food chain. Cs with properties similar to potassium is known to be strongly accumulated in the clays of upper soil horizons. While excavation of contaminated soil cannot be feasible for the whole contaminated surfaces (huge volumes to be cleaned-up), in situ methods could provide a sustainable and low cost solution. Phytoextraction is one of a few solutions for in situ remediation of soils contaminated by trace elements and it preserves the quality of agricultural soils. However, many improvements are still needed to enhance phytoextraction effectiveness. The combination of bioaugmentation (soil inoculation with exogenous microorganisms) with phytoextraction is likely to increase the bioaccessibility of radionuclides and their accumulation in plants. The role of bacteria on soil-pollutants can be direct (direct metal complexation) and/or indirect (weathering of clays adsorbing Cs). This study aims to provide more specifically a mechanistic understanding of the bacterial mobilization of Cs from soil with the prospect of soil bioremediation. Bacterial metabolites of Pseudomonas fluorescens (ATCC 17400) were supplied to illite spiked with 0.1 and 1 mM of Cs. Purified siderophores including pyoverdine from P. fluorescens, or the whole metabolites from the bacterial culture supernatant were compared to low molecular weight organic acids (LMWOA) (citric and oxalic acids) at 0.04 mM, or synthetic chelants, i.e., acetohydroxamic acid (AHA) and desferrioxamine mesylate (DFOM) ranging from 50 µM up to 250 µM. The release of Cs and the structural alteration of illite (release of Al, Fe and Si) were monitored. When compared to the control, no release of Cs from illite was observed with LMWOA. On the contrary, a slight release of Cs was shown with AHA and DFOM (9 % and 22 %, respectively). The highest release was shown with the bacterial supernatant and the purified pyoverdine (39 % and 43 %, respectively). The purified pyoverdine and the bacterial metabolites were also able to complex Fe from illite and to a lesser extent Al. These results demonstrated that Cs is likely to be indirectly released from illite by P. fluorescens producing chelating agents involved in its alteration.

Chronology of magmatism and mineralization in the Kassandra mining area, Greece: The potentials and limitations of dating hydrothermal illites

NASA Astrophysics Data System (ADS)

Gilg, H. Albert; Frei, Robert

1994-05-01

Various geochronological methods ( U/Pb, Rb/Sr, and K/Ar) have been applied to constrain the timing of magmatism and polymetallic mineralization in the Kassandra mining district, northern Greece. These data provide the first geochronological evidence that porphyry copper mineralization, proximal copper skarns, and distal high-temperature carbonate-hosted Pb-Zn-Ag-Au replacement ores formed contemporaneously and probably within less than 2 million years. Polymetallic mineralization is temporally related to the emplacement of granodioritic to quartz dioritic porphyries (24-25 Ma) that postdate the largest post-tectonic intrusion of the area, the Stratoni granodiorite (27.9 ± 1.2 Ma). Andesite porphyry dikes, which crosscut the Pb-Zn-Ag-Au ores and associated alterations, represent the last magmatic phase in the area (19.1 ± 0.6 Ma) and did not contribute to metal concentration. The combination of K/Ar, Rb/Sr, and oxygen isotope studies of hydrothermal illite-rich clays and careful granulometric analysis constrains the reliability of these geochronological methods and emphasizes the importance of characterizing the post-formational history of the sample. We identify various processes which partly disturbed the K/Ar and Rb/Sr system of some clays, such as retrograde alteration by heated meteoric waters, superimposed supergene illitization, and resetting of both isotopic systems due to a hydrothermal overprint related to the intrusion of the andesite porphyry. Our data, however, suggest that diffusive Ar loss from the finest clay fractions (< 0.6 μm) during cooling of the hydrothermal system probably played the most important role in the disturbance of the K/Ar system. Conventional K/Ar ages of < 2 μm fractions from high-temperature illites (> 200°C), therefore, do not give reliable formation ages. The loss of Ar may be used to model the cooling history of the hydrothermal system applying the concept of closure temperatures ( DODSON, 1973). 40K- 40Ar rad isochrons of natural, coarser grained (> 0.6 μm) size fractions of illites from single samples, even when slightly contaminated with feldspars, may yield meaningful ages either of the formation or of a reheating event. The Rb/Sr dating of hydrothermal clays is sensitive to contamination by adsorbed strontium, which may not be cogenetic with the clay, as well as feldspars, which may not have been homogenized isotopically by the illitization process.

Thickness distributions and evolution of growth mechanisms of NH4-illite from the fossil hydrothermal system of Harghita Bai, Eastern Carpathians, Romania

USGS Publications Warehouse

Bobos, Iuliu; Eberl, Dennis D.

2013-01-01

The crystal growth of NH4-illite (NH4-I) from the hydrothermal system of Harghita Bãi (Eastern Carpathians) was deduced from the shapes of crystal thickness distributions (CTDs). The 4-illite-smectite (I-S) interstratified structures (R1, R2, and R3-type ordering) with a variable smectite-layer content. The NH4-I-S (40–5% S) structures were identified underground in a hydrothermal breccia structure, whereas the K-I/NH4-I mixtures were found at the deepest level sampled (−110 m). The percentage of smectite interlayers generally decreases with increasing depth in the deposit. This decrease in smectite content is related to the increase in degree of fracturing in the breccia structure and corresponds to a general increase in mean illite crystal thickness. In order to determine the thickness distributions of NH4-I crystals (fundamental illite particles) which make up the NH4-I-S interstratified structures and the NH4,-I/K-I mixtures, 27 samples were saturated with Li+ and aqueous solutions of PVP-10 to remove swelling and then were analyzed by X-ray diffraction. The profiles for the mean crystallite thickness (Tmean) and crystallite thickness distribution (CTD) of NH4-I crystallites were determined by the Bertaut-Warren-Averbach method using the MudMaster computer code. The Tmean of NH4-I from NH4-I-S samples ranges from 3.4 to 7.8 nm. The Tmean measured for the NH4-I/K-I mixture phase ranges from 7.8 nm to 11.7 nm (NH4-I) and from 12.1 to 24.7 nm (K-I).The CTD shapes of NH4-I fundamental particles are asymptotic and lognormal, whereas illites from NH4-I/K-I mixtures have bimodal shapes related to the presence of two lognormal-like CTDs corresponding to NH4-I and K-I.The crystal-growth mechanism for NH4-I samples was simulated using the Galoper code. Reaction pathways for NH4-I crystal nucleation and growth could be determined for each sample by plotting their CTD parameters on an α–β2 diagram constructed using Galoper. This analysis shows that NH4-I crystals underwent simultaneous nucleation and growth, followed by surface-controlled growth without simultaneous nucleation.

Identification of remagnetization processes in Paleozoic sedimentary rocks of the northeast Rhenish Massif in Germany by K-Ar dating and REE tracing of authigenic illite and Fe oxides

NASA Astrophysics Data System (ADS)

Zwing, A.; Clauer, N.; Liewig, N.; Bachtadse, V.

2009-06-01

This study combines mineralogical, chemical (rare earth elemental (REE)) and isotopic (K-Ar) data of clay minerals as well as chemical compositions (major and REE) of Fe oxide leachates from remagnetized Palaeozoic sedimentary rocks from NE Rhenish Massif in Germany, for which the causes of remagnetization are not yet clear. The dominant carrier of the syntectonic, pervasive Carboniferous magnetization is magnetite. The Middle Devonian clastic rocks record an illitization event at 348 ± 7 Ma probably connected to a major magmatic event in the Mid-German Crystalline Rise, whereas a second illitization episode at 324 ± 3 Ma is coeval to the northward migrating deformation through the Rhenish Massif, being only detected in Upper Devonian and Lower Carboniferous rocks. The age of that younger illitization is not significantly different from that of the remagnetization, which, however, is not restricted to the upper part of the orogenic belt, but affects also the Middle Devonian strata. The REE patterns of the Fe-enriched leachates support two mineralization episodes with varied oxidation-reduction conditions outlined by varied Eu and Ce anomalies. This is not compatible with a unique, pervasive migration of orogenic fluids on a regional scale to explain the remagnetization in the studied region. While clay diagenesis and remagnetization are time-equivalent in Upper Devonian and Lower Carboniferous rocks, they are not so in Middle Devonian rocks. Transformation of smectite into illite cannot, therefore, account for the growth of associated authigenic magnetite, which must have been triggered by a different process. Since remagnetization and deformation ages are similar, the mechanism could relate to local physical conditions such as pressure solution and changing pore fluid pressure due to tectonic stress as well as to chemical conditions such as changing composition of the pore fluids.

Unravelling the Paleoenvironmental and Diagenetic History of Fluviolacustrine Sediments from a Northern Kenya Rift Basin Through Analysis of HSPDP West Turkana-Kaitio Core Material

NASA Astrophysics Data System (ADS)

Rabideaux, N. M.; Chaudhary, M. S.; Deocampo, D.; Feibel, C. S.; Cohen, A. S.

2016-12-01

The Hominin Sites and Paleolakes Drilling Project (HSPDP) collected sediment cores from six rift basins in Ethiopia and Kenya. The goal of HSPDP is to construct high-resolution records of environmental change, and to understand how those changes relate to early human evolution and cultural adaptations. The West Turkana-Kaitio (WTK) site was targeted due to the abundant archeological and paleontological artifacts and fossils discovered around the basin. We conducted XRD and XRF analyses on HSPDP-WTK core material to construct a high-resolution record of paleoenvironmental conditions in the Kenya Rift during the Early Pleistocene ( 1.9-1.35 Ma). Mineralogical and geochemical trends were also used to identify the diagenetic history of fluviolacustrine sediments in the basin. The bulk mineralogy is comprised of mostly detrital feldspars, muscovite, α-quartz, and carbonates. Zeolites are present in intervals throughout the core, possibly suggesting pulses of increased salinity. Oxides and S-bearing minerals are abundant from 100-170 mbs, which may be indicative of redox and or hydrothermal processes in that interval. The lowermost portion of the core contains α- and β-quartz, pyrite and zeolites, suggesting either low-oxygen saline conditions or hydrothermal activity. Oriented clay analysis indicated multiple intervals of diagenesis, with the illitization of smectite related to hydrothermal and or microbial activity. Clay analysis provided evidence for a low degree of illitization in the upper portion of the core, whereas mixed-layered illite-smectite (I/S) contained 30-50% illite proximal to fault breccia and up to 70% illite below the faulted section, indicative of significant alteration in the lowermost portion of the core. Coupled mineralogical and geochemical analysis revealed a complex alteration history in the basin indicated by: 1) the presence of mixed-layer I/S throughout the 216 m core; 2) pronounced alteration proximal to faulting; and 3) authigenic silicates and pyrite in the basal section of the core.

Environment of ore deposition in the Creede mining district, San Juan Mountains, Colorado; Part IV, source of fluids, from oxygen, hydrogen, and carbon isotope studies

USGS Publications Warehouse

Bethke, P.M.; Rye, R.O.

1979-01-01

The hydrogen isotopic composition of fluids responsible for formation of the near-surface silver-base metal vein deposits at Creede was measured by direct analysis of inclusion fluids in sphalerite, quartz, and rhodochrosite and was estimated from analyses of illite and chlorite. The oxygen isotopic composition was determined directly on inclusion fluids in sphalerite and was estimated from analyses of quartz, illite, rhodochrosite, siderite, and adularia. The carbon isotopic composition was estimated from analyses of rhodochrosite and siderite. The ranges in isotopic composition for water and CO2 in the fluids associated with the formation of each of the minerals is given below (number of determinations given in parentheses):Mineral delta D (sub H2) O ppm delta 18 O (sub H2) O ppm delta 13 C (sub CO2) ppmSphalerite -81 to -54 (4) -10.1 to -4.5 (4)Quartz -97 to -86 (4) -5.9 to 1.8 (18)Illite -62 to -50 (8) -1.6 to 1.2(7)Chlorite -64 to -55 (10) -2.2 to 0.8 (10)Adularia 4.2 (1)Rhodochrosite -82 to -78 (2) 4.2 to 9.4 (9) -5.7 to -4.2 (9)Siderite 4.9 to 9.9 (6) -6.9 to -2.7 (6)The delta D (sub H2) O and delta 18 O (sub H2) O values of fluids associated with the formation of sphalerite, quartz, illite/chlorite, and carbonate minerals differ substantially from one another, and these differences appear to have been maintained throughout the depositional history, regardless of the positions of the minerals in the paragenetic sequence.The data suggest that waters from three coexisting reservoirs fed the vein system alternately and episodically during vein formation, and apparently there was little mixing of the fluids from the different reservoirs. The hydrogen, oxygen, and carbon isotope data suggest that the carbonate waters were deep seated, probably dominantly magmatic, in origin. The sphalerite and illite/chlorite waters must have been dominantly meteoric in origin and substantially oxygen shifted by exchange with the volcanic country rocks. The quartz waters were also oxygen shifted meteoric waters but were some 40 per mil lower in deuterium content than the sphalerite and illite/chlorite waters.We propose that the quartz fluids entered the vein system from reservoirs beneath the mountainous areas to the north in the vicinity of the present Continental Divide, but that the sphalerite and illite/chlorite fluids entered the vein system from a topographically low area to the south along the structural moat of the Creede caldera. The difference in delta D between the two meteoric waters may reflect differences in altitude of the recharge areas for the two reservoirs or may be clue to isotopic evolution of the closed-basin lake and interstitial waters in the moat surrounding the Creede caldera.

The exchangeable fraction of selectively sorbed 137Cs in soils and natural sorbents as a function of the K+ and NH{4/+} concentrations

NASA Astrophysics Data System (ADS)

Stepina, I. A.; Popov, V. E.

2011-06-01

The exchangeable portion of the selectively sorbed 137Cs extractable by a 1 M ammonium acetate solution (α Ex ) for soils, illite, bentonite, and tripolite was found to increase with the increasing concentration of the competitive cation M+ (K+ or NH{4/+}) and can be approximated by a logarithmic relationship. For clinoptilolite, the values of α Ex did not depend on the concentration of M+. The expression 1 - α Ex ( C M= n )/α Ex ( C M = 16) as a function of the M+ concentration (where α Ex ( C M= n ) is the α Ex value at the competitive cation concentration equal to 16 mmol/dm3) was proposed to compare the dependence of α Ex on the concentration of K+ or NH{4/+}in different sorbents. For soils and illite, these dependences almost coincided, which indicated that the selective sorption of 137Cs in soils is determined by the presence of illite-group minerals.

Diagenetic contrast of sandstones in hydrocarbon prospective Mesozoic rift basins (Ethiopia, UK, USA)

NASA Astrophysics Data System (ADS)

Wolela, A.

2014-11-01

Diagenetic studied in hydrocarbon-prospective Mesozoic rift basins were carried out in the Blue Nile Basin (Ethiopia), Ulster Basin (United Kingdom) and Hartford Basin (United States of America). Alluvial fan, single and amalgamated multistorey meandering and braided river, deep and shallow perennial lake, shallow ephemeral lake, aeolian and playa mud-flat are the prominent depositional environments. The studied sandstones exhibit red bed diagenesis. Source area geology, depositional environments, pore-water chemistry and circulation, tectonic setting and burial history controlled the diagenetic evolution. The diagenetic minerals include: facies-related minerals (calcrete and dolocrete), grain-coating clay minerals and/or hematite, quartz and feldspar overgrowths, carbonate cements, hematite, kaolinite, illite-smectite, smectite, illite, chlorite, actinolite, laumontite, pyrite and apatite. Diversity of diagenetic minerals and sequence of diagenetic alteration can be directly related to depositional environment and burial history of the basins. Variation in infiltrated clays, carbonate cements and clay minerals observed in the studied sandstones. The alluvial fan and fluviatile sandstones are dominated by kaolinite, illite calcite and ferroan calcite, whereas the playa and lacustrine sandstones are dominated by illite-smectite, smectite-chlorite, smectite, chlorite, dolomite ferroan dolomite and ankerite. Albite, pyrite and apatite are predominantly precipitated in lacustrine sandstones. Basaltic eruption in the basins modified mechanically infiltrated clays to authigenic clays. In all the studied sandstones, secondary porosity predominates over primary porosity. The oil emplacement inhabited clay authigenesis and generation of secondary porosity, whereas authigenesis of quartz, pyrite and apatite continued after oil emplacement.

Role of minerals in thermal alteration of organic matter. II - A material balance

NASA Technical Reports Server (NTRS)

Tannenbaum, Eli; Huizinga, Bradley J.; Kaplan, I. R.

1986-01-01

The paper presents the results of pyrolysis experiments which were carried out on Green River and Monterey Formation kerogens with and without calcite, illite, or montmorillonite at 300 C for 2 to 1,000 hours under dry and hydrous conditions. The data reveal significant differences in the products generated by pyrolysis of kerogens with and without minerals. Both illite and montmorillonite adsorb a considerable portion of the generated bitumen. In the case of calcite, the pyrolysis products are similar to those from kerogen heated alone, and bitumen adsorption is negligible.

Role of Microbes in the Smectite-to-Illite Reaction

USGS Publications Warehouse

Kim, J.; Dong, H.; Seabaugh, J.; Newell, Steven W.; Eberl, D.D.

2004-01-01

Temperature, pressure, and time have been thought to control the smectiteto-illite (S-I) reaction, an important diagenetic process used for petroleum exploration. We demonstrated that microorganisms can promote the S-I reaction by dissolving smectite through reduction of structural FE(III) at room temperature and 1 atmosphere within 14 days. This reaction typically requires conditions of 300?? to 350??C, 100 megapascals, and 4 to 5 months in the absence of microbial activity. These results challenge the conventional concept of the S-I reaction and of reaction kinetic models.

Role of microbes in the smectite-to-illite reaction

NASA Technical Reports Server (NTRS)

Kim, Jinwook; Dong, Hailiang; Seabaugh, Jennifer; Newell, Steven W.; Eberl, Dennis D.

2004-01-01

Temperature, pressure, and time have been thought to control the smectite-to-illite (S-I) reaction, an important diagenetic process used for petroleum exploration. We demonstrated that microorganisms can promote the S-I reaction by dissolving smectite through reduction of structural Fe(III) at room temperature and 1 atmosphere within 14 days. This reaction typically requires conditions of 300 degrees to 350 degrees C, 100 megapascals, and 4 to 5 months in the absence of microbial activity. These results challenge the conventional concept of the S-I reaction and of reaction kinetic models.

Chlorite, Biotite, Illite, Muscovite and Feldspar Dissolution Kinetics at Variable pH and Temperatures up to 280 deg C

DOE Data Explorer

Carroll, Susan; Smith, Megan M.; Lammers, Kristin

2017-02-24

Chemical reactions pose an important but poorly understood threat to EGS long-term success because of their impact on fracture permeability. This report summarizes the dissolution rate equations for layered silicates where data were lacking for geothermal systems. Here we report updated rate laws for chlorite (Carroll and Smith 2013), biotite (Carroll and Smith, 2015), illite (Carroll and Smith, 2014), and for muscovite. Also included is a spreadsheet with rate data and rate equations for use in reactive transport simulators.

Water adsorption constrained Frenkel-Halsey-Hill adsorption activation theory: Montmorillonite and illite

NASA Astrophysics Data System (ADS)

Hatch, Courtney D.; Greenaway, Ann L.; Christie, Matthew J.; Baltrusaitis, Jonas

2014-04-01

Fresh mineral aerosol has recently been found to be effective cloud condensation nuclei (CCN) and contribute to the number of cloud droplets in the atmosphere due to the effect of water adsorption on CCN activation. The work described here uses experimental water adsorption measurements on Na-montmorillonite and illite clay to determine empirical adsorption parameters that can be used in a recently derived theoretical framework (Frenkel-Halsey-Hill Activation Theory, FHH-AT) that accounts for the effect of water adsorption on CCN activation. Upon fitting the Frenkel-Halsey-Hill (FHH) adsorption model to water adsorption measurements, we find FHH adsorption parameters, AFHH and BFHH, to be 98 ± 22 and 1.79 ± 0.11 for montmorillonite and 75 ± 17 and 1.77 ± 0.11 for illite, respectively. The AFHH and BFHH values obtained from water adsorption measurements differ from values reported previously determined by applying FHH-AT to CCN activation measurements. Differences in FHH adsorption parameters were attributed to different methods used to obtain them and the hydratable nature of the clays. FHH adsorption parameters determined from water adsorption measurements were then used to calculate the critical super-saturation (sc) for CCN activation using FHH-AT. The relationship between sc and the dry particle diameter (Ddry) gave CCN activation curve exponents (xFHH) of -0.61 and -0.64 for montmorillonite and illite, respectively. The xFHH values were slightly lower than reported previously for mineral aerosol. The lower exponent suggests that the CCN activity of hydratable clays is less sensitive to changes in Ddry and the hygroscopicity parameter exhibits a broader variability with Ddry compared to more soluble aerosols. Despite the differences in AFHH, BFHH and xFHH, the FHH-AT derived CCN activities of montmorillonite and illite are quite similar to each other and in excellent agreement with experimental CCN measurements resulting from wet-generated clay aerosol. This study illustrates that FHH-AT using adsorption parameters constrained by water adsorption is a simple, valid method for predicting CCN activation of fresh clay minerals and provides parameters that can be used in atmospheric models to study the effect of mineral dust aerosol on cloud formation and climate.

Genesis and significance of the silico-aluminous nodules in the Ordovician of the Montagne Noire and the Massif Armoricain (France)

NASA Astrophysics Data System (ADS)

Becq-Giraudon, Jean-François; Bouillé, Suzanne; Chauvel, Jean-Jacques

1992-04-01

Siliceous nodules of the Arenigian of the Montagne Noire (southern France) and the Massif Armoricain (western France) are made up of quartz, illite and chlorite with secondary apatite and, less frequently, dolomite. Diffractometrical and geochemical data indicate that the chlorite is a chamosite (trioctahedral 2:1 chlorite), whose development may be accompanied by that of apatite and diminution of illite. Three types of nodules are defined: Type 1, siliceous nodules, with more than 85% of SiO 2, very frequent in the Montagne Noire; Type II, nodules made of a micaceous siltstone with chlorite matrix, abundant in the Massif Armoricain but present also in the Montagne Noire; Type III, chloritic nodules with a finely globular structure, especially developed in the Massif armoricain but observed in the Montagne Noire as well. The nodules are always poorer in illite than their host sediments and often show traces of the initial sediments. Their formation occurs after the deposition and prior to the development of foliation. The frequent presence of undistorted fossil remains suggests an early formation linked to the physico-chemical modifications occurring in an unconsolidated sediment around a decaying organism. The post-depositional mineralogical evolution should have started with an illite/dolomite assemblage and end up with a chamosite-dominant one, under cold climatic conditions. The simultaneous presence of the three types of nodules in the same formation, or even in the same beds, shows that this mineralogical differentiation is not strictly related to the diagenetic and metamorphic transformation of this material.

Natural and ion-exchanged illite clays reduce bacterial burden and inflammation in cutaneous meticillin-resistant Staphylococcus aureus infections in mice

PubMed Central

Otto, Caitlin C.; Kilbourne, Jacquelyn

2016-01-01

Discoveries associated with antibacterial activity of hydrated clays necessitate assessments of in vivo efficacy, practical use and safety. Surface properties of clays can lead to variations in the composition and abundance of bound compounds or ions, thus affecting antibacterial activity. Since exchangeable metal ions released from the clay surface are responsible for in vitro antibacterial activity, we evaluated the in vivo antibacterial efficacy of four natural clays (one illite clay, two montmorillonite clays and one kaolinite clay) and three ion-exchanged, antibacterial clays against superficial, cutaneous meticillin-resistant Staphylococcus aureus (MRSA) infections in mice. Superficial, cutaneous wounds on the back of SKH1-Elite mice were generated and subsequently infected with MRSA. Following twice daily applications of a hydrated clay poultice to infected wounds for 7 days, we observed significant differences in the in vivo antibacterial efficacy between different types of clays. The natural and ion-exchanged illite clays performed best, as measured by bacterial load, inflammatory response and gross wound morphology with significant decreases in bacterial viability and dermatitis. Topical application of kaolinite clay was the least effective, resulting in the lowest decrease in bacterial load and exhibiting severe dermatitis. These data suggest that specific types of clays may offer a complementary and integrative strategy for topically treating MRSA and other cutaneous infections. However, since natural clays exhibit in vitro antibacterial variability and vary vastly in surface chemistries, adsorptive/absorptive characteristics and structural composition, the properties and characteristics of illite clays could aid in the development of standardized and customized aluminosilicates for topical infections. PMID:26508716

Timing and conditions of clay fault gouge formation on the Naxos detachment (Cyclades, Greece)

NASA Astrophysics Data System (ADS)

Mancktelow, N.; Zwingmann, H.; Mulch, A.

2016-10-01

Clay fault gouge from the Naxos detachment (locally up to 1.0-1.5 m thick) is reported and dated for the first time. K-Ar ages on eight clay size fractions from the detachment and a minor fault in the immediate footwall have a narrow range, from 10.3 to 9.0 Ma, with an average of 9.7 ± 0.5 Ma (±1σ). These results are in excellent accord with regional and local age constraints, independently demonstrating the reliability of the method. Hydrogen δD values fall in the range -89 to -95‰, indicating interaction with infiltrating meteoric water during gouge formation, which is consistent with deposition of freshwater sediments in the hanging wall at the same time. Clay mineralogy in the detachment gouge is predominantly mixed layer illite-smectite with subordinate 1 M illite and kaolinite but without higher-temperature 2 M1 illite/mica. Clay fault gouge predominantly formed over a limited time and temperature range, potentially acting as a weak lubricant promoting movement on the Naxos detachment, with correspondingly rapid exhumation and cooling of the underlying footwall.

Mesozoic clay diagenesis in the Appalachian Plateau

NASA Astrophysics Data System (ADS)

Boles, A.; Mulch, A.; van der Pluijm, B.

2017-12-01

Integrated investigation of authigenic clays in the Appalachian Plateau of the northeastern US Midcontinent using X-ray goniometry, Rietveld-method based illite polytype analysis, and 40Ar/39Ar geochronology yields novel insights about the structural diagenetic history of the North American sedimentary cover sequence. Texture analysis by High Resolution X-ray Texture Goniometry records the presence of a bedding-parallel diagenetic fabric, corresponding to a burial depth of 2-5 km. New development of polytype modeling using BGMN®, a quantitative X-ray powder diffraction forward modeling and whole-pattern matching program matches mineralic characteristic of illite at those depths and reduces uncertainty estimates in age analysis. Based on dating size fractions, the diagenetic age is constrained to 225-250 Ma (Triassic) by four authigenic illite samples, reflecting protracted, regional diagenesis in the area. Preliminary H isotopic analysis points to a surface-derived diagenetic fluid with δD values ranging from -48 to -72‰ (in the range of predicted Pangea meteoric fluid), with a dependence on proximity to the Appalachian Mountains that may reflect a rain shadow effect.

Illite Dissolution Rates and Equation (100 to 280 dec C)

DOE Data Explorer

Carroll, Susan

2014-10-17

The objective of this suite of experiments was to develop a useful kinetic dissolution expression for illite applicable over an expanded range of solution pH and temperature conditions representative of subsurface conditions in natural and/or engineered geothermal reservoirs. Using our new data, the resulting rate equation is dependent on both pH and temperature and utilizes two specific dissolution mechanisms (a “neutral” and a “basic” mechanism). The form of this rate equation should be easily incorporated into most existing reactive transport codes for to predict rock-water interactions in EGS shear zones.

Illitization of Potassium, Cesium, and Ammonium Exchanged Smectite

NASA Astrophysics Data System (ADS)

Mills, M. M.; Wang, Y.; Payne, C.; Sanchez, A. C.; Boisvert, L.; Matteo, E. N.

2017-12-01

Bentonite clay is a primary choice for engineered barrier systems within geologic repositories for disposal of radioactive wastes due to its low permeability at saturated states, warranting diffusion as the dominant transport mechanism, and large swelling pressures that promote sealing. In order to predict how well the barrier will function over time at repository relevant temperatures, it is important to understand thermal alteration effects on montmorillonite, better known as smectite, a main constituent of bentonite. One type of thermal alteration is the conversion to illite, when exposed to elevated temperatures and a sufficient amount of potassium ions, thereby weakening barrier functions. To facilitate the conversion of smectite to illite and examine the influence of interlayer cations, illitization experiments on cation exchanged smectite were performed within hydrothermal reaction vessels over one week timescales. The <2um fraction of a Na-rich smectite clay was first exchanged with 1M Cs, K, and NH4 salt solutions and further exposed to hydrous pyrolysis using a 1M KCl solution with various solid to liquid ratios at 200°C. Multiple analysis techniques were used to characterize the altered clay and identify extent of conversion, such as XRD, cation exchange capacity, and morphology changes by SEM. The pore-water chemistry was also analyzed by ICP-OES to detect any dissolved products and silica content. Results suggest the conversion rate is relatively fast, occurring within days, and is dependent on not only the amount of K, but also dissolved silica concentration related to total solid in solution. Sandia National Laboratories is a multimission laboratory managed and operated by National Technology and Engineering Solutions of Sandia LLC, a wholly owned subsidiary of Honeywell International Inc. for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-NA0003525. SAND2017-7856A

Laser probe /sup 40/Ar//sup 39/Ar and conventional K/Ar dating of illites associated with the McClean Uranium deposits, N. Saskatchewan, Canada

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bray, C.J.; Spooner, E.T.C.; Hall, C.M.

Mineralization at McClean occurs in elongate pods at the unconformity between the Athabasca sandstone sequence and the underlying Archean/Aphebian basement. Laser probe /sup 40/Ar//sup 39/Ar and conventional K/Ar dates were obtained on illites from the following environments (i) alteration halo around high grade U(-Ni-Co) mineralization, (ii) recrystallized sedimentary layers within the sandstone sequence, (iii) interstitial to quartz grains in sandstone, and (iv) regolith. The alteration halo illites gave ages between 1321+/-44 and 1002+/-33 Ma (n=20) which are in good agreement with published U-Pb dates on other U deposits in the area. One sample was analyzed twice, and gave a significantmore » age difference of 20 Ma. Hence the age range is interpreted as being either a reflection of variable argon retentivity or due to continued hydrothermal activity (i.e. U mineralization) or a combination of both. Dates obtained on (ii), (iii) and (iv) were 1438-1038 (n=8), 1459-1113 (n=3) and 1482-1262 (n=6) Ma respectively. The older ages are in good agreement with a published Rb-Sr whole rock age of 1470 Ma on tuffaceous sediments from the Athabasca group. The spread to younger ages is interpreted as due to resetting by the hot (approx. 200/sup 0/C) formation water which transported the U, and variable argon retentivity. Diffusion studies on a single sample of illite from the sedimentary sequence indicate a low blocking temperature of about 140/sup 0/C and imply that there have been very low temperatures in the area for the last 1000 Ma.« less

Distributions of clay minerals in surface sediments of the middle Bay of Bengal: Source and transport pattern

NASA Astrophysics Data System (ADS)

Li, Jingrui; Liu, Shengfa; Shi, Xuefa; Feng, Xiuli; Fang, Xisheng; Cao, Peng; Sun, Xingquan; Wenxing, Ye; Khokiattiwong, Somkiat; Kornkanitnan, Narumol

2017-08-01

The clay mineral contents in 110 surface sediment samples collected from the middle of the Bay of Bengal were analyzed by X-ray diffraction (XRD) to investigate the provenance and transport patterns. The illite content was highest, followed by chlorite, kaolinite and then smectite, with average weight percent distributions of 52%, 22%, 14% and 12%, respectively. Illite and chlorite had similar distribution pattern, with higher contents in the northern and central areas and lower contents in the southern area, whereas smectite showed the opposite distribution pattern. Kaolinite show no obvious higher or lower areas and the southern ;belt; was one of the highest content areas. Based on the spatial distribution characteristics and cluster analysis results, the study area can be classified into two provinces. Province I covers the southwestern area and contains high concentrations of illite and smectite sediments. Province II covers most sites and is also characterized by high concentrations of illite, but the weight percent of smectite is only half of that of province I. According to a quantitative estimate using end-member clay minerals contents, the relative contributions from the Himalayan source and the Indian source are 63% and 37% on average, respectively. Integrative analysis indicates that the hydrodynamic environment in the study area, especially the turbidity and surface monsoonal circulation, plays an important role in the spatial distribution and dispersal of the clay fraction in the sediments. The sediments in province I are mainly from the Indian source transported by the East Indian Coastal Current (EICC) and the surface monsoon circulation with minor contributions from the Himalayan source while the sediments in province II are mainly from the Himalayan source transported by turbidity and surface monsoonal circulation with little contribution from Indian river materials.

Depositional and diagenetic processes of Qa Khanna playa, North Jordan basaltic plateau, Jordan

NASA Astrophysics Data System (ADS)

Howari, F. M.; Banat, K. M.; Abu-Salha, Y. A.

2010-09-01

The present study explored mineral occurrences and sediment characteristics of playas from northern Jordan and explained depositional and diagenetic processes as reflected from bulk chemistry and sedimentary structures. Mudcracks of different sizes and shape patterns, laminations, intersediment vesicles, and bioturbation pipes are the main sedimentary structures. Plagioclase, olivine, orthopyroxene, nepheline and other opaque minerals are all of detrital origin, and are derived from the basaltic bedrocks surrounding the studied playa. Evaporites are very rare; they are represented only by trace amounts of gypsum. The identified clay minerals in the clay fraction of the studied sediments, arranged according to their decreasing abundances are palygorskite, illite, kaolinite, smectite and chlorite. The elemental abundances were tied to clay, CaCO 3 and nearby igneous rocks. The type of clay minerals, the high pH values of the studied sediments, and the considerable incorporation of Mg and K in palygorskite and illite respectively, may strongly reflect a high evaporative and alkaline environment under arid to semi-arid conditions in an ephemeral lake of the Qa Khanna. Concentrations and distributions of both major and trace elements are essentially controlled by the clay mineralogy and the calcium carbonate content; Ca is mainly incorporated in the CaCO 3, which is either generated authigenically or by aeolian deposition. Fe and K are incorporated and fixed by illite under an evaporative and alkaline environment. Mg is incorporated in palygorskite while Mn is adsorbed on various clay minerals. Sr substitutes for Ca in the aeolian CaCO 3 and its presence in the studied sediments is independent of the prevailing conditions during the playa evolution. Rb substitutes for K in illite under the prevailing chemical conditions in the studied playa.

Understanding the sorption mechanisms of aflatoxin B1 to kaolinite, illite, and smectite clays via a comparative computational study.

PubMed

Kang, Fuxing; Ge, Yangyang; Hu, Xiaojie; Goikavi, Caspar; Waigi, Michael Gatheru; Gao, Yanzheng; Ling, Wanting

2016-12-15

In current adsorption studies of biotoxins to phyllosilicate clays, multiply weak bonding types regarding these adsorptions are not well known; the major attractive forces, especially for kaolinite and illite, are difficult to be identified as compared to smectite with exchangeable cations. Here, we discriminated the bonding types of aflatoxin B1 (AFB1) contaminant to these clays by combined batch experiment with model computation, expounded their bonding mechanisms which have been not quantitatively described by researchers. The observed adsorbent-to-solution distribution coefficients (K d ) of AFB1 presented in increasing order of 18.5-37.1, 141.6-158.3, and 354.6-484.7L/kg for kaolinite, illite, and smectite, respectively. Normalization of adsorbent-specific surface areas showed that adsorption affinity of AFB1 is mainly dependent on the outside surfaces of clay aggregates. The model computation and test of ionic effect further suggested that weakly electrostatic attractions ((Si/Al-OH) 2 ⋯(OC) 2 ) are responsible for AFB1-kaolinite adsorption (K d , 18.5-37.1L/kg); a moderate electron-donor-acceptor attraction ((CO) 2 ⋯K + ⋯(O-Al) 3 ) is related to AFB1-illite adsorption (K d , 141.6-158.3L/kg); a strong calcium-bridging linkage ((CO) 2 ⋯Ca 2+ ⋯(O-Si) 4 ) is involved in AFB1-smectite adsorption (K d , 354.6-484.7L/kg). Changes in Gibbs free energy (ΔG°) suggested that the computed result is reliable, providing a good reproduction of AFB1-clay interaction. Copyright © 2016 Elsevier B.V. All rights reserved.

Clay minerals related to the circulation of geothermal fluids in boreholes at Rittershoffen (Alsace, France)

NASA Astrophysics Data System (ADS)

Vidal, Jeanne; Patrier, Patricia; Genter, Albert; Beaufort, Daniel; Dezayes, Chrystel; Glaas, Carole; Lerouge, Catherine; Sanjuan, Bernard

2018-01-01

Two geothermal wells, GRT-1 and GRT-2, were drilled into the granite at Rittershoffen (Alsace, France) in the Upper Rhine Graben to exploit geothermal resources at the sediment-basement interface. Brine circulation occurs in a permeable fracture network and leads to hydrothermal alteration of the host rocks. The goal of the study was to characterize the petrography and mineralogy of the altered rocks with respect to the permeable fracture zones in the granitic basement. As clay minerals are highly reactive to hydrothermal alteration, they can be used as indicators of present-day and paleo-circulation systems. Special attention has been paid to the textural, structural and chemical properties of these minerals. The fine-grained clay fraction (< 5 μm) was analyzed around the originally permeable fracture zones to observe the crystal structure of clay minerals using X-ray diffraction. Chemical microanalysis of the clay minerals was performed using scanning electron microscopy coupled with energy dispersive X-ray spectroscopy. The occurrences of mixed layers illite-smectite ( 10% smectite) provide a promising guide for identifying the fracture zones that control the present-day circulation of geothermal fluids in the Rittershoffen wells. However, multistage paleo-circulation systems could lead to an abundance of heterogeneous and fine-grained illitic minerals that could plug the fracture system. The permeability of fracture zones in the GRT-1 well was likely reduced because of an intense illitization, and the well was stimulated. The occurrence of chlorite in the permeable fracture zones of GRT-2 is indicative of less intense illitization, and the natural permeability is much higher in GRT-2 than in GRT-1.

Phanerozoic polyphase orogenies recorded in the northeastern Okcheon Belt, Korea from SHRIMP U-Pb detrital zircon and K-Ar illite geochronologies

NASA Astrophysics Data System (ADS)

Jang, Yirang; Kwon, Sanghoon; Song, Yungoo; Kim, Sung Won; Kwon, Yi Kyun; Yi, Keewook

2018-05-01

We present the SHRIMP U-Pb detrital zircon and K-Ar illite 1Md/1M and 2M1 ages, suggesting new insight into the Phanerozoic polyphase orogenies preserved in the northeastern Okcheon Belt, Korea since the initial basin formation during Neoproterozoic rifting through several successive contractional orogens. The U-Pb detrital zircon ages from the Early Paleozoic strata of the Taebaeksan Zone suggest a Cambrian maximum deposition age, and are supported by trilobite and conodont biostratigraphy. Although the age spectra from two sedimentary groups, the Yeongwol and Taebaek Groups, show similar continuous distributions from the Late Paleoproterozoic to Early Paleozoic ages, a Grenville-age hiatus (1.3-0.9 Ga) in the continuous stratigraphic sequence from the Taebaek Group suggests the existence of different peripheral clastic sources along rifted continental margin(s). In addition, we present the K-Ar illite 1Md/1M ages of the fault gouges, which confirm fault formation/reactivation during the Late Cretaceous to Early Paleogene (ca. 82-62 Ma) and the Early Miocene (ca. 20-18 Ma). The 2M1 illite ages, at least those younger than the host rock ages, provide episodes of deformation, metamorphism and hydrothermal effects related to the tectonic events during the Devonian (ca.410 Ma) and Permo-Triassic (ca. 285-240 Ma). These results indicate that the northeastern Okcheon Belt experienced polyphase orogenic events, namely the Okcheon (Middle Paleozoic), Songrim (Late Paleozoic to Early Mesozoic), Daebo (Middle Mesozoic) and Bulguksa (Late Mesozoic to Early Cenozoic) Orogenies, reflecting the Phanerozoic tectonic evolution of the Korean Peninsula along the East Asian continental margin.

Clay mineralogical record on the upper continental slope of the northwestern South China Sea since the Last Glacial Maximum

NASA Astrophysics Data System (ADS)

CHEN, Q.; Liu, Z.; Stattegger, K.

2012-12-01

Clay mineralogy of two gravity cores (18428 and 18429) on the upper continental slope of the northwestern South China Sea was investigated in order to understand terrigenous sediment sources and to evaluate the contribution from the Red River since the Late Glacial Maximum. Planktonic foraminiferal oxygen isotope and carbonate stratigraphies suggest that Core 18428 is constrained in Holocene while Core 18429 covers the period of MIS 1-2. Clay mineral assemblages of two cores are composed mainly of smectite (18-57%) and illite (21-41%), with minor chlorite (12-21%) and kaolinite (8-26%). In despite of relatively constant values of illite crystallinity, ranging among 0.14°-0.20° Δ2θ, the time series variation in clay mineral distributions indicates a strong glacial-interglacial shift. Contents of illite, chlorite, and kaolinite (Core 18429) in the Holocene are lower than in the glacial period, and vice versa for the smectite content. The provenance analysis based on clay mineralogy suggests the Red River as a predominant sedimentary source of illite, chlorite, and kaolinite during all the depositional period of MIS 1-2. The sea level change actually controlled the variations of clay mineral assemblages on the upper slope since the Last Glacial Maximum. When the sea level was low during the last glacial period, more terrigenous sediments from the Red River could reach the continental slope in the northwestern South China Sea. However, when the sea level is closed to the present situation during the Holocene, most of Red River sediments could be trapped in the Gulf of Tonkin, instead of draining in the deep South China Sea.

HYDROTHERMAL MINERALOGY OF RESEARCH DRILL HOLE Y-3, YELLOWSTONE NATIONAL PARK, WYOMING.

USGS Publications Warehouse

Bargar, Keith E.; Beeson, Melvin H.

1984-01-01

The approximate paragenetic sequence of hydrothermal minerals in the Y-3 U. S. Geological Survey research diamond-drill hole in Lower Geyser Basin, Yellowstone National Park, Wyoming, is: hydrothermal chalcedony, hematite, pyrite, quartz, clay minerals (smectite and mixed-layer illite-smectite), calcite, chlorite, fluorite, pyrite, quartz, zeolite minerals (analcime, dachiardite, laumontite, stilbite, and yugawaralite), and clay minerals (smectite and mixed-layer illite-smectite). A few hydrothermal minerals that were identified in drill core Y-3 (lepidolite, aegirine, pectolite, and truscottite) are rarely found in modern geothermal areas. The alteration minerals occur primarily as vug and fracture fillings that were deposited from cooling thermal water. Refs.

Chlorite, Biotite, Illite, Muscovite, and Feldspar Dissolution Kinetics at Variable pH and Temperatures up to 280 C

DOE Office of Scientific and Technical Information (OSTI.GOV)

Carroll, S.; Smith, M.; Lammers, K.

2016-10-05

Summary Sheet silicates and clays are ubiquitous in geothermal environments. Their dissolution is of interest because this process contributes to scaling reactions along fluid pathways and alteration of fracture surfaces, which could affect reservoir permeability. In order to better predict the geochemical impacts on long-term performance of engineered geothermal systems, we have measured chlorite, biotite, illite, and muscovite dissolution and developed generalized kinetic rate laws that are applicable over an expanded range of solution pH and temperature for each mineral. This report summarizes the rate equations for layered silicates where data were lacking for geothermal systems.

Effects of smectite on the oil-expulsion efficiency of the Kreyenhagen Shale, San Joaquin Basin, California, based on hydrous-pyrolysis experiments

USGS Publications Warehouse

Lewan, Michael D.; Dolan, Michael P.; Curtis, John B.

2014-01-01

The amount of oil that maturing source rocks expel is expressed as their expulsion efficiency, which is usually stated in milligrams of expelled oil per gram of original total organic carbon (TOCO). Oil-expulsion efficiency can be determined by heating thermally immature source rocks in the presence of liquid water (i.e., hydrous pyrolysis) at temperatures between 350°C and 365°C for 72 hr. This pyrolysis method generates oil that is compositionally similar to natural crude oil and expels it by processes operative in the subsurface. Consequently, hydrous pyrolysis provides a means to determine oil-expulsion efficiencies and the rock properties that influence them. Smectite in source rocks has previously been considered to promote oil generation and expulsion and is the focus of this hydrous-pyrolysis study involving a representative sample of smectite-rich source rock from the Eocene Kreyenhagen Shale in the San Joaquin Basin of California. Smectite is the major clay mineral (31 wt. %) in this thermally immature sample, which contains 9.4 wt. % total organic carbon (TOC) comprised of type II kerogen. Compared to other immature source rocks that lack smectite as their major clay mineral, the expulsion efficiency of the Kreyenhagen Shale was significantly lower. The expulsion efficiency of the Kreyenhagen whole rock was reduced 88% compared to that of its isolated kerogen. This significant reduction is attributed to bitumen impregnating the smectite interlayers in addition to the rock matrix. Within the interlayers, much of the bitumen is converted to pyrobitumen through crosslinking instead of oil through thermal cracking. As a result, smectite does not promote oil generation but inhibits it. Bitumen impregnation of the rock matrix and smectite interlayers results in the rock pore system changing from water wet to bitumen wet. This change prevents potassium ion (K+) transfer and dissolution and precipitation reactions needed for the conversion of smectite to illite. As a result, illitization only reaches 35% to 40% at 310°C for 72 hr and remains unchanged to 365°C for 72 hr. Bitumen generation before or during early illitization in these experiments emphasizes the importance of knowing when and to what degree illitization occurs in natural maturation of a smectite-rich source rock to determine its expulsion efficiency. Complete illitization prior to bitumen generation is common for Paleozoic source rocks (e.g., Woodford Shale and Retort Phosphatic Shale Member of the Phosphoria Formation), and expulsion efficiencies can be determined on immature samples by hydrous pyrolysis. Conversely, smectite is more common in Cenozoic source rocks like the Kreyenhagen Shale, and expulsion efficiencies determined by hydrous pyrolysis need to be made on samples that reflect the level of illitization at or near bitumen generation in the subsurface.

Altering wettability to recover more oil from tight formations

DOE PAGES

Brady, Patrick V.; Bryan, Charles R.; Thyne, Geoffrey; ...

2016-06-03

We describe here a method for chemically modifying fracturing fluids and overflushes to chemically increase oil recovery from tight formations. Oil wetting of tight formations is usually controlled by adhesion to illite, kerogen, or both; adhesion to carbonate minerals may also play a role. Oil-illite adhesion is sensitive to salinity, dissolved divalent cation content, and pH. We measure oil-rock adhesion with middle Bakken formation oil and core to verify a surface complexation model of reservoir wettability. The agreement between the model and experiments suggests that wettability trends in tight formations can be quantitatively predicted and that fracturing fluid and overflushmore » compositions can be individually tailored to increase oil recovery.« less

Altering wettability to recover more oil from tight formations

DOE Office of Scientific and Technical Information (OSTI.GOV)

Brady, Patrick V.; Bryan, Charles R.; Thyne, Geoffrey

We describe here a method for chemically modifying fracturing fluids and overflushes to chemically increase oil recovery from tight formations. Oil wetting of tight formations is usually controlled by adhesion to illite, kerogen, or both; adhesion to carbonate minerals may also play a role. Oil-illite adhesion is sensitive to salinity, dissolved divalent cation content, and pH. We measure oil-rock adhesion with middle Bakken formation oil and core to verify a surface complexation model of reservoir wettability. The agreement between the model and experiments suggests that wettability trends in tight formations can be quantitatively predicted and that fracturing fluid and overflushmore » compositions can be individually tailored to increase oil recovery.« less

Comparative study of microfacies variation in two samples from the Chittenango member, Marcellus shale subgroup, western New York state, USA

DOE Office of Scientific and Technical Information (OSTI.GOV)

Balulla, Shama, E-mail: shamamohammed77@outlook.com; Padmanabhan, E., E-mail: eswaran-padmanabhan@petronas.com.my; Over, Jeffrey, E-mail: over@geneseo.edu

This study demonstrates the significant lithologic variations that occur within the two shale samples from the Chittenango member of the Marcellus shale formation from western New York State in terms of mineralogical composition, type of lamination, pyrite occurrences and fossil content using thin section detailed description and field emission Scanning electron microscope (FESEM) with energy dispersive X-Ray Spectrum (EDX). This study is classified samples as laminated clayshale and fossiliferous carbonaceous shale. The most important detrital constituents of these shales are the clay mineral illite and chlorite, quartz, organic matter, carbonate mineral, and pyrite. The laminated clayshale has a lower amountmore » of quartz and carbonate minerals than fossiliferous carbonaceous shale while it has a higher amount of clay minerals (chlorite and illite) and organic matter. FESEM analysis confirms the presence of chlorite and illite. The fossil content in the laminated clayshale is much lower than the fossiliferous carbonaceous shale. This can provide greater insights about variations in the depositional and environmental factors that influenced its deposition. This result can be compiled with the sufficient data to be helpful for designing the horizontal wells and placement of hydraulic fracturing in shale gas exploration and production.« less

Effect of organic matter on CO(2) hydrate phase equilibrium in phyllosilicate suspensions.

PubMed

Park, Taehyung; Kyung, Daeseung; Lee, Woojin

2014-06-17

In this study, we examined various CO2 hydrate phase equilibria under diverse, heterogeneous conditions, to provide basic knowledge for successful ocean CO2 sequestration in offshore marine sediments. We investigated the effect of geochemical factors on CO2 hydrate phase equilibrium. The three-phase (liquid-hydrate-vapor) equilibrium of CO2 hydrate in the presence of (i) organic matter (glycine, glucose, and urea), (ii) phyllosilicates [illite, kaolinite, and Na-montmorillonite (Na-MMT)], and (iii) mixtures of them was measured in the ranges of 274.5-277.0 K and 14-22 bar. Organic matter inhibited the phase equilibrium of CO2 hydrate by association with water molecules. The inhibition effect decreased in the order: urea < glycine < glucose. Illite and kaolinite (unexpandable clays) barely affected the CO2 hydrate phase equilibrium, while Na-MMT (expandable clay) affected the phase equilibrium because of its interlayer cations. The CO2 hydrate equilibrium conditions, in the illite and kaolinite suspensions with organic matter, were very similar to those in the aqueous organic matter solutions. However, the equilibrium condition in the Na-MMT suspension with organic matter changed because of reduction of its inhibition effect by intercalated organic matter associated with cations in the Na-MMT interlayer.

Mineralogical, chemical and K-Ar isotopic changes in Kreyenhagen Shale whole rocks and <2 µm clay fractions during natural burial and hydrous-pyrolysis experimental maturation

USGS Publications Warehouse

Clauer, Norbert; Lewan, Michael D.; Dolan, Michael P.; Chaudhuri, Sambhudas; Curtis, John B.

2014-01-01

Large amounts of smectite layers in the illite–smectite mixed layers of the pyrolyzed outcrop <2 μm fraction remain during thermal experiments, especially above 310 °C. With no illitization detected above 310 °C, smectite appears to have inhibited rather than promoted generation of expelled oil from decomposition of bitumen. This hindrance is interpreted to result from bitumen impregnating the smectite interlayer sites and rock matrix. Bitumen remains in the <2 μm fraction despite leaching with H2O2. Its presence in the smectite interlayers is apparent by the inability of the clay fraction to fully expand or collapse once bitumen generation from the thermal decomposition of the kerogen is completed, and by almost invariable K–Ar ages confirming for the lack of any K supply and/or radiogenic 40Ar removal. This suggests that once bitumen impregnates the porosity of a progressively maturing source rock, the pore system is no longer wetted by water and smectite to illite conversion ceases. Experimental attempts to evaluate the smectite conversion to illite should preferentially use low-TOC rocks to avoid inhibition of the reaction by bitumen impregnation.

Late Miocene to Pleistocene Mineralogy of ODP Site 1146

NASA Astrophysics Data System (ADS)

Arnold, E. M.

2001-12-01

ODP Site 1146 (19° 27.40'N, 116° 16.37'E, 2092 m depth) was drilled on the continental slope of the South China Sea. A composite section, comprised of three stratigraphic units, extends down to 640 mcd. Unit 1 is late Pliocene to Pleistocene nannofossil clay (0 - 243 mcd); Unit 2, middle Miocene to Late Pliocene foraminifera - nannofossil - clay mixed sediment (243 - 553 mcd); Unit 3, early to middle Miocene nannofossil clay (553 - 642 mcd). This study reports the < 2 μ m mineralogy from the late Miocene through early Pleistocene. Samples were analyzed at approximately 1.5 m intervals from 150 to 225 mcd, and 1 m intervals from 225 to 440 mcd, with an age resolution of ~25 ka and ~35 ka, respectively. Illite, chlorite, quartz and plagioclase concentrations decrease with increasing depth through Unit 1. Kaolinite and calcite concentrations increase with depth, while smectite values are constant in this unit. Illite, quartz and plagioclase show high variability in Unit 1 compared with the underlying Unit 2. Unit 2 has more uniform sediment composition, with constant illite, chlorite, and quartz concentrations. Kaolinite concentration increases with depth, following a drop in concentration across the Unit 1/2 boundary. Plagioclase concentration shows a small, steady decrease throughout this unit. Smectite concentration does not change across the Unit 1/2 boundary, decreases to a steady low value from 310 - 400 mcd, and increases again towards the bottom. The mineralogy of sediments recovered at Site 1146 suggest a classic pattern of source region aridification from the middle Pliocene through the Pleistocene, indicated in Unit 1 mineralogy as a decrease in kaolinite with decreasing depth, concomitant with an increase in quartz, plagioclase, illite and chlorite. The mineral variability in this interval suggests glacial - interglacial control of the terrigenous sedimentation. The sediment sources and source area weathering regimes were relatively constant throughout Unit 2, as indicated by low mineral variability and relatively constant mineral concentrations.

Mineralogical compositions of fault rocks from surface ruptures of Wenchuan earthquake and implication of mineral transformation during the seismic cycle along Yingxiu-Beichuan fault, Sichuan Province, China

NASA Astrophysics Data System (ADS)

Dang, Jiaxiang; Zhou, Yongsheng; He, Changrong; Ma, Shengli

2018-06-01

There are two co-seismic bedrock surface ruptures from the Mw 7.9 Wenchuan earthquake in the northern and central parts of the Beichuan-Yingxiu fault, Sichuan Province, southwest China. In this study, we report on the macrostructure of the fault rocks and results from X-ray powder diffraction analysis of minerals from rocks in the fault zone. The most recent fault gouge (the gouge produced by the most recent co-seismic fault movement) in all the studied outcrops is dark or grayish-black, totally unconsolidated and ultrafine-grained. Older fault gouges in the same outcrops are grayish or yellowish and weakly consolidated. X-ray powder diffraction analysis results show that mineral assemblages in both the old fault gouge and the new fault gouge are more complicated than the mineral assemblages in the bedrock as the fault gouge is rich in clay minerals. The fault gouge inherited its major rock-forming minerals from the parent rocks, but the clay minerals in the fault gouge were generated in the fault zone and are therefore authigenic and synkinematic. In profiles across the fault, clay mineral abundances increase as one traverses from the bedrock to the breccia to the old gouge and from the old gouge to the new gouge. Quartz and illite are found in all collected gouge samples. The dominant clay minerals in the new fault gouge are illite and smectite along the northern part of the surface rupture and illite/smectite mixed-layer clay in the middle part of the rupture. Illite/smectite mixed-layer clay found in the middle part of the rupture indicates that fault slip was accompanied by K-rich fluid circulation. The existence of siderite, anhydrite, and barite in the northern part of the rupture suggests that fault slip at this locality was accompanied by acidic fluids containing ions of Fe, Ca, and Ba.

Controlling weathering and erosion intensity on the southern slope of the Central Himalaya by the Indian summer monsoon during the last glacial

NASA Astrophysics Data System (ADS)

Kuwahara, Yoshihiro; Masudome, Yukiko; Paudel, Mukunda Raj; Fujii, Rie; Hayashi, Tatsuya; Mampuku, Mami; Sakai, Harutaka

2010-03-01

This paper reports the results of clay mineral analysis (the amount of clay fraction, clay mineral assemblages, illite crystallinity) of samples collected from a drilled core (Rabibhawan (RB) core) located in the west-central part of the Kathmandu Basin on the southern slope of the Central Himalaya. The amount of clay fraction in the core sediments between 12 m and 45 m depth (corresponding to ca. 17-76 ka), which belong to the Kalimati Formation, is variable and shows three clay-poor zones (19-31 ka, 44-51 ka, and 66-75 ka). The variations correspond with those of illite crystallinity index (Lanson index (LI) and modified Lanson index (MLI)) and kaolinite/illite ratio as well as the fossil pollen and diatom records reported by previous workers. These data reveal the following transformations occurring during the weathering process in this area: micas(mainlymuscovite)→illite(→illite-smectitemixedlayermineral(R=1))→kaolinite The sedimentation rate (~ 50 cm/kyr) of clay-poor zones that correspond to dry climate intervals is only half that of clay-rich zones (~ 120 cm/kyr) that correspond to wet climate intervals, indicating weakened chemical weathering and erosion and low suspended discharge during dry climate intervals. The clay-poor zones commonly show unique laminite beds with very fine, authigenic calcite, which was probably precipitated under calm and high calcite concentration conditions caused by low precipitation and run-off. The variations between dry and wet conditions in this area as deduced from clay minerals appear to follow the Indian Summer Monsoon Index (ISMI) (30°N-30°S, 1 July) and northern hemisphere summer insolation (NHSI) signals (30°N) at 1 July, especially during the dry climate zones, whereas the wet maxima of the wet climate zones somewhat deviate from the strongest NHSI. On the other hand, the dry-wet records lead markedly the SPECMAP stack (by about 5000 years). These results suggest that the Indian summer monsoon precipitation was strongly controlled by the NHSI or summer insolation difference between the Himalayan-Tibetan Plateau and the subtropical Indian Ocean, showing a major fluctuation on the 23,000 years precessional cycle, and that it was not driven by changes in high-latitude ice volume, although the records of clay mineral indices during the wet intervals leave a question that other factors, in addition to insolation forcing, may play important roles in weathering, erosion, and sedimentation processes.

Molecular modeling of the effects of 40Ar recoil in illite particles on their K-Ar isotope dating

NASA Astrophysics Data System (ADS)

Szczerba, Marek; Derkowski, Arkadiusz; Kalinichev, Andrey G.; Środoń, Jan

2015-06-01

The radioactive decay of 40K to 40Ar is the basis of isotope age determination of micaceous clay minerals formed during diagenesis. The difference in K-Ar ages between fine and coarse grained illite particles has been interpreted using detrital-authigenic components system, its crystallization history or post-crystallization diffusion. Yet another mechanism should also be considered: natural 40Ar recoil. Whether this recoil mechanism can result in a significant enough loss of 40Ar to provide observable decrease of K-Ar age of the finest illite crystallites at diagenetic temperatures - is the primary objective of this study which is based on molecular dynamics (MD) computer simulations. All the simulations were performed for the same kinetic energy (initial velocity) of the 40Ar atom, but for varying recoil angles that cover the entire range of their possible values. The results show that 40Ar recoil can lead to various deformations of the illite structure, often accompanied by the displacement of OH groups or breaking of the Si-O bonds. Depending on the recoil angle, there are four possible final positions of the 40Ar atom with respect to the 2:1 layer at the end of the simulation: it can remain in the interlayer space or end up in the closest tetrahedral, octahedral or the opposite tetrahedral sheet. No simulation angles were found for which the 40Ar atom after recoil passes completely through the 2:1 layer. The energy barrier for 40Ar passing through the hexagonal cavity from the tetrahedral sheet into the interlayer was calculated to be 17 kcal/mol. This reaction is strongly exothermic, therefore there is almost no possibility for 40Ar to remain in the tetrahedral sheet of the 2:1 layer over geological time periods. It will either leave the crystal, if close enough to the edge, or return to the interlayer space. On the other hand, if 40Ar ends up in the octahedral sheet after recoil, a substantially higher energy barrier of 55 kcal/mol prevents it from leaving the TOT layer over geological time. Based on the results of MD simulations, the estimates of the potential effect of 40Ar recoil on the K-Ar dating of illite show that some of 40Ar is lost and the loss is substantially dependent on the crystallite dimensions. The 40Ar loss can vary from 10% for the finest crystallites (two 2:1 layers thickness and <0.02 μm in diameter) to close to zero for the thickest and largest (in the ab plane) ones. Because the decrease of the K-Ar estimated age is approximately proportional to the 40Ar loss, the finer crystallites show lower apparent age than the coarser ones, although the age of crystallization is assumed equal for all the crystallites. From the model it is also clear that the lack of K removal from illite fringes (potentially Ar-free) strongly increases the apparent age differences among crystallites of different size.

Alteration mineralogy and geochemistry as an exploration tool for detecting basement heat sources in sedimentary basins

NASA Astrophysics Data System (ADS)

Uysal, Tonguc; Gasparon, Massimo; van Zyl, Jacobus; Wyborn, Doone

2010-05-01

The Cooper Basin located in South Australia and Queensland hosts some of the hottest granites in the world at economic drilling depths (240°C at 3.5 km). Investigating the mechanism of heat-producing element enrichment in the Cooper Basin granite is crucial for understanding hot-dry rock geothermal systems and developing exploration strategies. Trace element (by ICP-MS) and stable isotope geochemistry of whole rock granite samples and hydrothermal phyllosilicate alteration minerals separated from the granite and overlying sandstones and mudstones of the Cooper Basin were examined in detail. Granite core samples from relatively shallow depths in Moomba 1 and Big Lake 1 are strongly altered with pervasive sericite (illite) and quartz precipitation, probably associated with intense micro-fracturing and veining. The intensity of hydrothermal alteration is less in deeper samples from Mcleod 1, Jolokia and Habanero 1. Highly altered granites from former holes are substantially enriched in lithophile elements, particularly in Cs, Rb, Be, Th, U and rare earth elements (REE) relative to the upper continental crust (UCC). U and Th contents with concentrations of up to 30 and 144 ppm, respectively, are 10 and 13 times higher than those of the UCC. Comparison of the trace element composition of the same samples dissolved by open beaker acid digestion and high-pressure acid bomb digestion (to dissolve zircon) shows that zircon is not the main repository of U and Th in the Cooper Basin granite. Instead, we propose that the enrichment of heat-producing elements was promoted by a regional hydrothermal event leading to the precipitation of U and Th- bearing minerals such as illite, K-feldspar and thorite. Crystallinity index (illite crystallinity) of the sericite indicates hydrothermal temperatures ranging from 250°C (in Moomba 1 and Big Lake 1) to 350°C (in McLeod 1 and Jolokia 1). In the overlying sedimentary rocks, crystallinity of authigenic illites translates to lower crystallisation temperatures (150-200°C). Normalised REE patterns of the mostly altered granite samples show a strong negative Ce anomaly, signifying oxidation of trivalent Ce to less soluble tetravalent Ce. Oxygen and hydrogen isotope compositions of illites from the granites and sedimentary rocks are very similar, with d18O = -1.8 per mill to +2.7 per mill; δD = -99 per mill to -121 per mill for granites and d18O = +2.3 per mill to +9.7 per mill, dD = -78 per mill to -119 per mill for sedimentary rocks. The calculated oxygen and hydrogen isotope compositions of fluids in equilibrium with the illites are depleted in 18O and deuterium, comparable to those of waters reported for most high-latitude sedimentary basins. Hence, stable isotope data of alteration minerals in the granite and the overlying sedimentary rocks suggest the operation of a hydrothermal system involving high latitude meteoric waters during extensional tectonism in the Cooper Basin region. Investigation of alteration mineralogy and geochemistry of relatively shallow sedimentary sections (generally intersected in previously drilled petroleum holes) represents a potentially strong tool to evaluate the presence of a geothermal heat source in the basement of sedimentary basins.

Geology of the epithermal Ag-Au Huevos Verdes vein system and San José district, Deseado massif, Patagonia, Argentina

NASA Astrophysics Data System (ADS)

Dietrich, Andreas; Gutierrez, Ronald; Nelson, Eric P.; Layer, Paul W.

2012-03-01

The San José district is located in the northwest part of the Deseado massif and hosts a number of epithermal Ag-Au quartz veins of intermediate sulfidation style, including the Huevos Verdes vein system. Veins are hosted by andesitic rocks of the Bajo Pobre Formation and locally by rhyodacitic pyroclastic rocks of the Chon Aike Formation. New 40Ar/39Ar constraints on the age of host rocks and mineralization define Late Jurassic ages of 151.3 ± 0.7 Ma to 144.7 ± 0.1 Ma for volcanic rocks of the Bajo Pobre Formation and of 147.6 ± 1.1 Ma for the Chon Aike Formation. Illite ages of the Huevos Verdes vein system of 140.8 ± 0.2 and 140.5 ± 0.3 Ma are 4 m.y. younger than the volcanic host rock unit. These age dates are among the youngest reported for Jurassic volcanism in the Deseado massif and correlate well with the regional context of magmatic and hydrothermal activity. The Huevos Verdes vein system has a strike length of 2,000 m, with several ore shoots along strike. The vein consists of a pre-ore stage and three main ore stages. Early barren quartz and chalcedony are followed by a mottled quartz stage of coarse saccharoidal quartz with irregular streaks and discontinuous bands of sulfide-rich material. The banded quartz-sulfide stage consists of sulfide-rich bands alternating with bands of quartz and bands of chlorite ± illite. Late-stage sulfide-rich veinlets are associated with kaolinite gangue. Ore minerals are argentite and electrum, together with pyrite, sphalerite, galena, chalcopyrite, minor bornite, covellite, and ruby silver. Wall rock alteration is characterized by narrow (< 3 m) halos of illite and illite/smectite next to veins, grading outward into propylitic alteration. Gangue minerals are dominantly massive quartz intergrown with minor to accessory adularia. Epidote, illite, illite/smectite, and, preferentially at deeper levels, Fe-chlorite gangue indicate near-neutral pH hydrothermal fluids at temperatures of >220°C. Kaolinite occurring with the late sulfide-rich veinlet stage indicates pH < 4 and a temperature of <200°C. The Huevos Verdes system has an overall strike of 325°, dipping on average 65° NE. The orientations of individual ore shoots are controlled by vein strike and intersecting north-northwest-striking faults. We propose a structural model for the time of mineralization of the San José district, consisting of a conjugate shear pair of sinistral north-northwest- and dextral west-northwest-striking faults that correspond to R and R' in the Riedel shear model and that are related to master faults (M) of north-northeast-strike. Veins of 315° strike can be interpreted as nearly pure extensional fractures (T). Variations in vein strike predict an induced sinistral shear component for strike directions of >315°, whereas strike directions of <315° are predicted with an induced dextral strike-slip movement. The components of the structural model appear to be present on a regional scale and are not restricted to the San José district.

Modelling of clay diagenesis using a combined approach of crystalchemistry and thermochemistry: a case study in the smectite illitization.

NASA Astrophysics Data System (ADS)

Geloni, Claudio; Previde Massara, Elisabetta; Di Paola, Eleonora; Ortenzi, Andrea; Gherardi, Fabrizio; Blanc, Philippe

2017-04-01

Diagenetic transformations occurring in clayey and arenaceous sediments is investigated in a number of hydrocarbon reservoirs with an integrated approach that combines mineralogical analysis, crystalchemistry, estimation of thermochemical parameters of clay minerals, and geochemical modelling. Because of the extremely variable crystalchemistry of clays, especially in the smectite - illite compositional range, the estimation of thermochemical parameters of site-specific clay-rich rocks is crucial to investigate water-rock equilibria and to predict mineralogical evolutionary patterns at the clay-sandstone interface. The task of estimating the thermochemical properties of clay minerals and predicting diagenetic reactions in natural reservoirs is accomplished through the implementation of an informatized, procedure (IP) that consists of: (i) laboratory analysis of smectite, illite and mixed layers (I/S) for the determination of their textural characteristics and chemical composition; (ii) estimation of the thermodynamic and structural parameters (enthalpy, entropy, and free energy of formation, thermal capacity, molar volume, molar weight) with a MS Excel tool (XLS) specifically developed at the French Bureau of Geological and Mining Researches (BRGM); (iii) usage of the SUPCRT (Johnson et al., 1992) software package (thereinafter, SSP) to derive log K values to be incorporated in thermodynamic databases of the standard geochemical codes; (iv) check of the consistency of the stability domains calculated with these log K values with relevant predominance diagrams; (v) final application of geochemical and reactive transport models to investigate the reactive mechanisms under different thermal conditions (40-150°C). All the simulations consider pore waters having roughly the same chemical composition of reservoir pore waters, and are performed with The Geochemist Workbench (Bethke and Yeakel, 2015), PHREEQC (Parkhurst, 1999) and TOUGHREACT (Xu, 2006). The overall procedure benefits from: (i) (minor) improvements of the I/O structure of the SSP; (ii) the development of a suite of python scripts to automate the steps needed to augment the thermodynamic database by integrating the external information provided by potential users with the XLS tool and the SSP; (iii) the creation of specific outputs to allow for more convenient handling and inspection of computed parameters of the thermodynamic database. A case study focused on non-isothermal smectite-illite transformation is presented to show the capability of our numerical models to account for clay compaction under 1D geometry conditions. This model considers fluid flow driven by the compaction of a clay layer, and chemistry-fluid flow mutual feedback with the underlying sandstone during the advancement of the diagenesis. Due to this complex interaction, as a result of the smectite-illite transformation in the clays, significant quartz cementation affects the sandstone adjacent to the compacting clay.

Diagenesis of clay mineral assemblages in the Shikoku Basin: Inputs to the Nankai Trough megathrust and seismogenic zone

NASA Astrophysics Data System (ADS)

Underwood, M.; Guo, J.; Song, C.

2012-12-01

One of the essential components of the Nankai Trough Seismogenic Zone Experiment (NanTroSEIZE) is to document the composition and diagenetic alteration of sedimentary inputs to the subduction zone of SW Japan. Two sites were drilled seaward of the trench during IODP Expeditions 322 and 333 to demonstrate how those subduction inputs have been influenced by the basement topography of Shikoku Basin. Site C0011 was drilled on the NW flank of Kashinosaki Knoll, and Site C0012 is located near the seamount's summit. The lithostratigraphy expands and condenses from site to site, but the clay mineral assemblages are nearly identical when comparisons are made among coeval units. The early history of sedimentation (middle to late Miocene) was dominated by expandable clay minerals of the smectite group. Contents of smectite in strata older than 5.3 Ma typically exceed 65% of the clay-size fraction, and there are dozens of bentonite layers (altered volcanic ash) interbedded with the hemipelagic mudstones and turbidites. Those percentages amount to >45 wt-% smectite in the bulk mudstone. Volcanic sources for the Miocene clay probably included the ancestral Izu-Bonin island arc, the Izu-Honshu collision zone, and anomalous near-trench magma bodies in the Outer Zone of Honshu and Shikoku Island. As sedimentation progressed into the Pliocene and Pleistocene, mud supplies to the Shikoku Basin shifted increasingly to detrital illite and chlorite eroded from the uplifted accretionary complex (Outer Zone). At Site C0011, the younger hemipelagic-pyroclastic facies (upper Shikoku Basin) contains an average of 43% smectite, 36% illite, and 18% kaolinite + chlorite in the clay-size fraction. At Site C0012, comparable values are S = 51%, I = 32%, and K+C = 14%. XRD results show no evidence of smectite-to-illite diagenesis seaward of the trench, although it is important to note that Site C0011 was abandoned before reaching basaltic basement. We can predict the extent of smectite-to-illite diagenesis using simple kinetic models that account for differences in heat flow from the flank to the summit of Kashinosaki Knoll and rapid burial of Shikoku Basin facies beneath the Quaternary trench wedge. Our modeling results support the notion that illitization does not progress to detectable levels (>20% I in mixed-layer clay) until after the Shikoku Basin deposits are subducted beneath the frontal megathrust. That absence of pre-subduction diagenesis is important to consider when assessing the potential for fluid production and fluid overpressures deeper down-dip along the megathrust, as well as for identifying the potential sources for freshening of interstitial fluids.

Microstructural and mineral analysis on the fault gouge in the coseismic shear zone of the 2008 M w 7.9 Wenchuan earthquake

NASA Astrophysics Data System (ADS)

Yuan, Ren-mao; Zhang, Bing-liang; Xu, Xi-wei; Lin, Chuan-yong; Han, Zhu-jun

2015-07-01

The 2008 M w 7.9 Wenchuan earthquake formed two coseismic surface rupture zones with the trend of N35°E, known as the Beichuan-Yingxiu rupture and the Pengguan rupture. The Beichuan-Yingxiu rupture is the principle one with abundant fault gouge development along its length. In the exploratory trench at the Saba village along the Beichuan-Yingxiu rupture, the new fault gouge zone is only ~3 mm wide, which suggests that fault slip was constrained in a very narrow zone. In this study, we thus carried out detailed microstructural and mineral component analysis on the oriented fault gouge samples from the Saba exploratory trench to understand their features and geological implication. The results show that different microstructures of localized brittle deformation can be observed in the fault gouges, including Y-shear, R1-shear, R2-shear, P-shear as well as tension fracture, bookshelf glided structure and so on. These microstructures are commonly recognized as the product of seismic fault slipping. Furthermore, within the area between two parallel Y-shears of the fault gouge, a few of microstructures of distributed ductile deformations were developed, such as P-foliation, elongation and asymmetrical trailing structure of detrital particles. The microstructure features of fault gouges implicate the thrust movement of the fault during the Wenchuan earthquake. In addition, the fault gouge has less quartz and feldspar and more clay than the surrounding rocks, which indicates that some quartz and feldspar in the surrounding rocks were transformed into clay, whereas the fault gouge has more illite and less illite/montmorillonite mixed layers than the surrounding rocks, which shows that the illite/montmorillonite mixed layer was partly converted into illite due to temperature increasing induced by coseismic fault slipping friction (also being affected partly by the chemical action of solutions). Such microstructures features and mineral component changes recorded the information of fault slip and provide criterions for discussing the genesis of fault gouge and recognition of the direction of fault movement.

Rheological properties of purified illite clays in glycerol/water suspensions

NASA Astrophysics Data System (ADS)

Dusenkova, I.; Malers, J.; Berzina-Cimdina, L.

2015-04-01

There are many studies about rheological properties of clay-water suspensions, but no published investigations about clay-glycerol suspensions. In this work apparent viscosity of previously purified illite containing clay fraction < 2 μm and glycerol/water suspensions were investigated. Carbonates were removed by dissolution in hydrochloric and citric acids and other non-clay minerals were almost totally removed by centrifugation. All obtained suspensions behaved as shear-thinning fluids with multiple times higher viscosity than pure glycerol/water solutions. Reduction of clay fraction concentration by 5% decreased the apparent viscosity of 50% glycerol/water suspensions approximately 5 times. There was basically no difference in apparent viscosity between all four 50% glycerol/water suspensions, but in 90% glycerol/water suspensions samples from Iecava deposit showed slightly higher apparent viscosity, which could be affected by the particle size distribution.

The influence of continuous rice cultivation and different waterlogging periods on morphology, clay mineralogy, Eh, pH and K in paddy soils.

PubMed

Bahmanyar, M A

2007-09-01

The effect of different rice cultivation periods on the properties of selected soils in alluvial plain were studied in Mazandaran province (north of Iran) in 2004. Soils were sampled form 0, 6, 16, 26 and over 40 years rice cultivation fields. In each treatment three soil profiles and six nearby auger holes were studied. The present study results indicated that continuous rice cultivation have changed soil moisture regime from xeric to aquic, soil color from brown to grayish, surface horizons from mollic to ochric epipedon and soil structure changed from granular or blocky to massive. Therefore, the soil order has changed from Mollisols to Inceptisols. No illuviation and eluviation of clay minerals occurred as a consequence of rice cultivation. X-ray diffraction analysis showed that clay minerals in non-rice cultivated field were illite, vermiculite, montmorillonite, kaolinite and chlorite, but in rice field were illite, montmorillonite, kaolinite and chlorite, respectively. In contrast of montmorillonite, the amount of illite and vermiculite have been decreased by increasing periods of rice cultivation. The pH values of the saturated soil surface in six weeks past plantation have shifted toward neutrality. While Eh value of non-paddy soils were about +90 mv, surface horizons of paddy soils at field conditions had Eh value about +40, -12, -84, -122 mv, respectively. The amounts of organic matter and available Fe, Mn, Zn and Cu were increased whereas available K was decreased in paddy soils.

Alteration in the Madera Limestone and Sandia Formation from core hole VC-1, Valles caldera, New Mexico

USGS Publications Warehouse

Keith, T.E.C.

1988-01-01

Core hole VC-1 penetrated the southwestern ring fracture zone of the 1.1 Ma Valles caldera and at a depth of 333 m intersected the top of the Paleozoic section including the Abo Formation, Madera Limestone, and Sandia Formation, reaching a total depth of 856 m. The Paleozoic rocks, which consist of thin-bedded limestone, siltstone, mudstone, sandstone, and local conglomerate, are overlain by volcanic rocks of the caldera moat that are less than 0.6 Ma. Diagenetic and at least three hydrothermal alteration stages were identified in the Madera Limestone and Sandia Formation. Diagenetic clay alteration was pervasive throughout the sedimentary rocks. Volcanic activity at 16.5 Ma and continuing through the formation of the Valles caldera resulted in high thermal gradients, which caused recrystallization of diagenetic clay minerals. Interstratified smectite-illite is the most diagnostic clay mineral throughout the section; structurally, the illite component in the ordered interstratified illite-smectite changes gradationally from 70% at the top of the Madera Limestone to 95% at the base of the section in the Sandia Formation. Pyrite that occurs as small clots and lenses as well as finely disseminated is interpreted as being of diagenetic origin, especially in organic-rich beds. Low permeability of much of the paleozoic section precluded the deposition of hydrothermal minerals except in fractures and intergranular space in some of the more permeable sandstone and brecciated horizons. Three stages of hydrothermal mineral deposition are defined. -from Author

Mathematical modelling of anisotropy of illite-rich shale

USGS Publications Warehouse

Chesnokov, E.M.; Tiwary, D.K.; Bayuk, I.O.; Sparkman, M.A.; Brown, R.L.

2009-01-01

The estimation of illite-rich shale anisotropy to account for the alignment of clays and gas- or brine-filled cracks is presented via mathematical modelling. Such estimation requires analysis to interpret the dominance of one effect over another. This knowledge can help to evaluate the permeability in the unconventional reservoir, stress orientation, and the seal capacity for the conventional reservoir. Effective media modelling is used to predict the elastic properties of the illite-rich shale and to identify the dominant contributions to the shale anisotropy. We consider two principal reasons of the shale anisotropy: orientation of clay platelets and orientation of fluid-filled cracks. In reality, both of these two factors affect the shale anisotropy. The goal of this study is, first, to separately analyse the effect of these two factors to reveal the specific features in P- and S-wave velocity behaviour typical of each of the factors, and, then, consider a combined effect of the factors when the cracks are horizontally or vertically aligned. To do this, we construct four models of shale. The behaviour of P- and S-wave velocities is analysed when gas- and water-filled cracks embedded in a host matrix are randomly oriented, or horizontally or vertically aligned. The host matrix can be either isotropic or anisotropic (of VTI symmetry). In such a modelling, we use published data on mineralogy and clay platelet alignment along with other micromechanical measurements. In the model, where the host matrix is isotropic, the presence of a singularity point (when the difference VS1 - VS2 changes its sign) in shear wave velocities is an indicator of brine-filled aligned cracks. In the model with the VTI host matrix and horizontally aligned cracks filled with gas, an increase in their volume concentration leads to that the azimuth at which the singularity is observed moves toward the symmetry axis. In this case, if the clay content is small (around 20 per cent), the singularity point may even vanish. The Thomsen parameters are helpful in fluid type indication in shale. An indicator of gas-filled aligned cracks is ?? > ??. If aligned cracks in illite-rich shale are brine-filled, ?? < ??. Negative value of ?? indicates brine-filled cracks in illite-rich shale. A shale with brine-filled cracks exhibits higher Vp/Vs ratio in the vertical direction as compared to the gas-filled shale. A disorientation of clay platelets and brine-filled cracks may lead to that the singularity point is absent for brine-saturated shale as well. In this case one can also observe ?? > ?? and decreased values of Vp/Vs in the vertical direction as in the case of gas-filled cracks. In the presence of vertically aligned cracks, shales exhibit distinctly revealed features of orthorhombic symmetry. The results have important applications where seismic measurements are applied to predict the maturity state of the shale. ?? 2009 The Authors Journal compilation ?? 2009 RAS.

Clay mineral formation and transformation in rocks and soils

USGS Publications Warehouse

Eberl, D.D.

1983-01-01

Three mechanisms for clay mineral formation (inheritance, neoformation, and transformation) operating in three geological environments (weathering, sedimentary, and diagenetic-hydrothermal) yield nine possibilities for the origin of clay minerals in nature. Several of these possibilities are discussed in terms of the rock cycle. The mineralogy of clays neoformed in the weathering environment is a function of solution chemistry, with the most dilute solutions favoring formation of the least soluble clays. After erosion and transportation, these clays may be deposited on the ocean floor in a lateral sequence that depends on floccule size. Clays undergo little reaction in the ocean, except for ion exchange and the neoformation of smectite; therefore, most clays found on the ocean floor are inherited from adjacent continents. Upon burial and heating, however, dioctahedral smectite reacts in the diagenetic environment to yield mixed-layer illite-smectite, and finally illite. With uplift and weathering, the cycle begins again. Refs.

Role of minerals in the thermal alteration of organic matter. I - Generation of gases and condensates under dry condition

NASA Technical Reports Server (NTRS)

Tannenbaum, E.; Kaplan, I. R.

1985-01-01

Pyrolysis experiments conducted at 200 and 300 C on kerogen and bitumen from the Monterey formation and on the Green River Formation kerogen with montmorillonite, illite, and calcite added are described. The pyrolysis products are identified and gas and condensate analyses are performed. A catalytic effect is detected in the pyrolysis of kerogen with montmorillonite; however, illite and calcite display no catalytic activity. The increased production of C1-C6 hydrocarbons and the dominance of branched hydrocarbons in the C4-C6 range reveals a catalytic influence. It is observed that the catalysis of montmorillonite is greater during bitumen pyrolysis than for kerogen, and catalysis with minerals affects the production of CO2. It is concluded that a mineral matrix is important in determining the type and amount of gases and condensates forming from organic matter under thermal stress.

Steranes and triterpanes generated from kerogen pyrolysis in the absence and presence of minerals

NASA Technical Reports Server (NTRS)

Tannenbaum, E.; Ruth, E.; Kaplan, I. R.

1986-01-01

Changes in the degree of isomerization of steranes and triterpanes during kerogen pyrolysis in the absence or presence of minerals are described. Kerogen from a Monterey Formation diatomite core sample was pyrolyzed under reduced pressure at 300 C for 2-1000 hrs in the presence or absence of calcite, illite, and montmorillonite. It is observed that the extent of isomerization of biomakers in C-20 in 14 alpha(H), 17 alpha(H)-steranes, at C-22 in 17 alpha(H), 21 beta(H)-hopanes and of 17 beta(H), 21 beta(H)-hopanes correlates to early diagenetic stages in rock extracts from sedimentary basins, and faster isomerization for steranes and triterpanes in the bitumen then for those in the kerogen structure are detected. The effects of the minerals on the isomerization reactions are examined; calcite inhibits, and illite and montmorillonite catalyze the reactions.

Water and Sediment Quality in the Yukon River Basin, Alaska, During Water Year 2005

DTIC Science & Technology

2007-01-01

Disordered Kaolinite 0.6 0.5 0.4 0.7 0.6 1.0 0.4 Ferruginous smectite 7.4 9.5 6.1 4.9 9.4 10.6 12.4 Illite + Smectite 6.8 4.8 5.2 6.6 6.6 5.5 4.9...64.7 Clays: Goethite 0.1 0.1 0.3 0.1 0.1 0.3 0.1 Disordered Kaolinite 0.6 0.9 0.3 0.7 0.9 0.6 0.7 Ferruginous smectite 7.0 6.8 7.1...7.9 7.6 16.4 15.7 Illite + Smectite 10.2 7.7 8.1 7.9 6.8 1.2 3.2 Chlorite 8.0 9.5 9.6 9.4 10.7 10.8 12.2 Muscovite (2M1) 4.1 6.0 5.2 4.8 4.1 4.8

Characterization of mineral phases of agricultural soil samples of Colombian coffee using Mössbauer spectroscopy and X-ray diffraction

NASA Astrophysics Data System (ADS)

Rodríguez, Humberto Bustos; Lozano, Dagoberto Oyola; Martínez, Yebrayl Antonio Rojas; Pinilla, Marlene Rivera; Alcázar, German Antonio Pérez

2012-03-01

Soil chemical analysis, X-ray diffraction (XRD) and Mössbauer spectrometry (MS) of 57Fe were used to characterize mineral phases of samples taken from the productive layer (horizon A) of agricultural coffee soil from Tolima (Colombia). Chemical analysis shows the chemical and textural parameters of samples from two different regions of Tolima, i.e., Ibagué and Santa Isabel. By XRD phases like illite (I), andesine (A) and quartz (Q) in both samples were identified. The quantity of these phases is different for the two samples. The MS spectra taken at room temperature were adjusted by using five doublets, three of them associated to Fe + 3 type sites and the other two to Fe + 2 type sites. According to their isomer shift and quadrupole splitting the presence of phases like illite (detected by DRX), nontronite and biotite (not detected by XRD) can be postulated.

Aggregation Rates of Sediments (Montmorillonite, Kaolinite, Illite and Goethite) with the Enveloped Φ6 Bacteriophage

NASA Astrophysics Data System (ADS)

Katz, A.; Block, K. A.; Peña, S.; Alimova, A.; Gottlieb, P.

2015-12-01

The interaction between sediments and viruses has been studied extensively from the prospective of virus survivability and infectivity. However, the role of soil organisms, including viruses in C and N sequestration in soil has not been studied as extensively. Φ6, a member of the cystoviridae family, is a bacteriophage that infects Pseudomonas syringae, a common plant pathogen known to readily form biofilms.The small mineral fraction (< 0.2 μm) of soil and Φ6 are colloidal particles, therefore aggregation can be explained by DLVO (Derjaguin & Landau, Verwey & Overbeek) theory. Time-resolved visible-light turbidity measurements were used to calculate the heteroaggregation rates of Φ6 with the sediments. Samples were suspended in a low-concentration cation buffer so that the kinetics were in the reaction limited cluster aggregation (RLCA) regime in where the probability of two particles adhering after collision is determined by the interaction forces between the particles.At neutral pH to slightly acidic pH, Φ6 is slightly negatively charged; montmorillonite and illite are negatively charged; and kaolinite and goethite are positively charged. In isolation, neither Φ6 nor the sediments aggregated in the modified buffer. However, in mixtures, Φ6 and montmorillonite, and Φ6 and illite, exhibited increases in turbidity, indicating heteroaggregation. Neither Φ6 and kaolinite, nor Φ6 and goethite, exhibited increased turbidity upon mixing indicating little or no aggregation. These results suggest that the interaction of the virus with the sediments is governed by hydrophobic rather than electrostatic forces. Heteroaggregation rates were calculated from the time rate of change of the turbidity.

Effect of clay content and mineralogy on frictional sliding behavior of simulated gouges: binary and ternary mixtures of quartz, illite, and montmorillonite

USGS Publications Warehouse

Tembe, Sheryl; Lockner, David A.; Wong, Teng-Fong

2010-01-01

We investigated the frictional sliding behavior of simulated quartz-clay gouges under stress conditions relevant to seismogenic depths. Conventional triaxial compression tests were conducted at 40 MPa effective normal stress on saturated saw cut samples containing binary and ternary mixtures of quartz, montmorillonite, and illite. In all cases, frictional strengths of mixtures fall between the end-members of pure quartz (strongest) and clay (weakest). The overall trend was a decrease in strength with increasing clay content. In the illite/quartz mixture the trend was nearly linear, while in the montmorillonite mixtures a sigmoidal trend with three strength regimes was noted. Microstructural observations were performed on the deformed samples to characterize the geometric attributes of shear localization within the gouge layers. Two micromechanical models were used to analyze the critical clay fractions for the two-regime transitions on the basis of clay porosity and packing of the quartz grains. The transition from regime 1 (high strength) to 2 (intermediate strength) is associated with the shift from a stress-supporting framework of quartz grains to a clay matrix embedded with disperse quartz grains, manifested by the development of P-foliation and reduction in Riedel shear angle. The transition from regime 2 (intermediate strength) to 3 (low strength) is attributed to the development of shear localization in the clay matrix, occurring only when the neighboring layers of quartz grains are separated by a critical clay thickness. Our mixture data relating strength degradation to clay content agree well with strengths of natural shear zone materials obtained from scientific deep drilling projects.

Origin and diagenesis of clay minerals in relation to sandstone paragenesis: An example in eolian dune reservoirs and associated rocks, Permian upper part of the Minnelusa Formation, Powder River basin, Wyoming

DOE Office of Scientific and Technical Information (OSTI.GOV)

Pollastro, R.M.; Schenk, C.J.

Eolian dune sandstones are the principal reservoir rocks in the Permian upper part of the Minnelusa Formation, Powder River basin, Wyoming. These sandstones formed as shorelines retreated and dunes migrated across siliciclastic sabkhas. Sandstones are mainly quartzarenites; on average, clay minerals constitute about 5 wt.% the whole rock. Although present in minor amounts, clay minerals play an important role in the diagenetic evolution of these sandstones. Allogenic clay minerals are present in shaly rock fragments and laminae. Early infiltration of clays into porous sabkha sands commonly form characteristic menisei or bridges between framework grains or, when more extensive, form coatingsmore » or rims on grain surfaces. Authigenic clays include nearly pure smectite, mixed-layer illite/smectite (I/S), and late diagenetic illite and corrensite; these clay minerals are present as pore-lining cements. In addition to the deposition and neoformation of clay minerals throughout sandstone paragenesis, the conversion of smectite to illite occurred as temperatures increased with progressive burial. A temperature of 103C is calculated at a present depth of 3,200 m using a geothermal gradient of 30C/km and a mean annual surface temperature of 7C. After correction for uplift and erosion (250 m), the maximum calculated temperature for the conversion of all random I/S to ordered I/S is 100C. This calculated temperature is in excellent agreement with temperatures of 100-110C implied from I/S geothermometry.« less

[Analysis of XRD spectral characteristics of soil clay mineral in two typical cultivated soils].

PubMed

Zhang, Zhi-Dan; Luo, Xiang-Li; Jiang, Hai-Chao; Li, Qiao; Shen, Cong-Ying; Liu, Hang; Zhou, Ya-Juan; Zhao, Lan-Po; Wang, Ji-Hong

2014-07-01

The present paper took black soil and chernozem, the typical cultivated soil in major grain producing area of Northeast, as the study object, and determinated the soil particle composition characteristics of two cultivated soils under the same climate and location. Then XRD was used to study the composition and difference of clay mineral in two kinds of soil and the evolutionary mechanism was explored. The results showed that the two kinds of soil particles were composed mainly of the sand, followed by clay and silt. When the particle accumulation rate reached 50%, the central particle size was in the 15-130 microm interval. Except for black soil profile of Shengli Xiang, the content of clay showed converse sequence to the central particle in two soils. Clay accumulated under upper layer (18.82%) in black soil profile while under caliche layer (17.41%) in chernozem profile. Clay content was the least in parent material horizon except in black profile of Quanyanling. Analysis of clay XRD atlas showed that the difference lied in not only the strength of diffraction peak, but also in the mineral composition. The main contents of black soil and chernozem were both 2 : 1 clay, the composition of black soil was smectite/illite mixed layer-illite-vermiculite and that of chernozem was S/I mixture-illite-montmorillonite, and both of them contained little kaolinite, chlorite, quartz and other primary mineral. This paper used XRD to determine the characteristics of clay minerals comprehensively, and analyzed two kinds of typical cultivated soil comparatively, and it was a new perspective of soil minerals study.

Geochemistry of volcanogenic clayey marine sediments from the Hazar-Maden Basin (Eastern Turkey)

NASA Astrophysics Data System (ADS)

Akkoca, Dicle Bal; Kürüm, Sevcan; Huff, Warren D.

2013-12-01

The Hazar-Madeıı Basin sediments were deposited along the southern branch of the Neotethys Ocean margin during Late Maastrichtian-Middle Eocene times. X-ray powder diffraction (XRD), ICP-AES, ICP-MS and scanning electron microscopy (SEM) were performed on samples of the Upper Maastrichtian-Middle Eocene Hazar Group and the Middle Eocene Maden Complex from the Hazar-Maden Basin to investigate the main effects of depositional envi- ronmental parameters in three sections belonging to deeper marine (slope), proximal arc volcanic (Mastarhill and Yukaribag sections) and shallow platform marine (Sebken section) settings. Marine sediments contain clay minerals (smectite, smectite/chlorite, chlorite, illite, interstratified illite/smectite, illite/chlorite, palygorskite), clinoptilolite, quartz, feldspar, calcite, dolomite, opal-CT and hematite. The clays are dominated by iron-rich smectites. La, Zr and Th concentrations are high in the shallow marginal Sebken section where the terrestrial detrital contribution is significant, while Sc and Co are more dominant in the deeper marine (slope) Yukaribag section, which is represented by basic-type volcanism and a higher contribution of hydrothermal phases. In a chondrite-normalized REE diagram, the negative Eu anomaly in samples from Sebken, the section which was deposited in a shallow marine environment, is less significant than that of the other two sections indicating the presence of a high terrestrial contribution in that part of the basin. A decrease in LREE v/HREEiV and Lajv/Ybv, LaiV/Sin v ratios from Sebken to Mastarhill and the Yukaribag sections indi- cates deepening of the basin and an increasing contribution of volcanism in that direction.

Ocurrence and genesis of kaolinite in sedimentary deposits from the Southern Iberian Range (Spain)

NASA Astrophysics Data System (ADS)

Bauluz, B.; Mayayo, M. J.; Yuste, A.; Fernández-Nieto, C.; González López, J. M.

2003-04-01

The kaolinite-rich clay deposits from the Southern Iberian Range (Spain) correspond to continental clay-sandy series developed during Lower Cretaceous times. The clay deposits are mined by ceramic industry nowadays, and are intercalated with coal levels (lignites) that are also mined for energetic purposes. We have characterized by XRD, optical, and electronic microscopy (SEM, TEM) the mineralogical composition of a set of 55 samples, emphasizing in the kaolinite features: texture, morphology, crystallinity, and composition. Studied rocks (lutites, limolites, and sandstones) are composed by different proportions of quartz, kaolinite, muscovite, and illite, with minor K-feldspar, pyrite and siderite. The XRD study shows that, in comparison to micaceous phases, kaolinite particles are preferentially concentrated in the finest fractions of the rocks, indicating a lower crystal size. In addition, electron microscopy observations show that kaolinite occurs in four distinct modes: (a) as subhedral-anhedral flakes (<20 μm) that are the major component of the lutites. This kaolinite shows a disordered type (XRD). Chemical composition of kaolinite and illite particles (TEM/AEM) show a broad compositional variation. Some of the particles correspond to kaolinite and illite compositions, but most of the analyses indicate intermediate compositions, suggesting the occurrence of submicroscopic intergrowths of kaolinite and illite. The detection of low Ca contents in some analyses indicate the presence of smectite phases in these intergrowths. Probably, this kaolinite was formed by alteration of aluminosilicates (micas and K-feldspars) in the source area of the sediments. (b) as flakes filling pyritized plants in some dark lutites. (c) as subhedral and hexagonal plates, up to 5 μm in size, in sandstones. They are replacing K-feldspar fragments with clear evidence of alteration under SEM. The kaolinites display a high degree of order. (d) as booklets of pseudo-hexagonal plates of kaolinite and muscovite-type mica. These aggregates, up to 30 μm thick, appears mainly in limolites. The growth of kaolinite between the cleavage layers of pre-existing detrital mica resulted in a net increase in volume of the original grain. The delicate fabrics of these intergrowths suggest an in situ origin. The modes (b), (c) and (d) would have an authigenic origin, being K-feldspar one of the source of components for their formation during the early stages of the diagenesis.

Clay alteration and gold deposition in the genesis and blue star deposits, Eureka County, Nevada

USGS Publications Warehouse

Drews-Armitage, S. P.; Romberger, S.B.; Whitney, C.G.

1996-01-01

The Genesis and Blue Star sedimentary rock-hosted gold deposits occur within the 40-mile-long Carlin trend and are located in Eureka County, Nevada. The deposits are hosted within the Devonian calcareous Popovich Formation, the siliciclastic Rodeo Creek unit and the siliciclastic Vinini Formation. The host rocks have undergone contact metamorphism, decalcification, silicification, argillization, and supergene oxidation. Detailed characterization of the alteration patterns, mineralogy, modes of occurrence, and associated geochemistry of clay minerals resulted in the following classifications: least altered rocks, found distal to the orebody, consisting of both metamorphosed and unmetamorphosed host rock that has not been completely decalcified; and altered rocks, found proximal to the orebody that have been decalcified. Altered rocks are classified further into the following groups based on clay mineral content: silicic, 1 to 10 percent clay; silicicargillic, 10 to 35 percent clay; and argillic, 35 to 80 percent clay. Clay species identified are 1M illite, 2M1 illite, kaolinite, halloysite, and dioctahedral smectite. An early hydrothermal event resulted in the precipitation of euhedral kaolinite and at least one generation of silica. This event occurred contemporaneously with decalcification which increased rock permeability and porosity. A second clay alteration event resulted in the precipitation of hydrothermal 1M illite which replaced hydrothermal kaolinite and is associated with gold deposition. Silver and silica deposition is also associated with this phase of hydrothermal alteration. Hydrothermal alteration was followed by supergene alteration which resulted in the formation of supergene kaolinite, halloysite, and smectite as well as the oxidation of iron-bearing minerals. Supergene clays are concentrated along faults, dike margins, and within rocks containing carbonate. Gold mineralization is not associated with supergene clay minerals within the Genesis and Blue Star deposits. Rocks classified as silicic-argillic in the Popovich Formation represent the most significant gold host. Silicicargillic rocks commonly exhibit bedding-parallel alteration zones. This pattern of alteration indicates that stratigraphy as well as northwest-trending structures played a significant role in the migration of gold-bearing fluids. Based on K-Ar age determinations of hydrothermal 1M illite associated with gold, the main event of mineralization in the Genesis and Blue Star deposits occurred between 93 and 100 Ma, during mid-Cretaceous time.

Chemistry, mineralogy and alteration intensity of hydrothermal altered Mt Unzen conduit rocks (Shimabara/Japan)

NASA Astrophysics Data System (ADS)

Hess, Kai-Uwe; Yilmaz, Tim; Gilg, H. Albert; Janots, Emilie; Mayer, Klaus; Nakada, Setsuya; Dingwell, Donald

2017-04-01

Investigations were carried out on hydrothermally altered coherent dacitic dykes samples from (USDP-4) drill core at Mt Unzen stratovolcano (Shimabara/Japan). XRF, XRD, EMPA, C-O-isotope, hot-cathode CL and SEM analysis led to insights concerning chemistry, mineralogy, and intensity and type of alteration as well as the origin of carbonate-precipitating fluids. Additionally a textural characterization of the occurring replacement features in the volcanic conduit rocks was performed. The occurrence of the main secondary phases such as chlorite, pyrite, carbonates, and R1 (Reichweite parameter) illite-smectite and kaolinite group minerals indicate a weak to moderate propylitic to phyllic hydrothermal alteration. The dacitic samples of the dykes show different hydrothermal alteration features: (i) carbonate and chlorite pseudomorphs after hornblende as well as core and zonal textures due to replacement of plagioclase by R1 illite-smectite as well as kaolinite group minerals, (ii) colloform banded fracture fillings and fillings in dissolution vugs, and (iii) chlorite, R1 illite-smectite as well as kaolinite group minerals in the groundmass. Late chlorite veins crosscut precipitates of R1 illite-smectite as well as kaolinite group minerals. Carbonates in fractures and in pseudomorphs after hornblende comprise iron-rich dolomite solid solutions ("ankerite") and calcite. Isotopic values indicate a hydrothermal-magmatic origin for the carbonate formation. The chlorite-carbonate-pyrite index (CCPI) and the Ishikawa alteration index (AI), applied to the investigated samples show significant differences (CCPI=52.7-57.8; AI=36.1-40.6) indicating their different degree of alteration. According to Nakada et al., 2005, the C13 to C16 dykes represent the feeder dyke from the latest eruption (1991-1995) whereas C8 represents an earlier dyke feeder dyke from an older eruption. Weakest alteration, which was obtained in samples C16-1-5 and C13-2-5, correlates with the alteration degree of the pristine dome rocks. The highest CCPI value was determined for sample C14-1-5 and the highest AI value was determined for sample C15-2-6. The degrees of alteration do not indicate highest alteration of the samples C8-1-2 and C8-2-1 from the older dykes.

Effects of smectite to illite transformation on the frictional strength and sliding stability of intact marine mudstones

USGS Publications Warehouse

Saffer, Demian M.; Lockner, David A.; McKiernan, Alex

2012-01-01

At subduction zones, earthquake nucleation and coseismic slip occur only within a limited depth range, known as the “seismogenic zone”. One leading hypothesis for the upper aseismic-seismic transition is that transformation of smectite to illite at ∼100–150°C triggers a change from rate-strengthening frictional behavior that allows only stable sliding, to rate weakening behavior considered a prerequisite for unstable slip. Previous studies on powdered gouges have shown that changes in clay mineralogy alone are unlikely to control this transition, but associated fabric and cementation developed during diagenesis remain possible candidates. We conducted shearing experiments designed specifically to evaluate this hypothesis, by using intact wafers of mudstone from Ocean Drilling Program Site 1174, offshore SW Japan, which have undergone progressive smectite transformation in situ. We sheared specimens along a sawcut in a triaxial configuration, oriented parallel to bedding, at normal stresses of ∼20–150 MPa and a pore pressure of 1 MPa. During shearing, we conducted velocity-stepping tests to measure the friction rate parameter (a-b). Friction coefficient ranges from 0.28–0.40 and values of (a-b) are uniformly positive; both are independent of clay transformation progress. Our work represents the most direct and comprehensive test of the clay transformation hypothesis to date, and suggests that neither illitization, nor accompanying fabric development and cementation, trigger a transition to unstable frictional behavior. We suggest that strain localization, in combination with precipitation of calcite and quartz, is a viable alternative that is consistent with both field observations and recent conceptual models of a heterogeneous seismogenic zone.

Holocene debris flows on the Colorado Plateau: The influence of clay mineralogy and chemistry

USGS Publications Warehouse

Webb, R.H.; Griffiths, P.G.; Rudd, L.P.

2008-01-01

Holocene debris flows do not occur uniformly on the Colorado Plateau province of North America. Debris flows occur in specific areas of the plateau, resulting in general from the combination of steep topography, intense convective precipitation, abundant poorly sorted material not stabilized by vegetation, and the exposure of certain fine-grained bedrock units in cliffs or in colluvium beneath those cliffs. In Grand and Cataract Canyons, fine-grained bedrock that produces debris flows contains primarily single-layer clays - notably illite and kaolinite - and has low multilayer clay content. This clay-mineral suite also occurs in the colluvium that produces debris flows as well as in debris-flow deposits, although unconsolidated deposits have less illite than the source bedrock. We investigate the relation between the clay mineralogy and major-cation chemistry of fine-grained bedrock units and the occurrence of debris flows on the entire Colorado Plateau. We determined that 85 mapped fine-grained bedrock units potentially could produce debris flows, and we analyzed clay mineralogy and major-cation concentration of 52 of the most widely distributed units, particularly those exposed in steep topography. Fine-grained bedrock units that produce debris flows contained an average of 71% kaolinite and illite and 5% montmorillonite and have a higher concentration of potassium and magnesium than nonproducing units, which have an average of 51% montmorillonite and a higher concentration of sodium. We used multivariate statistics to discriminate fine-grained bedrock units with the potential to produce debris flows, and we used digital-elevation models and mapped distribution of debris-flow producing units to derive a map that predicts potential occurrence of Holocene debris flows on the Colorado Plateau. ?? 2008 Geological Society of America.

Mineralogy of Fluvio-Lacustrine Sediments Investigated by Curiosity during the Prime Mission: Implications for Diagenesis

NASA Astrophysics Data System (ADS)

Rampe, E. B.; Morris, R. V.; Bish, D. L.; Vaniman, D. T.; Bristow, T.; Chipera, S.; Blake, D. F.; Ming, D. W.; Farmer, J.; Morrison, S. M.; Treiman, A. H.; Achilles, C.; Crisp, J.; Des Marais, D. J.; Downs, R. T.; Morookian, J. M.; Sarrazin, P.; Spanovich, N.; Yen, A.

2014-12-01

The Mars Science Laboratory rover Curiosity investigated sedimentary rocks that were deposited in a diversity of fluvio-lacustrine settings. The entire science payload was employed to characterize the mineralogy and chemistry of the Sheepbed mudstone at Yellowknife Bay and the Windjana sandstone at the Kimberley. Data from the CheMin instrument, a transmission X-ray diffractometer, were used to determine the quantitative mineralogy of both samples. The Sheepbed mudstone contains detrital basaltic minerals, calcium sulfates, iron oxides or hydroxides, iron sulfides, trioctahedral smectite, and amorphous material. The mineral assemblage and chemical data from APXS suggest that the trioctahedral smectite and magnetite formed authigenically as a result of alteration of olivine. The apparent lack of higher-grade phyllosilicates (e.g., illite and chlorite) and the presence of anhydrite indicate diagenesis at ~50-80 ºC. The mineralogy of the Windjana sandstone is different than the Sheepbed mudstone. Windjana contains significant abundances of K-feldspar, low- and high-Ca pyroxenes, magnetite, phyllosilicates, and amorphous material. At least two distinct phyllosilicate phases exist: a 10 Å phase and a component that is expanded with a peak at ~11.8 Å. The identity of the expanded phase is currently unknown, but could be a smectite with interlayer H2O, and the 10 Å phase could be illite or collapsed smectite. Further work is necessary to characterize the phyllosilicates, but the presence of illite could suggest that Windjana experienced burial diagenesis. Candidates for the cementing agents include fine-grained phyllosilicates, Fe-oxides, and/or amorphous material. Interpretations of CheMin data from the Windjana sandstone are ongoing at the time of writing, but we will present an estimate of the composition of the amorphous material from mass balance calculations using the APXS bulk chemistry and quantitative mineralogy from CheMin.

Mineralogy of Fluvio-Lacustrine Sediments Investigated by Curiosity During the Prime Mission: Implications for Diagenesis

NASA Technical Reports Server (NTRS)

Rampe, Elizabeth B.; Morris, R. V.; Bish, D. L.; Vaniman, D. T.; Bristow, T. F.; Chipera, S. J.; Blake, D. F.; Ming, D. W.; Farmer, J. D.; Morrison, S. M.;

Measurement of clay surface areas by polyvinylpyrrolidone (PVP) sorption and its use for quantifying illite and smectite abundance

USGS Publications Warehouse

Blum, A.E.; Eberl, D.D.

2004-01-01

A new method has been developed for quantifying smectite abundance by sorbing polyvinylpyrrolidone (PVP) on smectite particles dispersed in aqueous solution. The sorption density of PVP-55K on a wide range of smectites, illites and kaolinites is ~0.99 mg/m2, which corresponds to ~0.72 g of PVP-55K per gram of montmorillonite. Polyvinylpyrrolidone sorption on smectites is independent of layer charge and solution pH. PVP sorption on SiO2, Fe2O3 and ZnO normalized to the BET surface area is similar to the sorption densities on smectites. γ-Al2O3, amorphous Al(OH)3 and gibbsite have no PVP sorption over a wide range of pH, and sorption of PVP by organics is minimal. The insensitivity of PVP sorption densities to mineral layer charge, solution pH and mineral surface charge indicates that PVP sorption is not localized at charged sites, but is controlled by more broadly distributed sorption mechanisms such as Van der Waals’ interactions and/or hydrogen bonding. Smectites have very large surface areas when dispersed as single unit-cell-thick particles (~725 m2/g) and usually dominate the total surface areas of natural samples in which smectites are present. In this case, smectite abundance is directly proportional to PVP sorption. In some cases, however, the accurate quantification of smectite abundance by PVP sorption may require minor corrections for PVP uptake by other phases, principally illite and kaolinite. Quantitative XRD can be combined with PVP uptake measurements to uniquely determine the smectite concentration in such samples.

Studies on thermal reactions and sintering behaviour of red clays by irreversible dilatometry

NASA Astrophysics Data System (ADS)

Anil, Asha; Misra, S. N.; Misra, N. M.

2018-05-01

Thermal behavior of clays strongly influences that of ceramic bodies made thereof and hence, its study is must for assessing its utility in ceramic products as well as to set the body composition. Irreversible dilatometry is an effective thermal analysis tool for evaluating thermal reactions as well as sintering behavior of clays or clay based ceramic bodies. In this study, irreversible dilatometry of four red clay samples (S, M, R and G) of Gujarat region, which vary in their chemical and mineralogical compositions was carried out using a Dilatometer and compared. Chemical analysis and XRD of red clays were carried out. XRD showed that major clay minerals in S, M and R clays are kaolinite. However, clay marked R and G showed presence of both kaolinite and illite and /muscovite. Presence of non-clay minerals such as hematite, quartz, anatase were also observed in all clays. XRD results were in agreement with chemical analyses results. Rational analyses showed variation in amount of clay and non-clay minerals in red clay samples. Evaluation of dilatometric curves showed that clay marked as S, M and R exhibit patterns typical for kaolinitic clays. Variation in linear expansion (up to 550°C) and shrinkage (above 550°C) between these three clays was found to be related to difference in amount of quartz and kaolinite respectively. However, dilatometric curve of G exhibit a pattern similar to that for an illitic clay. This study confirmed that sintering of investigated kaolinitic and illitic and / muscovitic red clays initiates at above 1060°C and 860°C respectively and this behaviour strongly depends upon type and amount of minerals and their chemical compositions.

Organic and clay mineral diagenesis in Neogene sediments of western Taiwan

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hsueh, C.M.

1985-01-01

Three deep wells (two in the northern region and one in the southern region) with completion depths of over 5000m have been selected and the rock samples thoroughly examined. The TOC data of most samples studied are less than 1%, which is the TOC of an average shale. The low TOC is unfavorable for the Neogene sediments in western Taiwan as good source rocks. The data of C,H elemental analysis and Rock-Eval pyrolysis imply that the quality of kerogen in the northern region inclines to type II wet-gas prone, and in the southern region inclines to type III dry-gas prone.more » The maturity parameters of bitumen ratio, vitrinite reflectance, Tmax of Rock-Eval pyrolysis, and TTI of Lopatin's method show that the threshold of the oil-generative zone (about 0.6% Ro) in the northern region is in middle Miocene (about 3000m) and in the southern region is in lower Pliocene (about 4500m). The result of clay mineral analysis reveals that the transformation of smectitic clays to ordered mixed-layered smectite-illite can be identified and correlated with 0.6% Ro vitrinite reflectance. The illite crystallinity values are in the range of incipient to weak metamorphism and decrease with burial depth implying that the source area of low-grade metamorphic rocks has been uplifted rapidly so that the erosion from the exposed source area where the metamorphic grade became higher and higher was sufficiently fast to prevent weathering of illite. The Neogene sediments studied would not be expected to generate substantial amounts of oil. However, it can be expected that the pre-Miocene sediments in the northern region and the pre-Pliocene sediments in the southern region should have generated substantial amounts of gas at deeper depths.« less

Link between Indian monsoon rainfall and physical erosion in the Himalayan system during the Holocene

NASA Astrophysics Data System (ADS)

Joussain, Ronan; Liu, Zhifei; Colin, Christophe; Duchamp-Alphonse, Stéphanie; Yu, Zhaojie; Moréno, Eva; Fournier, Léa.; Zaragosi, Sébastien; Dapoigny, Arnaud; Meynadier, Laure; Bassinot, Franck

2017-09-01

Mineralogical and geochemical analyses conducted on cores located on the active channel-levee system of the northern Bengal Fan are used to establish changes in the weathering pattern and the sediment transport of the Himalayan system, and evaluate the effect of Indian summer monsoon rainfall during the Holocene. Our data indicate that during the Holocene, sediments from the northern Bengal Fan originate mainly from the G-B river system without any significant changes in the relative contribution of these rivers. From 9.8 to around 6 ka, relatively low smectite/(illite+chlorite) ratios and relatively high K/Si* ratios indicate high physical denudation rates of the Himalayan highlands together with a rapid transfer of the detrital material to the Bengal Fan. The period between 9.2 and 7 ka is associated to lower values of K/Si* and corresponds to the maximum of Indian monsoon rainfall which indicates a more important chemical weathering material that rapidly transits by the G-B river system without a long storage in the Indo-Gangetic plain. From 6.0 ka to present day, higher smectite/(illite+chlorite) ratio and lower K/Si* ratio document a gradual increase of sediments originated from the Indo-Gangetic plain, characterized by higher degree of chemical weathering. During the last 2.5 ka, the drastic increase in the smectite/(illite+chlorite) ratio could be associated to enhanced alteration of the plain soils due to anthropogenic activity. The comparison of mineralogical and geochemical data with previous reconstructions of the Indian monsoon dynamic indicates a rapid response of erosion and sediment transfer of the G-B river system to changes of monsoon rainfall intensity.

Mineralogy, structural control and age of the Incachule Sb epithermal veins, the Cerro Aguas Calientes collapse caldera, Central Puna

NASA Astrophysics Data System (ADS)

Salado Paz, Natalia; Petrinovic, Iván; Do Campo, Margarita; Brod, José Affonso; Nieto, Fernando; da Silva Souza, Valmir; Wemmer, Klauss; Payrola, Patricio; Ventura, Roberto

2018-03-01

The Incachule Sb epithermal veins is located near to the N-E rim of the Cerro Aguas Calientes collapse caldera (17.5-10.8 Ma), in the geologic province of Puna, Salta- Argentina. It is hosted in Miocene felsic volcanic rocks with continental arc signature. The district includes twelve vein systems with mineralization of Sb occurring in hydrothermal breccias and stockwork. The veins are composed of quartz-sulfide with pyrite, stibnite and arsenopyrite. All around the veins, wall rocks are variably altered to clay minerals and sulfates in an area of around 2.5 km wide by more than 7 km long. The hydrothermal alterations recognized are: silicic, phyllic and argillic. The veins are characterized by high contents of Sb, As, and Tl and intermediate contents of Pb-Zn-Cu, and traces of Ag and Au. Homogenization and ice-melting temperatures of fluid inclusions vary from 125 °C to 189 °C and -2.4 °C to -0.8 °C. The isotopic data indicated a range of δ34S -3.04‰ to +0.72‰ consistent with a magmatic source for sulfur. We present the firsts K-Ar ages for hydrothermal illite/smectite mixed layers (I/SR1, 60% illite layers) and illite that constrain the age of the ore deposit (8.5-6.7 ± 0.2 Ma). The data shown here, let characterized the Incachule district as a shallow low sulfidation epithermal system hosted in a collapse caldera. Our data also indicate that mineralization is structurally controlled by a fault system related to the 10.3 Ma collapse of Aguas Calientes caldera. The interpreted local stress field is consistent with the regional one.

Clay Mineralogy of AN Alluvial Aquifer in a Mountainous, Semiarid Terrain, AN Example from Rifle, Colorado

NASA Astrophysics Data System (ADS)

Elliott, W. C.; Lim, D.; Zaunbrecher, L. K.; Pickering, R. A.; Williams, K. H.; Navarre-Sitchler, A.; Long, P. E.; Noel, V.; Bargar, J.; Qafoku, N. P.

2015-12-01

Alluvial sediments deposited along the Colorado River corridor in the semi-arid regions of central to western Colorado can be important hosts for legacy contamination including U, V, As and Se. These alluvial sediments host aquifers which are thought to provide important "hot spots" and "hot moments" for microbiological activity controlling organic carbon processing and fluxes in the subsurface. Relatively little is known about the clay mineralogy of these alluvial aquifers and the parent alluvial sediments in spite of the fact that they commonly include lenses of silt-clay materials. These lenses are typically more reduced than coarser grained materials, but zones of reduced and more oxidized materials are present in these alluvial aquifer sediments. The clay mineralogy of the non-reduced parent alluvial sediments of the alluvial aquifer located in Rifle, CO (USA) is composed of chlorite, smectite, illite, kaolinite and quartz. The clay mineralogy of non-reduced fine-grained materials at Rifle are composed of the same suite of minerals found in the sediments plus a vermiculite-smectite intergrade that occurs near the bottom of the aquifer near the top of the Wasatch Formation. The clay mineral assemblages of the system reflect the mineralogically immature character of the source sediments. These assemblages are consistent with sediments and soils that formed in a moderately low rainfall climate and suggestive of minimal transport of the alluvial sediments from their source areas. Chlorite, smectite, smectite-vermiculite intergrade, and illite are the likely phases involved in the sorption of organic carbon and related microbial redox transformations of metals in these sediments. Both the occurrence and abundance of chlorite, smectite-vermiculite, illite and smectite can therefore exert an important control on the contaminant fluxes and are important determinants of biogeofacies in mountainous, semiarid terrains.

Combined structural analysis and dating of authigenic/synkinematic illite: A step towards unravelling brittle faulting processes in time and space

NASA Astrophysics Data System (ADS)

Viola, Giulio

2017-04-01

Faulting accommodates momentous deformation and its style reflects the complex interplay of often transient processes such as friction, fluid flow and rheological changes within generally dilatant systems. Brittle faults are thus unique archives of the stress state and the physical and chemical conditions at the time of both initial strain localization and subsequent slip(s) during structural reactivation. Opening those archives, however, may be challenging due to the commonly convoluted (if not even chaotic) nature of brittle fault architectures and fault rocks. This is because, once formed, faults are extremely sensitive to variations in stress field and environmental conditions and are prone to readily slip in a variety of conditions, also in regions affected by only weak, far-field stresses. The detailed, multi-scalar structural analysis of faults and of fault rocks has to be the starting point for any study aiming at reconstructing the complex framework of brittle deformation. However, considering that present-day exposures of faults only represent the end result of the faults' often protracted and heterogeneous histories, the obtained structural and mechanical results have to be integrated over the life span of the studied fault system. Dating of synkinematic illite/muscovite to constrain the time-integrated evolution of faults is therefore the natural addition to detailed structural studies. By means of selected examples it will be demonstrated how careful structural analysis integrated with illite characterization and K-Ar dating allows the high-resolution reconstruction of brittle deformation histories and, in turn, multiple constraints to be placed on strain localization, deformation mechanisms, fluid flow, mineral alteration and authigenesis within actively deforming brittle fault rocks. Complex and long brittle histories can thus be reconstructed and untangled in any tectonic setting.

Preliminary report on the clay mineralogy of the Upper Devonian Shales in the southern and middle Appalachian Basin

USGS Publications Warehouse

Hosterman, John W.; Loferski, Patricia J.

1978-01-01

The distribution of kaolinite in parts of the Devonian shale section is the most significant finding of this work. These shales are composed predominately of 2M illite and illitic mixed-layer clay with minor amounts of chlorite and kaolinite. Preliminary data indicate that kaolinite, the only allogenic clay mineral, is present in successively older beds of the Ohio Shale from south to north in the southern and middle parts of the Appalachian basin. This trend in the distribution of kaolinite shows a paleocurrent direction to the southwest. Three well-known methods of preparing the clay fraction for X-ray diffraction analysis were tested and evaluated. Kaolinite was not identified in two of the methods because of layering due to differing settling rates of the clay minerals. It is suggested that if one of the two settling methods of sample preparation is used, the clay film be thin enough for the X-ray beam to penetrate the entire thickness of clay.

Phase-dependent phytoavailability of thallium--a synthetic soil experiment.

PubMed

Vaněk, Aleš; Mihaljevič, Martin; Galušková, Ivana; Chrastný, Vladislav; Komárek, Michael; Penížek, Vít; Zádorová, Tereza; Drábek, Ondřej

2013-04-15

The study deals with the environmental stability of Tl-modified phases (ferrihydrite, goethite, birnessite, calcite and illite) and phytoavailability of Tl in synthetically prepared soils used in a model vegetation experiment. The data presented here clearly demonstrate a strong relationship between the mineralogical position of Tl in the model soil and its uptake by the plant (Sinapis alba L.). The maximum rate of Tl uptake was observed for plants grown on soil containing Tl-modified illite. In contrast, soil enriched in Ksat-birnessite had the lowest potential for Tl release and phytoaccumulation. Root-induced dissolution of synthetic calcite and ferrihydrite in the rhizosphere followed by Tl mobilization was detected. Highly crystalline goethite was more stable in the rhizosphere, compared to ferrihydrite, leading to reduced biological uptake of Tl. Based on the results obtained, the mineralogical aspect must be taken into account prior to general environmental recommendations in areas affected by Tl. Copyright © 2013 Elsevier B.V. All rights reserved.

The magnetic fabrics of experimentally deformed artificial clay-water dispersions

NASA Astrophysics Data System (ADS)

Richter, Carl; Frisch, Wolfgang; Ratschbacher, Lothar; Schwarz, Hans-Ulrich

1991-12-01

The development of magnetic fabrics in artificial clay-water dispersions and natural, hematite-bearing mudstones is investigated in plane-strain pure shear laboratory experiments under strain rates of 1.6 × 10 -5 and 2 × 10 -4s-1. The mixtures contain 0,15, 30 and 45% chlorite in an illite matrix, and 0, 1, 3, 6 and 8% magnetite in a kaolin matrix. Shortening up to 40% is imposed. The resulting fabrics show the following characteristics: (1) In the clay mixtures, the principal susceptibility axes ( kmax ≥ kint ≥ kmin) rotate away from the well defined initial fabric orientations into the princip strain directions ( e1 ≥ e2 ≥ e3) at strains > 30%. (2) Both mineralogical composition and initial magnetic fabric, but not the applied strain, influence the magnitudes of the principal susceptibility axes. (3) The illite-chlorite mixture series show an almost linear correlation between mineral concentration and susceptibility magnitudes. (4) Magnetite dominates the fabric of the magnetite-kaolin mixtures; the fabric is independent of the magnetite concentration.

The role of minerals in the thermal alteration of organic matter. IV - Generation of n-alkanes, acyclic isoprenoids, and alkenes in laboratory experiments

NASA Technical Reports Server (NTRS)

Huizinga, Bradley J.; Tannenbaum, Eli; Kaplan, Isaac R.

1987-01-01

The effect of common sedimentary minerals (illite, Na-montmorillonite, or calcite) under different water concentrations on the generation and release of n-alkanes, acyclic isoprenoids, and select alkenes from oil-prone kerogens was investigated. Matrices containing Green River Formation kerogen or Monterey Formation kerogen, alone or in the presence of minerals, were heated at 200 or 300 C for periods of up to 1000 hours, and the pyrolysis products were analyzed. The influence of the first two clay minerals was found to be critically dependent on the water content. Under the dry pyrolysis conditions, both minerals significantly reduced alkene formation; the C12+ n-alkanes and acyclic isoprenoids were mostly destroyed by montmorillonite, but underwent only minor alteration with illite. Under hydrous conditions (mineral/water of 2/1), the effects of both minerals were substantially reduced. Calcite had no significant effect on the thermal evolution of the hydrocarbons.

Deconvoluting complex structural histories archived in brittle fault zones

NASA Astrophysics Data System (ADS)

Viola, G.; Scheiber, T.; Fredin, O.; Zwingmann, H.; Margreth, A.; Knies, J.

2016-11-01

Brittle deformation can saturate the Earth's crust with faults and fractures in an apparently chaotic fashion. The details of brittle deformational histories and implications on, for example, seismotectonics and landscape, can thus be difficult to untangle. Fortunately, brittle faults archive subtle details of the stress and physical/chemical conditions at the time of initial strain localization and eventual subsequent slip(s). Hence, reading those archives offers the possibility to deconvolute protracted brittle deformation. Here we report K-Ar isotopic dating of synkinematic/authigenic illite coupled with structural analysis to illustrate an innovative approach to the high-resolution deconvolution of brittle faulting and fluid-driven alteration of a reactivated fault in western Norway. Permian extension preceded coaxial reactivation in the Jurassic and Early Cretaceous fluid-related alteration with pervasive clay authigenesis. This approach represents important progress towards time-constrained structural models, where illite characterization and K-Ar analysis are a fundamental tool to date faulting and alteration in crystalline rocks.

Late Quarternary Sedimentation in the Eastern Angola Basin.

DTIC Science & Technology

1973-11-01

Angola diapir field. Illite and montmorillonite are abundant in the southern part of the basin, reflecting the source in soils of South West Africa and...northward transport in the Benguela Current system. Kaolinite dominates the clay-mineral assemblage in the north-central part of the basin

Thermal Properties of Soils

DTIC Science & Technology

1981-12-01

plagio - clase feldspar and pyroxene. The tine fraction may Surface area and its effects contain the clay "sheet" minerals (i.e. kaolinite. illite...Pyroxene, Kaoliniwe Unified By By Ortho. Plagio . amphibole, Basic clay min. Hematite Soil Soil soil petrogr. X.ray clase clase and Igneous and clay and no

Mineralogical control of soil organic carbon persistence at the multidecadal time scale

NASA Astrophysics Data System (ADS)

Lutfalla, Suzanne; Barré, Pierre; Bernard, Sylvain; Le Guillou, Corentin; Chenu, Claire

2015-04-01

One of the current challenges in understanding the long term persistence of organic carbon in soils is to assess how mineral surfaces, especially at small scale, can stabilize soil organic carbon (SOC). The question we address in this work is whether different mineral species stabilize different types of SOC. Here we used the unique opportunity offered by long term bare fallows to study in situ C dynamics in several fine fractions of a silty loam soil. Indeed, with no vegetation i.e. no external input of fresh C, the plant-free soil of the Versailles 42 Plots (INRA, France) has been progressively enriched in persistent SOC during the 80 years of bare fallow. To separate mineral phases of the clay size fraction we performed a size fractionation on samples taken from 4 different plots at 5 different dates (0, 10, 22, 52, and 79 years after the beginning of the BF) and analyzed the SOC in the different fractions thus obtained. First, the clay fraction (< 2 µm) was isolated by wet sieving and centrifugation in water. Then, the clay fraction was further separated into 3 size fractions by centrifugation: fine clay (< 0.05 µm), intermediate clay (0.05 - 0.2 µm), and coarse clay (0.2 - 2 µm). X-ray diffraction was used to determine the mineralogy of the phases and we found that the coarse clay fraction on the one hand and fine and intermediate clay fractions on the other hand exhibited contrasted mineralogies. Fine and intermediate clay fractions contained almost exclusively smectite and mixed-layered illite/smectite minerals whereas coarse clays contained also discrete illite and kaolinite on top of smectite and illite/smectite. We carried out CHN elemental analysis to study the C and nitrogen dynamics with time in the different fractions. And synchrotron based spectroscopy and microscopy (NEXAFS bulk and STXM at the carbon K edge of 280 eV, CLS Saskatoon, Canada) was used to get information on the distribution and the chemical speciation of the SOC in fractions with contrasted mineralogies. Data analysis is still ongoing and full results will be presented at EGU. First results show that the dynamics and quality of the SOC differ in the different clay fractions. SOC decay was greater in coarse clays compared to intermediate clays, SOC in the coarse clay fraction displaying more diversity than in the other fractions. SOC persistence at the multidecadal timescale also seems to be mineral dependent: smectite being more efficient at protecting carbon compared to illite.

Minerals and clay minerals assemblages in organic-rich facies: the case study of the Sinemurian-Pliensbachian carbonate deposits of the western Lusitanian Basin (Portugal)

NASA Astrophysics Data System (ADS)

Caniço, Ana; Duarte, Luís V.; Silva, Ricardo L.; Rocha, Fernando; Graciano Mendonça Filho, João

2015-04-01

The uppermost Sinemurian-Pliensbachian series of the western part of the Lusitanian Basin is composed by hemipelagic carbonates particularly enriched in organic matter. Great part of this succession, considered to be one of the most important potential source rock intervals of Portugal, crops out in the S. Pedro de Moel and Peniche sectors, belonging to the Água de Madeiros and Vale das Fontes formations. In this study, supported by a detailed and integrated stratigraphic framework, we analyzed 98 marly samples (whole-rock mineralogy and clay minerals assemblages) from the aforementioned formations in the S. Pedro de Moel and Peniche sectors. X-ray Diffraction analysis followed the standard procedures and the semi-quantification of the different mineral phases was calculated using MacDiff 4.2.6. The goals of this work are to demonstrate the vertical variability of the mineral composition of these two units and investigate the relationship between the clay minerals assemblages and the content in organic matter (Total organic carbon: TOC). Besides the abundance of calcite and phyllosilicates, whole-rock mineralogy revealed the presence of quartz, potassium feldspar, dolomite, and pyrite (trace amounts). Other minerals like anhydrite, barite and gypsum occur sporadically. The clay minerals assemblages are dominated by illite+illite/smectite mixed-layers (minimum of 59%), always associated with kaolinite (maximum of 37%) and chlorite (maximum of 25%); sporadically smectite occurs in trace amounts. Generally, high TOC levels (i.e., black shale facies with TOC reaching up to 22 wt.% in both units, see Duarte et al., 2010), show a major increase in chlorite and kaolinite (lower values of illite+illite/smectite mixed layers). A kaolinite enrichment is also observed just above the Sinemurian-Pliensbachian boundary (base of Praia da Pedra Lisa Member of Água de Madeiros Formation; values varying between 30 and 37%). This event is associated with a second-order regressive phase, and marks the disappearance of the organic-rich facies and increase of carbonate sedimentation. This enrichment was likely favored by the development of more humid conditions at the Sinemurian-Pliensbachian transition. References Duarte, L.V., Silva, R.L., Oliveira, L.C.V., Comas-Rengifo, M.J., Silva, F. 2010. Organic-rich facies in the Sinemurian and Pliensbachian of the Lusitanian Basin, Portugal: Total Organic Carbon distribution and relation to transgressive-regressive facies cycles. Geologica Acta 8, 325-340.

Modeling selenate adsorption behavior on oxides, clay minerals, and soils using the triple layer model

USDA-ARS?s Scientific Manuscript database

Selenate adsorption behavior was investigated on amorphous aluminum oxide, amorphous iron oxide, goethite, clay minerals: kaolinites, montmorillonites, illite, and 18 soil samples from Hawaii, and the Southwestern and the Midwestern regions of the US as a function of solution pH. Selenate adsorpti...

Modeling selenite adsorption envelopes on oxides, clay minerals, and soils using the triple layer model

USDA-ARS?s Scientific Manuscript database

Selenite adsorption behavior was investigated on amorphous aluminum and iron oxides, clay minerals: kaolinite, montmorillonite, and illite, and 45 surface and subsurface soil samples from the Southwestern and Midwestern regions of the USA as a function of solution pH. Selenite adsorption decreased ...

POLISHING INDUSTRIAL WASTE STREAM EFFLUENTS USING FLY ASH - NATURAL CLAY SORBENT COMBINATION

EPA Science Inventory

A laboratory evaluation of the use of acidic and basic fly ashes, bentonite, bauxite, illite, kaolinite, zeolite, vermiculite, and activated alumina is presented for polishing a 3.8 x 10 to the 6th power liters per day waste stream from the feldspar mining and processing industry...

Information Communications Technology Support to Reconstruction and Development: Some Observations from Afghanistan

DTIC Science & Technology

2007-06-01

banditry. Afghan women are still among the worst off in the world: most are illite many have no access to healthcare, and child and forced marriages...Cyber security » Virus and spyware protection, intrusion detection-protection, firewalls » Control use of pirated software and porn surfing by

A comprehensive laboratory study on the immersion freezing behavior of illite NX particles: a comparison of 17 ice nucleation measurement techniques

NASA Astrophysics Data System (ADS)

Hiranuma, N.; Augustin-Bauditz, S.; Bingemer, H.; Budke, C.; Curtius, J.; Danielczok, A.; Diehl, K.; Dreischmeier, K.; Ebert, M.; Frank, F.; Hoffmann, N.; Kandler, K.; Kiselev, A.; Koop, T.; Leisner, T.; Möhler, O.; Nillius, B.; Peckhaus, A.; Rose, D.; Weinbruch, S.; Wex, H.; Boose, Y.; DeMott, P. J.; Hader, J. D.; Hill, T. C. J.; Kanji, Z. A.; Kulkarni, G.; Levin, E. J. T.; McCluskey, C. S.; Murakami, M.; Murray, B. J.; Niedermeier, D.; Petters, M. D.; O'Sullivan, D.; Saito, A.; Schill, G. P.; Tajiri, T.; Tolbert, M. A.; Welti, A.; Whale, T. F.; Wright, T. P.; Yamashita, K.

2015-03-01

Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice-nucleating particles. However, an intercomparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques. Within the framework of INUIT (Ice Nuclei Research Unit), we distributed an illite-rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature (T), cooling rate and nucleation time. A total of 17 measurement methods were involved in the data intercomparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while 10 other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing data set was evaluated using the ice nucleation active surface-site density, ns, to develop a representative ns(T) spectrum that spans a wide temperature range (-37 °C < T < -11 °C) and covers 9 orders of magnitude in ns. In general, the 17 immersion freezing measurement techniques deviate, within a range of about 8 °C in terms of temperature, by 3 orders of magnitude with respect to ns. In addition, we show evidence that the immersion freezing efficiency expressed in ns of illite NX particles is relatively independent of droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature dependence and weak time and size dependence of the immersion freezing efficiency of illite-rich clay mineral particles enabled the ns parameterization solely as a function of temperature. We also characterized the ns(T) spectra and identified a section with a steep slope between -20 and -27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below -27 °C. While the agreement between different instruments was reasonable below ~ -27 °C, there seemed to be a different trend in the temperature-dependent ice nucleation activity from the suspension and dry-dispersed particle measurements for this mineral dust, in particular at higher temperatures. For instance, the ice nucleation activity expressed in ns was smaller for the average of the wet suspended samples and higher for the average of the dry-dispersed aerosol samples between about -27 and -18 °C. Only instruments making measurements with wet suspended samples were able to measure ice nucleation above -18 °C. A possible explanation for the deviation between -27 and -18 °C is discussed. Multiple exponential distribution fits in both linear and log space for both specific surface area-based ns(T) and geometric surface area-based ns(T) are provided. These new fits, constrained by using identical reference samples, will help to compare IN measurement methods that are not included in the present study and IN data from future IN instruments.

A comprehensive laboratory study on the immersion freezing behavior of illite NX particles: a comparison of seventeen ice nucleation measurement techniques

NASA Astrophysics Data System (ADS)

Hiranuma, N.; Augustin-Bauditz, S.; Bingemer, H.; Budke, C.; Curtius, J.; Danielczok, A.; Diehl, K.; Dreischmeier, K.; Ebert, M.; Frank, F.; Hoffmann, N.; Kandler, K.; Kiselev, A.; Koop, T.; Leisner, T.; Möhler, O.; Nillius, B.; Peckhaus, A.; Rose, D.; Weinbruch, S.; Wex, H.; Boose, Y.; DeMott, P. J.; Hader, J. D.; Hill, T. C. J.; Kanji, Z. A.; Kulkarni, G.; Levin, E. J. T.; McCluskey, C. S.; Murakami, M.; Murray, B. J.; Niedermeier, D.; Petters, M. D.; O'Sullivan, D.; Saito, A.; Schill, G. P.; Tajiri, T.; Tolbert, M. A.; Welti, A.; Whale, T. F.; Wright, T. P.; Yamashita, K.

2014-08-01

Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice nucleating particles (INPs). However, an inter-comparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques. Within the framework of INUIT (Ice Nucleation research UnIT), we distributed an illite rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature (T), cooling rate and nucleation time. Seventeen measurement methods were involved in the data inter-comparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while ten other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing dataset was evaluated using the ice nucleation active surface-site density (ns) to develop a representative ns(T) spectrum that spans a wide temperature range (-37 °C < T < -11 °C) and covers nine orders of magnitude in ns. Our inter-comparison results revealed a discrepancy between suspension and dry-dispersed particle measurements for this mineral dust. While the agreement was good below ~ -26 °C, the ice nucleation activity, expressed in ns, was smaller for the wet suspended samples and higher for the dry-dispersed aerosol samples between about -26 and -18 °C. Only instruments making measurement techniques with wet suspended samples were able to measure ice nucleation above -18 °C. A possible explanation for the deviation between -26 and -18 °C is discussed. In general, the seventeen immersion freezing measurement techniques deviate, within the range of about 7 °C in terms of temperature, by three orders of magnitude with respect to ns. In addition, we show evidence that the immersion freezing efficiency (i.e., ns) of illite NX particles is relatively independent on droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature-dependence and weak time- and size-dependence of immersion freezing efficiency of illite-rich clay mineral particles enabled the ns parameterization solely as a function of temperature. We also characterized the ns (T) spectra, and identified a section with a steep slope between -20 and -27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below -27 °C. A multiple exponential distribution fit is expressed as ns(T) = exp(23.82 × exp(-exp(0.16 × (T + 17.49))) + 1.39) based on the specific surface area and ns(T) = exp(25.75 × exp(-exp(0.13 × (T + 17.17))) + 3.34) based on the geometric area (ns and T in m-2 and °C, respectively). These new fits, constrained by using an identical reference samples, will help to compare IN measurement methods that are not included in the present study and, thereby, IN data from future IN instruments.

Stanford-USGS shrimp-RG ion microprobe: A new approach to determining the distribution of trace elements in coal

USGS Publications Warehouse

Kolker, A.; Wooden, J.L.; Persing, H.M.; Zielinski, R.A.

2000-01-01

The distribution of Cr and other trace metals of environmental interest in a range of widely used U.S. coals was investigated using the Stanford-USGS SHRIMP-RG ion microprobe . Using the oxygen ion source, concentrations of Cr (11 to 176 ppm), V (23 to 248 ppm), Mn (2 to 149 ppm), Ni (2 to 30 ppm), and 13 other elements were determined in illite/smectite, a group of clay minerals commonly present in coal. The results confirm previous indirect or semi-quantitative determinations indicating illite/smectite to be an important host of these metals. Calibration was achieved using doped aluminosilicate-glass synthetic standards and glasses prepared from USGS rock standards. Grains for analysis were identified optically, and confirmed by 1) precursory electron microprobe analysis and wavelength-dispersive compositional mapping, and 2) SHRIMP-RG major element data obtained concurrently with trace element results. Follow-up investigations will focus on the distribution of As and other elements that are more effectively ionized with the cesium primary beam currently being tested.

The tectonic significance of K/Ar illite fine-fraction ages from the San Luis Formation (Eastern Sierras Pampeanas, Argentina)

NASA Astrophysics Data System (ADS)

Wemmer, Klaus; Steenken, André; Müller, Stefan; de Luchi, Mónica G. López; Siegesmund, Siegfried

2011-04-01

The Sierra de San Luis forms the southern tip of the Eastern Sierras Pampeanas in central Argentina. Two narrow belts of low-grade phyllites and quartz arenites, i.e. the San Luis Formation, have accommodated part of the strain-related differential exhumation of the medium- to high-grade metamorphic domains that constitute to the basement complex of the sierra. Eleven phyllite samples were subjected to the K/Ar fine-fraction dating technique. Results are interpreted in relation to the Kübler index of the illites, which indicate epimetamorphic conditions for the majority of the samples. Obtained ages between 330 and 290 Ma cover a period of compressional tectonics in the late Mississippian (Visean/Serpukhovian boundary) followed by the subsidence during the formation of the Paganzo Basin in the provinces of La Rioja and San Luis. These tectonic movements are coincident with the Toco orogeny in northern Chile and southern Bolivia. This suggests that the older K/Ar ages document the compressional stage and that younger ages record the cooling of the basement during the subsequent extensional uplift of the basement.

Chemical remagnetization and clay diagenesis: testing the hypothesis in the Cretaceous sedimentary rocks of northwestern Montana

NASA Astrophysics Data System (ADS)

Gill, J. D.; Elmore, R. D.; Engel, M. H.

Although the migration of fluids is a likely agent of remagnetization for some chemical remanent magnetizations (CRMs), widespread CRMs, which occur in rocks that have not been altered by externally derived fluids, need to explained by another mechanism. We are testing clay diagenesis as a remagnetization mechanism for such CRMs by comparing results from Mesozoic strata in the disturbed belt of Montana where the rocks contain ordered illite/smectite that formed by moderate heating as a result of thrust loading, with equivalent strata on the adjacent Sweetgrass Arch which contain unaltered smectite-rich clay mineral assemblages. The results indicate that the magnetization in the rocks in the Sweetgrass Arch is weak and dominated by a modern viscous component. In contrast, the disturbed belt rocks have higher magnetic intensities and contain a prefolding or early synfolding, reversed tertiary magnetization that is interpreted to be a CRM residing in magnetite and perhaps pyrrhotite. A presence-absence test and the timing of acquisition for the CRM suggest that magnetite authigenesis could be related to the smectite-to-illite conversion.

Ore deposits and epithermal evidences associated with intra-magmatic faults at Aïn El Araâr-Oued Belif ring structure (NW of Tunisia)

NASA Astrophysics Data System (ADS)

Aissa, Wiem Ben; Aissa, Lassaâd Ben; Amara, Abdesslem Ben Haj; Tlig, Said; Alouani, Rabah

2017-03-01

Hydrothermal ore deposits at Aïn El Araâr-Oued Belif location are classified as epithermal deposits type. The ore bodies are hosted by upper Turonian (8-9 M.y) volcanic rhyodacitic complex. Polymetallic sulfide orebodies are mainly concentrated within intra-magmatic faults. Petrographic, XRD, and TEM-STEM investigations revealed that ore minerals are essentially, arsenopyrite, pyrite, chalcopyrite, pyrrhotite, hematite, goethite and magnetite with Au, Ag and Pt trace metals. Gangue minerals are mainly adularia, quartz, sericite, alunite, tridymite, chlorite, phlogopite and smectite. Epithermal alteration is well zoned with four successive characteristic zones: (1) zone of quartz-adularia-sericite and rare alunite; (2) zone of kaolinite and plagioclase albitization; (3) intermediate zone of illite-sericite; (4) sapropelic alteration type zone of chlorite-smectite and rare illite. This can be interpreted as a telescoping of two different acidity epithermal phases; low sulfidation (adularia-sericite) and high sulfidation (quartz-alunite), separated in time or due to a gradual increase of fluids acidity and oxicity within the same mineralization phase. Brecciated macroscopic facies with fragments hosting quartz-adularia-sericite minerals (low-sulfidation phase) without alunite, support the last hypothesis. Geodynamic context and mineral alteration patterns are closely similar to those of Maria Josefa gold mine at SE of Spain which exhibit a volcanic-hosted epithermal ore deposit in a similar vein system, within rhyolitic ignimbrites, altered to an argillic assemblage (illite-sericite abundant and subordinate kaolinite) that grades outwards into propylitic alteration (Sanger-von Oepen et al. (1990)). Mineralogical and lithologic study undertaken in the volcanic host rock at Aïn El Araâr-Oued Belif reveals a typical epithermal low-sulfidation and high-sulfidation ore deposits with dominance of low-sulfidation. Host rocks in these systems range from silicic to intermediate for adularia-sericite type (low sulfidation) to rhyodacite for quartz-alunite type (high sulfidation).

Clay-mineral suites, sources, and inferred dispersal routes: Southern California continental shelf

USGS Publications Warehouse

Hein, J.R.; Dowling, J.S.; Schuetze, A.; Lee, H.J.

2003-01-01

Clay mineralogy is useful in determining the distribution, sources, and dispersal routes of fine-grained sediments. In addition, clay minerals, especially smectite, may control the degree to which contaminants are adsorbed by the sediment. We analyzed 250 shelf sediment samples, 24 river-suspended-sediment samples, and 12 river-bed samples for clay-mineral contents in the Southern California Borderland from Point Conception to the Mexico border. In addition, six samples were analyzed from the Palos Verdes Headland in order to characterize the clay minerals contributed to the offshore from that point source. The <2 ??m-size fraction was isolated, Mg-saturated, and glycolated before analysis by X-ray diffraction. Semi-quantitative percentages of smectite, illite, and kaolinite plus chlorite were calculated using peak areas and standard weighting factors. Most fine-grained sediment is supplied to the shelf by rivers during major winter storms, especially during El Nin??o years. The largest sediment fluxes to the region are from the Santa Ynez and Santa Clara Rivers, which drain the Transverse Ranges. The mean clay-mineral suite for the entire shelf sediment data set (26% smectite, 50% illite, 24% kaolinite+chlorite) is closely comparable to that for the mean of all the rivers (31% smectite, 49% illite, 20% kaolinite+chlorite), indicating that the main source of shelf fine-grained sediments is the adjacent rivers. However, regional variations do exist and the shelf is divided into four provinces with characteristic clay-mineral suites. The means of the clay-mineral suites of the two southernmost provinces are within analytical error of the mineral suites of adjacent rivers. The next province to the north includes Santa Monica Bay and has a suite of clay minerals derived from mixing of fine-grained sediments from several sources, both from the north and south. The northernmost province clay-mineral suite matches moderately well that of the adjacent rivers, but does indicate some mixing from sources in adjacent provinces.

Evidence for low-grade metamorphism, hydrothermal alteration, and diagenesis on Mars from phyllosilicate mineral assemblages

USGS Publications Warehouse

Ehlmann, Bethany L.; Mustard, John F; Clark, Roger N.; Swayze, Gregg A.; Murchie, Scott L.

2011-01-01

The enhanced spatial and spectral resolution provided by the Compact Reconnaissance Imaging Spectrometer for Mars (CRISM) on the Mars Reconnaissance Orbiter (MRO) has led to the discovery of numerous hydrated silicate minerals on Mars, particularly in the ancient, cratered crust comprising the southern highlands. Phases recently identified using visible/near-infrared spectra include: smectite, chlorite, prehnite, high-charge phyllosilicates (illite or muscovite), the zeolite analcime, opaline silica, and serpentine. Some mineral assemblages represent the products of aqueous alteration at elevated temperatures. Geologic occurrences of these mineral assemblages are described using examples from west of the Isidis basin near the Nili Fossae and with reference to differences in implied temperature, fluid composition, and starting materials during alteration. The alteration minerals are not distributed homogeneously. Rather, certain craters host distinctive alteration assemblages: (1) prehnite-chlorite-silica, (2) analcime-silica-Fe,Mg-smectite-chlorite, (3) chlorite-illite (muscovite), and (4) serpentine, which furthermore has been found in bedrock units. These assemblages contrast with the prevalence of solely Fe,Mg-smectites in most phyllosilicate-bearing terrains on Mars, and they represent materials altered at depth then exposed by cratering. Of the minerals found to date, prehnite provides the clearest evidence for subsurface, hydrothermal/metamorphic alteration, as it forms only under highly restricted conditions (T = 200–400ºC). Multiple mechanisms exist for forming the other individual minerals; however, the most likely formation mechanisms for the characteristic mineralogic assemblages observed are, for (1) and (2), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in basalt; for (3), transformation of trioctahedral smectites to chlorite and dioctahedral smectites to illite during diagenesis; and for (4), low-grade metamorphism or hydrothermal (<400ºC) circulation of fluids in ultramafic rocks. Evidence for high-grade metamorphism at elevated pressures or temperatures >400ºC has not been found.

Diagenesis and reservoir quality of the Lower Cretaceous Quantou Formation tight sandstones in the southern Songliao Basin, China

NASA Astrophysics Data System (ADS)

Xi, Kelai; Cao, Yingchang; Jahren, Jens; Zhu, Rukai; Bjørlykke, Knut; Haile, Beyene Girma; Zheng, Lijing; Hellevang, Helge

2015-12-01

The Lower Cretaceous Quantou Formation in the southern Songliao Basin is the typical tight oil sandstone in China. For effective exploration, appraisal and production from such a tight oil sandstone, the diagenesis and reservoir quality must be thoroughly studied first. The tight oil sandstone has been examined by a variety of methods, including core and thin section observation, XRD, SEM, CL, fluorescence, electron probing analysis, fluid inclusion and isotope testing and quantitative determination of reservoir properties. The sandstones are mostly lithic arkoses and feldspathic litharenites with fine to medium grain size and moderate to good sorting. The sandstones are dominated by feldspar, quartz, and volcanic rock fragments showing various stages of disintegration. The reservoir properties are quite poor, with low porosity (average 8.54%) and permeability (average 0.493 mD), small pore-throat radius (average 0.206 μm) and high displacement pressure (mostly higher than 1 MPa). The tight sandstone reservoirs have undergone significant diagenetic alterations such as compaction, feldspar dissolution, quartz cementation, carbonate cementation (mainly ferrocalcite and ankerite) and clay mineral alteration. As to the onset time, the oil emplacement was prior to the carbonate cementation but posterior to the quartz cementation and feldspar dissolution. The smectite to illite reaction and pressure solution at stylolites provide a most important silica sources for quartz cementation. Carbonate cements increase towards interbedded mudstones. Mechanical compaction has played a more important role than cementation in destroying the reservoir quality of the K1q4 sandstone reservoirs. Mixed-layer illite/smectite and illite reduced the porosity and permeability significantly, while chlorite preserved the porosity and permeability since it tends to be oil wet so that later carbonate cementation can be inhibited to some extent. It is likely that the oil emplacement occurred later than the tight rock formation (with the porosity close to 10%). However, thicker sandstone bodies (more than 2 m) constitute potential hydrocarbon reservoirs.

To what extent clay mineralogy affects soil aggregation? Consequences for soil organic matter stabilization

NASA Astrophysics Data System (ADS)

Fernandez-Ugalde, O.; Barré, P.; Hubert, F.; Virto, I.; Chenu, C.; Ferrage, E.; Caner, L.

2012-12-01

Aggregation is a key process for soil functioning as it influences C storage, vulnerability to erosion and water holding capacity. While the influence of soil organic C on aggregation has been documented, much less is known about the role of soil mineralogy. Soils usually contain a mixture of clay minerals with contrasted surface properties, which should result on different abilities of clay minerals to aggregation. We took advantage of the intrinsic mineral heterogeneity of a temperate Luvisol to compare the role of clay minerals (illite, smectite, kaolinite, and mixed-layer illite-smectite) in aggregation. In a first step, grassland and tilled soil samples were fractionated in water in aggregate-size classes according to the hierarchical model of aggregation (Tisdall and Oades, 1982). Clay mineralogy and organic C in the aggregate-size classes were analyzed. The results showed that interstratified minerals containing swelling phases accumulated in aggregated fractions (>2 μm) compared to free clay fractions (<2 μm) in the two land-uses. The accumulation increased from large macro-aggregates (>500 μm) to micro-aggregates (50-250 μm). C concentration and C/N ratio followed the opposite trend. These results constitute a clay mineral-based evidence for the hierarchical model of aggregation, which postulates an increasing importance of the reactivity of clay minerals in the formation of micro-aggregates compared to larger aggregates. In the latter aggregates, formation relies on the physical enmeshment of particles by fungal hyphae, and root and microbial exudates. In a second step, micro-aggregates from the tilled soil samples were submitted to increasingly disaggregating treatments by sonication to evaluate the link between their water stability and clay mineralogy. Micro-aggregates with increasing stability showed an increase of interstratified minerals containing swelling phases and C concentration for low intensities of disaggregation (from 0 to 5 J mL-1). This suggests that swelling phases promote their stability. Swelling phases and organic C decreased for greater intensities of disaggregation. These results and the SEM images taken at different disaggregation intensities indicate that when increasing disaggregation intensity above 5 J mL-1, the recovered material consists on sand particles covered by physical coatings of illite and kaolinite. Our results show that different clay minerals have different contribution to soil aggregation. Swelling phases are especially important for water-stable aggregates formation, whereas illite and kaolinite can either contribute to aggregation or been coated to sand grains in "mineral aggregates", without porosity and organic C protection capability. In conclusion, soils with large proportion of swelling clay minerals have greater potential for carbon storage by occlusion in aggregates and greater resistance to erosion. Tisdall JM, Oades JM (1982) Organic matter and water-stable aggregates in soils. J Soil Sci 62: 141-163.

Sorption of Sr, Co and Zn on illite: Batch experiments and modelling including Co in-diffusion measurements on compacted samples

NASA Astrophysics Data System (ADS)

Montoya, V.; Baeyens, B.; Glaus, M. A.; Kupcik, T.; Marques Fernandes, M.; Van Laer, L.; Bruggeman, C.; Maes, N.; Schäfer, T.

2018-02-01

Experimental investigations on the uptake of divalent cations (Sr, Co and Zn) onto illite (Illite du Puy, Le-Puy-en-Velay, France) were carried out by three different international research groups (Institute for Nuclear Waste Disposal, KIT (Germany), Group Waste & Disposal, SCK-CEN, (Belgium) and Laboratory for Waste Management, PSI (Switzerland)) in the framework of the European FP7 CatClay project. The dependence of solid-liquid distribution ratios (Rd values) on pH at trace metal conditions (sorption edges) and on the metal ion concentration (sorption isotherms) was determined in dilute suspensions of homo-ionic Na-illite (Na-IdP) under controlled N2 atmosphere. The experimental results were modelled using the 2 Site Protolysis Non Electrostatic Surface Complexation and Cation Exchange (2SPNE SC/CE) sorption model. The sorption of Sr depends strongly on ionic strength, while a rather weak pH dependence is observed in a pH range between 3 and 11. The data were modelled with cation exchange reactions, taking into account competition with H, K, Ca, Mg and Al, and surface complexation on weak amphotheric edge sites at higher pH values. The sorption of Co on Na-IdP, however, is strongly pH dependent. Cation exchange on the planar sites and surface complexation on strong and weak amphoteric edge sites were used to describe the Co sorption data. Rd values for Co derived from in-diffusion measurements on compacted Na-IdP samples (bulk-dry density of 1700 kg m-3) between pH 5.0 and 9.0 are in good agreement with the batch sorption data. The equivalence of both approaches to measure sorption was thus confirmed for the present test system. In addition, the results highlight the importance of both major and minor surface species for the diffusive transport behaviour of strongly sorbing metal cations. While surface complexes at the edge sites determine largely the Rd value, the diffusive flux may be governed by those species bound to the planar sites, even at low fractional occupancies. The pH dependent sorption determined for trace Zn concentrations showed large Rd values across the entire pH range with almost no dependence on the background electrolyte concentration. Additional sorption experiments carried out at substantial fractional Zn loadings demonstrated that the selectivity for the exchange of Na+ for Zn2+ at the planar sites could not explain the large Rd values measured at low pH and trace Zn concentrations. This suggests that another mechanism is ruling Zn uptake under these conditions.

Distribution of clay minerals on the Alaskan margin near Barrow Canyon revealed by Diffuse Spectral Reflectance measurements

NASA Astrophysics Data System (ADS)

Orsburn, C.; Ortiz, J. D.; Polyak, L.; Grebmeier, J. M.; Darby, D.

2007-12-01

Sediment clay mineral assemblages provide an excellent means of assessing the provenance of Arctic sediment due to the variety of sediment transport mechanisms at work and the existence of distinct weathering sources from differing bedrock geology. During HOTRAX Leg 1 aboard the USCG Ice breaker Healy (cruise HLY0501), we collected jumbo piston cores on the Alaskan margin near Barrow Canyon which provide detailed Holocene sedimentary records. Measurements of Diffuse Spectral Reflectance (DSR) were collected at 1cm resolution from the split surface of the cores using a Minolta CM-2600d UV/VIS spectrophotometer (400-700nm wavelength range; 10nm resolution; 3mm spot size). To interpret the resulting downcore records, we present a preliminary study using 28 coretop sediment samples collected by the Shelf-Basin Interaction program in 2004 arrayed in four transects across the shelf near Barrow Canyon. The samples were analyzed using an ASD Labspec Pro FR UV/VIS/NIR spectrometer (250-2500nm wavelength range, 2-10nm resolution; 20mm spot size). Our results indicate that the measurements from the two instruments are offset by constant factors, but can be easily compared. To estimate the clay mineralogy of the cores, we decomposed the matrix of DSR measurements from the coretop and downcore samples using principle component analysis and compared the resulting factor score patterns with mineral diffuse spectral reflectance signatures from known samples measured in our lab or available from version 5 of the USGS Digital Spectral Library. The three leading modes extracted by principle component analysis of the downcore samples are applicable to the coretops. We infer that the first principle component mode relates to smectite, the second to chlorite, and the third to a mixture of illite and goethite (herein referred to as illite - goethite). The geographic and bathymetric trends in the coretop data indicate that (1) the smectite and illite - goethite components both increase with depth and reach greater values in the two western transects than in the two eastern transects closest to the coast and Barrow Canyon, (2) the smectite and illite- goethite components are anticorrelated in the two western transects, but not in the two eastern transects, (3) chlorite decreases with depth and is highest in the two transects closest to Barrow Canyon. These results suggest that the chlorite on the Alaskan margin is transported by nearshore currents from the Bering Straight and then by bottom currents flowing through the Barrow Canyon. Accordingly, we interpret downcore chlorite peaks inferred from DSR measurements in our sediment cores as evidence of times of enhanced input of Pacific water to the Alaskan Margin.

Oxygen and hydrogen isotope geochemistry of Cretaceous bentonites and shales from the Disturbed Belt, Montana

NASA Astrophysics Data System (ADS)

Eslinger, Eric V.; Yeh, Hsueh-Wen

1986-01-01

The mineralogy, δO 18, and δD of the <0.1 μm fraction of 22 Cretaceous bentonites and the mineralogy and δO 18 of the < 0.1 μm fraction of 14 adjacent shales collected from outcrops in the Sweetgrass Arch and Disturbed Belt, Montana, have been determined. Mixed-layer illite/smectite (I/S) is the dominant mineral in the bulk bentonite and usually the only mineral in the < 0.1 μm fraction. I/S is also the major clay mineral in the shales. The diagenetic grade in bentonite is qualitatively given by the percentage of illite layers in I/S, which varies from 2 to 25 (Sweetgrass Arch) to as high as 95 (Disturbed Belt). δO 18 of < 0.1 μm bentonite generally decreases from about +20%. to about +13%. with increasing diagenetic grade. On a plot of δD versus δO 18, data for the < 0.1 μm bentonite define a field that generally parallels, but falls on the meteoric water line side of the smectite-water line (Savin and Epstein, 1970). δO 18 of bulk bentonite is 1 to 3%. more negative than the δO 18 of the < 0.1 μm fraction, due to the presence of volcanic quartz and feldspar. δO 18 of several size fractions of clay-sized quartz separated from the bentonite varies from +11%. to +24%., and, in a given bentonite, generally increases with decreasing grain size. Among the different bentonites, the δO 18 range of the different grain sizes decreases as the percentage of illite layers in the coexisting I/S increases. The δO 18 of 0.1-0.5 μm shale quartz is generally 1 to 4%. more positive than clay-sized quartz from an adjacent bentonite, and the δO 18 of < 0.1 μm I/S concentrate of shales is generally < 1 to 4%. more negative than the < 0.1 μm I/S from an adjacent bentonite. Isotopic temperatures, interpreted to be maximum burial temperatures, range between about 160°C (shale), to about 250°C (bentonite). The isotopic data can be interpreted using the stages: 1) deposition of volcanic glassy ash containing some quartz and feldspar; 2) devitrification into mostly 100% expandable smectite with a δO 18 of about 20%. and δD of -60 to -80%.; 3) tectonic burial beneath thrust sheets in the Disturbed Belt region which induced elevated temperatures that allowed oxygen and hydrogen isotope reequilibration as the percentage of illite layers in I/S increased and diagenetic quartz formed; and 4) exhumation of the strata with preservation of O 18/O 16 and D/H attained during burial.

Mid-Holocene Strengthening of the Bering Strait Inflow to the Arctic and its Linkage With the North Atlantic Subpolar Gyre Circulation

NASA Astrophysics Data System (ADS)

Yamamoto, M.; Nam, S. I.; Polyak, L.; Kobayashi, D.; Suzuki, K.; Irino, T.; Shimada, K.

2017-12-01

The Bering Strait inflow (BSI) is an important element of the Arctic Ocean circulation system. We report records of the chlorite/illite ratios in three sediment cores from the northern Chukchi Sea providing insights into the long-term dynamics of the BSI during the Holocene. The BSI approximation by the chlorite/illite record, despite a considerable geographic variability, consistently shows intensified flow from the Bering Sea to the Arctic during the middle Holocene, which is attributed primarily to the effect of higher atmospheric pressure over the Aleutian Basin. The intensified BSI was associated with decrease in sea-ice concentrations and increase in marine production, as indicated by biomarker concentrations, suggesting a major influence of the BSI on sea-ice and biological conditions in the Chukchi Sea. Multi-century to millennial fluctuations, presumably controlled by solar activity, were also identified. This middle Holocene strengthening of the BSI was coeval with intense subpolar gyre circulation in the North Atlantic. We propose that the BSI is linked with the North Atlantic circulation via an atmospheric teleconnection between the Aleutian and Icelandic Lows.

Exploration of geo-mineral compounds in granite mining soils using XRD pattern data analysis

NASA Astrophysics Data System (ADS)

Koteswara Reddy, G.; Yarakkula, Kiran

2017-11-01

The purpose of the study was to investigate the major minerals present in granite mining waste and agricultural soils near and away from mining areas. The mineral exploration of representative sub-soil samples are identified by X-Ray Diffractometer (XRD) pattern data analysis. The morphological features and quantitative elementary analysis was performed by Scanning Electron Microscopy-Energy Dispersed Spectroscopy (SEM-EDS).The XRD pattern data revealed that the major minerals are identified as Quartz, Albite, Anorthite, K-Feldspars, Muscovite, Annite, Lepidolite, Illite, Enstatite and Ferrosilite in granite waste. However, in case of agricultural farm soils the major minerals are identified as Gypsum, Calcite, Magnetite, Hematite, Muscovite, K-Feldspars and Quartz. Moreover, the agricultural soils neighbouring mining areas, the minerals are found that, the enriched Mica group minerals (Lepidolite and Illite) the enriched Orthopyroxene group minerals (Ferrosilite and Enstatite). It is observed that the Mica and Orthopyroxene group minerals are present in agricultural farm soils neighbouring mining areas and absent in agricultural farm soils away from mining areas. The study demonstrated that the chemical migration takes place at agricultural farm lands in the vicinity of the granite mining areas.

Correlation between thermal behavior of clays and their chemical and mineralogical composition: a review

NASA Astrophysics Data System (ADS)

Dwi Yanti, Evi; Pratiwi, I.

2018-02-01

Clay's abundance has been widely used as industrial raw materials, especially ceramic and tile industries. Utilization of these minerals needs a thermal process for producing ceramic products. Two studies conducted by Septawander et al. and Chin C et al., showed the relationship between thermal behavior of clays and their chemical and mineralogical composition. Clays are characterized by XRD analysis and thermal analysis, ranging from 1100°C to 1200°C room temperature. Specimen of raw materials of clay which is used for the thermal treatment is taken from different geological conditions and formation. In raw material, Quartz is almost present in all samples. Halloysite, montmorillonite, and feldspar are present in Tanjung Morawa raw clay. KC and MC similar kaolinite and illite are present in the samples. The research illustrates the interrelationships of clay minerals and chemical composition with their heat behavior. As the temperature of combustion increases, the sample reduces a significant weight. The minerals which have undergone a transformation phase became mullite, cristobalite or illite and quartz. Under SEM analysis, the microstructures of the samples showed irregularity in shape; changes occurred due the increase of heat.

A comprehensive laboratory study on the immersion freezing behavior of illite NX particles. A comparison of 17 ice nucleation measurement techniques

DOE Office of Scientific and Technical Information (OSTI.GOV)

Hiranuma, Naruki; Augustin-Bauditz, Stefanie; Bingemer, Heinz

Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice-nucleating particles. However, an intercomparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques.more » Within the framework of INUIT (Ice Nuclei Research Unit), we distributed an illite-rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature ( T), cooling rate and nucleation time. A total of 17 measurement methods were involved in the data intercomparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while 10 other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing data set was evaluated using the ice nucleation active surface-site density, n s, to develop a representative n s( T) spectrum that spans a wide temperature range (-37 °C < T < -11 °C) and covers 9 orders of magnitude in n s. In general, the 17 immersion freezing measurement techniques deviate, within a range of about 8 °C in terms of temperature, by 3 orders of magnitude with respect to n s. In addition, we show evidence that the immersion freezing efficiency expressed in n s of illite NX particles is relatively independent of droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature dependence and weak time and size dependence of the immersion freezing efficiency of illite-rich clay mineral particles enabled the n s parameterization solely as a function of temperature. We also characterized the n s( T) spectra and identified a section with a steep slope between -20 and -27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below -27 °C. While the agreement between different instruments was reasonable below ~ -27 °C, there seemed to be a different trend in the temperature-dependent ice nucleation activity from the suspension and dry-dispersed particle measurements for this mineral dust, in particular at higher temperatures. For instance, the ice nucleation activity expressed in n s was smaller for the average of the wet suspended samples and higher for the average of the dry-dispersed aerosol samples between about -27 and -18 °C. Only instruments making measurements with wet suspended samples were able to measure ice nucleation above -18 °C. A possible explanation for the deviation between -27 and -18 °C is discussed. Multiple exponential distribution fits in both linear and log space for both specific surface area-based n s( T) and geometric surface area-based n s( T) are provided. These new fits, constrained by using identical reference samples, will help to compare IN measurement methods that are not included in the present study and IN data from future IN instruments.« less

A comprehensive laboratory study on the immersion freezing behavior of illite NX particles. A comparison of 17 ice nucleation measurement techniques

DOE PAGES

Hiranuma, Naruki; Augustin-Bauditz, Stefanie; Bingemer, Heinz; ...

2015-03-06

Immersion freezing is the most relevant heterogeneous ice nucleation mechanism through which ice crystals are formed in mixed-phase clouds. In recent years, an increasing number of laboratory experiments utilizing a variety of instruments have examined immersion freezing activity of atmospherically relevant ice-nucleating particles. However, an intercomparison of these laboratory results is a difficult task because investigators have used different ice nucleation (IN) measurement methods to produce these results. A remaining challenge is to explore the sensitivity and accuracy of these techniques and to understand how the IN results are potentially influenced or biased by experimental parameters associated with these techniques.more » Within the framework of INUIT (Ice Nuclei Research Unit), we distributed an illite-rich sample (illite NX) as a representative surrogate for atmospheric mineral dust particles to investigators to perform immersion freezing experiments using different IN measurement methods and to obtain IN data as a function of particle concentration, temperature ( T), cooling rate and nucleation time. A total of 17 measurement methods were involved in the data intercomparison. Experiments with seven instruments started with the test sample pre-suspended in water before cooling, while 10 other instruments employed water vapor condensation onto dry-dispersed particles followed by immersion freezing. The resulting comprehensive immersion freezing data set was evaluated using the ice nucleation active surface-site density, n s, to develop a representative n s( T) spectrum that spans a wide temperature range (-37 °C < T < -11 °C) and covers 9 orders of magnitude in n s. In general, the 17 immersion freezing measurement techniques deviate, within a range of about 8 °C in terms of temperature, by 3 orders of magnitude with respect to n s. In addition, we show evidence that the immersion freezing efficiency expressed in n s of illite NX particles is relatively independent of droplet size, particle mass in suspension, particle size and cooling rate during freezing. A strong temperature dependence and weak time and size dependence of the immersion freezing efficiency of illite-rich clay mineral particles enabled the n s parameterization solely as a function of temperature. We also characterized the n s( T) spectra and identified a section with a steep slope between -20 and -27 °C, where a large fraction of active sites of our test dust may trigger immersion freezing. This slope was followed by a region with a gentler slope at temperatures below -27 °C. While the agreement between different instruments was reasonable below ~ -27 °C, there seemed to be a different trend in the temperature-dependent ice nucleation activity from the suspension and dry-dispersed particle measurements for this mineral dust, in particular at higher temperatures. For instance, the ice nucleation activity expressed in n s was smaller for the average of the wet suspended samples and higher for the average of the dry-dispersed aerosol samples between about -27 and -18 °C. Only instruments making measurements with wet suspended samples were able to measure ice nucleation above -18 °C. A possible explanation for the deviation between -27 and -18 °C is discussed. Multiple exponential distribution fits in both linear and log space for both specific surface area-based n s( T) and geometric surface area-based n s( T) are provided. These new fits, constrained by using identical reference samples, will help to compare IN measurement methods that are not included in the present study and IN data from future IN instruments.« less

Fe-SAPONITE and Chlorite Growth on Stainless Steel in Hydrothermal Engineered Barrier Experiments

NASA Astrophysics Data System (ADS)

Cheshire, M. C.; Caporuscio, F. A.; McCarney, M.

2012-12-01

The United States recently has initiated the Used Fuel Disposition campaign to evaluate various generic geological repositories for the disposal of high-level, spent nuclear fuel within environments ranging from hard-rock, salt/clay, to deep borehole settings. Previous work describing Engineered Barrier Systems (EBS) for repositories focused on low temperature and pressure conditions. The focus of this experimental work is to characterize the stability and alteration of a bentonite-based EBS with different waste container materials in brine at higher heat loads and pressures. All experiments were run at ~150 bar and 125 to 300 C for ~1 month. Unprocessed bentonite from Colony, Wyoming was used in the experiments as the clay buffer material. The redox conditions for each system were buffered along the magnetite-iron oxygen fugacity univariant curve using Fe3O4 and Feo filings. A K-Na-Ca-Cl-based salt solution was chosen to replicate deep groundwater compositions. The experimental mixtures were 1) salt solution-clay; 2) salt solution -clay-304 stainless steel; and 3) salt solution -clay-316 stainless steel with a water/bentonite ratio of ~9. Mineralogy and aqueous geochemistry of each experiment was evaluated to monitor the reactions that took place. No smectite illitization was observed in these reactions. However, it appears that K-smectite was produced, possibly providing a precursor to illitization. It is unclear whether reaction times were sufficient for bentonite illitization at 212 and 300 C or whether conditions conducive to illite formation were obtained. The more notable clay mineral reactions occurred at the stainless steel surfaces. Authigenic chlorite and Fe-saponite grew with their basal planes near perpendicular to the steel plate, forming a 10 - 40 μm thick 'corrosion' layer. Partial dissolution of the steel plates was the likely iron source for chlorite/saponite formation; however, dissolution of the Feo/Fe3O4 may also have acted as an iron source, with the steel plates acting as a substrate for chlorite/saponite growth. Trace amounts of pyrite in the bentonite appeared to have reacted to form H2S gas and pentlandite ((Ni,Fe)8S9). Mineral growth on the waste containers was influenced by the container, buffer, and fluid compositions, in addition to pressure and temperature conditions. No significant mineralogical changes were apparent away from the steel-smectite interface. Results of this research show that the waste container may act as a substrate for mineral growth in response to corrosion. However, it is presently unknown whether chlorite and Fe-saponite will act as passivating agents or whether their presence will facilitate further corrosion of the waste containers. The role of these Fe-rich minerals on the stability of steel canisters at elevated heat loads is currently under investigation. LA-UR-12-23845

Oreshoot zoning in the Carlin-type Betze orebody, Goldstrike Mine, Eureka County, Nevada

USGS Publications Warehouse

Peters, Stephen G.; Ferdock, Gregory C.; Woitsekhowskaya, Maria B.; Leonardson, Robert; Rahn, Jerry

1998-01-01

Field and laboratory investigations of the giant Betze gold orebody, the largest Carlin-type deposit known, in the north-central Carlin trend, Nevada document that the orebody is composed of individual high-grade oreshoots that contain different geologic, mineralogic, and textural characteristics. The orebody is typical of many structurally controlled Carlin-type deposits, and is hosted in thin-bedded, impure carbonate or limy siltstone, breccia bodies, and intrusive or calc-silicate rock. Most ores in the Betze orebody are highly sheared or brecciated and show evidence of syndeformational hydrothermal deposition. The interplay between rock types and pre- and syn-structural events accounts for most of the distribution and zoning of the oreshoots. Hydrothermal alteration is scale dependent, either in broad, pervasive alteration patterns, or in areas related to various oreshoots. Alteration includes decarbonatization (~decalcification) of carbonate units, argillization (illite-clay), and silicification. Patterns of alteration zoning in and surrounding the Betze orebody define a large porous, dilated volume of rock where high fluid flow predominated. Local restriction of alteration to narrow illite- and clay-rich selvages around unaltered marble or calc-silicate rock phacoids implies that fluid flow favored permeable structures and deformed zones. Gold mainly is present as disseminated sub-micron-sized particles, commonly associated with Asñrich pyrite, although one type of oreshoot contains micron-size free gold. Oreshoots form a three-dimensional zoning pattern in the orebody within a WNW-striking structural zone of shearing and shear folding, termed the Dillon deformation zone (DDZ). Main types of oreshoots are: (1) rutile-bearing siliceous oreshoots; (2) illite-clay-pyrite oreshoots; (3) realgar- and orpiment-bearing oreshoots; (4) stibnite-bearing siliceous oreshoots; and (5) polymetallic oreshoots. Zoning patterns result from paragenetically early development of illite-clay-pyrite oreshoots during movement along the DDZ, and subsequent silicification and brecciation, associated with formation of the realgar- and orpiment-bearing, and stibnite-bearing oreshoots. Additional shear movement along the DDZ followed. Polymetallic oreshoots, which contain minerals rich in Hg, Cu, Zn, Ag, and native Au, were the last ores to form and overprint most earlier oreshoots. Ore textures, gouge, phyllonitic rock, alteration style, and previously documented isotopic and fluid-inclusion data, all indicate a weakly to moderately saline fluid that ascended and cooled during structural displacements. Changing conditions, due to water-wall rock reactions and P-T changes during deformation, are probably responsible for fluid variation that resulted in zoning of the different oreshoots during dynamic interaction of the Au-bearing fluid with the wall rock. This investigation indicates that isolated As-, Sb-, and Hg-rich ores are separate parts of a larger single gold system. This large gold system was contemporaneous with post-Jurassic brittle-ductile deformation, on the basis of deformed mineralized pods of the Jurassic Goldstrike pluton, and large-scale hydrothermal flow, and together they appear to be an integral part of the formation of some Carlin-type gold deposits in north-central Nevada.

Particle size and X-ray analysis of Feldspar, Calvert, Ball, and Jordan soils

NASA Technical Reports Server (NTRS)

Chapman, R. S.

1977-01-01

Pipette analysis and X-ray diffraction techniques were employed to characterize the particle size distribution and clay mineral content of the feldspar, calvert, ball, and jordan soils. In general, the ball, calvert, and jordan soils were primarily clay size particles composed of kaolinite and illite whereas the feldspar soil was primarily silt-size particles composed of quartz and feldspar minerals.

Incremental fold tests of remagnetized carbonate rocks

NASA Astrophysics Data System (ADS)

Van Der Voo, R.; van der Pluijm, B.

2017-12-01

Many unmetamorphosed carbonates all over the world are demonstrably remagnetized, with the age of the secondary magnetizations typically close to that of the nearest orogeny in space and time. This observation did not become compelling until the mid-1980's, when the incremental fold test revealed the Appalachian carbonates to carry a syn-deformational remanence of likely Permian age (Scotese et al., 1982, Phys. Earth Planet. Int., v. 30, p. 385-395; Cederquist et al., 2006, Tectonophysics v. 422, p. 41-54). Since that time scores of Appalachian and Rocky Mountain carbonate rocks have added results to the growing database of paleopoles representing remagnetizations. Late Paleozoic remagnetizations form a cloud of results surrounding the reference poles of the Laurentian APWP. Remagnetizations in other locales and with inferred ages coeval with regional orogenies (e.g., Taconic, Sevier/Laramide, Variscan, Indosinian) are also ubiquitous. To be able to transform this cornucopia into valuable anchor-points on the APWP would be highly desirable. This may indeed become feasible, as will be explained next. Recent studies of faulted and folded carbonate-shale sequences have shown that this deformation enhances the illitization of smectite (Haines & van der Pluijm, 2008, Jour. Struct. Geol., v. 30, p. 525-538; Fitz-Diaz et al., 2014, International Geol. Review, v. 56, p. 734-755). 39Ar-40Ar dating of the authigenic illite (neutralizing any detrital illite contribution by taking the intercept of a mixing line) yields, therefore, the age of the deformation. We know that this date is also the age of the syndeformational remanence; thus we have the age of the corresponding paleopole. Results so far are obtained for the Canadian and U.S. Rocky Mountains and for the Spanish Cantabrian carbonates (Tohver et al., 2008, Earth Planet. Sci. Lett., v. 274, p. 524-530) and make good sense in accord with geological knowledge. Incremental fold tests are the tools used for this determination, with plots of the precision parameter (k) versus percent unfolding. Analyses of these plots are carried out to detect whether there is a systematic combination of tilting (=folding) and oroclinal rotations in eastern Mexico.

Direct evidence for organic carbon preservation as clay-organic nanocomposites in a Devonian black shale; from deposition to diagenesis

NASA Astrophysics Data System (ADS)

Kennedy, Martin John; Löhr, Stefan Carlos; Fraser, Samuel Alex; Baruch, Elizabeth Teresa

2014-02-01

The burial of marine sourced organic carbon (OC) in continental margin sediments is most commonly linked to oceanographic regulation of bottom-water oxygenation (anoxia) and/or biological productivity. Here we show an additional influence in the Devonian Woodford Shale, in which OC occurs as nanometer intercalations with specific phyllosilicate minerals (mixed-layer illite/smectite) that we term organo-mineral nanocomposites. High resolution transmission electron microscopic (HRTEM) images provide direct evidence of this nano-scale relationship. While discrete micron-scale organic particles, such as Tasmanites algal cysts, are present in some lamina, a strong relation between total organic carbon (TOC) and mineral surface area (MSA) over a range of 15% TOC indicate that the dominant association of organic carbon is with mineral surfaces and not as discrete pelagic grains, consistent with HRTEM images of nanocomposites. Where periods of oxygenation are indicated by bioturbation, this relationship is modified by a shift to lower OC loading on mineral surfaces and reduced MSA variability likely resulting from biological mixing and homogenization of the sediment, oxidative burn down of OC and/or stripping of OC from minerals in animal guts. The TOC-MSA relationship extends across a range of burial depths and thermal maturities into the oil window and persists through partial illitization. Where illitization occurs, the loss of mineral surface area associated with the collapse of smectite interlayer space results in a systematic increase in TOC:MSA and reorganization of organic carbon and clays into nano-scale aggregates. While the Woodford Shale is representative of black shale deposits commonly thought to record heightened marine productivity and/or anoxia, our results point to the importance of high surface area clay minerals for OC enrichment. Given that the vast majority of these clay minerals are formed in soils before being transported to continental margin settings, their mineralogy and attendant preservative potential is primarily a function of continental climate and provenance making these deposits a sensitive recorder of land as well as oceanographic change.

Sedimentary environment and diagenesis of the Lower Cretaceous Chaswood Formation, southeastern Canada: The origin of kaolin-rich mudstones

NASA Astrophysics Data System (ADS)

Pe-Piper, Georgia; Dolansky, Lila; Piper, David J. W.

2005-07-01

The Lower Cretaceous fluvial sandstone-mudstone succession of the Chaswood Formation is the proximal equivalent of offshore deltaic rocks of the Scotian Basin that are reservoirs for producing gas fields. This study interprets the mineralogical consequences of Cretaceous weathering and early diagenesis in a 130-m core from the Chaswood Formation in order to better understand detrital and diagenetic minerals in equivalent rocks offshore. Mineralogy was determined by X-ray diffraction, electron microprobe analysis and scanning electron microscopy. The rocks can be divided into five facies associations: light gray mudstone, dark gray mudstone, silty mudstone and muddy sandstone, sorted sandstone and conglomerate, and paleosols. Facies transitions in coarser facies are related to deposition in and near fluvial channels. In the mudstones, they indicate an evolutionary progression from the dark gray mudstone facies association (swamps and floodplain soils) to mottled paleosols (well-drained oxisols and ultisols following syntectonic uplift). Facies transitions and regional distribution indicate that the light gray mudstone facies association formed from early diagenetic oxidation and alteration of the dark gray mudstone facies association, probably by meteoric water. Principal minerals in mudstones are illite/muscovite, kaolinite, vermiculite and quartz. Illite/muscovite is of detrital origin, but variations in abundance show that it has altered to kaolinite in the light gray mudstone facies association and in oxisols. Vermiculite developed from the weathering of biotite and is present in ultisols. The earliest phase of sandstone cementation in reducing conditions in swamps and ponds produced siderite nodules and framboidal pyrite, which were corroded and oxidized during subsequent development of paleosols. Kaolinite is an early cement, coating quartz grains and as well-crystallized, pore-filling booklets that was probably synchronous with the formation of the light gray mudstone facies association. Later illite and barite cement indicate a source of abundant K and Ba from formation water. This late diagenesis of sandstone took place when the Chaswood Formation was in continuity with the main Scotian Basin, prior to Oligocene uplift of the eastern Scotian Shelf. Findings of this study are applicable to other mid-latitude Cretaceous weathering and early diagenetic environments.

Sorption of Cm(III) and Eu(III) onto clay minerals under saline conditions: Batch adsorption, laser-fluorescence spectroscopy and modeling

NASA Astrophysics Data System (ADS)

Schnurr, Andreas; Marsac, Rémi; Rabung, Thomas; Lützenkirchen, Johannes; Geckeis, Horst

2015-02-01

The present work reports experimental data for trivalent metal cation (Cm/Eu) sorption onto illite (Illite du Puy) and montmorillonite (Na-SWy-2) in NaCl solutions up to 4.37 molal (m) in the absence of carbonate. Batch sorption experiments were carried out for a given ionic strength at fixed metal concentration (mEu = 2 × 10-7 m, labeled with 152Eu for γ-counting) and at a constant solid to liquid ratio (S:L = 2 g/L) for 3 < pHm < 12 (pHm = -log mH+). The amount of clay sorbed Eu approaches almost 100% (with log KD > 5) for pHm > 8, irrespective of the NaCl concentration. Variations in Eu uptake are minor at elevated NaCl concentrations. Time-resolved laser fluorescence spectroscopy (TRLFS) studies on Cm sorption covering a wide range of NaCl concentrations reveal nearly identical fluorescence emission spectra after peak deconvolution, i.e. no significant variation of Cm surface speciation with salinity. Beyond the three surface complexes already found in previous studies an additional inner-sphere surface species with a fluorescence peak maximum at higher wavelength (λ ∼ 610 nm) could be resolved. This new surface species appears in the high pH range and is assumed to correspond to a clay/curium/silicate complex as already postulated in the literature for kaolinite. The 2 site protolysis non-electrostatic surface complexation and cation exchange sorption model (2SPNE SC/CE) was applied to describe Eu sorption data by involving the Pitzer and SIT (specific ion interaction) formalism in the calculation of the activities of dissolved aqueous species. Good agreement of model and experiment is achieved for sorption data at pHm < 6 without the need of adjusting surface complexation constants. For pHm > 6 in case of illite and pHm > 8 in case of montmorillonite calculated sorption data systematically fall below experimental data with increasing ionic strength. Under those conditions sorption is almost quantitative and deviations must be discussed considering uncertainties of measured Eu concentrations in the range of analytical detection limits.

Long-term variations of clay mineral composition in the Andaman Sea (IODP Exp. 353 Site U1447): preliminary result

NASA Astrophysics Data System (ADS)

Lee, J.; Khim, B. K.; Cho, H. G.; Kim, S.; 353 Scientists, I. E.

2016-12-01

Clay mineral studies in the Bengal Fan have allowed the reconstruction of the erosional history of the Himalayan-Tibetan complex since the Early Miocene. Several factors such as climate change and tectonic activity are important for the erosion rate of the Himalaya-Tibet complex. IODP Expedition 353 Site U1447 (10°47.4'N, 93°00'E; 1391 mbsl) was drilled on a ridge 45 km offshore Little Andaman Island in the Andaman Sea, penetrating to total depths of 738 m. Riverine sediments supplied mainly by the Irrawaddy and Salween (draining the Indo-Burman Ranges; smectite-rich) and the Ganga/Brahmaputra (draining the Himalaya; illite-rich) via the surface currents have been known to deposit in the Andaman Sea. We measured clay minerals of 38 sediment samples collected from 150 to 737 m CSF-A at Site U1447 in order to reveal long-term variation patterns of clay minerals and their controlling factors. Age reconstruction of Site U1447 aided by shipboard biostratigraphic and paleomagnetic data defined the study interval spanning from the Late Miocene ( 10 Ma) to Early Pleistocene ( 1.25 Ma). At this interval, clay minerals consist mainly of smectite (28-61% with an average of 47%) followed by illite (20-41% with an average of 29%), kaolinite (9-19% with an average of 14%), and chlorite (5-15% with an average of 10%). Variation of clay mineral compositions is divided into three stages; almost consistent variations of all clay minerals (from 750 to 570 m CSF-A; 10.0 to 7.5 Ma), gradual decrease of smectite and increase of illite and chlorite (from 570 to 400 m CSF-A; 7.5 to 4.5 Ma), and great fluctuation of all clay minerals (from 400 to 150 m CSF-A; 4.5 to 1.1 Ma). Such long-term clay mineral changes may be related to provenance switches, tectonic evolution of the source regions, climatic variations, degree of volcanism with basin evolution, sedimentation history by sea level changes or some combination of these factors.

Advances in authigenic silicate geochemistry: Evidence for Precessional Control of Pleistocene Lake Salinity at Olduvai Gorge, Tanzania

NASA Astrophysics Data System (ADS)

Deocampo, D.; Simpson, A. J.; Cuadros, J.; Beverly, E.; Ashley, G. M.; Delaney, J. S.; Longstaffe, F. J.

2017-12-01

Magnesium enrichment of authigenic clays is an indicator of elevated salinity in hydrologically closed lake basins. Studies at Olduvai Gorge over the last four decades have shown that chemically-precipitated clay minerals form a substantial portion of the sedimentary succession, in some intervals even dominating the sediment. Outcrops of lacustrine mud in two localities near the depocenter were examined using a new geochronological framework based on Ar/Ar dating of volcaniclastic sanidine (Deino, 2012). Olduvai's clay mineralogy is dominated by 2:1 clays, including smectite, illite, and interstratified illite-smectite. Previous work has shown that clay alteration includes octahedral Mg-enrichment, Fe-reduction, K-fixation, and low-temperature illitization. Here we show that long term environmental conditions in Paleolake Olduvai indicated by sub-micron clay geochemistry were generally saline and alkaline between 1.78 and 1.92 Ma, but 6 episodes of freshened paleolake water are indicated by intervals of lower Mg content. Five of these freshening episodes occurred at peak climatic precession. The sub-micron clay geochemistry agrees with infrared spectroscopy and whole-rock geochemical compositions, and the same stratigraphic variation is observed at both localities, separated laterally by 330m. Preliminary analyses show that the <0.1µm clay mineral δ18Oclay suggest a δ18OH2O range of about -4 to +3‰ (SMOW) through this stratigraphic interval. No significant correlation is found with elemental composition, but lighter isotopic values are associated stratigraphically with geochemically defined freshening events. This suggests that isotopic and elemental equilibrium may not be reached at the same time, or that diagenetic events may have differentially altered the isotopic record. The environmental changes recorded in the Olduvai sediments occurred at a time when zonal Walker circulation increasingly affected global climate, new stone technologies emerged, and the genus Homo spread beyond Africa. Unraveling the details of mineralogical records such as those at Olduvai will be important in characterizing details of continental Quaternary environmental change, particularly in stratigraphic intervals where biotic proxies are unavailable.

Past environmental/climatic changes in the northern part of the South China Sea, input from multi-proxy analysis of core MD12-3432

NASA Astrophysics Data System (ADS)

Chen, Quan; Kissel, Catherine; Liu, Zhifei

2017-04-01

In the South China Sea, the magnetic component of marine sediment is a powerful recorder of paleoenvironmental changes linked to the regional and global climate. Based on the knowledge of the sedimentary signature of the potential sources for terrigenous sediments, the composition of marine sediments can be used to decipher the different mechanisms, forcing, and transport vectors. We report here the analysis of the magnetic properties combined with sortable silt and clay mineralogy of a 51 m long sedimentary sequence retrieved from the northern South China Sea and covering the last 400 ka. Magnetic minerals with different coercivities (magnetite, pyrrhotite and hematite) are mixed in the sequence and their relative concentration varies with time. Glacial low sea-levels reduce the land-site distance and they are illlustrated by higher concentrations in magnetites and iron-sulfides (pyrrhotite) related to the sediments previously deposited on the continental shelf and re-worked by the river. This is accompanied by increasing kaolinite content within the clay assemblage (Pearl River signature) and by coarser grains. Superimposed to this eccentricity periodicity, hematite content and smectite/(illite+chlorite) ratio present a predominant precession periodicity synchronous with the northern hemisphere summer insolation changes and therefore with that of the East Asian summer monsoon. Events of high hematite content, in phase with finer grains, coincide with precession lows, while smectite/(illite+chlorite) ratio is maximum during precession highs. Knowing that smectite is mainly produced by contemporaneous chemical weathering intensity in Luzon, we use the smectite/(illite+chlorite) ratio as a tracer for increasing weathering rate in Luzon, in turn related to enhanced East Asian summer monsoon. Hematite is not produced in large amount on adjacent lands and its association with fine sediment grains suggests that its periodic supply is related to the eolian dust transported from the Central China deserts to the studied site. Higher hematite content at this latitude may therefore be used as a tracer for weak East Asian summer monsoon intensity.

Growth of thermophilic and hyperthermophilic Fe(III)-reducing microorganisms on a ferruginous smectite as the sole electron acceptor.

PubMed

Kashefi, Kazem; Shelobolina, Evgenya S; Elliott, W Crawford; Lovley, Derek R

2008-01-01

Recent studies have suggested that the structural Fe(III) within phyllosilicate minerals, including smectite and illite, is an important electron acceptor for Fe(III)-reducing microorganisms in sedimentary environments at moderate temperatures. The reduction of structural Fe(III) by thermophiles, however, has not previously been described. A wide range of thermophilic and hyperthermophilic Archaea and Bacteria from marine and freshwater environments that are known to reduce poorly crystalline Fe(III) oxides were tested for their ability to reduce structural (octahedrally coordinated) Fe(III) in smectite (SWa-1) as the sole electron acceptor. Two out of the 10 organisms tested, Geoglobus ahangari and Geothermobacterium ferrireducens, were not able to conserve energy to support growth by reduction of Fe(III) in SWa-1 despite the fact that both organisms were originally isolated with solid-phase Fe(III) as the electron acceptor. The other organisms tested were able to grow on SWa-1 and reduced 6.3 to 15.1% of the Fe(III). This is 20 to 50% less than the reported amounts of Fe(III) reduced in the same smectite (SWa-1) by mesophilic Fe(III) reducers. Two organisms, Geothermobacter ehrlichii and archaeal strain 140, produced copious amounts of an exopolysaccharide material, which may have played an active role in the dissolution of the structural iron in SWa-1 smectite. The reduction of structural Fe(III) in SWa-1 by archaeal strain 140 was studied in detail. Microbial Fe(III) reduction was accompanied by an increase in interlayer and octahedral charges and some incorporation of potassium and magnesium into the smectite structure. However, these changes in the major element chemistry of SWa-1 smectite did not result in the formation of an illite-like structure, as reported for a mesophilic Fe(III) reducer. These results suggest that thermophilic Fe(III)-reducing organisms differ in their ability to reduce and solubilize structural Fe(III) in SWa-1 smectite and that SWa-1 is not easily transformed to illite by these organisms.

Growth of Thermophilic and Hyperthermophilic Fe(III)-Reducing Microorganisms on a Ferruginous Smectite as the Sole Electron Acceptor▿

PubMed Central

Kashefi, Kazem; Shelobolina, Evgenya S.; Elliott, W. Crawford; Lovley, Derek R.

2008-01-01

Recent studies have suggested that the structural Fe(III) within phyllosilicate minerals, including smectite and illite, is an important electron acceptor for Fe(III)-reducing microorganisms in sedimentary environments at moderate temperatures. The reduction of structural Fe(III) by thermophiles, however, has not previously been described. A wide range of thermophilic and hyperthermophilic Archaea and Bacteria from marine and freshwater environments that are known to reduce poorly crystalline Fe(III) oxides were tested for their ability to reduce structural (octahedrally coordinated) Fe(III) in smectite (SWa-1) as the sole electron acceptor. Two out of the 10 organisms tested, Geoglobus ahangari and Geothermobacterium ferrireducens, were not able to conserve energy to support growth by reduction of Fe(III) in SWa-1 despite the fact that both organisms were originally isolated with solid-phase Fe(III) as the electron acceptor. The other organisms tested were able to grow on SWa-1 and reduced 6.3 to 15.1% of the Fe(III). This is 20 to 50% less than the reported amounts of Fe(III) reduced in the same smectite (SWa-1) by mesophilic Fe(III) reducers. Two organisms, Geothermobacter ehrlichii and archaeal strain 140, produced copious amounts of an exopolysaccharide material, which may have played an active role in the dissolution of the structural iron in SWa-1 smectite. The reduction of structural Fe(III) in SWa-1 by archaeal strain 140 was studied in detail. Microbial Fe(III) reduction was accompanied by an increase in interlayer and octahedral charges and some incorporation of potassium and magnesium into the smectite structure. However, these changes in the major element chemistry of SWa-1 smectite did not result in the formation of an illite-like structure, as reported for a mesophilic Fe(III) reducer. These results suggest that thermophilic Fe(III)-reducing organisms differ in their ability to reduce and solubilize structural Fe(III) in SWa-1 smectite and that SWa-1 is not easily transformed to illite by these organisms. PMID:17981937

Spectroscopic mapping of the white horse alunite deposit, Marysvale volcanic field, Utah: Evidence of a magmatic component

USGS Publications Warehouse

Rockwell, B.W.; Cunningham, C.G.; Breit, G.N.; Rye, R.O.

2006-01-01

Previous studies have demonstrated that the replacement alunite deposits just north of the town of Marysvale, Utah, USA, were formed primarily by low-temperature (100??-170?? C), steam-heated processes near the early Miocene paleoground surface, immediately above convecting hydrothermal plumes. Pyrite-bearing propylitically altered rocks occur mainly beneath the steam-heated alunite and represent the sulfidized feeder zone of the H2S-dominated hydrothermal fluids, the oxidation of which at higher levels led to the formation of the alunite. Maps of surface mineralogy at the White Horse deposit generated from Airborne Visible/Infrared Imaging Spectrometer (AVIRIS) data were used in conjunction with X-ray diffraction studies of field samples to test the accuracy and precision of AVIRIS-based mineral mapping of altered rocks and demonstrate the utility of spectroscopic mapping for ore deposit characterization. The mineral maps identified multiple core zones of alunite that grade laterally outward to kaolinite. Surrounding the core zones are dominantly propylitically altered rocks containing illite, montmorillonite, and chlorite, with minor pyrite, kaolinite, gypsum, and remnant potassium feldspar from the parent rhyodacitic ash-flow tuff. The AVIRIS mapping also identified fracture zones expressed by ridge-forming selvages of quartz + dickite + kaolinite that form a crude ring around the advanced argillic core zones. Laboratory analyses identified the aluminum phosphate-sulfate (APS) minerals woodhouseite and svanbergite in one sample from these dickite-bearing argillic selvages. Reflectance spectroscopy determined that the outer edges of the selvages contain more dickite than do the medial regions. The quartz + dickite ?? kaolinite ?? APS-mineral selvages demonstrate that fracture control of replacement processes is more prevalent away from the advanced argillic core zones. Although not exposed at the White Horse deposit, pyrophyllite ?? ordered illite was identified using AVIRIS in localized, superimposed conduits within propylitically altered rocks in nearby alteration systems of similar age and genesis that have been eroded to deeper levels. The fracture zones bearing pyrophyllite, illite, dickite, natroalunite, and/or APS minerals indicate a magmatic component in the dominantly steam-heated system. ?? 2006 Society of Economic Geologists, Inc.

Hydrothermal Alteration of the Mt Unzen Conduit (Shimabara/Japan)

NASA Astrophysics Data System (ADS)

Yilmaz, T. I.; Mayer, K.; Hess, K. U.; Janots, E.; Gilg, H. A.; Dingwell, D. B.

2016-12-01

Investigations were carried out on hydrothermally altered coherent dacitic dykes samples from (USDP-4) drill core at Mt Unzen stratovolcano (Shimabara/Japan). XRF, XRD, EMPA, and C-O-isotope analysis led to insights concerning chemistry, mineralogy, and intensity of alteration as well as the origin of carbonate-precipitating fluids. Additionally a textural characterization of the occurring replacement features in the magma conduit zone was performed. The occurrence of the main secondary phases such as chlorite, pyrite, carbonates, and R1 (Reichweite parameter) illite-smectite indicate a weak to moderate propylitic to phyllic hydrothermal alteration. The dacitic samples of the dykes show different hydrothermal alteration features: (i) carbonate pseudomorphs after hornblende as well as core and zonal textures due to replacement of plagioclase by R1 illite-smectite, (ii) colloform banded fracture fillings and fillings in dissolution vugs, and (iii) chlorite and R1 illite-smectite in the groundmass. Carbonates in fractures comprise iron-rich dolomite solid solutions ("ankerite") and calcite. Isotopic values of d13Cvpdb = -4.59 ± 0.6‰ and d18Ovpdb = -21.73 ± 0.5‰ indicate a hydrothermal-magmatic origin for the carbonate formation. The chlorite-carbonate-pyrite index (CCPI) and the Ishikawa alteration index (AI), applied to the investigated samples show significant differences (CCPI=52.7-57.8; AI=36.1-40.6) indicating their different degree of alteration. According to Nakada et al., 2005, the C13 to C16 dykes represent the feeder dyke from the latest eruption (1991-1995) whereas C8 represents an earlier dyke feeder dyke from an older eruption. Weakest conduit alteration, which was obtained in samples C16-1-5 and C13-2-5, correlates with the alteration degree of the pristine dome rocks. Highest CCPI value was determined for sample C14-1-5 and the highest AI value was determined for sample C15-2-6. The degrees of alteration do not indicate highest alteration of the samples C8-1-2 and C8-2-1 from the older dykes.

Micro- and Nanostructures of SAFOD Core Samples - First Results

NASA Astrophysics Data System (ADS)

Janssen, C.; Wirth, R.; Rybacki, E.; Naumann, R.; Kemnitz, H.; Wenk, H.; Dresen, G. H.

2009-12-01

Microstructures and chemical composition of ultra-cataclastic rocks from the San Andreas Fault drill hole (SAFOD) were examined using TEM, SEM and XRD analyses. The ultra-cataclasites are mainly composed of quartz, clay minerals (illite/smectite, chlorite), feldspar (plagioclase) and calcite with grain sizes between 200 nm and 500 μm. In particular we found: (1) amorphous materials, identified by transmission electron microscopy. Chemical analyses suggest that all amorphous material was formed by comminution (crush-origin) of fragments rather than by melting (melt-origin) and that the observed amorphous phases may act as hydrodynamic lubricating layers that reduce friction in the San Andreas Fault. (2) Pressure solution seams and localized precipitation of hydrous mixed-layered clay minerals suggest intensive dissolution-precipitation processes. These may lead to a thin film covering slip surfaces. (3) Authigenic clay minerals forming a flocculated fabric. (4) The fine-grained (< 1μm) gouge matrix contains clasts (feldspar, quartz) and is frequently cut by fault-related veins. The veins are filled with calcite or quartz. Observed micorstructures in the fine-grained matrix suggest comminution and sliding of the nanoscale grains. Open pore spaces up to 2.25 μm3 have been formed during and after deformation within the gouge matrix. These were possibly filled with hydrothermal fluids at elevated pore fluid pressure preventing closure. (5) Detrital quartz and feldspar grains are partly dissolved and replaced by authigenic illite-smectite (I-S) mixed-layer clay minerals. TEM imaging of these grains reveal that initial alteration processes started within pores and small fissures of grains. The crystallographic-preferred orientation of illite and I/S grains is rather weak with a maximum m.r.d. (multiples of random orientation) of 2.3. (6) Some older fault-related vein-calcites show evidence for intense intracrystalline plasticity (deformation twins and dislocation creep). Dislocation densities in calcite grains indicate a local maximum stress of about 40 MPa. The younger fault-related vein-calcite generation with elongated to fibrous habit suggests slow opening by aseismic slip. These crystals are not fractured or twinned (or only less); indicating that healing processes (cementation) outlasted deformation.

Multidecadal persistence of organic matter in soils: insights from spatially resolved investigations at the submicrometer scale

NASA Astrophysics Data System (ADS)

Lutfalla, Suzanne; Barré, Pierre; Bernard, Sylvain; Le Guillou, Corentin; Alléon, Julien; Chenu, Claire

2016-04-01

Better understanding the mechanisms responsible for the pluri-decadal persistence of carbon in soils requires well constraining the dynamics, the distribution and the chemical nature of both the soil organic carbon (SOC) and the associated mineral phases. The question we address in this work is whether different mineral species lead to different organo-mineral interactions and stabilize different quantities of SOM and different types of SOC. Here, benefiting from the unique opportunity offered by an INRA long term bare fallow (LTBF) experiment having started in 1928 in Versailles (France), we report the in-situ characterization of SOC dynamics in four clay fractions of this silty loam soil (total clays [TC, <2μm], coarse clays [CC, 0.2-2μm], intermediate clays [IC, 0.05-0.2μm] and fine clays [FC, 0-0.05μm]). The IC and FC fractions only contain smectite and illite/smectite mixed-layered clay minerals while the CC fraction also contains illite and kaolinite. In the absence of any carbon input, the plant-free LTBF clay fractions from Versailles progressively lost SOC during the first 50 years of the experiment, until they reached a seemingly stable concentration. Of note, the investigated clay fractions did not lose the same amount of SOC and do not exhibit the same final carbon concentrations. The decrease of the organic C:N ratios with LTBF duration corresponds to a progressive enrichment in N-rich SOC for all fractions which can be attributed to microbial material. Even though the speciation of SOC appears to only slightly evolve with LTBF duration, an enrichment in carboxyl and carbonyl groups is revealed by bulk-scale C-NEXAFS data for SOC from all clay fractions. In addition, STXM-based NEXAFS investigations at the submicrometer scale reveal three types of SOC-clay assemblages in addition to clay-free SOC and organic-free clays. While SOC appears mostly adsorbed onto clay surfaces within the IC and FC fractions, other protection mechanisms occur within the CC fraction. Altogether, the present study suggests that smectite have more efficient protection capabilities than those of illite and kaolinite.

The Cretaceous glauconitic sandstones of Abu Tartur, Egypt

NASA Astrophysics Data System (ADS)

Pestitschek, Brigitte; Gier, Susanne; Essa, Mahmoud; Kurzweil, Johannes

2010-05-01

The Abu Tartur mine is located in the Western Desert of Egypt, 50 km west of El Kharga City. Geologically, the Abu Tartur plateau is built by a sequence of Upper Cretaceous (Campanian - Maastrichtian) phosphorites, black shales and glauconitic sandstones. The phosphate deposits are of great economic importance and have been mined since their discovery in 1967. Outcrop sections were measured, sampled, sedimentologically characterized and described. One specific glaucony layer was investigated mineralogically and chemically in detail and compared to a subsurface sample from the mine. Two depositional regimes can be interpreted based on sedimentary architecture and structures: 1) a deeper-water hemipelagic environment, where phosphorites and organic carbon-rich shales were deposited and 2) a shallower, prograding higher energy shelf environment with glauconies. From a sequence stratigraphic perspective 1) was deposited during the transgressive systems tract and the early highstand while 2) was deposited during the remaining highstand and a lowstand prograding wedge (Glenn & Arthur, 1990). Petrographic and SEM investigations show that the glaucony grains are of authochtonous origin. XRF, EMPA and thin-section analyses show that the glaucony grains from the outcrop differ significantly in their chemical composition, morphology and color from the grains of the mine sample. The fresh glauconies are enriched in Fe2O3 and K2O compared to the surface samples. XRD analyses of the clay fraction of the six outcrop samples and the mine sample show that the grains consist of illite(glauconite)/smectite mixed-layers, with more illite layers (80 %) in the mine sample. The charge distribution diagram muscovite-pyrophyllite-celadonite shows a clear trend from smectitic glaucony to illitic glaucony, the mine sample plots exactly in the field for glauconites. All these features indicate that the surface samples are strongly altered by weathering and that glauconite progressively transforms into iron-rich illte/smectite mixed layers and then into smectites. For any chemical and mineralogical characterization of glauconites at surface, these weathering effects have to be taken into consideration. GLENN, C. R. & ARTHUR, M. A. (1990): Anatomy and origin of a Cretaceous phosphorites-greensand giant, Egypt. Sedimentology, 37, 123-154.

Carbon sequestration in depleted oil shale deposits

DOEpatents

Burnham, Alan K; Carroll, Susan A

2014-12-02

A method and apparatus are described for sequestering carbon dioxide underground by mineralizing the carbon dioxide with coinjected fluids and minerals remaining from the extraction shale oil. In one embodiment, the oil shale of an illite-rich oil shale is heated to pyrolyze the shale underground, and carbon dioxide is provided to the remaining depleted oil shale while at an elevated temperature. Conditions are sufficient to mineralize the carbon dioxide.

Investigation into Suitability of Geopolymers (Illite & Metakaolin) for the Space Environment

DTIC Science & Technology

2012-09-13

most disastrous if a spacecraft telescope made of a hybrid composite mirror with a geopolymer adhesive became distorted or damaged on orbit due to...background According to the Dictionary of Composite Materials Technology, (Lee 1989) a geopolymer is defined as: “A family of refractory ceramics...polysilicates to form polymeric Si-O-Al bonds”. Geopolymers and geopolymer composites are a relatively newly defined class of ceramic materials whose

In-place oil shale resources in the saline-mineral and saline-leached intervals, Parachute Creek Member of the Green River Formation, Piceance Basin, Colorado

USGS Publications Warehouse

Birdwell, Justin E.; Mercier, Tracey J.; Johnson, Ronald C.; Brownfield, Michael E.; Dietrich, John D.

2014-01-01

A recent U.S. Geological Survey analysis of the Green River Formation of the Piceance Basin in western Colorado shows that about 920 and 352 billion barrels of oil are potentially recoverable from oil shale resources using oil-yield cutoffs of 15 and 25 gallons per ton (GPT), respectively. This represents most of the high-grade oil shale in the United States. Much of this rich oil shale is found in the dolomitic Parachute Creek Member of the Green River Formation and is associated with the saline minerals nahcolite and halite, or in the interval where these minerals have been leached by groundwater. The remaining high-grade resource is located primarily in the underlying illitic Garden Gulch Member of the Green River Formation. Of the 352 billion barrels of potentially recoverable oil resources in high-grade (≥25 GPT) oil shale, the relative proportions present in the illitic interval, non-saline R-2 zone, saline-mineral interval, leached interval (excluding leached Mahogany zone), and Mahogany zone were 3.1, 4.5, 36.6, 23.9, and 29.9 percent of the total, respectively. Only 2 percent of high-grade oil shale is present in marginal areas where saline minerals were never deposited.

Experimental verification of the steric-entropic mode of retention in centrifugal field-flow fractionation using illite clay plates.

PubMed

Tadjiki, Soheyl; Beckett, Ronald

2018-02-23

The commonly used theory to describe the normal Brownian mode of field-flow fractionation (FFF) assumes the particles to be point masses and hence the shape is ignored. Beckett and Giddings extended this theory to include the effect of thin rods and discs being forced very close to the accumulation wall. By including the decrease in the entropy this causes, they derived new expressions for the retention of such nonspherical particles in FFF. The steric-entropic theory predicts that when the sample cloud thickness is less than the major dimension of the rods or discs then particles elute earlier than predicted by the Brownian mode theory. This leads to an underestimation of the buoyant mass and equivalent spherical diameter calculated from FFF data. In this paper we report for the first time experimental data for the retention of thin illite particles in centrifugal FFF that agrees well with these steric-entropic predictions. Not only do the size distributions calculated using the Brownian mode theory shift to lower size when the field is increased but the shift in the retention ratio of the peak maxima of the FFF fractograms could be predicted fairly accurately by the steric-entropic equations. Copyright © 2018 Elsevier B.V. All rights reserved.

Hydrothermal alteration of deep fractured granite: Effects of dissolution and precipitation

NASA Astrophysics Data System (ADS)

Nishimoto, Shoji; Yoshida, Hidekazu

2010-03-01

This paper investigates the mineralogical effects of hydrothermal alteration at depth in fractures in granite. A fracture accompanied by an alteration halo and filled with clay was found at a depth of 200 m in a drill core through Toki granite, Gifu, central Japan. Microscopic observation, XRD, XRF, EPMA and SXAM investigations revealed that the microcrystalline clays consist of illite, quartz and pyrite and that the halo round the fracture can be subdivided into a phyllic zone adjacent to the fracture, surrounded by a propylitic zone in which Fe-phyllosilicates are present, and a distinctive outer alteration front characterized by plagioclase breakdown. The processes that result in these changes took place in three successive stages: 1) partial dissolution of plagioclase with partial chloritization of biotite; 2) biotite dissolution and precipitation of Fe-phyllosilicate in the dissolution pores; 3) dissolution of K-feldspar and Fe-phyllosilicate, and illite precipitation associated with development of microcracks. These hydrothermal alterations of the granite proceed mainly by a dissolution-precipitation process resulting from the infiltration of hydrothermal fluid along microcracks. Such infiltration causes locally high mobility of Al and increases the ratio of fluid to rock in the alteration halo. These results contribute to an understanding of how granitic rock becomes altered in orogenic fields such as the Japanese island arc.

Causes and consequences of the great strength variability among soft Nankai accretionary prism sediments from offshore SW-Japan

NASA Astrophysics Data System (ADS)

Stipp, Michael; Schumann, Kai; Leiss, Bernd; Ullemeyer, Klaus

2014-05-01

The Nankai Trough Seismogenic Zone Experiment of the International Ocean Discovery Program (IODP) is the very first attempt to drill into the seismogenic part of a subduction zone. Offshore SW-Japan the oceanic Philippine sea plate is subducted beneath the continental Eurasian plate causing earthquakes of magnitude 8.0 to 8.5 and related tsunamis with a recurrence rate of 80-100 years. For the tsunamigenic potential of the forearc slope and accreted sediments their mechanical strength, composition and fabrics have been investigated. 19 drill core samples of IODP Expeditions 315, 316 and 333 were experimentally deformed in a triaxial cell under consolidated and undrained conditions at confining pressures of 400-1000 kPa, room temperature, axial shortening rates of 0.01-9.0 mm/min, and up to an axial strain of ˜64% (Stipp et al., 2013). With respect to the mechanical behavior, two distinct sample groups could be distinguished. Weak samples from the upper and middle forearc slope of the accretionary prism show a deviatoric peak stress after only a few percent strain (< 10%) and a continuous stress decrease after a maximum combined with a continuous increase in pore pressure. Strong samples from the accretionary prism toe display a constant residual stress at maximum level or even a continuous stress increase together with a decrease in pore pressure towards high strain (Stipp et al., 2013). Synchrotron texture and composition analysis of the experimentally deformed and undeformed samples using the Rietveld refinement program MAUD indicates an increasing strength of the illite and kaolinite textures with increasing depth down to 523 m below sea floor corresponding to a preferred mineral alignment due to compaction. Experimentally deformed samples have generally stronger textures than related undeformed core samples and they show also increasing strength of the illite and kaolinite textures with increasing axial strain. Mechanically weak samples have a bulk clay plus calcite content of 31-65 vol.-% and most of their illite, kaolinite, smectite and calcite [001]-pole figures have maxima >1.5 mrd. Strong samples which were deformed to approximately the same amount of strain (up to 40%) have no calcite and a bulk clay content of 24-36 vol.-%. Illite, kaolinite and smectite [001]-pole figure maxima are mostly <1.5 mrd, except for one sample which was deformed to a considerably higher strain (64%). The higher clay and calcite content and the stronger textures of the mechanically weak samples can be related to a collapsing pore space of the originally flocculated clay aggregates. This process is insignificant in the strong samples from the prism toe, for which deformation would tend to involve large rock volumes and lead to strain dissipation. The weak samples from the forearc slope which become even weaker with increasing strain may provoke mechanical runaway situations allowing for earthquake rupture, surface breakage and tsunami generation. Stipp, M., Rolfs, M., Kitamura, Y., Behrmann, J.H., Schumann, K., Schulte-Kortnack, D. and Feeser, V. 2013. G-Cubed 14/11, doi: 10.1002/ggge.20290.

Mineralogy and thermal properties of clay from Slatina (Ub, Serbia)

NASA Astrophysics Data System (ADS)

Milosevic, Maja; Logar, Mihovil; Kaludjerovic, Lazar; Jelic, Ivana

2017-04-01

The "Slatina" deposit, Ub, Serbia was opened in 1965 and represents one of few deposits exploited by "Kopovi" a.d., Ub, company. Deposit is composed of clay layers belonging to Neogene sediments that are widespread transgressive over granitoid rocks of Cer mountain and Paleozoic and Mesozoic sediments. Clay is mostly of illite-montmorillonite-kaolinite type and they are generally used as ceramic materials while some of the layers are used as fire-resistant materials. In this study we present mineralogical and thermal characterization of two samples to determine their application as industrial materials. Chemical and mineral composition was determined using inductively coupled plasma optical emission spectroscopy (ICP-OES), X-ray diffraction (XRD) on powder and oriented samples, infrared spectroscopy (IR) and granulometry. Cationic exchange capacity (CEC) and specific surface area (SSA) was determined using spectrophotometry and methylene blue (MB). Thermal properties where determined by gravimetry (120, 350, 600 and 1000 oC) and differential thermal analysis (DTA). Quantitative mineral composition obtained by Rietveld refinement of combined chemical and XRD data shows that the sample 1(SC) is mainly smectite-illite (45%) and kaolinite (14%) clay with 19% of quartz, 10% feldspars and 7% of limonite, while sample 2(SV) is smectite-illite (43%) and kaolinite (11%) clay with 10% of quartz, 15% feldspars and 7% of limonite. Both samples have low content of impurities (carbonate minerals). Medium grain size (μm) goes from 1.02 (SSA = 104 m2/g) for sample 1(SC) to 0.71 (SSA = 117 m2/g) for sample 2(SV) while their CEC is 12.7 and 14.9 mmol/100g for 1(SC) and 2(SV) respectively. IR spectra of the samples shows larger amount of smectite clays with quartz and carbonate minerals for both samples which is in accordance with XRD data. DTA data shows couple of events that are endothermic. First one (100-200 oC) is associated with loss of moisture and constitutive water, second (300-400 oC) with iron hydroxide minerals, third (500-600 oC) with smectite clay content with smaller separate bands of kaolinite clays while events between 800-900 oC correspond to carbonate minerals. Loss of mass after gravimetry measurement at given temperatures shows that the samples have significant amount of water in their structure (≈3 wt% (120 oC)) with larger weight loss at 600 oC (3.06 and 3.37 wt%) while total weight loss is 9.12 and 9.08 wt% for 1(SC) and 2(SV) respectively. The studied clays from "Slatina" deposit have a medium content of smectite-illite minerals with smaller amount of kaolinite mineral together with quartz and feldspars. Based on their mineral composition and characteristics, possible application should be in different types of ceramic and construction industries. REFERENCES - M. Milošević, M. Logar, B. Dojčinović, A. Rosić and S. Erić, 2016, Diffuse reflectance spectra of methylene blue adsorbed on different types of clay samples, Clay Minerals, (2016) 5, 1-15

Bioreduction of Fe-bearing clay minerals and their reactivity toward pertechnetate (Tc-99)

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bishop, Michael E.; Dong, Hailiang; Kukkadapu, Ravi K.

2011-07-01

99Technetium (99Tc) is a fission product of uranium-235 and plutonium-239 and poses a high environmental hazard due to its long half-life (t1/2 = 2.13 x 105 y), abundance in nuclear wastes, and environmental mobility under oxidizing conditions [i.e., Tc(VII)]. Under reducing conditions, Tc(VII) can be reduced to insoluble Tc(IV). Ferrous iron [Fe(II)], either in aqueous form or in mineral form, has been used to reduce Tc(VII) to Tc(IV). However, the reactivity of Fe(II) from clay minerals, other than nontronite, toward immobilization of Tc(VII) and its role in retention of reduced Tc(IV) have not been investigated. In this study the reactivitymore » of a suite of clay minerals toward Tc(VII) reduction and immobilization was evaluated. The clay minerals chosen for this study included five members in the smectite-illite (S-I) series, (montmorillonite, nontronite, rectorite, mixed layered I-S, and illite), chlorite, and palygorskite. Fe-oxides were removed from these minerals with a modified dithionite-citrate-bicarbonate (DCB) procedure. The total Fe content of these clay minerals, after Fe-oxide removal, ranged from 0.7 to 30.4% by weight, and the Fe(III)/Fe(total) ratio ranged from 44.9 to 98.5%. X-ray diffraction (XRD) and Mössbauer spectroscopy results showed that after Fe oxide removal the clay minerals were free of Fe-oxides. Scanning electron microscopy (SEM) revealed that little dissolution occurred during the DCB treatment. Bioreduction experiments were performed in bicarbonate buffer (pH-7) with Fe(III) in the clay minerals as the sole electron acceptor, lactate as the sole electron donor, and Shewanella Putrifaciens CN32 cells as mediators. In select tubes, anthraquinone-2,6-disulfate (AQDS) was added as electron shuttle to facilitate electron transfer. The extent of Fe(III) bioreduction was the highest for chlorite (~43 wt%) and the lowest for palygorskite (~4.17 wt%). In the S-I series, NAu-2 was the most reducible (~31 %) and illite the least (~0.4 %). The extent and initial rate of bioreduction were positively correlated with the percent smectite in the S-I series (i.e., layer expandability). Fe(II) in the bioreduced clay minerals subsequently was used to reduce Tc(VII) to Tc(IV) in PIPES buffer. Similar to the trend of bioreduction, in the S-I series, reduced smectite showed the highest reactivity toward Tc(VII), and reduced illite exhibited the least. The initial rate of Tc(VII) reduction, after normalization to clay and Fe(II) concentrations, was positively correlated with the percent smectite in the S-I series. Fe(II) in chlorite and palygorskite was also reactive toward Tc(VII) reduction. These data demonstrate that crystal chemical parameters (layer expandability, Fe and Fe(II) contents, and surface area etc.) play important roles in controlling the extent and rate of bioreduction and the reactivity toward Tc(VII) reduction. Reduced Tc(IV) resides within clay mineral matrix, and this association could minimize any potential of reoxidation over long term.« less

An Investigation of the Effects of Deposit Feeding Invertebrates on the Structural Properties of Clay Minerals.

DTIC Science & Technology

1981-07-01

Dennis M. Lavoie of NORDA for chemical analysis of clay minerals with the x-ray energy dispersive spectrometer. We thank Fred Bowles, Peter Fleischer...diffractograi of Nuculana acuta fecal pellet 11 residue (illite experiment). TABLES TABLE 1. X-ray energy dispersive spectrometer chemical 8 analysis for...inontmorillonite experiments. Counts for elements after background counts removed. TABLE 2. X-ray energy dispersive spectroneter chemical analysis 12 for

Program and Abstracts for Clay Minerals Society 28th Annual Meeting

NASA Technical Reports Server (NTRS)

1991-01-01

This volume contains abstracts that were accepted for presentation at the annual meeting. Some of the main topics covered include: (1) fundamental properties of minerals and methods of mineral analysis; (2) surface chemistry; (3) extraterrestrial clay minerals; (4) geothermometers and geochronometers; (5) smectite, vermiculite, illite, and related reactions; (6) soils and clays in environmental research; (7) kaolinite, halloysite, iron oxides, and mineral transformations; and (8) clays in lakes, basins, and reservoirs.

Composition and properties of the Pierre Shale and equivalent rocks, northern Great Plains region

USGS Publications Warehouse

Schultz, Leonard Gene; Tourtelot, H.A.; Gill, J.R.; Boerngen, J.G.

1980-01-01

The Pierre Shale and equivalent rocks of Late Cretaceous age consist in the east-central Dakotas of several hundred feet of offshore-marine shale and minor marl; in west-central Montana near the sediment source the equivalents of the Pierre Shale consist of several thousand feet of volcanic-rich and mostly nonmarine sediments; and in the area between, both types of rock are separated by tongues of nearshore-marine siltstone and sandstone that mark three major transgressions of the sea across the area. The major-, minor-, and trace-element composition was determined for 226 samples of these rocks, and the mineralogical composition was determined for 1,350 samples. Slurry pH, Atterberg limits, and grain and bulk densities were determined on some samples. The arithmetic mean, in percent, and standard deviation (in parentheses) of major and minor elements, mostly in shale and siltstone and excluding the 23 chemically analyzed bentonite samples, are as follows: SiO2 60.8 (7.9) Al2O3 14.4 (2.5) Fe2O3 3.4 (1.4) FeO 1.1 (1.2) MgO 2.2 (1.0) CaO 2.7 (0.48) Na2O 1.1 (0.56) K2O 2.4 (0.57) H2O- 3.2 (1.3) H2O+ 4.3 (1.2) TiO2 0.58 (0.12) P2O5 0.14 (0.073) S 0.37 (1.1) F 0.71 (0.15) Cl 0.16 (0.024) CO2 2.1 (7.0) C, organic 0.94 (1.8) The mean and standard deviation of minerals as determined by X-ray methods, excluding bentonite samples, is as follows: clay minerals, 53 (20); quartz, 24 (13); cristobalite, 1 (5); potassium-feldspar, 1 (2); plagioclase, 6 (7); anorthite content from 20 to 40 percent; calcite, 5 (14); dolomite, 4 (7); organic matter, 1 (2); and sparsely scattered gypsum, jarosite, pyrite, zeolites, augite, siderite, and probably minor amounts of hydrated iron-manganese (Fe-Mn) oxides. The mean and standard deviation of the clay-mineral fraction is as follows: mixed-layer illite-smectite, 70 (20); illite, 16 (9); chlorite, 3 (6); and kaolinite, 9 (13). The mixed-layer clay, except in the Montana disturbed belt, is a random interlayering of 20 to 60 percent illite-type layers, about 35 percent beidelite-type layers, and the remainder montmorillonite-type layers; chlorite or vermiculite layers are rare. Most bentonite differs from shale in its small quartz content, rarely more than a few percent, in the more calcic composition and hightemperature thermal state of its plagioclase, and in its rare kaolinite, near absence of chlorite, and lack of illite-either free or mixed layered with smectite. Bentonite commonly consists of more than 90 percent smectite in which montmorillonite is interlayered with a smaller amount of beidellite. The clay-mineral composition of marine rock, including proportions of layers in the dominant illite-smectite, averages about the same as in the nonmarine rock, though in the latter the composition is more variable. The average content of major chemical constituents also is closely similar, partly because the large clay content of fine-grained offshore-marine shale is balanced by the small clay content of nearshore-marine siltstone and sandstone. In addition, the alumina and alkalic elements in an average of 10 percent more clay in marine rock are partly balanced by these constituents in the 5 percent more feldspar in nonmarine rock. Much of the observed regional and stratigraphic variation in maj or constituents is the result of the three major east-west migrations of the depositional sites of nearshore-marine sandstone and siltstone. Dolomite is found almost exclusively in relatively coarse-grained rock, particularly in nearshore-marine siltstone where diagenetic dolomite is expected, but it is found almost as frequently in nonmarine siltstone. Amounts of minor constituents are nearly equal in marine and nonmarine rocks, except that pyrite and consequently sulfur are relatively sparse in nonmarine rock. Average amounts of organic matter found in marine and nonmarine rocks are nearly identical. However, organic matter in nonmarine rock occurs almost entirely in volumetric

The clay mineral and Sr-Nd isotopic composition for fine-grained fraction of sediments from northwestern South China Sea: implications for sediment provenance

NASA Astrophysics Data System (ADS)

Cai, G.

2013-12-01

*Guanqiang Cai caiguanqiang@sina.com Guangzhou Marine Geological Survey, Guangzhou, 510760, P.R. China As the largest marginal sea in the western pacific, the South China Sea (SCS) receives large amount of terrigenous material annually through numerous rivers from surrounding continents and islands, which make it as the good place for the study of source to sink process. Yet few studies put emphasis on the northwestern continental shelf and slope in the SCS, even though most of the detrital materials derived from the Red River and Hainan Island are deposited in this area, and northwestern shelf plays a significant role in directly linking the South China, the Indochina and the South China Sea and thus controlling the source to sink process of terrestrial sediment. We presented the clay mineral and Sr-Nd isotopic composition of fine-grained fraction for sediments from northwestern SCS, in order to identify sediment source and transportation. The results show that the clay mineral of northwestern SCS sediments are mainly illite (30%~59%), smectite (20%~40%) and kaolinite (8%~35%), with minor chlorite. The illite chemical index varies between 0.19 and 0.75 with an average of 0.49, indicating an intensive hydrolysis in the source region. The 87Sr/86Sr ratios of sediments range from 0.716288 to 0.734416 (average of 0.724659), and ɛ Nd(0) values range from -10.31 to -11.62 (average of -10.93), which suggest that the source rocks of these sediments are derived from continental crust. The Hainan Island is an important source for sediments deposited in the nearshore and western shelf, especially for illite, kaolinite and smectite clay minerals. Furthermore, the relatively high contents of kaolinite and smectite in sediments from eastern shelf and southern slope of Hainan Island are also controlled by the supply of terrigenous materials from Hainan, which cannot be resulted from sedimentary differentiation of the Pearl and Red river sediments. And the correlation analysis between smectite and Sr-Nd isotopic ratios imply that the smectite in sediments mainly come from chemical weathering products of old continental crust, rather than volcanic rocks of Luzon island.

Exploring the potential of phyllosilicate minerals as potassium fertilizers using sodium tetraphenylboron and intensive cropping with perennial ryegrass

PubMed Central

Li, Ting; Wang, Huoyan; Wang, Jing; Zhou, Zijun; Zhou, Jianmin

2015-01-01

In response to addressing potassium (K) deficiency in soil and decreasing agricultural production costs, the potential of K-bearing phyllosilicate minerals that can be directly used as an alternative K source has been investigated using sodium tetraphenylboron (NaTPB) extraction and an intensive cropping experiment. The results showed that the critical value of K-release rate and leaf K concentration was 3.30 g kg−1 h−1 and 30.64 g (kg dry matter)−1, respectively under the experimental conditions. According to this critical value, the maximum amount of released K that could be utilized by a plant with no K deficiency symptoms was from biotite (27.80 g kg−1) and vermiculite (5.58 g kg−1), followed by illite, smectite and muscovite with 2.76, 0.88 and 0.49 g kg−1, respectively. Ryegrass grown on phlogopite showed K deficiency symptoms during the overall growth period. It is concluded that biotite and vermiculite can be directly applied as a promising and sustainable alternative to the use of classical K fertilizers, illite can be utilized in combination with soluble K fertilizers, whereas muscovite, phlogopite and smectite may not be suitable for plant growth. Further field experiments are needed to assess the use of these phyllosilicate minerals as sources of K fertilizer. PMID:25782771

Multiple techniques for mineral identification of terrestrial evaporites relevant to Mars exploration

NASA Astrophysics Data System (ADS)

Stivaletta, N.; Dellisanti, F.; D'Elia, M.; Fonti, S.; Mancarella, F.

2013-05-01

Sulfates, commonly found in evaporite deposits, were observed on Mars surface during orbital remote sensing and surface exploration. In terrestrial environments, evaporite precipitation creates excellent microniches for microbial colonization, especially in desert areas. Deposits comprised of gypsum, calcite, quartz and silicate deposits (phyllosilicates, feldspars) from Sahara Desert in southern Tunisia contain endolithic colonies just below the rock surface. Previous optical observations verified the presence of microbial communities and, as described in this paper, spectral visible analyses have led to identification of chlorophylls belonging to photosynthetic bacteria. Spectral analyses in the infrared region have clearly detected the presence of gypsum and phyllosilicates (mainly illite and/or smectite), as well as traces of calcite, but not quartz. X-ray diffraction (XRD) analysis has identified the dominant presence of gypsum as well as that of other secondary minerals such as quartz, feldspars and Mg-Al-rich phyllosilicates, such as chlorite, illite and smectite. The occurrence of a small quantity of calcite in all the samples was also highlighted by the loss of CO2 by thermal analysis (TG-DTA). A normative calculation using XRD, thermal data and X-ray fluorescence (XRF) analysis has permitted to obtain the mineralogical concentration of the minerals occurring in the samples. The combination of multiple techniques provides information about the mineralogy of rocks and hence indication of environments suitable for supporting microbial life on Mars surface.

Ball clay and bentonite deposits of the central and western Gulf of Mexico Coastal Plain, United States

USGS Publications Warehouse

Hosterman, John W.

1984-01-01

The Gulf of Mexico Coastal Plain produces approximately 85 percent of the ball clay used in the United States. The best commercial-grade clay deposits are composed of poorly crystalline kaolinite and small amounts of Md illite and (or) smectite. Sand and silt and iron oxide minerals are virtually absent, but quartz is present in the clay-size fraction. The best grade ball clays are found as lenses limited to the Wilcox Group (Paleocene and lower Eocene) and Claiborne Group (middle Eocene). Reserves of ball clay are sufficient for the present, but because of the lenticular nature of the clay bodies, close-spaced drilling, detailed sampling, mineralogic analyses, and ceramic testing are needed to prove future reserves.Approximately 11 percent of the total bentonite produced in the United States comes from the Gulf Coast region. The commercial-grade bentonites are composed primarily of smectite with little or no Md illite and kaolinite. The nonclay impurities are quartz, feldspar, muscovite, biotite, calcite, dolomite, gypsum, and heulandite. Commercial bentonites occur in the Upper Cretaceous formations in Alabama and Mississippi, in Paleocene formations in Mississippi and Tennessee, and in Eocene and Miocene formations in Texas. The demand for low-swelling bentonite of the Gulf Coastal Plain has not increased along with the demand for swelling bentonite; therefore the reserves are adequate.

[Effects of Long-term Implementation of the Flow-Sediment Regulation Scheme on Grain and Clay Compositions of Inshore Sediments in the Yellow River Estuary].

PubMed

Wang, Miao-miao; Sun, Zhi-gao; Lu, Xiao-ning; Wang, Wei; Wang, Chuan-yuan

2015-04-01

Based on the laser particle size and X-ray diffraction (XRD) analysis, 28 sediment samples collected from the inshore region of the Yellow River estuary in October 2013 were determined to discuss the influence of long-term implementation of the flow-sediment regulation scheme (FSRS, initiated in 2002) on the distributions of grain size and clay components (smectite, illite, kaolinite and chlorite) in sediments. Results showed that, after the FSRS was implemented for more than 10 years, although the proportion of sand in inshore sediments of the Yellow River estuary was higher (average value, 23.5%) than those in sediments of the Bohai Sea and the Yellow River, silt was predominated (average value, 59.1%) and clay components were relatively low (average value, 17.4%). The clay components in sediments of the inshore region in the Yellow River estuary were close with those in the Yellow River. The situation was greatly changed due to the implementation of FSRS since 2002, and the clay components were in the order of illite > smectite > chlorite > kaolinite. This study also indicated that, compared to large-scale investigation in Bohai Sea, the local study on the inshore region of the Yellow River estuary was more favorable for revealing the effects of long-term implementation of the FSRS on sedimentation environment of the Yellow River estuary.

Cordão Formation: loess deposits in the southern coastal plain of the state of Rio Grande do Sul, Brazil.

PubMed

Lopes, Renato P; Dillenburg, Sergio R; Schultz, Cesar L

2016-01-01

Loess consists of silt-dominated sediments that cover ~10% of the Earth's surface. In southern South America it occurs in Argentina, Bolivia, Paraguay and Uruguay, and its presence in southern Brazil was never studied in detail. Here is proposed a new lithostratigraphic unit, Cordão Formation, consisting of loess deposits in the southern Brazilian coastal plain. It consists of fine-very fine silt with subordinate sand and clay, found mostly in lowland areas between Pleistocene coastal barriers. These sediments are pale-colored (10YR hue) and forms ~1,5-2,0 meter-thick stable vertical walls. The clay minerals include illite, smectite, interstratified illite/smectite and kaolinite, the coarser fraction is mostly quartz and plagioclase. Caliche and iron-manganese nodules are also present. The only fossils found so far are rodent teeth and a tooth of a camelid (Hemiauchenia paradoxa). Luminescence ages indicate that this loess was deposited in the latest Pleistocene, between ~30 and 10 kyrs ago, and its upper portion was modified by erosion and accumulation of clay and organic matter in the Holocene. The estimated accumulation rate was ~630 g/m2/year. The probable source of this loess is the Pampean Aeolian System of Argentina and it would have been deposited by the increased aeolian processes of the last glacial.

Immobilization of soil cadmium using combined amendments of illite/smectite clay with bone chars.

PubMed

Li, Hong; Ou, Jieyong; Wang, Xuedong; Yan, Zengguang; Zhou, Youya

2018-05-12

The widespread use of cadmium (Cd)-containing organic fertilizers is a source of heavy metal inputs to agricultural soils in suburban areas. Therefore, the research and development of new materials and technologies for the remediation of Cd-contaminated soil is of great significance and has the potential to guarantee the safety of agricultural products and the protection of human health. We performed pot experiments to determine the potential of combined amendments of illite/smectite (I/S) clay with bone chars for the remediation of Cd-contaminated agricultural soils in a suburban area of Beijing, China. The results showed that both diethylene triamine pentaacetic acid (DTPA)-extractable Cd in soil and the Cd in Brassica chinensis were significantly decreased by the application of 1, 2, or 5% combined amendments with various I/S and bone char (BC) ratios. The higher proportions of BC used in the combined amendments resulted in a better immobilization of soil Cd. The application of the 5% amendment that combined I/S with either pig or cattle BC resulted in the best immobilization. All of the combined amendments, regardless of the composition and ratio of the components, had no negative effects on the growth of B. chinensis. Therefore, it was concluded that combined amendments of I/S and BC have a good potential for remediating Cd-contaminated soils.

Treatment of boundary conditions in through-diffusion: A case study of (85)Sr(2+) diffusion in compacted illite.

PubMed

Glaus, M A; Aertsens, M; Maes, N; Van Laer, L; Van Loon, L R

2015-01-01

Valuable techniques to measure effective diffusion coefficients in porous media are an indispensable prerequisite for a proper understanding of the migration of chemical-toxic and radioactive micropollutants in the subsurface and geosphere. The present article discusses possible pitfalls and difficulties in the classical through-diffusion technique applied to situations where large diffusive fluxes of cations in compacted clay minerals or clay rocks occur. The results obtained from a benchmark study, in which the diffusion of (85)Sr(2+) tracer in compacted illite has been studied using different experimental techniques, are presented. It is shown that these techniques may yield valuable results provided that an appropriate model is used for numerical simulations. It is further shown that effective diffusion coefficients may be systematically underestimated when the concentration at the downstream boundary is not taken adequately into account in modelling, even for very low concentrations. A criterion is derived for quasi steady-state situations, by which it can be decided whether the simplifying assumption of a zero-concentration at the downstream boundary in through-diffusion is justified or not. The application of the criterion requires, however, knowledge of the effective diffusion coefficient of the clay sample. Such knowledge is often absent or only approximately available during the planning phase of a diffusion experiment. Copyright © 2015 Elsevier B.V. All rights reserved.

Sand and clay mineralogy of sal forest soils of the Doon Siwalik Himalayas

NASA Astrophysics Data System (ADS)

Mukesh; Manhas, R. K.; Tripathi, A. K.; Raina, A. K.; Gupta, M. K.; Kamboj, S. K.

2011-02-01

The peteromineralogical characterization of the soil was carried out for the 12 soil profiles exposed in the Shorea robusta dominated forests of the Siwalik forest division, Dehradun. The quartz was observed as the dominating light mineral fraction (64-80%) in all the profiles studied. Biotite, hornblende, zircon, tourmaline, rutile and opaques comprising of iron minerals constituted the heavy mineral fraction (20%). The mineralogy of both the sand and clay fractions revealed a mixed mineralogy. The clay minerals in the order of their dominance were vermiculite, illite, kaolinite and mixed layer minerals. The presence of vermiculite and illite in appreciable quantities indicates that these were synthesized from the K-rich soil solution, as orthoclase and micas were present in significant quantities in the sand minerals. The mineral suites identified in the study shows that the geological, climatological and topographical factors of the region collectively played a dominant role in their formation and transformation. After critical appraisal of the results, it may be deduced that the mineralogical composition, physicochemical properties and total elemental analysis of the soils do not show any deficiency of the bases and other plant nutrients in general. The inherent fertility of the soil is good as indicated by the sand and clay mineralogy of the soil and the biotite and feldspar together with the mica is an important source of nutrients for the vegetation in the soils of the Doon valley.

Geological and technological characterization of the Late Jurassic-Early Cretaceous clay deposits (Jebel Ammar, northeastern Tunisia) for ceramic industry

NASA Astrophysics Data System (ADS)

Ben M'barek-Jemaï, Moufida; Sdiri, Ali; Ben Salah, Imed; Ben Aissa, Lassaad; Bouaziz, Samir; Duplay, Joelle

2017-05-01

Late Jurassic-Lower Cretaceous clays of the Jebel Ammar study site were used as raw materials for potential applications in ceramic industry. Physico-chemical characterization of the collected samples was performed using atomic absorption spectroscopy, X-ray diffraction, thermogravimetry and dilatometry (Bugot's curve). Geotechnical study was also undertaken by the assessment of plasticity and liquidity limits. It was found that high concentrations of silica, alumina with SiO2/Al2O3 ratio characterized the studied clays; its high amounts of CaO and Fe2O3 in the Late Jurassic clays indicated their calcareous nature. In addition, technological tests indicated moderate to low plasticity values for the Late Jurassic and Lower Cretaceous clays, respectively. Clay fraction (<2 μm) reached 50% of the natural clay in some cases. Mineralogical analysis showed that Jurassic clays were dominated by smectite, illite and kaolinite, as clay mineral species; calcite was the main associated mineral. Lower Cretaceous clays were mainly composed of abundant illite accompanied by well-crystallized smectite and kaolinite. Kaolinite gradually increased upwards, reaching 70% of the total clay fraction (i.e. <2 μm). Quartz, calcite and feldspar were the main non-clay minerals. Based on these analyses, the clays meet technological requirements that would allow their use in the ceramic industry and for the manufacturing of ceramic tiles.

Physical and chemical characterization of Devonian gas shale. Quarterly status report, October 1-December 31, 1978

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zielinski, R.E.; Nance, S.W.

On shale samples from the WV-6 (Monongalia County, West Virginia) well, mean total gas yield was 80.4 ft/sup 3//ton. Mean hydrocarbon gas yield was 5.7 ft/sup 3//ton, 7% of total yield. Methane was the major hydrocarbon component and carbon dioxide the major nonhydrocarbon component. Oil yield was negligible. Clay minerals and organic matter were the dominant phases of the shale. Illite averages 76% of the total clay mineral content. This is detrital illite. Permeation of methane, parallel to the bedding direction for select samples from WV-5 (Mason County, West Virginia) well ranges from 10/sup -4/ to 10/sup -12/ darcys. Themore » permeability of these shales is affected by orgaic carbon content, density, particle orientation, depositional facies, etc. Preliminary studies of Devonian shale methane sorption rates suggest that these rates may be affected by shale porosity, as well as absorption and adsorption processes. An experimental system was designed to effectively simulate sorption of methane at natural reservoir conditions. The bulk density and color of select shales from Illinois, Appalachian and Michigan Basins suggest a general trend of decreasing density with increasing organic content. Black and grayish black shales have organic contents which normally exceed 1.0 wt %. Medium dark gray and gray shales generally have organic contents less than 1.0 wt %.« less

Two cation exchange models for direct and inverse modelling of solution major cation composition in equilibrium with illite surfaces

NASA Astrophysics Data System (ADS)

Tournassat, Christophe; Gailhanou, Hélène; Crouzet, Catherine; Braibant, Gilles; Gautier, Anne; Lassin, Arnault; Blanc, Philippe; Gaucher, Eric C.

2007-03-01

Na/K, Na/Ca and Na/Mg exchange isotherms were performed on the fine fraction (<2 μm) of Imt-2 illite samples at a total normality of about 0.005 mol/L in anionic chloride medium. The derived selectivity coefficients for Na/K, Na/Ca and Na/Mg were found to vary as a function of the exchanger composition and compared well with the data collected in the literature for similar experimental conditions. Two models were built to reproduce the data: the first was a multi(2)-site model with constant Gaines and Thomas selectivity coefficients; the second was a one-site model taking into account surface species activity coefficients. The results of the models were in rather good agreement with both our data and literature data. The multi-site model proved to be efficient in predicting the exchanger composition as a function of the Na/Ca/Mg/K concentrations in solution, whereas the one-site model proved to be a better approach to derive the Na/Ca/Mg/K concentrations in solution based on the knowledge of the exchanger composition and the total normality of the solution. The interest of this approach is illustrated by the need for major cation solute concentration predictions in compacted clay for the characterization of nuclear deep disposal host rock repositories.

Creep and Sliding in Clays Slopes: Mutual Effects of Interlayer Swelling and Ice Jacking.

DTIC Science & Technology

1984-01-11

chlorite 14% (6-21%) calcite 6,5% (1 - 15%) kaolinite 2% ( 1- 5%) dolomite 0,5% (0 - 4%) montmorillonite 23% (15-35%) Non clay phases 19% (15-30%) Clay...iconcretions, 200 mm coal lenses RE 3 4 Calcite N Quartz Feldspar Illite-muscovite Z Chlorite E Kaolinite montmori 1 loni te Fig. 10: Mineral content... montmorillonite , belong to a fluviatile fresh water cycle and are possibly influenced by volcanic ash falls. The series under investigation belongs to the upper

The Use 0f AVIRIS Imagery To Assess Clay Mineralogy And Debris-Flow Potential In Cataract Canyon, Utah: A Preliminary Report

NASA Technical Reports Server (NTRS)

Rudd, Lawrence; Merenyi, Erzsebet

2004-01-01

Worldwide debris flows destroy property and take human lives every year (Costa, 1984). As a result of extensive property damage and loss of life there is a pressing need to go beyond just describing the nature and extent of debris flows as they occur. Most of the research into debris-flow initiation has centered on rainfall, slope angle, and existing debris-flow deposits (Costa and Wieczorek, 1987). The factor of source lithology has been recently addressed by studies in the sedimentary terranes of Grand Canyon (Webb et al., 1996; Griffiths et al., 1996) and on the Colorado Plateau as a whole.3 On the Colorado Plateau shales dominated by kaolinite and illite clays are significantly more likely to be recent producers of debris-flows than are shales in which smectite clays dominate.3 Establishing the location of shales and colluvial deposits containing kaolinite and illite clays in sedimentary terranes on the Colorado Plateau is essential to predicting where debris flows are likely to occur. AVIRIS imagery can be used to distinguish between types of clay minerals (Chabrillat et al., 2001), providing the basis for surface-materials maps. The ultimate product of this study will be a model that can be used to estimate the debris-flow hazard in Cataract Canyon, Utah. This model will be based on GIS overlay analysis of debris-flow initiation factor maps, including surface-materials maps derived from AVIRIS data.

Supercritical CO2 uptake by nonswelling phyllosilicates

PubMed Central

Tokunaga, Tetsu K.; Ashby, Paul D.; Kim, Yongman; Voltolini, Marco; Gilbert, Benjamin; DePaolo, Donald J.

2018-01-01

Interactions between supercritical (sc) CO2 and minerals are important when CO2 is injected into geologic formations for storage and as working fluids for enhanced oil recovery, hydraulic fracturing, and geothermal energy extraction. It has previously been shown that at the elevated pressures and temperatures of the deep subsurface, scCO2 alters smectites (typical swelling phyllosilicates). However, less is known about the effects of scCO2 on nonswelling phyllosilicates (illite and muscovite), despite the fact that the latter are the dominant clay minerals in deep subsurface shales and mudstones. Our studies conducted by using single crystals, combining reaction (incubation with scCO2), visualization [atomic force microscopy (AFM)], and quantifications (AFM, X-ray photoelectron spectroscopy, X-ray diffraction, and off-gassing measurements) revealed unexpectedly high CO2 uptake that far exceeded its macroscopic surface area. Results from different methods collectively suggest that CO2 partially entered the muscovite interlayers, although the pathways remain to be determined. We hypothesize that preferential dissolution at weaker surface defects and frayed edges allows CO2 to enter the interlayers under elevated pressure and temperature, rather than by diffusing solely from edges deeply into interlayers. This unexpected uptake of CO2, can increase CO2 storage capacity by up to ∼30% relative to the capacity associated with residual trapping in a 0.2-porosity sandstone reservoir containing up to 18 mass % of illite/muscovite. This excess CO2 uptake constitutes a previously unrecognized potential trapping mechanism. PMID:29339499

Supercritical CO2 uptake by nonswelling phyllosilicates.

PubMed

Wan, Jiamin; Tokunaga, Tetsu K; Ashby, Paul D; Kim, Yongman; Voltolini, Marco; Gilbert, Benjamin; DePaolo, Donald J

2018-01-30

Interactions between supercritical (sc) CO 2 and minerals are important when CO 2 is injected into geologic formations for storage and as working fluids for enhanced oil recovery, hydraulic fracturing, and geothermal energy extraction. It has previously been shown that at the elevated pressures and temperatures of the deep subsurface, scCO 2 alters smectites (typical swelling phyllosilicates). However, less is known about the effects of scCO 2 on nonswelling phyllosilicates (illite and muscovite), despite the fact that the latter are the dominant clay minerals in deep subsurface shales and mudstones. Our studies conducted by using single crystals, combining reaction (incubation with scCO 2 ), visualization [atomic force microscopy (AFM)], and quantifications (AFM, X-ray photoelectron spectroscopy, X-ray diffraction, and off-gassing measurements) revealed unexpectedly high CO 2 uptake that far exceeded its macroscopic surface area. Results from different methods collectively suggest that CO 2 partially entered the muscovite interlayers, although the pathways remain to be determined. We hypothesize that preferential dissolution at weaker surface defects and frayed edges allows CO 2 to enter the interlayers under elevated pressure and temperature, rather than by diffusing solely from edges deeply into interlayers. This unexpected uptake of CO 2 , can increase CO 2 storage capacity by up to ∼30% relative to the capacity associated with residual trapping in a 0.2-porosity sandstone reservoir containing up to 18 mass % of illite/muscovite. This excess CO 2 uptake constitutes a previously unrecognized potential trapping mechanism. Copyright © 2018 the Author(s). Published by PNAS.

From illite/smectite clay to mesoporous silicate adsorbent for efficient removal of chlortetracycline from water.

PubMed

Wang, Wenbo; Tian, Guangyan; Zong, Li; Zhou, Yanmin; Kang, Yuru; Wang, Qin; Wang, Aiqin

2017-01-01

A series of mesoporous silicate adsorbents with superior adsorption performance for hazardous chlortetracycline (CTC) were sucessfully prepared via a facile one-pot hydrothermal reaction using low-cost illite/smectite (IS) clay, sodium silicate and magnesium sulfate as the starting materials. In this process, IS clay was "teared up" and then "rebuilt" as new porous silicate adsorbent with high specific surface area of 363.52m 2 /g (about 8.7 folds higher than that of IS clay) and very negative Zeta potential (-34.5mV). The inert SiOSi (Mg, Al) bonds in crystal framework of IS were broken to form Si(Al) O - groups with good adsorption activity, which greatly increased the adsorption sites served for holding much CTC molecules. Systematic evaluation on adsorption properties reveals the optimal silicate adsorbent can adsorb 408.81mg/g of CTC (only 159.7mg/g for raw IS clay) and remove 99.3% (only 46.5% for raw IS clay) of CTC from 100mg/L initial solution (pH3.51; adsorption temperature 30°C; adsorbent dosage, 3g/L). The adsorption behaviors of CTC onto the adsorbent follows the Langmuir isotherm model, Temkin equation and pseudo second-order kinetic model. The mesopore adsorption, electrostatic attraction and chemical association mainly contribute to the enhanced adsorption properties. As a whole, the high-efficient silicate adsorbent could be candidates to remove CTC from the wastewater with high amounts of CTC. Copyright © 2016. Published by Elsevier B.V.

Supercritical CO 2 uptake by nonswelling phyllosilicates

DOE PAGES

Wan, Jiamin; Tokunaga, Tetsu K.; Ashby, Paul D.; ...

2018-01-16

Interactions between supercritical (sc) CO 2 and minerals are important when CO 2 is injected into geologic formations for storage and as working fluids for enhanced oil recovery, hydraulic fracturing, and geothermal energy extraction. It has previously been shown that at the elevated pressures and temperatures of the deep subsurface, scCO 2 alters smectites (typical swelling phyllosilicates). However, less is known about the effects of scCO 2 on nonswelling phyllosilicates (illite and muscovite), despite the fact that the latter are the dominant clay minerals in deep subsurface shales and mudstones. Our studies conducted by using single crystals, combining reaction (incubationmore » with scCO 2 ), visualization [atomic force microscopy (AFM)], and quantifications (AFM, X-ray photoelectron spectroscopy, X-ray diffraction, and off-gassing measurements) revealed unexpectedly high CO 2 uptake that far exceeded its macroscopic surface area. Results from different methods collectively suggest that CO 2 partially entered the muscovite interlayers, although the pathways remain to be determined. We hypothesize that preferential dissolution at weaker surface defects and frayed edges allows CO 2 to enter the interlayers under elevated pressure and temperature, rather than by diffusing solely from edges deeply into interlayers. This unexpected uptake of CO 2, can increase CO 2 storage capacity by up to ~30% relative to the capacity associated with residual trapping in a 0.2-porosity sandstone reservoir containing up to 18 mass % of illite/muscovite. This excess CO 2 uptake constitutes a previously unrecognized potential trapping mechanism.« less

Effect of minerals on accumulation of Cs by fungus Saccaromyces cerevisiae.

PubMed

Ohnuki, Toshihiko; Sakamoto, Fuminori; Yamasaki, Shinya; Kozai, Naofumi; Shiotsu, Hiroyuki; Utsunomiya, Satoshi; Watanabe, Naoko; Kozaki, Tamotsu

2015-06-01

The accumulation of Cs by unicellular fungus of Saccharomyces cerevisiae in the presence of minerals has been studied to elucidate the role of microorganisms in the migration of radioactive Cs in the environment. Two different types of experiments were employed: experiments using stable Cs to examine the effect of a carbon source on the accumulation of Cs, and accumulation experiments of radioactive Cs from agar medium containing (137)Cs and zeolite, vermiculite, phlogopite, smectite, mica, or illite as mineral supplements. In the former type of experiments, the Cs-accumulated cells were analyzed by scanning electron microscopy equipped with energy dispersive X-ray analysis (SEM-EDS). In the latter type, the radioactivity in the yeast cells was measured by an autoradiography technique. When a carbon source was present, higher amounts of Cs accumulated in the cells than in the resting condition without a carbon source. Analyses with SEM-EDS showed that no mineral formed on the cell surface. These results indicate that the yeast cells accumulate Cs by adsorption on the cell surface and intracellular accumulation. In the presence of minerals in the agar medium, the radioactivity in the yeast cells was in the order of mica > smectite, illite > vermiculite, phlogopite, zeolite. This order is inversely correlated to the ratio of the concentration of radioactive Cs between the minerals and the medium solution. These results strongly suggest that the yeast accumulates radioactive Cs competitively with minerals. Copyright © 2015 Elsevier Ltd. All rights reserved.

Clay mineralogy of surface sediments as a tool for deciphering river contributions to the Cariaco Basin (Venezuela)

NASA Astrophysics Data System (ADS)

Bout-Roumazeilles, V.; Riboulleau, A.; du Châtelet, E. Armynot; Lorenzoni, L.; Tribovillard, N.; Murray, R. W.; Müller-Karger, F.; Astor, Y. M.

2013-02-01

The mineralogical composition of 95 surface sediment samples from the Cariaco Basin continental shelf and Orinoco delta was investigated in order to constrain the clay-mineral main provenance and distribution within the Cariaco Basin. The spatial variability of the data set was studied using a geo-statistical approach that allows drawing representative clay-mineral distribution maps. These maps are used to identify present-day dominant sources for each clay-mineral species in agreement with the geological characteristics of the main river watersheds emptying into the basin. This approach allows (1) identifying the most distinctive clay-mineral species/ratios that determine particle provenance, (2) evaluating the respective contribution of local rivers, and (3) confirming the minimal present-day influence of the Orinoco plume on the Cariaco Basin sedimentation. The Tuy, Unare, and Neveri Rivers are the main sources of clay particles to the Cariaco Basin sedimentation. At present, the Tuy River is the main contributor of illite to the western part of the southern Cariaco Basin continental shelf. The Unare River plume, carrying smectite and kaolinite, has a wide westward propagation, whereas the Neveri River contribution is less extended, providing kaolinite and illite toward the eastern Cariaco Basin. The Manzanares, Araya, Tortuga, and Margarita areas are secondary sources of local influence. These insights shed light on the origin of present-day terrigenous sediments of the Cariaco Basin and help to propose alternative explanations for the temporal variability of clay mineralogy observed in previously published studies.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wan, Jiamin; Tokunaga, Tetsu K.; Ashby, Paul D.

Interactions between supercritical (sc) CO 2 and minerals are important when CO 2 is injected into geologic formations for storage and as working fluids for enhanced oil recovery, hydraulic fracturing, and geothermal energy extraction. It has previously been shown that at the elevated pressures and temperatures of the deep subsurface, scCO 2 alters smectites (typical swelling phyllosilicates). However, less is known about the effects of scCO 2 on nonswelling phyllosilicates (illite and muscovite), despite the fact that the latter are the dominant clay minerals in deep subsurface shales and mudstones. Our studies conducted by using single crystals, combining reaction (incubationmore » with scCO 2 ), visualization [atomic force microscopy (AFM)], and quantifications (AFM, X-ray photoelectron spectroscopy, X-ray diffraction, and off-gassing measurements) revealed unexpectedly high CO 2 uptake that far exceeded its macroscopic surface area. Results from different methods collectively suggest that CO 2 partially entered the muscovite interlayers, although the pathways remain to be determined. We hypothesize that preferential dissolution at weaker surface defects and frayed edges allows CO 2 to enter the interlayers under elevated pressure and temperature, rather than by diffusing solely from edges deeply into interlayers. This unexpected uptake of CO 2, can increase CO 2 storage capacity by up to ~30% relative to the capacity associated with residual trapping in a 0.2-porosity sandstone reservoir containing up to 18 mass % of illite/muscovite. This excess CO 2 uptake constitutes a previously unrecognized potential trapping mechanism.« less

Exploration and geology of the Karangahake and Rahu epithermal Au-Ag deposits, Hauraki Goldfield

USGS Publications Warehouse

Simpson, Mark P.; Stevens, Murray R; Mauk, Jeffrey L.; Harris, Matthew C; Stuart, Alistair G J

2016-01-01

Karangahake was the third largest gold producer in the Hauraki goldfield. In 2009, New Talisman Gold mines was granted a mining permit, and plans are underway to commence underground mine development of the Maria vein, which has a maiden Ore Reserve (consistent with the 2012 JORC Code) of 28 800 oz Au and 127 800 oz Ag. Exploration drilling at Rahu, located 2 km north of Karangahake has identified polymictic hydrothermal breccias and quartz veins that are strongly gold anomalous. Some quartz vein clasts within the breccia have up to 8.7 g/t Au, suggesting the presence of higher grade quartz vein(s) either below or directly adjacent to the breccias. A controlled source audio-frequency magnetotelluric (CSAMT) survey at Rahu revealed that strongly resistive zones extend below the Barbara and Eunice anomalies to at least 300 m depth and likely correspond to areas of increased silicification, breccias and/or veins. Future drilling will focus on these targets. Detailed geophysical, alteration and fluid inclusion studies have been undertaken at Karangahake, Rahu and Ascot (c 1 km NW of Rahu). Karangahake and Rahu both occur within a broad demagnetised zone, c 4.2 × 2.7 km, in which magnetite has been destroyed by strong hydrothermal alteration. At Karangahake, andesite and overlying minor rhyolite are replaced by adularia, chlorite, illite, pyrite, plus minor albite, epidote and calcite, which have formed from upwelling chloride waters that at depth were hotter than 280°C. At Rahu, localised adularia coupled with complex distributions of illite and interstratified illite-smectite, suggest cooler (c 180° to 240°C) and more focused fluid flow, as well as inferred cool groundwater influx. Fluid inclusion data suggest veins at Karangahake, Rahu and Ascot formed beneath palaeowater tables at 920 m, 440 m and 430 m relative to current sea level (asl), respectively. At Ascot, the presence of silica sinter at 135 m asl, which formed at the palaeosurface, is shallower compared to the fluid inclusion depth estimate and suggests that the palaeowater table here rose some 300 m during hydrothermal activity due to burial, resulting in overprinting. This overprint may also have occurred at Karangahake and Rahu, but the evidence is inconclusive; although burial during hydrothermal activity could explain the exceptional 700 m vertical range of mineralisation at Karangahake and raises the possibility of concealed mineralisation at depth elsewhere within the Karangahake alteration envelope.

Influence of Compositional Variations on Floc Size and Strength

NASA Astrophysics Data System (ADS)

Yin, H.; Tan, X.; Reed, A. H.; Furukawa, Y.; Zhang, G.

2010-12-01

Clay-biopolymer micro aggregates or flocs are abundant in waters, including rivers, lakes, and oceans. Owing to their small size and charged surfaces, fine-grained inorganic sediment particles, mainly clays, interact actively with organic substances, such as organic matter and biogenic polymers, to form aggregates or flocs, typically in the size of 10-1000 μm. The flocs in ocean waters are also termed “marine snow”. These flocs are typically porous, tenuous, and soft in nature. During transport in suspension, they may breakdown and decrease in size if the turbulent shear stress exceeds their strength. They may also collide and form larger ones if the shear stress is relatively small. Since flocs of different size and structure settle at different velocities, understanding their strength is also of essential importance for sediment hydrodynamics, transport, and management. Our study focuses on investigating the influence of compositional variations on floc size and strength so that a better understanding of floc dynamics can be achieved. A laser diffraction-based Cilas® particle size and shape analyzer with controllable fluid circulation velocity was employed to conduct floc size measurements and shape imaging, the latter achieved by a high resolution inverted optical microscope, which is also installed with the size analyzer. Totally two clay minerals, kaolinite and illite, were tested as the model inorganic solid skeleton minerals for floc formation, and two biopolymers, anionic xanthan gum and neutral guar gum, were chosen as analogs of naturally occurring organic matter or biopolymers to simulate clay-biopolymer floc formation. Moreover, the concentration of both organic and inorganic phases was varied. The floc breakage or tensile strength was indirectly estimated by the varied fluid flow velocity in the particle size analyzer’s circulation system. For each individual composition, stable flocs were formed by three different fluid circulating velocities, resulting in different shearing stress in the fluid. Experimental results show that organic biopolymers can have profound influences on clay flocculation process and the resultant floc size and strength. Anionic xanthan gum tends to form smaller and weaker clay-biopolymer flocs than neutral guar gum, because the Coulombic repulsion forces develop between the two negatively charged constituents. Illite results in stronger clay-guar flocs than kaolinite, probably due to the relatively higher negative charges on illite surface. Generally, a bimodal distribution of floc size frequency was observed for all types of flocs. The maxim floc sizes range from 10-30 μm for kaolinite-xanthan flocs to 250-300 μm for kaolinite-guar flocs at a weight ratio of 1:1.

Optical Properties of Natural Minerals in the Far-Infrared

NASA Astrophysics Data System (ADS)

Long, Larry Lavern

The reflectivity of natural mineral powders were measured in the far infrared. The complex indices of refraction were then determined by Kramers-Kronig analysis or dispersive analysis. The samples were constructed by pressing the powdered sample into a 13 mm diameter pellet. A few of the samples that were measured were kaolin, illite, and montmorillonite, clay samples that could not be obtained in large single crystals. For calcite and gypsum crystals a comparison between the single crystal measurements and powder measurements was done to determine the effect of sample preparation on the measured spectra.

Effects of clay minerals on transport of graphene oxide in saturated porous media.

PubMed

Lu, Taotao; Xia, Tianjiao; Qi, Yu; Zhang, Chengdong; Chen, Wei

2017-03-01

The presence of kaolinite, montmorillonite, and illite in packed quartz sand inhibited the transport of graphene oxide to different degrees. Transport inhibition was exerted mainly by the presence of positively charged sites on clay edges (which served as favorable deposition sites), whereas the effects on the overall particle-collector interaction energy and flow path were small. Kaolinite exhibited the most significant transport-inhibition effects because of its high percentage of edge area. Environ Toxicol Chem 2017;36:655-660. © 2016 SETAC. © 2016 SETAC.

Distribution of clay minerals in surface sediments of the western Gulf of Thailand: Sources and transport patterns

NASA Astrophysics Data System (ADS)

Shi, Xuefa; Liu, Shengfa; Fang, Xisheng; Qiao, Shuqing; Khokiattiwong, Somkiat; Kornkanitnan, Narumol

2015-06-01

A high density sampling program during two joint China-Thailand scientific cruises in 2011-2012 included collection of 152 gravity box cores in the Gulf of Thailand (GoT). Samples from the top 5 cm of each core were analyzed by X-ray diffraction for clay mineral content. Several systemic analytical approaches were applied to examine the distribution pattern and the constraint factors of clay minerals in the surface sediments of the western GoT. The clay minerals mainly comprise illite, kaolinite, chlorite and smectite, having the average weight percent distributions of 50%, 34%, 14% and 2%, respectively. Based on the spatial distribution characteristics and statistical results, the study area can be classified into three provinces. Province I contains high concentrations of smectite, and covers the northern GoT, sediments in this province are mainly from rivers discharging into the upper GoT, especially the Chao Phraya and Mae Klong Rivers. Sediments in Province II are characterized by higher values of illite, located in the central GoT, where fine sediments are contributed by the Mekong River and from the South China Sea. Province Ш, in the coastal regions of southwestern GoT close to Malaysia, exhibits a clay mineral assemblage with complex distribution patterns, and may contain terrestrial materials from the Mae Klong River as well as re-suspended sediments. Results of integrative analysis also demonstrate that the hydrodynamic environment in the study area, especially the seasonal various circumfluence and eddies, play an important role in the spatial distribution and dispersal of clay fraction in sediments.

New Location of Chicxulub's Impact Ejecta in Central Belize.

NASA Astrophysics Data System (ADS)

Ocampo, A.; Ames, D.; Pope, K.; Smit, J.

2003-04-01

Chicxulub ejecta composed of altered glass, accretionary lapilli, and pebble to cobble sized carbonate clasts are found in the Cayo District of central Belize, about 500 km southeast of the Chicxulub impact crater centre. The ejecta layer, found near the town of Armenia, in central Belize, is about 4 m thick, and rests unconformably on a deeply weathered Cretaceous land surface, of the Barton Creek Formation dolomite. There are similarities between these ejecta and the basal bed (spheroid bed) of the continuous ejecta blanket deposits (Albion Formation) found in northern Belize and southern Quintana Roo, Mexico, 340-360 km from Chicxulub. Although, the spheroid bed in the Armenia location exhibits an exceptional state of impact glass preservation, than that found in Northern Belize. Overlying the bed with glass and lapilli is a 5-m-thick layer of limestone pebbles and cobbles, which contain altered glass and shocked quartz in the matrix. The well-rounded limestone pebbles and cobbles show striated and amygdaloidal textures. We interpret the central Belize spheroid bed deposit with accretionary lapilli as ejecta deposited by the rapidly expanding vapour plume, and may contain carbonate condensates. The altered glass component consists of an inter-stratified illite-smectite mixed layer clay dominated by illite. The overlying pebble and cobble bed may be a later deposit containing re-worked ejecta, or a lateral extension of the coarse ejecta beds found in northern Belize. This new impact ejecta deposit, found in central Belize ~500 km from Chicxulub, emphasizes the importance of volatile-rich target rock and the dispersal of ejecta by the expanding vapour plume.

Detecting the thermal aureole of a magmatic intrusion in immature to mature sediments: a case study in the East Greenland Basin (73°N)

NASA Astrophysics Data System (ADS)

Aubourg, Charles; Techer, Isabelle; Geoffroy, Laurent; Clauer, Norbert; Baudin, François

2014-01-01

The Cretaceous and Triassic argillaceous rocks from the passive margin of Greenland have been investigated in order to detect the thermal aureole of magmatic intrusions, ranging from metric dyke to kilometric syenite pluton. Rock-Eval data (Tmax generally <468 °C), vitrinite reflectance data (R0 < 0.9 per cent) and illite cristallinity data (ICI > 0.3), all indicate a maximum of 5 km burial for the argillaceous rocks whatever the distance to an intrusion. The K-Ar dating of the clays <2 μm fraction suggests that illites are mostly detrital, except near magmatic intrusions where younger ages are recorded. To get more information about the extent of the thermal aureole, rock magnetism data were determined. At distance away from the thermal aureole of the syenite intrusion, Triassic argillaceous rocks reveal a standard magnetic assemblage compatible with their burial (R0 ˜ 0.4 per cent). It is constituted essentially by neoformed stoichiometric magnetite (Fe3O4). In contrast, within the thermal aureole of the magmatic intrusions, the Cretaceous argillaceous rocks contain micron-sized pyrrhotite (Fe7S8), firmly identified through the recognition of Besnus transition at 35 K. The thermal demagnetization of natural remanence carried by this pyrrhotite shows a diagnostic `square shouldered' pattern, indicating a narrow grain size distribution of pyrrhotite. The extension of this diagnostic pyrrhotite maps a ˜10-km-thick aureole around the syenitic pluton. Away from this aureole, the magnetic assemblage is diagnostic of those found in argillaceous rocks where organic matter is mature.

Distribution and composition of gold in porphyry gold systems: example from the Biely Vrch deposit, Slovakia

NASA Astrophysics Data System (ADS)

Koděra, Peter; Kozák, Jaroslav; Brčeková, Jana; Chovan, Martin; Lexa, Jaroslav; Jánošík, Michal; Biroň, Adrián; Uhlík, Peter; Bakos, František

2018-03-01

The Biely Vrch deposit in the Western Carpathians is assigned to the shallow, sulfide-poor porphyry gold deposit type and has an exceptionally low Cu/Au ratio. According to 3-D geochemical models, there is a limited spatial correlation between Au and Cu due to the primary introduction of gold by a salt melt and Cu by low-density vapor. Despite a rough spatial correlation of gold grades with quartz stockwork intensity, gold is hosted mostly by altered rock, exclusively in native form. Three main gold mineral assemblages were recognized here. In the deepest parts of the system, the K- and Ca-Na silicate gold assemblage is associated with minerals of high-temperature alteration (plagioclase, K-feldspar, actinolite), with gold grades and fineness depending on depth and potassium content of the host rock: K-silicate alteration hosts the lowest fineness gold ( 914), whereas Ca-Na silicate alteration has the highest ( 983). The intermediate argillic gold assemblage is the most widespread, with gold hosted mainly by chlorite, illite, smectite, and interstratified illite-chlorite-smectite minerals. The gold fineness is mostly variable (875-990) and inherited from the former gold mineral assemblages. The latest advanced argillic gold assemblage has its gold mostly in kaolinite. The extremely high fineness ( 994) results from gold remobilization by late-stage aqueous magmatic-hydrothermal fluids. Uncommon bonanza-grade appears where the earlier gold mineral assemblages were further enriched by this remobilized gold. Primary precipitation of gold occurred during ascent and cooling of salt melts at 450 to 309 °C, mostly during retrograde quartz solubility.

Understanding Copper Isotope Behavior in the High Temperature Magmatic-Hydrothermal Porphyry Environment

NASA Astrophysics Data System (ADS)

Gregory, Melissa J.; Mathur, Ryan

2017-11-01

Copper stable isotope geochemistry has the potential to constrain aspects of ore deposit formation once variations in the isotopic data can be related to the physiochemical conditions during metal deposition. This study presents Cu isotope ratios for samples from the Pebble porphyry Cu-Au-Mo deposit in Alaska. The δ65Cu values for hypogene copper sulfides range from -2.09‰ to 1.11‰ and show linear correlations with the δ18O isotope ratios calculated for the fluid in equilibrium with the hydrothermal alteration minerals in each sample. Samples with sodic-potassic, potassic, and illite alteration display a negative linear correlation between the Cu and O isotope results. This suggests that fractionation of Cu isotopes between the fluid and precipitating chalcopyrite is positive as the hydrothermal fluid is evolving from magmatic to mixed magmatic-meteoric compositions. Samples with advanced argillic alteration display a weak positive linear correlation between Cu and O isotope results consistent with small negative fluid-chalcopyrite Cu isotope fractionation during fluid evolution. The hydrothermal fluids that formed sodic-potassic, potassic, and illite alteration likely transported Cu as CuHS0. Hydrothermal fluids that resulted in advanced argillic alteration likely transport Cu as CuCl2-. The pH conditions also control Cu isotope fractionation, consistent with previous experimental work. Larger fractionation factors were found between fluids and chalcopyrite precipitating under neutral conditions contrasting with small fractionation factors calculated between fluids and chalcopyrite precipitating under acidic conditions. Therefore, this study proposes that hydrothermal fluid compositions and pH conditions are related to Cu isotope variations in high temperature magmatic-hydrothermal deposits.

Late Eocene clay boron-derived paleosalinity in the Qaidam Basin and its implications for regional tectonics and climate

NASA Astrophysics Data System (ADS)

Ye, Chengcheng; Yang, Yibo; Fang, Xiaomin; Zhang, Weilin

2016-12-01

The Qaidam Basin, located on the northeastern Tibetan Plateau and containing Cenozoic sediments with a maximum thickness of 12,000 m, is an ideal place to study the phased uplift of the NE Tibetan Plateau and regional climate change. The estimation of the paleosalinity of sedimentary environments not only helps to evaluate the evolution of lakes in this region but offers insights into contemporaneous climate change. We present detailed geochemical and mineralogical investigations from the lacustrine interval of the Hongliugou section in the northern Qaidam Basin to reconstruct salinity fluctuations in the paleolake during the late Eocene era ( 42.0-35.5 Ma). The clay mineral assemblages mainly contain smectite, illite, chlorite, kaolinite and irregular illite/smectite mixed layers. Clay boron-derived paleosalinity estimates (equivalent boron content, Couch's paleosalimeter and B/Ga ratios) along with other proxies sensitive to salinity changes (e.g., Rb/K ratios and ostracod assemblages) collectively indicate an overall brackish sedimentary environment with a higher-salinity period at approximately 40.0-39.2 Ma. This higher-salinity period indicates a more arid environment and is probably related to global cooling. However, the global cooling in late Eocene cannot explain the overall stable long-term salinity pattern, implying that other factors exist. We propose that the migration of the Yiliping depression depocenter in the northern Qaidam and increased orographic rainfall induced by late Eocene tectonic activity at the northern margin of the basin might have partly offset the increase in salinity driven by global cooling.

Linking preferred orientations to elastic anisotropy in Muderong Shale, Australia

DOE PAGES

Kanitpanyacharoen, Waruntorn; Vasin, Roman; Wenk, Hans -Rudolf; ...

2015-01-01

The significance of shales as unconventional hydrocarbon reservoirs, nuclear waste repositories, and geological carbon storage has opened new research frontiers in geophysics. Among many of its unique physical properties, elastic anisotropy has long been investigated by both experimental and computational approaches. Here we calculate elastic properties of Cretaceous Muderong Shale from Australia with a self-consistent averaging method based on microstructural information. The volume fraction and crystallographic preferred orientation distributions of constituent minerals are based on synchrotron X-ray diffraction experiments. Aspect ratios of minerals and pores, determined from scanning electron microscopy (SEM), are introduced in the self-consistent averaging. Our analysis suggestsmore » that phyllosilicates (i.e., illite-mica, illite-smectite, kaolinite, and chlorite) are dominant with ~70 vol.%. The shape of clay platelets displays an average aspect ratio of 0.05. These platelets are aligned parallel to the bedding plane with a rather high degree of preferred orientation. The estimated porosity at ambient pressure is ~17 vol.% and is divided into equiaxial pores and flat pores with an average aspect ratio of 0.01. Our model shows results (e.g. at pressure of ~50 MPa with C 11 = 26.3; C 13 =12.5; C 33 = 18.2; C 44 = 2.8; C 66 = 6.8 [GPa]) that compare satisfactorily with values derived from ultrasonic velocity measurements (C 11 = 26.6; C 13 = 16.2; C 33 = 18.3; C 44 = 4.5; C 66 = 8.8 [GPa]), confirming the validity and reliability of our approximations and averaging approach.« less

The Lower Silurian Osmundsberg K-bentonite. Part II: Mineralogy, geochemistry, chemostratigraphy and tectonomagmatic significance

USGS Publications Warehouse

Huff, W.D.; Bergstrom, Stig M.; Kolata, Dennis R.; Sun, H.

1998-01-01

The Lower Silurian Osmundsberg K-bentonite is a widespread ash bed that occurs throughout Baltoscandia and parts of northern Europe. This paper describes its characteristics at its type locality in the Province of Dalarna, Sweden. It contains mineralogical and chemical characteristics that permit its regional correlation in sections elsewhere in Sweden as well as Norway, Estonia, Denmark and Great Britain. The < 2 ??m clay fraction of the Osmundsberg bed contains abundant kaolinite in addition to randomly ordered (RO) illite/smectite (I/S). Modelling of the X-ray diffraction tracings showed the I/S consists of 18% illite and 82 % smectite. The high smectite and kaolinite content is indicative of a history with minimal burial temperatures. Analytical data from both pristine melt inclusions in primary quartz grains as well as whole rock samples can be used to constrain both the parental magma composition and the probable tectonic setting of the source volcanoes. The parental ash was dacitic to rhyolitic in composition and originated in a tectonically active collision margin setting. Whole rock chemical fingerprinting of coeval beds elsewhere in Baltoscandia produced a pronounced clustering of these samples in the Osmundsberg field of the discriminant analysis diagram. This, together with well-constrained biostratigraphic and lithostratigraphic data, provides the basis for regional correlation and supports the conclusion that the Osmundsberg K-bentonite is one of the most extensive fallout ash beds in the early Phanerozoic. The source volcano probably lay to the west of Baltica as part of the subduction complex associated with the closure of Iapetus.

Electron paramagnetic resonance, scanning electron microscopy with energy dispersion X-ray spectrometry, X-ray powder diffraction, and NMR characterization of iron-rich fired clays.

PubMed

Presciutti, Federica; Capitani, Donatella; Sgamellotti, Antonio; Brunetti, Brunetto Giovanni; Costantino, Ferdinando; Viel, Stéphane; Segre, Annalaura

2005-12-01

The aim of this study is to clarify the structure of an iron-rich clay and the structural changes involved in the firing process as a preliminary step to get information on ancient ceramic technology. To this purpose, illite-rich clay samples fired at different temperatures were characterized using a multitechnique approach, i.e., by electron paramagnetic resonance, scanning electron microscopy with electron dispersion X-ray spectrometry, X-ray powder diffraction, magic angle spinning and multiple quantum magic angle spinning NMR. During firing, four main reaction processes occur: dehydration, dehydroxylation, structural breakdown, and recrystallization. When the results are combined from all characterization methods, the following conclusions could be obtained. Interlayer H2O is located close to aluminum in octahedral sites and is driven off at temperatures lower than 600 degrees C. Between 600 and 700 degrees C dehydroxylation occurs whereas, between 800 and 900 degrees C, the aluminum in octahedral sites disappears, due to the breakdown of the illite structure, and all iron present is oxidized to Fe3+. In samples fired at 1000 and 1100 degrees C iron clustering was observed as well as large single crystals of iron with the occurrence of ferro- or ferrimagnetic effects. Below 900 degrees C the aluminum in octahedral sites presents a continuous distribution of chemical shift, suggesting the presence of slightly distorted sites. Finally, over the whole temperature range, the presence of at least two tetrahedral aluminum sites was revealed, characterized by different values of the quadrupolar coupling constant.

Occurrence and origin of minerals in a chamosite-bearing coal of Late Permian age, Zhaotong, Yunnan, China

USGS Publications Warehouse

Dai, S.; Chou, C.-L.

2007-01-01

The minerals found in the no.5 coal (Late Permian) from the Zhaotong Coalfield, Yunnan Province, southwestern China, have been examined and found to consist mainly of kaolinite, pyrite, chamosite, quartz, and calcite, with trace amounts of illite and mixed-layer illite-smectite. The proportion of chamosite in clay minerals ranges from 32 to 56 wt%, with an average of 46 wt%. Chamosite is distributed not only in collodetrinite, but also occurs as cell fillings in fusinite, semifusinite, and telinite. The high content and mode of occurrence of chamosite in this mine indicate its formation by interaction of kaolinite with Fe-Mg-rich fluids during early diagenesis. Except for a minor amount of terfigenous quartz, most quartz is of authigenic origin and formed from kaolinite desilication. The calcite content of the no. 5 coal is 1.4-6.3% (with an average of 3%) and is distributed in collodetrinite and as cell fillings of coal-forming plants. Calcite originated from seawater invasion during peat accumulation. Pyrite occurs in several ways: as massive, framboidal, isolated enhedral/ anhedral, and euhedral forms. In addition, the presence of a large amount of pyritized red algae provides strong evidence of seawater invasion during peat accumulation. The red algae may have played an important role in the enrichment of sulfur in the coal. The characteristic assemblage of minerals in this mine resulted from a unique basinal environment in which the mineral matter was derived from a basaltic source region, volcanic activity, and seawater transgression during coal formation.

Provenance of Holocene sediment on the Chukchi-Alaskan margin based on combined diffuse spectral reflectance and quantitative X-Ray Diffraction analysis

USGS Publications Warehouse

Ortiz, J.D.; Polyak, L.; Grebmeier, J.M.; Darby, D.; Eberl, D.D.; Naidu, S.; Nof, D.

2009-01-01

Sediment clay and silt mineral assemblages provide an excellent means of assessing the provenance of fine-grained Arctic sediment especially when a unique mineral assemblage can be tied to specific source areas. The diffuse spectral reflectance (DSR) first derivative measurements and quantitative X-Ray Diffraction (qXRD) on a high-resolution sediment core from the continental slope north of Alaska constrain the sediment mineralogy. DSR results are augmented by measurements on several adjacent cores and compared to surface sediment samples from the northern Alaskan shelf and slope. Using Principal Component Analysis (PCA), we infer that the three leading DSR modes relate to mixtures of smectite + dolomite, illite + goethite, and chlorite + muscovite. This interpretation is consistent with the down core qXRD results. While the smectite + dolomite, and illite + goethite factors show increased variability down core, the chlorite + muscovite factor had highest positive loadings in the middle Holocene, between ca. 6.0 and 3.6??ka. Because the most likely source of the chlorite + muscovite suite in this vicinity lies in the North Pacific, we argue that the oscillations in chlorite + muscovite values likely reflect an increase in the inflow of Pacific water to the Arctic through the Bering Strait. The time interval of this event is associated in other parts of the globe with a non-linear response of the climate system to the decrease in insolation, which may be related to changes in water exchange between the Pacific and Arctic Ocean. ?? 2009 Elsevier B.V.

Chemical composition and geologic history of saline waters in Aux Vases and Cypress Formations, Illinois Basin

USGS Publications Warehouse

Demir, I.; Seyler, B.

1999-01-01

Seventy-six samples of formation waters were collected from oil wells producing from the Aux Vases or Cypress Formations in the Illinois Basin. Forty core samples of the reservoir rocks were also collected from the two formations. Analyses of the samples indicated that the total dissolved solids content (TDS) of the waters ranged from 43,300 to 151,400 mg/L, far exceeding the 35,400 mg/mL of TDS found in typical seawater. Cl-Br relations suggested that high salinities in the Aux Vases and Cypress formation waters resulted from the evaporation of original seawater and subsequent mixing of the evaporated seawater with concentrated halite solutions. Mixing with the halite solutions increased Na and Cl concentrations and diluted the concentration of other ions in the formation waters. The elemental concentrations were influenced further by diagenetic reactions with silicate and carbonate minerals. Diagenetic signatures revealed by fluid chemistry and rock mineralogy delineated the water-rock interactions that took place in the Aux Vases and Cypress sandstones. Dissolution of K-feldspar released K into the solution, leading to the formation of authigenic illite and mixed-layered illite/smectite. Some Mg was removed from the solution by the formation of authigenic chlorite and dolomite. Dolomitization, calcite recrystallization, and contribution from clay minerals raised Sr levels significantly in the formation waters. The trend of increasing TDS of the saline formation waters with depth can be explained with density stratification. But, it is difficult to explain the combination of the increasing TDS and increasing Ca/Na ratio with depth without invoking the controversial 'ion filtration' mechanism.

Mineralogical, chemical and K-Ar isotopic changes in Kreyenhagen Shale whole rocks and <2 μm clay fractions during natural burial and hydrous-pyrolysis experimental maturation

NASA Astrophysics Data System (ADS)

Clauer, N.; Lewan, M. D.; Dolan, M. P.; Chaudhuri, S.; Curtis, J. B.

2014-04-01

Progressive maturation of the Eocene Kreyenhagen Shale from the San Joaquin Basin of California was studied by combining mineralogical and chemical analyses with K-Ar dating of whole rocks and <2 μm clay fractions from naturally buried samples and laboratory induced maturation by hydrous pyrolysis of an immature outcrop sample. The K-Ar age decreases from 89.9 ± 3.9 and 72.4 ± 4.2 Ma for the outcrop whole rock and its <2 μm fraction, respectively, to 29.7 ± 1.5 and 21.0 ± 0.7 Ma for the equivalent materials buried to 5167 m. The natural maturation does not produce K-Ar ages in the historical sense, but rather K/Ar ratios of relative K and radiogenic 40Ar amounts resulting from a combined crystallization of authigenic and alteration of initial detrital K-bearing minerals of the rocks. The Al/K ratio of the naturally matured rocks is essentially constant for the entire depth sequence, indicating that there is no detectable variation in the crystallo-chemical organization of the K-bearing alumino-silicates with depth. No supply of K from outside of the rock volumes occurred, which indicates a closed-system behavior for it. Conversely, the content of the total organic carbon (TOC) content decreases significantly with burial, based on the progressive increasing Al/TOC ratio of the whole rocks. The initial varied mineralogy and chemistry of the rocks and their <2 μm fractions resulting from differences in detrital sources and depositional settings give scattered results that homogenize progressively during burial due to increased authigenesis, and concomitant increased alteration of the detrital material. Hydrous pyrolysis was intended to alleviate the problem of mineral and chemical variations in initially deposited rocks of naturally matured sequences. However, experiments on aliquots from thermally immature Kreyenhagen Shale outcrop sample did not mimic the results from naturally buried samples. Experiments conducted for 72 h at temperatures from 270 to 365 °C did not induce significant changes at temperatures above 310 °C in the mineralogical composition and K-Ar ages of the rock and <2 μm fraction. The K-Ar ages of the <2 μm fraction range from 72.4 ± 4.2 Ma in the outcrop sample to 62.4 ± 3.4 Ma in the sample heated the most at 365 °C for 216 h. This slight decrease in age outlines some loss of radiogenic 40Ar, together with losses of organic matter as oil, gas, and aqueous organic species. Large amounts of smectite layers in the illite-smectite mixed layers of the pyrolyzed outcrop <2 μm fraction remain during thermal experiments, especially above 310 °C. With no illitization detected above 310 °C, smectite appears to have inhibited rather than promoted generation of expelled oil from decomposition of bitumen. This hindrance is interpreted to result from bitumen impregnating the smectite interlayer sites and rock matrix. Bitumen remains in the <2 μm fraction despite leaching with H2O2. Its presence in the smectite interlayers is apparent by the inability of the clay fraction to fully expand or collapse once bitumen generation from the thermal decomposition of the kerogen is completed, and by almost invariable K-Ar ages confirming for the lack of any K supply and/or radiogenic 40Ar removal. This suggests that once bitumen impregnates the porosity of a progressively maturing source rock, the pore system is no longer wetted by water and smectite to illite conversion ceases. Experimental attempts to evaluate the smectite conversion to illite should preferentially use low-TOC rocks to avoid inhibition of the reaction by bitumen impregnation.

Geology and Refractory Clay Deposits of the Haldeman and Wrigley Quadrangles, Kentucky

USGS Publications Warehouse

Patterson, Sam H.; Hosterman, John W.; Huddle, John Warfield

1962-01-01

The Haldeman and Wrigley 7th-minute quadrangles are near the western edge of the eastern Kentucky coal field and cover an area of approximately 117 square miles in parts of Carter, Rowan, Elliott, and Morgan Counties, Ky. The rocks exposed in the two quadrangles are of Early and Late Mississippian and Early and Middle Pennsylvanian age. The Mississippian rocks are composed of the thick Brodhead formation, which consists of siltstone and shale, and eleven thin marine limestone and shale formations, having an aggregate thickness of about 150 feet. The Lee and Breathitt formations, of Pennsylvanian age, consist of sandstone, siltstone, and shale; they also contain thin beds of coal and several beds of underclay, including the economically important Olive Hill clay bed of Crider, 1913. Pennsylvanian rocks include beds of both continental and marine origin. The eleven thin Mississippian formations and the upper-most part of the thick Brodhead formation are truncated by a prominent unconformity on which rocks of Pennsylvanian age rest. The rocks occupy a region of gentle dips between the Cincinnati arch and the Appalachian Mountains. Refractory clay deposits are in the Olive Hill clay bed, which occurs in the lower part of the Lee formation. The Olive Hill clay bed is discontinuous and consists of a series of irregularly shaped lenses. The bed is approximately two-thirds semifiint clay and one-third flint clay, and it contains minor amounts of plastic clay. Some of the flint clay is nearly pure kaolinite, but the semi flint and plastic clay consists of mixtures of kaolinite, illite, and mixed-layer clay minerals. The structure of the kaolinite ranges from highly crystalline to very poorly crystalline 'fireclay' type. The degree of crystallinity of the kaolinite and the hardness of the clay vary inversely with the amount of illite and mixed-layer clay minerals present. The nearly pure kaolinite is believed to have formed by the removal of alkalies and some silica fram mixtures of kaolinite, illite, and mixed-layer clays by leaching in swamps to the deposition of the beds overlying the clay. The refractory properties of the clay vary directly with the purity of the kaolinite, and refractoriness decreases as the proportions of illite and mixed-layer clays increase. Certain nonclay minerals, chiefly siderite, pyrite, and iron oxide-bearing minerals, also act as fiuxes, reducing the refractory properties of the clay. The entire resources of clay in the Olive Hill clay bed are roughly and tentatively estimated to include 105,000,000 tons in the Haldeman quadrangle and 175,000,000 tons in the Wrigley quadrangle. Much of this clay is of poor quality and the amount that is better than the minimum requirements for use in refractories is probably about 30,000,000 tons. Only a fraction of this tonnage is suitable for superheat-duty products. Limestone is the only nonmetallic mineral resource other than refractory clay that has been developed in the two quadrangles, but 1arge amounts of shale suitable for use in making lightweight aggregate and structural clay products may also be present. Most of the limestone, which is quarried. in both quadrangles, is used for road-metal, concrete aggregate, and agriculture stone, but some of the limestone is of the quality that would be suitable for other uses. Virtually all the Mississippian Beech Creek limestone of Malott, 1919 which is as much as 18 feet thick, consists of high-calcium limestone. Shale beds that appear most favoralble for making lightweight aggregate are in the shale facies of the Lee formation of Pennsylvanian age. Shale that is probably suitable for structural clay products is present in the shale flacles of the Lee formation and in the Muldraugh formation of Mississippian age. Several dry holes have been drilled in search for oil and gas within the area of the two quadrangles. Though no commercial production was ever attained, one well furnished a supply of gas f

Seawater Hydraulics: Development and Evaluation of an Experimental Diver Tool System.

DTIC Science & Technology

1984-02-01

wrench was operated, it ran irregularly and with low power; third, the motor would not always tart when the valve was actuated . Investigation revealed...I’’r Iulticctlic.4X N (4M144 i , I1.401 . (L(It I A,-- II N1I I I \\k RI Cit I X I)H ( 4 Wit IN ( N I (41lnson. XXaisli,, iot , D)4 NI I M4 I lid. Ill...its primary distribution lists. SUBJECT CATEGORIES 28 ENERGY/POWER GENERATION 29 Thermal conservation (thermal engineering of buildings. HVAC I SHORE

Use of digital Munsell color space to assist interretation of imaging spectrometer data: Geologic examples from the northern Grapevine Mountains, California and Nevada

NASA Technical Reports Server (NTRS)

Kruse, F. A.; Knepper, D. H., Jr.; Clark, R. N.

1986-01-01

Techniques using Munsell color transformations were developed for reducing 128 channels (or less) of Airborne Imaging Spectrometer (AIS) data to a single color-composite-image suitable for both visual interpretation and digital analysis. Using AIS data acquired in 1984 and 1985, limestone and dolomite roof pendants and sericite-illite and other clay minerals related to alteration were mapped in a quartz monzonite stock in the northern Grapevine Mountains of California and Nevada. Field studies and laboratory spectral measurements verify the mineralogical distributions mapped from the AIS data.

Clay minerals behaviour in thin sandy clay-rich lacustrine turbidites (Lake Hazar, Turkey)

NASA Astrophysics Data System (ADS)

El Ouahabi, Meriam; Hubert-Ferrari, Aurelia; Lamair, Laura; Hage, Sophie

2017-04-01

Turbidites have been extensively studied in many different areas using cores or outcrop, which represent only an integrated snapshot of a dynamic evolving flow. Laboratory experiments provide the missing relationships between the flow characteristics and their deposits. In particular, flume experiments emphasize that the presence of clay plays a key role in turbidity current dynamics. Clay fraction, in small amount, provides cohesive strength to sediment mixtures and can damp turbulence. However, the degree of flocculation is dependent on factors such as the amount and size of clay particles, the surface of clay particles, chemistry and pH conditions in which the clay particles are dispersed. The present study focuses on thin clayey sand turbidites found in Lake Hazar (Turkey) occurring in stacked thin beds. Depositional processes and sources have been previously studied and three types were deciphered, including laminar flows dominated by cohesion, transitional, and turbulence flow regimes (Hage et al., in revision). For the purpose of determine the clay behavior in the three flow regimes, clay mineralogical, geochemical measurements on the cores allow characterising the turbidites. SEM observations provide further information regarding the morphology of clay minerals and other clasts. The study is particularly relevant given the highly alkaline and saline water of the Hazar Lake. Clay minerals in Hazar Lake sediments include kaolinite (1:1-type), illite and chlorite (2:1-type). Hazar lake water is alkaline having pH around 9.3, in such alkaline environment, a cation-exchange reaction takes place. Furthermore, in saline water (16‰), salts can act as a shield and decrease the repulsive forces between clay particle surfaces. So, pH and salt content jointly impact the behaviour of clays differently. Since the Al-faces of clay structures have a negative charge in basic solutions. At high pH, all kaolinite surfaces become negative-charged, and then kaolinite particles are dispersed, and the suspension is stabilized supported by our SEM observations. In alkaline water, kaolinite reveals a lower degree of consolidation. While, alkaline water has no measurable effect on illite and chlorite surface properties due to the absence of modifications in charge. Illite and chlorite form with other clasts clusters or aggregate structures in suspension when the particle interactions are dominated by attractive energies were formed. The aggregate structure plays a major part in the flow behavior of clay suspensions. Flocs will immobilize the suspending medium, and give rise to increasing viscosity and yield strength of the suspension. S. Hage, A. Hubert-Ferrari, L. Lamair, U. Avşar, M. El Ouahabi, M. Van Daele, F. Boulvain, M.A. Bahri, A. Seret, Al. Plenevaux. Flow dynamics at the origin of thin sandy clay-rich lacustrine turbidites: Examples from Lake Hazar, Turkey, submitted to Sedimentology, in revision.

A preliminary study of older hot spring alteration in Sevenmile Hole, Grand Canyon of the Yellowstone River, Yellowstone Caldera, Wyoming

USGS Publications Warehouse

Larson, Peter B.; Phillips, Allison; John, David A.; Cosca, Michael A.; Pritchard, Chad; Andersen, Allen; Manion, Jennifer

2009-01-01

Erosion in the Grand Canyon of the Yellowstone River, Yellowstone Caldera (640 ka), Wyoming, has exposed a cross section of older hydrothermal alteration in the canyon walls. The altered outcrops of the post-collapse tuff of Sulphur Creek (480 ka) extend from the canyon rim to more than 300 m beneath it. The hydrothermal minerals are zoned, with an advanced argillic alteration consisting of an association of quartz (opal) + kaolinite ± alunite ± dickite, and an argillic or potassic alteration association with quartz + illite ± adularia. Disseminated fine-grained pyrite or marcasite is ubiquitous in both alteration types. These alteration associations are characteristic products of shallow volcanic epithermal environments. The contact between the two alteration types is about 100 m beneath the rim. By analogy to other active geothermal systems including active hydrothermal springs in the Yellowstone Caldera, the transition from kaolinite to illite occurred at temperatures in the range 150 to 170 °C. An 40Ar/39Ar age on alunite of 154,000 ± 16,000 years suggests that hydrothermal activity has been ongoing since at least that time. A northwest-trending linear array of extinct and active hot spring centers in the Sevenmile Hole area implies a deeper structural control for the upflowing hydrothermal fluids. We interpret this deeper structure to be the Yellowstone Caldera ring fault that is covered by the younger tuff of Sulphur Creek. The Sevenmile Hole altered area lies at the eastern end of a band of hydrothermal centers that may mark the buried extension of the Yellowstone Caldera ring fault across the northern part of the Caldera.

Exploring Nested Reaction Fronts to Understand How Oxygen Cracks Rocks, Carbonic and Sulfuric Acids Dissolve Rocks, and Water Transports Rocks during Weathering

NASA Astrophysics Data System (ADS)

Brantley, S. L.; Gu, X.; Sullivan, P. L.; Kim, H.; Stinchcomb, G. E.; Lebedeva, M.; Balashov, V. N.

2016-12-01

To first order, weathering is the reaction of rocks with oxidants (oxygen, nitrate, etc.), acids (carbonic, sulfuric, and organic acids), and water. To explore weathering we have been studying the depth intervals in soils, saprolite, and weathering rock where mineral reactions are localized - "reaction fronts". We limit the study to ridges or catchments in climates where precipitation is greater than potential evapotranspiration. For example, in the Susquehanna Shale Hills Critical Zone Observatory, we observe reaction fronts that generally define very rough surfaces in 3D that mimic the land surface topography, although with lower relief. Overall, the fronts form nested curved surfaces. In Shale Hills, the deepest reaction fronts are oxidation of pyrite, and dissolution of carbonate. The carbonate is inferred to dissolve at least partly due to the sulfuric acid produced by the pyrite. In addition to pyrite, chlorite also starts to oxidize at the water table. We hypothesize that these dissolution and oxidation reactions open pores and cause microfracturing that open the rock to infiltration of advecting meteoric waters. At much shallower depths, illite is observed to dissolve. In Shale Hills, these reaction fronts - pyrite, carbonate, illite - separate over meters beneath the ridges. Such separated reaction fronts have also been observed in other fractured lithologies where oxidation is the deepest reaction and is associated with weathering-induced fractures. In contrast, in some massive mafic rocks, reaction fronts are almost co-located. By studying the geometry of reaction fronts, it may be possible to elucidate the relative importance of how oxygen cracks rocks; carbonic, organic, and sulfuric acids dissolve rocks; and water mobilizes rock materials during weathering.

Reactivity of clay minerals with acids and alkalies

USGS Publications Warehouse

Carroll, Dorothy; Starkey, Harry C.

1971-01-01

One-g samples of a montmorillonite, a metabentonite, an illite, two kaolinites, and three halloysites were treated with 50 ml of hydrochloric acid (6⋅45 N, 1:1), acetic acid (4⋅5 N, 1:3), sodium hydroxide (2⋅8 N), sodium chloride solution (pH 6⋅10; Na = 35‰; Cl = 21⋅5‰), and natural sea water (pH 7⋅85; Na = 35⋅5‰; Cl = 21⋅ 5‰) for a 10-day period in stoppered plastic vials. The supernatant solutions were removed from the clay minerals and analyzed for SiO2, Al2O3, CaO, MgO, Na2O, and K2O. All the solutions removed some SiO2, Al2O3, and Fe2O3 from the samples, but the quantities were small. Sodium hydroxide attacked the kaolin group minerals more strongly than it did montmorillonite, metabentonite, or illite. Halloysite was more strongly attacked by hydrochloric acid than was any of the other experimental minerals. Hydrochloric acid removed iron oxide coatings from soil clay minerals, but acetic acid did not remove them completely. The samples most strongly attacked by HCl and NaOH were examined by X-ray diffraction. Acid treatment did not destroy the structure of the clays, but the halloysite structure was partially destroyed. Sodium hydroxide attacked the halloysite structure, as shown by chemical analysis and X-ray diffraction. These experiments show that treatment in dilute acids has no harmful effect in the preparation of clays for X-ray diffraction. Acetic acid is preferred to hydrochloric acid for this purpose. Hydrochloric acid cleans clay minerals by removing free iron oxide from the surface; acetic acid is less effective.

Altered volcanic ash layers of the Late Cretaceous San Felipe Formation, Sierra Madre Oriental (Northeastern Mexico): Usbnd Pb geochronology, provenance and tectonic setting

NASA Astrophysics Data System (ADS)

Velasco-Tapia, Fernando; Martínez-Paco, Margarita; Iriondo, Alexander; Ocampo-Díaz, Yam Zul Ernesto; Cruz-Gámez, Esther María; Ramos-Ledezma, Andrés; Andaverde, Jorge Alberto; Ostrooumov, Mikhail; Masuch, Dirk

2016-10-01

A detailed petrographic, geochemical, and Usbnd Pb geochronological study of altered volcanic ash layers, collected in eight outcrops of the Late Cretaceous San Felipe Formation (Sierra Madre Oriental, Northeastern Mexico), has been carried out. The main objectives have been: (1) to establish a deposit period, and (2) to propose a reliable provenance-transport-deposit-diagenetic model. These volcano-sedimentary strata represent the altered remains of vitreous-crystalline ash (main grains: quartz + K-feldspar (sanidine) + Na-plagioclase + zircon + biotite; groundmass: glass + calcite + clinochlore + illite) deposited and preserved in a shallow, relatively large in area, open platform environment. Major and trace element geochemistry indicate that parent volcanism was mainly rhyodacitic to rhyolitic in composition. Discrimination diagrams suggest a link to continental arc transitional to extension tectonic setting. Usbnd Pb geochronology in zircon has revealed that the volcanic ash was released from their sources approximately during the range 84.6 ± 0.8 to 73.7 ± 0.3 Ma, being transported to the depocenters. Burial diagenesis process was marked by: (a) a limited recycling, (b) the partial loss of original components (mainly K-feldspar, plagioclase, biotite and glass), and (c) the addition of quartz, calcite, illite and clinochlore. The location of the source area remains uncertain, although the lack of enrichment in Zr/Sc ratio suggests that ashes were subjected to relatively fast and short-distance transport process. El Peñuelo intrusive complex, at 130-170 km west of the depocenters, is the nearest known zone of active magmatism during the Upper Cretaceous. This intermediate to felsic pluton, characterized by a geochemical affinity to post-orogenic tectonic setting, could be linked to the volcanic sources.

Continental weathering as a driver of Late Cretaceous cooling: new insights from clay mineralogy of Campanian sediments from the southern Tethyan margin to the Boreal realm

NASA Astrophysics Data System (ADS)

Chenot, Elise; Deconinck, Jean-François; Pucéat, Emmanuelle; Pellenard, Pierre; Guiraud, Michel; Jaubert, Maxime; Jarvis, Ian; Thibault, Nicolas; Cocquerez, Théophile; Bruneau, Ludovic; Razmjooei, Mohammad J.; Boussaha, Myriam; Richard, James; Sizun, Jean-Pierre; Stemmerik, Lars

2018-03-01

New clay mineralogical analyses have been performed on Campanian sediments from the Tethyan and Boreal realms along a palaeolatitudinal transect from 45° to 20°N (Danish Basin, North Sea, Paris Basin, Mons Basin, Aquitaine Basin, Umbria-Marche Basin and Tunisian Atlas). Significant terrigenous inputs are evidenced by increasing proportions of detrital clay minerals such as illite, kaolinite and chlorite at various levels in the mid- to upper Campanian, while smectitic minerals predominate and represented the background of the Late Cretaceous clay sedimentation. Our new results highlight a distinct latitudinal distribution of clay minerals, with the occurrence of kaolinite in southern sections and an almost total absence of this mineral in northern areas. This latitudinal trend points to an at least partial climatic control on clay mineral sedimentation, with a humid zone developed between 20° and 35°N. The association and co-evolution of illite, chlorite and kaolinite in most sections suggest a reworking of these minerals from basement rocks weathered by hydrolysis, which we link to the formation of relief around the Tethys due to compression associated with incipient Tethyan closure. Diachronism in the occurrence of detrital minerals between sections, with detrital input starting earlier during the Santonian in the south than in the north, highlights the northward progression of the deformation related to the anticlockwise rotation of Africa. Increasing continental weathering and erosion, evidenced by our clay mineralogical data through the Campanian, may have resulted in enhanced CO2 consumption by silicate weathering, thereby contributing to Late Cretaceous climatic cooling.

Kaolinite, illite and quartz dissolution in the karstification of Paleozoic sandstones of the Furnas Formation, Paraná Basin, Southern Brazil

NASA Astrophysics Data System (ADS)

Melo, Mário Sérgio de; Guimarães, Gilson Burigo; Chinelatto, Adilson Luiz; Giannini, Paulo César Fonseca; Pontes, Henrique Simão; Chinelatto, Adriana Scoton Antonio; Atencio, Daniel

2015-11-01

Karstification processes in sandstones of the Furnas Formation, Silurian to Devonian of the Paraná Basin, have been described since the mid-twentieth century. However, some geologists still doubt the idea of true karst in sandstones. Studies carried out in the Campos Gerais region, Paraná State, Southern Brazil, aimed at investigating the nature of erosion processes in Furnas Formation and the role of the dissolution in the development of their notorious erosive features and underground cavities. These studies have led to the recognition of dissolution macro to micro features ('furnas', caves, ponds, sinks, ruiniform relief on cliffs and rocky surfaces, grain corrosion, speleothems, mineral reprecipitation and incrustation). The analysis (scanning electron microscopy, energy dispersive spectrometry and x-ray diffractometry) of sandstones and their alterites has indicated significant dissolution of clay cement along with discrete quartz grain dissolution. This mesodiagenetic cement (kaolinite and illite) is dissolved and reprecipitated as clay minerals with poorly developed crystallinity along with other minerals, such as variscite and minerals of the alunite supergroup, suggesting organic participation in the processes of dissolution and incrustation. The mineral reprecipitation usually forms centimetric speleothems, found in cavities and sheltered rocky surfaces. The cement dissolution associated with other factors (fractures, wet weather, strong hydraulic gradient, antiquity of the landforms) leads to the rock arenisation, the underground erosion and the appearance of the karst features. Carbonate rocks in the basement may locally be increasing the karst forms in the overlying Furnas Formation. The recognition of the karst character of the Furnas Formation sandstones has important implications in the management of underground water resources (increasingly exploited in the region), in the use of the unique geological heritage and in the prevention of geo-environmental accidents resulting from underground erosion phenomena.

The effect of moisture on the methane adsorption capacity of shales: A study case in the eastern Qaidam Basin in China

NASA Astrophysics Data System (ADS)

Wang, Lu; Yu, Qingchun

2016-11-01

This study investigated the effects of moisture on high-pressure methane adsorption in carboniferous shales from the Qaidam Basin, China. The shale characteristics, including the organic/inorganic compositions and pore structure (volume and surface) distribution, were obtained using various techniques. Gibbs adsorption measurements were performed over a pressure range up to 6 MPa and temperatures of 308.15 K on dry samples and moisture-equilibrated samples to analyze the correlations between organic/inorganic matter, pore structure, and moisture content on the methane sorption capacity. Compared to dry samples, the sorption capacity of wet samples (0.44-2.52% of water content) is reduced from 19.7 ± 5.3% to 36.1% ± 6.1%. Langmuir fitting is conducted to investigate moisture-dependent variations of adsorbed methane density, Langmuir pressure, and volume. By combining the pore volume and surface distribution analyses, our observations suggested that the main competition sites for CH4-H2O covered pores of approximately 2-7 nm, whereas the effective sites for methane and water were predominantly distributed within smaller (<4 nm) and larger pores (>10 nm), respectively. Regarding the compositional correlations, the impact of moisture on the amount of adsorbed methane shows a roughly linearly decreasing trend with increasing TOC content ranging from 0.62 to 2.88%, whereas the correlation between the moisture effect and various inorganic components is more complicated. Further fitting results indicate that illite/smectite mixed formations are closely related to the methane capacity, whereas the illite content show an evident connection to the pore structural (volume and surface) variations in the presence of moisture.

[X-ray diffraction (XRD) and near infrared spectrum (NIR) analysis of the soil overlying the Bairendaba deposit of the Inner Mongolia Grassland].

PubMed

Luo, Song-ying; Cao, Jian-jin; Wu, Zheng-quan

2014-08-01

The soil samples uniformly overlying the Bairendaba deposit of the Inner Mongolia grassland were collected, and ana- lyzed with X-ray diffraction (XRD) and near infrared spectrum (NIR), for exploring the origins of the soil from the, grassland mining area and the relationship with the underground rock. The results show that the samp]s consist of quartz, graphite, carbonate, hornblende, mica, chlorite, montmorillonite, illite, berlinite, diaspore, azurite, hen tite, etc. These indicate that the soil samples were not only from the weathering products of the surface rock, but also from the underground rock mass and the alteration of the wall rock. The azurite and the hematite contained in the soil, mainly coming from the oxidation zone of the orebodies, can be used as the prospecting marks. The alteration mineral assemblage is mainly chlorite-illite-montmorillonite and it experienced the alteration process of potassic alteration-->silicification-->carbonatization-->silk greisenization-->clayization. Also, the wall rock alteration and the physical weathering processes can be accurately restored by analyzing the combination of the alteration minerals, which can provide important reference information for the deep ore prospecting and the ore deposit genesis study, improving the rate of the prospecting. The XRD and NIR with the characteristics of the economy and quickness can be used for the identification of mineral composition of soil, and in the study of mineral and mineral deposits. Especially, NIR has its unique superiority, that is, its sample request is low, and it can analyze a batch of samples quickly. With the development of INR, it will be more and more widely applied in geological field, and can play an important role in the ore exploration.

A review of the surface features and properties, surfactant adsorption and floatability of four key minerals of diasporic bauxite resources.

PubMed

Zhang, Ningning; Nguyen, Anh V; Zhou, Changchun

2018-04-01

Diasporic bauxite represents one of the major aluminum resources. Its upgrading for further processing involves a separation of diaspore (the valuable mineral) from aluminosilicates (the gangue minerals) such as kaolinite, illite, and pyrophyllite. Flotation is one of the most effective ways to realize the upgrading. Since flotation is a physicochemical process based on the difference in the surface hydrophobicity of different components, determining the adsorption characteristics of various flotation surfactants on the mineral surfaces is critical. The surfactant adsorption properties of the minerals, in turn, are controlled by the surface chemistry of the minerals, while the latter is related to the mineral crystal structures. In this paper, we first discuss the crystal structures of the four key minerals of diaspore, kaolinite, illite, and pyrophyllite as well as the broken bonds on their exposed surfaces after grinding. Next, we summarize the surface chemistry properties such as surface wettability and surface electrical properties of the four minerals, and the differences in these properties are explained from the perspective of mineral crystal structures. Then we review the adsorption mechanism and adsorption characteristics of surfactants such as collectors (cationic, anionic, and mixed surfactants), depressants (inorganic and organic), dispersants, and flocculants on these mineral surfaces. The separation of diaspore and aluminosilicates by direct flotation and reverse flotation are reviewed, and the collecting properties of different types of collectors are compared. Furthermore, the abnormal behavior of the cationic flotation of kaolinite is also explained in this section. This review provides a strong theoretical support for the optimization of the upgrading of diaspore bauxite ore by flotation and the early industrialization of the reverse flotation process. Copyright © 2018 Elsevier B.V. All rights reserved.

Extraction of hydrothermal alterations from ASTER SWIR data from east Zanjan, northern Iran

NASA Astrophysics Data System (ADS)

Azizi, H.; Tarverdi, M. A.; Akbarpour, A.

2010-07-01

The use of satellite images for mineral exploration has been very successful in pointing out the presence of minerals such as smectite and kaolinite which are important in the identification of hydrothermal alterations. Shortwave infrared (SWIR) bands from Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) with the wavelength of ASTER SWIR bands between 1.65 and 2.43 μm has a good potential for mapping a hydrothermal alteration minerals such as alunite, pyrophyllite, kaolinite, illite-muscovite-sericite, and carbonate. In this range, hydroxide minerals which have been produced by hydrothermal alteration exhibit good absorption compared to shorter or longer wavelengths. In this research which aims to remove atmospheric and topographic effects from ASTER SWIR data, the authors used the log-residual method (LRM) with the minimum noise fraction (MNF) transformation to create a pixel purity index (PPI) which was used to extract the most spectrally pure pixels from multispectral images. Spectral analyses of the clay mineralogy of the study area (east Zanjan, in northern Iran) were obtained by matching the unknown spectra of the purest pixels to the U.S. Geological Survey (USGS) mineral library. Three methods, spectral feature fitting (SFF), spectral angle mapping (SAM), and binary encoding (BE) were used to generate a score between 0 and 1, where a value of 1 indicates a perfect match showing the exact mineral type. In this way, it was possible to identify certain mineral classes, including chlorite, carbonate, calcite-dolomite-magnesite, kaolinite-smectite, alunite, and illite. In this research, two main propylitic and phyllic-argillic zones could be separated using their compositions of these minerals. These two alteration zones are important for porphyry copper deposits and gold mineralization in this part of Iran.

Effect of Mineral and Microbe Interactions on Biomass Yield

NASA Astrophysics Data System (ADS)

Pena, S. A.; Block, K. A.; Katz, A.; Gottlieb, P.

2016-12-01

The ecological feedback of microbes (bacteria and viruses) in association with minerals is virtually unexplored in the context of characterizing how carbon cycles in the terrestrial ecosystem. These interactions include the ability for bacteriophage to control bacteria populations, the ability of minerals to provide a substrate for bacteria growth, and the effect of minerals on bacteriophage viability. We investigate bacteriophage aggregation with minerals in the clay size fraction (< 0.2 µm) as well as the interaction between bacteriophage and mineral biofilms. In our virus experiments, bacteriophage Φ6 was suspended with the minerals smectite, illite, kaolinite, and goethite at low divalent cation concentrations so aggregation was in the reaction limited colloidal aggregation (RLCA) regime, at neutral pH and room temperature conditions. Virus remained viable at a 1:1 virus-clay ratio for clays, and at an approximate 100:1 ratio for goethite. However, the number of plaque forming units was reduced by 99%. Electron micrographs show viable as well as partially disassembled virus, similar to the results found by Block et al. 2014. We found that inactivation of a 4 x 1011 cm-3 concentration of bacteriophage Φ6 by smectite, illite, kaolinite, and goethite, required a minimum sediment concentration of 1.5 x 1011 cm-3, 1.4 x 1011 cm-3, 2.5 x 1011 cm-3, and 1.1 x 109 cm-3, respectively. Mineral biofilms were generated by suspension of tropical soil clays with gram-positive and gram-negative microbes and characterized by x-ray diffraction and imaged by electron microscopy (SEM and TEM). Mineral biomass produced by gram negative organisms were subjected to virus infection to determine influence of minerals on community resilience. Lastly, we report biomass yield in each instance to quantify the influence of mineral composition on total biomass production.

Phosphoric acid purification through different raw and activated clay materials (Southern Tunisia)

NASA Astrophysics Data System (ADS)

Trabelsi, Wafa; Tlili, Ali

2017-05-01

This study concerns the purification of Tunisian phosphoric acid produced by the Tunisian Chemical Group (TCG), using raw and activated clays materials from Southern Tunisia. The Gafsa basin clays samples (Jebel Hamadi (JHM); Jebel Stah (JS) and the El Hamma sample (Jebel Aïdoudi (JAD)) were activated with 3 M, HCl solution. Phosphoric acid purification was performed on raw and activated clays. Mineralogical characterisation was carried out using the X-ray powder diffraction method and infrared absorption spectroscopy. Textural changes between raw and activated clays were identified using SEM observations and specific surface analysis. Jebel Hamadi clays were almost dominated by smectite associated with kaolinite and illite traces, while Jebel Stah and Jebel Aïdoudi clays were composed of the association of smectite, illite and kaolinite. It is worth noting that the position of the smectite (001) reflection increased after the acidic activation in all studied samples, indicating the relaxation of the smectite structure along the c-axis. This was corroborated by the increasing specific surface area of the clay particles with the activation process. The specific surface area was close to 50 m2/g and 200 m2/g, for raw and activated materials, respectively. The maximum phosphoric acid purification was obtained by using activated clays with 3 N HCl for 4 h. This performance correlated with the maximum of the external specific surface area which generated strong acid sites. Furthermore, the best results of phosphoric acids purification from TCG were obtained at a specific consumption equivalent to 30 Kg of clay/ton of P2O5. These results showed that the best phosphoric acid purification was yielded by Jebel Aïdoudi clay. In all cases, the highest organic carbon reduction rates in the phosphoric acid after filtration were obtained at 90°C.

Isolation of phyllosilicate-iron redox cycling microorganisms from an illite-smectite rich hydromorphic soil.

PubMed

Shelobolina, Evgenya; Konishi, Hiromi; Xu, Huifang; Benzine, Jason; Xiong, Mai Yia; Wu, Tao; Blöthe, Marco; Roden, Eric

2012-01-01

The biogeochemistry of phyllosilicate-Fe redox cycling was studied in a Phalaris arundinacea (reed canary grass) dominated redoximorphic soil from Shovelers Sink, a small glacial depression near Madison, WI. The clay size fraction of Shovelers Sink soil accounts for 16% of the dry weight of the soil, yet contributes 74% of total Fe. The dominant mineral in the clay size fraction is mixed layer illite-smectite, and in contrast to many other soils and sediments, Fe(III) oxides are present in low abundance. We examined the Fe biogeochemistry of Shovelers Sink soils, estimated the abundance of Fe redox cycling microorganisms, and isolated in pure culture representative phyllosilicate-Fe oxidizing and reducing organisms. The abundance of phyllosilicate-Fe reducing and oxidizing organisms was low compared to culturable aerobic heterotrophs. Both direct isolation and dilution-to-extinction approaches using structural Fe(II) in Bancroft biotite as a Fe(II) source, and O(2) as the electron acceptor, resulted in recovery of common rhizosphere organisms including Bradyrhizobium spp. and strains of Cupriavidus necator and Ralstonia solanacearum. In addition to oxidizing biotite and soluble Fe(II) with O(2), each of these isolates was able to oxidize Fe(II) in reduced NAu-2 smectite with [Formula: see text] as the electron acceptor. Oxidized NAu-2 smectite or amorphous Fe(III) oxide served as electron acceptors for enrichment and isolation of Fe(III)-reducing microorganisms, resulting in recovery of a strain related to Geobacter toluenoxydans. The ability of the recovered microorganisms to cycle phyllosilicate-Fe was verified in an experiment with native Shovelers Sink clay. This study confirms that Fe in the native Shovelers Sink clay is readily available for microbial redox transformation and can be cycled by the Fe(III)-reducing and Fe(II)-oxidizing microorganisms recovered from the soil.

Oscillation of mineral compositions in Core SG-1b, western Qaidam Basin, NE Tibetan Plateau

PubMed Central

Fang, Xiaomin; Li, Minghui; Wang, Zhengrong; Wang, Jiuyi; Li, Jiao; Liu, Xiaoming; Zan, Jinbo

2016-01-01

Uplift of the Tibetan Plateau since the Late Miocene has greatly affected the nature of sediments deposited in the Qaidam Basin. However, due to the scarcity of continuously dated sediment records, we know little about how minerals responded to this uplift. In order to understand this response, we here present results from the high-resolution mineral profile from a borehole (7.3–1.6 Ma) in the Basin, which shows systematic oscillations of various evaporite and clay minerals that can be linked to the variation of regional climate and tectonic history. In particular, x-ray diffraction (XRD) analyses show that carbonate minerals consist mainly of calcite and aragonite, with minor ankerite and dolomite. Evaporates consist of gypsum, celesite and halite. Clay minerals are principally Fe-Mg illite, mixed layers of illite/smectite and chlorite, with minor kaolinite and smectite. Following implications can be drawn from the oscillations of these minerals phases: (a) the paleolake was brackish with high salinity after 7.3 Ma, while an abrupt change in the chemical composition of paleolake water (e.g. Mg/Ca ratio, SO42− concentration, salinity) occurred at 3.3 Ma; (b) the three changes at ~6.0 Ma, 4.5–4.1 Ma and 3.3 Ma were in response to rapid erosions/uplift of the basin; (c) pore water or fluid was Fe/Mg-rich in 7.3–6.0 Ma, Mg-rich in 6.0–4.5 Ma, and K-rich in 4.1–1.6 Ma; and (d) evaporation rates were high, but weaker than today’s. PMID:27625177

Geochemical evidences for palaeoclimatic fluctuations at the Triassic-Jurassic boundary: southwestern margin of the Neotethys in the Salt Range, Pakistan

NASA Astrophysics Data System (ADS)

Iqbal, Shahid; Wagreich, Michael; Jan, Irfanullah; Kürschner, Wolfram Michael; Gier, Susanne

2017-04-01

The Triassic-Jurassic boundary interval reveals a change from warm-arid to a warm and humid climate in the Tethyan domain. Sea-level reconstruction records across the European basins during this interval reveal an end-Triassic global regression event and is linked to the Central Atlantic Magmatic Province (CAMP) activity and Pangaea breakup. In the Tethyan Salt Range of Pakistan a succession of Upper Triassic dolomites/green-black mudstones (Kingriali Formation), overlying quartzose sandstone, mudstones, laterites and Lower Jurassic conglomerates/pebbly sandstones (Datta Formation) provides information on the palaeoclimatic evolution of the area. Preliminary palynological results from the mudstones indicate a Rhaetian age for the Kingriali Formation and a Hettangian age for the Datta Formation. X-ray diffraction (XRD) analysis of the mudstones (upper part of the Kingriali Formation) indicates the presence of mainly illite while kaolinite is a minor component. The kaolinite content, a reflection of the advanced stage of chemical weathering and hence warm-humid conditions, increases up-section in the overlying sandstone-mudstone succession. The overlying laterite-bauxite horizons lack illite/smectite and are entirely composed of kaolinite, boehmite and haematite. At places these kaolinite rich horizons are mined in the area (Western Salt Range). The bulk rock geochemistry of the succession confirms a similar trend. The Chemical Index of Alteration (CIA) displays an increasing trend from the Upper Triassic shales (CIA 75-80) through the overlying sandstones/mudstones-laterites to the overlying quartz rich sandstones and mudstones (CIA 90-97). The overall results for the succession reveal an increasing chemical maturity trend (increase in the intensity of chemical weathering) from Rhaetian to Hettangian thereby supporting a change from warm-arid to a warm-humid palaeoclimate, probably extreme greenhouse conditions.

Environmental effect and genetic influence: a regional cancer predisposition survey in the Zonguldak region of Northwest Turkey

NASA Astrophysics Data System (ADS)

Kadir, Selahattin; Önen-Hall, A. Piril; Aydin, S. Nihal; Yakicier, Cengiz; Akarsu, Nurten; Tuncer, Murat

2008-03-01

The Cretaceous-Eocene volcano-sedimentary units of the Zonguldak region of the western Black Sea consist of subalkaline andesite and tuff, and sandstone dominated by smectite, kaolinite, accessory chlorite, illite, mordenite, and analcime associated with feldspar, quartz, opal-CT, amphibole, and calcite. Kaolinization, chloritization, sericitization, albitization, Fe-Ti-oxidation, and the presence of zeolite, epidote, and illite in andesitic rocks and tuffaceous materials developed as a result of the degradation of a glass shards matrix, enclosed feldspar, and clinopyroxene-type phenocrysts, due to alteration processes. The association of feldspar and glass with smectite and kaolinite, and the suborientation of feldspar-edged, subparallel kaolinite plates to fracture axes may exhibit an authigenic smectite or kaolinite. Increased alteration degree upward in which Al, Fe, and Ti are gained, and Si, Na, K, and Ca are depleted, is due to the alteration following possible diagenesis and hydrothermal activities. Micromorphologically, fibrous mordenite in the altered units and the presence of needle-type chrysotile in the residential buildings in which cancer cases lived were detected. In addition, the segregation pattern of cancer susceptibility in the region strongly suggested an environmental effect and a genetic influence on the increased cancer incidence in the region. The most likely diagnosis was Li-Fraumeni syndrome, which is one of the hereditary cancer predisposition syndromes; however, no mutations were observed in the p53 gene, which is the major cause of Li-Fraumeni syndrome. The micromorphology observed in the altered units in which cancer cases were detected may have a role in the expression of an unidentified gene, but does not explain alone the occurrence of cancer as a primary cause in the region.

Mineralogy, morphology, and textural relationships in coatings on quartz grains in sediments in a quartz-sand aquifer

USGS Publications Warehouse

Zhang, Shouliang; Kent, Douglas B.; Elbert, David C.; Shi, Zhi; Davis, James A.; Veblen, David R.

2011-01-01

Mineralogical studies of coatings on quartz grains and bulk sediments from an aquifer on Western Cape Cod, Massachusetts, USA were carried out using a variety of transmission electron microscopy (TEM) techniques. Previous studies demonstrated that coatings on quartz grains control the adsorption properties of these sediments. Samples for TEM characterization were made by a gentle mechanical grinding method and focused ion beam (FIB) milling. The former method can make abundant electron-transparent coating assemblages for comprehensive and quantitative X-ray analysis and the latter technique protects the coating texture from being destroyed. Characterization of the samples from both a pristine area and an area heavily impacted by wastewater discharge shows similar coating textures and chemical compositions. Major constituents of the coating include Al-substituted goethite and illite/chlorite clays. Goethite is aggregated into well-crystallized domains through oriented attachment resulting in increased porosity. Illite/chlorite clays with various chemical compositions were observed to be mixed with goethite aggregates and aligned sub-parallel to the associated quartz surface. The uniform spatial distribution of wastewater-derived phosphorus throughout the coating from the wastewater-contaminated site suggests that all of the coating constituents, including those adjacent to the quartz surface, are accessible to groundwater solutes. Both TEM characterization and chemical extraction results indicate there is a significantly greater amount of amorphous iron oxide in samples from wastewater discharge area compared to those from the pristine region, which might reflect the impact of redox cycling of iron under the wastewater-discharge area. Coating compositions are consistent with the moderate metal and oxy-metalloid adsorption capacities, low but significant cation exchange capacities, and control of iron(III) solubility by goethite observed in reactive transport experimental and modeling studies conducted at the site.

Mineralogy, geochemistry, and palynology of modern and late Tertiary mangrove deposits in the Barreiras Formation of Mosqueiro Island, northeastern Pará state, eastern Amazonia

NASA Astrophysics Data System (ADS)

Behling, Hermann; da Costa, Marcondes Lima

2004-12-01

A coastal environment has been interpreted from 110 cm thick mudstone deposits found at the base of a 10 m immature laterite profile, which forms the modern coastal cliff on Mosqueiro Island in northeastern Pará state, northern Brazil. The late Tertiary sediment deposits of the Barreiras Formation are studied by multi-element geochemistry and pollen analyses. The mineralogical and geochemical results show that the gray, organic-rich deposits are composed of kaolinite, quartz, and illite/muscovite, as well as pyrite and anatase. They are rich in SiO 2, Al 2O 3, and some FeO. The composition is homogenous, indicating that the detritus source area is formed of lateritic soils derived from acid rock composition. Their chemical composition, including trace elements, is somewhat comparable to continental shale, and the values are below the upper continental Earth crust composition. The pollen analytical data document that the mudstone deposits were formed by an ancient mangrove ecosystem. Mineralogical, geochemical, and pollen analytical data obtained from late Tertiary mangrove deposits are compared with modern mangrove deposits from the Bragança Peninsula of the northeastern coast of Pará state. Although the pollen composition of the deposits is very similar to the modern one, the geochemical and mineralogical composition is different. Smectite was only found in the modern deposit; illite/mica occurs in the ancient deposit, along with Mg, K, and Na. The pollen signature and detrital minerals (kaolinite, quartz and anatase) found in both mangrove deposits show that during the Miocene, a humid tropical climate condition prevailed, similar to modern conditions.

Mössbauer studies on some Argentinian soil: Mollisols from Bahia Blanca

NASA Astrophysics Data System (ADS)

Saragovi, C.; Labenski, F.; Duhalde, S. M.; Acebal, S.; Venegas, R.

1994-12-01

Clay fractions of a Mollisol sample as is, treated with ammonium oxalate (AO), with dithionite-citrate-bicarbonate (DCB) and with dithionite-ethilene-diamine-tetraacetic acid (D-EDTA) methods, were studied. Illite-montmorillonites together with hematites, goethites and maghemites, all of the AI-substituted and with a wide range of sizes, were identified. It is found that the AO attack extracts little iron, whereas the other two attacks extract the magnetic signal. Furthermore, the DCB attack facilitates the reduction of the Fe3+ ions, while the D-EDTA method does not. Instead, this attack extracts more clay mineral Fe ions. A comparison with large grain soil samples is made.

Geothermometry, geochronology, and mass transfer associated with hydrothermal alteration of a rhyolitic hyaloclastite from Ponza Island, Italy

USGS Publications Warehouse

Altaner, S.P.; Ylagan, R.F.; Savin, S.M.; Aronson, J.L.; Belkin, H.E.; Pozzuoli, A.

2003-01-01

A rhyolitic hyaloclastite from Ponza Island, Italy, was hydrothermally altered, producing four distinct alteration zones based on X-ray diffraction mineralogy and field textures: (1) nonpervasive argillic zone; (2) propylitic zone; (3) silicic zone; and (4) sericitic zone. The unaltered hyaloclastite is volcanic breccia with clasts of vesiculated obsidian in a matrix of predominantly pumice lapilli. Incomplete alteration of the hyaloclastite resulted in the nonpervasive argillic zone, characterized by smectite and disordered opal-CT. The other three zones exhibit more complete alteration of the hyaloclastite. The propylitic zone is characterized by mixed-layer illite-smectite (I-S) with 10 to 85% I, mordenite, opal-C, and authigenic K-feldspar (akspar). The silicic zone is characterized by I-S with ???90% I, pure illite, quartz, akspar, and occasional albite. The sericitic zone consists primarily of I-S with ???66% I, pure illite, quartz, and minor akspar and pyrite. K/Ar dates of I-S indicate hydrothermal alteration occurred at 3.38 ?? 0.08 Ma. Oxygen isotope compositions of I-S systematically decrease from zones 1 to 4. In the argillic zone, smectite has ??18 O values of 21.7 to 22.0??? and I-S from the propylitic, silicic, and sericitic zones ranges from 14.5 to 16.3???, 12.5 to 14.0???, and 8.6 to 11.9???, respectively. ??18 O values for quartz from the silicic and sericitic zones range from 12.6 to 15.9???. By use of isotope fractionation equations and data from authigenic quartz-hosted primary fluid inclusions, alteration temperatures ranged from 50 to 65 ??C for the argillic zone, 85 to 125 ??C for the propylitic zone, 110 to 210 ??C for the silicic zone, and 145 to 225 ??C for the sericitic zone. Fluid inclusion data and calculated ??18 O water values indicate that hydrothermal fluids were seawater dominated. Mass-transfer calculations indicate that hydrothermal alteration proceeded in a relatively open chemical system and alteration in the sericitic zone involved the most extensive loss of chemical species, especially Si. Systematic gains in Mg occur in all alteration zones as a result of I-S clay mineral formation, and systematic losses of Na, Ca, and K occur in most zones. With the exception of Ca, calculations of mass transfer associated with hydrothermal alteration on Ponza agree with chemical fluxes observed in laboratory experiments involving hydrothermal reactions of rhyolite and seawater. The anomalous Ca loss at Ponza may be due to hydrothermal formation of anhydrite and later low-temperature dissolution. On the basis of Mg enrichments derived from circulating seawater, we estimate the following minimum water/rock ratios: 9, 3, 6, and 9 for the argillic, propylitic, silicic, and sericitic zones, respectively. Hydrothermal fluid pH for the propylitic and silicic zones was neutral to slightly basic and relatively acidic for the sericitic zone as a result of condensation of carbonic and perhaps other acids. Copyright ?? 2003 Elsevier Science Ltd.

The importance of XRD analysis in provenance and palaeoenvironmental studies of the Piedras de Afilar Formation, Neoproterozoic of Uruguay

NASA Astrophysics Data System (ADS)

Pamoukaghlian, K.; Poiré, D. G.; Gaucher, C.; Uriz, N.; Cingolani, C.; Frigeiro, P.

2009-04-01

The Piedras de Afilar Formation crops out in the southeast part of Uruguay, forming part of the Tandilia Terrane (sensu Bossi et al. 2005). Pamoukaghlian et al. (2006) and Gaucher et al. (2008) have published δ13C, δ18O and U/Pb SHRIMP results, which indicate a Neoproterozoic age for this formation. The palaeoenvironment has been defined as a shallow marine platform based on the presence of interference ripples, hummocky and mega-hummocky cross-stratification. X-ray diffraction (XRD) analyses help to better constrain the palaeoenvironment: the presence of chlorite/smectite found in black shales, suggest a reducing environment, and abundant illite indicates a cold to temperate climate. Provenance studies have been undertaken that utilise a combination of detailed palaeocurrent measurements, petrographic descriptions, XRD analyses, and geochemical isotopic analyses, including U/Pb SHRIMP determinations. Mineral compositional diagrams for sandstones suggest a stable cratonic provenance. Palaeocurrents are mainly from the NNE, indicating a provenance from the cratonic areas of the Tandilia Terrane. The illite crystal index indicates diagenetic to low-metamorphic conditions for the sequence; this is important to confirm that the identified minerals are authigenic. Clay minerals identified by XRD analysis of sandstones from the siliciclastic member are illite (80 - 90%), kaolinite (5 - 10%), and chlorite (5 - 10%). This is consistent with a provenance from the cratonic areas (quartz-feldspar dominated rock types). Isotopic analyses have been undertaken to provide better constraints on the tectonic setting. U/Pb SHRIMP ages for the youngest zircons are 990 Ma (Gaucher et al. 2008), and the basal granite (Granito de la Paz) is 2056 ± 11 Ma (Hartmann et al. 2001), suggesting a provenance from the Archaean basement for the Piedras de Afilar Formation, like its counterparts in the Rio de la Plata Craton. References Bossi, J., Piñeyro, D., Cingolani, C. (2005). El límite norte del Terreno Piedra Alta (Uruguay). Importancia de la faja milonítica sinestral de Colonia. Actas XVI Congreso Argentino de Geología, de La Plata. Gaucher, C., Poiré, D.G., Finney, S.C., Valencia, V.a., Blanco, G., Pamoukaghlian, K., Gómez Peral, L. (2008). Detrital zircón ages of Neoproterozoic sedimentary successions in Uruguay and Argentina: Insights into the geological evolution of the Rio de la Plata Craton. Precambrian Research. Hartmann, L.A., Campal, N., Santos, J.O., Mc. Neughton, N.J., Schipilov, A., Lafon, J.M. (2001). Archean crust in the Rio de la Plata Craton, Uruguay - SHRIMP U-Pb zircon reconnaissance geochronology. Journal of South American Earth Science, 14, 557-570. Pamoukaghlian, K., Gaucher, C., Bossi, J., Sial, N., Poire, D.G. (2006). First C and O isotopic data for the Piedras de Afilar Formation, Tandilia Terrane, Uruguay: their bearing on correlation and age. Fifth South American Symposium on Isotope Geology, Punta del Este.

Smectite clays of Serbia and their application in adsorption of organic dyes

NASA Astrophysics Data System (ADS)

Milošević, Maja; Logar, Mihovil

2014-05-01

Colorants and dyes are currently available in over a 100.000 different species and several biggest industries are using them daily in their manufacture processes (textile, cosmetics, food industry, etc.). Since colorants are easily dissoluble in water they pass through filter membranes without further decomposing and in that manner they end up in the environment. The main goal of this work is to apply certain methods in determining the suitability of individual clay in adsorbing and removing colorants from polluted waters. For this study we have chosen four different raw clays from three regions in Serbia: Svrljig (B), Bogovina (Bo) and Slatina-Ub (C and V) and as colorant - methylene blue dye (MB (MERCK, for analytical purposes)). Experiments where carried out to determine the sample structure (XRD and IR), grain size (granulometry), cationic exchange capacity (CEC via spectrophotometry using MB) and adsorption capabilities (spectrophotometry and fluorimetry using MB). XRD and IR data are showing that the samples are smectite clays where samples B i Bo are mainly montmorillonite while C and V are montmorillonite-illite clays. Granulometric distribution results indicate that samples B i Bo have smaller grain size, less that 1μ (over 60%) whereas the samples C and V are more coarse grained (40% over 20μ). This grain distribution is affecting their specific surface area in the manner that those coarse grained samples have smaller specific surface area. Cationic exchange capacity determined with methylene blue indicate that montmorillonite samples have larger CEC (B = 37 meq/100g, Bo = 50 meq/100g) and montmorillonite-illite samples smaller CEC (V = 5 meq/100g, V = 3 meq/100g). Fluorimetry measurement results gave us a clear distinction between those with higher and smaller adsorption capability. Montmorillonite samples (B and Bo) with higher CEC values and smaller grain size are adsorbing large amounts of methylene blue witch is visible by absence of fluorimetric band corresponding to methylene blue. Montmorillonite-illite samples with smaller CEC values and coarser grain size are adsorbing very small amounts of methylene blue from the suspension which is visible by appearance of the methylene blue band. Untreated, raw smectite clays of Serbia are efficient adsorbent material for removal of dyes from polluted waters. Samples from two regions especially, Bogovina and Svrljig, are showing favorable adsorption results and they are representing good raw materials for purification of waste-waters containing dyes. References: - Jović-Jovičić, N., Milutinović-Nikolić, A., Gržetić, I., Jovanović, D.; Organobentonite as efficient textile dye sorbent; Chem. Eng. Technol. 2008, 31, No. 4, 567-574 - Žunić, M.J., Milutinović-Nikolić, A.D., Jović-Jovičić, N.P., Banković, P.T., Mojović, Z.D., Manojlović, D.D., Jovanović, D.M.; Modified bentonite as adsorbent and catalyst for purification of wastewaters containing dyes; Hem. ind. 2010, 64 ,No. 3, 193-199

The laser microprobe mass analyser for determining partitioning of minor and trace elements among intimately associated macerals: an example from the Swallow Wood coal bed, Yorkshire, UK

USGS Publications Warehouse

Lyons, P.C.; Morelli, J.J.; Hercules, D.M.; Lineman, D.; Thompson-Rizer, C. L.; Dulong, F.T.

1990-01-01

A study of the elemental composition of intimately associated coal macerals in the English Swallow Wood coal bed was conducted using a laser microprobe mass analyser, and indicated a similar trace and minor elemental chemistry in the vitrinite and cutinite and a different elemental signature in the fusinite. Three to six sites were analysed within each maceral during the study by laser micro mass spectrometry (LAMMS). Al, Ba, Ca, Cl, Cr, Dy, F, Fe, Ga, K, Li, Mg, Na, S, Si, Sr, Ti, V, and Y were detected by LAMMS in all three macerals but not necessarily at each site analysed. The signal intensities of major isotopic peaks were normalized to the signal intensity of the m z 85 peak (C7H) to determine the relative minor- and trace-element concentrations among the three dominant macerals. The vitrinite and the cutinite were depleted in Ba, Ca, Dy, Li, Mg, Sr, and Y relative to their concentrations observed in the fusinite. The cutinite was distinguished over vitrinite by less Ti, V, Cr and Ca, and K Ca $ ??1 (relative signal intensities). The fusinite, relative to the cutinite and vitrinite, was relatively depleted in Cr, Sc, Ti, and V. The fusinite, as compared with both the cutinite and vitrinite, was relatively enriched in Ba, Ca, Dy, Li, Mg, Sr, and Y, and also showed the most intense m z 64, 65, 66 signals (possibly S2+, HS2+, H2S2+, respectively). The LAMMS data indicate a common source for most elements and selective loss from the maceral precursors in the peat or entrapment of certain elements as mineral matter, most likely during the peat stage or during early diagenesis. The relatively high amounts of Ba, Ca, Dy, Li, Mg, Sr, and Y in the fusinite are consistent with micron and submicron mineral-matter inclusions such as carbonates and Ca-Al phosphates (probably crandallite group minerals). Mineralogical data on the whole coal, the LAMMS chemistry of the vitrinite and cutinite, and scanning electron microscopy/energy dispersive X-ray analysis (SEM/EDAX) of the elements in the macerals are consistent with the presence of micron and submicron inclusions of clays such as kaolinite, illite, and Ca-rich or Ca-bearing minerals (e.g. calcite, Ca-Al phosphates, and illite) which are different in kind and proportions in the three macerals. The variance as measured by the F-statistic for all three macerals indicates generally a nonuniform distribution of minor and trace elements in all three macerals, thus supporting a mineral-matter (inorganic) origin of the elements analysed. Exceptions are Al, K, Fe, Ga, and Sr in the vitrinite and cutinite, which is consistent with organic complexing or a uniform distribution of micron or submicron mineral matter such as illite and phosphate(s). ?? 1990.

Sediment mineralogy based on visible and near-infrared reflectance spectroscopy

USGS Publications Warehouse

Jarrard, R.D.; Vanden Berg, M.D.; ,

2006-01-01

Visible and near-infrared spectroscopy (VNIS) can be used to measure reflectance spectra (wavelength 350-2500 nm) for sediment cores and samples. A local ground-truth calibration of spectral features to mineral percentages is calculated by measuring reflectance spectra for a suite of samples of known mineralogy. This approach has been tested on powders, core plugs and split cores, and we conclude that it works well on all three, unless pore water is present. Initial VNIS studies have concentrated on determination of relative proportions of carbonate, opal, smectite and illite in equatorial Pacific sediments. Shipboard VNIS-based determination of these four components was demonstrated on Ocean Drilling Program Leg 199. ?? The Geological Society of London 2006.

Effets thermique et hydrothermal de la coulée de basalte triasico-liasique sur les argiles du bassin d'Argana (Maroc)Thermal and hydrothermal effects of Triassic Liassic basalt flow deposition on clays (Agana Basin, Morocco)

NASA Astrophysics Data System (ADS)

Daoudi, Lahcen; Pot de Vin, Jean-Luc

Thermal and hydrothermal effects of Triassic-Liassic basalt flow deposition on sedimentary series of the Argana Basin are responsible for major modifications in detrital clays, until 20 m in depth. It expressed by transformation of detrital smectite to corrensite and moreover to chlorite, and by increasing illite crystallinity. On the 2 m of sediments located immediately under the flow, magnesium-rich hydrothermal fluids have caused precipitation of new mineral phases. To cite this article: L. Daoudi, J.-L. Pot de Vin, C. R. Geoscience 334 (2002) 463-468.

Effect of carboxymethyl cellulose and ionic strength on stability of mineral suspensions in potash ore flotation systems.

PubMed

Pawlik, M; Laskowski, J S; Ansari, A

2003-04-15

The adsorption of sodium carboxymethyl cellulose from aqueous solutions varying in ionic strength from that of distilled water to 50% NaCl/KCl brine (about 3.5 mol/dm(3)) onto illite and dolomite has been studied. The purpose of this work was to investigate the solvency effects in the phenomena underlying the potash flotation process that is carried out in saturated brine. Based on viscosity measurements, the adsorption results were analyzed in terms of a simple model of polymer macromolecules in solution. Suspension stability measurements carried out concomitantly with adsorption tests showed the ranges of carboxymethyl cellulose concentration over which the tested suspensions either were aggregated or were restabilized.

Chemical and mineralogical analysis of devonian black-shale samples from Martin County, Kentucky; Carroll and Washington counties, Ohio; Wise County, Virginia; and Overton County, Tennessee, U.S.A.

USGS Publications Warehouse

Leventhal, J.S.; Hosterman, J.W.

1982-01-01

Core samples of Devonian shales from five localities in the Appalachian basin have been analyzed chemically and mineralogically. The amounts of major elements are similar; however, the minor constituents, organic C, S, phosphate and carbonate show ten-fold variations in amounts. Trace elements Mo, Ni, Cu, V, Co, U, Zn, Hg, As and Mn show variations in amounts that can be related to the minor constituents. All samples contain major amounts of quartz, illite, two types of mixed-layer clays, and chlorite in differing quantities. Pyrite, calcite, feldspar and kaolinite are also present in many samples in minor amounts. Dolomite, apatite, gypsum, barite, biotite and marcasite are present in a few samples in trace amounts. Trace elements listed above are strongly controlled by organic C with the exception of Mn which is associated with carbonate minerals. Amounts of organic C generally range from 3 to 6%, and S is in the range of 2-5%. Amounts of trace elements show the following general ranges in ppm (parts per million): Co, 20-40; Cu, 40-70; U, 10-40; As, 20-40; V, 150-300; Ni, 80-150; high values are as much as twice these values. The organic C was probably the concentrating agent, and the organic C and sulfide S together created an environment that immobilized and preserved these trace elements. Closely spaced samples showing an abrupt transition in color also show changes in organic C, S and trace-element contents. Several associations exist between mineral and chemical content. Pyrite and marcasite are the only minerals found to contain sulfide-S. In general, the illite-chlorite mixed-layer clay mineral shows covariation with organic C if calcite is not present. The enriched trace elements are not related to the clay types, although the clay and organic matter are intimately associated as the bulk fabric of the rock. ?? 1982.

Radiometric Dating of Folds: A new approach to determine the timing of deformation at shallow-crustal conditions, with examples from the Mexican Fold-Thrust Belt

NASA Astrophysics Data System (ADS)

Fitz Diaz, E.; van der Pluijm, B. A.

2012-12-01

We are developing a robust method to obtain absolute ages of folds that were formed at shallow crustal conditions. The method takes advantage of illite neocrystallization in folded, clay-bearing layers and the ability to obtain accurate retention and total gas ages from small size fractions using encapsulated Ar analysis, analogous to prior work on fault gouge dating. We illustrate our approach in folded Cretaceous shale-bentonitic layers that are interbedded with carbonates of the Zimapán and the Tampico-Misantla cretaceous basins in central-eastern Mexico. Basinal carbonates were buried by syntectonic turbidites and inverted during the formation of the Mexican Fold-Thrust in the Late Cretaceous. Results were obtained from four chevron folds that are representative of different stages of deformation, burial/temperature conditions and location within this thin-skinned orogenic wedge: two from the Zimapán Basin (Folds 1 and 2) in the west and two from the Tampico-Misantla Basin (Folds 3 and 4) in the east. Mineralogic compositions and variations in illite-polytypes, crystallite-size (CS) and Ar/Ar ages were obtained from size fractions in limbs and hinges of folded layers. Ar retention ages produce a folding age of ~81 Ma for Fold 1 and ~69 Ma for Fold 2, which are fully consistent with stratigraphic limits from syn-orogenic turbidities and observed overprinting events in the Mexican Fold-Thrust Belt. The total gas age of Fold 3, on the easternmost margin of the Tampico-Misantla Basin is similar to that of Fold 2, indicating that the second event is regional in scale. In addition to presenting a new, reliable method to constrain the timing of local deformation, we interpret folding and associated clay neo-mineralization in terms of the regional burial history, and localization and propagation of deformation within a heterogeneous orogenic wedge involving progressive deformation of two basins separated by a platform block.

Experimental and theoretical studies of the effect of temperature on supercritical CO2 adsorption on illite

NASA Astrophysics Data System (ADS)

Joewondo, N.; Zhang, Y.; Prasad, M.

2016-12-01

Sequestration of carbon dioxide in shale has been a subject of interest as the result of the technological advancement in gas shale production. The process involves injection of CO2 to enhance methane recovery and storing CO2 in depleted shale reservoir at elevated pressures. To better understand both shale production and carbon storage one must study the physical phenomena acting at different scales that control the in situ fluid flow. Shale rocks are complex systems with heterogeneous structures and compositions. Pore structures of these systems are in nanometer scales and have significant gas storage capacity and surface area. Adsorption is prominent in nanometer sized pores due to the high attraction between gas molecules and the surface of the pores. Recent studies attempt to find correlation between storage capacity and the rock composition, particularly the clay content. This study, however, focuses on the study of supercritical adsorption of CO2 on pure clay sample. We have built an in-house manometric experimental setup that can be used to study both the equilibrium and kinetics of adsorption. The experiment is conducted at isothermal condition. The study of equilibrium of adsorption gives insight on the storage capacity of these systems, and the study of the kinetics of adsorption is essential in understanding the resistance to fluid transport. The diffusion coefficient, which can be estimated from the dynamic experimental results, is a parameter which quantify diffusion mobility, and is affected by many factors including pressure and temperature. The first part of this paper briefly discusses the study of both equilibrium and kinetics of the CO2 adsorption on illite. Both static and dynamic measurements on the system are compared to theoretical models available in the literature to estimate the storage capacity and the diffusion time constants. The main part of the paper discusses the effect of varying temperature on the static and dynamic experimental results.

Diagenetic history of the Surma Group sandstones (Miocene) in the Surma Basin, Bangladesh

NASA Astrophysics Data System (ADS)

Rahman, M. Julleh Jalalur; McCann, Tom

2012-02-01

This study examines the various diagenetic controls of the Miocene Surma Group sandstones encountered in petroleum exploration wells from the Surma Basin, which is situated in the northeastern part of the Bengal Basin, Bangladesh. The principal diagenetic minerals/cements in the Surma Group sandstones are Fe-carbonates (with Fe-calcite dominating), quartz overgrowths and authigenic clays (predominantly chlorite, illite-smectite and minor kaolin). The isotopic composition of the carbonate cement revealed a narrow range of δ 18O values (-10.3‰ to -12.4‰) and a wide range of δ 13C value (+1.4‰ to -23.1‰). The δ 13C VPDB and δ 18O VPDB values of the carbonate cements reveal that carbon was most likely derived from the thermal maturation of organic matter during burial, as well as from the dissolution of isolated carbonate clasts and precipitated from mixed marine-meteoric pore waters. The relationship between the intergranular volume (IGV) versus cement volume indicates that compaction played a more significant role than cementation in destroying the primary porosity. However, cementation also played a major role in drastically reducing porosity and permeability in sandstones with poikilotopic, pore-filling blocky cements formed in early to intermediate and deep burial areas. In addition to Fe-carbonate cements, various clay minerals including illite-smectite and chlorite occur as pore-filling and pore-lining authigenic phases. Significant secondary porosity has been generated at depths from 2500 m to 4728 m. The best reservoir rocks found at depths of 2500-3300 m are well sorted, relatively coarse grained; more loosely packed and better rounded sandstones having good porosities (20-30%) and high permeabilities (12-6000 mD). These good quality reservoir rocks are, however, not uniformly distributed and can be considered to be compartmentalized as a result of interbedding with sandstone layers of low to moderate porosities, low permeabilities owing to poor sorting and extensive compaction and cementation.

Co-evolution of monsoonal precipitation in East Asia and the tropical Pacific ENSO system since 2.36 Ma: New insights from high-resolution clay mineral records in the West Philippine Sea

NASA Astrophysics Data System (ADS)

Yu, Zhaojie; Wan, Shiming; Colin, Christophe; Yan, Hong; Bonneau, Lucile; Liu, Zhifei; Song, Lina; Sun, Hanjie; Xu, Zhaokai; Jiang, Xuejun; Li, Anchun; Li, Tiegang

2016-07-01

Clay mineralogical analysis and scanning electron microscope (SEM) analysis were performed on deep-sea sediments cored on the Benham Rise (core MD06-3050) in order to reconstruct long-term evolution of East Asian Summer Monsoon (EASM) rainfall in the period since 2.36 Ma. Clay mineralogical variations are due to changes in the ratios of smectite, which derive from weathering of volcanic rocks in Luzon Island during intervals of intensive monsoon rainfall, and illite- and chlorite-rich dusts, which are transported from East Asia by winds associated with the East Asian Winter Monsoon (EAWM). Since Luzon is the main source of smectite to the Benham Rise, long-term consistent variations in the smectite/(illite + chlorite) ratio in core MD06-3050 as well as ODP site 1146 in the Northern South China Sea suggest that minor contributions of eolian dust played a role in the variability of this mineralogical ratio and indicate strengthening EASM precipitation in SE Asia during time intervals from 2360 to 1900 kyr, 1200 to 600 kyr, and after 200 kyr. The EASM rainfall record displays a 30 kyr periodicity suggesting the influence of El Niño-Southern Oscillation (ENSO). These intervals of rainfall intensification on Luzon Island are coeval with a reduction in precipitation over central China and an increase in zonal SST gradient in the equatorial Pacific Ocean, implying a reinforcement of La Niña-like conditions. In contrast, periods of reduced rainfall on Luzon Island are associated with higher precipitation in central China and a weakening zonal SST gradient in the equatorial Pacific Ocean, thereby suggesting the development of dominant El Niño-like conditions. Our study, therefore, highlights for the first time a long-term temporal and spatial co-evolution of monsoonal precipitation in East Asia and of the tropical Pacific ENSO system over the past 2.36 Ma.

Experimental Evaluation of pH and Temperature Effects on the Adsorption of Boron onto Clay Minerals

NASA Astrophysics Data System (ADS)

Hoenisch, B.; Marone, D.; Ruprecht, J.

2017-12-01

Modeling the secular evolution of the concentration [B] and isotopic composition (δ11B) of boron in seawater is hampered by limited constraints on the relative sources (i.e. riverine input of weathering products, hydrothermal convection at mid-ocean ridges and fluids expelled from accretionary prisms) and sinks (i.e. alteration of the oceanic crust, adsorption onto clays, and co-precipitation in carbonates) of boron to and from the ocean. Clays remove approximately 28% of total boron from the ocean and quantification of this sink thus represents a major factor for reconstructing the secular evolution of seawater [B] and δ11B over the Cenozoic. However, the relative strength of the clay sink could have been much smaller in the early Cenozoic compared to today, because borate ion as the charged species is preferentially adsorbed onto detrital clays over boric acid, and because the relative abundance of borate in seawater should have been lower under the more acidic conditions of the early Cenozoic. In addition, different clay minerals tend to fractionate boron isotopes differentially, and the relative composition of clay minerals has varied in the past with the dominant climate and weathering patterns on the continents. We have conducted a range of pH (7.5-8.4) and temperature (3-32°C) experiments with four clay minerals (Kaolinite, Illite, Montmorillonite and Chlorite), to build on previously published but limited experimental data. Similar to a previous study and as expected based on the relative abundance of borate ion in seawater, boron adsorption onto these clays increases at higher pH and lower temperatures, but whereas Montmorillonite and Illite absorb similar quantities of boron, Kaolinite is most and Chlorite least efficient in this process. We are now in the process of characterizing the boron isotope fractionation associated with these adsorption experiments.

Soft X-ray spectromicroscopy study of mineral-organic matter associations in pasture soil clay fractions.

PubMed

Chen, Chunmei; Dynes, James J; Wang, Jian; Karunakaran, Chithra; Sparks, Donald L

2014-06-17

There is a growing acceptance that associations with soil minerals may be the most important overarching stabilization mechanism for soil organic matter. However, direct investigation of organo-mineral associations has been hampered by a lack of methods that can simultaneously characterize organic matter (OM) and soil minerals. In this study, STXM-NEXAFS spectroscopy at the C 1s, Ca 2p, Fe 2p, Al 1s, and Si 1s edges was used to investigate C associations with Ca, Fe, Al, and Si species in soil clay fractions from an upland pasture hillslope. Bulk techniques including C and N NEXAFS, Fe K-edge EXAFS spectroscopy, and XRD were applied to provide additional information. Results demonstrated that C was associated with Ca, Fe, Al, and Si with no separate phase in soil clay particles. In soil clay particles, the pervasive C forms were aromatic C, carboxyl C, and polysaccharides with the relative abundance of carboxyl C and polysaccharides varying spatially at the submicrometer scale. Only limited regions in the soil clay particles had aliphatic C. Good C-Ca spatial correlations were found for soil clay particles with no CaCO3, suggesting a strong role of Ca in organo-mineral assemblage formation. Fe EXAFS showed that about 50% of the total Fe in soils was contained in Fe oxides, whereas Fe-bearing aluminosilicates (vermiculite and Illite) accounted for another 50%. Fe oxides in the soil were mainly crystalline goethite and hematite, with lesser amounts of poorly crystalline ferrihydrite. XRD revealed that soil clay aluminosilicates were hydroxy-interlayered vermiculite, Illite, and kaolinite. C showed similar correlation with Fe to Al and Si, implying a similar association of Fe oxides and aluminosilicates with organic matter in organo-mineral associations. These direct microscopic determinations can help improve understanding of organo-mineral interactions in soils.

Formation of stable nanocomposite clays from small peptides reacted with montmorillonite and illite-smectite mixed layer clays

NASA Astrophysics Data System (ADS)

Block, K. A.; Katz, A.; LeBlanc, J.; Peña, S.; Gottlieb, P.

2015-12-01

Understanding how organic compounds interact with clay minerals and which functional groups result in the strongest bonds is pivotal to achieving a better understanding of how mineral composition affects the residence time of carbon and nitrogen in soils. In this work, we describe how small peptides derived from tryptone casein digest are dissolved and suspended with clay minerals to examine the nature of OM adsorption to mineral surfaces and the resulting effect on clay mineral structure. XRD analyses indicate that peptides intercalation results in expansion of the d001 spacing of montmorillonite (Mt) and the smectite component of a 70-30 illite-smectite mixed layer clay (I-S) and poorer crystallinity overall as a result of exfoliation of tactoids. Peptide adsorption is concentration-dependent, however, surface adsorption appears to mediate interlayer adsorption in Mt reaching a maximum of 16% of the mass of the organoclay complex, indicating that at a critical concentration, peptide intercalation will supersede surface adsorption resulting in a more stable attachment. In I-S the degree of surface adsorption and intercalation is proportional to concentration, however, surface adsorption is not a priming mechanism for interlayer adsorption. Thermogravimetric analysis of the organoclay complexes determined by TGA coupled to GC-MS indicate that the most prominent product species measured was 1-(1-Trimethylsiloxyethenyl)-3-trimethylsiloxy-benzene, likely from tryptophan monomer decomposition. The compound was detected over a broad temperature range, greater than 300 oC, during pyrolysis and suggests a carbon-silicon covalent bond formed between the peptide and tetrahedral layers in the clay. An additional silicon-bearing VOC detected at lower pyrolysis temperature by GC was N,N-Diethyl-1-(trimethylsilyl)-9,10-didehydroergoline-8-carboxamide, likely derived from a lysine-bearing peptide derivative. We hypothesize that hydrophobic (non-ionic) peptides react with silanol at the clay platelet edges to induce exfoliation and subsequent formation of stable nanocomposite clays.

Scaling Effects of Cr(VI) Reduction Kinetics. The Role of Geochemical Heterogeneity

DOE Office of Scientific and Technical Information (OSTI.GOV)

Wang, Li; Li, Li

2015-10-22

The natural subsurface is highly heterogeneous with minerals distributed in different spatial patterns. Fundamental understanding of how mineral spatial distribution patterns regulate sorption process is important for predicting the transport and fate of chemicals. Existing studies about the sorption was carried out in well-mixed batch reactors or uniformly packed columns, with few data available on the effects of spatial heterogeneities. As a result, there is a lack of data and understanding on how spatial heterogeneities control sorption processes. In this project, we aim to understand and develop modeling capabilities to predict the sorption of Cr(VI), an omnipresent contaminant in naturalmore » systems due to its natural occurrence and industrial utilization. We systematically examine the role of spatial patterns of illite, a common clay, in determining the extent of transport limitation and scaling effects associated with Cr(VI) sorption capacity and kinetics using column experiments and reactive transport modeling. Our results showed that the sorbed mass and rates can differ by an order of magnitude due to of the illite spatial heterogeneities and transport limitation. With constraints from data, we also developed the capabilities of modeling Cr(VI) in heterogeneous media. The developed model is then utilized to understand the general principles that govern the relationship between sorption and connectivity, a key measure of the spatial pattern characteristics. This correlation can be used to estimate Cr(VI) sorption characteristics in heterogeneous porous media. Insights gained here bridge gaps between laboratory and field application in hydrogeology and geochemical field, and advance predictive understanding of reactive transport processes in the natural heterogeneous subsurface. We believe that these findings will be of interest to a large number of environmental geochemists and engineers, hydrogeologists, and those interested in contaminant fate and transport, water quality and water composition, and natural attenuation processes in natural systems.« less

Characterization of Heat-treated Clay Minerals in the Context of Nuclear Waste Disposal

NASA Astrophysics Data System (ADS)

Matteo, E. N.; Wang, Y.; Kruichak, J. N.; Mills, M. M.

2015-12-01

Clay minerals are likely candidates to aid in nuclear waste isolation due to their low permeability, favorable swelling properties, and high cation sorption capacities. Establishing the thermal limit for clay minerals in a nuclear waste repository is a potentially important component of repository design, as flexibility of the heat load within the repository can have a major impact on the selection of repository design. For example, the thermal limit plays a critical role in the time that waste packages would need to cool before being transferred to the repository. Understanding the chemical and physical changes, if any, that occur in clay minerals at various temperatures above the current thermal limit (of 100 °C) can enable decision-makers with information critical to evaluating the potential trade-offs of increasing the thermal limit within the repository. Most critical is gaining understanding of how varying thermal conditions in the repository will impact radionuclide sorption and transport in clay materials either as engineered barriers or as disposal media. A variety of repository-relevant clay minerals (illite, mixed layer illite/smectite, and montmorillonite), were heated for a range of temperatures between 100-1000 °C. These samples were characterized to determine surface area, mineralogical alteration, and cation exchange capacity (CEC). Our results show that for conditions up to 500 °C, no significant change occurs, so long as the clay mineral remains mineralogically intact. At temperatures above 500 °C, transformation of the layered silicates into silica phases leads to alteration that impacts important clay characteristics. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's Nation Nuclear Security Administration under contract DE-AC04-94AL85000. SAND Number: SAND2015-6524 A

A non-invasive spectroscopic study to evaluate both technological features and conservation state of two types of ancient Roman coloured bricks.

PubMed

Scatigno, C; Prieto-Taboada, N; Preite Martinez, M; Conte, A M; Madariaga, J M

2018-06-07

The study of both original and decaying compounds is relevant in understanding the chemistry behind the deterioration processes, above all in open museum contexts where environmental stressors affect the artefacts. In this sense, a combination of non-invasive spectroscopy techniques (Raman spectroscopy, μ-X-ray fluorescence and X-ray diffraction) was applied on an ancient Roman building (130 CE), the "Casa di Diana" Mithraeum at Ostia Antica archaeological site. The aim is to study the raw materials, manufacturing and decaying products of the two observed types of Roman fired bricks (red and yellow) that compose the building. The present study estimates an illite raw material of carbonate-bearing marine clay likely referring to the common deposits of central/southern Italy, which contain calcite as accessory phase and a-plastic fraction constituted by quartz, feldspar and opaques. This clay material was added with volcanic temper characterised by abundant clinopyroxene and analcime (from analcimization of leucite) that are typical of the Roman Province volcanism. The firing would be probably the result of oxidizing conditions, as proved by the hematite presence. Thanks to the existence of specific neoformed mineral phases during firing it was possible to assess different temperatures ranges. In detail, the red/orange bricks, for the existence of gehlenite (formed from calcite and its reaction with silicates), were fired at 800-900 °C range; whereas, the yellow ones are characterised by the lack of gehlenite and the disappearance of illite/muscovite, which indicates firing temperature at over 900 °C. Regarding the decaying products, the gypsum covers most of the surface of most bricks, both red and the yellow ones, but these latter are more susceptible to environmental stressors (sulphates and carbonates). Therefore, this work points out how by integrated non-invasive approaches it is possible trace back to original firing temperature, technology of manufacture, interpreting ceramic data. Copyright © 2018 Elsevier B.V. All rights reserved.

Characterization and origin of spongillite-hosting sediment from João Pinheiro, Minas Gerais, Brazil

NASA Astrophysics Data System (ADS)

Almeida, A. C. S.; Varajão, A. F. D. C.; Gomes, N. S.; Varajão, C. A. C.; Volkmer-Ribeiro, C.

2010-03-01

Spongillite from João Pinheiro, Minas Gerais, Brazil is mainly known for its use in brick production and in the refractory industry. Very few studies have focused on its geological context. Spongillite-rich deposits occur in shallow ponds on a karstic planation surface developed on rocks of the Neoproterozoic São Francisco Supergroup. Cenozoic siliciclastic sediments are related to this surface. A field study of these deposits and analysis of multispectral images showed a SE-NW preferential drainage system at SE, suggesting that Mesozoic Areado Group sandstones were the source area of the spongillite-hosting sediments. Mineralogical and textural characterization by optical microscopic analysis, X-ray diffraction (XRD), differential and gravimetric thermal analysis (DTA-GTA), infrared spectroscopy (IR) and scanning electron microscopy (SEM) of seven open-pit spongillite-rich deposits (Avião, Carvoeiro, Vânio, Preguiça, Divisa, Severino, Feijão) showed a sedimentological similarity between the deposits. They are lens-shaped and are characterized at the bottom by sand facies, in the middle by spicules-rich muddy-sand facies and at the top by organic matter-rich muddy-sand facies. Petrographically, the spongillite-hosting sediments and the siliclastic sediments of the Areado Group show detrital phases with similar mineralogical and textural features, such as the presence of well-sorted quartz grains and surface features of abrasion typical of aeolian reworking that occurred in the depositional environment in which the sandstones of the Areado Group were formed. Detrital heavy minerals, such as staurolite, zircon, tourmaline, and clay minerals, such as kaolinite, low amounts of illite, scarce chlorite and mixed-layer chlorite/smectite and illite/smectite occur in the spongillite-hosting sediments and in sandstones from the Areado Group. In both formations, staurolite has similar chemical composition. These mineralogical and textural features show that the sediments of the Areado Group constitute the main source of the pond sediments that host spongillite.

Nitrogen Concentrations and Isotopic Compositions of Seafloor-Altered Terrestrial Basaltic Glass: Implications for Astrobiology

PubMed Central

Banerjee, N.R.; Izawa, M.R.M.; Kobayashi, K.; Lazzeri, K.; Ranieri, L.A.; Nakamura, E.

2018-01-01

Abstract Observed enrichments of N (and the δ15N of this N) in volcanic glasses altered on Earth's modern and ancient seafloor are relevant in considerations of modern global N subduction fluxes and ancient life on Earth, and similarly altered glasses on Mars and other extraterrestrial bodies could serve as valuable tracers of biogeochemical processes. Palagonitized glasses and whole-rock samples of volcanic rocks on the modern seafloor (ODP Site 1256D) contain 3–18 ppm N with δ15Nair values of up to +4.5‰. Variably altered glasses from Mesozoic ophiolites (Troodos, Cyprus; Stonyford volcanics, USA) contain 2–53 ppm N with δ15N of −6.3 to +7‰. All of the more altered glasses have N concentrations higher than those of fresh volcanic glass (for MORB, <2 ppm N), reflecting significant N enrichment, and most of the altered glasses have δ15N considerably higher than that of their unaltered glass equivalents (for MORB, −5 ± 2‰). Circulation of hydrothermal fluids, in part induced by nearby spreading-center magmatism, could have leached NH4+ from sediments then fixed this NH4+ in altering volcanic glasses. Glasses from each site contain possible textural evidence for microbial activity in the form of microtubules, but any role of microbes in producing the N enrichments and elevated δ15N remains uncertain. Petrographic analysis, and imaging and chemical analyses by scanning electron microscopy and scanning transmission electron microscopy, indicate the presence of phyllosilicates (smectite, illite) in both the palagonitized cracks and the microtubules. These phyllosilicates (particularly illite), and possibly also zeolites, are the likely hosts for N in these glasses. Key Words: Nitrogen—Nitrogen isotope—Palagonite—Volcanic glass—Mars. Astrobiology 18, 330–342. PMID:29106312

Weathering of the New Albany Shale, Kentucky, USA: I. Weathering zones defined by mineralogy and major-element composition

USGS Publications Warehouse

Tuttle, M.L.W.; Breit, G.N.

2009-01-01

Comprehensive understanding of chemical and mineralogical changes induced by weathering is valuable information when considering the supply of nutrients and toxic elements from rocks. Here minerals that release and fix major elements during progressive weathering of a bed of Devonian New Albany Shale in eastern Kentucky are documented. Samples were collected from unweathered core (parent shale) and across an outcrop excavated into a hillside 40 year prior to sampling. Quantitative X-ray diffraction mineralogical data record progressive shale alteration across the outcrop. Mineral compositional changes reflect subtle alteration processes such as incongruent dissolution and cation exchange. Altered primary minerals include K-feldspars, plagioclase, calcite, pyrite, and chlorite. Secondary minerals include jarosite, gypsum, goethite, amorphous Fe(III) oxides and Fe(II)-Al sulfate salt (efflorescence). The mineralogy in weathered shale defines four weathered intervals on the outcrop-Zones A-C and soil. Alteration of the weakly weathered shale (Zone A) is attributed to the 40-a exposure of the shale. In this zone, pyrite oxidization produces acid that dissolves calcite and attacks chlorite, forming gypsum, jarosite, and minor efflorescent salt. The pre-excavation, active weathering front (Zone B) is where complete pyrite oxidation and alteration of feldspar and organic matter result in increased permeability. Acidic weathering solutions seep through the permeable shale and evaporate on the surface forming abundant efflorescent salt, jarosite and minor goethite. Intensely weathered shale (Zone C) is depleted in feldspars, chlorite, gypsum, jarosite and efflorescent salts, but has retained much of its primary quartz, illite and illite-smectite. Goethite and amorphous FE(III) oxides increase due to hydrolysis of jarosite. Enhanced permeability in this zone is due to a 14% loss of the original mass in parent shale. Denudation rates suggest that characteristics of Zone C were acquired over 1 Ma. Compositional differences between soil and Zone C are largely attributed to illuvial processes, formation of additional Fe(III) oxides and incorporation of modern organic matter.

Architecture and reservoir quality of low-permeable Eocene lacustrine turbidite sandstone from the Dongying Depression, East China

NASA Astrophysics Data System (ADS)

Munawar, Muhammad Jawad; Lin, Chengyan; Chunmei, Dong; Zhang, Xianguo; Zhao, Haiyan; Xiao, Shuming; Azeem, Tahir; Zahid, Muhammad Aleem; Ma, Cunfei

2018-05-01

The architecture and quality of lacustrine turbidites that act as petroleum reservoirs are less well documented. Reservoir architecture and multiscale heterogeneity in turbidites represent serious challenges to production performance. Additionally, establishing a hierarchy profile to delineate heterogeneity is a challenging task in lacustrine turbidite deposits. Here, we report on the turbidites in the middle third member of the Eocene Shahejie Formation (Es3), which was deposited during extensive Middle to Late Eocene rifting in the Dongying Depression. Seismic records, wireline log responses, and core observations were integrated to describe the reservoir heterogeneity by delineating the architectural elements, sequence stratigraphic framework and lithofacies assemblage. A petrographic approach was adopted to constrain microscopic heterogeneity using an optical microscope, routine core analyses and X-ray diffraction (XRD) analyses. The Es3m member is interpreted as a sequence set composed of four composite sequences: CS1, CS2, CS3 and CS4. A total of forty-five sequences were identified within these four composite sequences. Sand bodies were mainly deposited as channels, levees, overbank splays, lobes and lobe fringes. The combination of fining-upward and coarsening-upward lithofacies patterns in the architectural elements produces highly complex composite flow units. Microscopic heterogeneity is produced by diagenetic alteration processes (i.e., feldspar dissolution, authigenic clay formation and quartz cementation). The widespread kaolinization of feldspar and mobilization of materials enhanced the quality of the reservoir by producing secondary enlarged pores. In contrast, the formation of pore-filling authigenic illite and illite/smectite clays reduced its permeability. Recovery rates are higher in the axial areas and smaller in the marginal areas of architectural elements. This study represents a significant insight into the reservoir architecture and heterogeneity of lacustrine turbidites, and the understanding of compartmentalization and distribution of high-quality sand reservoirs can be applied to improve primary and secondary production in these fields.

Improvement of nitrogen utilization and soil properties by addition of a mineral soil conditioner: mechanism and performance.

PubMed

Yan, Xiaodan; Shi, Lin; Cai, Rumeng

2018-01-01

A mineral soil conditioner (MSC) composed of activated potash feldspar, gypsum, and calcium carbonate and containing an amount of available mineral nutrients, is shown to be effective for plant growth and acidic soil amelioration. In this study, a field test was conducted over four rice seasons by examining treatment with control check (CK), MSC, biological active carbon, and lime to investigate the nitrogen-use efficiency and mechanism of soil characteristic variations due to the desilicification and allitization of soil as well as the unrestrained use of nitrogen (N) fertilizer in recent years. Influences of MSC on the xylem sap intensity and mean rice yields were evaluated, and the soil type was also analyzed using the FactSage 6.1 Reaction, phase diagram, and Equilib modules. The results of the field trial showed that MSC application increased the xylem sap intensity and nitrogen export intensity by 37.33-39.85% and 31.40-51.20%, respectively. A significant increase (5.63-15.48%) in mean grain yields was achieved with MSC application over that with biological active carbon and lime application. The effects of MSC had a tendency to increase with time in the field experiment results, and grain yields increased after the initial application. The new formation of clay minerals exhibits a significant influence on [Formula: see text] fixation, especially for 2:1 phyllosilicates with illite, owing to the interlayers of the clay minerals. Our preliminary results showed that kaolinite, the main 1:1 phyllosilicate clay mineral in ferralsol, transformed to illite at room temperature as a consequence of the presence of H 4 SiO 4 and available K + supplied by MSC. This indicated that improving the soil quality combined with reducing N losses from soils is an efficient way to control non-point source pollution from agriculture without the risk of decreased in grain yield.

Water uptake of clay and desert dust aerosol particles at sub- and supersaturated water vapor conditions.

PubMed

Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona; Gysel, Martin; Weingartner, Ernest; Lohmann, Ulrike; Baltensperger, Urs; Cziczo, Daniel J

2009-09-28

Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of atmospheric interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation (SS) with respect to liquid water. In this study the subsaturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols were determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as well as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were investigated. Aerosols were generated both with a wet and a dry disperser. The water uptake was parameterized via the hygroscopicity parameter kappa. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived kappa values between 0.00 and 0.02 (the latter corresponds to a particle consisting of 96.7% by volume insoluble material and approximately 3.3% ammonium sulfate). Pure clay aerosols were generally found to be less hygroscopic than natural desert dust particles. The illite and montmorillonite samples had kappa approximately 0.003. The kaolinite samples were less hygroscopic and had kappa=0.001. SD (kappa=0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (kappa=0.007) and ATD (kappa=0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles. Thus, the generation method is critically important when presenting such data. These results indicate any atmospheric processing of a fresh mineral dust particle which leads to the addition of more than approximately 3% soluble material will significantly enhance its hygroscopicity and CCN activity.

Cover sequences at the northern margin of the Antongil Craton, NE Madagascar

USGS Publications Warehouse

Bauer, W.; Walsh, G.J.; De Waele, B.; Thomas, Ronald J.; Horstwood, M.S.A.; Bracciali, L.; Schofield, D.I.; Wollenberg, U.; Lidke, D.J.; Rasaona, I.T.; Rabarimanana, M.H.

2011-01-01

The island of Madagascar is a collage of Precambrian, generally high-grade metamorphic basement domains, that are locally overlain by unmetamorphosed sedimentary rocks and poorly understood low-grade metasediments. In the Antalaha area of NE Madagascar, two distinct cover sequences rest on high-grade metamorphic and igneous basement rocks of the Archaean Antongil craton and the Neoproterozoic Bemarivo belt. The older of these two cover sequences, the Andrarona Group, consists of low-grade metasedimentary rocks. The younger sequence, the newly defined Ampohafana Formation, consists of unmetamorphosed sedimentary rocks. The Andrarona Group rests on Neoarchaean granites and monzogranites of the Antongil craton and consists of a basal metagreywacke, thick quartzites and an upper sequence of sericite-chlorite meta-mudstones, meta-sandstones and a volcaniclastic meta-sandstone. The depositional age of the volcaniclastic meta-sandstone is constrained in age by U–Pb laser-ablation ICP-MS analyses of euhedral zircons to 1875 ± 8 Ma (2σ). Detrital zircons of Archaean and Palaeoproterozoic age represent an input from the Antongil craton and a newly defined Palaeoproterozoic igneous unit, the Masindray tonalite, which underlies the Andrarona Group, and yielded a U–Pb zircon age of 2355 ± 11 Ma (2σ), thus constraining the maximum age of deposition of the basal part of the Andrarona Group. The Andrarona Group shows a low-grade metamorphic overprint in the area near Antalaha; illite crystallinity values scatter around 0.17°Δ2Θ CuKα, which is within the epizone. The Ampohafana Formation consists of undeformed, polymict conglomerate, cross-bedded sandstone, and red mudstone. An illite crystallinity value of >0.25°Δ2Θ CuKα obtained from the rocks is typical of the diagenetic zone. Occurrences of rhyodacite pebbles in the Ampohafana Formation and the intrusion of a basaltic dyke suggest a deposition in a WSW-ENE-trending graben system during the opening of the Indian Ocean in the Upper Cretaceous, that was characterized by extensive rhyolitic to basaltic magmatism along Madagascar's eastern coast.

Pedogenesis of a catena of the Farmdale-Sangamon Geosol complex in the north central United States

USGS Publications Warehouse

Jacobs, P.M.; Konen, M.E.; Curry, B. Brandon

2009-01-01

The Farmdale-Sangamon Geosol pedocomplex consists of the Sangamon Geosol and the overlying Farmdale Geosol, which form the most extensive terrestrial record of the last interglacial to glacial transition in the Midwest United States. The geosol complex formed for upwards of 100??ka, extending from the end of MIS 6 through 4 for the Sangamon Geosol, then the Farmdale Geosol for during a brief episode at the end of MIS 3 following slow accumulation and pedogenic modification of eolian silt deposited on top of the Sangamon Geosol. Our study site consists of a buried paleo-hillslope transect that forms a catena, enabling evaluation of slope effects on interglacial-scale soil formation. The Sangamon Geosol is formed in calcareous and illitic glaciogenic sediment. Along the catena the Sangamon Geosol profiles display some morphological changes, namely in terms of colors that we interpret as indicators of differences in drainage. Most thickness and horizonation characteristics are similar all along the transect, with intact upper sola horizons (AE and E horizons) that overlie clay-enriched Bt horizons. The Bt horizons contain abundant clay that exists as illuvial clay coatings, matrix infills, and as mosaic-speckled domains. The clay originated both by in situ weathering and through illuviation from the clay depleted upper sola. Slope does not appear to affect Bt characteristics beyond redder hues of the matrix and clay coatings in the upper slope position. With depth, effects of carbonate leaching and infilling of clay in the matrix decrease and clay coatings are restricted to walls of voids adjacent to aggregates. Clay mineralogy shows illite depletion, but no interstratified kaolinite-expandable minerals, indicating the degree of weathering is not as great as is typical of Sangamon Geosol profiles formed in loess or in glaciogenic sediment of the central Illinois type area. Clay mineralogy is also stratified with depth, coincident with particle size, which probably indicates sorting of layers of illitic dolomite and shale. Variation of horizon and profile characteristics appears to largely be a function of particle size variability and stratification than topographic position in the catena. The influence of hillslope position on soil redistribution during formation of the Sangamon Geosol appears negligible given the uniformity of upper solum horizon thickness and sandy particle size characteristics, so we conclude that a bioturbation and rainwash origin of the upper solum and the texture contrast in these profiles is not the best process model explanation. We suggest that the base-rich nature of these soils led to ecosystem characteristics that discouraged erosion and encouraged infiltration and a lessivage-type origin of the texture contrast. No convincing evidence of MIS 6 through MIS 4 loess occurs at this site. The Farmdale Geosol formed in the Robein Silt, which is Roxana Silt (MIS 3 loess) that was redistributed downslope. The Robein Silt is thicker and finer in the topographic low and indicates the cooler and forested environmental conditions during MIS 3 were conducive to downslope movement of soil and also produced greater differences in drainage-induced soil morphological changes in the Farmdale Geosol. ?? 2009 Elsevier B.V. All rights reserved.

Re-evaluation of the petrogenesis of the Proterozoic Jabiluka unconformity-related uranium deposit, Northern Territory, Australia

NASA Astrophysics Data System (ADS)

Polito, Paul A.; Kurt Kyser, T.; Thomas, David; Marlatt, Jim; Drever, Garth

2005-11-01

The world class Jabiluka unconformity-related uranium deposit in the Alligator Rivers Uranium Field, Australia, contains >163,000 tons of contained U3O8. Mineralization is hosted by shallow-to-steeply dipping basement rocks comprising graphitic units of chlorite-biotite-muscovite schist. These rocks are overlain by flat-lying coarse-grained sandstones belonging to the Kombolgie Subgroup. The deposit was discovered in 1971, but has never been mined. The construction of an 1,150 m decline into the upper eastern sector of the Jabiluka II deposit combined with closely spaced underground drilling in 1998 and 1999 allowed mapping and sampling from underground for the first time. Structural mapping, drill core logging and petrographic studies on polished thin sections established a detailed paragenesis that provided the framework for subsequent electron microprobe and X-ray diffraction, fluid inclusion, and O-H, U-Pb and 40Ar/39Ar isotope analysis. Uranium mineralization is structurally controlled within semi-brittle shears that are sub-conformable to the basement stratigraphy, and breccias that are developed within the hinge zone of fault-related folds adjacent to the shears. Uraninite is intimately associated with chlorite, sericite, hematite ± quartz. Electron microprobe and X-ray diffraction analysis of syn-ore illite and chlorite indicates a mineralization temperature of 200°C. Pre- and syn-ore minerals extracted from the Kombolgie Subgroup overlying the deposit and syn-ore alteration minerals in the Cahill Formation have δ18Ofluid and δ D fluid values of 4.0±3.7 and -27±17‰, respectively. These values are indistinguishable from illite separates extracted from diagenetic aquifers in the Kombolgie Subgroup up to 70 km to the south and east of the deposit and believed to be the source of the uraniferous fluid. New fluid inclusion microthermometry data reveal that the mineralising brine was saline, but not saturated. U-Pb and 207Pb/206Pb ratios of uraninite by laser-ablation ICP-MS suggest that massive uraninite first precipitated at ca. 1,680 Ma, which is coincident with the timing of brine migration out from the Kombolgie Subgroup as indicated by 40Ar/39Ar ages of 1,683±11 Ma from sandstone-hosted illite. Unmineralized breccias cemeted by chlorite, quartz and sericite cross-cut the mineralized breccias and are in turn cut by straight-sided, high-angle veins of drusy quartz, sulphide and dolomite. U-Pb and 207Pb/206Pb ratios combined with fluid inclusion and stable isotope data indicate that these post-ore minerals formed when mixing between two fluids occurred sometime between ca. 1,450 and 550 Ma. Distinct 207Pb/206Pb age populations occur at ca. 1,302±37, 1,191±27 and 802±57 Ma, which respectively correlate with the intrusion of the Maningkorrirr/Mudginberri phonolitic dykes and the Derim Derim Dolerite between 1,370 and 1,316 Ma, the amalgamation of Australia and Laurentia during the Grenville Orogen at ca. 1,140 Ma, and the break-up of Rodinia between 1,000 and 750 Ma.

Does velocity-strengthening to velocity-weakening transition really determine the updip limit of the seismogenic zone in subduction megathrusts?

NASA Astrophysics Data System (ADS)

Shimamoto, T.

2009-12-01

Understanding the mechanisms of thrust-type earthquakes in subduction zones is the primary target of seismogenic-zone drilling project in Nankai Trough. Drilling into the upper part of the seismogenic zone is attempted, so that understanding the processes controlling the updip limit of the seismogenic zone is becoming a more specific target. A commonly accepted notion is that the onset of seismic behavior is due to a change in velocity strengthening to velocity weakening property of fault zone (see Saffer & Marone, 2003, EPSL ). Smectite-illite transformation had been a fashionable hypothesis for such a transition because the transformation is likely to occur near the updip limit of the seismogenic zone. However, Saffer & Marone recognized velocity-strengthening behavior of illite gouge questioning the smectite-illite transformation as the primary cause for the updip limit of seismic zone. They explored other possibilities that might cause a change in the velocity dependency of friction. I want to address the problem from a different angle. Progress in high-velocity friction in the last 15 years has demonstrated that nearly all faults exhibit dramatic weakening at high slip rates and large displacements. The weakening is indeed greater than the changes in friction at slow slip rates by more than one order of magnitude, and the slip- and velocity-weakening of faults at high velocities is likely to control the dynamic fault motion during large earthquakes. Thus by combining abundant work on rate-and-state dependent friction at slow slip rates and recent high-velocity friction studies, a possibility emerges in that the rate-and-state friction at slow slip rates controls the earthquake nucleation, whereas intermediate to high-velocity friction dictates the growth processes into a large earthquake. Taiwan Chi-Chi earthquake in 1999 is very interesting in this regard because Tanikawa & Shimamoto (2008, JGR ) recognized velocity-strengthening properties for gouge from the northern part of the Chelungpu fault (velocity weakening for gouge from the south). The northern part of the fault should be aseismic according to a traditional view for earthquakes in velocity-weakening regime, whereas the northern part displaced much more at higher slip rates with lower frequencies than in southern part. Permeability of fault gouge is lower in the north than in the south by one to two orders of magnitude, so that high-velocity weakening is more pronounced in the north due to more effective thermal pressurization than in the south. Thus Tanikawa & Shimamoto proposed a scenario that the Chi-Chi earthquake started from the southern part of Chelungpu fault with velocity-weakening property and that the earthquake rupture grew more in the north due to high-velocity weakening. Noda & Lapusta (2009, JPGU meeting ) demonstrated by dynamic modeling that such a scenario is indeed possible. I propose that such a scenario is applicable to shallow subduction zone where earthquake rupture comes from deeper parts. This change in view will change the scope of laboratory work, modeling, and even ways of looking at faults in accretionary prism such as Shimanto belt. Those problems will be elaborated in my presentation.

Alteration, adsorption and nucleation processes on clay-water interfaces: Mechanisms for the retention of uranium by altered clay surfaces on the nanometer scale

NASA Astrophysics Data System (ADS)

Schindler, Michael; Legrand, Christine A.; Hochella, Michael F.

2015-03-01

Nano-scale processes on the solid-water interface of clay minerals control the mobility of metals in the environment. These processes can occur in confined pore spaces of clay buffers and barriers as well as in contaminated sediments and involve a combination of alteration, adsorption and nucleation processes of multiple species and phases. This study characterizes nano-scale processes on the interface between clay minerals and uranyl-bearing solution near neutral pH. Samples of clay minerals with a contact pH of ∼6.7 are collected from a U mill and mine tailings at Key Lake, Saskatchewan, Canada. The tailings material contains Cu-, As-, Co-, Mo-, Ni-, Se-bearing polymetallic phases and has been deposited with a surplus of Ca(OH)2 and Na2CO3 slaked lime. Small volumes of mill-process solutions containing sulfuric acid and U are occasionally discharged onto the surface of the tailings and are neutralized after discharge by reactions with the slaked lime. Transmission electron microscopy (TEM) in combination with the focused ion beam (FIB) technique and other analytical methods (SEM, XRD, XRF and ICP-OES) are used to characterize the chemical and mineralogical composition of phases within confined pore spaces of the clay minerals montmorillonite and kaolinite and in the surrounding tailings material. Alteration zones around the clay minerals are characterized by different generations of secondary silicates containing variable proportions of adsorbed uranyl- and arsenate-species and by the intergrowth of the silicates with the uranyl-minerals cuprosklodowskite, Cu[(UO2)2(SiO3OH)2](H2O)6 and metazeunerite, Cu[(UO2)(AsO4)2](H2O)8. The majority of alteration phases such as illite, illite-smectite, kaolinite and vermiculite have been most likely formed in the sedimentary basin of the U-ore deposit and contain low amounts of Fe (<5 at.%). Iron-enriched Al-silicates or illite-smectites (Fe >10 at.%) formed most likely in the limed tailings at high contact pH (∼10.5) and their structure is characterized by a low degree of long-range order. Adsorption of U and nucleation of metazeunerite and cuprosklodowskite are strongly controlled by the presence of the adsorbed oxy-anion species arsenate and silica on the Fe-enriched silicates. Heterogeneous nucleation of nano-crystals of the uranyl minerals occurs most likely on adsorption sites of binary uranyl-, arsenate- and silica-complexes as well as on ternary uranyl-arsenate or uranyl-silicate complexes. The uranyl minerals occur as aggregates of misoriented nano-size crystals and are the result of supersaturated solutions and a high number of nucleation sites that prevented the formation of larger crystals through Oswald ripening. The results of this study provide an understanding of interfacial nano-scale processes between uranyl species and altered clay buffers in a potential Nuclear Waste repository as similar alteration conditions of clays may occur in a multi-barrier system.

ROLE OF PRESSURE IN SMECTITE DEHYDRATION - EFFECTS ON GEOPRESSURE AND SMECTITE-TO-ILLITE TRANSFORMATION.

USGS Publications Warehouse

Colten-Bradley, Virginia

1987-01-01

Evaluation of the effects of pressure on the temperature of interlayer water loss (dehydration) by smectites under diagenetic conditions indicates that smectites are stable as hydrated phases in the deep subsurface. Hydraulic and differential pressure conditions affect dehydration differently. The temperature of dehydration increase with pore fluid pressure and interlayer water density. The temperatures of dehydration increase with pore fluid pressure and interlayer water density. The temperatures of dehydration under differential-presssure conditions are inversely related to pressure and interlayer water density. The model presented assumes the effects of pore fluid composition and 2:1 layer reactivity to be negligible. Agreement between theoretical and experimental results validate this assumption. Additional aspects of the subject are discussed.

Stable isotopic evidence for fluid flow and fluid/rock interaction during thrust faulting in Pumpkin Valley shale and Rome Formation, east Tennessee

DOE Office of Scientific and Technical Information (OSTI.GOV)

Butler, B.K.; Haase, C.S.

1989-08-01

The Pumpkin Valley Shale and the underlying Rome Formation form the lower portions of the Copper Creek and White Oak Mountain thrust sheets in east Tennessee. The Pumpkin Valley Shale consists of shale and mudstone with subordinate amounts of interbedded siltstone. The Rome Formation is composed predominantly of sandstone with interbedded shale and siltstone toward the base of the formation. The percentage of illite increases from 20% to over 80% of the bulk clay mineralogy toward the base of the section. Porosity is occluded by quartz, phyllosilicate, and calcite cements. Both formations contain calcite-filled and, less commonly, quartz-filled Alleghenian fracturesmore » and joints.« less

Mineralogical, crystallographic and morphological characteristics of natural kaolins from the Ivory Coast (West Africa)

NASA Astrophysics Data System (ADS)

Sei, J.; Morato, F.; Kra, G.; Staunton, S.; Quiquampoix, H.; Jumas, J. C.; Olivier-Fourcade, J.

2006-10-01

Thirteen clay samples from four deposits in the Ivory Coast (West Africa) were studied using X-ray diffraction, thermogravimetric analysis and chemical analysis. Mineralogical, crystallographic and morphological characteristics of these samples are given. Kaolinite is the principal mineral but other minerals are present in small quantities: illite, quartz, anatase and iron oxides (oxides and oxyhydroxides). The crystallographic, morphological and surface characteristics are influenced by the presence of these impurities. In particular, the presence of iron oxides was associated with reduced structural ordering and thermal stability of kaolinite and increased specific surface area. These clays could be used in the ceramics industry to make tiles and bricks, and also in agronomy as supports for chemical fertilizers or for environmental protection by immobilising potentially toxic waste products.

A method for the concentration of fine-grained rutile (TiO2) from sediment and sedimentary rocks by chemical leaching

USGS Publications Warehouse

Commeau, Judith A.; Valentine, Page C.

1991-01-01

Most of the sample analyzed by the method described were marine muds collected from the Gulf of Maine (Valentine and Commeau, 1990). The silt and clay fraction (up to 99 wt% of the sediment) is composed of clay minerals (chiefly illite-mica and chlorite), silt-size quartz and feldspar, and small crystals (2-12 um) of rutile and hematite. The bulk sediment samples contained an average of 2 to 3 wt percent CaCO3. Tiher samples analyzed include red and gray Carboniferous and Triassic sandstones and siltstones exposed around the Bay of Fundy region and Paleozoic sandstones, siltstones, and shales from northern Maine and New Brunswick. These rocks are probable sources for the fine-grained rutile found in the Gulf of Maine.

Geotechnical properties of sediments from North Pacific and Northern Bermuda Rise

DOE Office of Scientific and Technical Information (OSTI.GOV)

Silva, A J; Laine, E P; Lipkin, J

1980-01-01

Studies of geotechnical properties for the Sub-seabed Disposal Program have been oriented toward sediment characterization related to effectiveness as a containment media and determination of detailed engineering behavior. Consolidation tests of the deeper samples in the North Pacific clays indicate that the sediment column is normally consolidated. The in-situ coefficient of permeability (k) within the cored depth of 25 meters is relatively constant at 10/sup -7/ cm/sec. Consolidated undrained (CIU) triaxial tests indicate stress-strain properties characteristic of saturated clays with effective angles of friction of 35/sup 0/ for smectite and 31/sup 0/ for illite. These results are being used inmore » computer modeling efforts. Some general geotechnical property data from the Bermuda Rise are also discussed.« less

Outcrop analogue study of Permocarboniferous geothermal sandstone reservoir formations (northern Upper Rhine Graben, Germany): impact of mineral content, depositional environment and diagenesis on petrophysical properties

NASA Astrophysics Data System (ADS)

Aretz, Achim; Bär, Kristian; Götz, Annette E.; Sass, Ingo

2016-07-01

The Permocarboniferous siliciclastic formations represent the largest hydrothermal reservoir in the northern Upper Rhine Graben in SW Germany and have so far been investigated in large-scale studies only. The Cenozoic Upper Rhine Graben crosses the Permocarboniferous Saar-Nahe Basin, a Variscan intramontane molasse basin. Due to the subsidence in this graben structure, the top of the up to 2-km-thick Permocarboniferous is located at a depth of 600-2900 m and is overlain by Tertiary and Quaternary sediments. At this depth, the reservoir temperatures exceed 150 °C, which are sufficient for geothermal electricity generation with binary power plants. To further assess the potential of this geothermal reservoir, detailed information on thermophysical and hydraulic properties of the different lithostratigraphical units and their depositional environment is essential. Here, we present an integrated study of outcrop analogues and drill core material. In total, 850 outcrop samples were analyzed, measuring porosity, permeability, thermal conductivity and thermal diffusivity. Furthermore, 62 plugs were taken from drillings that encountered or intersected the Permocarboniferous at depths between 1800 and 2900 m. Petrographic analysis of 155 thin sections of outcrop samples and samples taken from reservoir depth was conducted to quantify the mineral composition, sorting and rounding of grains and the kind of cementation. Its influence on porosity, permeability, the degree of compaction and illitization was quantified. Three parameters influencing the reservoir properties of the Permocarboniferous were detected. The strongest and most destructive influence on reservoir quality is related to late diagenetic processes. An illitic and kaolinitic cementation and impregnation of bitumina document CO2- and CH4-rich acidic pore water conditions, which are interpreted as fluids that migrated along a hydraulic contact from an underlying Carboniferous hydrocarbon source rock. Migrating oil and acidic waters led to the dissolution of haematite cements in the lower Permocarboniferous formations. During the Eocene, subsidence of the Upper Rhine Graben porosities and permeabilities of the sandstones of these formations were strongly reduced to 2.5 % and 3.2 × 10-18 m2. The second important influence on reservoir quality is the distinct depositional environment and its influence on early diagenetic processes. In early stage diagenesis, the best influence on reservoir properties exhibits a haematite cementation. It typically occurs in eolian sandstones of the Kreuznach Formation (Upper Permocarboniferous) and is characterized by grain covering haematite coatings, which are interpreted to inhibit cementation, compaction and illitization of pore space during burial. Eolian sandstones taken from outcrops and reservoir depths exhibit the highest porosities (16.4; 12.3 %) and permeabilities (2.0 × 10-15; 8.4 × 10-16 m2). A third important influence on reservoir quality is the general mineral composition and the quartz content which is the highest in the Kreuznach Formation with 73.8 %. Based on the integrated study of depositional environments and diagenetic processes, reservoir properties of the different Permocarboniferous formations within the northern Upper Rhine Graben and their changes with burial depth can be predicted with satisfactory accuracy. This leads to a better understanding of the reservoir quality and enables an appropriate well design for exploration and exploitation of these geothermal resources.

Decoding recent mud-volcano activity in the westernmost Mediterranean: Evidence from sediment/porewater data and geochemical modeling

NASA Astrophysics Data System (ADS)

López-Rodríguez, Carmina; Martínez-Ruíz, Francisca; Mogollón, José M.; Comas, Menchu; Nieto, Fernando; Böning, Philipp; Pahnke, Katharina; Sapart, Célia; De Lange, Gert J.

2017-04-01

Recent studies have demonstrated the occurrence of active mud volcanism in the West Alboran Basin. Though most of the mud volcanoes (MVs) discovered in this region are dormant, a few structures evidence active hydrocarbon venting, as Carmen MV. This study focuses on sedimentological and geochemical investigations on one piston core, GP05PC, recovered from the summit of Carmen MV during the Gasalb-Pelagia cruise (2011). Although the full core consists of mud breccia sediments, a dramatic change occurs between enhanced methane concentrations in its lowermost and dissolved SO42- in its uppermost sediments. At the boundary of 150 cm, methane is oxidized and sulphate reduced. In the lowermost interval, the depletion of major elements (i.e., Ca2+ and Mg2+), the enrichment of trace species (i.e., Li+ and B) and the radiogenic 87Sr all point to a deep fluid source. The δ18Opw and δDpw compositions of pore water (5.7‰ and -10‰ VSMOW, respectively) together with the mineralogical results (presence of randomly insterstrafied (R0) illite-smectite minerals (I/S) to more illitic (>50% I) and ordered ones (R1-R3)) indicate smectite to illite transformation at greater depth and support smectite dehydration as the main porewater freshening mechanism. Water formation temperatures calculated through the application of empirical geo-thermometers (K-Na, K-Mg and K-Ca) together with the presence from I/S mixed layers (R3) suggest that fluids were generated at temperatures 100-200°C. This temperature indicates that, under a regional geothermal gradient, the fluid source originates from 8 km depth. From an adjacent borehole it is known that sedimentary units of Early to Middle Miocene age occur at that depth (Jurado and Comas et al., 1992). The δ13Cmethane and δDmethane composition of methane (-59‰ VPDB and -184‰ VSMOW, respectively) of the deepest sample also may be associated to a thermogenic origin. The absence of hemipelagic sediment draping, the distinctive seawater-like pore water composition in the uppermost part of the mud breccia together with the abrupt transition to the interval with typical deep-source fluid composition, all point to a very recent mud and associated gas-expulsion. Such outburst leads to the downward intrusion of seawater coincident with the episode of gas-bubble expulsion. A numerical transport-reaction model has been applied to the distinctively kink-shaped pore water Cl, SO42-CH4, and other profiles in core GP05PC, to derive the very recent timing for this eruption event (López-Rodríguez et al., 2017). References: Jurado, M. J. and Comas, M. C. (1992). Well log interpretation and seismic character of the Cenozoic sequence in the Northern Alboran Sea, Geo-Marine Letters, 12, 129-136. López-Rodríguez, C., Martínez-Ruíz, F., Mogollón, J.M., Comas, M. Nieto, F, Böning P.H., Pahnke, K., Sapart, C. and De Lange, G.J. (2017). Evidence for a 2000 AD +/- 3 yr mud/methane discharge event in the westernmost Mediterranean (based on sediment/pore water data and modelling). Manuscript submitted for publication.

The Mid-Cretaceous Frontier Formation near the Moxa Arch, southwestern Wyoming

USGS Publications Warehouse

Mereweather, E.A.; Blackmon, P.D.; Webb, J.C.

1984-01-01

The Frontier Formation in the Green River Basin of Wyoming, Utah, and Colorado, consists of sandstone, siltstone, and shale, and minor conglomerate, coal, and bentonite. These strata were deposited in several marine and nonmarine environments during early Late Cretaceous time. At north-trending outcrops along the eastern edge of the overthrust belt, the Frontier is of Cenomanian, Turonian, and early Coniacian age, and commonly is about 610 m (2,000 ft) thick. The formation in that area conformably overlies the Lower Cretaceous Aspen Shale and is divided into the following members, in ascending order: Chalk Creek, Coalville, Allen Hollow, Oyster Ridge Sandstone, and Dry Hollow. In west-trending outcrops on the northern flank of the Uinta Mountains in Utah, the Frontier is middle and late Turonian, and is about 60 m (200 ft) thick. These strata disconformably overlie the Lower Cretaceous Mowry Shale. In boreholes on the Moxa arch, the upper part of the Frontier is of middle Turonian to early Coniacian age and unconformably overlies the lower part of the formation, which is early Cenomanian at the south end and probably Cenomanian to early Turonian at the north end. The Frontier on the arch thickens northward from less than 100 m (328 ft) to more than 300 m (984 ft) and conformably overlies the Mowry. The marine and nonmarine Frontier near the Uinta Mountains, marine and mnmarine beds in the upper part of the formation on the Moxa arch and the largely nonmarine Dry Hollow Member at the top of the Frontier in the overthrust belt are similar in age. Older strata in the formation, which are represented by the disconformable basal contact of the Frontier near the Uinta Mountains, thicken northward along the Moxa arch and westward between the arch and the overthrust belt. The large changes in thickness of the Frontier in the Green River Basin were caused mainly by differential uplift and truncation of the lower part of the formation during the early to middle Turonian and by the shoreward addition of progressively younger sandstone units at the top of the formation during the late Turonian and early Coniacian. The sandstone in cores of the Frontier, from boreholes on the Moxa arch and the northern plunge of the Rock Springs uplift, consists of very fine grained and fine-grained litharenites and sublitharenites that were deposited in deltaic and shallow-water marine environments. These rocks consist mainly of quartz, chert, rock fragments, mixed-layer illite-smectite, mica-illite, and chlorite. Samples of the sandstone have porosities of 4.7 to 23.0 percent and permeabilities of 0.14 to 6.80 millidarcies, and seem to represent poor to fair reservoir beds for oil and gas. The shale in cores of the Frontier Formation and the overlying basal Hilliard Shale, from the Moxa arch, Rock Springs uplift, and overthrust belt, was deposited in deltaic and offshore-marine environments. Samples of the shale are composed largely of quartz, micaillite, mixed-layer illite-smectite, kaolin, and chlorite. They also contain from 0.27 to 4.42 percent organic carbon, in humic and sapropelic organic matter. Most of the sampled shale units are thermally mature, in terms of oil generation, and a few probably are source rocks for oil and gas.

MINERALOGY, PETROGRAPHY, AND RADIOACTIVITY OF REPRESENTATIVE SAMPLES OF CHATTANOOGA SHALE

DOE Office of Scientific and Technical Information (OSTI.GOV)

Bates, T.F.; Strahl, E.O.

1957-01-01

Qualitative and quantitative mineralogical studies of the Chattanooga Shale are in progress. Problems of separation and analysis of mineral and organic components are difficult because the rock is fine-grained. However, the applicaiion of light and electron microscopy, x-ray diffraction, nuclear-track study, and other methods has provided data of interest. Megascopically, the shalc is a massive chocolate-brown sediment which displays faint indications of lamination. Some pyrite lenses, nodules, and crystals and a few mica flakes are large enough to be seen with a hand lens. In thin section the rock is seen to consist of grains of quartz and feldspar inmore » a matrix of yellow to red--brown organic material, which incorporates shreds of mica and probably clay particles and is dotted by small clusters of pyrite. Larger organic fragments with associated pyrite are common and take various forms. Individual mineral particles range from pyrite cubes less than 0.15 micron on a side to quartz and feldspar grains as large as 0.10 mm. X-ray studies show the clay minerals to be illite, kaolinite, and chlorite in decreasing order of abundance. Tourmaline, zircon, and apatite are the characteristic heavy minerals of the sediment. Quantitative studies, accomplished by a combination of chemical and mineralogical methods, have shown the composition of a batch sample of this rock to be approxiinately: 22% quartz, 9% feldspar, 31% illite and kaolinite, 22% organic matter, 11% pyrite and marcasite, 2% chlorite, 2% iron oxides, and l% tourmaline, zircon, and apatite. Alphatrack studies of cniulsion-covered thin sections indicate that no uranium mineral is present. Approximately 70% of the uranium atoms is randomly distributed throughout the finegrained matrix of the rock, whereas another 25% is concentrated in organic-pyrite-clay complexes such as pyrite nodules and discrete organic bodies. In unweathered samples there is no relationship between uranium distribution and textural fcatures such as bedding. The data indicate that the uranium was precipitated from sea water under reducing conditions and has not been redistributed following compaction of the sediment. (auth)« less

Investigating the Thermal Limit of Clay Minerals for Applications in Nuclear Waste Repository Design

NASA Astrophysics Data System (ADS)

Matteo, E. N.; Miller, A. W.; Kruichak, J.; Mills, M.; Tellez, H.; Wang, Y.

2013-12-01

Clay minerals are likely candidates to aid in nuclear waste isolation due to their low permeability, favorable swelling properties, and high cation sorption capacities. Establishing the thermal limit for clay minerals in a nuclear waste repository is a potentially important component of repository design, as flexibility of the heat load within the repository can have a major impact on the selection of repository design. For example, the thermal limit plays a critical role in the time that waste packages would need to cool before being transferred to the repository. Understanding the chemical and physical changes that occur in clay minerals at various temperatures above the current thermal limit (of 100 °C) can enable decision-makers with information critical to evaluating the potential trade-offs of increasing the thermal limit within the repository. Most critical is gaining understanding of how varying thermal conditions in the repository will impact radionuclide sorption and transport in clay materials either as engineered barriers or as disposal media. A variety of clays (illite, mixed layer illite/smectite, montmorillonite, and palygorskite) were heated for a range of temperatures between 100-500 °C. These samples were characterized by a variety of methods, including nitrogen adsorption, x-ray diffraction, thermogravimetric analysis, barium chloride exchange for cation exchange capacity (CEC), and iodide sorption. The nitrogen porosimetry shows that for all the clays, thermally-induced changes in BET surface area are dominated by collapse/creation of the microporosity, i.e. pore diameters < 17 angstroms. Changes in micro porosity (relative to no heat treatment) are most significant for heat treatments 300 °C and above. Alterations are also seen in the chemical properties (CEC, XRD, iodide sorption) of clays, and like pore size distribution changes, are most significant above 300 °C. Overall, the results imply that changes seen in pores size distribution correlate with cation exchange capacity and cation exchange processes. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's Nation Nuclear Security Administration under contract DE-AC04-94AL85000. SAND Number: 2013-6352A.

Smectite Dehydration, Membrane Filtration, and Pore-Water Freshening in Deep Ultra-Low Permeability Formations: Deep Processes in the Nankai Accretionary Wedge

NASA Astrophysics Data System (ADS)

Brown, K. M.; Sample, J. C.; Even, E.; Poeppe, D.; Henry, P.; Tobin, H. J.; Saffer, D. M.; Hirose, T.; Toczko, S.; Maeda, L.

2014-12-01

We address the fundamental questions surrounding the nature of water and chemical transport processes deep within sedimentary basin and accretionary-wedge environments. Consolidation and permeability studies conducted to 165 MPa (~10km depth) indicate that ultra-tight clay formations (10-18 m2 to10-21 m2) can substantially modify the fluids migrating through then. Pore-water extractions conducted on smectite/illite rich core samples obtained from 1-3 km depths at IODP (NanTroSEIZE, Chikyu) deep-riser drilling Site C0002, at the elevated loads required to squeeze waters from such deeply buried sediment (stresses up to 100 MPa),resulted in anomalous patterns of sequential freshening with progressive loading. More accurate laboratory investigations (both incremental loading and Constant Rate of Strain test) revealed that such freshening initiates above 20 MPa and progresses with consolidation to become greater than 20% by effective normal load of 165 MPa. Log-log plots of stress vs. hydraulic conductivity reveal that trends remain linear to elevated stresses and total porosities as low at 14%. The implications are that stress induced smectite dehydration and/or membrane filtration effects cause remarkable changes in pore water chemistry with fluid migration through deep, tight, clay-rich formations. These changes should occur in addition to any thermally induced diagenetic and clay-dehydration effects on pore water chemistry. Work is progressing to evaluate the impact of clay composition and temperature to ascertain if purely illitic compositions show similar trends and if the mass fractionation of water and other isotopes also occurs. Such studies will ascertain if the presence of smectite is a prerequisite for freshening or if membrane filtration is a major process in earth systems containing common clay minerals. The results have major implications for interpretations of mass chemical balances, pore water profiles, and the hydrologic, geochemical, and stress state controls on deep system behavior in all deep accretionary wedge and basin environments where clays are abundant. This research used samples provided by the International Ocean Discovery Program (IODP).

New mineralogical and geochemical evidence for the Middle Eocene Climatic Optimum (MECO) in the Neo-Tethys (Central Turkey)

NASA Astrophysics Data System (ADS)

Rego, E. S.; Jovane, L.; Giorgioni, M.; Hein, J. R.; Sant'Anna, L. G.; Rodelli, D.; Özcan, E.; Frontalini, F.; Coccioni, R.

2016-12-01

The Middle Eocene Climatic Optimum (MECO) is one of several climate warming events that occurred during the Paleogene. It started at 40.5 Ma and produced a global temperature increase over a period of 500 kyr. However, the duration and the d13C signature of this event are not consistent with the models commonly proposed to explain warming events in the Cenozoic, and thus challenge our understanding of carbon cycling and climatic processes. Here we present data of a new section from central Turkey, recording the MECO in the eastern part of the Neo-Tethys. The stratigraphic extent and continuity, as well as the exceptional preservation of various types of microfossils, allow us to obtain a multi-proxy record of unprecedented high resolution for this interval. We integrate data from stable isotopes, X-ray diffraction mineralogy, XRF chemistry, and magnetic properties to obtain a complete paleoclimatic and paleoceanographic reconstruction. Stable isotopes (d13C and d18O) allow us to clearly define the geochemical signature of the MECO. A divergence between the d18O curves of the shallow- and deep-water dwelling planktonic foraminifera after the event suggests a more stratified water column in the Neo-Tethys. Bulk and clay mineralogy reveal changing weathering conditions on land. Higher amounts of chlorite and illite (physical weathering) occur prior and after the event, while the MECO interval displays greater amounts of illite and smectite (chemical weathering). Additionally, the inverse relationship between detrital minerals and calcite suggests that carbonate productivity might have suffered at that time, or an increase in detrital input could have diluted the carbonate fraction. An increase in ARM and magnetic particle grain size also suggests an increase in productivity or preservation of biogenic magnetite. Our results confirm the global nature of the MECO, affecting both oceans and continents. However, different from other events, warming conditions were not produced by a sudden release of greenhouse gasses, but probably by a change in circulation amplified by orbital forcing.

The Western North American Cretaceous-Tertiary (K-T) boundary interval and its content of shock-metamorphosed minerals: Implications concerning the K-T boundary impact-extinction theory

NASA Technical Reports Server (NTRS)

Izett, G. A.

1988-01-01

At 20 sites in the Raton Basin of Colorado and New Mexico, and at several other sites in Wyoming, Montana, and Canada, a pair of claystone units, an Ir abundance anomaly, and a concentration of shock-metamorphosed minerals mark the palynological K-T boundary. The K-T boundary claystone, which is composed of kaolinite and small amounts of illite/smectite mixed-layer clay, is similar in most respects to kaolinite tonstein layers in coal beds. At some, but not all, K-T boundary localities, the boundary claystone contains solid kaolinite and hollow and solid goyazite spherules, 0.05 to 1.2 mm in diameter. The upper unit, the K-T boundary impact layer, consists chiefly of kaolinite and various amounts of illite/smectite mixed-layer clay. The impact layer and boundary claystone are similar chemically, except that the former has slightly more Fe, K, Ba, Cr, Cu, Li, V, and Zn than the latter. The facts that the boundary claystone and impact layer contain anomalous amounts of Ir, comprise a stratigraphic couplet at Western North American sites, and form thin, discrete layers, similar to air-fall units (volcanic or impact), suggest that the claystone units are of impact origin. Significantly, the impact layer contains as much as 2 percent clastic mineral grains, about 30 percent of which contain multiple sets of shock lamellae. Only one such concentration of shocked minerals has been found near the K-T boundary. The type of K-T boundary shock-metamorphosed materials (quartzite and metaquartzite) in the impact layer and the lack of shock lamellae in quartz and feldspar of pumice lapilli and granitic xenoliths in air-fall pumice units of silicic tuffs, such as the Bishop Tuff, eliminate the possibility that the shock-metamorphosed minerals in the K-T impact layer are of volcanic origin. The global size distribution and abundance of shock-metamorphosed mineral grains suggest that the K-T impact occurred in North America.

Rb-Sr and K-Ar age of globular phyllosilicates and biostratigraphy of the Riphean deposits of the Olenek Uplift (North Siberia)

NASA Astrophysics Data System (ADS)

Zaitseva, T. S.; Gorokhov, I. M.; Semikhatov, M. A.; Ivanovskaya, T. A.; Kuznetsov, A. B.; Dorzhieva, O. V.

2017-11-01

This work presents results of the complex mineralogical, geochemical, and isotope-geochronological investigation of globular dioctahedral 2: 1 phyllosilicates (GPS) of the illite-glauconite series from the Riphean sequences of the Olenek Uplift. It is established that GPS (glauconite, Al-glauconite, Fe-illite) in deposits of the Arymass, Debengda, and Khaipakh formations are represented by mixed-layer varieties of two types: (1) with relatively low (<10%) and (2) higher (10-20%) contents of expandable layers. Among the mixed-layer varieties are those with disordered alternation of micaceous and smectite layers (R = 0), as well as with tendency to ordering (R ≥ 1). The parameter b of an elementary cell of minerals varies from 9.18 to 9.72 Å. The Rb-Sr age dating of GPS was first carried out in combination with the calculation of theoretical pattern of the cation distribution in the mineral structure and comparison of the calculation results obtained with the Mössbauer and IR spectroscopy data. This approach is based on the assumption that development and evolution of isotope systems in GPS are synchronous with the evolution of the crystalline structure of the mineral at various stages of the geological and geochemical history of the development of sedimentary units. Analysis of the obtained data allows us to state that the structural features of the Riphean GPS from the Olenek section reflect the early diagenetic stages of the formation of the minerals studied. The 87Sr/86Sr initial ratios in the studied sediments are consistent with the range of variations in this ratio in the Middle Riphean Ocean (0.7049-0.7061). The Rb-Sr and K-Ar ages of the GPS of the Arymass (1305 ± 8 and 1302 Ma, respectively), Debengda (1265 ± 12 and 1284 ± 22 Ma), and Khaipakh (1172 ± 18 and 1112 ± 24 Ma) formations in the Olenek Uplift section are close to the accumulation time of corresponding deposits and, correspondingly, have significance for stratigraphic correlations.

Pore water evolution in sandstones of the Groundhog Coalfield, northern Bowser Basin, British Columbia

NASA Astrophysics Data System (ADS)

Cookenboo, H. O.; Bustin, R. M.

1999-01-01

The succession of sandstone cements in chert and volcanic lithic arenites and wackes from the northern Bowser Basin of British Columbia comprises a record of diagenesis in shallow marine, deltaic, and coastal plain siliciclastic sediments that pass through the oil window and reach temperatures near the onset of metamorphism. The succession of cements is consistent with seawater in the sandstones mixing with acid waters derived from dewatering of interbedded organic rich muds. Sandstone cement paragenesis includes seven discrete cement stages. From earliest to latest the cement stages are: (1) pore-lining chlorite; (2) pore-lining to pore-filling illite; (3) pore-filling kaolinite; (4) oil migration through some of the remaining connected pores; (5) chlorite dissolution; (6) quartz cement; and (7) calcite cement. These seven cement stages are interpreted as a record of the evolution of pore waters circulating through the sandstones after burial. The earliest cement stages, as well as the depositional environments, are compatible with seawater as the initial pore fluid. Seawater composition changed during transport through the sandstones, first by loss of Mg 2+ and Fe 2+ during chlorite precipitation (stage 1). Dewatering of interbedded organic-rich mudstones probably added Mg 2+ and Fe 2+ to partially buffer the loss of these cations to chlorite. Acids produced during breakdown of organic matter are presumed to have mixed into sandstone pore fluids due to further compaction of the muds, leading to reduction of initial alkalinity. Reduction in alkalinity, in turn, favours change from chlorite to illite precipitation (stage 2), and finally to kaolinite (stage 3). Pore waters likely reached their peak acidity at the time of oil migration (stage 4). Chlorite dissolution (stage 5) and quartz precipitation (stage 6) occurred when pores were filled by these hydrocarbon-bearing and presumably acidic fluids. Fluid inclusions in fracture-filling quartz cements contain petroleum, high-pressure methane, and methane-rich aqueous solutions. Homogenization temperatures from primary two-phase inclusions are consistent with quartz cementation during progressive heating between approximately 100 and 200°C. Following quartz precipitation, alkaline pore waters were re-established, as evidenced by late-stage calcite cement (stage 7).

Integrating petrography, mineralogy and hydrochemistry to constrain the influence and distribution of groundwater contributions to baseflow in poorly productive aquifers: insights from Gortinlieve catchment, Co. Donegal, NW Ireland.

PubMed

Caulfield, John; Chelliah, Merlyn; Comte, Jean-Christophe; Cassidy, Rachel; Flynn, Raymond

2014-12-01

Identifying groundwater contributions to baseflow forms an essential part of surface water body characterisation. The Gortinlieve catchment (5 km(2)) comprises a headwater stream network of the Carrigans River, itself a tributary of the River Foyle, NW Ireland. The bedrock comprises poorly productive metasediments that are characterised by fracture porosity. We present the findings of a multi-disciplinary study that integrates new hydrochemical and mineralogical investigations with existing hydraulic, geophysical and structural data to identify the scales of groundwater flow and the nature of groundwater/bedrock interaction (chemical denudation). At the catchment scale, the development of deep weathering profiles is controlled by NE-SW regional scale fracture zones associated with mountain building during the Grampian orogeny. In-situ chemical denudation of mineral phases is controlled by micro- to meso-scale fractures related to Alpine compression during Palaeocene to Oligocene times. The alteration of primary muscovite, chlorite (clinochlore) and albite along the surfaces of these small-scale fractures has resulted in the precipitation of illite, montmorillonite and illite-montmorillonite clay admixtures. The interconnected but discontinuous nature of these small-scale structures highlights the role of larger scale faults and fissures in the supply and transportation of weathering solutions to/from the sites of mineral weathering. The dissolution of primarily mineral phases releases the major ions Mg, Ca and HCO3 that are shown to subsequently form the chemical makeup of groundwaters. Borehole groundwater and stream baseflow hydrochemical data are used to constrain the depths of groundwater flow pathways influencing the chemistry of surface waters throughout the stream profile. The results show that it is predominantly the lower part of the catchment, which receives inputs from catchment/regional scale groundwater flow, that is found to contribute to the maintenance of annual baseflow levels. This study identifies the importance of deep groundwater in maintaining annual baseflow levels in poorly productive bedrock systems. Copyright © 2014 Elsevier B.V. All rights reserved.

Tectonic uplift-influenced monsoonal changes promoted hominin occupation of the Luonan Basin: Insights from a loess-paleosol sequence, eastern Qinling Mountains, central China

NASA Astrophysics Data System (ADS)

Fang, Qian; Hong, Hanlie; Zhao, Lulu; Furnes, Harald; Lu, Huayu; Han, Wen; Liu, Yao; Jia, Zhuoyue; Wang, Chaowen; Yin, Ke; Algeo, Thomas J.

2017-08-01

Quaternary soil deposits from northern and southern China are distinctly different, reflecting variability of the East Asian monsoon north and south of the Qinling Mountains. Coeval sediments from the transitional climatic zone of central China, which are little studied to date, have the potential to improve our understanding of Quaternary monsoon changes and associated influences on hominin occupation of this region. Here, we investigate in detail a well-preserved and continuous Quaternary loess-paleosol sequence (Shangbaichuan) from the Luonan Basin, using a variety of weathering indices including major and trace element ratios, clay mineralogy, and Fe-oxide mineralogy. The whole-rock samples display similar rare earth element patterns characterized by upper continental crustal ratios: (La/Yb)N ≈ 9.5 and Eu/Eu* ≈ 0.65. Elemental data such as (La/Yb)N, La/Th and Eu/Eu* ratios show a high degree of homogeneity, suggesting that dust in the source region may have been thoroughly mixed and recycled, resulting in all samples having a uniform initial composition. Indices for pedogenic weathering such as Na/K, Ba/Sr, Rb/Sr, CIA, CIW, CPA, PIA, kaolinite/illite, (kaolinite + smectite)/illite, and hematite/(hematite + goethite) exhibit similar secular trends and reveal a four-stage accumulation history. The indices also indicate that the climate was warmer and wetter during the most recent interglacial stage, compared with coeval environments of the Chinese Loess Plateau. Secular changes in weathering intensity can be related to stepwise uplift of the Qinling Mountains and variation in East Asian monsoon intensity, both of which played significant roles in controlling climate evolution in the Luonan Basin. Furthermore, intensified aridity and winter monsoon strength in dust source areas, as evidenced by mineralogic and geochemical changes, may have been due to the mid-Pleistocene climate transition. Based on temporal correlation of warmer and wetter climatic conditions with more frequent hominin occupation, we infer that the paleoclimate in the eastern Qinling Mountains remained mild and favorable during glacial stages of the Late Quaternary, thus promoting early human settlement.

Tectonothermal evolution of the Triassic flysch in the Bayan Har Orogen, Tibetan plateau

NASA Astrophysics Data System (ADS)

Wang, Hejing; Rahn, Meinert; Zhou, Jian

2018-01-01

The Bayan Har Orogen comprises a major part of the "Qingzang-Dianxi fold region" in western China. It preserves important information of the tectono-thermal evolution covering the time span from the closure of the Paleo-Tethys Ocean up to the formation of the Himalayas. Low temperature metamorphic indicators, such as mineral assemblages, illite "crystallinity" (IC), chlorite "crystallinity" (CC), illite polytype, b-cell dimension of K-white micas, geothermometry of selected minerals were analyzed. The values of Kübler index (KI) of the Triassic flysch in the Bayan Har Orogen range from 0.23-1.63°Δ2θ while Árkai index (ÁI) in a range of 0.21-0.60°Δ2θ. Iso-thermal zones mapped with KI describe a pair of anchizones and an anchiregion within the Bayan Har Orogen: the "Giant Yushu Anchizone" in the southwest (extending > 750 km long and 100 km wide), the "Zaling-Eling-Lakes Anchizone" in the center (about 150 km long and 40 km wide) and the "Xing-Tong-Zhe Anchiregion" in the northeast (covering an area of roughly 60,000 km2). They are separated by diagenetic zones. Peak metamorphic conditions are estimated around 280-330 °C and a low to intermediate (N. New Hampshire) pressure type. A slight change with increasing then decreasing pressure was observed from SW to NE. The relationship between anchimetamorphic pattern of Triassic flysch and large-scale folds and faults indicates syn- to post structural metamorphism. Compression at the end of the Triassic, induced by the interaction of the Tarim, North China and Indian blocks caused the closure of the Paleo-Tethys Ocean and led to the folding of the Triassic flysch within the Paleo-Tethys Ocean basin. Anchimetamorphism may have been caused by crustal thickening of > 10 km due to an accretionary wedge setting and a temperature increase in those rocks due to burial. Such a regional metamorphic pattern would provide important information for reconstruction of palaeotectonic-palaeogeograph and the evolutionary history of Tibetan plateau.

Characterization of feed coal and coal combustion products from power plants in Indiana and Kentucky

DOE Office of Scientific and Technical Information (OSTI.GOV)

Brownfield, M.E.; Affolter, R.H.; Cathcart, J.D.

1999-07-01

The US Geological Survey, Kentucky Geological Survey, and the University of Kentucky Center for Applied Energy Research are collaborating with Indiana and Kentucky utilities to determine the physical and chemical properties of feed coal and coal combustion products (CCP) from three coal-fired power plants. These three plants are designated as Units K1, K2, and I1 and burn high-, moderate-, and low-sulfur coals, respectively. Over 200 samples of feed coal and CCP were analyzed by various chemical and mineralogical methods to determine mode of occurrence and distribution of trace elements in the CCP. Generally, feed coals from all 3 Units containmore » mostly well-crystallized kaolinite and quartz. Comparatively, Unit K1 feed coals have higher amounts of carbonates, pyrite and sphalerite. Unit K2 feed coals contain higher kaolinite and illite/muscovite when compared to Unit K1 coals. Unit I1 feed coals contain beta-form quartz and alumino-phosphates with minor amounts of calcite, micas, anatase, and zircon when compared to K1 and K2 feed coals. Mineralogy of feed coals indicate that the coal sources for Units K1 and K2 are highly variable, with Unit K1 displaying the greatest mineralogic variability; Unit I1 feed coal however, displayed little mineralogic variation supporting a single source. Similarly, element contents of Units K1 and K2 feed coals show more variability than those of Unit I1. Fly ash samples from Units K1 and K2 consist mostly of glass, mullite, quartz, and spines group minerals. Minor amounts of illite/muscovite, sulfates, hematite, and corundum are also present. Spinel group minerals identified include magnetite, franklinite, magnesioferrite, trevorite, jacobisite, and zincochromite. Scanning Electron Microscope analysis reveals that most of the spinel minerals are dendritic intergrowths within aluminum silicate glass. Unit I1 fly ash samples contain glass, quartz, perovskite, lime, gehlenite, and apatite with minor amounts of periclase, anhydrite, carbonates, pyroxenes, and spinels. The abundant Ca mineral phases in the Unit I1 fly ashes are attributed to the presence of carbonate, clay and phosphate minerals in the coal.« less

Development and Application of a Paleomagnetic/Geochemical Method for Constraining the Timing of Burial Diagenetic Events

DOE Office of Scientific and Technical Information (OSTI.GOV)

Elmore, Richard D.; Engel, Michael H.

2006-01-05

Studies of diagenesis caused by fluid migration or other events are commonly hindered by a lack of temporal control. Our results to date demonstrate that a paleomagnetic/geochemical approach can be used to date fluid migration as well as burial diagenetic events. Our principal working hypothesis is that burial diagenetic processes (e.g., maturation of organic-rich sediments and clay diagenesis) and the migration of fluids can trigger the authigenesis of magnetic mineral phases. The ages of these events can be constrained by comparing chemical remanent magnetizations (CRMs) to independently established Apparent Polar Wander Paths. Whilst geochemical (e.g. stable isotope and organic analyses)more » and petrographic studies provide important clues for establishing these relationships, the ultimate test of this hypothesis requires the application of independent dating methods to verify the paleomagnetic ages. Towards this end, we have used K-Ar dating of illitization as an alternative method for constraining the ages of magnetic mineral phases in our field areas. We have made significant progress toward understanding the origin and timing of chemical remagnetization related to burial diagenetic processes. For example, a recently completed field study documents a relationship between remagnetization and the maturation of organic matter (Blumstein et al., 2004). We have tested the hypothesized connection between clay diagenesis and remagnetization by conducting K-Ar dating of authigenic illites in units in Scotland and Montana with CRMs (e.g., Elliott et al., 2006a; Elliott et al., 2006b). We have also developed a fluid related model for alteration and remagnetization of Appalachian red beds that involves reduction and mobilization of iron phases by hydrocarbons and precipitation of authigenic hematite as a result of the introduction of meteoric fluid recharge (Cox et al., 2005). In addition, our recent studies of fluid-related CRMs along faults in Scotland provide information on the timing and origin of fluid flow events along the Moine and Great Glen faults (Parnell et al., 2004; Blumstein et al., 2005; Elmore et al., 2006).« less

Structure and clay mineralogy: borehole images, log interpretation and sample analyses at Site C0002 Nankai Trough accretionary prism

NASA Astrophysics Data System (ADS)

Jurado, Maria Jose; Schleicher, Anja

2015-04-01

Our research focused on the characterization of fracture and fault structures from the deep Nankai Trough accretionary prism in Japan. Logging Data and cuttings samples from the two most recent International Ocean Discovery Program (IODP) Expeditions 338 and 348 of the NanTroSEIZE project were analyzed by Logging While Drilling (LWD) oriented images, geophysical logs and clay mineralogy. Both expeditions took place at Site C0002, but whereas Hole C0002F (Expedition 338) was drilled down to 2004.5 mbsf, Hole C0002N and C0002P (Expedition 348) reached a depth of 2325.5 mbsf and 3058.8 mbsf respectively. The structural interpretation of borehole imaging data illustrates the deformation within the fractured and faulted sections of the accretionary prism. All drill holes show distinct areas of intense fracturing and faulting within a very clay-dominated lithology. Here, smectite and illite are the most common clay minerals, but the properties and the role they may play in influencing the fractures, faults and folds in the accretionary prism is still not well understood. When comparing clay mineralogy and fracture/fault areas in hole C0002F (Expedition 338), a trend in the abundance of illite and smectite, and in particular the swelling behavior of smectite is recognizable. In general, the log data provided a good correlation with the actual mineralogy and the relative abundance of clay. Ongoing postcruise preliminary research on hole C0002 N and C0002P (Expedition 348) should confirm these results. The relationship between fracture and fault structures and the changes in clay mineralogy could be explained by the deformation of specific areas with different compaction features, fluid-rock interaction processes, but could also be related to beginning diagenetic processes related to depth. Our results show the integration of logging data and cutting sample analyses as a valuable tool for characterization of petrophysical and mineralogical changes of the structures of the Nankai accretionary prism. This is critical for our understanding of clay-fluid interaction and mechanical properties duing fault displacements and seismogenesis.

Effects of detrital influx in the Pennsylvanian Upper Freeport peat swamp

USGS Publications Warehouse

Ruppert, L.F.; Stanton, R.W.; Blaine, Cecil C.; Eble, C.F.; Dulong, F.T.

1991-01-01

Quartz cathodoluminescence properties and mineralogy of three sets of samples and vegetal and/ or miospore data from two sets of samples from the Upper Freeport coal bed, west-central Pennsylvania, show that detrital influence from a penecontemporaneous channel is limited to an area less than three km from the channel. The sets of samples examined include localities of the coal bed where (1) the coal is thin, split by partings, and near a penecontemporaneous fluvial channel, (2) the coal is relatively thick and located approximately three km from the channel, and (3) the coal is thick and located approximately 12 km from the channel. Samples from locality 1 (nearest the channel) have relatively high-ash yields (low-temperature ash average = 27.3% on a pyrite- and calcite-free basis) and high proportions of quartz and clay minerals. The quartz is primarily detrital, as determined by cathodoluminescent properties, and the ratio of kaolinite to illite is low. In addition, most of the plant remains and miospores indicate peat-forming plants that required low nutrient levels for growth. In contrast, samples from localities 2 and 3, from the more interior parts of the bed, contained predominantly authigenic quartz grains nd yielded low-temperature ash values of less than 14% on a pyrite- and calcite-free basis. The low-temperature ash contains low concentrations of quartz and clay minerals and the ratio of kaolinite to illite is relatively high. Although intact core was not available for paleobotanical analyses, another core collected within 1 km from locality 3 contained plant types interpreted to have required high nutrient levels for growth. These data indicate that mineral formation is dominated by authigenic processes in interior parts of the coal body. Some of the authigenic quartz may have been derived from herbaceous ferns as indicated by patterns in the palynological and paleobotanical data. In contrast, detrital processes appeared to be limited to in areas directly adjacent to the penecontemporaneous channel where the coal bed is high in ash, split by mineral-rich partings, and of little or no economic value. ?? 1991.

Experimental Insights into Multiphase (H2O-CO2) Fluid-Rock Interactions in Geothermal Systems

NASA Astrophysics Data System (ADS)

Kaszuba, J. P.; Lo Re, C.; Martin, J.; McPherson, B. J.; Moore, J. N.

2012-12-01

Integrated hydrothermal experiments and geochemical modeling elucidate fluid-rock interactions and reaction pathways in both natural and anthropogenic systems, including enhanced geothermal systems (EGS) in which CO2 is introduced as a working fluid. Experiments are conducted in rocker bombs and flexible Au-Ti reaction cells. Individual experiments require one to three months to complete; intensive in-situ fluid/gas sampling gauges reaction progress. Investigation of granitic reservoirs and associated vein minerals are broadly based on the Roosevelt Hot Springs thermal area, Utah, USA. The granite consists of subequal amounts of quartz, perthitic K-feldspar (~25% wt% albite and 75% wt% K-feldspar), and oligoclase (An23), and 4 wt% Fe-rich biotite. Vein minerals include epidote and chlorite (clinochlore). Experiments are conducted at 250°C and 25 to 45 MPa. Each experiment uses mineral powders (75 wt% of rock mass, ground to <45 um) to increase reactivity and also mineral pieces (0.1-0.7 cm in size) to promote petrologic evaluation of mineral reactions. The water (I ≈ 0.1 molal) initially contains millimolal quantities of SiO2, Al, Ca, Mg, K, SO4, and HCO3 and is designed to be saturated with all of the minerals present at the start of each experiment. Excess CO2 is injected to saturate the water and maintain an immiscible supercritical fluid phase. The entire evolutionary path of the natural system is not replicated at laboratory scales. Instead, experiments define a segment of the reaction path and, in combination with geochemical modeling, provide clear trajectories towards equilibrium. Reaction of granite+water yields illite+zeolite; smectite subsequently precipitates in response to CO2 injection. Reaction of granite+epidote+water yields illite+zeolite+smectite; zeolite does not precipitate after CO2 is injected. Water in all experiments become saturated with chalcedony. Carbonate minerals do not precipitate but are predicted as final equilbrium products. Enhanced Geothermal Systems are expected to follow similar reaction pathways and produce metastable minerals during initial development.

Effective strength of incoming sediments and its implications for plate boundary propagation: Nankai and Costa Rica as type examples of accreting vs. erosive convergent margins

NASA Astrophysics Data System (ADS)

Kopf, Achim

2013-11-01

The location of the seaward tip of a subduction thrust controls material transfer at convergent plate margins, and hence global mass balances. At approximately half of those margins, the material of the subducting plate is completely underthrust so that no accretion or even subduction erosion takes place. Along the remaining margins, material is scraped off the subducting plate and added to the upper plate by frontal accretion. We here examine the physical properties of subducting sediments off Costa Rica and Nankai, type examples for an erosional and an accretionary margin, to investigate which parameters control the level where the frontal thrust cuts into the incoming sediment pile. A series of rotary-shear experiments to measure the frictional strength of the various lithologies entering the two subduction zones were carried out. Results include the following findings: (1) At Costa Rica, clay-rich strata at the top of the incoming succession have the lowest strength (μres = 0.19) while underlying calcareous ooze, chalk and diatomite are strong (up to μres = 0.43; μpeak = 0.56). Hence the entire sediment package is underthrust. (2) Off Japan, clay-rich deposits within the lower Shikoku Basin inventory are weakest (μres = 0.13-0.19) and favour the frontal proto-thrust to migrate into one particular horizon between sandy, competent turbidites below and ash-bearing mud above. (3) Taking in situ data and earlier geotechnical testing into account, it is suggested that mineralogical composition rather than pore-pressure defines the position of the frontal thrust, which locates in the weakest, clay mineral-rich (up to 85 wt.%) materials. (4) Smectite, the dominant clay mineral phase at either margin, shows rate strengthening and stable sliding in the frontal 50 km of the subduction thrust (0.0001-0.1 mm/s, 0.5-25 MPa effective normal stress). (5) Progressive illitization of smectite cannot explain seismogenesis, because illite-rich samples also show velocity strengthening at the conditions tested.

Fingerprinting Persistent Turbidity in Sheep Creek Reservoir, Owhyee, Nevada

NASA Astrophysics Data System (ADS)

Ransom, R. N.; Hooper, R. L.; Kerner, D.; Nicols, S.

2007-12-01

Sheep Creek Reservoir near Owyhee, NV is historically a quality rainbow trout fishery. Persistent high-turbidity has been an issue since a major storm event in 2005 resulted in surface water runoff into the Reservoir. The high turbidity is adversely impacting the quality of the fishery. Initial turbidity measurements in 2005 were upwards of 80NTU and these numbers have only decreased to 30NTU over the past two summers. Field parameters indicate the turbidity is associated with high total suspended solids (TSS) and not algae. Five water samples collected from around the reservoir during June, 2007 indicated uniform TSS values in the range of 5 to 12mg/L and oriented powder x-ray diffraction(XRD) and transmission electron microscopy(TEM) analyses of suspended sediment shows very uniform suspended particulate mineralogy including smectite, mixed layer illite/smectite (I/S), discrete illite, lesser amounts of kaolin, sub-micron quartz and feldspar. Diatoms represent a ubiquitous but minor component of the suspended solids. Six soil samples collected from possible source areas around the reservoir were analyzed using both XRD and TEM to see if a source area for the suspended solids could be unambiguously identified. Soils on the east side of the reservoir contain smectite and mixed layer I/S but very little of the other clays. The less than 2 micron size fraction from soils collected from a playa on the topographic bench immediately to the west of the reservoir show a mineralogic finger-print essentially identical to the current suspended sediment. The suspended sediment probably originates on the bench to the west of the reservoir and cascades into the reservoir over the topographic break during extreme storm events. The topographic relief, short travel distance and lack of a suitable vegetated buffer zone to the west are all consistent with a primary persistent suspended sediment source from the west. Identification of the sediment source allows for design of a cost effective remediation plan that includes minimizing future loading of the reservoir with soils capable of producing extended turbidity.

Gram-negative Biomass in Clay Minerals Analogs: Testing Habitability Potential for the 2011 Mars Science Laboratory Mission

NASA Astrophysics Data System (ADS)

Bonaccorsi, R.; McKay, C. P.

2009-12-01

Landing sites of next missions to Mars i.e., the US 2011 Mars Science Laboratory (MSL11) and the ESA2016 Pasteur ExoMars, will include phyllosilicate outcrops as targets for investigating the geological and biological history of that planet. In this context, we present a study assessing the living biomass and habitability potential in mineralogical Mars analogs such as phyllosilicates and hematite-rich deposits encompassing a broad arid-hyper-arid climate range (annual rainfall <0.2 to ~700mm/y). Samples from the Atacama Desert (Chile), the Death Valley (CA), and the California Coast (USA) were analyzed for microbial lipopolysaccharide (LPS) as proxy for Gram-negatives biomass with the Limulus-Amebocite-Lysate (LAL) assay. Mineral phases were identified using X-Ray-Diffraction (XRD). These samples resulted to contain phyllosilicate phases similar to those identified, or inferred [1], on the surface of Mars by the OMEGA-Mars/Express [e.g., 2], the Mars Reconnaissance Orbiter (MRO) instruments (HiRISE and CRISM) [3]. Basic observations were: 1) there is no systematic pattern in biomass content of clays vs. non-clays (oxidized) materials from the study sites; 2) Atacama desiccation polygons (muscovite and kaolinite) and contiguous hematite-rich hyper-arid deposits contain the lowest biomass, i.e., ~104to-105 cells/g, respectively; 3) the hyper-arid clays contain three-order magnitude lower Gram-negative biomass than those (montmorillonite, illite, and chlorite) from the arid Death Valley site (~107cells/g); and 4) finally, the Gram-negative (~107cells/g) of clay minerals-rich materials from the arid site is about the same than that (~1.5 to ~3.0 x 107cells/g) of water-saturated massive deposits (kaolinite, illite, and vermiculite) from the wetter California coast. Results from this investigation will help testing for the habitability potential of phyllosilicate deposits sampled by the MSL11 Mission. REFERENCES:[1] Bibring et al., 2006, Science 312:400-404; [2] Wang et al., 2006 JGR E02S16 Vol.111; [3] Bishop et al., 2008. Science, 321,830-833.

Preliminary Results from an Assimilation of Saharan Dust Using TOMS Radiances and the GOCART Model

NASA Technical Reports Server (NTRS)

Weaver, C. J.; daSilva, Arlindo; Ginoux, Paul; Torres, Omar; Einaudi, Franco (Technical Monitor)

2000-01-01

At NASA Goddard we are developing a global aerosol data assimilation system that combines advances in remote sensing and modeling of atmospheric aerosols. The goal is to provide high resolution, 3-D aerosol distributions to the research community. Our first step is to develop a simple assimilation system for Saharan mineral aerosol. The Goddard Chemistry and Aerosol Radiation model (GOCART) provides accurate 3-D mineral aerosol size distributions. Surface mobilization, wet and dry deposition, convective and long-range transport are all driven by assimilated fields from the Goddard Earth Observing System Data Assimilation System, GEOS-DAS. Our version of GOCART transports sizes from .08-10 microns and only simulates Saharan dust. We draw the assimilation to two observables in this study: the TOMS aerosol index (Al) which is directly related to the ratio of the 340 and 380 radiances and the 380 radiance alone. The forward model that simulates the observables requires the aerosol optical thickness, the single scattering albedo and the height of the aerosol layer from the GOCART fields. The forward model also requires a refractive index for the dust. We test three index values to see which best fits the TOMS observables. These are 1) for Saharan dust reported by Patterson, 2) for a mixture of Saharan dust and a highly reflective material (sea salt or sulfate) and 3) for pure illite. The assimilation works best assuming either pure illite or the dust mixture. Our assimilation cycle first determines values of the aerosol index (Al) and the radiance at 380 nm based on the GOCART aerosol fields. Differences between the observed and GOCART model calculated Al and 380 nm radiance are first analyzed horizontally using the Physical-space Statistical Analysis System (PSAS). A quasi-Newton iteration is then performed to produce analyzed 3D aerosol fields according to parameterized background and observation error covariances. We only assimilate observations into the the GOCART model over regions of Africa and the Atlantic where mineral aerosols are dominant and carbonaceous aerosols are minimal.

Development of weathering profile of a forest hillslope in clay-rich sedimentary system

NASA Astrophysics Data System (ADS)

Nicklas, R. W.; Kim, H.; Bishop, J. K.; Rempe, D. M.

2012-12-01

Hillslopes are an essential element to the understanding of landscape evolution, storm flow generation and biogeochemical processes. Since 2008, extensive studies of climate variables, vegetation, soil moisture, subsurface hydrology, and water chemistry have taken place at a small forested hillslope, "Rivendell", at the Angelo Coast Range Reserve located at the headwaters of the Eel River, California. Here we report on the signature of weathering processes through analysis of core and soil samples collected during well drilling campaigns. Core samples from multiple depths at four wells (at creek edge, mid-slope, up-slope, and ridge-top) were selected and include 1) soil; 2) unsaturated fractured/ weathered zone; 3) zone of seasonal water table fluctuation within weathered bedrock; and 4) chronically saturated fresh bedrock zone. We also include soil samples from a groundwater seep located at the toe of the slope. The mineralogy of these samples was identified using X-ray diffraction. Samples were analyzed for salt and Ca(Mg)CO3 concentrations, and cation exchange capacity using Milli-Q water and acetic acid extraction and BaCl2-NH4Cl treatments, respectively. To further quantify the mineral dissolution and secondary mineral precipitation, a sequential extraction of trace metals were conducted - 1) exchangeable using MgCl2; 2) bound to carbonates using NaOAc; 3) bound to Fe-Mn oxides using NH2OH HCl; and 4) bound to organic matters using H2O2 and HNO3. The total elemental contents were determined using HF-HNO3-HClO4 dissolution. The mineralogy of the fresh bedrock zone showed similar patterns throughout the site -for clay minerals, chlorite, illite, interstratified illite/smectite were dominant; K-feldspar dominated the primary minerals. Shallow (<30 cm) soils had kaolinite, and chlorite was absent in some samples. CaCO3 was also predominantly found in the fresh bedrock zone and progressively increased with depth. The depletion profile of major cations (Ca, Na, Mg, K, and Si) and trace metals (Fe, Mn and Al) show the mineral dissolution fronts. K-feldspar, chlorite and CaCO3 dissolution and secondary mineral precipitation are thus the major processes that are critical to the interpretation of groundwater chemistry.

Mineralogy and geochemistry of a superhigh-organic-sulfur coal, Yanshan Coalfield, Yunnan, China: Evidence for a volcanic ash component and influence by submarine exhalation

USGS Publications Warehouse

Dai, S.; Ren, D.; Zhou, Y.; Chou, C.-L.; Wang, X.; Zhao, L.; Zhu, Xudong

2008-01-01

The mineralogy and geochemistry of a superhigh-organic-sulfur (SHOS) coal of Late Permian age from the Yanshan Coalfield, Yunnan Province, southwestern China, have been studied using optical microscope, low-temperature ashing plus X-ray diffraction analysis, scanning electron microscope equipped with energy-dispersive X-ray spectrometer, a sequential chemical extraction procedure, and inductively coupled plasma mass spectrometry. The M9 Coal from the Yanshan Coalfield is a SHOS coal that has a total sulfur content of 10.12%-11.30% and an organic sulfur content of 8.77%-10.30%. The minerals in the coal consist mainly of high-temperature quartz, sanidine, albite, muscovite, illite, pyrite, and trace amounts of kaolinite, plagioclase, akermanite, rutile, and dawsonite. As compared with ordinary worldwide (bituminous coals and anthracite) and Chinese coals, the M9 Coal is remarkably enriched in B (268????g/g), F (841????g/g), V (567????g/g), Cr (329????g/g), Ni (73.9????g/g), Mo (204????g/g), and U (153????g/g). In addition, elements including Se (25.2????g/g), Zr (262????g/g), Nb (20.1????g/g), Cd (2.07????g/g), and Tl (2.03????g/g) are also enriched in the coal. Occurrence of high-temperature quartz, sanidine, muscovite, and illite in the M9 Coal is evidence that there is a volcanic ash component in the coal that was derived from acid volcanic ashes fallen into the swamp during peat accumulation. Occurrence of albite and dawsonite in the coal and strong enrichment of some elements, including F, S, V, Cr, Ni, Mo and U, are attributed to the influence by submarine exhalation which invaded along with seawater into the anoxic peat swamp. Abundances of lithophile elements, including rare earth elements, Nb, Y, Zr, and TiO2, indicate that the silicate minerals in the coal were derived from the northern Vietnam Upland to the south of the basin. ?? 2008 Elsevier B.V. All rights reserved.

Water uptake of clay and desert dust aerosol particles at sub- and supersaturated water vapor conditions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Herich, Hanna; Tritscher, Torsten; Wiacek, Aldona

2009-11-01

Airborne mineral dust particles serve as cloud condensation nuclei (CCN), thereby influencing the formation and properties of warm clouds. It is therefore of particular interest how dust aerosols with different mineralogy behave when exposed to high relative humidity (RH) or supersaturation with respect to liquid water similar to atmospheric conditions. In this study the sub-saturated hygroscopic growth and the supersaturated cloud condensation nucleus activity of pure clays and real desert dust aerosols was determined using a hygroscopicity tandem differential mobility analyzer (HTDMA) and a cloud condensation nuclei counter (CCNC), respectively. Five different illite, montmorillonite and kaolinite clay samples as wellmore » as three desert dust samples (Saharan dust (SD), Chinese dust (CD) and Arizona test dust (ATD)) were used. Aerosols were generated both with a wet and a dry disperser and the water uptake was parameterized via the hygroscopicity parameter, κ. The hygroscopicity of dry generated dust aerosols was found to be negligible when compared to processed atmospheric aerosols, with CCNC derived κ values between 0.00 and 0.02. The latter value can be idealized as a particle consisting of 96.7% (by volume) insoluble material and ~3.3% ammonium sulfate. Pure clay aerosols were found to be generally less hygroscopic than real desert dust particles. All illite and montmorillonite samples had κ~0.003, kaolinites were least hygroscopic and had κ=0.001. SD (κ=0.023) was found to be the most hygroscopic dry-generated desert dust followed by CD (κ=0.007) and ATD (κ=0.003). Wet-generated dust showed an increased water uptake when compared to dry-generated samples. This is considered to be an artifact introduced by redistribution of soluble material between the particles while immersed in an aqueous medium during atomization, thus indicating that specification of the generation method is critically important when presenting such data. Any atmospheric processing of fresh mineral dust which leads to the addition of more than ~3% soluble material is expected to significantly enhance hygroscopicity and CCN activity.« less

Lithologic Control on Secondary Clay Mineral Formation in the Valles Caldera, New Mexico

NASA Astrophysics Data System (ADS)

Caylor, E.; Rasmussen, C.; Dhakal, P.

2015-12-01

Understanding the transformation of rock to soil is central to landscape evolution and ecosystem function. The objective of this study was to examine controls on secondary mineral formation in a forested catchment in the Catalina-Jemez CZO. We hypothesized landscape position controls the type of secondary minerals formed in that well-drained hillslopes favor Si-poor secondary phases such as kaolinite, whereas poorly drained portions of the landscape that collect solutes from surrounding areas favor formation of Si-rich secondary phases such as smectite. The study focused on a catchment in Valles Caldera in northern New Mexico where soils are derived from a mix of rhyolitic volcanic material, vegetation includes a mixed conifer forest, and climate is characterized by a mean annual precipitation of ~800 mm yr-1 and mean annual temperature of 4.5°C. Soils were collected at the soil-saprolite boundary from three landscape positions, classified as well drained hillslope, poorly drained convergent area, and poorly drained hill slope. Clay fractions were isolated and analyzed using a combination of quantitative and qualitative x-ray diffraction (XRD) analyses and thermal analysis. Quantitative XRD of random powder mounts indicated the presence of both primary phases such as quartz, and alkali and plagioclase feldspars, and secondary phases that include illite, Fe-oxyhydroxides including both goethite and hematite, kaolinite, and smectite. The clay fractions were dominated by smectite ranging from 36-42%, illite ranging from 21-35%, and kaolinite ranging from 1-8%. Qualitative XRD of oriented mounts confirmed the presence of smectite in all samples, with varying degrees of interlayering and interstratification. In contrast to our hypothesis, results indicated that secondary mineral assemblage was not strongly controlled by landscape position, but rather varied with underlying variation in lithology. The catchment is underlain by a combination of porphorytic rhyolite and hydrothermally altered rhyolitic tuff, with an intrusion of Paleozoic sandstone. Smectite content was generally greater in areas underlain by the tuff and likely represent a combination of both diagenic smectite formed by hydrothermal alteration of volcanic glass and authigenic smectites formed in the soils via chemical weathering.

Hydrothermal alteration of graywacke and basalt by 4 molal NaCl.

USGS Publications Warehouse

Rosenbauer, R.J.; Bischoff, J.L.; Radtke, A.S.

1983-01-01

Rock-water interaction experiments were carried out at 350oC and 500 bar at a 1/10 rock/fluid ratio using 4 molal NaCl brine. Reaction of brine and greywacke lead to the conversion of illite, dolomite and quartz to albite and smectite. In the process, the rock gained Na and released Ca, K, heavy metals and CO2 to solution. Metal mobilization was found to primarily depend on acidity which was produced by Na metasomatism and by dedolomitization. Reaction of brine and basalt produced only minor alteration in which some smectite and little albite formed. No significant acidity was produced nor did metals become mobilized. Production of acidity during albitization depends entirely on the phase being altered. Albitization of greywacke produces H+ whereas the albitization of basalt apparently consumes this ion. -J.E.S.

Aqueous geochemistry on Mars: Possible clues from salts and clays in SNC meteorites

NASA Technical Reports Server (NTRS)

Gooding, James L.

1992-01-01

All subgroups of the shergottite, nakhlite, and chassignite (SNC) meteorites contain traces of water precipitated minerals that include various combinations of carbonates, sulfates, halides, ferric oxides, and aluminosilicate clays of preterrestrial origin. Oxygen three-isotope analysis of thermally extracted bulk water has confirmed that at least some of the water in SNC's is, indeed, extraterrestrial. A mixture of aqueous precipitates found in the SNC's, comprising smectite, illite, and gypsum (with minor halite +/- calcite and hematite), provides a self-consistent, though not unique, model for the bulk elemental composition of surface sediments at the Viking Lander sites. Therefore, if the salts and clays in SNC's are truly linked to aqueous alteration and soil formation on Mars, then the suite of SNC secondary minerals might provide the best currently available insight into near-surface martian chemistry.

Polymerization on the rocks: beta-amino acids and arginine

NASA Technical Reports Server (NTRS)

Liu, R.; Orgel, L. E.; Bada, J. L. (Principal Investigator)

1998-01-01

We have studied the accumulation of long oligomers of beta-amino acids on the surface of minerals using the 'polymerization on the rocks' protocol. We find that long oligopeptides of beta-glutamic acid which cannot be formed in homogeneous aqueous solution are accumulated efficiently on the surface of hydroxylapatite using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide (EDAC) as condensing agent. The EDAC-induced oligomerization of aspartic acid on hydroxylapatite proceeds even more efficiently. Hydroxylapatite can also facilitate the ligation of the tripeptide (glu)3. The 'polymerization on the rocks' scenario is not restricted to negatively-charged amino acids. Oligoarginines are accumulated on the surface of illite using carbonyldiimidizole (CDI) as condensing agent. We find that FeS2 catalyzes the CDI-induced oligomerization of arginine, although it does not adsorb oligoarginines. These results are relevant to the formation of polypeptides on the primitive earth.

Hydrothermal alteration of sediments associated with surface emissions from the Cerro Prieto geothermal field

DOE Office of Scientific and Technical Information (OSTI.GOV)

Valette-Silver, J.N.; Esquer P., I.; Elders, W.A.

1981-01-01

A study of the mineralogical changes associated with these hydrothermal vents was initiated with the aim of developing possible exploration tools for geothermal resources. The Cerro Prieto reservoir has already been explored by extensive deep drilling so that relationships between surface manifestations and deeper hydrothermal processes could be established directly. Approximately 120 samples of surface sediments were collected both inside and outside of the vents. The mineralogy of the altered sediments studied appears to be controlled by the type of emission. A comparison between the changes in mineralogy due to low temperature hydrothermal activity in the reservoir, seen in samplesmore » from boreholes, and mineralogical changes in the surface emission samples shows similar general trends below 180 C: increase of quartz, feldspar and illite, with subsequent disappearance of kaolinite, montmorillonite, calcite and dolomite. These mineral assemblages seem to be characteristic products of the discharge from high intensity geothermal fields.« less

Hydrogen and oxygen isotope exchange reactions between clay minerals and water

USGS Publications Warehouse

O'Neil, J.R.; Kharaka, Y.K.

1976-01-01

The extent of hydrogen and oxygen isotope exchange between clay minerals and water has been measured in the temperature range 100-350?? for bomb runs of up to almost 2 years. Hydrogen isotope exchange between water and the clays was demonstrable at 100??. Exchange rates were 3-5 times greater for montmorillonite than for kaolinite or illite and this is attributed to the presence of interlayer water in the montmorillonite structure. Negligible oxygen isotope exchange occurred at these low temperatures. The great disparity in D and O18 exchange rates observed in every experiment demonstrates that hydrogen isotope exchange occurred by a mechanism of proton exchange independent of the slower process of O18 exchange. At 350?? kaolinite reacted to form pyrophyllite and diaspore. This was accompanied by essentially complete D exchange but minor O18 exchange and implies that intact structural units in the pyrophyllite were inherited from the kaolinite precursor. ?? 1976.

Synthesis of long Prebiotic Oligomers on Mineral Surfaces

NASA Technical Reports Server (NTRS)

Ferris, James P.; Hill, Aubrey R., Jr.; Liu, Rihe; Orgel, Leslie E.

1996-01-01

Most theories of the origin of biological organization assume that polymers with lengths in the range of 30-60 monomers are needed to make a genetic system viable. But it has not proved possible to synthesize plausibly prebiotic polymers this long by condensation in aqueous solution, because hydrolysis competes with polymerization. The potential of mineral surfaces to facilitate prebiotic polymerization was pointed out long ago. Here we describe a system that models prebiotic polymerization by the oligomerization of activated monomers -both nucleotides and amino acids. We find that whereas the reactions in solution produce only short oligomers (the longest typically being a 10-mer), the presence of mineral surfaces (montmorillonite for nucleotides, illite and hydroxylapatite for amino adds) induces the formation of oligomers up to 55 monomers long. These are formed by successive "feedings" with the monomers; polymerization takes place on the mineral surfaces in a manner akin to solid-phase synthesis of biopolymers.

Soda Creek springs - metamorphic waters in the eastern Alaska Range

USGS Publications Warehouse

Richter, D.H.; Donaldson, D.E.; Lamarre, R.A.

1973-01-01

The Soda Creek springs are a group of small, cold mineral springs on the southern flank of the eastern Alaska Range. The spring waters contain anomalous concentrations of carbon dioxide, sodium, chlorine, sulfate, boron, and ammonia and are actively precipitating deposits of calcite and aragonite. Sparingly present in these deposits are mixed-layer illite-montmorillonite clays and zeolite minerals. Low-temperaturemetamorphic reactions in subjacent marine sedimentary rocks of Jurassic and Cretaceous age may have produced the fluids and silicate minerals. With only a few exceptions, cool bicarbonate-rich springs in Alaska are concentrated south of the Denali fault system in south-central Alaska, southeastern Alaska, and along the Kaltag-Tintina fault system. These areas are characterized by active or recently activetectonism, major faults and folds, and an abundance of marine sedimentary rocks.

Methods for enhancing mapping of thermal fronts in oil recovery

DOEpatents

Lee, David O.; Montoya, Paul C.; Wayland, Jr., James R.

1987-01-01

A method for enhancing the resistivity contrasts of a thermal front in an oil recovery production field as measured by the CSAMT technique is disclosed. This method includes the steps of: (a) preparing a CSAMT-determined topological resistivity map of the production field; (b) introducing a solution of a dopant material into the production field at a concentration effective to alter the resistivity associated with the thermal front; said dopant material having a high cation exchange capacity which might be selected from the group consisting of montmorillonite, illite, and chlorite clays; said material being soluble in the connate water of the production field; (c) preparing a CSAMT-determined topological resistivity map of the production field while said dopant material is moving therethrough; and (d) mathematically comparing the maps from step (a) and step (c) to determine the location of the thermal front. This method is effective with the steam flood, fire flood and water flood techniques.

A study of the hydrothermal alteration in Paleoproterozoic volcanic centers, São Félix do Xingu region, Amazonian Craton, Brazil, using short-wave infrared spectroscopy

NASA Astrophysics Data System (ADS)

da Cruz, Raquel Souza; Fernandes, Carlos Marcello Dias; Villas, Raimundo Netuno Nobre; Juliani, Caetano; Monteiro, Lena Virgínia Soares; de Almeida, Teodoro Isnard Ribeiro; Lagler, Bruno; de Carvalho Carneiro, Cleyton; Misas, Carlos Mario Echeverri

2015-10-01

Hypogene hydrothermal minerals have been identified by short-wave infrared spectroscopy in hydrothermally altered rocks from the Sobreiro and Santa Rosa formations, which belong to a Paleoproterozoic volcano-plutonic system in Amazonian craton. Three clay minerals are spectrally recognized: montmorillonite, kaolinite, and illite. The integration of these data with those available in the literature, including gold occurrences, suggests that those rocks are hydrothermal products of both volcanic thermal sources and later crustal intrusions, as evidenced by variable styles of propylitic, sericitic, potassic, and intermediate argillic alteration. The influence of meteoric fluids is emphasized. This low cost exploratory technique, which can be applied to hand samples, seems to be promising in the separation of hydrothermally altered volcano-plutonic centers in regions submitted to severe weathering conditions, in addition to aid elaborating models for prospecting mineral deposits.

Impact of Adsorption on Gas Transport in Nanopores.

PubMed

Wu, Tianhao; Zhang, Dongxiao

2016-03-29

Given the complex nature of the interaction between gas and solid atoms, the development of nanoscale science and technology has engendered a need for further understanding of gas transport behavior through nanopores and more tractable models for large-scale simulations. In the present paper, we utilize molecular dynamic simulations to demonstrate the behavior of gas flow under the influence of adsorption in nano-channels consisting of illite and graphene, respectively. The results indicate that velocity oscillation exists along the cross-section of the nano-channel, and the total mass flow could be either enhanced or reduced depending on variations in adsorption under different conditions. The mechanisms can be explained by the extra average perturbation stress arising from density oscillation via the novel perturbation model for micro-scale simulation, and approximated via the novel dual-region model for macro-scale simulation, which leads to a more accurate permeability correction model for industrial applications than is currently available.

Clay mineral type effect on bacterial enteropathogen survival in soil.

PubMed

Brennan, Fiona P; Moynihan, Emma; Griffiths, Bryan S; Hillier, Stephen; Owen, Jason; Pendlowski, Helen; Avery, Lisa M

2014-01-15

Enteropathogens released into the environment can represent a serious risk to public health. Soil clay content has long been known to have an important effect on enteropathogen survival in soil, generally enhancing survival. However, clay mineral composition in soils varies, and different clay minerals have specific physiochemical properties that would be expected to impact differentially on survival. This work investigated the effect of clay materials, with a predominance of a particular mineral type (montmorillonite, kaolinite, or illite), on the survival in soil microcosms over 96 days of Listeria monocytogenes, Salmonella Dublin, and Escherichia coli O157. Clay mineral addition was found to alter a number of physicochemical parameters in soil, including cation exchange capacity and surface area, and this was specific to the mineral type. Clay mineral addition enhanced enteropathogen survival in soil. The type of clay mineral was found to differentially affect enteropathogen survival and the effect was enteropathogen-specific. © 2013.

Numerical modeling of the impact of temperature on the behavior of minerals in the Soultz-sous-Forêts enhanced geothermal system

NASA Astrophysics Data System (ADS)

Van Ngo, Viet; Lucas, Yann; Clément, Alain; Fritz, Bertrand

2015-04-01

Operation of the enhanced geothermal system (EGS) requires to re-inject fluid, after heat exchange at the surface to the energy production, into the geothermal reservoir. This cold re-injected fluid can cause a strong disequilibrium with the fluid and granitic rock within the geothermal reservoir and then implies the possible dissolution/precipitation of minerals. The hydrothermal alterations include the transformation of plagioclase, biotite and K-feldspar and the precipitation of various secondary minerals. The major sealing phases observed in the main fracture zones are quartz, calcite, and clay minerals. These mineralogical transformations may modify the porosity, permeability and fluid pathways of the geothermal reservoir. In the Soultz-sous-Forêts EGS (Alsace, France), the hydraulic connection between the injection well and the production well is quite poor. Therefore, understanding the impact of changes in temperature, which are caused by the re-injected fluid, on the behavior of minerals (especially for the main newly-formed minerals such as quartz, calcite and clay minerals) is a critical preliminary step for the long-term prediction of their evolution. The approach used in the present work is typically based on a geochemical code, called THERMA, which enables to calculate the changes in equilibrium constants of all primary and secondary minerals and aqueous species as a function of temperature. Our model accounted for a wide range of different mineral groups in order to make sure a large freedom for the numerical calculations. The modeling results showed that when the temperature of geothermal reservoir is cooled down, quartz, calcite, illites, galena and pyrite have tendency towards equilibrium state, which indicates that they are precipitated under the geothermal conditions. In contrast, other minerals including plagioclase, K-feldspar and biotite remained unsaturated. These behaviors of minerals were further illustrated by the Khorzinsky stability diagrams, which are based on the activities of different species such as H4SiO4, Ca2+, Mg2+, and Al3+ and take into account partial CO2 pressure,. The modeling results further suggested that we should pay a special attention to the main minerals (e.g., quartz, calcite and illites) when studying the changes in porosity and permeability of the geothermal reservoir. This study was preparing a simulation of water-rock interaction processes related to these temperature conditions.

Heteroaggregation of Silver Nanoparticles with Clay Minerals in Aqueous System

NASA Astrophysics Data System (ADS)

Liu, J.; Burrow, E.; Hwang, Y.; Lenhart, J.

2013-12-01

Nanoparticles are increasingly being used in industrial processes and consumer products that exploit their beneficial properties and improve our daily lives. Nevertheless, they also attract attention when released into natural environment due to their potential for causing adverse effects. The fate and transport of nanoparticles in aqueous systems have been the focus of intense study. However, their interactions with other natural particles have received only limited attention. Clay minerals are ubiquitous in most aquatic systems and their variably charged surfaces can act as deposition sites that can alter the fate and transport of nanoparticles in natural aqueous environments. In this study, we investigated the homoaggregation of silver nanoparticles with different coating layers and their heteroaggregation behavior with clay minerals (illite, kaolinite, montmorillonite) in neutral pH solutions. Silver nanoparticles with a nominal diameter of 80 nm were synthesized with three different surface coating layers: uncoated, citrate-coated and Tween-coated. Illite (IMt-2), kaolinite (KGa-2), and montmorillonite (SWy-2) were purchased from the Clay Mineral Society (Indiana) and pretreated to obtain monocationic (Na-clay) and dicationic (Ca-clay) suspensions before the experiments. The change in hydrodynamic diameter as a function of time was monitored using dynamic light scattering (DLS) measurements in order to evaluate early stage aggregation as a function of electrolyte concentration in both the homo- and heteroaggregation scenarios. A shift in the critical coagulation concentration (CCC) values to lower electrolyte concentrations was observed in binary systems, compared to single silver nanoparticle and clay systems. The results also suggest more rapid aggregation in binary system during the early aggregation stage when compared to the single-particle systems. The behavior of citrate-coated silver nanoparticles was similar to that of the bare particles, while the Tween-coated silver nanoparticles showed high stability in both single and binary systems. There were no significant differences in early stage aggregation kinetics observed inthe Na-clay-nanoparticle or Ca-clay-nanoparticle systems, which suggested that the CCC values of the single Na- or Ca-clay suspensions depend only on the electrolyte concentration, not the original cations on the clay surface. These results provide a basic idea for understanding the heteroaggregation of different silver nanoparticles and clays, which can be utilized in further study of fate and transport of engineered nanoparticles in natural aqueous system.

Practical characterization of eolian reservoirs for development: Nugget Sandstone, Utah—Wyoming thrust belt

NASA Astrophysics Data System (ADS)

Lindquist, Sandra J.

1988-04-01

The Jurassic eolian Nugget Sandstone of the Utah-Wyoming thrust belt is a texturally heterogeneous formation with anisotropic reservoir inherited primarily from the depositional environment. Original reservoir quality has been reduced somewhat by cementation and slightly enhanced by dissolution. Low-permeability, gouge-filled micro-faults compartmentalize the formation, whereas intermittently open fractures provide effective permeability paths locally. Where productive, the Nugget Sandstone ranges from approximately 800 to 1050 ft (244-320 m) thick at subsurface depths of 7500 to 15,000 ft (2286-4572 m). Porosity ranges from several percent to 25%, and permeability covers five orders of magnitude from hundredths of milliDarcies to Darcies. Some Nugget reservoirs are fully charged with hydrocarbons. Different stratification types have unique depositional textures, primary and diagenetic mineralogies, and deformational fabrics resulting in characteristic porosity, permeability, permeability directionality, and pore geometry attributes. Such characteristics can be determined from core analysis, mercury injection, nuclear magnetic resonance, conventional log, dipmeter and production data. Nugget dune deposits (good reservoir facies) primarily consist of grainflow and wind-ripple cross-strata, the former of which have the better reservoir quality and the lesser heterogeneity in bedding texture. High-permeability facies are commonly affected by local quartz and nodular carbonate cementation, chlorite (and lesser illite) precipitation, and minor framework and cement dissolution. Gouge-filled micro-faults are the predominant deformational overprint. Interdune, sand-sheet, and other water-associated deposits (poor reservoir facies) are characterized by low-angle wind-ripple laminae and more irregular bedding, some of which is associated with damp or wet conditions. Water-associated Nugget stratification generally contains the finest grained depositional textures and has the poorest reservoir properties. These non-dune facies contain intergranular micritic carbonate and illite precipitates and are most affected by compaction and pressure solution phenomena. Open types of fractures are somewhat more likely in this lower permeability rock. Depositional models incorporating dune morphologies, facies distribution, permeability directionality, and theoretical concepts regarding dune migration through time are useful in delineating correlative intervals most likely to have continuity and potential communication of reservoir properties. Stratigraphic models can be adapted for reservoir simulation studies and also can be utilized in solving structural resolution problems if correlatable vertical sequences and relatively consistent cross-strata orientations exist.

Evolution of Continental Environments and Chemical Weathering in the Western Himalayan Foreland Basin since 11 Ma

NASA Astrophysics Data System (ADS)

Zhou, P.; Clift, P. D.; Murray, R. W.; Blusztajn, J.; Ireland, T. J.; Feakins, S. J.; Liddy, H.

2017-12-01

The Asian monsoon is the dominant climatic phenomena in Southwest Asia and as the primary source of moisture is one of the major controls over the processes of chemical weathering, especially in the Himalayan foreland basin. The sedimentary records of the eastern Arabian Sea mostly reflect the evolving erosion and chemical weathering processes in the source mountains and foreland basin, with limited input from peninsular India. Analysis of the geochemistry of sediments from International Ocean Discovery Program (IODP) Sites U1456 and U1457 allow us to investigate how chemical weathering may relate to evolving environments and the intensity of the precipitation in the Indus catchment since 11 Ma. We employed X-ray diffraction methods to quantify clay mineral assemblages from the core samples of these two sites. kaolinite/(chlorite+illite) and illite crystallinity show a general long-term trend towards less chemical weathering from 10 Ma to 5 Ma. Meanwhile, the high-resolution hematite/goethite records were acquired from visible diffuse reflectance spectrophotometry from both Sites U1457 and U1456 show a general increase in hematite/goethite, This may represent a long-term drying of the climate and/or an increase in seasonality since 10 Ma, consistent with the long-term trend in carbon isotope values known from the Siwalik Group of the Himalayan foreland. In particular, there is an increase in the relative portion of hematite starting at 8.2 Ma with a subsequent decrease at 6.7 Ma, and a further notable increase after 5.7 Ma. Bulk sediment geochemistry allows us to calculate the Chemical Index of Alteration (CIA) as well other geochemical indices such as K/Al. Both these proxies indicate a strong decrease in chemical weathering intensity at 8.2 Ma, followed by a rapid increase in the degree of alteration after 7.8 Ma followed by a gradual decrease until 6.6 Ma. In general, drier/more seasonal conditions are associated with less chemical weathering over this critical transition. Sedimentary provenance does not drive the variations in weathering indices across most of the record. We therefore interpret the degree of chemical weathering in the floodplains of the Indus River as a record of changing monsoon precipitation (amount and seasonality) within the Indus catchment.

Environment and Climate Changes during the Holocene: Inferred from Sedimentary Record/Proxies of a Paleodelta Region, Southwest Coast of India

NASA Astrophysics Data System (ADS)

Allu, N. C.; Prakash, V.; Gautam, P. K.; Bera, S. K.

2014-12-01

This work explains the sedimentation history and environment and climate changes during the Holocene along the southwest coast of India. The area is characterized by various landforms such as lagoons, barrier islands, beach ridges, paleostrandlines, alluvial plains, marshy lands and flood plains. Paleodelta, located at the mouth of the modern Periyar River is an important geomorphic marker. A borehole of 40 m depth was drilled in the paleodelta and sediment samples were recovered at different depth intervals. Paleoclimate and paleo-environment were inferred based on geochronology, textural and geotechnical parameters, clay minerals, and pollen analysis results. The bottom of the borehole represents an age of ~ 12 ka BP. Sediments exhibit coarsening texture upwards of the borehole, with fine mud and peat intercalations at the bottom. Six litho facies - muddy sand, sand, sandy mud, silty sand, sandy silt, and mud - were recorded. Geotechnical properties comprising moisture content, organic carbon, plasticity index record high values, whereas low bulk density associated with a low critical shear stress, are recorded. An increase in illite and to a lesser degree smectite with concomitant decrease in kaolinite is observed. Sediment texture represents a major change of depositional environment from marine to fluvial sedimentary facies during the major sea level fall i.e., after 7 ka B.P. The present sea level attained during 4-5 ka B.P; major rise of sea level has taken place from 7-11 ka BP and regression during 7 - 5 ka B.P. These transgression and regression phases introduced the changes in the environment of deposition. The monsoon was dynamic and more intense after the major fall of sea level causing the fluctuations in the fluvial facies. Upward coarsening of grain size in the borehole indicates change in sediment deposition due to increased hydrodynamic conditions and strong fluvial action, which can be linked to marine regression. Geotechnical properties suggest textural changes and sedimentary facies. An upward increase in smectite and kaolinite and decreasing illite supports major fall in sea level and also the aridity. Pollen record of sediment strata supports the paleo-environment dominated by the presence of semi-evergreen type of mangrove plants during mid- to early-Holocene times.

On the origin of mixed-layered clay minerals from the San Andreas Fault at 2.5-3 km vertical depth (SAFOD drillhole at Parkfield, California)

NASA Astrophysics Data System (ADS)

Schleicher, A. M.; Warr, L. N.; van der Pluijm, B. A.

2009-02-01

A detailed mineralogical study is presented of the matrix of mudrocks sampled from spot coring at three key locations along the San Andreas Fault Observatory at depth (SAFOD) drill hole. The characteristics of authigenic illite-smectite (I-S) and chlorite-smectite (C-S) mixed-layer mineral clays indicate a deep diagenetic origin. A randomly ordered I-S mineral with ca. 20-25% smectite layers is one of the dominant authigenic clay species across the San Andreas Fault zone (sampled at 3,066 and 3,436 m measured depths/MD), whereas an authigenic illite with ca. 2-5% smectite layers is the dominant phase beneath the fault (sampled at 3,992 m MD). The most smectite-rich mixed-layered assemblage with the highest water content occurs in the actively deforming creep zone at ca. 3,300-3,353 m (true vertical depth of ca. 2.7 km), with I-S (70:30) and C-S (50:50). The matrix of all mudrock samples show extensive quartz and feldspar (both plagioclase and K-feldspar) dissolution associated with the crystallization of pore-filling clay minerals. However, the effect of rock deformation in the matrix appears only minor, with weak flattening fabrics defined largely by kinked and fractured mica grains. Adopting available kinetic models for the crystallization of I-S in burial sedimentary environments and the current borehole depths and thermal structure, the conditions and timing of I-S growth can be evaluated. Assuming a typical K+ concentration of 100-200 ppm for sedimentary brines, a present-day geothermal gradient of 35°C/km and a borehole temperature of ca. 112°C for the sampled depths, most of the I-S minerals can be predicted to have formed over the last 4-11 Ma and are probably still in equilibrium with circulating fluids. The exception to this simple burial pattern is the occurrence of the mixed layered phases with higher smectite content than predicted by the burial model. These minerals, which characterize the actively creeping section of the fault and local thin film clay coating on polished brittle slip surfaces, can be explained by the influence of either cooler fluids circulating along this segment of the fault or the flow of K+-depleted brines.

Clay minerals trap hydrogen in the Earth's crust: Evidence from the Cigar Lake uranium deposit, Athabasca

NASA Astrophysics Data System (ADS)

Truche, Laurent; Joubert, Gilles; Dargent, Maxime; Martz, Pierre; Cathelineau, Michel; Rigaudier, Thomas; Quirt, David

2018-07-01

Hydrogen (H2)-rich fluids are observed in a wide variety of geologic settings including gas seeps in serpentinized ultramafic rocks, sub-seafloor hydrothermal vents, fracture networks in crystalline rocks from continental and oceanic crust, and volcanic gases. Natural hydrogen sources can sustain deep microbial ecosystems, induce abiotic hydrocarbons synthesis and trigger the formation of prebiotic organic compounds. However, due to its extreme mobility and small size, hydrogen is not easily trapped in the crust. If not rapidly consumed by redox reactions mediated by bacteria or suitable mineral catalysts it diffuses through the rocks and migrates toward the surface. Therefore, H2 is not supposed to accumulate in the crust. We challenge this view by demonstrating that significant amount of H2 may be adsorbed by clay minerals and remain trapped beneath the surface. Here, we report for the first time H2 content in clay-rich rocks, mainly composed of illite, chlorite, and kaolinite from the Cigar Lake uranium ore deposit (northern Saskatchewan, Canada). Thermal desorption measurements reveal that H2 is enriched up to 500 ppm (i.e. 0.25 mol kg-1 of rock) in these water-saturated rocks having a very low total organic content (<0.5 wt%). Such hydrogen uptake is comparable and even exceeds adsorbed methane capacities reported elsewhere for pure clay minerals or shales. Sudoite (Al-Mg di-trioctahedral chlorite) is probably the main mineral responsible for H2 adsorption in the present case. The presence of multiple binding sites in interlinked nanopores between crystal layers of illite-chlorite particles offers the ideal conditions for hydrogen sorption. We demonstrate that 4 to 17% of H2 produced by water radiolysis over the 1.4-Ga-lifetime of the Cigar Lake uranium ore deposit has been trapped in the surrounding clay alteration haloes. As a result, sorption processes on layered silicates must not be overlooked as they may exert an important control on the fate and mobility of H2 in the crust. Furthermore, the high capacity of clay minerals to sorb molecular hydrogen may also open up new opportunities for exploration of unexpected energy resources and for H2 storage based on geo-inspired materials.

Adsorption and Desorption of Cesium in Clay Minerals: Effects of Natural Organic Matter and pH

NASA Astrophysics Data System (ADS)

Yoon, Hongkyu; Ilgen, Anastasia; Mills, Melissa; Lee, Moo; Seol, Jeung Gun; Cho, Nam Chan; Kang, Hyungyu

2017-04-01

Cesium (Cs) released into the environment (e.g., Fukushima accident) poses significant environmental concerns and remediation challenges. A majority of Cs in the environment have remained within the surface soils due to the strong adsorption affinity of Cs towards clay minerals. Different clay minerals have different bonding sites, resulting in various adsorption mechanisms at nanometer scale. For example, the illite commonly has a basal spacing of 1.0 nm, but becomes wider to 1.4 nm once other cations exchange with K in the interlayer site. Cs adsorbs into these expanded wedged zone strongly, which can control its mobility in the environment. In addition, natural organic matter (NOM) in the surface soils can interact with clay minerals, which can modify the mechanisms of Cs adsorption on the clay minerals by blocking specific adsorption sites and/or providing Cs adsorption sites on NOM surface. In this work, three representative clay minerals (illite, vermiculite, montmorillonite) and humic acid (HA) are used to systematically investigate the adsorption and desorption behavior of Cs. We performed batch adsorption experiments over a range of Cs concentrations on three clay minerals with and without HA, followed by sequential desorption batch testing. We tested desorption efficiency as a function of initial adsorbed Cs concentration, HA content, sodium concentration, and pH. The sequential extraction results are compared to the structural changes in clay minerals, measured using extended X-ray absorption fine structure spectroscopy (EXAFS) and aberration-corrected (scanning) transmission electron microscopy (TEM) - energy dispersive X-ray spectroscopy (EDX). Hence, this work aims to identify the mechanisms of Cs fixation at the nanometer (or atomic-) scale as a function of the clay mineral properties (e.g. expandability, permanent surface charge) and varying organic matter content at different pH values and to enhance our atomic-scale mechanistic understanding of the clay mineral interactions with cesium in the presence of NOM. The expandability of clay minerals and effect of HA addition on Cs adsorption and desorption are highlighted to address the efficiency of Cs removal schemes from contaminated soils. Sandia National Laboratories is a multi-mission laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-AC04-94AL85000.

Provenance analysis and thermo-dynamic studies of multi-type Holocene duricrusts (1700 BC) in the Sua Salt Pan, NE Botswana

NASA Astrophysics Data System (ADS)

Dill, Harald G.; Dohrmann, R.; Kaufhold, S.; Techmer, A.

2014-08-01

Multi-type duricrusts, composed of silcretes, calcretes, halcretes and sulcretes developed during the Holocene at the northern rim of the Sua Salt Pan, NE Botswana. They were investigated for their light (quartz/chalcedony, feldspar, analcime, clinoptilolite, calcite, kaolinite/halloysite, illite-smectite mixed-layers, halite) and heavy minerals (baryte, clinozoisite-epidote s.s.s., amphibole, corundum, tourmaline, ilmenite, rutile, sphene, kyanite, andalusite, staurolite, garnet, zircon, apatite, monazite, cassiterite, garnet, biotite) using petrographic microscopy, X-ray fluorescence and diffraction analyses, radio-carbon dating, scanning electron microscopy equipped with an EDX-system, cation exchange capacity and infrared spectroscopy. Detrital minerals predominantly derived from the erosion of rocks belonging to the Archaean Basement Complex, the Stormberg Volcanites and the Kalahari sediments. Of particular interest to exploration geologists, geikielite-enriched ilmenite fragments are a hint to kimberlitic pipes. Biodetritus was derived from invertebrates and from vertebrates (fish bones?). A man-made impact on the heavy mineral suite has to be invoked from small fragments of cassiterite fragments that derived from processing of sulfidic and pegmatitic Sn-bearing ore. In the salt-pan-derived duricrusts mainly the aeolian and to a lesser degree fluvial inputs were responsible for the concentration of clasts in these multi-type duricrusts. Moreover, their variegated mineralogy enables us to constrain the physical-chemical regime, prevalently as to the pH and the chemical composition of the major constituents. All duricrusts developed in a self-sufficient chemically closed system where quartz and feldspar provided the elements Si, Na, K, Ca, and Ba to produce the encrustations. The spatial and temporal trend in the Sua Salt Pan rim encrustations may be described as follows: (1) sulcrete-silcretes, (2) silcretes with kaolinite-group minerals towards more recent stages at the rim and smectite-illite mixed-layers and clinoptilolite towards the basin center, (3) calcretes with analcite towards the basin center, (4) halcretes (and soda ash at a more central position). In the sulcrete-silcrete facies the pH decreases from pH 14 down to 4. In the calcretes and halcretes it increases from pH 8 to pH > 13. marking a chemical hiatus between stages 1 plus 2 and stages 3 plus 4. Mineral assemblages forming more basinward tend to have derived from more alkaline fluids than those near the edge of the salt pan.

Reactive alteration of Mt. Simon sandstone during CO2-rich brine injection: A coupled experimental and modeling study

NASA Astrophysics Data System (ADS)

Dávila Ordoñez, M. G.; Zahasky, C.; Crandall, D.; Druhan, J. L.

2017-12-01

Thus far, one million metric tons of CO2 have been injected into the lower Mt. Simon formation as part of the Decatur CO2 Capture and Storage Project. Micro-seismic events were observed within the CO2 plume both during and after pressurization associated with the primary injection. The Mt. Simon reservoir rock consists of 76.5 wt.% quartz, 2.1 wt.% calcite, 17.3 wt.% K-feldspar, 1.1 wt.% chlorite, 0.7 wt.% illite and lesser extents of siderite, kaolinite, dolomite and marcasite, and is thus anticipated to become geochemically altered by exposure to acidified CO2-rich brine. However, the extent to which the geochemical reactivity contributes to structural weakening is unknown. To explore relationships between the principle geochemical reactions, evolution of fluid transport properties and physical alteration, we performed a series of flow-through experiments using Mt. Simon core (5 cm diameter, ranging from 4.3 - 8.6 cm length) and fluids representative of acidified reservoir brine. Experiments were operated under P = 1450 bar, Pconfining = 1900 - 3000 bar and T = 53 ºC conditions, and flow rates varied from 0.08 to 5.00 mL h-1 over a period of 166 h. A 2D reactive transport code (Crunch-Tope) was used to simulate these experiments, constrained by measured time series aqueous concentrations of Ca, Mg, S, Si, K and Fe and pH during the CO2-rich brine interaction. The model domain was divided into 30 nodes in x at a spacing of 0.12 cm, and 40 nodes in y at a spacing of 0.22 cm, and initial permeability measured for the core was specified and allowed to evolve over the course of the simulation using measured flow rate as a constraint. All relevant kinetic and thermodynamic reaction parameters were obtained from the literature. Solute time series from both experiments and simulations indicated that the acidified brine introduced continuously into the column promoted dissolution of K-feldspar, chloride, illite, pyrite and calcite, and the precipitation of Ca-, Fe- and Si -bearing secondary phases, resulting in a net porosity increase at the inlet. Despite this opening of the inlet pore space, permeability decreased over the length of the column (kfinal/kinitial = 0.76), thus altering local resistance to fluid phase pressure gradients.

How the Assumed Size Distribution of Dust Minerals Affects the Predicted Ice Forming Nuclei

NASA Technical Reports Server (NTRS)

Perlwitz, Jan P.; Fridlind, Ann M.; Garcia-Pando, Carlos Perez; Miller, Ron L.; Knopf, Daniel A.

2015-01-01

The formation of ice in clouds depends on the availability of ice forming nuclei (IFN). Dust aerosol particles are considered the most important source of IFN at a global scale. Recent laboratory studies have demonstrated that the mineral feldspar provides the most efficient dust IFN for immersion freezing and together with kaolinite for deposition ice nucleation, and that the phyllosilicates illite and montmorillonite (a member of the smectite group) are of secondary importance.A few studies have applied global models that simulate mineral specific dust to predict the number and geographical distribution of IFN. These studies have been based on the simple assumption that the mineral composition of soil as provided in data sets from the literature translates directly into the mineral composition of the dust aerosols. However, these tables are based on measurements of wet-sieved soil where dust aggregates are destroyed to a large degree. In consequence, the size distribution of dust is shifted to smaller sizes, and phyllosilicates like illite, kaolinite, and smectite are only found in the size range 2 m. In contrast, in measurements of the mineral composition of dust aerosols, the largest mass fraction of these phyllosilicates is found in the size range 2 m as part of dust aggregates. Conversely, the mass fraction of feldspar is smaller in this size range, varying with the geographical location. This may have a significant effect on the predicted IFN number and its geographical distribution.An improved mineral specific dust aerosol module has been recently implemented in the NASA GISS Earth System ModelE2. The dust module takes into consideration the disaggregated state of wet-sieved soil, on which the tables of soil mineral fractions are based. To simulate the atmospheric cycle of the minerals, the mass size distribution of each mineral in aggregates that are emitted from undispersed parent soil is reconstructed. In the current study, we test the null-hypothesis that simulating the presence of a large mass fraction of phyllosilicates in dust aerosols in the size range 2 m, in comparison to a simple model assumption where this is neglected, does not yield a significant effect on the magnitude and geographical distribution of the predicted IFN number. Results from sensitivity experiments are presented as well.

Sequence-stratigraphic controls on sandstone diagenesis: An example from the Williams Fork formation, Piceance Basin, Colorado

NASA Astrophysics Data System (ADS)

Aboktef, Adel

This study documents the distribution of diagenetic alterations in Williams Fork fluvial sandstones, assess sequence stratigraphic controls on diagenetic features, and addresses diagenetic impacts on porosity. Petrographic point counts of 220 thin sections from six wells forms the database. The near absence of potassium feldspar and volcanic rock fragments in the lower Williams Fork interval and increasing plagioclase content upward represent changes in sediment provenance rather than stratigraphic variability in diagenesis. The lower Williams Fork sands are from sedimentary sources whereas middle and upper Williams Fork sands include input from magmatic arcs and basement uplifts. Compaction, early and late cementation, dissolution, and replacement by calcite or clay minerals combined to alter Williams Fork sandstones. Infiltration of clays occurred prior to any burial. Chlorite, quartz, non-ferroan calcite, compaction and dissolution features, and kaolinite formed during eo-diagenesis at <70°C. More quartz, compaction and dissolution features, plus albite, illite, mixed-layer illite/smectite, ferroan calcite, and dolomite formed in the meso-diagenetic realm (>70°C). Four of these features show spatial variability with respect to systems tracts. Infiltrated clays are concentrated in lowstand systems tracts (LST) and highstand systems tracts (HST) because accommodation space rose slow or fell during deposition of those sands, which led to prolonged sand body exposure on floodplain and ample opportunities for downward percolation of mud during flood events. Concentration of pseudomatrix (mud intraclasts) in HST and LST deposits resulted from floodplain erosion when base-level fell with decreasing accommodation space. Authigenic chlorite formed in the HST and transgressive systems tracts (TST) of the upper half of the Williams Fork Formation because volcanic clasts are abundant in that interval. Quartz overgrowths are more likely to exceed 7% in TST deposits for reasons that are unknown. High total clay content (infiltrated, grain coatings, pseudomatrix) does inhibit quartz overgrowths in all systems tracts. Williams Fork sandstones form low-permeability tight-gas reservoirs. Primary porosity was almost entirely destroyed by compaction and cementation. Reservoir rock resulted from one of two pathways. Eogenetic authigenic chlorite and/or calcite inhibited quartz cementation, minimized compaction and protected some primary porosity. Alternately, dissolution of framework grains or cements created secondary porosity. The later pathway tends to be the more dominant.

Thermal Expansivity Between 150 and 800°C of Hydrothermally Altered Conduit Dyke Samples from USDP-4 Drill Core (Mt Unzen, Shimabara, Japan)

NASA Astrophysics Data System (ADS)

Yilmaz, T. I.; Hess, K. U.; Vasseur, J.; Wadsworth, F. B.; Gilg, H. A.; Nakada, S.; Dingwell, D. B.

2017-12-01

When hot magma intrudes the crust, the surrounding rocks expand. Similarly, the cooling magma contracts. The expansion and contraction of these multiphase materials is not simple and often requires empirical constraint. Therefore, we constrained the thermal expansivity of Unzen dome and conduit samples using a NETZSCH® DIL 402C. Following experiments, those samples were scanned using a Phoenix v|tome|x m to observe the cracks that may have developed during the heating and cooling. The dome samples do not show petrological or chemical signs of alteration. However, the alteration of the conduit dykes is represented by the occurrence of the main secondary phases such as chlorite, sulfides, carbonates, R1 (Reichweite parameter) illite-smectite, and kaolinite. These alteration products indicate an (I) early weak to moderate argillic magmatic alteration, and a (II) second stage weak to moderate propylitic hydrothermal alteration. The linear thermal expansion coefficient aL of the dome material is K-1 between 150° and 800°C and shows a sharp peak of up to K-1 around the alpha-beta-quartz-transition ( 573°C). In contrast, aL of the hydrothermally altered conduit samples starts to increase around 180° and reaches K-1 at 400°C. We interpret this effect as being due to the water content of the kaolinite and the R1 illite-smectite, which induces larger expansions per degree temperature change. Furthermore, the altered conduit samples show a more pronounced increases of aL between 500 and 650°C of up to peaks at K-1, which is generated by the breakdown of chlorite, iron-rich dolomite solid solutions, calcite, and pyrite. We use a 1D conductive model of heat transfer to explore how the country rock around the Unzen conduit zone would heat up after intrusion. In turn, we convert these temperature profiles to thermal stress profiles, assuming the edifice is largely undeformable. We show that these high linear thermal expansion coefficients of the hydrothermally altered conduit rocks may large induce thermal stresses in the surrounding host rock and therefore promotes cracking, which may in turn lead to edifice instability.

Microbe-Clay Mineral Reactions and Characterization Techniques

NASA Astrophysics Data System (ADS)

Dong, H.; Zhang, G.; Ji, S.; Jaisi, D.; Kim, J.

2008-12-01

Clays and clay minerals are ubiquitous in soils, sediments, and sedimentary rocks. They play an important role in environmental processes such as nutrient cycling, plant growth, contaminant migration, organic matter maturation, and petroleum production. The changes in the oxidation state of the structural iron in clay minerals, in part, control their physical and chemical properties in natural environments, such as clay particle flocculation, dispersion, swelling, hydraulic conductivity, surface area, cation and anion exchange capacity, and reactivity towards organic and inorganic contaminants. The structural ferric iron [Fe(III)] in clay minerals can be reduced either chemically or biologically. Many different chemical reductants have been tried, but the most commonly used agent is dithionite. Biological reductants are bacteria, including dissimilatory iron reducing prokaryotes (DIRP) and sulfate-reducing bacteria (SRB). A wide variety of DIRP have been used to reduce ferric iron in clay minerals, including mesophilic, thermophilic, and hyperthermophilic prokaryotes. Multiple clay minerals have been used for microbial reduction studies, including smectite, nontronite (iron-rich smectite variety), illite, illite/smectite, chlorite, and their various mixtures. All these clay minerals are reducible by microorganisms under various conditions with smectite (nontronite) being the most reducible. The reduction extent and rate of ferric iron in clay minerals are measured by wet chemistry, and the reduced clay mineral products are typically characterized with chemical methods, X-ray diffraction, scanning and transmission electron microscopy, Mössbauer spectroscopy, Fourier Transform Infrared Spectroscopy (FTIR), UV-vis spectroscopy, and synchrotron-based techniques (such as EXAFS). Microbially reduced smectites (nontronites) have been found to be reactive in reducing a variety of organic and inorganic contaminants. Degradable organic contaminants include pesticides, solvents, explosives, and nitroaromatic and polychlorinated compounds. Inorganic contaminants include Cr(VI), U(VI), and Tc(VII). Despite significant efforts, our understanding of mechanisms of chemical and microbial reduction of ferric iron in clay minerals is still limited. While some studies have presented evidence for a solid-state reduction mechanism, others argue that the clay mineral structure dissolves when the extent of reduction is higher (greater than 30 percent). The electron transfer process is also dependent on the reducing agent. While chemical reduction of ferric iron appears to occur at the basal surfaces, bacteria appear to attack clay minerals at the edges.

Automation and heat transfer characterization of immersion mode spectroscopy for analysis of ice nucleating particles

NASA Astrophysics Data System (ADS)

Beall, Charlotte M.; Stokes, M. Dale; Hill, Thomas C.; DeMott, Paul J.; DeWald, Jesse T.; Prather, Kimberly A.

2017-07-01

Ice nucleating particles (INPs) influence cloud properties and can affect the overall precipitation efficiency. Developing a parameterization of INPs in global climate models has proven challenging. More INP measurements - including studies of their spatial distribution, sources and sinks, and fundamental freezing mechanisms - must be conducted in order to further improve INP parameterizations. In this paper, an immersion mode INP measurement technique is modified and automated using a software-controlled, real-time image stream designed to leverage optical changes of water droplets to detect freezing events. For the first time, heat transfer properties of the INP measurement technique are characterized using a finite-element-analysis-based heat transfer simulation to improve accuracy of INP freezing temperature measurement. The heat transfer simulation is proposed as a tool that could be used to explain the sources of bias in temperature measurements in INP measurement techniques and ultimately explain the observed discrepancies in measured INP freezing temperatures between different instruments. The simulation results show that a difference of +8.4 °C between the well base temperature and the headspace gas results in an up to 0.6 °C stratification of the aliquot, whereas a difference of +4.2 °C or less results in a thermally homogenous water volume within the error of the thermal probe, ±0.2 °C. The results also show that there is a strong temperature gradient in the immediate vicinity of the aliquot, such that without careful placement of temperature probes, or characterization of heat transfer properties of the water and cooling environment, INP measurements can be biased toward colder temperatures. Based on a modified immersion mode technique, the Automated Ice Spectrometer (AIS), measurements of the standard test dust illite NX are reported and compared against six other immersion mode droplet assay techniques featured in Hiranuma et al. (2015) that used wet suspensions. AIS measurements of illite NX INP freezing temperatures compare reasonably with others, falling within the 5 °C spread in reported spectra. The AIS as well as its characterization of heat transfer properties allows higher confidence in accuracy of freezing temperature measurement, allows higher throughput of sample analysis, and enables disentanglement of the effects of heat transfer rates on sample volumes from time dependence of ice nucleation.

Impacts on seafloor geology of drilling disturbance in shallow waters.

PubMed

Corrêa, Iran C S; Toldo, Elírio E; Toledo, Felipe A L

2010-08-01

This paper describes the effects of drilling disturbance on the seafloor of the upper continental slope of the Campos Basin, Brazil, as a result of the project Environmental Monitoring of Offshore Drilling for Petroleum Exploration--MAPEM. Field sampling was carried out surrounding wells, operated by the company PETROBRAS, to compare sediment properties of the seafloor, including grain-size distribution, total organic carbon, and clay mineral composition, prior to drilling with samples obtained 3 and 22 months after drilling. The sampling grid used had 74 stations, 68 of which were located along 7 radials from the well up to a distance of 500 m. The other 6 stations were used as reference, and were located 2,500 m from the well. The results show no significant sedimentological variation in the area affected by drilling activity. The observed sedimentological changes include a fining of grain size, increase in total organic carbon, an increase in gibbsite, illite, and smectite, and a decrease in kaolinite after drilling took place.

Polymerization on the rocks: theoretical introduction

NASA Technical Reports Server (NTRS)

Orgel, L. E.; Bada, J. L. (Principal Investigator)

1998-01-01

It is difficult if not impossible to synthesize long polymers of amino acids, nucleotides, etc., in homogeneous aqueous solution. We suggest that long polymers were synthesized on the surface of minerals in a prebiotic process analogous to solid-phase synthesis. Provided that the affinity of a mineral for an oligomer increases with the length of the oligomer, adsorption must become essentially irreversible for sufficiently long oligomers. Irreversibly adsorbed oligomers may be elongated indefinitely by repeated cycles in which the mineral with its adsorbed oligomers is first incubated with activated monomers and then washed free of deactivated monomer and side-products. We discuss in some detail the formation of oligomers of negatively-charged amino acids such as glutamic acid on anion-exchange minerals such as hydroxylapatite or illite. We show that the average length of adsorbed oligomers at steady state, n, depends on the balance between the rate of chain elongation and the rate of hydrolysis, and we derive a very approximate formula for n.

Fault dating in the Canadian Rocky Mountains: Evidence for late Cretaceous and early Eocene orogenic pulses

USGS Publications Warehouse

van der Pluijm, B.A.; Vrolijk, P.J.; Pevear, D.R.; Hall, C.M.; Solum, J.

2006-01-01

Fault rocks from the classic Rocky Mountain foreland fold-and-thrust belt in south-western Canada were dated by Ar analysis of clay grain-size fractions. Using X-ray diffraction quantification of the detrital and authigenic component of each fraction, these determinations give ages for individual faults in the area (illite age analysis). The resulting ages cluster around 72 and 52 Ma (here called the Rundle and McConnell pulses, respectively), challenging the traditional view of gradual forward progression of faulting and thrust-belt history of the area. The recognition of spatially and temporally restricted deformation episodes offers field support for theoretical models of critically stressed wedges, which result in geologically reasonable strain rates for the area. In addition to regional considerations, this study highlights the potential of direct dating of shallow fault rocks for our understanding of upper-crustal kinematics and regional tectonic analysis of ancient orogens. ?? 2006 Geological Society of America.

Analysis of 19th century ceramic fragments excavated from Pirenópolis (Goiás, Brazil) using FT-IR, Raman, XRF and SEM

NASA Astrophysics Data System (ADS)

Freitas, Renato P.; Coelho, Filipe A.; Felix, Valter S.; Pereira, Marcelo O.; de Souza, Marcos André Torres; Anjos, Marcelino J.

2018-03-01

This study used Raman, FT-IR and XRF spectroscopy and SEM to analyze ceramic fragments dating from the 19th century, excavated from an old farm in the municipality of Pirenópolis, Goiás, Brazil. The results show that the samples were produced in an open oven at a firing temperature below 500 °C, using raw materials including kaolinite, hematite, magnetite, quartz, microcline, albite, anhydrite, calcite, illite, orthoclase and MnO2. Although the analyses showed similarities in the manufacturing process and the presence of many minerals was common in all samples, multivariate statistical methods (PCA) allowed a more detailed assessment of similarities and differences in the mineral composition of the samples. The results of the PCA showed that the samples excavated in one of the slave quarters (senzalas) group with those excavated at the farmhouse, where the landowner lived, which indicates a paternalistic attitude towards captives, including the sharing of ceramic materials of everyday use.

Frictional melting of clayey gouge during seismic fault slip: Experimental observation and implications

NASA Astrophysics Data System (ADS)

Han, Raehee; Hirose, Takehiro; Jeong, Gi Young; Ando, Jun-ichi; Mukoyoshi, Hideki

2014-08-01

Clayey gouges are common in fault slip zones at shallow depths. Thus, the fault zone processes and frictional behaviors of the gouges are critical to understanding seismic slip at these depths. We conducted rotary shear tests on clayey gouge (~41 wt % clay minerals) at a seismic slip rate of 1.3 m/s. Here we report that the gouge was melted at 5 MPa of normal stress and room humidity conditions. The initial local melting was followed by melt layer formation. Clay minerals (e.g., smectite and illite) and plagioclase were melted and quenched to glass with numerous vesicles. Both flash heating and bulk temperature increases appear to be responsible for the melting. This observation of clayey gouge melting is comparable to that of natural faults (e.g., Chelungpu fault, Taiwan). Due to heterogeneous fault zone properties (e.g., permeability), frictional melting may be one of the important processes in clayey slip zones at shallow depths.

Development and Application of a Paleomagnetic/Geochemical Method for Constraining the Timing of Burial Diagenetic and Fluid

DOE Office of Scientific and Technical Information (OSTI.GOV)

Elmore, Richard D.; Engel, Michael H.

2005-03-10

Studies of diagenesis caused by fluid migration or other events are commonly hindered by a lack of temporal control. Our results to date demonstrate that a paleomagnetic/geochemical approach can be used to date fluid migration as well as burial diagenetic events. Our principal working hypothesis is that burial diagenetic processes (e.g., maturation of organic-rich sediments and clay diagenesis) and the migration of fluids can trigger the authigenesis of magnetic mineral phases. The ages of these events can be constrained by comparing chemical remanent magnetizations (CRMs) to independently established Apparent Polar Wander Paths. While geochemical (e.g. stable isotope and organic analyses)more » and petrographic studies provide important clues for establishing these relationships, the ultimate test of this hypothesis requires the application of independent dating methods to verify the paleomagnetic ages. Towards this end, we have used K-Ar dating of illitization as an alternative method for constraining the ages of magnetic mineral phases in our field areas.« less

Effect of sewage sledge and their bio-char on some soil qualities

NASA Astrophysics Data System (ADS)

Fathi, Hamed; Movahedi Naeini, Seyed Alireza; Mirzanejad, Mojan

2015-04-01

Bio char (BC) application as a soil amendment has achieved much interest and has been found that considerably improves soil nutrient status and crop yields on poor soils. However, information on the effect of BC on illitic soils in temperate climates is still insufficient. The primary objective in this study was to assess the influence of biochar on the soil physical properties, nutrient status and plant production. The result may also provide a reference for the use of biochars as a solution in agricultural waste management when sludge with considerable load of pathogens are involved. Soybean was already grown one year and will be repeated one more year with same treatments. The investigated soil properties included soil water content and mechanical resistance, pH, electrical conductivity (EC), calcium- acetate-lactate (CAL)-extractable P (PCAL) and K (KCAL), C, N, and nitrogen-supplying potential (NSP). The results show soil water content, potassium uptake and plant yield were increased. Heating sludge removed all pathogens and soybean yield was increased by 6%.

The Leaching of Aluminium In Spanish Clays, Coal Mining Wastes and Coal Fly Ashes by Sulphuric Acid.

NASA Astrophysics Data System (ADS)

Fernández, A. M.; Ibáñez, J. L.; Llavona, M. A.; Zapico, R.

The acid leaching of aluminium from several non traditional ores, bayerite, kaolinite, different clays, coal mining wastes and coal fly ashes, and the kinetic of their dissolution are described. The effects of time, temperature, acid concentration, sample calcination, particle size were examined. The leaching of aluminium is dependent on acid concentration and strongly on temperature. Generally, the time to reach a fixed percentage of dissolution decreases with increasing acid concentration in the range 6% to 40% acid by weight. On clays and coal mining wastes a good relation between Al removal and ratio kaolinite/illite was also observed at all temperatures and acid concentration tested. Coal fly ashes are particles that were heated at very high temperatures in the power station and Al compounds were transformed into mullite and so Al recovery was minor. Several rate equations describing the kinetics of the leach reaction were discussed and Kinetic parameters and activation energy values of samples are presented.

A volcanic connection between the Pennsylvanian of the Mid-Continent and Appalachian regions

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lyons, P.C.; Congdon, R.D.; Outerbridge, W.F.

1993-02-01

Until now, it has not been possible to find key beds that precisely connect the Pennsylvanian section in the Mid-Continent and Appalachian regions. Altered volcanic ash deposits (tonsteins) offer the potential for high-precision stratigraphic correlation. The Fire Clay tonstein which is chemically distinct from the other five Middle Pennsylvanian tonstein beds in the central Appalachian basin, has a unimodal, rhyolitic fingerprint'' based on glass-inclusion data (n = 109) from volcanic quartz. This tonstein has been correlated over a distance of about 400 km in KY, WV, VA, and TN. Analyses of glass inclusions (n = 12) in volcanic quartz frommore » a mixed-layer (illite/smectite) tonstein (K-bentonite) from near the Morrowan-Atokan boundary, recovered from cuttings in Arkansas wells (Phillips Petroleum Co., [number sign]2, Johnson City; Carter Oil Co., [number sign]1 Williams, Conway City), are identical, within the limits of analytical precision, to those from the Fire Clay tonstein.« less

Methods for enhancing mapping of thermal fronts in oil recovery

DOEpatents

Lee, D.O.; Montoya, P.C.; Wayland, J.R. Jr.

1984-03-30

A method for enhancing the resistivity contrasts of a thermal front in an oil recovery production field as measured by the controlled source audio frequency magnetotelluric (CSAMT) technique is disclosed. This method includes the steps of: (1) preparing a CSAMT-determined topological resistivity map of the production field; (2) introducing a solution of a dopant material into the production field at a concentration effective to alter the resistivity associated with the thermal front; said dopant material having a high cation exchange capacity which might be selected from the group consisting of montmorillonite, illite, and chlorite clays; said material being soluble in the conate water of the production field; (3) preparing a CSAMT-determined topological resistivity map of the production field while said dopant material is moving therethrough; and (4) mathematically comparing the maps from step (1) and step (3) to determine the location of the thermal front. This method is effective with the steam flood, fire flood and water flood techniques.

Mössbauer study of Fe mineralogy with respect to rank, type and Colombian carboniferous zone

NASA Astrophysics Data System (ADS)

Caballero, F. Reyes; Martínez Ovalle, S. A.; Díaz Lagos, M.; Gómez, O. P.; Blandón, A.

2017-11-01

The transmission mode of Fe-57 Mössbauer spectroscopy was used to identify iron bearing minerals and establish relationships between and among these minerals and the ranks and types of various carboniferous zones in Colombia. Maceral and mineral compositions vary significantly among Colombian carboniferous zones. These variations determine some of the final characteristics and potential uses of coal, and therefore significantly contribute to defining coal quality. A comparison of spectroscopy results shows that the thermal maturity of the Colombian coals ranges from lignite to semianthracite. Similarities and differences exist with respect to conventional parameters. The coals of Córdoba and Cauca have higher sulfur contents > 2 % ash contents. Iron bearing minerals identified included pyrite, which was, found everywhere, and illite, ankerite, siderite, iron sulfates were found in particular areas. Coals from Valle del Cauca, Córdoba, Caldas and Santander are characterized by oxidation of pyrite and its transformation into ferrous or ferric sulfate.

Terrigenous sediment supply along the Chilean continental margin: modern regional patterns of texture and composition

NASA Astrophysics Data System (ADS)

Lamy, F.; Hebbeln, D.; Wefer, G.

The regional patterns of texture and composition of modern continental slope and pelagic sediments off Chile between 25°S and 43°S reflect the latitudinal segmentation of geological, morphological, and climatic features of the continental hinterland. Grain-size characteristics are controlled by the grain-size of source rocks, the weathering regime, and mode of sediment input (eolian off northern Chile vs fluvial further south). Bulk-mineral assemblages reveal a low grade of maturity. Regional variations are governed by the source-rock composition of the different geological terranes and the relative source-rock contribution of the Coastal Range and Andes, as controlled by the continental hydrology. The relative abundance of clay minerals is also predominantly influenced by the source-rock composition and partly by continental smectite neoformation. Latitudinal variations of illite crystallinities along the Chilean continental slope (and west of the Peru-Chile trench) clearly reflect modifications of the weathering regime which correspond to the strong climatic zonation of Chile.

DOE Office of Scientific and Technical Information (OSTI.GOV)

Garimella, Sarvesh; Kristensen, Thomas Bjerring; Ignatius, Karolina

The SPectrometer for Ice Nuclei (SPIN) is a commercially available ice nucleating particle (INP) counter manufactured by Droplet Measurement Technologies in Boulder, CO. The SPIN is a continuous flow diffusion chamber with parallel plate geometry based on the Zurich Ice Nucleation Chamber and the Portable Ice Nucleation Chamber. This study presents a standard description for using the SPIN instrument and also highlights methods to analyze measurements in more advanced ways. It characterizes and describes the behavior of the SPIN chamber, reports data from laboratory measurements, and quantifies uncertainties associated with the measurements. Experiments with ammonium sulfate are used to investigatemore » homogeneous freezing of deliquesced haze droplets and droplet breakthrough. Experiments with kaolinite, NX illite, and silver iodide are used to investigate heterogeneous ice nucleation. SPIN nucleation results are compared to those from the literature. A machine learning approach for analyzing depolarization data from the SPIN optical particle counter is also presented (as an advanced use). Altogether, we report that the SPIN is able to reproduce previous INP counter measurements.« less

Mineralogy of ash of some American coals: variations with temperature and source

USGS Publications Warehouse

Mitchell, R.S.; Gluskoter, H.J.

1976-01-01

Ten samples of mineral-matter residue were obtained by the radio-frequency low-temperature ashing of subbituminous and bituminous coals. The low-temperature ash samples were then heated progressively from 400 ??C to 1400 ??C at 100 ??C intervals. Mineral phases present at each temperature interval were determined by X-ray diffraction analyses. The minerals originally present in the coals (quartz, kaolinite, illite, pyrite, calcite, gypsum, dolomite, and sphalerite) were all altered to higher temperature phases. Several of these phases, including kaolinite, metakaolinite, mullite, anhydrite, and anorthite, were found only in limited temperature ranges. Therefore the temperature of formation of the ashes in which they occur may be determined. Mineralogical differences were observed between coal samples from the Rocky Mountain Province, the Illinois Basin, and the Appalachians; and as a result of these mineralogical differences, different high-temperature phases resulted as the samples were heated. However, regional generalizations cannot be made until a greater number of samples have been studied. ?? 1976.

Microbial reduction of Fe(III)-bearing clay minerals in the presence of humic acids

NASA Astrophysics Data System (ADS)

Liu, Guangfei; Qiu, Shuang; Liu, Baiqing; Pu, Yiying; Gao, Zhanming; Wang, Jing; Jin, Ruofei; Zhou, Jiti

2017-03-01

Both Fe(III)-bearing clay minerals and humic acids (HAs) are abundant in the soils and sediments. Previous studies have shown that bioreduction of structural Fe(III) in clay minerals could be accelerated by adding anthraquinone compound as a redox-active surrogate of HAs. However, a quinoid analogue could not reflect the adsorption and complexation properties of HA, and little is known about the effects of real HAs at environmental concentration on bioreduction of clay minerals. Here, it was shown that 10-200 mg l-1 of natural or artificially synthesized HAs could effectively stimulate the bioreduction rate and extent of Fe(III) in both iron-rich nontronite NAu-2 and iron-deficient montmorillonite SWy-2. After adsorption to NAu-2, electron-transfer activities of different HA fractions were compared. Additionally, Fe(II) complexation by HAs also contributed to improvement of clay-Fe(III) bioreduction. Spectrosopic and morphological analyses suggested that HA addition accelerated the transformation of NAu-2 to illite, silica and siderite after reductive dissolution.

Constraining the alteration history of a Late Cretaceous Patagonian volcaniclastic bentonite-ash-mudstone sequence using K-Ar and 40Ar/39Ar isotopes

NASA Astrophysics Data System (ADS)

Warr, L. N.; Hofmann, H.; van der Pluijm, B. A.

2017-01-01

Smectite is typically considered unsuitable for radiometric dating, as argon (40Ar) produced from decay of exchangeable potassium (40K) located in the interlayer sites can be lost during fluid-rock interaction and/or during wet sample preparation in the laboratory. However, age analysis of Late Cretaceous Argentinian bentonites and associated volcaniclastic rocks from Lago Pellegrini, Northern Patagonia, indicates that, in the case of these very low-permeability rocks, the radioactive 40Ar was retained and thus can provide information on smectite age and the timing of rock alteration. This study presents isotopic results that indicate the ash-to-bentonite conversion and alteration of the overlying tuffaceous mudstones in Northern Patagonia was complete 13-17 my after middle Campanian sedimentation when the system isotopically closed. The general absence of illite in these smectite-rich lithologies reflects the low activity of K and the low temperature (<60 °C) of the formation waters that altered the parent ash.

Lithology, reservoir properties, and burial history of portion of Gammon Shale ( Cretaceous), southwestern North Dakota.

USGS Publications Warehouse

Gautier, D.L.

1981-01-01

In the northern Great Plains, large quantities of biogenic methane are contained at shallow depths in Cretaceous marine mudstones. The Gammon Shale and equivalents of the Milk River Formation in Canada are typical. At Little Missouri field, Gammon reservoirs consist of discontinuous lenses and laminae of siltstone, enclosed by silty clay shale. Large amounts of allogenic clay, including highly expansible mixed-layer illite-smectite cause great water sensitivity and high water-saturation values. Studies show that the Gammon has not undergone thermal conditions sufficient for oil or thermal gas generation. The scarcity of authigenic silicates suggests that diagenesis has been inhibited by the presence of free methane. Shale layers are practically impermeable whereas siltstone microlenses are porous (30-40%) and have permeabilities on the order of 3-30 md. Organic matter in the low-permeability reservoirs served as the source of biogenic methane, and capillary forces acted as the trapping mechanism for gas accumulation. Much of the Gammon interval is potentially economic. -from Author

Physico-chemistry and geochemistry of Balengou clay deposit (West Cameroon) with inference to an argillic hydrothermal alteration

NASA Astrophysics Data System (ADS)

Tassongwa, Bernard; Eba, François; Njoya, Dayirou; Tchakounté, Jacqueline Numbem; Jeudong, Narcisse; Nkoumbou, Charles; Njopwouo, Daniel

2017-09-01

Field description and sampling along two pits, granulometry, Atterberg limits, mineralogical (XRD, FTIR, DSC & TGA) and geochemical analyses of the Balengou clays help to determine their characteristics and the genesis of the deposit. The mineralogical composition is comprised of halloysite-kaolinite, quartz, montmorillonite, hematite, anatase, feldspar, zircon, chromite, and apatite. Gibbsite and illite occur at the shallow and deep depth, respectively. Dikes of sand-poor clays contain also cristobalite and tridymite. Pairs of elements Rb-Ba, Rb-Sr, Nb-Ta, Ta-Zr, TiO2-Zr display good positive correlations (R2 > 0.85). REE patterns are highly fractionated (LaN up to 3312, LaN/YbN: 19-10) and are marked by deep Ce and Eu negative anomalies. Immobile element canonical ratios indicate that the protoliths were commendite/pantelerite, rhyolite and dacite, or their plutonic equivalents. Mineralogical and geochemical features lead to the suggestion that the clays derived from an advanced argillic hydrothermal alteration.

Effects of simulated clay gouges on the sliding behavior of Tennessee sandston

NASA Astrophysics Data System (ADS)

Shimamoto, Toshihiko; Logan, John M.

1981-06-01

The effects of simulated fault gouge on the sliding behavior of Tennessee sandstone are studied experimentally with special reference to the stabilizing effect of clay minerals mixed into the gouge. About 30 specimens with gouge composed of pure clays, of homogeneously mixed clay and anhydrite, or of layered clay and anhydrite, along a 35° precut are deformed dry in a triaxial apparatus at a confining pressure of 100 MPa, with a shortening rate of about 5 · 10 -4/sec, and at room temperature. Pure clay gouges exhibit only stable sliding, and the ultimate frictional strength is very low for bentonite (mont-morillonite), intermediate for chlorite and illite, and considerably higher for kaolinite. Anhydrite gouge shows violent stick-slip at 100 MPa confining pressure. When this mineral is mixed homogeneously with clays, the frictional coefficient of the mixed gouge, determined at its ultimate frictional strength, decreases monotonically with an increase in the clay content. The sliding mode changes from stick-slip to stable sliding when the frictional coefficient of the mixed clay-anhydrite gouge is lowered down below 90-95% of the coefficient of anhydrite gouge. The stabilizing effect of clay in mixed gouge is closely related to the ultimate frictional strength of pure clays; that is, the effect is conspicuous only for a mineral with low frictional strength. Only 15-20% of bentonite suppresses the violent stick-slip of anhydrite gouge. In contrast, violent stick-slip occurs even if the gouge contains as much as 75% of kaolinite. The behavior of illite and chlorite is intermediate between that of kaolinite and bentonite. Bentonite—anhydrite two-layer gouge exhibits stable sliding even when the bentonite content is only 5%. Thus, the presence of a thin, clay-rich layer in a fault zone stabilizes the behavior much more effectively than do the clay minerals mixed homogeneously with the gouge. This result brings out the mechanical significance of internal structures of a fault zone in understanding the effects of intrafault materials on the fault motion. Based on the present experimental results incorporated with some other experimental data, it is argued that although the stabilizing effect of montmorillonite and vermiculite is indeed remarkable at room temperature, the effect should be much less pronounced at elevated temperatures, due perhaps to the dewatering of the clays. In most geological environments where shallow earthquakes occur, the stabilizing effect of clays is probably not so conspicuous as to completely suppress the unstable motion of a fault.

Selenium isotope fractionation during adsorption onto the modified clay minerals

NASA Astrophysics Data System (ADS)

Xu, W.; Jianming, Z.; Tan, D.; Qin, H.

2016-12-01

Currently, Selenium (Se) isotopes have been used as a paleoenvironmental proxy to trace Se evolution in Ancient Ocean. And many researchers considered the variation of Se isotopes in nature mainly result from the reduction of Se oxyanion, while Se isotope fractionation during adsorption onto minerals was rarely reported. Therefore, based on the previous studies [1, 2], we used three common clay minerals in supergene environment: montmorillonite, illite and kaolinite as an adsorbent to study Se isotope fractionation during adsorption. Before doing adsorption experiments, the adsorbent were modified as Na-clay minerals to remove the possibility of interference of Ca2+, Fe3+, Fe2+ as well as organic matters. A batch adsorption experiments were carried out at room temperature (23 ±2 °) under N2 atmosphere, initial Se concentration (SeO32-/ SeO42-) was respectively 200ng and 100ng, the solution ionic strength was 0.1mol/L NaCl; the ratio of liquid to solid is 2g / L, and pH = 5. Experimental results showed that adsorption reached a steady state during 48h, and the maximum adsorption for SeO32- was larger than SeO42-. The isotope data showed that SeO42- adsorbed onto three clay minerals didn't present obvious Se isotope fractionation, generally δ82/78Se is less than 0.1 ‰. Meanwhile, SeO32- during adsorption process also didn't show the significant fractionation, less than 0.3 ‰. However, interestingly, for SeO32- the δ82/78Se values of solution during adsorption onto kaolinite underwent a process of increasing by 0.5‰ compared to the initial solution and then decreasing to 0.3‰. We speculated the reason may not be related to the surface charge of the clay minerals, but mostly with the layered structure of clay minerals. Montmorillonite and illite are 2: 1; kaolinite is 1: 1 layered structure. The different layered structure may influence the isotope fraction between Se oxyanions and clay minerals. These still needs further and more experiments to definitely explain this phenomenon. This work was financially supported by National Key Basic Research Program of China (2014CB238903) and Natural Science Foundation of China (41473028, 41273029). [1] D. Peak et al. Soil Science Society of America Journal. 2006, 192-203. [2] T. Missana et al. Journal of Colloid and Interface Science. 2009, 334, 132-138.

Application of Spectral Gamma Ray for Lithofacies and Paleo-environmental Interpretation: A Case Study from the Late Ordovician Glaciogenic Deposits, Saudi Arabia

NASA Astrophysics Data System (ADS)

Alqubalee, Abdullah; Abdullatif, Osman; Babalola, Lamidi

2017-04-01

This study is an integral part of multidisciplinary research being carried out on the Late Ordovician Sarah Formation in the Rub' Al-Khali Basin, Saudi Arabia. Sarah Formation proved to be important target for tight gas reservoir in Saudi Arabia. This study integrates lithofacies characteristics and spectral Gamma Ray of core samples so as to identify and differentiate among different depositional environments. Thorium (Th, ppm) and potassium (K, %) are acquired with approximately a reading point per inch using high-resolution Spectral Core Gamma. The cores description and analysis from six exploratory wells revealed four depositional environments ranging from the glaciofluvial, glaciolacustrine delta, subglacial to the nearshore environments. Based on lithofacies and geochemical analysis of the core samples, four groups of lithofacies including sandstone (G1), claystone and/or argillaceous sandstone (G2), calcareous and/or evaporitic sandstone (G3), and diamictites (G4) were recognized in each well. The bivariate plots of Th and K were used to delineate the minerals contents in each core and environment. The results showed that the G1 facies of the nearshore and glaciofluvial environments are characterized by similar distribution patterns of these elements exhibiting lower clay minerals variations than that in the other groups of lithofacies. These patterns consist of two mineral groups, the first one includes illite and montmorillonite clay minerals while the second one includes mica, glauconite, and feldspar. By contrast, G1 and G2 lithofacies of the glaciolacustrine delta environment are characterized by a range of clay minerals. However, G3 of this environment exhibits similar pattern of the nearshore and the glaciofluvial environments This is because the grains of G3 are cemented by anhydrite rather than by clays. Based on the lithological characteristic, matrix-supported and clast-supported diamictites were identified in the subglacial environment. The differences between these two lithofacies were clearly detected using Th/K plot. Both diamictites are characterized by a range of minerals including illite, mixed layer clays, glauconite, and feldspar. The matrix-supported diamictites contain higher proportions of these minerals. This study indicates that the relationship between Th and K can be used to predict the types of lithofacies and clay contents in different glaciogenic depositional environments. In addition, it can be used to predict the relative amounts of the clay minerals in each lithofacies. In turn, identifying the types and the amounts of clay minerals in lithofacies facilitate the prediction of reservoir quality and eventually lead to enhancement of their development and productivity.

Weathering of the New Albany Shale, Kentucky: II. Redistribution of minor and trace elements

USGS Publications Warehouse

Tuttle, M.L.W.; Breit, G.N.; Goldhaber, M.B.

2009-01-01

During weathering, elements enriched in black shale are dispersed in the environment by aqueous and mechanical transport. Here a unique evaluation of the differential release, transport, and fate of Fe and 15 trace elements during progressive weathering of the Devonian New Albany Shale in Kentucky is presented. Results of chemical analyses along a weathering profile (unweathered through progressively weathered shale to soil) describe the chemically distinct pathways of the trace elements and the rate that elements are transferred into the broader, local environment. Trace elements enriched in the unweathered shale are in massive or framboidal pyrite, minor sphalerite, CuS and NiS phases, organic matter and clay minerals. These phases are subject to varying degrees and rates of alteration along the profile. Cadmium, Co, Mn, Ni, and Zn are removed from weathered shale during sulfide-mineral oxidation and transported primarily in aqueous solution. The aqueous fluxes for these trace elements range from 0.1 g/ha/a (Cd) to 44 g/ha/a (Mn). When hydrologic and climatic conditions are favorable, solutions seep to surface exposures, evaporate, and form Fe-sulfate efflorescent salts rich in these elements. Elements that remain dissolved in the low pH (<4) streams and groundwater draining New Albany Shale watersheds become fixed by reactions that increase pH. Neutralization of the weathering solution in local streams results in elements being adsorbed and precipitated onto sediment surfaces, resulting in trace element anomalies. Other elements are strongly adsorbed or structurally bound to solid phases during weathering. Copper and U initially are concentrated in weathering solutions, but become fixed to modern plant litter in soil formed on New Albany Shale. Molybdenum, Pb, Sb, and Se are released from sulfide minerals and organic matter by oxidation and accumulate in Fe-oxyhydroxide clay coatings that concentrate in surface soil during illuviation. Chromium, Ti, and V are strongly correlated with clay abundance and considered to be in the structure of illitic clay. Illite undergoes minimal alteration during weathering and is concentrated during illuvial processes. Arsenic concentration increases across the weathering profile and is associated with the succession of secondary Fe(III) minerals that form with progressive weathering. Detrital fluxes of particle-bound trace elements range from 0.1 g/ha/a (Sb) to 8 g/ha/a (Mo). Although many of the elements are concentrated in the stream sediments, changes in pH and redox conditions along the sediment transport path could facilitate their release for aqueous transport.

Spatially resolved nanoscale observations of soil carbon multidecadal persistence

NASA Astrophysics Data System (ADS)

Lutfalla, S.; Chenu, C.; Bernard, S.; Le Guillou, C.; Barré, P.

2015-12-01

Assessing how mineral surfaces, especially at small scale, can protect soil organic carbon (SOC) from biodegradation is crucial. The question we address in this work is whether different mineral species lead to different organo-mineral interactions and stabilize different quantities of SOM and different types of SOC. Here we used the unique opportunity offered by long term bare fallows (BF) to study in situ C dynamics in several fine fractions of a silty loam soil. With no vegetation i.e. no external input of fresh C, the plant-free soil of the Versailles 42 Plots (INRA, France) has been progressively enriched in persistent SOC during the 80 years of BF. Contrasted mineral phases of the clay size fraction were isolated by size fractionation on samples from 5 different dates (0, 10, 22, 52, and 79 years after the beginning of the BF, four field replicates per date). Four fractions were studied: total clays (< 2 μm), and three sub fractions in the clay (fine clay: 0 - 0.05 μm, intermediate clay: 0.05 - 0.2 μm, and coarse clay: 0.2 - 2 μm). X-ray diffraction analyses showed contrasted mineralogies in the fine and intermediate clay (smectite and mixed layered illite/smectite) as opposed to the coarse clay (smectite, illite, kaolinite and mixed layered I/S). We performed CHN elemental analysis and synchrotron based spectroscopy and microscopy (NEXAFS bulk and STXM at the carbon K edge of 280 eV, CLS Saskatoon, Canada) to study the dynamics, the distribution and the chemical speciation of the SOC in these fractions. The quantity of C appears to be stabilized after 50 years of BF, even though the dynamics are different for the three clay fractions. Indeed, coarse and intermediate clays have the same final C content but coarse clays lose more C. Fine clay experiences the highest C losses and displays the highest final C content suggesting that fine clays contained more labile C and more persistent C. In all fractions, C:N ratios are really low (below 8) and are decreasing with time, evidencing the dominant presence of microbial SOC. STXM-NEXAFS data shows that, in the fine and intermediate clay fractions, during the first 50 years of BF all mineral particles are associated with SOC. On the contrary, in the coarse clays, SOC displays more diversity: the chemical signature is more diverse and mineral particles not associated with SOC appear more quickly.

Percolation of diagenetic fluids in the Archaean basement of the Franceville basin

NASA Astrophysics Data System (ADS)

Mouélé, Idalina Moubiya; Dudoignon, Patrick; Albani, Abderrazak El; Cuney, Michel; Boiron, Marie-Christine; Gauthier-Lafaye, François

2014-01-01

The Palaeoproterozoic Franceville basin, Gabon, is mainly known for its high-grade uranium deposits, which are the only ones known to act as natural nuclear fission reactors. Previous work in the Kiéné region investigated the nature of the fluids responsible for these natural nuclear reactors. The present work focuses on the top of the Archaean granitic basement, specifically, to identify and date the successive alteration events that affected this basement just below the unconformity separating it from the Palaeoproterozoic basin. Core from four drill holes crosscutting the basin-basement unconformity have been studied. Dating is based on U-Pb isotopic analyses performed on monazite. The origin of fluids is discussed from the study of fluid inclusion planes (FIP) in quartz from basement granitoids. From the deepest part of the drill holes to the unconformable boundary with the basin, propylitic alteration assemblages are progressively replaced by illite and locally by a phengite + Fe chlorite ± Fe oxide assemblage. Illitic alteration is particularly strong along the sediment-granitoid contact and is associated with quartz dissolution. It was followed by calcite and anhydrite precipitation as fracture fillings. U-Pb isotopic dating outlines three successive events: a 3.0-2.9-Ga primary magmatic event, a 2.6-Ga propylitic alteration and a late 1.9-Ga diagenetic event. Fluid inclusion microthermometry suggests the circulation of three types of fluids: (1) a Na-Ca-rich diagenetic brine, (2) a moderately saline (diagenetic + meteoric) fluid, and (3) a low-salinity fluid of probable meteoric origin. These fluids are similar to those previously identified within the overlying sedimentary rocks of the Franceville basin. Overall, the data collected in this study show that the Proterozoic-Archaean unconformity has operated as a major flow corridor for fluids circulation, around 1.9 Ga. highly saline diagenetic brines; hydrocarbon-rich fluids derived from organic matter-rich formations; a low-salinity fluid likely of meteoric origin migrating through the granitic basement; mineralizing fluids resulting from the mixing of fluids 1 and 3; high-temperature fluids resulting from the natural nuclear reactor environment (Mathieu et al., 2000). The present paper attempts to characterize the succession of alteration events that have affected the top of the basement below the Palaeoproterozoic sediment unconformity. Are these alterations related to early post-magmatic to hydrothermal events, to palaeoweathering, or to late infiltration of diagenetic brines from the overlying basin? Our study, carried out on drill core samples from Kiéné, is supported by petrographic investigation, new fluid inclusion data and U-Pb geochronology on monazite.

Badlands in humid regions - redbed desertification in Nanxiong Basin, China

NASA Astrophysics Data System (ADS)

Yan, Luobin; Hua, Peng; Simonson, Scott

2016-04-01

The redbed badlands in Nanxiong City, China, well represent badlands in humid regions. The erosion rate in humid regions is much higher than that in arid regions and can reach 1 cm per month during the summer. The purpose of this study is to introduce the research of badlands in China, which have not been extensively studied so far, and to compare the badlands between arid and humid regions. Furthermore, the aim is to study the impact of mineralogical and chemical composition on the disintegration of soft rock in Nanxiong Basin badlands. For the purpose of this study field observations, sampling, and digging profiles were done. The mineralogical and chemical compositions of the Nanxiong Basin badland lithologies were determined by XRD, XRF and thin sections. Weathering resistance, process of weathering, and disintegration features were studied by weathering experiments under natural conditions. Weathering profiles can be easily divided into four layers: regolith, a strongly weathered layer, a poorly weathered layer, and an unweathered sediment. The depth of the weathering profile is influenced by the weathering resistance of the soft rock. Weathering resistance affects the erosion rate and evolution of landforms in badlands by influencing the rate from unweathered rock to regolith. Analyzed sediments have high content of illite and illite-smectite interstratifications. This composition of clay minerals together with poor sediment consolidation jointly leads to weathering prone sediment. The weathering and disintegration of soft rock in Nanxiong Basin badlands has a close relationship with rainfall. Sheet erosion, a kind of solid-liquid phase flow, formed in the regolith of the badland during rainfall events and can be the most instrumental to erosion. The mineral composition and liquidity plasticity index were also analyzed, and the results show that the regolith are low liquid limit silts with liquid limit of 21%-25%, plastic limit of 13%-18% and plasticity index of 6.5%-11%. Sheet erosion will occur when rainfall splash destroys the original structure of the badland slopes with the impermeable siltstone underneath and with the high porosity regolith. In China, the badlands in redbed areas have been called the extreme "redbed desertification". Our preliminary research concerning Nanxiong Basin badlands puts forward the concepts of "redbed deserts" and "redbed desertification". Based on the field work, the mechanism of redbed desertification depends on the lithological features, natural impacts, and human activities. The trigger for formation of the redbed badlands desertification are complex, but mainly influenced by activities such as severe reclamation, forest fires, tree planting disturbances, dry-land degradation, acquirement of topsoil, etc.

A kinetics database and scripts for PHREEQC

NASA Astrophysics Data System (ADS)

Hu, B.; Zhang, Y.; Teng, Y.; Zhu, C.

2017-12-01

Kinetics of geochemical reactions has been increasingly used in numerical models to simulate coupled flow, mass transport, and chemical reactions. However, the kinetic data are scattered in the literature. To assemble a kinetic dataset for a modeling project is an intimidating task for most. In order to facilitate the application of kinetics in geochemical modeling, we assembled kinetics parameters into a database for the geochemical simulation program, PHREEQC (version 3.0). Kinetics data were collected from the literature. Our database includes kinetic data for over 70 minerals. The rate equations are also programmed into scripts with the Basic language. Using the new kinetic database, we simulated reaction path during the albite dissolution process using various rate equations in the literature. The simulation results with three different rate equations gave difference reaction paths at different time scale. Another application involves a coupled reactive transport model simulating the advancement of an acid plume in an acid mine drainage site associated with Bear Creek Uranium tailings pond. Geochemical reactions including calcite, gypsum, and illite were simulated with PHREEQC using the new kinetic database. The simulation results successfully demonstrated the utility of new kinetic database.

Global distribution of clay-size minerals on land surface for biogeochemical and climatological studies

PubMed Central

Ito, Akihiko; Wagai, Rota

2017-01-01

Clay-size minerals play important roles in terrestrial biogeochemistry and atmospheric physics, but their data have been only partially compiled at global scale. We present a global dataset of clay-size minerals in the topsoil and subsoil at different spatial resolutions. The data of soil clay and its mineralogical composition were gathered through a literature survey and aggregated by soil orders of the Soil Taxonomy for each of the ten groups: gibbsite, kaolinite, illite/mica, smectite, vermiculite, chlorite, iron oxide, quartz, non-crystalline, and others. Using a global soil map, a global dataset of soil clay-size mineral distribution was developed at resolutions of 2' to 2° grid cells. The data uncertainty associated with data variability and assumption was evaluated using a Monte Carlo method, and validity of the clay-size mineral distribution obtained in this study was examined by comparing with other datasets. The global soil clay data offer spatially explicit studies on terrestrial biogeochemical cycles, dust emission to the atmosphere, and other interdisciplinary earth sciences. PMID:28829435

Temporal change in fallout {sup 137}Cs in terrestrial and aquatic systems: A whole ecosystem approach

DOE Office of Scientific and Technical Information (OSTI.GOV)

Smith, J.T.; Elder, D.G.; Fesenko, S.V.

1999-01-01

During the years after a nuclear accident, the bioavailability and environmental mobility of radiocesium declines markedly, resulting in large changes in contamination of foodstuffs, vegetation, and surface waters. Predicting such changes is crucial to the determination of potential doses to affected populations and therefore to the implementation of radiological countermeasures. The authors have analyzed 77 data sets of radiocesium ({sup 137}Cs) activity concentrations in milk, vegetation, and surface waters after the Chernobyl accident. Their results show that the rate of decline in {sup 137}Cs during the years after Chernobyl is remarkably consistent in all three ecosystem components, having a meanmore » effective half-life, T{sub eff} {approx} 2 years. By comparing changes in {sup 137}Cs availability with rates of diffusion of {sup 40}K (a close analogue) into the lattice of an illitic clay the authors have, for the first time, directly linked changes in the environmental availability of {sup 137}Cs to fixation processes at a mechanistic level. These changes are consistent with declines in the exchangeable fraction of {sup 137}Cs in soils.« less

Visual classification of very fine-grained sediments: Evaluation through univariate and multivariate statistics

USGS Publications Warehouse

Hohn, M. Ed; Nuhfer, E.B.; Vinopal, R.J.; Klanderman, D.S.

1980-01-01

Classifying very fine-grained rocks through fabric elements provides information about depositional environments, but is subject to the biases of visual taxonomy. To evaluate the statistical significance of an empirical classification of very fine-grained rocks, samples from Devonian shales in four cored wells in West Virginia and Virginia were measured for 15 variables: quartz, illite, pyrite and expandable clays determined by X-ray diffraction; total sulfur, organic content, inorganic carbon, matrix density, bulk density, porosity, silt, as well as density, sonic travel time, resistivity, and ??-ray response measured from well logs. The four lithologic types comprised: (1) sharply banded shale, (2) thinly laminated shale, (3) lenticularly laminated shale, and (4) nonbanded shale. Univariate and multivariate analyses of variance showed that the lithologic classification reflects significant differences for the variables measured, difference that can be detected independently of stratigraphic effects. Little-known statistical methods found useful in this work included: the multivariate analysis of variance with more than one effect, simultaneous plotting of samples and variables on canonical variates, and the use of parametric ANOVA and MANOVA on ranked data. ?? 1980 Plenum Publishing Corporation.

Syn-deformational features of Carlin-type Au deposits

USGS Publications Warehouse

Peters, S.G.

2004-01-01

Syn-deformational ore deposition played an important role in some Carlin-type Au deposits according to field and laboratory evidence, which indicates that flow of Au-bearing fluids was synchronous with regional-scale deformation events. Gold-related deformation events linked to ore genesis were distinct from high-level, brittle deformation that is typical of many epithermal deposits. Carlin-type Au deposits, with brittle-ductile features, most likely formed during tectonic events that were accompanied by significant fluid flow. Interactive deformation-fluid processes involved brittle-ductile folding, faulting, shearing, and gouge development that were focused along illite-clay and dissolution zones caused by hydrothermal alteration. Alteration along these deformation zones resulted in increased porosity and enhancement of fluid flow, which resulted in decarbonated, significant dissolution, collapse, and volume and mass reduction. Carlin-type Au deposits commonly are hosted in Paleozoic and Mesozoic sedimentary rocks (limestone, siltstone, argillite, shale, and quartzite) on the margins of cratons. The sedimentary basins containing the host rocks underwent tectonic events that influenced the development of stratabound, structurally controlled orebodies. Published by Elsevier Ltd.

Clay minerals in sediments of Portuguese reservoirs and their significance as weathering products from over-eroded soils: a comparative study of the Maranhão, Monte Novo and Divor Reservoirs (South Portugal)

NASA Astrophysics Data System (ADS)

Fonseca, Rita M. F.; Barriga, Fernando J. A. S.; Conceição, Patrícia I. S. T.

2010-12-01

The Southern region of Portugal is subjected to several forms of over-erosion. Most leached products, mainly composed of fine particles containing nutrients, metals or pesticides, are easily transported by river flows. When these are hindered by a physical barrier such as a dam, the particulate load accumulates on the bottom of the reservoirs, often leading to a pronounced decrease of water quality. Bottom sediments from three reservoirs were subjected to grain-size analysis and a study of clay minerals by X-ray diffraction. Most sediments contain a diverse set of clay minerals, mostly illites, smectites, chlorites and kaolinites. The nature of the clay minerals reflects the nature of the parent rocks. During the cycles of transport and temporary deposition, they may undergo significant chemical and physical transformations, which lead to an increase of expandable properties and therefore, to a higher cationic exchange capacity, determining its important role as vehicles of environmental pollutants.

Effect of sewage sledge and their bio-char on some soil qualities in Second year cropping

NASA Astrophysics Data System (ADS)

fathi dokht, hamed; Movahedi Naeini, Seyed Alireza; Dordipor, Esmaeil; mirzanejad, moujan

2016-04-01

Bio char (BC) application as a soil amendment has achieved much interest and has been found that considerably improves soil nutrient status and crop yields on poor soils. However, information on the effect of BC on illitic soils in temperate climates is still insufficient. The primary objective in this study was to assess the influence of sewage sledge and their bio-char on the soil physical properties, nutrient status and plant production in Second year cropping. The result may also provide a reference for the use of biochars as a solution in agricultural waste management when sludge with considerable load of pathogens are involved. Soybean was already grown one year and will be repeated one more year with same treatments. The investigated soil properties included soil water content and mechanical resistance, pH, electrical conductivity (EC), calcium- acetate-lactate (CAL)-extractable P (PCAL) and K (KCAL), C, N, and nitrogen-supplying potential (NSP). The results show soil water content, potassium uptake and plant yield were increased. Heating sludge removed all pathogens and soybean yield was increased by 7%.

Bricks in historical buildings of Toledo City: characterisation and restoration

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lopez-Arce, Paula; Garcia-Guinea, Javier; Gracia, Mercedes

2003-01-15

Two different types of ancient bricks (12th to 14th centuries) collected from historical buildings of Toledo (Spain) were characterised by optical microscopy, scanning electron microscopy/energy-dispersive X-ray spectrometers (SEM/EDS), electron probe microanalysis (EM), X-ray diffraction (XRD), differential thermal analysis (DTA) and {sup 57}Fe-Moessbauer spectroscopy. Physical properties such as water absorption and suction, porosity, density and compression strength were also determined. Several minerals found in the brick matrix, such as garnet, let us infer raw material sources; calcite, dolomite, illite and neoformed gehlenite and diopside phases, on temperature reached in firing; secondary calcite, on first cooling scenarios; and manganese micronodules, on latemore » pollution environments. XRD and DTA of original and refired samples supply information about firing temperatures. Additional data on firing conditions and type of the original clay are provided by the Moessbauer study. Physical properties of both types of bricks were compared and correlated with raw materials and fabric and firing technology employed. The physicochemical characterisation of these bricks provides valuable data for restoration purposes to formulate new specific bricks using neighbouring raw materials.« less

The SPectrometer for Ice Nuclei (SPIN): An instrument to investigate ice nucleation

DOE PAGES

Garimella, Sarvesh; Kristensen, Thomas Bjerring; Ignatius, Karolina; ...

2016-07-06

The SPectrometer for Ice Nuclei (SPIN) is a commercially available ice nucleating particle (INP) counter manufactured by Droplet Measurement Technologies in Boulder, CO. The SPIN is a continuous flow diffusion chamber with parallel plate geometry based on the Zurich Ice Nucleation Chamber and the Portable Ice Nucleation Chamber. This study presents a standard description for using the SPIN instrument and also highlights methods to analyze measurements in more advanced ways. It characterizes and describes the behavior of the SPIN chamber, reports data from laboratory measurements, and quantifies uncertainties associated with the measurements. Experiments with ammonium sulfate are used to investigatemore » homogeneous freezing of deliquesced haze droplets and droplet breakthrough. Experiments with kaolinite, NX illite, and silver iodide are used to investigate heterogeneous ice nucleation. SPIN nucleation results are compared to those from the literature. A machine learning approach for analyzing depolarization data from the SPIN optical particle counter is also presented (as an advanced use). Altogether, we report that the SPIN is able to reproduce previous INP counter measurements.« less

Short-wave infrared reflectance investigation of sites of paleobiological interest: applications for Mars exploration.

PubMed

Brown, Adrian; Walter, Malcolm; Cudahy, Thomas

2004-01-01

Rover missions to the rocky bodies of the Solar System and especially to Mars require lightweight, portable instruments that use minimal power, require no sample preparation, and provide suitably diagnostic mineralogical information to an Earth-based exploration team. Short-wave infrared (SWIR) spectroscopic instruments such as the Portable Infrared Mineral Analyser (PIMA, Integrated Spectronics Pty Ltd., Baulkham Hills, NSW, Australia) fulfill all these requirements. We describe an investigation of a possible Mars analogue site using a PIMA instrument. A survey was carried out on the Strelley Pool Chert, an outcrop of stromatolitic, silicified Archean carbonate and clastic succession in the Pilbara Craton, interpreted as being modified by hydrothermal processes. The results of this study demonstrate the capability of SWIR techniques to add significantly to the geological interpretation of such hydrothermally altered outcrops. Minerals identified include dolomite, white micas such as illite-muscovite, and chlorite. In addition, the detection of pyrophyllite in a bleached and altered unit directly beneath the succession suggests acidic, sulfur-rich hydrothermal activity may have interacted with the silicified sediments of the Strelley Pool Chert.

Observations on Cretaceous abyssal hills in the northeast Pacific

USGS Publications Warehouse

Eittreim, S.L.; Piper, D.Z.; Chezar, H.; Jones, D.R.; Kaneps, A.

1984-01-01

An abyssal hills area of 50 ?? 60 km in the northeast Pacific was studied using bottom transponder navigation, closely spaced survey lines, and long-traverse oblique photography. The block-faulted north-south hills are bounded by scarps, commonly with 40?? slopes. On these steep scarps sedimentation is inhibited and pillow basalts often crop out. An ash layer of high acoustic reflectivity at about 7 m subbottom depth blankets the area. This ash occurs in multiple beds altered to phillipsite and is highly consolidated. A 24 m.y. age for the ash is based on ichthyolith dates from samples in the overlying sediments. Acoustically transparent Neogene sediments above the ash are thickest in trough bottoms and are absent or thin on steep slopes. These Neogene sediments are composed of pale-brown pelagic clays of illite, quartz, smectite, chlorite and kaolinite. Dark-brown pelagic clays, rich in smectite and amorphous iron oxides, underlie the Neogene surficial sediments. Manganese nodules cover the bottom in varying percentages. The nodules are most abundant near basement outcrops and where the subbottom ash layer is absent. ?? 1984.

Slides showing quantitative models for mineral-resource assessment of the Rolla 1 degree x 2 degrees Quadrangle, Missouri

USGS Publications Warehouse

Walker, Kim-Marie; Jenson, S.K.; Francica, J.R.; Hastings, D.A.; Trautwein, C.M.; Pratt, W.P.

1983-01-01

Th.is report consists of nineteen 35-mm color slides sh.owing digital synthesis and quantitative modeling of five geologic recognition criteria for assessment of Mississippi Valley-type resource potential in the Rolla 1° x 2° quadrangle, Missouri. The digital synthesis and quantitative modeling (Pratt and others, 1982) was done to supplement an earlier manual synthesis and evaluation (Pratt, 1981). The five criteria synthesized in this study, and the sources of data used, are that most known deposits are: In dolomite of the Bonneterre Formation, near the limestone-dolomite interface, which is defined as ls:dol = 1:16 (Thacker and Anderson, 1979; Kisvarsanyi, 1982);Near areas where insoluble residues of "barren" Bonneterre Formation contain anomalously high amounts of base metals (Erickson and others, 1978);Near areas of faults and fractures in the Bonneterre Formation or in underlying rocks (Pratt, 1982);In "brown rock" (finely crystalline brown dolomite) near the interface with "white rock" (coarsely recrystallized, white or very light gray, vuggy, illite-bearing dolomite) (Kisvarsanyi, 1982);Near or within favorably situated digitate reef-complex facies (Kisvarsanyi , 1982).

Water-rock interaction and geochemistry of groundwater from the Ain Azel aquifer, Algeria.

PubMed

Belkhiri, Lazhar; Mouni, Lotfi; Tiri, Ammar

2012-02-01

Hydrochemical, multivariate statistical, and inverse geochemical modeling techniques were used to investigate the hydrochemical evolution within the Ain Azel aquifer, Algeria. Cluster analysis based on major ion contents defined 3 main chemical water types, reflecting different hydrochemical processes. The first group water, group 1, has low salinity (mean EC = 735 μS/cm). The second group waters are classified as Cl-HCO(3)-alkaline earth type. The third group is made up of water samples, the cation composition of which is dominated by Ca and Mg with anion composition varying from dominantly Cl to dominantly HCO(3) plus SO(4). The varifactors obtained from R-mode FA indicate that the parameters responsible for groundwater quality variations are mainly related to the presence and dissolution of some carbonate, silicate, and evaporite minerals in the aquifer. Inverse geochemical modeling along groundwater flow paths indicates the dominant processes are the consumption of CO(2), the dissolution of dolomite, gypsum, and halite, along with the precipitation of calcite, Ca-montmorillonite, illite, kaolinite, and quartz. © Springer Science+Business Media B.V. 2011

CO2–rock–brine interactions in Lower Tuscaloosa Formation at Cranfield CO2 sequestration site, Mississippi, U.S.A.

USGS Publications Warehouse

Lu, Jiemin; Kharaka, Yousif K.; Thordsen, James J.; Horita, Juske; Karamalidis, Athanasios; Griffith, Craig; Hakala, J. Alexandra; Ambats, Gil; Cole, David R.; Phelps, Tommy J.; Manning, Michael A.; Cook, Paul J.; Hovorka, Susan D.

2012-01-01

A highly integrated geochemical program was conducted at the Cranfield CO2-enhanced oil recovery (EOR) and sequestration site, Mississippi, U.S.A.. The program included extensive field geochemical monitoring, a detailed petrographic study, and an autoclave experiment under in situ reservoir conditions. Results show that mineral reactions in the Lower Tuscaloosa reservoir were minor during CO2 injection. Brine chemistry remained largely unchanged, which contrasts with significant changes observed in other field tests. Field fluid sampling and laboratory experiments show consistently slow reactions. Carbon isotopic composition and CO2 content in the gas phase reveal simple two-end-member mixing between injected and original formation gas. We conclude that the reservoir rock, which is composed mainly of minerals with low reactivity (average quartz 79.4%, chlorite 11.8%, kaolinite 3.1%, illite 1.3%, concretionary calcite and dolomite 1.5%, and feldspar 0.2%), is relatively unreactive to CO2. The significance of low reactivity is both positive, in that the reservoir is not impacted, and negative, in that mineral trapping is insignificant.

Smectite diagenesis, pore-water freshening, and fluid flow at the toe of the Nankai wedge

USGS Publications Warehouse

Brown, K.M.; Saffer, D.M.; Bekins, B.A.

2001-01-01

The presence of low-chloride fluids in the lowermost sediments drilled at Ocean Drilling Program Site 808, at the Nankai accretionary wedge, has been considered as prime evidence for long-distance, lateral fluid flow from depth. Here, we re-evaluate the potential role of in situ reaction of smectite (S) to illite (I) in the genesis of this low chloride anomaly. This reaction is known to be occurring at Site 808, with both the S content and S to I ratio in the mixed layer clays decreasing substantially with depth. We show that the bulk of the chloride anomaly can generate by in situ clay dehydration, particularly if pre-reaction smectite abundances (Ai) approach ?? 10-15% of the bulk sediment. The Ai values, however, are not well constrained. At Ai values < 10-15%, an additional source of low-Cl fluid centered close to the de??collement could be required. Thus, there remains the important possibility that the observed low-Cl anomaly is a compound effect of both lateral flow and in situ smectite dehydration. ?? 2001 Elsevier Science B.V. All rights reserved.

What Makes a Natural Clay Antibacterial?

PubMed Central

Williams, Lynda B.; Metge, David W.; Eberl, Dennis D.; Harvey, Ronald W.; Turner, Amanda G.; Prapaipong, Panjai; Poret-Peterson, Amisha T.

2011-01-01

Natural clays have been used in ancient and modern medicine, but the mechanism(s) that make certain clays lethal against bacterial pathogens has not been identified. We have compared the depositional environments, mineralogies, and chemistries of clays that exhibit antibacterial effects on a broad spectrum of human pathogens including antibiotic resistant strains. Natural antibacterial clays contain nanoscale (<200 nm), illite-smectite and reduced iron phases. The role of clay minerals in the bactericidal process is to buffer the aqueous pH and oxidation state to conditions that promote Fe2+ solubility. Chemical analyses of E. coli killed by aqueous leachates of an antibacterial clay show that intracellular concentrations of Fe and P are elevated relative to controls. Phosphorus uptake by the cells supports a regulatory role of polyphosphate or phospholipids in controlling Fe2+. Fenton reaction products can degrade critical cell components, but we deduce that extracellular processes do not cause cell death. Rather, Fe2+ overwhelms outer membrane regulatory proteins and is oxidized when it enters the cell, precipitating Fe3+ and producing lethal hydroxyl radicals. PMID:21413758

Paleoproterozoic volcanic centers of the São Félix do Xingu region, Amazonian craton, Brazil: Hydrothermal alteration and metallogenetic potential

NASA Astrophysics Data System (ADS)

da Cruz, Raquel Souza; Fernandes, Carlos Marcello Dias; Villas, Raimundo Netuno Nobre; Juliani, Caetano; Monteiro, Lena Virgínia Soares; Lagler, Bruno; Misas, Carlos Mario Echeverri

2016-06-01

Geological, petrographic, scanning electron microscopy, and X-ray diffraction studies revealed hydrothermalized lithotypes evidenced by overprinted zones of potassic, propylitic, sericitic, and intermediate argillic alterations types, with pervasive and fracture-controlled styles, in Paleoproterozoic volcano-plutonic units of the São Félix do Xingu region, Amazonian craton, northern Brazil. The Sobreiro Formation presents propylitic (epidote + chlorite + carbonate + clinozoisite + sericite + quartz ± albite ± hematite ± pyrite), sericitic (sericite + quartz + carbonate), and potassic (potassic feldspar + hematite) alterations. The prehnite-pumpellyite pair that is common in geothermal fields also occurs in this unit. The Santa Rosa Formation shows mainly potassic (biotite + microcline ± magnetite), sericitic (sericite + quartz + carbonate ± chlorite ± gold), and intermediate argillic (montmorillonite + kaolinite/halloysite + illite) alterations. These findings strongly suggest the involvement of magma-sourced and meteoric fluids and draw attention to the metallogenetic potential of these volcanic units for Paleoproterozoic epithermal and rare and base metal porphyry-type mineralizations, similar to those already identified in other portions of the Amazonian craton.

New particle dependant parameterizations of heterogeneous freezing processes.

NASA Astrophysics Data System (ADS)

Diehl, Karoline; Mitra, Subir K.

2014-05-01

For detailed investigations of cloud microphysical processes an adiabatic air parcel model with entrainment is used. It represents a spectral bin model which explicitly solves the microphysical equations. The initiation of the ice phase is parameterized and describes the effects of different types of ice nuclei (mineral dust, soot, biological particles) in immersion, contact, and deposition modes. As part of the research group INUIT (Ice Nuclei research UnIT), existing parameterizations have been modified for the present studies and new parameterizations have been developed mainly on the basis of the outcome of INUIT experiments. Deposition freezing in the model is dependant on the presence of dry particles and on ice supersaturation. The description of contact freezing combines the collision kernel of dry particles with the fraction of frozen drops as function of temperature and particle size. A new parameterization of immersion freezing has been coupled to the mass of insoluble particles contained in the drops using measured numbers of ice active sites per unit mass. Sensitivity studies have been performed with a convective temperature and dew point profile and with two dry aerosol particle number size distributions. Single and coupled freezing processes are studied with different types of ice nuclei (e.g., bacteria, illite, kaolinite, feldspar). The strength of convection is varied so that the simulated cloud reaches different levels of temperature. As a parameter to evaluate the results the ice water fraction is selected which is defined as the relation of the ice water content to the total water content. Ice water fractions between 0.1 and 0.9 represent mixed-phase clouds, larger than 0.9 ice clouds. The results indicate the sensitive parameters for the formation of mixed-phase and ice clouds are: 1. broad particle number size distribution with high number of small particles, 2. temperatures below -25°C, 3. specific mineral dust particles as ice nuclei such as illite or montmorillonite. Coupled cases of deposition and contact freezing show that they are hardly in competition because of differences in the preferred particle sizes. In the contact mode, small particles are less efficient for collisions as well as less efficient as ice nuclei so that these are available for deposition freezing. On the other hand, immersion freezing is the dominant process when it is coupled with deposition freezing. As it is initiated earlier the formed ice particles consume water vapor for growing. The competition of combined contact and immersion freezing leads to lower ice water contents because more ice particles are formed via the immersion mode. In general, ice clouds and mixed-phase clouds with high ice water fractions are not directly the result of primary ice formation but of secondary ice formation and growth of ice particles at the expense of liquid drops.

Geochemical and technological characterization of clays of Corumbataí Formation, Paraná Basin, in the state of São Paulo, Brazil for the application in the ceramic industry.

NASA Astrophysics Data System (ADS)

Christofoletti, Sergio Ricardo; Torres Moreno, Maria Margarita; Batezelli, Alessandro; Zanardo, Antenor

2014-05-01

The Corumbataí Formation is a geological unit of the Paraná Basin comprises a range of predominantly argillaceous facies. These clays are important from an economic point of view, because they represent important mineral deposits suppliers of raw materials for the ceramic industry in the production of ceramic tiles.The study presents preliminary results of a research that aims to study the clays municipalities Tambaú, Ferreira and Santa Rosa of Viterbo in the State of São Paulo for their application and diversification of ceramic products. The methodology used was based on a detailed description of facies using the methodology in principles of analysis of Basin Miall (1984), followed by mineralogical identification by X-ray Diffraction, chemical analysis of major elements by X-ray Fluorescence and technological tests ceramic. According to the geological surveys of mines studied through columnar sections were identified the following lithofacies from base to top: Massive, Laminated, Intercalated and Altered. The mineralogy present on these lithofacies is composed by minerals: quartz, microclineo, albite, calcite, dolomite and hematite and by clay minerals illite, kaolinite and montmorillonite. The quartz represents the mineral more present in diffraction and occurs with d001 of 3.33Å in all lithofacies studied. The illite clay mineral represents the most frequent in studied samples presenting d 001 10Å in three conditions (natural, heated and treated with ethylene glycol) in which the blade was subjected to the analysis of X-ray diffraction, the presence of kaolinite or montmorillonite occurs or not in samples. It was observed a increased frequency of some minerals in the lithofacies studied, carbonates (calcite and dolomite), hematite and feldspar occurring in the intermediate portions of the profile with a predominance in lithofacies Intercalated. The illita clay mineral occurs throughout the profile, but with greater frequency in the lithofacies Massive and Laminated. The clay minerals kaolinite and montmorillonite occur in portions intermediate and top of the profiles studied in the intercalated and altered lithofacies. The chemical results of major elements by X-ray fluorescence confirmed the mineralogical results, with average values of 63.74 % of SiO2, 12.50 of Al2O3, 4.35% of of K2O, 0.45% of Na2O, 2,72% of CaO and 1,87 of MgO. The results chemical and mineralogical subsidized testing and ceramic formulations due to be executed later so defining the main applications of these clays in the production of ceramic products. The authors acknowledge the finantial support of Fundação de Amparo à Pesquisa do Estado de São Paulo-FAPESP, (Process, number 2012/24219-9).

Rapakivi texture: An indication of the crystallization of hydrosilicates, II

NASA Astrophysics Data System (ADS)

Elliston, John N.

1985-05-01

Rapakivi granites have puzzled all who have seriously studied them. Typical rapakivi texture is a mixture of variously mantled, non-mantled or partly mantled, concentrically zoned, plastically distorted, fragmented, reaggregated, large and small ovoids. Commonly they are potash feldspar often mantled by, and having a variable content of plagioclase. Some display remarkable sphericity. In form, composition, zoning sequence, and crystallization pattern each ovoid reflects an individual development. Up to five concentric internal plagioclase rims have been observed and some ovoids may be isolated in autoliths and wall-rocks. Anomalies and contradictions arise from any assumption of genesis from a cooling melt. The recorded objective data imply that the "magma" from which rapakivi textures develop had similar diffusive and rheological properties to those of a partly dewatered macromolecular paste or a mixture of gelatinous hydrosilicates. As indicated by deep oil wells this system is found at somewhat elevated temperatures at considerable depths within accumulated sediments. In addition to the very specific diffusive and rheological properties of such partly dewatered sediments, the system has as its major components normal solvated macromolecules of mixed clays, silica gels and hydrous ferromagnesian minerals which are characterised by distinctive particle sizes and geometric shapes (platelets, spheres and rods, respectively). Thixotropic liquefaction and intrusion of such concentrated gelatinous "magma" or sediment paste introduces relative movement between the component macromolecules whereby they can reduce surface energy by interaction to assume a "close-packed" condition and aggregate during laminar flow into macro-accretions comprised essentially of their respective particle shapes. Syneresis of these precursor accretions desorbs ions, including the small montmorillonite particles behaving as a colloidal electrolyte. These diffuse from the illitic cores to form a montmorillonite-rich rim which it is suggested crystallizes together with the illitic cores to form mantled or polymantled feldspar ovoids. Crystallization of the rapakivi massif is associated with strong temperature rise stemming from exothermic crystallization of the close-packed metastable colloids. This follows the development of the characteristic texture. The rounded and rimmed precursor accretions are formed during earlier lower-temperature episodes of thixotropic liquefaction which are isothermal. The fluidity is an earlier event. There is high temperature dependent on the rate of water loss but no molten stage. Forty-six typical features of rapakivi texture are described and illustrated, each of which is directly attributable to specific interactions in an alternately dynamic and static colloidal system. Individual correlation between each observed distinctive feature of the rapakivi texture and the well-documented physico-chemical process is complete. For sediment-derived granites, therefore, the rapakivi texture can confidently be assumed to be an indication of the crystallization of their sedimentary hydrosilicate precursors.

Differences and similarities between behavior of Fukushima-derived and Chernobyl-derived radiocesium in the environment

NASA Astrophysics Data System (ADS)

Konoplev, Alexei; Nanba, Kenji; Onda, Yuichi; Golosov, Valentin; Wakiyama, Yoshifumi; Takase, Tsugiko; Yoschenko, Vasyl; Zheleznyak, Mark

2016-04-01

The mobility and bioavailability of radiocesium (r-Cs) of accidental origin is governed by the ratio of its chemical forms in fallout and site-specific environmental characteristics determining the rates of leaching, fixation-remobilization, as well as sorption-desorption of the mobile fraction (its solid-liquid distribution). R-Cs in the environment is strongly bound to soil and sediment particles containing micaceous clay minerals (illite, vermiculite, etc.). This is associated with two basic processes - high selective reversible sorption and fixation. Climate and geographical conditions for Fukushima Prefecture of Japan and Chernobyl zone differ. For example, the catchments of the Chernobyl zone are flat and characterized by low slopes, while Fukushima's watersheds are hilly with steep slopes. Annual precipitation also differs substantially, with annual average for Fukushima about 3 times higher than at Chernobyl. The soils on the north-east coast of the Honshu island that were primarily affected by the radioactive contamination from the Fukushima Daiichi nuclear power plant (FDNPP) accident differ significantly from the Chernobyl zone soils. The proportion of clays such as illite, vermiculite etc. is 20-30% at Fukushima, which is higher than in the sandy loam soils of the Chernobyl zone. In addition to the landscape differences, the speciation of r-Cs in fallout was also different between Fukushima and Chernobyl. It is a challenge to compare r-Cs behavior in FDNPP and Chernobyl zones. Comparative analysis has been carried out for r-Cs wash-off parameters and the distribution coefficient Kd in rivers and surface runoff on Fukushima and Chernobyl contaminated areas for the first years after the accidents. The r-Cs distribution coefficient in Fukushima rivers was 1-2 orders of magnitude higher than correspondent values for rivers and surface runoff of the Chernobyl zone. This suggests higher ability of Fukushima soils and sediments to bind r-Cs. The normalized dissolved wash-off coefficients for Fukushima river watersheds are 1-2 orders of magnitude lower than corresponding values for the Chernobyl zone. Normalized particulate wash-off coefficients are comparable for Fukushima and Chernobyl. The effective dispersion coefficients in the Fukushima soils were found to be relatively high (2-10 cm2/year) as compared to Chernobyl values. Investigation and analysis of Fukushima-derived r-Cs distribution in soils of Niida river catchment has led to identify accumulation zones of contaminated sediments on the floodplain. Contaminated sediment accumulation is one of the most important factors for predicting r-Cs redistribution on a catchment and its fluvial transport, and is also relevant for decision making on remediation options of contaminated territories.

Effect of organic matter properties, clay mineral type and thermal maturity on gas adsorption in organic-rich shale systems

USGS Publications Warehouse

Zhang, Tongwei; Ellis, Geoffrey S.; Ruppel, Stephen C.; Milliken, Kitty; Lewan, Mike; Sun, Xun; Baez, Luis; Beeney, Ken; Sonnenberg, Steve

2013-01-01

A series of CH4 adsorption experiments on natural organic-rich shales, isolated kerogen, clay-rich rocks, and artificially matured Woodford Shale samples were conducted under dry conditions. Our results indicate that physisorption is a dominant process for CH4 sorption, both on organic-rich shales and clay minerals. The Brunauer–Emmett–Teller (BET) surface area of the investigated samples is linearly correlated with the CH4 sorption capacity in both organic-rich shales and clay-rich rocks. The presence of organic matter is a primary control on gas adsorption in shale-gas systems, and the gas-sorption capacity is determined by total organic carbon (TOC) content, organic-matter type, and thermal maturity. A large number of nanopores, in the 2–50 nm size range, were created during organic-matter thermal decomposition, and they significantly contributed to the surface area. Consequently, methane-sorption capacity increases with increasing thermal maturity due to the presence of nanopores produced during organic-matter decomposition. Furthermore, CH4 sorption on clay minerals is mainly controlled by the type of clay mineral present. In terms of relative CH4 sorption capacity: montmorillonite ≫ illite – smectite mixed layer > kaolinite > chlorite > illite. The effect of rock properties (organic matter content, type, maturity, and clay minerals) on CH4 adsorption can be quantified with the heat of adsorption and the standard entropy, which are determined from adsorption isotherms at different temperatures. For clay-mineral rich rocks, the heat of adsorption (q) ranges from 9.4 to 16.6 kJ/mol. These values are considerably smaller than those for CH4 adsorption on kerogen (21.9–28 kJ/mol) and organic-rich shales (15.1–18.4 kJ/mol). The standard entropy (Δs°) ranges from -64.8 to -79.5 J/mol/K for clay minerals, -68.1 to -111.3 J/mol/K for kerogen, and -76.0 to -84.6 J/mol/K for organic-rich shales. The affinity of CH4 molecules for sorption on organic matter is stronger than for most common clay minerals. Thus, it is expected that CH4 molecules may preferentially occupy surface sites on organic matter. However, active sites on clay mineral surfaces are easily blocked by water. As a consequence, organic-rich shales possess a larger CH4-sorption capacity than clay-rich rocks lacking organic matter. The thermodynamic parameters obtained in this study can be incorporated into model predictions of the maximum Langmuir pressure and CH4- sorption capacity of shales under reservoir temperature and pressure conditions.

Frictional behaviour of exhumed subduction zone sediments from the Shimanto Belt, Japan, at in-situ P-T conditions and implications for megathrust seismogenesis

NASA Astrophysics Data System (ADS)

den Hartog, Sabine; Niemeijer, Andre; Saffer, Demian; Marone, Chris

2014-05-01

Seismogenesis on subduction zone megathrusts is generally thought to be limited to a region between the ~100-150°C isotherms, at ~5-15 km depth, and the ~350°C isotherm, typically at ~40 km depth. This zone is bounded at its up-dip and down-dip limits by aseismic zones. However, in recent years it has been discovered that very low frequency earthquakes (VLFE) and non-destructive Slow Slip Events (SSEs) or slow earthquakes nucleate in these presumed aseismic regions. Slip on megathrusts is likely to localize in the weak subducted sediments along the plate interface, which implies that the fault material is derived at least in part from these sediments. Therefore, understanding the depth distribution of seismicity and SSEs on megathrusts requires knowledge of the frictional behaviour of metapelites. We investigated such behaviour by performing shear experiments on natural megathrust fault gouges, derived from exhumed subduction zone sediments and faults exposed in the Shimanto Belt on Shikoku Island, Japan. These gouges correspond to peak paleo-temperatures of 105°C to 280°C, representing different stages in the diagenetic and metamorphic evolution of the subducted sediments, covering the shallow aseismic zone as well as the seismogenic zone. The composition of all gouges was dominated by illite/muscovite, with smaller amounts of quartz, feldspar and chlorite. We sheared these gouges at low displacement rates (0.1-100 micron/s) to address the nucleation of megathrust earthquakes and SSEs, using either a double-direct (biaxial) shear machine or a rotary shear machine. The double-direct shear experiments were performed at room temperature, 5% relative humidity and 50 MPa normal stress. The rotary shear experiments, in turn, were conducted at the sample-specific, approximate peak in-situ P-T conditions, i.e. the P-T conditions corresponding to the maximum burial depth of these samples. At room temperature, samples from different peak paleo-temperatures showed similar frictional behaviour, with near-neutral velocity dependence, i.e. stable or aseismic behaviour. When deformed at their approximate in-situ peak P-T conditions, on the other hand, the samples showed a progressive transition from strong velocity-strengthening (stable) behaviour at 105°C (notably at 10-100 micron/s), to velocity-weakening (unstable) behaviour at 280°C. The results at elevated P-T conditions match previous results on simulated illite-quartz analogue fault gouges and imply a broad transition in the slip stability of subduction megathrusts from stable (velocity-strengthening), to unstable (velocity-weakening) with increasing depth, in agreement with seismological observations.

The Eocene-Oligocene sedimentary record in the Chesapeake Bay impact structure: Implications for climate and sea-level changes on the western Atlantic margin

USGS Publications Warehouse

Schulte, P.; Wade, B.S.; Kontny, A.; ,

2009-01-01

A multidisciplinary investigation of the Eocene-Oligocene transition in the International Continental Scientific Drilling Program (ICDP)-U.S. Geological Survey (USGS) Eyreville core from the Chesapeake Bay impact basin was conducted in order to document environmental changes and sequence stratigraphic setting. Planktonic foraminifera and calcareous nannofossil biostratigraphy indicate that the Eyreville core includes an expanded upper Eocene (Biozones E15 to E16 and NP19/20 to NP21, respectively) and a condensed Oligocene-Miocene (NP24-NN1) sedimentary sequence. The Eocene-Oligocene contact corresponds to a =3-Ma-long hiatus. Eocene- Oligocene sedimentation is dominated by great diversity and varying amounts of detrital and authigenic minerals. Four sedimentary intervals are identified by lithology and mineral content: (1) A 30-m-thick, smectite- and illite-rich interval directly overlies the Exmore Formation, suggesting long-term reworking of impact debris within the Chesapeake Bay impact structure. (2) Subsequently, an increase in kaolinite content suggests erosion from soils developed during late Eocene warm and humid climate in agreement with data derived from other Atlantic sites. However, the kaolinite increase may also be explained by change to a predominant sediment input from outside the Chesapeake Bay impact structure caused by progradation of more proximal facies belts during the highstand systems tract of the late Eocene sequence E10.Spectral analysis based on gamma-ray and magnetic susceptibility logs suggests infl uence of 1.2 Ma low-amplitude oscillation of the obliquity period during the late Eocene. (3) During the latest Eocene (Biozones NP21 and E16), several lithological contacts (clay to clayey silt) occur concomitant with a prominent change in the mineralogical composition with illite as a major component: This lithological change starts close to the Biozone NP19/20-NP21 boundary and may correspond to sequence boundary E10-E11 as observed in other northwest Atlantic margin sections. It could result from a shift to more distal depositional environments and condensed sedimentation during maximum fl ooding, rather than refl ecting a climatic change in the hinterland. The distinct 1% increase of the oxygen isotopes may correspond to the short-term latest Eocene "precursor isotope event." (4) The abrupt increase of sediment grainsize, carbonate content, and abundance of authigenic minerals (glauconite) across the major unconformity that separates Eocene from Oligocene sediments in the Eyreville core refl ects deposition in shallower settings associated with erosion, winnowing, and reworking. Sediments within the central crater were affected by the rapid eustatic sea-level changes associated with the greenhouse-icehouse transition, as well as by an abrupt major uplift event and possibly enhanced current activity on the northwestern Atlantic margin. ?? 2009 The Geological Society of America.

Infrared Spectroscopy for Rapid Characterization of Drill Core and Cutting Mineralogy

NASA Astrophysics Data System (ADS)

Calvin, W. M.; Kratt, C.; Kruse, F. A.

2009-12-01

Water geochemistry can vary with depth and location within a geothermal reservoir, owing to natural factors such as changing rock type, gas content, fluid source and temperature. The interaction of these variable fluids with the host rock will cause well known changes in alteration mineral assemblages that are commonly factored into the exploration of hydrothermal systems for economic metals, but are less utilized with regard to mapping borehole geology for geothermal energy production. Chemistry of geothermal fluids and rock alteration products can impact production factors such as pipeline corrosion and scaling and early studies explored the use of both silica and chlorites as geothermometers. Infrared spectroscopy is particularly good at identifying a wide variety of alteration minerals, especially in discrimination among clay minerals, with no sample preparation. The technique has been extensively used in the remote identification of materials, but is not commonly used on drill core or chips. We have performed several promising pilot studies that suggest the power of the technique to sample continuously and provide mineral logs akin to geophysical ones. We have surveyed a variety of samples, including drill chip boards, boxed core, and drill cuttings from envelopes, sample bottles and chip trays. This work has demonstrated that core and drill chips can be rapidly surveyed, acquiring spectra every few to tens of cm of section, or the vertical resolution of the chip tray (typically 10 feet). Depending on the sample type we can acquire spectral data over thousands of feet depth at high vertical resolution in a fraction of the time that is needed for traditional analytical methods such as XRD or TEM with better accuracy than traditional geologic drill or chip logging that uses visual inspection alone. We have successfully identified layered silicates such as illite, kaolinite, montmorillonite chlorite and prehnite, zeolites, opal, calcite, jarosite and iron oxides and hydroxides in geothermal drill samples. We are currently developing automated analysis techniques to convert this detailed spectral logging data into high-vertical-resolution mineral depth profiles that can be linked to lithology, stratigraphy, fracture zones and potential for geothermal production. Also in development are metrics that would link mapped mineralogy to known geothermometers such as Na-K, Mg depletion, discrimination among illite, montmorillonite, and beidellite, and kaolinite crystallinity. Identification of amorphous and crystalline silica components (chalcedony, crystobalite and quartz) can also constrain silica geothermometry. The degree of alteration and some mineral types have been shown to be a proxy for host rock permeability, natural circulation, and the potential for reservoir sealing. Analysis of alteration intensity is also under way. We will present a synthesis of results to date.

Hydrothermal alteration and mass exchange in the hornblende latite porphyry, Rico, Colorado

USGS Publications Warehouse

Larson, P.B.; Cunningham, C.G.; Naeser, C.W.

1994-01-01

The Rico paleothermal anomaly, southwestern Colorado, records the effects of a large hydrothermal system that was active at 4 Ma. This hydrothermal system produced the deep Silver Creek stockwork Mo deposit, which formed above the anomaly's heat source, and shallower base and precious-metal vein and replacement deposits. A 65 Ma hornblende latite porphyry is present as widespread sills throughout the area and provided a homogenous material that recorded the effects of the hydrothermal system up to 8 km from the center. Hydrothermal alteration in the latite can be divided into a proximal facies which consists of two assemblages, quartz-illite-calcite and chlorite-epidote, and a distal facies which consists of a distinct propylitic assemblage. Temperatures were gradational vertically and laterally in the anomaly, and decreased away from the centra heat source. A convective hydrothermal plume, 3 km wide and at least 2 km high, was present above the stock-work molybdenum deposit and consisted of upwelling, high-temperature fluids that produced the proximal alteration facies. Distal facies alteration was produced by shallower cooler fluids. The most important shallow base and precious-metal vein deposits in the Rico district are at or close to the boundary of the thermal plume. Latite within the plume had a large loss of Na2O, large addition of CaO, and variable SiO2 exchante. Distal propylitized latite samples lost small amounts of Na2O and CaO and exchanged minor variable amounts of SiO2. The edge of the plume is marked by steep Na2O exchange gradients. Na2O exchange throughout the paleothermal anomaly was controlled by the reaction of the albite components in primary plagioclase and alkali feldspars. Initial feldspar alteration in the distal facies was dominated by reaction of the plagioclase, and the initial molar ratio of reactants (alkali feldspar albite component to plagioclase albite component) was 0.35. This ratio of the moles of plagioclase to alkali feldspar albite components that reacted evolved to 0.92 as the reaction progressed. Much of the alkali feldspar albite component in the proximal facies reacted while the, primary plagioclase was still unreacted, but the ratio for these assemblages increased to 1.51 when the plagioclase entered the reaction paragenesis. Plagioclase reaction during distal propylitic alteration resulted in pseudomorphic albite mixed with illite and a loss of Na2O. CaO is lost in the distal facies as hornblende reacts to chlorite, although some calcium may be fixed in calcite. CaO is added to the proximal facies as the quantity of chlorite replacing hornblende increases and epidote and calcite are produced. ?? 1994 Springer-Verlag.

The Marianas-San Marcos vein system: characteristics of a shallow low sulfidation epithermal Au-Ag deposit in the Cerro Negro district, Deseado Massif, Patagonia, Argentina

NASA Astrophysics Data System (ADS)

Vidal, Conrado Permuy; Guido, Diego M.; Jovic, Sebastián M.; Bodnar, Robert J.; Moncada, Daniel; Melgarejo, Joan Carles; Hames, Willis

2016-08-01

The Cerro Negro district, within the Argentinian Deseado Massif province, has become one of the most significant recent epithermal discoveries, with estimated reserves plus resources of ˜6.7 Moz Au equivalent. The Marianas-San Marcos vein system contains about 70 % of the Au-Ag resources in the district. Mineralization consists of Upper Jurassic (155 Ma) epithermal Au- and Ag-rich veins of low to intermediate sulfidation style, hosted in and genetically related to Jurassic intermediate composition volcanic rocks (159-156 Ma). Veins have a complex infill history, represented by ten stages with clear crosscutting relationships that can be summarized in four main episodes: a low volume, metal-rich initial episode (E1), an extended banded quartz episode with minor mineralization (E2), a barren waning stage episode (E3), and a silver-rich late tectonic-hydrothermal episode (E4). The first three episodes are interpreted to have formed at the same time and probably from fluids of similar composition: a 290-230 °C fluid dominated by meteoric and volcanic waters (-3‰ to -0‰ δ18Owater), with <3 % NaCl equivalent salinity and with a magmatic source of sulfur (-1 to -2 ‰ δ34Swater). Metal was mainly precipitated at the beginning of vein formation (episode 1) due to a combination of boiling at ˜600 to 800 m below the paleowater table, and associated mixing/cooling processes, as evidenced by sulfide-rich bands showing crustiform-colloform quartz, adularia, and chlorite-smectite banding. During episodes 2 and 3, metal contents progressively decrease during continuing boiling conditions, and veins were filled by quartz and calcite during waning stages of the hydrothermal system, and the influx of bicarbonate waters (-6 to -8.5 ‰ δ18Owater). Hydrothermal alteration is characterized by proximal illite, adularia, and silica zone with chlorite and minor epidote, intermediate interlayered illite-smectite and a distal chlorite halo. This assemblage is in agreement with measured fluid inclusion temperatures. A striking aspect of the Marianas-San Marcos vein system is that the high-grade/high-temperature veins are partially covered by breccia and volcaniclastic deposits of acidic composition, and are spatially associated with hot spring-related deposits and an advanced argillic alteration blanket. A telescoped model is therefore proposed for the Marianas-San Marcos area, where deeper veins were uplifted and eroded, and then partially covered by non-explosive, post-mineral rhyolitic domes and reworked volcaniclastic deposits, together with shallow geothermal features. The last tectonic-hydrothermal mineralization episode (E4), interpreted to have formed at lower temperatures, could be related to this late tectonic and hydrothermal activity.

Geochemistry of autochthonous and hypautochthonous siderite-dolomite coal-balls (Foord Seam, Bolsovian, Upper Carboniferous), Nova Scotia, Canada

USGS Publications Warehouse

Zodrow, E.L.; Lyons, P.C.; Millay, M.A.

1996-01-01

The 11-13 m thick Foord Seam in the fault-bounded Stellarton Basin, Nova Scotia, is the thickest seam from the Euramerican floral province known to contain coal-balls. In addition to the first discovery of autochthonous coal-balls in the Foord Seam, Nova Scotia, its shale parting also contains hypautochthonous coal-balls with histologically preserved plant structures. The coal-ball discovery helps fill a stratigraphic gap in coal-ball occurrences in the upper Carboniferous (Bolsovian) of Euramerica. The autochthonous and hypautochthonous coal-balls have a similar mineralogical composition and are composed of siderite (81-100%), dolomite-ankerite (0-19%), minor quartz and illite, and trace amounts of 'calcite'. Similar is also their permineralizing mineralogy, which consists of dolomite-ankerite and siderite. Their low pyrite content and carbonate mineralogy, and nonmarine origin, differentiates the Foord Seam coal-balls from other Euramerican coal-ball occurrences. A preliminary geochemical model, which is based on oxygen and carbon isotopic data, indicates that siderite in both the autochthonous and hypautochthonous coal-balls is of very early diagenetic (nonmarine) origin from 13C-enriched bicarbonate derived from bacterial methanogenesis of organic matter.

The inheritance of a Mesozoic landscape in western Scandinavia

PubMed Central

Fredin, Ola; Viola, Giulio; Zwingmann, Horst; Sørlie, Ronald; Brönner, Marco; Lie, Jan-Erik; Grandal, Else Margrethe; Müller, Axel; Margreth, Annina; Vogt, Christoph; Knies, Jochen

2017-01-01

In-situ weathered bedrock, saprolite, is locally found in Scandinavia, where it is commonly thought to represent pre-Pleistocene weathering possibly associated with landscape formation. The age of weathering, however, remains loosely constrained, which has an impact on existing geological and landscape evolution models and morphotectonic correlations. Here we provide new geochronological evidence that some of the low-altitude basement landforms on- and offshore southwestern Scandinavia are a rejuvenated geomorphological relic from Mesozoic times. K-Ar dating of authigenic, syn-weathering illite from saprolitic remnants constrains original basement exposure in the Late Triassic (221.3±7.0–206.2±4.2 Ma) through deep weathering in a warm climate and subsequent partial mobilization of the saprolitic mantle into the overlying sediment cascade system. The data support the bulk geomorphological development of west Scandinavia coastal basement rocks during the Mesozoic and later, long-lasting relative tectonic stability. Pleistocene glaciations played an additional geomorphological role, selectively stripping the landscape from the Mesozoic overburden and carving glacial landforms down to Plio–Pleistocene times. Saprolite K-Ar dating offers unprecedented possibilities to study past weathering and landscape evolution processes. PMID:28452366

DOE Office of Scientific and Technical Information (OSTI.GOV)

Kalyoncu, R.S.; Boyer, J.P.; Snyder, M.J.

Partial data on the characterization of Well 0-1 (Christian County, Kentucky) shales were first reported in the Fifth Quarterly Technical Progress Report on January 1978. This report presents all the characterization data and its analysis on the 0-1 shales. Coring of Well 0-1 was accomplished in October 1976. A total of 17 samples were obtained, 13 for Battelle and 4 for other DOE Contractors. Methane is almost the sole hydrocarbon gas present in these shales, with higher chain hydrocarbon gases nearly nonexistent. An apparent increase in hydrocarbon gas contents with shale depth is observed. Other organic contents (in the formmore » of carbon and hydrogen) also show an increase with increasing shale depth. An increase in hydrocarbon gas contents with carbon and hydrogen contents is also noticeable. Natural gas, carbon and hydrogen contents all vary inversely with bulk densities. 0-1 shales show low mercury intrusion porosities and very low to negligible gas permeabilities. Lithology of these shales is very similar to those previously reported, quartz being the most abundant single mineral. Illite and kaolin are the major clay minerals with a number of carbonates (nahcolite, sortite, siderite) present in moderate quantities. Pyrite is also observed in significant quantities.« less

Mineral particles content in recent snow at Summit (Greenland)

NASA Astrophysics Data System (ADS)

Drab, E.; Gaudichet, A.; Jaffrezo, J. L.; Colin, J. L.

The mineral insoluble fraction of snowpit samples collected at Summit is investigated, representing deposition from summer 1987 to summer 1991. We attempt to describe the particles which are observed in the series, with very large seasonal variations. Elemental, mineralogical and size distribution studies are carried out on four samples selected according to the chemical profile of the snowpit (two samples from spring and two from winter) using X-ray fluorescence spectrometry and analytical transmission electron microscopy. Results indicate a large predominance of the soil-derived particles originating from arid or semi-arid regions of the Northern Hemisphere. The mineralogy clearly indicates a high contribution for the muscovite-illite associated with a low kaolinite/chlorite ratio, together with the rather lack of smectite. This supports the hypothesis of an Asian source. Several other factors are consistent with this Asian source, like the recent climatology and the good timing between the Asian dust storms period and the peak of dust concentration in the ice. The mineralogy of the insoluble particles in the snow is similar between winter and spring, suggesting that the change of concentration between the seasons is more strongly linked to changes of atmospheric parameters than changes of the source regions.

Application of Principal Component Analysis to NIR Spectra of Phyllosilicates: A Technique for Identifying Phyllosilicates on Mars

NASA Technical Reports Server (NTRS)

Rampe, E. B.; Lanza, N. L.

2012-01-01

Orbital near-infrared (NIR) reflectance spectra of the martian surface from the OMEGA and CRISM instruments have identified a variety of phyllosilicates in Noachian terrains. The types of phyllosilicates present on Mars have important implications for the aqueous environments in which they formed, and, thus, for recognizing locales that may have been habitable. Current identifications of phyllosilicates from martian NIR data are based on the positions of spectral absorptions relative to laboratory data of well-characterized samples and from spectral ratios; however, some phyllosilicates can be difficult to distinguish from one another with these methods (i.e. illite vs. muscovite). Here we employ a multivariate statistical technique, principal component analysis (PCA), to differentiate between spectrally similar phyllosilicate minerals. PCA is commonly used in a variety of industries (pharmaceutical, agricultural, viticultural) to discriminate between samples. Previous work using PCA to analyze raw NIR reflectance data from mineral mixtures has shown that this is a viable technique for identifying mineral types, abundances, and particle sizes. Here, we evaluate PCA of second-derivative NIR reflectance data as a method for classifying phyllosilicates and test whether this method can be used to identify phyllosilicates on Mars.

Contents and occurrence of cadmium in the coals from Guizhou province, China.

PubMed

Song, Dangyu; Wang, Mingshi; Zhang, Junying; Zheng, Chuguang

2008-10-01

Eleven raw coal samples were collected from Liuzhi, Suicheng, Zunyi, Xingren, Xingyi, and Anlong districts in Guizhou Province, Southwest China. The content of cadmium (Cd) in coal was determined using inductively coupled plasma mass-spectrometry (ICP-MS). Cd contents ranged from 0.146 to 2.74 ppm (whole coal basis), with an average of 1.09 ppm. In comparison with the arithmetic means of Cd in Chinese coal (0.25 ppm), this is much higher. In order to find its occurrence in coal, float-sink analysis and a coal flotation test by progressive release were conducted on two raw coal samples. The content of the Cd and ash yield of the flotation products were determined. The organic matter was removed by low-temperature ashing (LTA). X-ray diffraction (XRD) was used to differentiate the main, minor, and trace minerals in the LTA from different flotation subproducts. Quartz, kaolinite, pyrite, and calcite were found to dominate the mineral matters, with a proportion of anatase, muscovite, and illite. Then quantitative analysis of minerals in LTA was conducted using material analysis using diffraction (MAUD) based on the Rietveld refinement method. Results show that Cd has a strong association with kaolinite.

Abundance and distribution of ultramafic microbreccia in Moses Rock Dike: Quantitative application of AIS data

NASA Technical Reports Server (NTRS)

Mustard, John F.; Pieters, Carle M.

1987-01-01

Moses Rock dike is a Tertiary diatreme containing serpentinized ultramafic microbreccia (SUM). Field evidence indicates the SUM was emplaced first followed by breccias derived from the Permian strata exposed in the walls of the diatreme and finally by complex breccias containing basement and mantle derived rocks. SUM is found primarily dispersed throughout the matrix of the diatreme. Moses Rock dike was examined with Airborne Imaging Spectrometer (AIS) to map the distribution and excess of SUM in the matrix and to better understand the nature of the eruption which formed this explosive volcanic feature. AIS data was calibrated by dividing the suite of AIS data by data from an internal standard area and then multiplying this relative reflectance data by the absolute bidirectional reflectance of a selected sample from the standard area which was measured in the lab. From the calibrated AIS data the minerals serpentine, gypsum, and illite as well as desert varnish and the lithologies SUM and other sandstones were identified. SUM distribution and abundance in the matrix of the diatreme were examined in detail and two distinct styles of SUM dispersion were observed. The two styles are discussed in detail.

Hyperspectral remote sensing applied to mineral exploration in southern Peru: A multiple data integration approach in the Chapi Chiara gold prospect

NASA Astrophysics Data System (ADS)

Carrino, Thais Andressa; Crósta, Alvaro Penteado; Toledo, Catarina Labouré Bemfica; Silva, Adalene Moreira

2018-02-01

Remote sensing is a strategic key tool for mineral exploration, due to its capacity of detecting hydrothermal alteration minerals or alteration mineral zones associated with different types of mineralization systems. A case study of an epithermal system located in southern Peru is presented, aimed at the characterization of mineral assemblies for discriminating potential high sulfidation epithermal targets, using hyperspectral imagery integrated with petrography, XRD and magnetic data. HyMap images were processed using the Mixture Tuned Matched Filtering (MTMF) technique for producing alteration map in the Chapi Chiara epithermal gold prospect. Extensive areas marked by advanced argillic alteration (alunite-kaolinite-dickite ± topaz) were mapped in detail, as well as limited argillic (illite-smectite) and propylitic (chlorite spectral domain) alteration. The magmatic-hydrothermal processes responsible for the formation of hypogene minerals were also related to the destruction of ferrimagnetic minerals (e.g., magnetite) of host rocks such as andesite, and the remobilization/formation of paramagnetic Fe-Ti oxides (e.g., rutile, anatase). The large alteration zones of advanced argillic alteration are controlled by structures related to a regional NW-SE trend, and also by local NE-SW and ENE-WSW ones.

Lake Chad sedimentation and environments during the late Miocene and Pliocene: New evidence from mineralogy and chemistry of the Bol core sediments

NASA Astrophysics Data System (ADS)

Moussa, Abderamane; Novello, Alice; Lebatard, Anne-Elisabeth; Decarreau, Alain; Fontaine, Claude; Barboni, Doris; Sylvestre, Florence; Bourlès, Didier L.; Paillès, Christine; Buchet, Guillaume; Duringer, Philippe; Ghienne, Jean-François; Maley, Jean; Mazur, Jean-Charles; Roquin, Claude; Schuster, Mathieu; Vignaud, Patrick; Brunet, Michel

2016-06-01

This study presents mineralogical and geochemical data from a borehole drilled near the locality of Bol (13°27‧N, 14°44‧E), in the eastern archipelago of the modern Lake Chad (Chad). Samples were taken from a ∼200 m long core section forming a unique sub-continuous record for Central Africa. Among these samples, 25 are dated between 6.4 and 2.4 Ma. Dominant minerals are clays (66% average) mixed with varying amounts of silt and diatomite. The clay fraction consists of Fe-beidellite (87% average), kaolinite, and traces of illite. Clay minerals originate from the erosion of the vertisols that surrounded the paleolake Chad. Sedimentological data indicate that a permanent lake (or recurrent lakes) existed from 6.7 until 2.4 Ma in the vicinity of Bol. By comparison with modern latitudinal distribution of vertisols in Africa the climate was Sudanian-like. Changes in the sedimentation rate suggest a succession of wetter and dryer periods during at least six million years in the region during the critical time period covering the Miocene-Pliocene transition.

Slip localization on the southern Alpine Fault, New Zealand

NASA Astrophysics Data System (ADS)

Barth, N. C.; Boulton, C.; Carpenter, B. M.; Batt, G. E.; Toy, V. G.

2013-06-01

of a detailed field study of the southern onshore portion of New Zealand's Alpine Fault reveal that for 75 km along-strike, dextral-normal slip on this long-lived structure is highly localized in phyllosilicate-rich fault core gouges and along their contact with more competent rocks. At three localities (Martyr River, McKenzie Creek, and Hokuri Creek), we document complete cross sections through the fault. New 40Ar/39Ar dates on mylonites, combined with microstructural and mechanical data on phyllosilicate-rich fault core gouges show that modern slip is localized onto a single, steeply dipping 1 to 12 m-thick fault core composed of impermeable (k = 10-20 to 10-22 m2), frictionally weak (μs = 0.12-0.37), velocity-strengthening, illite-chlorite, and saponite-chlorite-lizardite fault gouges. Fault core materials are (1) comparable to those of other major weak-cored faults (e.g., San Andreas Fault) and (2) most compatible with fault creep, despite paleoseismic evidence of quasiperiodic large magnitude earthquakes (Mw > 7) on this portion of the Alpine Fault. We conclude that frictional properties of gouges at the surface do not characterize the overall seismogenic behavior of the southern Alpine Fault.

Clay minerals and metal oxides strongly influence the structure of alkane-degrading microbial communities during soil maturation.

PubMed

Steinbach, Annelie; Schulz, Stefanie; Giebler, Julia; Schulz, Stephan; Pronk, Geertje J; Kögel-Knabner, Ingrid; Harms, Hauke; Wick, Lukas Y; Schloter, Michael

2015-07-01

Clay minerals, charcoal and metal oxides are essential parts of the soil matrix and strongly influence the formation of biogeochemical interfaces in soil. We investigated the role of these parental materials for the development of functional microbial guilds using the example of alkane-degrading bacteria harbouring the alkane monooxygenase gene (alkB) in artificial mixtures composed of different minerals and charcoal, sterile manure and a microbial inoculum extracted from an agricultural soil. We followed changes in abundance and community structure of alkane-degrading microbial communities after 3 and 12 months of soil maturation and in response to a subsequent 2-week plant litter addition. During maturation we observed an overall increasing divergence in community composition. The impact of metal oxides on alkane-degrading community structure increased during soil maturation, whereas the charcoal impact decreased from 3 to 12 months. Among the clay minerals illite influenced the community structure of alkB-harbouring bacteria significantly, but not montmorillonite. The litter application induced strong community shifts in soils, maturated for 12 months, towards functional guilds typical for younger maturation stages pointing to a resilience of the alkane-degradation function potentially fostered by an extant 'seed bank'.

Some engineering aspects of homoionized mixed clay minerals.

PubMed

Oren, Ali Hakan; Kaya, Abidin

2003-05-01

Many studies have been conducted to investigate the physicochemical behavior of pure clay minerals and predict their engineering performance in the field. In this study, the physicochemical properties of an artificial mixture of different clay minerals namely, 40-50% montmorillonite, 20-30% illite and 10-15% kaolin were investigated. The mixture was homoionized with sodium, Na+; calcium, Ca2+; and aluminum, Al3+. The engineering properties studied were consistency limits, sediment volume, compressibility behavior, and hydraulic conductivity. The results revealed that the liquid, plastic and shrinkage limits of soil increased with increasing cation valence. The hydraulic conductivity of the soil also increased with an increase in the valence of the cation at any given void ratio. Aluminum and sodium treated clays had the highest and the lowest modified compression index values, respectively. Furthermore, trivalent cation saturated clayey soil consolidates three times faster than that of monovalent and two times faster than that of divalent. These properties of the soils determined were, in general, similar to those of kaolinite rather than those of montmorillonite. The comparison of the results obtained with the published data in the literature revealed that the physicochemical behavior of the tested clay soil was, in general, similar to that of kaolinite.

Mineral mapping in the Maherabad area, eastern Iran, using the HyMap remote sensing data

NASA Astrophysics Data System (ADS)

Molan, Yusuf Eshqi; Refahi, Davood; Tarashti, Ali Hoseinmardi

2014-04-01

This study applies matched filtering on the HyMap airborne hyperspectral data to obtain the distribution map of alteration minerals in the Maherabad area and uses virtual verification to verify the results. This paper also introduces "moving threshold" which tries to find an appropriate threshold value to convert gray scale images, produced by mapping methods, to target and background pixels. The Maherabad area, located in the eastern part of the Lut block, is a Cu-Au porphyry system in which quartz-sericite-pyrite, argillic and propylitic alteration are most common. Minimum noise fraction transform coupled with a pixel purity index was applied on the HyMap images to extract the endmembers of the alteration minerals, including kaolinite, montmorillonite, sericite (muscovite/illite), calcite, chlorite, epidote, and goethite. Since there was no access to any portable spectrometer and/or lab spectral measurements for the verification of the remote sensing imagery results, virtual verification achieved using the USGS spectral library and showed an agreement of 83.19%. The comparison between the results of the matched filtering and X-ray diffraction (XRD) analyses also showed an agreement of 56.13%.

Hydrothermal alteration mapping using ASTER data in Baogutu porphyry deposit, China

NASA Astrophysics Data System (ADS)

Li, Q.; Zhang, B.; Lu, L.; Lin, Q.

2014-03-01

Remote sensing plays an important role in mineral exploration. One of its proven applications is extracting host-rock lithology and alteration zones that are related to porphyry copper deposits. An Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) was used to map the Baogutu porphyry deposit alteration area. A circular alteration mineral zoning pattern was clearly observed in the classification result of potassic, phyllic, argillic, propylitic zones. The potassic is characterized by biotite and anhydrite with an absorption feature centered at 1.94 and 2.1um. The phyllic zone is characterized by illite and sericite that indicates an intense Al-OH absorption feature centered at 2.20um. The narrower argillic zone including kaolinite and alunite displays a secondary Al-OH absorption feature at 2.17 um. The mineral assemblages of the outer propylitic zone are epidote, chlorite and calcite that exhibit absorption features at 2.335um.The performance of Principal Component Analysis(PCA), Minimum Noise Fraction (MNF), band ratio(BR) and Constrained Energy Minimization(CEM) has been evaluated. These techniques identified new prospects of porphyry copper mineralization in the study areas. These results indicate that ASTER is a powerful tool in the initial steps of mineral exploration.

Effects of pollution and bioleaching process on the mineral composition and texture of contaminated sediments of the Reconquista River, Argentina.

PubMed

Tufo, Ana E; Porzionato, Natalia F; Curutchet, Gustavo

2017-10-31

In this work, we report on the structural and textural changes in fluvial sediments from Reconquista River´s basin, Argentina, due to processes of contamination with organic matter and remediation by bioleaching. The original uncontaminated matrix showed quartz and phyllosilicates as the main primary mineral constituents and phases of interstratified illite-montmorillonite as secondary minerals. It was found that in contaminated sediments, the presence of organic matter in high concentration causes changes in the specific surface area, particle size distribution, size and distribution of micro and meso, and the morphology of the particles with respect to the uncontaminated sediment. After the bioleaching process, there were even greater changes in these parameters at the level of secondary mineral formation and the appearance of nanoparticles, which were confirmed by SEM. Especially, we found the formation of cementing substances such as gypsum, promoting the formation of macroporous aggregates and the weathering of clay components. Our results indicate that the bioleaching not only decreases the content of metals but also favors the formation of a material with improved characteristics for potential future applications.

Study of gamma spectrometry laboratory measurement in various sediment and vulcanic rocks

NASA Astrophysics Data System (ADS)

Nurhandoko, Bagus Endar B.; Kurniadi, Rizal; Rizka Asmara Hadi, Muhammad; Rizal Komara, Insan

2017-01-01

Gamma-ray spectroscopy is the quantitative study of the energy spectra of gamma-ray sources. This method is powerful to characterize some minerals, especially to differentiate rocks which contains among Potassium, Uranium, dan Thorium. Rock contains radioactive material which produce gamma rays in various energies and intensities. When these emissions are detected and analyzed with a spectroscopy system, a gamma-ray energy spectrum can be used as indicator for mineral content of rock. Some sediment and vulcanic rock have been collected from East Java Basin. Samples are ranging from Andesite vulcanics, Tuff, Shale, various vulcanic clay and Alluvial clay. We present some unique characteristics of gamma spectrometry in various sedimentar and vulcanic rocks of East Java Basins. Details contents of gamma ray spectra give enrichments to characterize sample of sediment and vulcanic in East Java. Weathered vulcanic clay has lower counting rate of gamma ray than alluvial deltaic clay counting rate. Therefore, gamma spectrometrometry can be used as tool for characterizing the enviroment of clay whether vulcanic or alluvial-deltaic. This phenomena indicates that gamma ray spectrometry can be as tool for characterizing the clay whether it tends to Smectite or Illite

Clay minerals and metal oxides strongly influence the structure of alkane-degrading microbial communities during soil maturation

PubMed Central

Steinbach, Annelie; Schulz, Stefanie; Giebler, Julia; Schulz, Stephan; Pronk, Geertje J; Kögel-Knabner, Ingrid; Harms, Hauke; Wick, Lukas Y; Schloter, Michael

2015-01-01

Clay minerals, charcoal and metal oxides are essential parts of the soil matrix and strongly influence the formation of biogeochemical interfaces in soil. We investigated the role of these parental materials for the development of functional microbial guilds using the example of alkane-degrading bacteria harbouring the alkane monooxygenase gene (alkB) in artificial mixtures composed of different minerals and charcoal, sterile manure and a microbial inoculum extracted from an agricultural soil. We followed changes in abundance and community structure of alkane-degrading microbial communities after 3 and 12 months of soil maturation and in response to a subsequent 2-week plant litter addition. During maturation we observed an overall increasing divergence in community composition. The impact of metal oxides on alkane-degrading community structure increased during soil maturation, whereas the charcoal impact decreased from 3 to 12 months. Among the clay minerals illite influenced the community structure of alkB-harbouring bacteria significantly, but not montmorillonite. The litter application induced strong community shifts in soils, maturated for 12 months, towards functional guilds typical for younger maturation stages pointing to a resilience of the alkane-degradation function potentially fostered by an extant ‘seed bank'. PMID:25535940

Sub-pixel mineral mapping using EO-1 Hyperion hyperspectral data

NASA Astrophysics Data System (ADS)

Kumar, C.; Shetty, A.; Raval, S.; Champatiray, P. K.; Sharma, R.

2014-11-01

This study describes the utility of Earth Observation (EO)-1 Hyperion data for sub-pixel mineral investigation using Mixture Tuned Target Constrained Interference Minimized Filter (MTTCIMF) algorithm in hostile mountainous terrain of Rajsamand district of Rajasthan, which hosts economic mineralization such as lead, zinc, and copper etc. The study encompasses pre-processing, data reduction, Pixel Purity Index (PPI) and endmember extraction from reflectance image of surface minerals such as illite, montmorillonite, phlogopite, dolomite and chlorite. These endmembers were then assessed with USGS mineral spectral library and lab spectra of rock samples collected from field for spectral inspection. Subsequently, MTTCIMF algorithm was implemented on processed image to obtain mineral distribution map of each detected mineral. A virtual verification method has been adopted to evaluate the classified image, which uses directly image information to evaluate the result and confirm the overall accuracy and kappa coefficient of 68 % and 0.6 respectively. The sub-pixel level mineral information with reasonable accuracy could be a valuable guide to geological and exploration community for expensive ground and/or lab experiments to discover economic deposits. Thus, the study demonstrates the feasibility of Hyperion data for sub-pixel mineral mapping using MTTCIMF algorithm with cost and time effective approach.

Mineralogy and diagenesis of low-permeability sandstones of Late Cretaceous age, Piceance Creek Basin, northwestern Colorado

USGS Publications Warehouse

Hansley, Paula L.; Johnson, Ronald C.

1980-01-01

This report presents preliminary results of a mineralogic and diagenetic study of some low-permeability sandstones from measured surface sections and cores obtained from drill holes in the Piceance Creek Basin of northwestern Colorado. A documentation of the mineralogy and diagenetic history will aid in the exploration for natural gas and in the development of recovery technology in these low-permability sandstones. These sandstones are in the nonmarine upper part of the Mesaverde Formation (or Group) of Late Cretaceous age and are separated from overlying lower Tertiary rocks by a major regional unconformity. Attention is focused on the sandstone units of the Ohio Creek Member, which directly underlies the unconformity; however, comparisons between the mineralogy of the Ohio Creek strata and that of the underlying sandstone units are made whenever possible. The Ohio Creek is a member of the Hunter Canyon Formation (Mesaverde Group) in the southwestern part of the basin, and the Mesaverde Formation in the southern and central parts of the basin. The detrital mineralogy is fairly constant throughout all of these nonrnarine Cretaceous sandstone units; however, in the southeastern part of the basin, there is an increase in percentage of feldspar, quartzite, and igneous rock fragments in sandstones of the Ohio Creek Member directly underlying the unconformity. In the southwestern part of the basin, sandstones of the Ohio Creek Member are very weathered and are almost-entirely comprised of quartz, chert, and kaolinite. A complex diagenetic history, partly related to the overlying unconformity, appears to be responsible for transforming these sandstones into potential gas reservoirs. The general diagenetic sequence for the entire Upper Cretaceous interval studied is interpreted to be (early to late): early(?) calcite cement, chlorite, quartz overgrowths, calcite cement, secondary porosity, analcime (surface only), kaolinite and illite, and late carbonate cements. Authigenic high-iron chlorite, which occurs on grain rims and in pore throats, is primarily responsible for the low-permeability of the subsurface sandstones of the Ohio Creek Member in the center of the basin. Kaolinite is the most abundant pore-filling authigenic clay in these sandstones, from the southwestern part of the basin and is responsible for their distinctive white-weathering color in outcrop. In the sandstones below the Ohio Creek Member, however, chlorite and kaolinite occur locally, and authigenic calcite and illite are more abundant. The occurrence and distribution of secondary porosity is one of the most important aspects of the diagenetic history of these sandstones. It is present as moldic intra- and intergranular porosity, as well as microporosity among authigenic clay pariicles. Although present locally in most sandstone units, secondary porosity is particularly common in the uppermost sandstone units and is interpreted to have formed primarily asa result ofweathering during the time represented by the Cretaceous-Tertiary unconformity.

Use of the Single Particle Soot Photometer (SP2) as a pre-filter for ice nucleation measurements: effect of particle mixing state and determination of SP2 conditions to fully vaporize refractory black carbon

NASA Astrophysics Data System (ADS)

Schill, Gregory P.; DeMott, Paul J.; Levin, Ezra J. T.; Kreidenweis, Sonia M.

2018-05-01

Ice nucleation is a fundamental atmospheric process that impacts precipitation, cloud lifetimes, and climate. Challenges remain to identify and quantify the compositions and sources of ice-nucleating particles (INPs). Assessment of the role of black carbon (BC) as an INP is particularly important due to its anthropogenic sources and abundance at upper-tropospheric cloud levels. The role of BC as an INP, however, is unclear. This is, in part, driven by a lack of techniques that directly determine the contribution of refractory BC (rBC) to INP concentrations. One previously developed technique to measure this contribution uses the Single Particle Soot Photometer (SP2) as a pre-filter to an online ice-nucleating particle counter. In this technique, rBC particles are selectively heated to their vaporization temperature in the SP2 cavity by a 1064 nm laser. From previous work, however, it is unclear under what SP2 conditions, if any, the original rBC particles were fully vaporized. Furthermore, previous work also left questions about the effect of the SP2 laser on the ice-nucleating properties of several INP proxies and their mixtures with rBC.To answer these questions, we sampled the exhaust of an SP2 with a Scanning Mobility Particle Sizer and a Continuous Flow Diffusion Chamber. Using Aquadag® as an rBC proxy, the effect of several SP2 instrument parameters on the size distribution and physical properties of particles in rBC SP2 exhaust were explored. We found that a high SP2 laser power (930 nW/(220 nm PSL)) is required to fully vaporize a ˜ 0.76 fg rBC particle. We also found that the exhaust particle size distribution is minimally affected by the SP2 sheath-to-sample ratio; the size of the original rBC particle, however, greatly influences the size distribution of the SP2 exhaust. The effect of the SP2 laser on the ice nucleation efficiency of Snomax®, NX-illite, and Suwannee River Fulvic Acid was studied; these particles acted as proxies for biological, illite-rich mineral dust, and brown carbon INPs, respectively. The original size distribution and ice nucleation efficiency of all non-rBC proxies were unaffected by the SP2 laser. Furthermore, the ice nucleation efficiencies of all proxies were not affected when externally mixed with rBC. These proxies, however, always show a reduction in ice-nucleating ability when internally mixed with rBC. We end this work with recommendations for users who wish to use the SP2 as a pre-filter to remove large rBC particles from an aerosol stream.

High cesium concentrations in groundwater in the upper 1.2 km of fractured crystalline rock - Influence of groundwater origin and secondary minerals

NASA Astrophysics Data System (ADS)

Mathurin, Frédéric A.; Drake, Henrik; Tullborg, Eva-Lena; Berger, Tobias; Peltola, Pasi; Kalinowski, Birgitta E.; Åström, Mats E.

2014-05-01

Dissolved and solid phase cesium (Cs) was studied in the upper 1.2 km of a coastal granitoid fracture network on the Baltic Shield (Äspö Hard Rock Laboratory and Laxemar area, SE Sweden). There unusually high Cs concentrations (up to 5-6 μg L-1) occur in the low-temperature (<20 °C) groundwater. The material includes water collected in earlier hydrochemical monitoring programs and secondary precipitates (fracture coatings) collected on the fracture walls, as follows: (a) hydraulically pristine fracture groundwater sampled through 23 surface boreholes equipped for the retrieval of representative groundwater at controlled depths (Laxemar area), (b) fracture groundwater affected by artificial drainage collected through 80 boreholes drilled mostly along the Äspö Hard Rock Laboratory (underground research facility), (c) surface water collected in local streams, a lake and sea bay, and shallow groundwater collected in 8 regolith boreholes, and (d) 84 new specimens of fracture coatings sampled in cores from the Äspö HRL and Laxemar areas. The groundwater in each area is different, which affects Cs concentrations. The highest Cs concentrations occurred in deep-seated saline groundwater (median Äspö HRL: 4.1 μg L-1; median Laxemar: 3.7 μg L-1) and groundwater with marine origin (Äspö HRL: 4.2 μg L-1). Overall lower, but variable, Cs concentrations were found in other types of groundwater. The similar concentrations of Cs in the saline groundwater, which had a residence time in the order of millions of years, and in the marine groundwater, which had residence times in the order of years, shows that duration of water-rock interactions is not the single and primary control of dissolved Cs in these systems. The high Cs concentrations in the saline groundwater is ascribed to long-term weathering of minerals, primarily Cs-enriched fracture coatings dominated by illite and mixed-layer clays and possibly wall rock micaceous minerals. The high Cs concentrations in the groundwater of marine origin are, in contrast, explained by relatively fast cation exchange reactions. As indicated by the field data and predicted by 1D solute transport modeling, alkali cations with low-energy hydration carried by intruding marine water are capable of (NH4+ in particular and K+ to some extent) replacing Cs+ on frayed edge (FES) sites on illite in the fracture coatings. The result is a rapid and persistent (at least in the order of decades) buildup of dissolved Cs concentrations in fractures where marine water flows downward. The identification of high Cs concentrations in young groundwater of marine origin and the predicted capacity of NH4+ to displace Cs from fracture solids are of particular relevance in the disposal of radioactive nuclear waste deep underground in crystalline rock.

Characterization of structures of the Nankai Trough accretionary prism from integrated analyses of LWD log response, resistivity images and clay mineralogy of cuttings: Expedition 338 Site C0002

NASA Astrophysics Data System (ADS)

Jurado, Maria Jose; Schleicher, Anja

2014-05-01

The objective of our research is a detailed characterization of structures on the basis of LWD oriented images and logs,and clay mineralogy of cuttings from Hole C0002F of the Nankai Trough accretionary prism. Our results show an integrated interpretation of structures derived from borehole images, petrophysical characterization on LWD logs and cuttings mineralogy. The geometry of the structure intersected at Hole C0002F has been characterized by the interpretation of oriented borehole resistivity images acquired during IODP Expedition 338. The characterization of structural features, faults and fracture zones is based on a detailed post-cruise interpretation of bedding and fractures on borehole images and also on the analysis of Logging While Drilling (LWD) log response (gamma radioactivity, resistivity and sonic logs). The interpretation and complete characterization of structures (fractures, fracture zones, fault zones, folds) was achieved after detailed shorebased reprocessing of resistivity images, which allowed to enhance bedding and fracture's imaging for geometry and orientation interpretation. In order to characterize distinctive petrophysical properties based on LWD log response, it could be compared with compositional changes derived from cuttings analyses. Cuttings analyses were used to calibrate and to characterize log response and to verify interpretations in terms of changes in composition and texture at fractures and fault zones defined on borehole images. Cuttings were taken routinely every 5 m during Expedition 338, indicating a clay-dominated lithology of silty claystone with interbeds of weakly consolidated, fine sandstones. The main mineralogical components are clay minerals, quartz, feldspar and calcite. Selected cuttings were taken from areas of interest as defined on LWD logs and images. The clay mineralogy was investigated on the <2 micron clay-size fraction, with special focus on smectite and illite minerals. Based on X-ray diffraction analysis measured at room temperature and a relative humidity of ~30%, we compared the shape and size of illite and smectite, as well as their water content and their polytypes. The comparison of cuttings mineralogy with logging while drilling (LWD) data allowed us to characterize structural, petrophysical and mineralogical properties at fracture and fault zones. We also analyzed the relationship between deformation structures and compositional and mineralogical changes. We established a correlation between observed results on clay mineralogy and log responses in relation with the structures and trends characterized on logging data. In general, the log data provide a good correlation with the actual mineralogy and the relative abundance of clay. In particular we analyzed trends characterized by smectite water layers as indication of compaction. These trends were correlated with log response (on sonic velocity) within Unit IV. Our results show the integration of logging data and cutting sample analyses as a valuable tool for characterization of petrophysical and mineralogical changes of the structures of the Nankai accretionary prism.

Lithological influences on contemporary and long-term regolith weathering at the Luquillo Critical Zone Observatory

USGS Publications Warehouse

Buss, Heather L.; Lara, Maria Chapela; Moore, Oliver; Kurtz, Andrew C.; Schulz, Marjorie S.; White, Arthur F.

2017-01-01

Lithologic differences give rise to the differential weatherability of the Earth’s surface and globally variable silicate weathering fluxes, which provide an important negative feedback on climate over geologic timescales. To isolate the influence of lithology on weathering rates and mechanisms, we compare two nearby catchments in the Luquillo Critical Zone Observatory in Puerto Rico, which have similar climate history, relief and vegetation, but differ in bedrock lithology. Regolith and pore water samples with depth were collected from two ridgetops and at three sites along a slope transect in the volcaniclastic Bisley catchment and compared to existing data from the granitic Río Icacos catchment. The depth variations of solid-state and pore water chemistry and quantitative mineralogy were used to calculate mass transfer (tau) and weathering solute profiles, which in turn were used to determine weathering mechanisms and to estimate weathering rates.Regolith formed on both lithologies is highly leached of most labile elements, although Mg and K are less depleted in the granitic than in the volcaniclastic profiles, reflecting residual biotite in the granitic regolith not present in the volcaniclastics. Profiles of both lithologies that terminate at bedrock corestones are less weathered at depth, near the rock-regolith interfaces. Mg fluxes in the volcaniclastics derive primarily from dissolution of chlorite near the rock-regolith interface and from dissolution of illite and secondary phases in the upper regolith, whereas in the granitic profile, Mg and K fluxes derive from biotite dissolution. Long-term mineral dissolution rates and weathering fluxes were determined by integrating mass losses over the thickness of solid-state weathering fronts, and are therefore averages over the timescale of regolith development. Resulting long-term dissolution rates for minerals in the volcaniclastic regolith include chlorite: 8.9 × 10−14 mol m−2 s−1, illite: 2.1 × 10−14 mol m−2 s−1 and kaolinite: 4.0 × 10−14 mol m−2 s−1. Long-term weathering fluxes are several orders of magnitude lower in the granitic regolith than in the volcaniclastic, despite higher abundances of several elements in the granitic regolith. Contemporary weathering fluxes were determined from net (rain-corrected) solute profiles and thus represent rates over the residence time of water in the regolith. Contemporary weathering fluxes within the granitic regolith are similar to the long-term fluxes. In contrast, the long-term fluxes are faster than the contemporary fluxes in the volcaniclastic regolith. Contemporary fluxes in the granitic regolith are generally also slightly faster than in the volcaniclastic. The differences in weathering fluxes over space and time between these two watersheds indicate significant lithologic control of chemical weathering mechanisms and rates.

Mineralogy and geochemistry of the Lokoundje alluvial clays from the Kribi deposits, Cameroonian Atlantic coast: Implications for their origin and depositional environment

NASA Astrophysics Data System (ADS)

Ndjigui, Paul-Désiré; Onana, Vincent Laurent; Sababa, Elisé; Bayiga, Elie Constantin

2018-07-01

The Lokoundje alluvial clay deposits are located at the left floodplain of the Lokoundje River, towards the estuary in the Kribi region. The mineralogical and geochemical features of the Lokoundje River fine-grained sediments have been reported using XRD, XRF, ICP-MS, and IR instruments in order to understand their provenance and depositional history. The Lokoundje watershed covers a surface area of about 5381 km2. The basement of this watershed is made up of gneisses, amphibolites, migmatites, charnockites, and pyroxenites from the Nyong and Ntem units, in the NW border of the Congo craton. The alluvial materials are about 100 cm thick and cover a total area of 1.4 km2. They are mainly plastic clays with silty-clayey texture and four colors (yellow, red yellow, white, and light grey). The mineral assemblage is composed of kaolinite, quartz, illite, gibbsite, goethite, rutile, and interstratified illite-vermiculite. The infra-red data associated with those of XRD portray the disordering of kaolinite. These materials are mostly constituted by SiO2 (44.33-69.19 wt%, av. = 51.17 wt% with n = 18) and Al2O3 (20.69-30.26 wt%, av. = 26.07 wt%) with very low Fe2O3 contents (1-7.71 wt%, av. = 3.35 wt%). The SiO2/Al2O3 ratio range between 1.46 and 4.1 (av. = 2.06). The alkali contents (Na2O + K2O) are below 5 wt%. ICV, CIA, PIA, and SiO2/Al2O3 portray high degree of chemical weathering in the source area as well as the maturity of sediments. The trace element behavior is quite different probably due to the mixed source rocks; Ba, Sr, Zn have high contents while several elements such as Th and U show low contents. The REE contents are also variable; their concentrations vary between 92 and 1065 ppm (av. = 307 ppm). The mineral assemblage associated with the geochemical data reveal that REE are mainly housed in clay minerals. The behavior of REE is also marked by the abundance of LREE (LREE/HREE = 19.69-34.62). The REE chondrite-normalized spectra confirm the LREE-abundance and exhibit negative Eu anomalies. The PAAS-normalized patterns reveal slight positive Eu anomalies and negative Ce anomalies. The (La/Yb)N values (3.30-8.43, av. = 5.71) display low degree of REE-fractionation in the Lokoundje watershed. The morphological, mineralogical, and geochemical features reveal that the fine-grained sediments derive from the intense weathering of mixed source. The disordering of kaolinite confirms that sediments were sorted during a long transportation before their deposition under oxic conditions (U/Th < 1.25; V/Cr < 2) in the floodplains near the Atlantic coast.

Potentially hazardous elements in coal: Modes of occurrence and summary of concentration data for coal components

USGS Publications Warehouse

Kolker, A.; Finkelman, R.B.

1998-01-01

Mode-of-occurrence data are summarized for 13 potentially hazardous elements (Be, Cr, Mn, Co, Ni, As, Se, Cd, Sb, Hg, Pb, Th, U) in coal. Recent work has refined mode-of-occurrence data for Ni, Cr, and As, as compared to previous summaries. For Cr, dominant modes of occurrence include the clay mineral illite, an amorphous CrO(OH) phase, and Cr-bearing spinels. Nickel is present in Fe-sulfides (pyrite and marcasite) and is also organically bound. Arsenic-bearing pyrite may be the dominant host of As in bituminous coals. Concentration data for the 13 HAPs, obtained primarily by quantitative microanalysis techniques, are compiled for mineral and organic portions of coal. HAPs element concentrations are greatest in Fe-sulfides, and include maxima of 2,300 ppm (Co), 4,500 ppm (Ni), 4.9wt.% (As), 2,000 ppm (Se), 171 ppm (Hg), and 5,500 ppm (Pb). Trace-element microanalysis is a significant refinement over bulk methods, and shows that there is considerable trace-element variation on a fine scale for a given coal, and from one coal to another. ?? 1998 OPA (Overseas Publishers Association) N.V. Published by license under the Gordon and Breach Science Publishers imprint.

A Comparative Study of T1 and T2 Relaxation in Shale

NASA Astrophysics Data System (ADS)

Keating, K.; Obasi, C. C.; Pashin, J. C.

2015-12-01

Nuclear magnetic resonance (NMR) relaxation measurement have been used extensively in petroleum and, more recently, in groundwater resource evaluation to estimate the porosity, pore-size distributions, permeability, fluid saturation, and fluid mobility. In shale, the transverse decay rate of NMR signal is sensitive to the microporosity, but is also affected by the paramagnetic contributions of clay and other iron-bearing minerals. Furthermore, contrasts in the magnetic susceptibility of the mineral matrix and pore fluids that result in an inhomogeneous magnetic field within the pore space results in an extra term in transverse relaxation. These issues can cause errors in NMR-based estimates of pore-size distribution and permeability. In this study we compare T1 and T2 relaxation time distributions in order to study the molecular mechanism of relaxation in brine-saturated mixtures of clay and other common minerals. We collected measurements on a range of mixtures of clay minerals common in shale (illite, glauconite, celadonite, chamosite, montmorillonite and kaolinite) and pyrite. To constrain the interpretation of the NMR data, we measured the magnetic susceptibility and surface area of all samples. We are confident that by accounting for the presence and variations of clay and pyrite in shale, we can substantially improve both the NMR estimate of pore-size distribution and permeability.

Clay mineral distribution and provenance in the Heuksan mud belt, Yellow Sea

NASA Astrophysics Data System (ADS)

Cho, Hyen Goo; Kim, Soon-Oh; Kwak, Kyeong Yoon; Choi, Hunsoo; Khim, Boo-Keun

2015-12-01

The Heuksan mud belt (HMB), located in the southeastern Yellow Sea, runs parallel to the southwest coast of Korea. In this study, the distribution and relative contribution of four major clay minerals are investigated using 101 surface sediment samples collected in the course of KIOST (2001, 2010, 2011) and KIGAM (2012) cruises, as well as 33 river sediment samples (four from the Huanghe River, three from the Changjiang River, and 26 from Korean rivers) in order to clarify the provenance of fine-grained sediments in the HMB. Based on this currently largest and most robust dataset available for interpretation, the clay mineral assemblages of the fine-grained sediments in the HMB are found to be on average composed of 64.7% illite, 17.9% chlorite, 11.4% kaolinite, and 5.9% smectite. Overall, the clay mineral assemblages are similar in both the northern and the southern parts of the HMB, although smectite seems to be relatively enriched in the southern part, whereas kaolinite is slightly more dominant in the northern part. This clearly indicates that the clays are mostly derived from Korean rivers and, in the southern part of the HMB, partly also from the Huanghe River in China. The new data thus confirm and strengthen the tentative interpretation of some earlier work based on a more limited dataset.

Global distribution of minerals in arid soils as lower boundary condition in dust models

NASA Astrophysics Data System (ADS)

Nickovic, Slobodan

2010-05-01

Mineral dust eroded from arid soils affects the radiation budget of the Earth system, modifies ocean bioproductivity and influences human health. Dust aerosol is a complex mixture of minerals. Dust mineral composition has several potentially important impacts to environment and society. Iron and phosphorus embedded in mineral aerosol are essential for the primary marine productivity when dust deposits over the open ocean. Dust also acts as efficient agent for heterogeneous ice nucleation and this process is dependent on mineralogical structure of dust. Recent findings in medical geology indicate possible role of minerals to human health. In this study, a new 1-km global database was developed for several minerals (Illite, Kaolinite, Smectite, Calcite, Quartz, Feldspar, Hematite and Gypsum) embedded in clay and silt populations of arid soils. For the database generation, high-resolution data sets on soil textures, soil types and land cover was used. Tin addition to the selected minerals, phosphorus was also added whose geographical distribution was specified from compiled literature and data on soil types. The developed global database was used to specify sources of mineral fractions in the DREAM dust model and to simulate atmospheric paths of minerals and their potential impacts on marine biochemistry and tropospheric ice nucleation.

Influence of depositional environment on diagenesis in St. Peter sandstone, Michigan basin

DOE Office of Scientific and Technical Information (OSTI.GOV)

Lundgren, C.E. Jr.; Barnes, D.A.

1989-03-01

The Middle Ordovician St. Peter Sandstone in the Michigan basin was deposited in marine peritidal to storm-dominated, outer shelf depositional environments that evolved in a regionally significant transgressive pattern. The formation is bounded by carbonate and shaly clastic strata of the Prairie du Chien Group below and is transitional to condensed sequence clastics and carbonates of the Glenwood Formation above. Sedimentologic and petrographic analysis of conventional core from 25 wells suggests that reservoir quality in the formation is strongly dependent on a complex diagenetic history, especially the nature and subsequent dissolution of intergranular carbonate in the sandstone. Petrographic evidence indicatesmore » that porosity in the formation formed by dissolution of precursor dolomite of various origins and, locally, the formation of pore-filling authigenic clay (chlorite-illite). Authigenic clay is the incongruent dissolution product of dolomite, detrital K-feldspar, and, possibly, muscovite and results in diminished reservoir quality where abundant in the St. Peter Sandstone. Authigenic clay is volumetrically more significant in the upper portions of the formation and is associated with higher concentrations of detrital K-feldspar. Depositional facies controlled the distribution and types of intergranular carbonate (now dolomite) and detrital K-feldspar in the St. Peter Sandstone and hence reservoir quality; both components were more significant in storm-shelf sandstone facies.« less

Mineralogical Characterization of the Miocene Olcese Formation, Southern San Joaquin Valley, California

NASA Astrophysics Data System (ADS)

Lopez, K. A.; Baron, D.; Guo, J.; Woolford, J. M.

2016-12-01

The early to middle Miocene Olcese Formation in the southern San Joaquin Valley of California consists of shallow marine shelf sands in its lower and upper parts, and non-marine, frequently pumiceous sands in its middle part, and varies in thickness up to 1800 ft. There is little known as to the origin, nature, quantity, and distribution of clay minerals throughout the formation. This study examined 95 sidewall core samples from three wells, as well as 388 cutting samples from four wells and 12 samples from 3 outcrops. Well samples were from depths between 1,800 and 4,000 ft. Qualitative and quantitative mineralogy including clay minerals of the sidewall samples and selected cutting samples was determined by powder X-ray diffraction (XRD). XRD analyses were supplemented by scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM-EDS) and petrographic microscopy of selected samples. The main minerals of bulk samples include composite clay, quartz, potassium feldspar/plagioclase, calcite, and clinoptilolite. Content of composite clay varies between 17% and 51%. The clay-size fraction is predominantly composed of smectite, illite, kaolinite and chlorite with smectite being the most abundant. Smectite and clinoptilolite may be the alteration products of deeper burial of volcanic materials. The formation permeability could be significantly lowered by these authigenic minerals.

Geochemical characteristics of Kırka (Sarıkaya) borate deposit, northwestern Anatolia, Turkey

NASA Astrophysics Data System (ADS)

Koçak, İ.; Koç, Ş.

2016-02-01

The Kırka borate deposit was deposited in a Miocene lacustrine basin which is closely associated with volcanic activity which lasted from Paleogene to the beginning of Quaternary. Borate mineralization alternates with claystone, mudstone, tuff and fine-layered limestone and mostly shows a lenticular structure. The mineral paragenesis is composed of borax, tincalconite, ulexite, kurnakovite, probertite, tunellite, colemanite, dolomite, smectite group minerals, illite and some firstly reported minerals for the Kırka deposit including hydrochloroborite, brianroulstonite, hilgardite-4M and searlesite minerals. In comparison to average values of earth crust, concentrations of Cs, Sr, Li, As and Se were significantly enriched with respective rates of 21, 15, 14, 3 and 188 folds. Regarding KY, KS1 and KS2 locations, there are differences in both element abundances and their geochemical tendencies which are attributed to variations in discharge regime and physico-chemical conditions of the depositional environment. Independent behaviour of B2O3 might indicate that boron is not associated with clays and carbonates and, therefore, most part of boron must be derived from volcanic activity (hydrothermal solutions, gases). REE data indicate that the Kırka borate deposit was formed in a sedimentary environment where highly alkaline (high pH) hydrothermal solutions also took part in borate precipitation process.

Desert Varnish - Preservation of Biofabrics/Implcations for Mars

NASA Technical Reports Server (NTRS)

Probst, Luke W.; Allen, Carlton C.; Thomas-Keprta, Kathie L.; Clemett, Simon J.; Longazo, Teresa G.; Nelman-Gonzalez, Mayra A.; Sams, Clarence

2002-01-01

Desert varnish is the orange to dark brown rind that accumulates on exposed rock surfaces in many arid environments. Samples from the Sonoran Desert of Arizona are composed predominantly of clays (illite, smectite) and Mn- and Fe- oxides (birnessite, hematite). Features that appear to be single organisms are found within the varnish and at the rock-varnish interface. Many of these features are embedded in films that strongly resemble the water-rich extracellular polysaccharides produced by diverse microorganisms. Most common are rod-shaped celllike objects, 0.5-2 microns in the longest dimension, located within the varnish coatings. Some of these objects are shown to contain amines by fluorescence microscopy. The rod-shaped objects are observed in various states of degradation, as indicated by C and S abundances. Rods with higher C and S abundances appear less degraded than those with lower concentrations of these two elements. Regions rich in apparent microbes are present, while other regions display Mn- and Fe-rich mineral fabrics with microbe-sized voids and no obvious cells. These textures are interpreted as biofabrics, preserved by the precipitation of Mn and Fe minerals. We are researching the preservation of biofabrics by desert varnish in Earth's geological record. Rock coatings may similarly preserve evidence of microbial life on the hyper-arid surface of Mars.

Derivation and calibration of semi-empirical gas geothermometers for Mahanagdong Geothermal Project, Philippines

DOE Office of Scientific and Technical Information (OSTI.GOV)

Sanchez, D.R.

1996-12-31

The dissolved CO{sub 2}, H{sub 2}S, and H{sub 2} gases in Mahanagdong aquifer fluids are controlled by specific gas-mineral equilibria. At temperature range of 250 to 310 {degrees}C, CO{sub 2} is buffered by clinozoisite + K-feldspar + calcite + muscovite (illite) + quartz mineral assemblage. For H{sub 2}S and H{sub 2} dissolved gases, they are more likely buffered by pyrrhotite + pyrite + magnetite mineral assemblage at similar temperature range. Calibration of five Mahanagdong (MG) gas geothermometers is presented, three of which used CO{sub 2}, H{sub 2}S, and H{sub 2} concentration in steam. The remaining two use CO{sub 2}/H{sub 2}more » and H{sub 2}S/H{sub 2} ratios. The calibration is based on the relation between gas content of drillhole discharges and measured aquifer temperatures. After establishing the gas content in the aquifer, gas concentrations were computed in steam after adiabatic boiling to atmospheric condition (100 {degrees}C), to obtain gas geothermometry functions. These functions could also be used in evaluating fraction of steam condensation and temperature of phase separation. A demonstration given the Mahanagdong fumarole data, indicates that there is generally a fair relation between computed temperatures using Mahanagdong gas geothermometers and the actual field trend`s temperatures.« less

Sorption of cadmium and lead by clays from municipal incinerator ash- water suspensions

USGS Publications Warehouse

Roy, W.R.; Krapac, I.G.; Steele, J.D.

1993-01-01

The effect of Cl complexation in extracts of a flue gas-scrubber incinerator fly ash sample on the sorption of Cd and Pb by kaolinite and illite was investigated using batch-sorption methods. In the pH range of 5 to 9, Cl complexation may reduce sorption and thus increase the mobility of these metals. When an ash-water suspension was acidified to pH 6.85, the dissolution of Cl and Ca essentially eliminated Cd sorption because of complexation and cationic competition. Cadmium would be considered as either mobile or very mobile under these conditions. Lead was not soluble in the pH- 6.85 suspension. At pH 12, the approximate pH of water in contact with flue gas-scrubber fly ash, Cd was essentially insoluble and Pb occurred as anionic Pb hydroxide. Anionic Pb was sorbed by the two clays, and the extent of sorption was not influenced by Cl or carbonate complexation. Sorption constants, derived from isotherms, suggested that Pb would be relatively immobile in saturated soil-water systems. The recent concern that highly alkaline, flue gas-scrubber fly ash may release environmentally significant concentrations of mobile Pb when placed in an ash-disposal site with a soil liner should be reevaluated in light of this study.

Mode of occurrence of chromium in four US coals

USGS Publications Warehouse

Huggins, Frank E.; Shah, N.; Huffman, G.P.; Kolker, A.; Crowley, S.; Palmer, C.A.; Finkelman, R.B.

2000-01-01

The mode of occurrence of chromium in three US bituminous coals and one US subbituminous has been examined using both X-ray absorption fine structure (XAFS) spectroscopy and a selective leaching protocol supplemented by scanning electron microscopy (SEM) and electron microprobe measurements. A synthesis of results from both methods indicates that chromium occurs principally in two forms in the bituminous coals: the major occurrence of chromium is associated with the macerals and is not readily leached by any reagent, whereas a second, lesser occurrence, which is leachable in hydrofluoric acid (HF), is associated with the clay mineral, illite. The former occurrence is believed to be a small particle oxyhydroxide phase (CrO(OH)). One coal also contained a small fraction (<5%) of the chromium in the form of a chromian magnetite, and the leaching protocol indicated the possibility of a similar small fraction of chromium in sulfide form in all three coals. There was little agreement between the two techniques on the mode of occurrence of chromium in the subbituminous coal; however, only a limited number of subbituminous coals have been analyzed by either technique. The chromium in all four coals was trivalent as no evidence was found for the Cr6+ oxidation state in any coal.

Schwertmannite stability in acidified coastal environments

NASA Astrophysics Data System (ADS)

Collins, Richard N.; Jones, Adele M.; Waite, T. David

2010-01-01

A combination of analytical and field measurements has been used to probe the speciation and cycling of iron in coastal lowland acid sulfate soils. Iron K-edge EXAFS spectroscopy demonstrated that schwertmannite dominated (43-77%) secondary iron mineralization throughout the oxidized and acidified soil profile, while pyrite and illite were the major iron-bearing minerals in the reduced potential acid sulfate soil layers. Analyses of contemporary precipitates from shallow acid sulfate soil groundwaters indicated that 2-line ferrihydrite, in addition to schwertmannite, is presently controlling secondary Fe(III) mineralization. Although aqueous pH values and concentrations of Fe(II) were seasonally high, no evidence was obtained for the Fe(II)-catalyzed crystallization of either mineral to goethite. The results of this study indicate that: (a) schwertmannite is likely to persist in coastal lowland acid sulfate soils on a much longer time-scale than predicted by laboratory experiments; (b) this mineral is less reactive in these types of soils due to surface-site coverage by components such as silicate and possibly, to a lesser extent, natural organic matter and phosphate and; (c) active water table management to promote oxic/anoxic cycles around the Fe(II)-Fe(III) redox couple, or reflooding of these soils, will be ineffective in promoting the Fe(II)-catalyzed transformation of either schwertmannite or 2-line ferrihydrite to crystalline iron oxyhydroxides.

Tellurium Distribution and Speciation in Contaminated Soils from Abandoned Mine Tailings: Comparison with Selenium.

PubMed

Qin, Hai-Bo; Takeichi, Yasuo; Nitani, Hiroaki; Terada, Yasuko; Takahashi, Yoshio

2017-06-06

The distribution and chemical species of tellurium (Te) in contaminated soil were determined by a combination of microfocused X-ray fluorescence (μ-XRF), X-ray diffraction (μ-XRD), and X-ray absorption fine structure (μ-XAFS) techniques. Results showed that Te was present as a mixture of Te(VI) and Te(IV) species, while selenium (Se) was predominantly present in the form of Se(IV) in the soil contaminated by abandoned mine tailings. In the contaminated soil, Fe(III) hydroxides were the host phases for Se(IV), Te(IV), and Te(VI), but Te(IV) could be also retained by illite. The difference in speciation and solubility of Se and Te in soil can result from different structures of surface complexes for Se and Te onto Fe(III) hydroxides. Furthermore, our results suggest that the retention of Te(IV) in soil could be relatively weaker than that of Te(VI) due to structural incorporation of Te(VI) into Fe(III) hydroxides. These findings are of geochemical and environmental significance for better understanding the solubility, mobility, and bioavailability of Te in the surface environment. To the best of our knowledge, this is the first study reporting the speciation and host phases of Te in field soil by the μ-XRF-XRD-XAFS techniques.

Mineralogical characterization of Greda clays and monitoring of their phase transformations on thermal treatment

NASA Astrophysics Data System (ADS)

Panduro, E. Chavez; Cabrejos, J. Bravo

2010-01-01

The mineralogical characterization of two clay samples from the Central Andean Region of Peru, denominated White Greda and Red Greda, is reported. These clays contain the clay minerals mica and illite respectively. Both clays were treated thermally in an oxidising atmosphere under controlled conditions up to 1,100°C with the purpose of obtaining information about structural changes that may be useful for pottery manufacture. X-ray fluorescence was used for the elemental characterization of the samples and X-ray diffractometry was used to determine the collapse and formation of the mineral phases present in the samples caused by thermal treatment. At temperatures above 1,000°C it is observed the formation of spinel in the case of White Greda and of hematite, corundum and cristobalite in the case of Red Greda. Room temperature transmission Mössbauer spectroscopy allowed the monitoring of the variation of the hyperfine parameters with the thermal treatment temperature; In the case of the evolution of the quadruple splitting of the paramagnetic Fe3 + sites with temperature, in both clays, the analyses reproduced results such as the “camel back” curve shape, found by other workers (Wagner and Wagner, Hyperfine Interact 154:35-82, 2004; Wagner and Kyek, Hyperfine Interact 154:5-33, 2004).

Reactive transport modelling of groundwater chemistry in a chalk aquifer at the watershed scale

NASA Astrophysics Data System (ADS)

Mangeret, A.; De Windt, L.; Crançon, P.

2012-09-01

This study investigates thermodynamics and kinetics of water-rock interactions in a carbonate aquifer at the watershed scale. A reactive transport model is applied to the unconfined chalk aquifer of the Champagne Mounts (France), by considering both the chalk matrix and the interconnected fracture network. Major element concentrations and main chemical parameters calculated in groundwater and their evolution along flow lines are in fair agreement with field data. A relative homogeneity of the aquifer baseline chemistry is rapidly reached in terms of pH, alkalinity and Ca concentration since calcite equilibrium is achieved over the first metres of the vadose zone. However, incongruent chalk dissolution slowly releases Ba, Mg and Sr in groundwater. Introducing dilution effect by rainwater infiltration and a local occurrence of dolomite improves the agreement between modelling and field data. The dissolution of illite and opal-CT, controlling K and SiO2 concentrations in the model, can be approximately tackled by classical kinetic rate laws, but not the incongruent chalk dissolution. An apparent kinetic rate has therefore been fitted on field data by inverse modelling: 1.5 × 10- 5 molchalk L - 1water year - 1. Sensitivity analysis indicates that the CO2 partial pressure of the unsaturated zone is a critical parameter for modelling the baseline chemistry over the whole chalk aquifer.

Clay-mineral assemblages from some levels of K-118 drill core of Maha Sarakham evaporites, northeastern Thailand

NASA Astrophysics Data System (ADS)

Suwanich, Parkorn

Clay-mineral assemblages in Middle Clastic, Middle Salt, Lower Clastic, Potash Zone, and Lower Salt, totalling 13 samples from K-118 drill core, in the Maha Sarakham Formation, Khorat Basin, northeastern Thailand were studied. The clay-size particles were separated from the water-soluble salt by water leaching. Then the samples were leached again in the EDTA solution and separated into clay-size particles by using the timing sedimentation. The EDTA-clay residues were divided and analyzed by using the XRD and XRF method. The XRD peaks show that the major-clay minerals are chlorite, illite, and mixed-layer corrensite including traces of rectorite? and paragonite? The other clay-size particles are quartz and potassium feldspar. The XRF results indicate Mg-rich values and moderate MgAl atom ratio values in those clay minerals. The variable Fe, Na, and K contents in the clay-mineral assemblages can explain the environment of deposition compared to the positions of the samples from the core. Hypothetically, mineralogy and the chemistry of the residual assemblages strongly indicate that severe alteration and Mg-enrichment of normal clay detritus occurred in the evaporite environment through brine-sediment interaction. The various Mg-enrichment varies along the various members reflecting whether sedimentation is near or far from the hypersaline brine.

Impact of monovalent cations on soil structure. Part II. Results of two Swiss soils

NASA Astrophysics Data System (ADS)

Farahani, Elham; Emami, Hojat; Keller, Thomas

2018-01-01

In this study, we investigated the impact of adding solutions with different potassium and sodium concentrations on dispersible clay, water retention characteristics, air permeability, and soil shrinkage behaviour using two agricultural soils from Switzerland with different clay content but similar organic carbon to clay ratio. Three different solutions (including only Na, only K, and the combination of both) were added to soil samples at three different cation ratio of soil structural stability levels, and the soil samples were incubated for one month. Our findings showed that the amount of readily dispersible clay increased with increasing Na concentrations and with increasing cation ratio of soil structural stability. The treatment with the maximum Na concentration resulted in the highest water retention and in the lowest shrinkage capacity. This was was associated with high amounts of readily dispersible clay. Air permeability generally increased during incubation due to moderate wetting and drying cycles, but the increase was negatively correlated with readily dispersible clay. Readily dispersible clay decreased with increasing K, while readily dispersible clay increased with increasing K in Iranian soil (Part I of our study). This can be attributed to the different clay mineralogy of the studied soils (muscovite in Part I and illite in Part II).

Colloid mobilization and seasonal variability in a semiarid headwater stream

USGS Publications Warehouse

Mills, Taylor J.; Suzanne P. Ancerson,; Bern, Carleton; Aguirre, Arnulfo; Derry, Louis A.

2017-01-01

Colloids can be important vectors for the transport of contaminants in the environment, but little is known about colloid mobilization at the watershed scale. We present colloid concentration, composition, and flux data over a large range of hydrologic conditions from a small watershed (Gordon Gulch) in the foothills of the Colorado Front Range. Colloids, consisting predominantly of Si, Fe, and Al, were present in most stream samples but were not detected in groundwater samples. Mineralogical and morphological analysis indicated that the colloids were composed of kaolinite and illite clays with lesser amounts of amorphous Fe-hydroxides. Although colloid composition remained relatively constant over the sampled flow conditions, colloid concentrations varied considerably and increased as ionic strength of stream water decreased. The highest concentrations occurred during precipitation events after extended dry periods. These observations are consistent with laboratory studies that have shown colloids can be mobilized by decreases in pore-water ionic strength, which likely occurs during precipitation events. Colloidal particles constituted 30 to 35% of the Si mass flux and 93 to 97% of the Fe and Al mass fluxes in the <0.45-µm fraction in the stream. Colloids are therefore a significant and often overlooked component of mass fluxes whose temporal variations may yield insight into hydrologic flowpaths in this semiarid catchment.

Hydrothermal Synthesis of Analcime from Kutingkeng Formation Mudstone

NASA Astrophysics Data System (ADS)

Hsiao, Yin-Hsiu; Chen, Kuan-Ting; Ray, Dah-Tong

2015-04-01

In southwest of Taiwan, the foothill located in Tainan-Kaohsiung city is the exposed area of Pliocene strata to early Pleistocene strata. The strata are about a depth of five thousand, named as Kutigkeng Formation. The outcrop of Kutigkeng Formation is typical badlands, specifically called 'Moon World.' It is commonly known as no important economic applications of agricultural land. The mineral compositions of Kutingkeng Formation are quartz, clay minerals and feldspar. The clay minerals consist of illite, clinochlore and swelling clays. To study how the phase and morphology of analcime formed by hydrothermal synthesis were affected, analcime was synthesized from the mudstone of Kutinkeng Formation with microwave hydrothermal reaction was investigated. The parameters of the experiment were the reaction temperature, the concentration of mineralizer, solids/liquid ratio and time. The sodium silicate (Na2SiO3) were used as mineralizer. The results showed that the analcime could be synthesized by hydrothermal reaction above 180° from Kutinkeng Formation mudstone samples. At the highest temperature (240°) of this study, the high purity analcime could be produced. When the concentration of Na2SiO3=3~6M, analcime could be synthesized at 240°. The best solids/liquid ratio was approximate 1 to 5. The hydrothermal reaction almost was completed after 4 hours.

Satellite-derived mineral mapping and monitoring of weathering, deposition and erosion

PubMed Central

Cudahy, Thomas; Caccetta, Mike; Thomas, Matilda; Hewson, Robert; Abrams, Michael; Kato, Masatane; Kashimura, Osamu; Ninomiya, Yoshiki; Yamaguchi, Yasushi; Collings, Simon; Laukamp, Carsten; Ong, Cindy; Lau, Ian; Rodger, Andrew; Chia, Joanne; Warren, Peter; Woodcock, Robert; Fraser, Ryan; Rankine, Terry; Vote, Josh; de Caritat, Patrice; English, Pauline; Meyer, Dave; Doescher, Chris; Fu, Bihong; Shi, Pilong; Mitchell, Ross

2016-01-01

The Earth’s surface comprises minerals diagnostic of weathering, deposition and erosion. The first continental-scale mineral maps generated from an imaging satellite with spectral bands designed to measure clays, quartz and other minerals were released in 2012 for Australia. Here we show how these satellite mineral maps improve our understanding of weathering, erosional and depositional processes in the context of changing weather, climate and tectonics. The clay composition map shows how kaolinite has developed over tectonically stable continental crust in response to deep weathering during northwardly migrating tropical conditions from 45 to 10 Ma. The same clay composition map, in combination with one sensitive to water content, enables the discrimination of illite from montmorillonite clays that typically develop in large depositional environments over thin (sinking) continental crust such as the Lake Eyre Basin. Cutting across these clay patterns are sandy deserts that developed <10 Ma and are well mapped using another satellite product sensitive to the particle size of silicate minerals. This product can also be used to measure temporal gains/losses of surface clay caused by periodic wind erosion (dust) and rainfall inundation (flood) events. The accuracy and information content of these satellite mineral maps are validated using published data. PMID:27025192

Adsorption of hydrogen gas and redox processes in clays.

PubMed

Didier, Mathilde; Leone, Laura; Greneche, Jean-Marc; Giffaut, Eric; Charlet, Laurent

2012-03-20

In order to assess the adsorption properties of hydrogen gas and reactivity of adsorbed hydrogen, we measured H(2)(g) adsorption on Na synthetic montmorillonite-type clays and Callovo-Oxfordian (COx) clayrock using gas chromatography. Synthetic montmorillonites with increasing structural Fe(III) substitution (0 wt %, 3.2 wt %, and 6.4 wt % Fe) were used. Fe in the synthetic montmorillonites is principally present as structural Fe(III) ions. We studied the concomitant reduction of structural Fe(III) in the clays using (57)Fe Mössbauer spectrometry. The COx, which mainly contains smectite/illite and calcite minerals, is also studied together with the pure clay fraction of this clayrock. Experiments were performed with dry clay samples which were reacted with hydrogen gas at 90 and 120 °C for 30 to 45 days at a hydrogen partial pressure close to 0.45 bar. Results indicate that up to 0.11 wt % of hydrogen is adsorbed on the clays at 90 °C under 0.45 bar of relative pressure. (57)Fe Mössbauer spectrometry shows that up to 6% of the total structural Fe(III) initially present in these synthetic clays is reduced upon adsorption of hydrogen gas. No reduction is observed with the COx sample in the present experimental conditions.

Geochemical Identification in Sediment Provenance during Glacial/Interglacial Period: the Southern Drake Passage

NASA Astrophysics Data System (ADS)

Park, Y. K.; Jung, J.; Lee, J. I.; Yoo, K. C.; Kim, J. W.

2016-12-01

Clay mineralogy and crystal size distribution in marine sediment is used for the indication of a sediment provenance and climatic changes. Objective of this study is to trace the sediment provenances in the Southern Drake Passage with clay mineralogy, elemental composition and crystal size distributions (CSDs) of clay mineral. In the present study, X-Ray Diffractometer (XRD) measurements showed that smectite, illite and chlorite are dominant phases. The semi-quantitative analysis showed that the relatively proportion of smectite is 50 - 60% in interglacial stage, 30 - 39% in glacial stage. Comparing with REE data, sediments supply was influenced by Weddell sea current and Antarctic Circumpolar Current (ACC). Moreover, elemental composition and microscopic analysis of smectites were carried by Transmission Electron Microscopy (TEM) and energy dispersive spectroscopy (EDS). The composition of smectite clay minerals were plotted on the tertiary diagram indicating that Smectite in Drake Passage was transported from three provenances: South Shetland island, east and west side of Antarctic peninsula during glacial - interglacial period. The CSDs of smectite also indicate the various source of smectite. The variation in the values of α (mean thickness) and β2 (shape or uniformity of the distribution) of smectite grain size will be discussed in terms of the sediment provenance.

Texture development in naturally compacted and experimentally deformed silty clay sediments from the Nankai Trench and Forearc, Japan

NASA Astrophysics Data System (ADS)

Schumann, Kai; Stipp, Michael; Leiss, Bernd; Behrmann, Jan H.

2014-12-01

The petrophysical properties of fine-grained marine sediments to a large extent depend on the microstructure and crystallographic preferred orientations (CPOs). In this contribution we show that Rietveld-based synchrotron texture analysis is a new and valuable tool to quantify textures of water-saturated fine-grained phyllosilicate-rich sediments, and assess the effects of compaction and tectonic deformation. We studied the CPO of compositionally almost homogeneous silty clay drillcore samples from the Nankai Accretionary Prism slope and the incoming Philippine Sea plate, offshore SW Japan. Basal planes of phyllosilicates show bedding-parallel alignment increasing with drillhole depth, thus reflecting progressive burial and compaction. In some samples calcite and albite display a CPO due to crystallographically controlled non-isometric grain shapes, or nannofossil tests. Consolidated-undrained experimental deformation of a suite of thirteen samples from the prism slope shows that the CPOs of phyllosilicate and calcite basal planes develop normal to the experimental shortening axis. There is at least a qualitative relation between CPO intensity and strain magnitude. Scanning electron micrographs show concurrent evolution of preferred orientations of micropores and detrital illite flakes normal to axial shortening. This indicates that the microfabrics are sensitive strain gauges, and contribute to anisotropic physical properties along with the CPO.

Influences of Sedimentary Environments and Volcanic Sources on Diagenetic Alteration of Volcanic Tuffs in South China.

PubMed

Gong, Nina; Hong, Hanlie; Huff, Warren D; Fang, Qian; Bae, Christopher J; Wang, Chaowen; Yin, Ke; Chen, Shuling

2018-05-16

Permian-Triassic (P-Tr) altered volcanic ashes (tuffs) are widely distributed within the P-Tr boundary successions in South China. Volcanic altered ashes from terrestrial section-Chahe (CH) and marine section-Shangsi (SS) are selected to further understand the influence of sedimentary environments and volcanic sources on diagenetic alterarion on volcanic tuffs. The zircon 206 Pb/ 238 U ages of the corresponding beds between two sections are almost synchronous. Sedimentary environment of the altered tuffs was characterized by a low pH and did not experience a hydrothermal process. The dominant clay minerals of all the tuff beds are illite-smectite (I-S) minerals, with minor chlorite and kaolinite. I-S minerals of CH (R3) are more ordered than SS (R1), suggesting that CH also shows a higher diagenetic grade and more intensive chemical weathering. Besides, the nature of the volcanism of the tuff beds studied is derived from different magma sources. The clay mineral compositions of tuffs have little relation with the types of source volcanism and the depositional environments. Instead, the degree of the mixed-layer clay minerals and the REE distribution are mainly dependent upon the sedimentary environments. Thus, the mixed-layer clay minerals ratio and their geochemical index can be used as the paleoenvironmental indicator.

Enrofloxacin uptake and retention on different types of clays

NASA Astrophysics Data System (ADS)

Wan, Miao; Li, Zhaohiu; Hong, Hanlie; Wu, Qingfeng

2013-11-01

The adsorption and retention of enrofloxacin (EN) on different types of clays was studied in batch tests under different pH, contact time, and initial concentration conditions. XRD and FTIR analyses were utilized to characterize EN adsorption and to elucidate mechanisms of EN adsorption. The EN adsorption equilibrium followed the Langmuir isotherm and reached capacities of 667, 228 and 20 mmol/kg at pH 4-5 on the montmorillonite (SWy-2), illite (IMt-2), and kaolinite (KGa-1b), respectively. The pseudo-second-order model fitted the EN sorption kinetics well. Although EN had a much lower adsorption capacity on KGa-1b compared to that on the other two clays, the adsorption rate constant was the fastest at 0.73 kg/mmol-h. Cation exchange interaction was attributed to the major mechanism for EN adsorption on SWy-2 and IMt-2, and non-electrostatic interactions attributed to EN adsorption when solution pH was above 7. Intercalation of EN molecules into the interlayer space of SWy-2 was confirmed by the XRD patterns after EN adsorption. In contrast, the basal spacing and intensity remained the same after EN adsorption on IMt-2 and KGa-1b, indicating that the EN adsorption on the non-swelling clays were limited to the external surfaces.

Evaluation of the healing activity of therapeutic clay in rat skin wounds.

PubMed

Dário, Giordana Maciel; da Silva, Geovana Gomes; Gonçalves, Davi Ludvig; Silveira, Paulo; Junior, Adilson Teixeira; Angioletto, Elidio; Bernardin, Adriano Michael

2014-10-01

The use of clays for therapeutic practice is widespread in almost all regions of the world. In this study the physicochemical and microbiological healing characteristics of a clay from Ocara, Brazil, popularly used for therapeutic uses, were analyzed. The presence of Ca, Mg, Al, Fe, and Si was observed, which initially indicated that the clay had potential for therapeutic use. The average particle size of the clay (26.3 μm) can induce the microcirculation of the skin and the XRD analysis shows that the clay is formed by kaolinite and illite, a swelling clay. During the microbiological evaluation there was the need to sterilize the clay for later incorporation into the pharmaceutical formula. The accelerated stability test at 50°C for 3 months has showed that the pharmaceutical formula remained stable with a shelf life of two years. After the stability test the wound-healing capacity of the formulation in rats was evaluated. It was observed that the treatment made with the formulation containing the Ocara clay showed the best results since the formula allowed greater formation of collagen fibers and consequent regeneration of the deep dermis after seven days of treatment and reepithelialization and continuous formation of granulation tissue at the 14th day. Copyright © 2014 Elsevier B.V. All rights reserved.

Palaeomagnetic dating of widespread remagnetization on the southeastern border of the French Massif Central and implications for fluid and Mississippi Valley-type mineralization

USGS Publications Warehouse

Henry, B.; Rouvier, H.; Goff, M.L.; Leach, D.; Macquar, J.-C.; Thibieroz, J.; Lewchuk, Michael T.

2001-01-01

Palaeomagnetic dating techniques have been applied to determine the age of fluid migration that produced the Mississippi Valley-type (MVT) Pb-Zn-Ba-F deposits in the Ce??vennes region of southern France. 15 sampling sites in two gently deformed areas around the Largentie??re and Croix-de-Pallie??res mines on the Ce??vennes border were selected for palaeomagnetic study. They yielded a very well-defined direction of remagnetization corresponding to an Early-Middle Eocene age. This remagnetization cannot be related to the formation of magnetic as a result of the transformation of smectite to illite because the latter has been well dated as a Mesozoic event. The magnetic overprint in this area is related to a chemical phenomenon during fluid migration. The age of remagnetization corresponds to a major uplift in the Pyre??ne??es mountains, located to the south of the Ce??vennes. This implies that fluid migration occurred from the south to the north as a result of hydraulic head established in the Pyre??ne??es orogenic belt during orogenesis and suggests that the MVT deposits in the Ce??vennes region formed from a gravity-driven fluid system as described by Garven & Freeze (1984a,b).

Remote Sensing Assessment of Soil Moisture, Soil Mineralogy and other Environmental Factors Influencing Mosquito-borne Infection Risks in the Lower Rio Grande Valley, U.S. - Mexico Border (Invited)

NASA Astrophysics Data System (ADS)

Hubbard, B. E.; Folger, H. W.; Page, W. R.

2010-12-01

A dengue fever outbreak occurred near Matamoros, Mexico along the Lower Rio Grande Valley during the summer of 2005 following heavy rainfall from Tropical Storm Gert and Hurricane Emily. This outbreak exemplifies the need for monitoring soil moisture and mapping soil permeability factors affecting the breeding and distribution of mosquito species capable of spreading disease. For example, the Rio Grande delta of South Texas and North Tamaulipas Mexico is inhabited by over 50 native and invasive species of mosquitoes capable of hosting Malaria, West Nile Virus and other types of human and livestock infecting Encephalitis. They range in ecological habitats from coastal salt marshes to freshwater riparian wetlands, tree holes and/or urban containers, flooded agricultural fields, and the many irrigation canals and ditches present throughout our study area. For this study, water-saturated and flooded soils were mapped using a “soil moisture availability” index (Mo) based on normalized difference vegetation index (NDVI) images and surface radiant and/or kinetic temperature images derived from multi-temporal Landsat-7 ETM+ and ASTER imagery. In particular, the Landsat-7 imagery covers ten cloud-free or minimal cloud cover acquisition dates during drought and wet periods of 2002, prior to the scan-line corrector failure in 2003. This includes one date (August 18, 2002) of co-orbital swath coverage between Landsat and ASTER, acquired after the land fall and dissipation of Tropical Storm Bertha (August 09, 2002). ASTER image dates used include those before and after the land fall of Hurricane Emily on July 20, 2005. The resulting maps show the distribution of relatively permeable (i.e. sandier) and impermeable soil types, the latter of which are dominated by clay-rich soils deposited in remnant interdistributary channels as channel-fill, and overbank flood deposits along the modern Rio Grande delta and portions of the (remapped) Pleistocene Beaumont coastal deltaic plain. Pools of standing rain water on impermeable soils can become ideal habitats for mosquito ovipositing and larval development between storms, which in turn can pose a higher risk for infection to humans and livestock animals. Because clay and other fine-grained minerals strongly affect a soil’s physical and chemical properties such as porosity, permeability and surface sealing/crusting upon saturation, 211 soil samples were collected at approximately 3-5 km sample spacing. The mineralogy of both the < 2 mm- and the < 2 micron-grain size fractions were then analyzed. The results show the distribution and relative abundance of kaolinite, illite and montmorillonite, for which we compare to ASTER remote sensing derived mineral maps based on drought period imagery (March 15, 2001), and airborne geophyisical data showing the distribution of radiometric K-bearing minerals (e.g. mainly illite/mica and orthoclase feldspar). The ASTER mineral maps show areas of clay-rich impermeable soils that are prone to ponding of standing water after storms. Our results show the utility of using remote sensing observations for mapping flood prone areas that may pose mosquito related health threats to both people and livestock on both sides of the border.

A multi proxy reconstruction of paleoproductivity of Cleland Lake British Columbia, Canada

NASA Astrophysics Data System (ADS)

Mihindukulasooriya, L. N.; Pompeani, D. P.; Ortiz, J. D.; Steinman, B. A.; Abbott, M. B.

2013-12-01

In small closed-basin lakes in semi arid regions, variations in precipitation/evaporation (P/E) balance affect the physical, biological, and chemical composition of the lake water and sediment. This study presents color reflectance, XRF derived elemental concentrations and δ18O values of carbonates (δ18Ocarb) in sediment cores from Cleland Lake, British Columbia to provide insight into paleolimnological variations during the past 7500 years. Principal Component (PC) 1 of the reflectance data, i.e, Illite+ sphalerite is used as a clay mineral proxy, and PC 4, diatoms+ cyanobacteria, is used as a paleoproductivity proxy. Lake paleoproductivity history is divided into three temporal periods, 400 to 2500 (denoted as P1), 2500 to 5000 (P2) and 5000 to 7500 (P3) calibrated years before present (Cal yr BP). Fe and Mn concentrations gradually increase during P3, reach high values during P2 and rapidly drop to the lowest values after 2600 Cal yr BP. Diatom abundances have a positive correlation with illite (r= 0.79, n=73 α=0.01) throughout the record. In contrast, negative correlations (table 1) exists between δ18Ocarb and diatom abundances during P2 and P3, indicating higher diatom abundance during wet periods. After 3000 cal yr BP, the correlation reverses (table 1), indicating low diatom abundance during wet periods. Variability in diatom abundances is greater than that of the δ18Ocarb values, indicating that factors other than the P/E balance affects phytoplankton abundance. P 1 is characterized by three periods (centered at 2500, 2100 and 1400 Cal yr BP) of predominantly low diatom abundance that occur simultaneously with low Mn and Cr concentrations. Low Mn and Cr levels may indicate intense reducing conditions, while the observed peaks in Ni and Cu concentration might indicate reducing conditions resulting from high rates of organic matter decomposition (Tribovillard et al., 2006). Contemporaneous with the abrupt δ18Ocarb depletion around 2600 Cal yr BP, trace metal concentrations (Fe, Cu, Ni and Zn) as well as nutrient (P, S) levels increase, suggesting a higher rate of groundwater inflow and mineral delivery. Despite these increases, diatom abundance remains low. This may indicate the competitive appearance of Cyanobacteria in place of diatoms. Three rapid increases in diatom abundances centered at 1500, 900 and 700 Cal yr BP are associated with peaks in Cr and δ18Ocarb. Cr enrichment and low Mn may indicate reducing conditions in the absence of free H2S (Tribovillard et al., 2006). Such conditions can develop due to restricted water mass renewal in a well stratified lake (Tribovillard et al., 2006). In contrast, around 900 Cal yr BP P, S and Si levels increase. Relatively high δ18Ocarb values at this time do not provide support for a groundwater associated inflow of nutrients to the lake. Therefore it is possible that this peak could have resulted from other climatic factors including higher wind speeds and a greater flux of fine clastic material.Table 1

Bentonite Clay Evolution at Elevated Pressures and Temperatures: An experimental study for generic nuclear repositories

NASA Astrophysics Data System (ADS)

Caporuscio, F. A.; Cheshire, M.; McCarney, M.

2012-12-01

The Used Fuel Disposition Campaign is presently engaged in looking at various generic repository options for disposal of used fuel. Of interest are the disposal of high heat load canisters ,which may allow for a reduced repository footprint. The focus of this experimental work is to characterize Engineered Barrier Systems (EBS) conditions in repositories. Clay minerals - as backfill or buffer materials - are critical to the performance of the EBS. Experiments were performed in Dickson cells at 150 bar and sequentially stepped from 125 oC to 300 oC over a period of ~1 month. An unprocessed bentonite from Colony, Wyoming was used as the buffer material in each experiment. An K-Ca-Na-Cl-rich brine (replicating deep Stripa groundwater) was used at a 9:1 water:rock ratio. The baseline experiment contained brine + clay, while three other experiments contained metals that could be used as waste form canisters (brine +clay+304SS, brine+clay+316SS, brine+clay+Cu). All experiments were buffered at the Mt-Fe oxygen fugacity univarient line. As experiment temperature increased and time progressed, pH, K and Ca ion concentrations dropped, while Si, Na, and SO4 concentrations increased. Silicon was liberated into the fluid phase (>1000 ppm) and precipitated during the quenching of the experiment. The precipitated silica transformed to cristobalite as cooling progressed. Potassium was mobilized and exchanged with interlayer Na, transitioning the clay from Na-montmorillonite to K-smectite. Though illitization was not observed in these experiments, its formation may be kinetically limited and longer-term experiments are underway to evaluate the equilibrium point in this reaction. Clinoptilolite present in the starting bentonite mixture is unstable above 150 oC. Hence, the zeolite broke down at high temperatures but recrystallized as the quench event occurred. This was borne out in SEM images that showed clinoptilolite as a very late stage growth mineral. Both experimental runs containing steel exhibit the generation of a chlorite / Fe-saponite layer at the clay-metal boundary. The formation of minor amounts of pentlandite [(Fe,Ni)9S8] also occurs on both steel plates. Chalcocite (Cu2S) formed as a corrosion product on the Cu plates. The two sulfide phases have been produced by the generation of H2S gas during the experimental runs. The H2S is formed by the breakdown of pyrite framboids at high temperature in the bentonite. Such experiments on representative EBS materials at elevated P,T repository conditions are providing useful information for generic repository studies. Lack of illite formation is common in clay experiments and may be related to kinetics or K concentration. Precipitated SiO2 may potentially seal heating cracks in the clay backfill. The chlorite layer generated on steel may act as a passivation material and prevent corrosion of the steel canister wall. Finally, even if zeolites break down during the high temperature thermal pulse of a repository, zeolites may form again as the repository inventory cools off and perform as radionuclide sorbing phases.

Composition, structure and properties of sediment thermal springs of Kamchatka

NASA Astrophysics Data System (ADS)

Shanina, Violetta; Smolyakov, Pavel; Parfenov, Oleg

2016-04-01

The paper deals with the physical and mechanical properties sediment thermal fields Mutnovsky, Lower Koshelevo and Bannyh (Kamchatka). This multi-component soils, mineral and chemical composition of which depends on the formation factors (pH, temperature, salinity of water, composition and structure of the host volcanic rocks). Samples Lower Koshelevo sediment thermal sources differ in the following composition: smectite, kaolinite, kaolinite-smectite mixed-mineral. Samples of sediment thermal springs Mutnovsky volcano in accordance with the X-ray analysis has the following composition: volcanic glass, crystalline sulfur, plagioclase, smectite, illite-smectite mixed, illite, chlorite, quartz, cristobalite, pyrite, melanterite, kaolinite. Natural moisture content samples of sediment thermal springs from 45 to 121%, hygroscopic moisture content of 1.3 to 3.7%. A large amount of native sulfur (up to 92%) and the presence of amorphous material gives low values of density of solid particles (up to 2.1 g/cm3) samples Mutnovskii thermal field. The values of the density of solids sediment Koshelevo and Bannyh hot springs close to those of the main components of mineral densities (up to 2.6-3.0 g/cm3). The results of the particle size distribution and microaggregate analysis of sediment thermal springs Lower Koshelevo field shows that the predominance observed of particles with a diameter from 0.05 mm to 0.25 mm, the coefficient of soil heterogeneity heterogeneous. In the bottom sediments of the thermal springs of the volcano Mutnovsky poorly traced predominance of one faction. Most prevalent fraction with particle size 0.01 - 0.05 mm. When analyzing the content in the soil microaggregates their content is shifted towards particles with a diameter of 0.25 mm. The contents of a large number of large (1-10 mm), porous rock fragments, due to the deposition of pyroclastic material from the eruptions of the last century. Present in large amounts rounded crystals of native sulfur associated with the rise of mixed solutions, formed at the boundary of secondary boil through faults to the surface thermal boiler (Bortnikova et al., 2009). Calculated flow index and plasticity, shows the classification in accordance with GOST 25100-2011. From these figures it is clear that all the sediments are sandy loam and are in a fluid state. A clear relationship between temperature, pH and particle size distribution of sediment thermal springs can not be traced, great importance is the geological evolution of the volcanic activity, hydrogeological conditions and the time factor. Therefore, samples with a currently active Mutnovsky volcano - sandy loam, sediments of the thermal springs Koshelevo fields are often to loams. The bottom sediments of thermal springs from the territory of the Lower Koshelevo thermal field in a natural occurrence in a state of higher yield strength, so they are an unstable surface, which may cause landslides. The bottom sediments of thermal springs are low explored subject of engineering geology, it is important to examine their properties to simulate the conditions of formation and the development of dangerous processes.

Surveying Clay Mineral Diversity in the Murray Formation, Gale Crater, Mars

NASA Technical Reports Server (NTRS)

Bristow, T.F.; Blake, D. F..; Vaniman, D. T.; Chipera, S. J.; Rampe, E. B.; Grotzinger, J. P.; McAdam, A. C.; Ming, D. W..; Morrison, S. M.; Yen, A. S.;

Investigating the behaviour of Mg isotopes during the formation of clay minerals

NASA Astrophysics Data System (ADS)

Wimpenny, Joshua; Colla, Christopher A.; Yin, Qing-Zhu; Rustad, James R.; Casey, William H.

2014-03-01

We present elemental and isotopic data detailing how the Mg isotope system behaves in natural and experimentally synthesized clay minerals. We show that the bulk Mg isotopic composition (δ26Mg) of a set of natural illite, montmorillonite and kaolinite spans a 2‰ range, and that their isotopic composition depends strongly on a balance between the relative proportions of structural and exchangeable Mg. After acid leaching, these natural clays become relatively enriched in isotopically heavy Mg by between 0.2‰ and 1.6‰. Results of exchange experiments indicate that the Mg that has adsorbed to interlayer spaces and surface charged sites is relatively enriched in isotopically light Mg compared to the residual clay. The isotopic composition of this exchangeable Mg (-1.49‰ to -2.03‰) is characteristic of the isotopic composition of Mg found in many natural waters. Further experiments with an isotopically characterized MgCl2 solution shows that the clay minerals adsorb this exchangeable Mg with little or no isotopic fractionation, although we cannot discount the possibility that the uptake of exchangeable Mg does so with a slight preference for 24Mg. To characterize the behaviour of Mg isotopes during clay mineral formation we synthesized brucite (Mg(OH)2), which we consider to be a good analogue for the incorporation of Mg into the octahedral sheet of Mg-rich clay minerals or into the brucitic layer of clays such as chlorite. In our experiment the brucite mineral becomes enriched in the heavy isotopes of Mg while the corresponding solution is always relatively enriched in isotopically light Mg. The system reaches a steady state after 10 days with a final fractionation factor (αsolid-solution) of 1.0005 at near-neutral pH. This result is consistent with the general consensus that secondary clay minerals preferentially take up isotopically heavy Mg during their formation. However our results also show that exchangeable Mg is an important component within bulk clay minerals and can have an important influence over the bulk clay δ26Mg value. Modeling shows that in certain soils or sediments where the percentage of exchangeable Mg is >30% and the isotopic composition of the exchangeable Mg is around -2‰, the generation of bulk δ26Mg values of <-0.5‰ is likely. On a broader scale, Mg-rich minerals such as smectite and illite are likely to impart a stronger control over the Mg budget in clay rich sediments, and their high structural Mg component is likely to result in bulk sediment δ26Mg values that are closer in composition to the UCC. Despite this, results of modeling, together with experimental observation suggests that the uptake of exchangeable Mg into these clay rich sediments could cause a decrease in the bulk δ26Mg value by up to ˜0.3-0.4‰. This should be accounted for when assessing the δ26Mg value of sediments on a crustal scale.

Fluid inclusions and preliminary studies of hydrothermal alteration in core hole PLTG-1, Platanares geothermal area, Honduras

USGS Publications Warehouse

Bargar, K.E.

1991-01-01

The Platanares geothermal area in western Honduras consists of more than 100 hot springs that issue from numerous hot-spring groups along the banks or within the streambed of the Quebrada de Agua Caliente (brook of hot water). Evaluation of this geothermal area included drilling a 650-m deep PLTG-1 drill hole which penetrated a surface mantling of stream terrace deposits, about 550 m of Tertiary andesitic lava flows, and Cretaceous to lower Tertiary sedimentary rocks in the lower 90 m of the drill core. Fractures and cavities in the drill core are partly to completely filled by hydrothermal minerals that include quartz, kaolinite, mixed-layer illite-smectite, barite, fluorite, chlorite, calcite, laumontite, biotite, hematite, marcasite, pyrite, arsenopyrite, stibnite, and sphalerite; the most common open-space fillings are calcite and quartz. Biotite from 138.9-m depth, dated at 37.41 Ma by replicate 40Ar/39 Ar analyses using a continuous laser system, is the earliest hydrothermal mineral deposited in the PLTG-1 drill core. This mid-Tertiary age indicates that at least some of the hydrothermal alteration encountered in the PLTG-1 drill core occured in the distant past and is unrelated to the present geothermal system. Furthermore, homogenization temperatures (Th) and melting-point temperatures (Tm) for fluid inclusions in two of the later-formed hydrothermal minerals, calcite and barite, suggest that the temperatures and concentration of dissolved solids of the fluids present at the time these fluid inclusions formed were very different from the present temperatures and fluid chemistry measured in the drill hole. Liquid-rich secondary fluid inclusions in barite and caicite from drill hole PLTG-1 have Th values that range from about 20??C less than the present measured temperature curve at 590.1-m depth to as much as 90??C higher than the temperature curve at 46.75-m depth. Many of the barite Th measurements (ranging between 114?? and 265??C) plot above the reference surface boiling-point curve for pure water assuming hydrostatic conditions; however, the absence of evidence for boiling in the fluid inclusions indicates that at the time the minerals formed, the ground surface must have been at least 80 m higher than at present and underwent stream erosion to the current elevation. Near-surface mixed-layer illite-smectite is closely associated with barite and appears to have formed at about the same temperature range (about 120?? to 200??C) as the fluid-inclusion Th values for barite. Fluid-inclusion Th values for calcite range between about 136?? and 213??C. Several of the calcite Th values are significantly lower than the present measured temperature curve. The melting-point temperatures (Tm) of fluid-inclusion ice yield calculated salinities, ranging from near zero to as much as 5.4 wt. % NaCl equivalent, which suggest that much of the barite and calcite precipitated from fluids of significantly greater salinity than the present low salinity Platanares hot-spring water or water produced from the drill hole. ?? 1991.

Accumulation and chemical states of radiocesium by fungus Saccharomyces cerevisiae

NASA Astrophysics Data System (ADS)

Ohnuki, Toshihiko; Sakamoto, Fuminori; Kozai, Naofumi; Yamasaki, Shinya; Yu, Qianqian

2014-05-01

After accident of Fukushima Daiichi Nuclear Power Plant, the fall-out radiocesium was deposited on the ground. Filamentous fungus is known to accumulate radiocesium in environment, even though many minerals are involved in soil. These facts suggest that fungus affect the migration behavior of radiocesium in the environment. However, accumulation mechanism of radiocesium by fungus is not understood. In the present study, accumulation and chemical states change of Cs by unicellular fungus of Saccharomyces cerevisiae have been studied to elucidate the role of microorganisms in the migration of radiocesium in the environment. Two different experimental conditions were employed; one is the accumulation experiments of radiocesium by S. cerevisiae from the agar medium containing 137Cs and a mineral of zeolite, vermiculite, smectite, mica, or illite. The other is the experiments using stable cesium to examine the chemical states change of Cs. In the former experiment, the cells were grown on membrane filter of 0.45 μm installed on the agar medium. After the grown cells were weighed, radioactivity in the cells was measured by an autoradiography technique. The mineral weight contents were changed from 0.1% to 1% of the medium. In the latter experiment, the cells were grown in the medium containing stable Cs between 1 mM and 10mM. The Cs accumulated cells were analyzed by SEM-EDS and EXAFS. The adsorption experiments of cesium by the cells under resting condition were also conducted to test the effect of cells metabolic activity. Without mineral in the medium, cells of S. cerevisiae accumulated 1.5x103 Bq/g from the medium containing 137Cs of 2.6x102 Bq/g. When mineral was added in the medium, concentration of 137Cs in the cells decreased. The concentration of 137Cs in the cells from the medium containing different minerals were in the following order; smectite, illite, mica > vermiculite > zeolite. This order was nearly the same as the inverse of distribution coefficient of mineral for 137Cs in the medium solution. The concentration of 137Cs in the cells lowered in the medium containing higher mineral content. These results indicate that radiocesium was competively accumulated in the cells with minerals in the soil. Higher concentration of stable Cs was accumulated in the cells in the metabolically active condition than in the resting cells condition. XAFS analyses showed that the k3-weighted extended-XAFS functions and the radial structural function of Cs accumulated by the cells in the metabolically active condition were similar to those in the resting condition, indicating that chemical states of the accumulated Cs were nearly the same between both conditions. These results indicate that the fungus accumulates radiocesium by competitively with minerals in the soils, and performs higher retardation of the migration of Cs in the metabolically active condition than the resting one. A part of this study is the results of "Multidisciplinary investigation on radiocesium fate and transport for safety assessment for interim storage and disposal of heterogeneous waste" carried out under the Initiatives for Atomic Energy Basic and Generic Strategic Research by the Ministry of Education, Culture, Sports, Science and Technology of Japan.

Regional polyphase deformation of the Eastern Sierras Pampeanas (Argentina Andean foreland): strengths and weaknesses of paleostress inversion

NASA Astrophysics Data System (ADS)

Traforti, Anna; Zampieri, Dario; Massironi, Matteo; Viola, Giulio; Alvarado, Patricia; Di Toro, Giulio

2016-04-01

The Eastern Sierras Pampeanas of central Argentina are composed of a series of basement-cored ranges, located in the Andean foreland c. 600 km east of the Andean Cordillera. Although uplift of the ranges is partly attributed to the regional Neogene evolution (Ramos et al. 2002), many questions remain as to the timing and style of deformation. In fact, the Eastern Sierras Pampeanas show compelling evidence of a long lasting brittle history (spanning the Early Carboniferous to Present time), characterised by several deformation events reflecting different tectonic regimes. Each deformation phase resulted in further strain increments accommodated by reactivation of inherited structures and rheological anisotropies (Martino 2003). In the framework of such a polyphase brittle tectonic evolution affecting highly anisotropic basement rocks, the application of paleostress inversion methods, though powerful, suffers from some shortcomings, such as the likely heterogeneous character of fault slip datasets and the possible reactivation of even highly misoriented structures, and thus requires careful analysis. The challenge is to gather sufficient fault-slip data, to develop a proper understanding of the regional evolution. This is done by the identification of internally consistent fault and fracture subsets (associated to distinct stress states on the basis of their geometric and kinematic compatibility) in order to generate a chronologically-constrained evolutionary conceptual model. Based on large fault-slip datasets collected in the Sierras de Cordoba (Eastern Sierras Pampeanas), reduced stress tensors have been generated and interpreted as part of an evolutionary model by considering the obtained results against: (i) existing K-Ar illite ages of fault gouges in the study area (Bense et al. 2013), (ii) the nature and orientation of pre-existing anisotropies and (iii) the present-day stress field due to the convergence of the Nazca and South America plates (main shortening oriented WSW-ENE). Although remarkable differences in reactivation mechanisms have been observed for the various studied lithological domains (schist, gneiss and granitic rocks), the brittle regional polyphase deformation of the Eastern Sierras Pampeanas appears to be dominated by two extensional episodes (σ3 oriented NE/ENE and WNW, respectively), which can be associated with Middle-Late Permian to Early Cretaceous tectonism, followed by a compressional paleostress (σ1 oriented ENE), which is compatible with the present day Andean convergence. Paleostress inversion techniques, despite all uncertainties involved, represent a robust approach to disentangle complex polyphase deformation histories both in term of reactivation mechanisms and strain partitioning. References: Bense, F. A., Wemmer, K., Löbens, S., & Siegesmund, S. (2013). Fault gouge analyses: K-Ar illite dating, clay mineralogy and tectonic significance-a study from the Sierras Pampeanas, Argentina. International Journal of Earth Sciences, 103, 189-218. Martino, R. D. (2003). Las fajas de deformación dúctil de las Sierras Pampeanas de Córdoba : Una reseña general. Revista de La Asociación Geológica Argentina, 58(4), 549-571. Ramos, V. A., Cristallini, E. O., & Perez, D. J. (2002). The Pampean flat-slab of the Central Andes. Journal of South American Earth Sciences, 15, 59-78.

Frictional properties of fault rocks along the shallow part of the Japan Trench décollement: insights from samples recovered during the Integrated Ocean Drilling Project Expedition 343 (the JFAST project)

NASA Astrophysics Data System (ADS)

Remitti, Francesca; Smith, Steven; Gualtieri, Alessandro; Di Toro, Giulio; Nielsen, Stefan

2014-05-01

The Japan Trench Fast Drilling Project (JFAST), Integrated Ocean Drilling Program (IODP) Expedition 343, successfully located and sampled the shallow slip zone of the Mw =9.0 Tohoku-Oki earthquake where the largest coseismic slip occurred (c. 50 m). Logging-while-drilling, core-sample observations and the analysis of temperature data recovered from a third borehole show that a thin (<5 m), smectite rich plate-boundary fault accommodated the large slip of the Tohoku-Oki Earthquake rupture, as well as most of the interplate motion at the drill site. Effective normal stress along the shallow plate-boundary fault is estimated to be c. 7 MPa. Single-velocity and velocity-stepping rotary-shear friction experiments on fault material were performed with the Slow to HIgh Velocity Apparatus (SHIVA) installed at INGV in Rome. Quantitative phase analysis using the combined Rietveld and R.I.R. method indicates that the starting material is mainly composed of smectite (56 wt%) and illite/mica (21 wt%) and minor quartz, kaolinite, plagioclase and K-feldspar. The amount of amorphous fraction has also been calculated and it is close to the detection limit. Each experiment used 3.5 g of loosely disaggregated gouge, following sieving to a particle size fraction <1 mm. Experiments were performed either 1) "room-dry" (40-60% humidity) at 8.5 MPa normal stress (one test at 12.5 MPa), or 2) "water-dampened" (0.5 ml distilled water added to the gouge layers) at 3.5 MPa normal stress. Slip velocities ranged over nearly seven orders of magnitude (10-5 - 3 m s-1). Total displacement is always less than 1 m. The peak and steady-state frictional strengths of the gouges are significantly lower under water-dampened conditions, with mean steady-state friction coefficients (μ, shear stress/normal stress) at all investigated velocities of 0.04<μ<0.1. This is consistent with the small measured frictional heat anomaly along the plate boundary fault ~1.5 years after the Tohoku-Oki earthquake. Under room-dry conditions the gouge material is velocity-strengthening at intermediate velocities (0.001 - 0.1 m s-1), but strongly velocity-weakening at > 0.1 m s-1. Instead, under water-dampened conditions, the gouge is velocity-neutral to velocity-weakening at all investigated velocities. In other words, the intermediate-velocity strengthening, which would probably act as a "barrier" to rupture propagation in the dry gouges, disappears in water-dampened gouges. This result is compatible with propagation of the Tohoku rupture to the trench, and also with large coseismic slip at shallow depths. Quantitative phase analysis using the combined Rietveld and R.I.R. method has been performed also on six post-experiment gouges for the determination of both the crystalline and amorphous fractions. Preliminary results show that the mineralogical assemblage is basically the same after the experiments, with both smectite and illite phases preserved, this suggests that the weakening mechanism operating in this material is active at low temperature.

Integrating remote sensing techniques at Cuprite, Nevada: AVIRIS, Thematic Mapper, and field spectroscopy

NASA Technical Reports Server (NTRS)

Hill, Bradley; Nash, Greg; Ridd, Merrill; Hauff, Phoebe L.; Ebel, Phil

1992-01-01

The Cuprite mining district in southwestern Nevada has become a test site for remote sensing studies with numerous airborne scanners and ground sensor data sets collected over the past fifteen years. Structurally, the Cuprite region can be divided into two areas with slightly different alteration and mineralogy. These zones lie on either side of a postulated low-angle structural discontinuity that strikes nearly parallel to US Route 95. Hydrothermal alternation at Cuprite was classified into three major zones: silicified, opalized, and argillized. These alteration types form a bulls-eye pattern east of the highway and are more linear on the west side of the highway making a striking contrast from the air and the imagery. Cuprite is therefore an ideal location for remote sensing research as it exhibits easily identified hydrothermal zoning, is relatively devoid of vegetation, and contains a distinctive spectrally diagnostic mineral suite including the ammonium feldspar buddingtonite, several types of alunite, different jarosites, illite, kaolinite, smectite, dickite, and opal. This present study brings a new dimension to these previous remote sensing and ground data sets compiled for Cuprite. The development of a higher resolution field spectrometer now provides the capability to combine extensive in-situ mineralogical data with a new geologic field survey and detailed Airborne Visible/Infrared Imaging Spectrometers (AVIRIS) images. The various data collection methods and the refinement of the integrated techniques are discussed.

Structural Investigation of Alkali Activated Clay Minerals for Application in Water Treatment Systems

NASA Astrophysics Data System (ADS)

Bumanis, G.; Bajare, D.; Dembovska, L.

2015-11-01

Alkali activation technology can be applied for a wide range of alumo-silicates to produce innovative materials with various areas of application. Most researches focuse on the application of alumo-silicate materials in building industry as cement binder replacement to produce mortar and concrete [1]. However, alkali activation technology offers high potential also in biotechnologies [2]. In the processes where certain pH level, especially alkaline environment, must be ensured, alkali activated materials can be applied. One of such fields is water treatment systems where high level pH (up to pH 10.5) ensures efficient removal of water pollutants such as manganese [3]. Previous investigations had shown that alkali activation technology can be applied to calcined clay powder and aluminium scrap recycling waste as a foam forming agent to create porous alkali activated materials. This investigation focuses on the structural investigation of calcined kaolin and illite clay alkali activation processes. Chemical and mineralogical composition of both clays were determined and structural investigation of alkali activated materials was made by using XRD, DTA, FTIR analysis; the microstructure of hardened specimens was observed by SEM. Physical properties of the obtained material were determined. Investigation indicates the essential role of chemical composition of the clay used in the alkali activation process, and potential use of the obtained material in water treatment systems.

Determination of layer-charge characteristics of smectites

USGS Publications Warehouse

Christidis, G.E.; Eberl, D.D.

2003-01-01

A new method for calculation of layer charge and charge distribution of smectites is proposed. The method is based on comparisons between X-ray diffraction (XRD) patterns of K-saturated, ethylene glycol-solvated, oriented samples and calculated XRD patterns for three-component, mixed-layer systems. For the calculated patterns it is assumed that the measured patterns can be modeled as random interstratifications of fully expanding 17.1 Å layers, partially expanding 13.5 Å layers and non-expanding 9.98 Å layers. The technique was tested using 29 well characterized smectites. According to their XRD patterns, smectites were classified as group 1 (low-charge smectites) and group 2 (high-charge smectites). The boundary between the two groups is at a layer charge of −0.46 equivalents per half unit-cell. Low-charge smectites are dominated by 17.1 Å layers, whereas high-charge smectites contain only 20% fully expandable layers on average. Smectite properties and industrial applications may be dictated by the proportion of 17.1 Å layers present. Non-expanding layers may control the behavior of smectites during weathering, facilitating the formation of illite layers after subsequent cycles of wetting and drying. The precision of the method is better than 3.5% at a layer charge of −0.50; therefore the method should be useful for basic research and for industrial purposes.

Relationship between mineralogy and porosity in seals relevant to geologic CO2 Sequestration

DOE Office of Scientific and Technical Information (OSTI.GOV)

Swift, Alexander; Anovitz, Lawrence; Sheets, Julia

2014-01-01

Porosity and permeability are key petrophysical variables that link the thermal, hydrological, geochemical, and geomechanical properties of subsurface formations. The size, shape, distribution, and connectivity of rock pores dictate how fluids migrate into and through micro- and nano-environments, then wet and react with accessible solids. Three representative samples of cap rock from the Eau Claire Formation, the prospective sealing unit that overlies the Mount Simon Sandstone, a potential CO 2 storage formation, were interrogated with an array of complementary methods. neutron scattering, backscattered-electron imaging, energydispersive spectroscopy, and mercury porosimetry. Results are presented that detail variations between lithologic types in totalmore » and connected nano- to microporosity across more than five orders of magnitude. Pore types are identified and then characterized according to presence in each rock type, relative abundance, and surface area of adjacent minerals, pore and pore-throat diameters, and degree of connectivity. We observe a bimodal distribution of porosity as a function of both pore diameter and pore-throat diameter. The contribution of pores at the nano- and microscales to the total and the connected porosity is a distinguishing feature of each lithology observed. Pore:pore-throat ratios at each of these two scales diverge markedly, being almost unity at the nanoscale regime (dominated by illitic clay and micas), and varying by one and a half orders of magnitude at the microscale within a clastic mudstone.« less

Geochemical characteristics of The Emet (Espey-Hisarcik) borate deposits, Kütahya, Turkey

NASA Astrophysics Data System (ADS)

Koçak, İ.; Koç, Ş.

2018-06-01

Nearly 72% world's borate reserves are in western part of Turkey. The Emet (Kütahya) deposit is one of these deposits. The Emet borate deposit, like other deposits in western Anatolia, was deposited in Miocene lacustrine environment whose formation coincides with volcanic activity started in Paleogene and lasted to the beginning of Quaternary. The borate ore displaying lenticular structure is alternated with claystone, marl, tuff and thin bedded limestone. The mineral paragenesis is composed of colemanite, hydroboracite, Veatchite, dolomite, calcite, montmorillonite and illite. The Emet borate deposit has been the subject of various geologic and mineralogical studies. In the present study major and trace element contents of 60 borate samples from this deposit are discussed. Among the trace elements, significant enrichment was found in As, Se, Sr, Cs, Sb and Li. Element correlations indicate volcanic source for boron (exhalations and hydrothermal solutions) whilst other elements are found to be derived from a terrestrial source. According to REE data, high Ce concentrations and anomalies are generally indicative of oxygenated depositional environment whilst low Ce contents facilitated the lake waters to be low oxygenated as a result of H2S-rich hydrothermal solutions. The weak negative anomaly detected only in the Hisarcık region is attributed to lacking of Eu contribution to the lake due to insufficient alteration on the continent.

The effect of various pozzolanic additives on the concrete strength index

NASA Astrophysics Data System (ADS)

Vitola, L.; Sahmenko, G.; Erdmane, D.; Bumanis, G.; Bajare, D.

2017-10-01

The concrete industry is searching continuously for new effective mineral additives to improve the concrete properties. Replacing cement with the pozzolanic additives in most cases has resulted not only in positive impact on the environment but also has improved strength and durability of the concrete. Effective pozzolanic additives can be obtained from natural resources such as volcanic ashes, kaolin and other sediments as well as from different production industries that create various by-products with high pozzolanic reactivity. Current research deals with effectiveness evaluation of various mineral additives/wastes, such as coal combustion bottom ash, barley bottom ash, waste glass and metakaolin containing waste as well as calcined illite clays as supplementary cementitious materials, to be used in concrete production as partial cement replacement. Most of the examined materials are used as waste stream materials with potential reactive effect on the concrete. Milling time and fineness of the tested supplementary material has been evaluated and effectiveness was detected. Results indicate that fineness of the tested materials has crucial effect on the concrete compressive strength index. Not in all cases the prolonged milling time can increase fineness and reactivity of the supplementary materials; however the optimal milling time and fineness of the pozolanic additives increased the strength index of concrete up to 1.16 comparing to reference, even in cases when cement was substituted by 20 w%.

Environmental implication of subaqueous lava flows from a continental Large Igneous Province: Examples from the Moroccan Central Atlantic Magmatic Province (CAMP)

NASA Astrophysics Data System (ADS)

El Ghilani, S.; Youbi, N.; Madeira, J.; Chellai, E. H.; López-Galindo, A.; Martins, L.; Mata, J.

2017-03-01

The Late Triassic-Early Jurassic volcanic sequence of the Central Atlantic Magmatic Province (CAMP) of Morocco is classically subdivided into four stratigraphic units: the Lower, Middle, Upper and Recurrent Formations separated by intercalated sediments deposited during short hiatuses in volcanic activity. Although corresponding to a Large Igneous Province formed in continental environment, it contains subaqueous lava flows, including dominant pillowed flows but also occasional sheet flows. We present a study of the morphology, structure and morphometry of subaqueous lava flows from three sections located at the Marrakech High-Atlas (regions of Aït-Ourir, Jbel Imzar and Oued Lhar-Herissane), as well as an analysis of the sediments, in order to characterize them and to understand their environmental meaning. The analysis of clays by the diffraction method X-ray revealed the presence of illite, mica, phengite, céladonite, talc and small amounts of quartz, hematite, calcite and feldspar, as well as two pairs of interbedded irregular (chlorite Smectite/chlorite-Mica). Fibrous minerals such as sepiolite and palygorskite were not detected. The peperite of Herissane region (Central High Atlas) provided an excellent overview on the factors favoring the magma-sediment interaction. These are the products of a mixture of unconsolidated or poorly consolidated sediments, low permeability with a low viscosity magma. The attempt of dating palynology proved unfortunately without results.

The potassic sedimentary rocks in Gale Crater, Mars, as seen by ChemCam Onboard Curiosity

USGS Publications Warehouse

Le Deit, Laetitia; Mangold, Nicolas; Forni, Olivier; Cousin, Agnes; Lasue, Jeremie; Schröder, Susanne; Wiens, Roger C.; Sumner, Dawn Y.; Fabre, Cecile; Stack, Katherine M.; Anderson, Ryan; Blaney, Diana L.; Clegg, Samuel M.; Dromart, Gilles; Fisk, Martin; Gasnault, Olivier; Grotzinger, John P.; Gupta, Sanjeev; Lanza, Nina; Le Mouélic, Stephane; Maurice, Sylvestre; McLennan, Scott M.; Meslin, Pierre-Yves; Nachon, Marion; Newsom, Horton E.; Payre, Valerie; Rapin, William; Rice, Melissa; Sautter, Violaine; Treiman, Alan H.

2016-01-01

The Mars Science Laboratory rover Curiosity encountered potassium-rich clastic sedimentary rocks at two sites in Gale Crater, the waypoints Cooperstown and Kimberley. These rocks include several distinct meters thick sedimentary outcrops ranging from fine sandstone to conglomerate, interpreted to record an ancient fluvial or fluvio-deltaic depositional system. From ChemCam Laser-Induced Breakdown Spectroscopy (LIBS) chemical analyses, this suite of sedimentary rocks has an overall mean K2O abundance that is more than 5 times higher than that of the average Martian crust. The combined analysis of ChemCam data with stratigraphic and geographic locations reveals that the mean K2O abundance increases upward through the stratigraphic section. Chemical analyses across each unit can be represented as mixtures of several distinct chemical components, i.e., mineral phases, including K-bearing minerals, mafic silicates, Fe-oxides, and Fe-hydroxide/oxyhydroxides. Possible K-bearing minerals include alkali feldspar (including anorthoclase and sanidine) and K-bearing phyllosilicate such as illite. Mixtures of different source rocks, including a potassium-rich rock located on the rim and walls of Gale Crater, are the likely origin of observed chemical variations within each unit. Physical sorting may have also played a role in the enrichment in K in the Kimberley formation. The occurrence of these potassic sedimentary rocks provides additional evidence for the chemical diversity of the crust exposed at Gale Crater.

Factors controlling Li concentration and isotopic composition in formation waters and host rocks of Marcellus Shale, Appalachian Basin

USGS Publications Warehouse

Phan, Thai T.; Capo, Rosemary C; Stewart, Brian W.; Macpherson, Gwen; Rowan, Elisabeth L.; Hammack, Richard W.

2015-01-01

In Greene Co., southwest Pennsylvania, the Upper Devonian sandstone formation waters have δ7Li values of + 14.6 ± 1.2 (2SD, n = 25), and are distinct from Marcellus Shale formation waters which have δ7Li of + 10.0 ± 0.8 (2SD, n = 12). These two formation waters also maintain distinctive 87Sr/86Sr ratios suggesting hydrologic separation between these units. Applying temperature-dependent illitilization model to Marcellus Shale, we found that Li concentration in clay minerals increased with Li concentration in pore fluid during diagenetic illite-smectite transition. Samples from north central PA show a much smaller range in both δ7Li and 87Sr/86Sr than in southwest Pennsylvania. Spatial variations in Li and δ7Li values show that Marcellus formation waters are not homogeneous across the Appalachian Basin. Marcellus formation waters in the northeastern Pennsylvania portion of the basin show a much smaller range in both δ7Li and 87Sr/86Sr, suggesting long term, cross-formational fluid migration in this region. Assessing the impact of potential mixing of fresh water with deep formation water requires establishment of a geochemical and isotopic baseline in the shallow, fresh water aquifers, and site specific characterization of formation water, followed by long-term monitoring, particularly in regions of future shale gas development.

Post-Metamorphic Thermal Anomaly across the Nacimiento Block, Central California: a Hydrothermal Overprint?

NASA Astrophysics Data System (ADS)

Lacroix, B.; Hughes, J.; Lahfid, A.; Delchini, S.

2017-12-01

The thermal history of the Nacimiento block located within the Franciscan Complex (California, USA) has been previously proposed based on both vitrinite reflectance (Rm) and illite cristallinity methods (Underwood et al., 1995). These authors suggest that the Nacimiento block is locally perturbed by a thermal anomaly (up to 300ºC), probably caused by post-metamorphic hydrothermal activity linked to the emplacement of an Au-deposit: the Los Burros Gold deposit. Although both thermal anomaly and deposit seem spatially correlated, their relationship is still poorly constrained. Detailed geological and structural mapping within the Los Burros Mining District (LBMD) coupled with a thermal study was conducted to better understand processes responsible for the anomalous temperatures recorded near the deposit. The regional maximum temperature reached by metasediments from the Nacimiento block have been first investigated using the Raman Spectroscopy of Carbonaceous Materials (RSCM) method. In addition, through careful fluid-inclusion and stable isotopes (O and C) studies on the deposit, the temperature and the potential source of the fluid responsible for the Los Burros Au-deposit emplacement were investigated. RSCM technique confirms the presence of a thermal anomaly in the range 260-320ºC near LBMD. However, our structural and petrographic results suggest that the thermal anomaly is not correlated to a post-metamorphic hydrothermal overprint but rather to a late, transpressive deformation uplifting buried metamorphic rocks.

Experimental Study of Cement - Sandstone/Shale - Brine - CO2 Interactions

PubMed Central

2011-01-01

Background Reactive-transport simulation is a tool that is being used to estimate long-term trapping of CO2, and wellbore and cap rock integrity for geologic CO2 storage. We reacted end member components of a heterolithic sandstone and shale unit that forms the upper section of the In Salah Gas Project carbon storage reservoir in Krechba, Algeria with supercritical CO2, brine, and with/without cement at reservoir conditions to develop experimentally constrained geochemical models for use in reactive transport simulations. Results We observe marked changes in solution composition when CO2 reacted with cement, sandstone, and shale components at reservoir conditions. The geochemical model for the reaction of sandstone and shale with CO2 and brine is a simple one in which albite, chlorite, illite and carbonate minerals partially dissolve and boehmite, smectite, and amorphous silica precipitate. The geochemical model for the wellbore environment is also fairly simple, in which alkaline cements and rock react with CO2-rich brines to form an Fe containing calcite, amorphous silica, smectite and boehmite or amorphous Al(OH)3. Conclusions Our research shows that relatively simple geochemical models can describe the dominant reactions that are likely to occur when CO2 is stored in deep saline aquifers sealed with overlying shale cap rocks, as well as the dominant reactions for cement carbonation at the wellbore interface. PMID:22078161

Use of laboratory simulated pyrolysis in tracing the history of sedimentary organic matter

NASA Technical Reports Server (NTRS)

Kaplan, I. R.; Tannenbaum, E.; Huizinga, B. E.

1986-01-01

Results from laboratory simulated pyrolyses experiments show that in addition to depth of burial, preservation of kerogen, and hence any morphologic structure in it, is also dependent on the mineral matrix with which it is associated. In the presence of clay minerals, and especially under dry conditions, extractable lipids released during kerogen decomposition are more rapidly destroyed than in the presence of calcite or chert matrices. The result is production of gas, polar bitumen and pyrobitumen and destruction of biomarkers. During such an early reorganization of the kerogen, the biomarker constituents can be destroyed, or unrecognizably altered. The above process of organic residues maturation appears to be inhibited in the presence of water and is significantly reduced where kerogen is hosted in limestones, dolomites or cherts. These minerals have been characteristically found to be the most reliable in yielding morphological fossils and small quantities of extractable bitumen in Archean and Proterozoic rocks. To understand the validity of chemical and morphological fossils, in the early geologic record, it will be necessary to understand the process of kerogen in sedimentary rocks. To test the role of various minerals on the preservation process, kerogen extracted from a variety of rocks has been heated together with montmorillonite, illite and calcite. The kinetics of the process has been monitored and the products quantitatively identified.

Correlation between magnetic susceptibility and mineral species along NWA-1 well, southern Tunisia: An overlap of the depositional environment, the climate, and the diagenesis

NASA Astrophysics Data System (ADS)

Mefteh, Samir; Essefi, Elhoucine; Yaich, Chokri; Jamoussi, Fakher; Medhioub, Mounir

2015-03-01

In order to distinguish the effects of diagenesis, the climate and the depositional environment, the magnetic properties were correlated with some minerals along the NWA-1 well, which crosses the southern subsurface from Cretaceous to Silurian successions. The MS along NWA-1 well shows major picks probably indicating a dramatic change of geochemical and mineralogical composition. Minor picks may be attributed to diagenetic transformations affecting some minerals. The mineralogical analysis shows the presence of illite, kaolinite with some traces of chlorite and smectite. Quartz, calcite, white feldspar, anorthite, dolomite, gypsum and pyrite are identified as associated minerals. The PCA of the different minerals and the magnetic susceptibility shows three different heterogeneous populations. In these populations, the traditional classification of magnetic minerals is not respected. For instance, diamagnetic minerals are positively correlated with MS. This correlation is through indirect causal relation extrapolating the temperature caused by the burial diagenesis. The aim is not totally reached because the handicap is twofold. The XRD diffraction is not able to identify the low amounts of magnetic minerals and the primary mineralogy and magnetic properties are radically modified by post-depositional processes. At the productive well of NWA-1, this overlap is further complicated by hydrocarbons, low grade metamorphism and remagnetization modifying the original magnetic signal.

Immersion freezing of internally and externally mixed mineral dust species analyzed by stochastic and deterministic models

NASA Astrophysics Data System (ADS)

Wong, B.; Kilthau, W.; Knopf, D. A.

2017-12-01

Immersion freezing is recognized as the most important ice crystal formation process in mixed-phase cloud environments. It is well established that mineral dust species can act as efficient ice nucleating particles. Previous research has focused on determination of the ice nucleation propensity of individual mineral dust species. In this study, the focus is placed on how different mineral dust species such as illite, kaolinite and feldspar, initiate freezing of water droplets when present in internal and external mixtures. The frozen fraction data for single and multicomponent mineral dust droplet mixtures are recorded under identical cooling rates. Additionally, the time dependence of freezing is explored. Externally and internally mixed mineral dust droplet samples are exposed to constant temperatures (isothermal freezing experiments) and frozen fraction data is recorded based on time intervals. Analyses of single and multicomponent mineral dust droplet samples include different stochastic and deterministic models such as the derivation of the heterogeneous ice nucleation rate coefficient (J­­het), the single contact angle (α) description, the α-PDF model, active sites representation, and the deterministic model. Parameter sets derived from freezing data of single component mineral dust samples are evaluated for prediction of cooling rate dependent and isothermal freezing of multicomponent externally or internally mixed mineral dust samples. The atmospheric implications of our findings are discussed.

Dolomitization of felsic volcaniclastic rocks in continental strata: A study from the Lower Cretaceous of the A'nan Sag in Er'lian Basin, China

NASA Astrophysics Data System (ADS)

Zhu, Shifa; Yue, Hui; Zhu, Xiaomin; Sun, Shuyang; Wei, Wei; Liu, Xin; Jia, Ye

2017-05-01

Dolomitization of fine-grained volcaniclastic rocks is common in the Lower Cretaceous of the A'nan Sag in the Er'lian Basin of China. Analysis of core samples shows that the organic-rich volcaniclastic rocks are mainly composed of reworked felsic volcanic materials and terrigenous clay minerals. The fine-grained volcaniclastic rocks can be divided into four types: volcaniclastic rocks without carbonatization, volcaniclastic rocks with ferroan dolomites, dolomitized and calcified volcaniclastic rocks, and calcified volcaniclastic rocks. The parent rocks of the volcaniclastic rocks have high silicon and potassium contents and low iron and magnesium contents, and are probably felsic magma of the calc-alkaline series. The average values of δ13CPDB of the carbonate minerals are about 3.13‰; the average values of δ18OPDB are about - 16.74‰. The compositions of C and O isotopes are probably influenced by bacterial methanogenesis. Iron, magnesium, and calcium are probably derived from illitization of terrigenous smectite. A model for dolomitization of felsic volcaniclastic rock is proposed, including three stages: 1) mixed sedimentation and bacterial methanogenesis (< 75 °C); 2) transformation of clay minerals (> 70 °C) and dolomitization (75 to 97 °C); and 3) dissolution. Late dissolution of authigenic carbonate minerals, creating abundant secondary pores, is significant for hydrocarbon accumulation.

Role of grain-size in phyllonitisation: Insights from mineralogy, microstructures, strain analyses and numerical modeling

NASA Astrophysics Data System (ADS)

Bose, Narayan; Dutta, Dripta; Mukherjee, Soumyajit

2018-07-01

Brittle Y- and P-planes exist in an exposure of greywacke in the Garhwal Lesser Himalaya, India. Although, Y-planes are well developed throughout, the P-planes are prominent only in some parts (domain-A), and not elsewhere (domain-B). To investigate why the P-planes developed selectively, the following studies were undertaken: 1. Clay-separated XRD analyses: clinochlore and illite are present in both the domains. 2. Strain analyses by Rf-φ method: it deduces strain magnitudes of ∼1.8 for the ductile deformed quartz grains from both the domains A and B. 3. Grain size analyses of quartz clasts: domain-A is mostly composed of finer grains (area up to 40,000 μm2), whereas domain-B consists of a population of coarser grains (area >45,000 μm2). A 2D finite element modeling of linear elastic material was performed using COMSOL software to investigate the control of grain-size variation on the generation brittle shear planes. The results of numerical modeling corroborate the known fact that an increase in grain-size reduces the elastic strain energy density. A broader grain-size distribution increases the effects of diffusion creep and resists the onset of dislocation creep. Thus, rocks with coarser grain population (domain B) tend to resist the generation of shear fractures, unlike their fine-grained counterpart (domain A).

On the past climate of the Dobrogea (Romania) during the late Quaternary as reflected by loess geochemistry

NASA Astrophysics Data System (ADS)

Duliu, Octavian G.; Tugulan, Liviu C.; Bojar, Ana-Voica; Dumitras, Delia; Zincovskaya, Inga; Culicov, Otilia A.; Frontasyeva, Marina V.

2015-04-01

Ten samples of loess and paleosoil collected from the Costinesti - Dobrogea (Romania) loess deposit that are covering a time span of about 690 ± 90 ky were analyzed by X-ray diffraction (XRD) , Instrumental Neutron Activation Analysis (INAA) and X-ray Fluorescence (XRF) in order to evidentiate the origin as well as the climatic conditions during the formation of loess material. The presence of illite and calcite, suggests reduced weathering. This was confirmed by further climate proxies as Chemical Index of Alteration (CIA) whose values are between 54.6 and 64.0, Chemical Index of Weathering (CIW) between 65.7 and 71.7 as well as Rb/Sr ratio between 0.26 and 0.47, lower than the neighboring Hungarian loess, but closer to the average Chinese and European loess. No statistical significant differences were observed between average values of loess and palaeosol samples regarding these proxies. The content of 27 trace elements, including 10 REE were, excepting Cr, Ni, Zr and Hf,very close to average rocks composition as Upper Continental Crust (UCC), North America Shale Composite (NASC) and Post-Archean Average Australian Shale (PAAS). Both mineralogical and geochemical data from Costinesti loess and palaeosol samples support a continental origin of loess material deposited in a rather arid and cold climate during the past 690 ± 90 ky.

Groundwater geochemistry in the Seminole Well Field, Cedar Rapids, Iowa

USGS Publications Warehouse

Boyd, Robert A.

1999-01-01

The City of Cedar Rapids obtains its municipal water supply from four well fields in an alluvial aquifer along the Cedar River in east-central Iowa. Since 1992, the City and the U.S. Geological Survey have cooperatively studied the groundwater-flow system and water chemistry near the well fields. The geochemistry in the alluvial aquifer near the Seminole Well Field was assessed to identify potentially reactive minerals and possible chemical reactions that produce observed changes in water chemistry. Calcite, dolomite, ferrihydrite, quartz, rhodochrosite, and siderite were identified as potentially reactive minerals by calculating saturation indexes. Aluminosiicate minerals including albite, Ca-montmorillonite, gibbsite, illite, K-feldspar, and kaolinite were identified as potentially reactive minerals using hypothetical saturation indexes calculated with an assumed dissolved aluminum concentration of 1 microgram per liter. Balanced chemical equations derived from inverse-modeling techniques were used to assess chemical reactions as precipitation percolates to the water table. Calcite dissolution was predominate, but aluminosilicate weathering, cation exchange, and redox reactions also likely occurred. Microbial-catalyzed redox reactions altered the chemical composition of water infiltrating from the Cedar River into the alluvial aquifer by consuming dissolved oxygen, reducing nitrate, and increasing dissolved iron and manganese concentrations. Nitrate reduction only occurred in relatively shallow (3 to 7 meters below land surface) groundwater near the Cedar River and did not occur in water infiltrating to deeper zones of the alluvial aquifer.

PM10 and Pb evolution in an industrial area of the Mediterranean basin

NASA Astrophysics Data System (ADS)

Vicente, A. B.; Jordán, M. M.; Pallarés, S.; Sanfeliu, T.

2007-02-01

The study area is highly industrialized, with businesses involved in the non-metal mineral products sector and ceramic industries (colors, frits and enamel manufacturing) standing out. Air quality evaluation was performed regarding atmospheric particles (PM10 fraction) and Pb in a Spanish coastal area during 2001 and 2002 in order to compare these values with other areas in the Mediterranean basin. Once the samples were collected, their PM10 fraction concentration levels were determined gravimetrically. A Pb analysis in air pollution filters was carried out by ICP-MS. The seasonal and weekly variabilities of these contaminants were also studied, with the objective of being able to explain their origin and thus minimize their possible damaging effects. A similar evolution of PM10 and Pb was observed in both years of the study. Higher PM10 concentrations have been detected during the months of June and July, lower values between March-May, August and October-December, and intermediate values in January and February. A similar tendency has been observed by other authors in European industrialized cities. Regarding Pb, the monthly mean remains constant during the entire year. In the study area, Pb represents 0.6% as a mean of the total PM10 mass, with a variation range between 0.1 and 5.1%. The major crystalline phases in PM10 were quartz, calcite, dolomite, illite, kaolinite and feldspars.

A note on the effect of fault gouge composition on the stability of frictional sliding

USGS Publications Warehouse

Summers, R.; Byerlee, J.

1977-01-01

The frictional properties of fault gouge have been studied at confining pressures to 6 kbars. If the gouge is composed of strong materials such as crushed granite or quartz sand, the frictional strength is high, and violent stick-slip occurs at confining pressures above approximately 1.5 kbars. If the gouge is composed of minerals such as illite, kaolinite, chlorite, or antigorite, which have weak bonding forces between the structural layers, the frictional strength is slightly lower, but violent stick-slip still occurs under high confining pressure. The expanding clays, montmorillonite and vermiculite, which have free water between their structural layers, slide stably at confining pressures as high as 6.25 kbars and exhibit low friction. A similar stable behavior with lowered strength is observed in water-saturated quartz sand when the water is confined within the fault zone during deformation. The results of this series of experiments support water being the stabilizing influence when it is either (1) trapped within or between rocks of low permeability and can provide a high pore pressure when the rocks are deformed, or (2) loosely bonded in a mineral structure, as in the hydrated clays, where it can produce a pseudo-pore pressure when the clay is compressed. In both these cases, the effective stress can be reduced and the deformation stabilized. ?? 1977.

The Role of Microbial Iron Reduction in the Formation of Proterozoic Molar Tooth Structures

NASA Astrophysics Data System (ADS)

Hodgskiss, M. S. W.; Kunzmann, M.; Halverson, G. P.; Poirier, A.

2016-12-01

Molar tooth structures are poorly understood early diagenetic, microspar-filled voids in clay-rich carbonate sediments. They are a common structure in sedimentary successions dating from 2600-720 Ma, but do not occur in rocks older or younger. Despite being volumetrically significant in carbonate rocks of this age, their formation and disappearance are poorly understood. Here, we present iron isotope data, supported by carbon and oxygen isotopes, major and minor element concentrations, and total organic carbon and pyrite contents for samples from ten regions spanning 1870-635 Ma. The iron isotopic composition of molar tooth structures is almost always lighter (modal depletion of 2‰) than the carbonate or siliciclastic components in the host sediment, whereas carbon isotopes are indistinguishable. We interpret the isotopically light iron in molar tooth structures to have been produced by microbial iron reduction utilising Fe-oxyhydroxides and smectites. The microbial conversion of smectite to illite results in a volume reduction of clay minerals ( 30%), while locally increasing pore water alkalinity. Therefore, this biogeochemical process is a viable mechanism to produce voids and subsequently precipitate carbonate minerals. The disappearance of molar tooth structures is likely linked to a combination of a decrease in smectite abundance, a decline in the marine DIC reservoir, and increase in the concentration of O2 in shallow seawater in the mid-Neoproterozoic.

Investigation on porosity and permeability change of Mount Simon sandstone (Knox County, IN, USA) under geological CO 2 sequestration conditions: a numerical simulation approach

DOE Office of Scientific and Technical Information (OSTI.GOV)

Zhang, Liwei; Soong, Yee; Dilmore, Robert M.

In this paper, a numerical model was developed to simulate reactive transport with porosity and permeability change of Mount Simon sandstone (samples from Knox County, IN) after 180 days of exposure to CO 2-saturated brine under CO 2 sequestration conditions. The model predicted formation of a high-porosity zone adjacent to the surface of the sample in contact with bulk brine, and a lower porosity zone just beyond that high-porosity zone along the path from sample/bulk brine interface to sample core. The formation of the high porosity zone was attributed to dissolution of quartz and muscovite/illite, while the formation of themore » lower porosity zone adjacent to the aforementioned high porosity zone was attributed to precipitation of kaolinite and feldspar. The model predicted a 40% permeability increase for the Knox sandstone sample after 180 days of exposure to CO 2-saturated brine, which was consistent with laboratory-measured permeability results. Model-predicted solution chemistry results were also found to be consistent with laboratory-measured solution chemistry data. Finally, initial porosity, initial feldspar content and the exponent n value (determined by pore structure and tortuosity) used in permeability calculations were three important factors affecting permeability evolution of sandstone samples under CO 2 sequestration conditions.« less