Illite-smectite Phases Research Articles

The Effect of K-Fertilization and Irrigation on the Composition of Cultivated Soils: Examples from Israel

Evaluation of soil sustainability should take into account chemical and mineralogical changes due to cultivation. Potassium (K) application is a key farming practice that may potentially affect phyllosilicate composition and soil properties. Irrigation is another agent that affects soil composition. This study aims to evaluate the imprints of cultivation on the chemical and mineralogical compositions of lowland soils under semi-arid and Mediterranean climate regimes and to assess them with the natural pedogenesis. The sites examined include two permanent plot experiments with crop rotation, and three single-plant plots. Cultivated, control, and fallow soils were analyzed for their chemical and mineralogical composition. The X-ray diffraction patterns of the clay fraction were decomposed to achieve quantitative detection of changes among the illite–smectite (IS) phases and in kaolinite amounts. In loamy and clayey soils dominated by IS phases, cultivation caused minor changes and diverse behavior of the IS phases. Yet, the K balance was negative under high fertilization levels and higher plant mass production. Fertilization enhanced the natural process of transforming IS into kaolinite and illite in the sandy soil, leading to a positive K balance. This study emphasizes the importance of IS minerals as a dynamic K pool that responds to plant needs.

Interstratified illite-smectite phases: formation mechanisms and practical applications

Secondary micas after smectite, including mix illite-smectite phases, can form in sediments by three mechanisms, each being specific to particular environments. As the process develops, the newly formed phases undergo structure ordering. Two mechanisms involve transformation of 2:1 mixed-layer structures, and the third is the growth of screw dislocations, with formation of ordered mix phases having a Reichweite parameter of R = 1 or R = 2. We propose methods for identifying such phases when they are present in small amounts or when their XRD patterns lack well-pronounced superperiodic reflections, as well as mathematical formalism for illitization modeling. The theoretical issues are illustrated with field examples, and the illitization mechanisms are discussed in terms of their possible practical applications.

Mass fluxes and clay mineral formation in soils developed on slope deposits of the Kowarski Grzbiet (Karkonosze Mountains, Czech Republic/Poland)

Weathering, mineral formation, and transformation processes along slopes are complex. In cool mountainous regions, undisturbed soil development with a strong vertical leaching element may abruptly change as a result of erosion, accumulation, lateral water fluxes and aeolian input. We investigated soils in the eastern Karkonosze Mountains that have developed on silicatic slope deposits. To date, illite, vermiculite and chlorite are the minerals that have been detected in the clay fraction. Although the climate and parent material should be favourable for the formation of smectites, expandable phases were not verified so far. We investigated if expandable phases could be detected and how they related to elemental fluxes along a short slope sequence (1142–1268ma.s.l. on the border between the Czech Republic and Poland). Mass balance calculations indicated intensive mineral weathering together with a significant leaching of Mg, Al, Ca and Mn on the shoulder and foot slope positions. In the middle zone, which has a concave or undulating surface shape, however, the mass balances of several elements (Na, K, Al, P) revealed a less pronounced leaching (corresponding to a lower degree of podsolization) and in some cases even accumulation. At all sites, mass balance calculations and detected soil minerals (e.g. the increase in illite towards the surface together with an increase in Al and K) indicate some aeolian input. Kaolinite was detected in all soil horizons. Its concentration slightly increased towards the soil surface. Together with the pronounced leaching of Ca, part of kaolinite originates from plagioclase weathering. Besides being a weathering product of primary minerals, part of the kaolinite is inherited from the parent material and probably is also due to aeolian input. In all soils, illite was being transformed into vermiculite and smectites (through regularly-interstratified illite-smectite phases). In addition, the content of chloritic components which increases with depth indicated their concurrent weathering and transformation into smectites. Amphibole also may have acted as a source of smectites. Not all smectite is being actively formed in the soil. Most likely due to slope processes (cover beds) that affected even the subsoil, some smectite has been transferred along the slope. Part of the smectite also seems to derive from the parent material. Active formation of expandable clay minerals is related to convex and planar landscape forms. This relationship suggests intense element leaching, inheritance from the parent material and cover bed mixing processes have contributed to the presence of smectite. Along the slope, zones with predominant vertical transport (shoulder, foot slopes) may repeatedly be interchanged with zones dominated by lateral transport (undulating slope, concave forms).

Changes in the structures of mixed-layer illite-smectite during flooding of terrigenous oil reservoirs

A difference-spectrum method is proposed for the qualitative assessment of changes of illite-smectite structures accompanying the flooding of oil reservoirs. The method permits one to get an open system and reduce the application of procedures based on Markov’s chain formalism. A computer simulation is made to obtain spectra by subtracting the spectrum of an ethylene glycol-saturated sample from the spectrum of an air-dried preparation throughout the entire range of concentrations of illite and smectite components with a short-range order factor R = 0 or R = 3.It has been established that only in the presence of filtration are the maximum and minimum of the spectra in the range of 12.5-9.4 A complicated by a number of local extrema, whose position is specified by the structure of intermediate phases. The flooding process first involves mixed-layer phases with R = 0, leading to a partial segregation of the structures into phase with one and two networks of interlayer H2O. When the secondary mica particles break, phases with R = 3 appear along the boundaries of nanoblocks, first only with 1 H2O and then only with 2 H2O in labile interspaces. Their coexistence with the phases R = 0 in the sample proves the existence of percolation effects due to two-phase filtration in the porous medium. The fully flooded reservoir is always dominated by a mechanical mixture of illite-smectite phases of different nature with R = 0 and with different ratios of components. Transformation of mica that can drastically reduce oil production begins long before the appearance of flooding zones, which are revealed by standard logging methods.

Transformation of Kaolinite into Smectite and Iron-Illite in Brazilian Mangrove Soils

This study investigated soil clay mineralogy of mangrove forests along the Brazilian coast in eight regions of different environmental characteristics, with a focus on the crystallochemical features and genesis of 2:1 phyllosilicates. Samples from two different depths (0–30 and 60–90 cm) and two clay size fractions (<2 and <0.2 μm) were studied. The analytical tools used were X-ray diffraction, Fourier-transform infrared spectroscopy, and transmission electron microscopy–energy dispersive spectroscopy (TEM-EDS). A complex assemblage was found in both fractions, including high proportions of kaolinite, illite (Fe-illite/glauconite), and smectite (Fe-beidellite, Fe-montmorillonite), minor amounts of gibbsite and quartz, and traces of K-feldspar, halloysite, and amphibole crystals (TEM-EDS data). Evidence of illite–smectite and possibly kaolinite–smectite mixed-layer phases was found in the <0.2-μm fraction. An authigenic transformation process likely taking place, from kaolinite to Fe-illite/glauconite, through transitory kaolinite–smectite and illite–smectite phases. The reaction is triggered by high Fe activity in solution generated by dissolution of Fe oxides and pyrite present in the sediment, at approximately neutral pH and high salt content in the water. Smectite illitization takes place by substitution of Al3+ for Si4+ in the tetrahedral sheet, of Fe and Mg2+ for Al3+ in the octahedral sheet, and progressive Fe reduction, all of which produces an increase in the layer charge and K uptake. The sequential nature of the transformation (kaolinite–smectite–illite) suggests a solid-state transformation process. Two unusual kaolinite-rich mangroves were found, indicating low reactivity or high deposition rate of continental sediments of soils derived from the Barreiras Group, dominated by kaolinite.

Роль механизмов образования вторичных слюд на характер структуры фаз иллит-смектит при обводнении коллекторов

Роль механизмов образования вторичных слюд на характер структуры фаз иллит-смектит при обводнении коллекторов

A reinvestigation of smectite illitization in experimental hydrothermal conditions: Results from X-ray diffraction and transmission electron microscopy

The hydrothermal reactivity of the <1 μm fraction, K-saturated SWy-2 Wyoming low-charge montmorillonite was studied in the 250-400 °C temperature range with reactions lasting between 5 and 120 days, with a solid/solution mass ratio of 1:10, and in 1 mol/L KCl solution. From X-ray diffraction (XRD) profile modeling results on K-saturated and ethylene-glycol solvated samples the illitization process appears to occur as a progressive replacement of expandable layers by layers with illitic behavior, in a single illite-smectite phase. However this treatment overestimates the amount of illite layers because of the presence of smectitic non-expandable layers. This was revealed by calcium exchange of the products, which causes re-expansion of the apparent illite layers. The illitization model then obtained consists of four phases with increasing illite content: discrete smectite, a randomly interstratified mixed-layered mineral (MLM) and two ordered MLMs that progressively replace the phases with less illite content. This polyphase model is consistent with results from transmission electron microscopy and chemical microanalysis, which show several types of particle morphology with different interlayer K content and Al-for-Si substitution that seem to correspond to the several phases detected by XRD. Thus, the actual illitization mechanism of smectite in our experiments is not a progressive reaction but a dissolution-precipitation process following the Ostwald step rule in which metastable smectite transforms into illite through a series of metastable illite-smectite phases.

Mineralogy of the clay fraction of water-stable aggregates from dark gray forest soil

Regular structural changes of mixed-layered illite-smectite phases depending on aggregate sizes were revealed by x-ray powder diffraction analysis in the clay fraction of water-stable aggregates of dark gray forest soil. They indicate the differences in the aggregation mechanisms at different depths of the soil profile, which are mutually related and restrict the growth of the water-stable aggregates in the lower part of the A1 horizon to a certain optimal size, because only the smectite surface (unlike the mica one) of the process-determining organomineral composites is capable of interacting. This ensures the kinetic stabilization of the soil as a system and its self-regulation ability.

Clay Mineral Changes in the Morrow Experimental Plots, University of Illinois

AbstractThe clay mineralogy of soil samples from the Morrow Plot Experiment (University of Illinois, Urbana Campus) was investigated. Analysis of soil samples taken at various intervals between 1913 and 1996 indicates that there is a significant influence of cropping method on the clay minerals in the soils. Curve decomposition methods were used to identify and follow the evolution of the different clay minerals: mica, illite and two randomly mixed-layered illite-smectite phases. The most striking difference is seen for continuous corn and corn-oats-hay rotations. Little change in clay mineralogy is seen in the rotation plot while a significant loss of illitic material from different phases was noted for the continuous-corn cultivation plots. Use of NPK fertilizer since 1955 appears to restore the clay mineralogy in continuous-corn cropping compared to that of the 1913 samples. From these data it appears that the I-S minerals play the role of a K buffer, becoming K-poor when the soil cannot furnish enough K from mineral reserves of detrital phases and K-rich when the soil is able to release enough K to enter into the I-S minerals, where it is available during a growing season, for plant growth.

Composition of clays along the continental shelf off Israel: contribution of the Nile versus local sources

The eastern Mediterranean sedimentary regime is dominated by sediment transport from the Nile River and its delta, but recent studies have also suggested a certain contribution of clay fraction from streams to the continental shelf and slope off Israel. In the present study we focused on clay fraction deposition along the inner (∼40–1000 m water depth) shelf of Israel in order to substantiate and quantify its different sources. For this purpose detailed XRD mineralogical determinations as well as chemical compositions of the clay (<2 μm) fraction of marine and continental sediments were used. The clay mineral composition of Israeli stream sediments is variable, with no distinct spatial or temporal trend, but within a limited assemblage. This clay assemblage is made up of illite–smectite (IS) phases (70–90%), kaolinite (5–25%) and illite (<10%) and is similar to that of the Nile. However, it is clearly distinguished by the type of the IS phases, which are derived mainly from Mesozoic outcrops and recent sediments/soils and are less expandable than those of the Nile, which are derived mainly from weathered basalt. The Nile-derived component is depleted in the marine clay fraction along the Israel coast, evidenced by a decrease of IS expandability and the Fe2O3/Al2O3 ratio, and an increase in the K2O/Al2O3, MgO/Al2O3 and CaO/Al2O3 ratios. The depletion is well pronounced north of Tel Aviv, where the largest coastal plain stream flows to the sea. A northward increase of carbonates in the clay fraction, and particularly of the bioskeletal component is indicated by the ratios of MgO and Sr to CaO. The contribution of the local streams to the shallow shelf marine clay fraction is estimated to be about 50%. A minor contribution of desert dust is identified by the relative increase in kaolinite in the marine sediments south of Tel Aviv.

Mineralogy of the &lt;2 μm fraction of three mixed-layer clays from southern and central Tunisia

AbstractThree clay minerals from southern and central Tunisia were characterized. Both XRD quantitative analysis and a chemical method were used to determine the mineralogical and physico-chemical characteristics of the &lt;2 μm clay fractions. The XRD, CEC and specific surface measurement analyses showed that the dominant phase in all samples is illite-smectite with kaolinite and traces of quartz also present. From quantitative XRD, the abundances of the minerals identified are consistent with the measured CEC, specific surface area and TG/DTA properties. Analysis by XRD also showed that the illite-smectite phases are composed of thin stacks (two to a maximum of ten layers per stack) of random illite-smectite and ordered (R1) illite-smectite. There is also some discrete illite.

Clay minerals as records of temperature conditions and duration of thermal anomalies in the Paris Basin, France: a reply to the discussion by Spötl et al.

AbstractSpötl et al. (1996) have re-examined studies published by us on clay materials of sandstones in the Paris Basin. They refute the XRD characterization, K-Ar dating and formation temperature of one of the interstratified illite-smectite phases identified and have provided an alternative explanation of the published results. However, the authors ignored some basic data provided in the publications under discussion, and they have not been able to explain readily why some of the data were discarded. Furthermore, part of their disagreement is unsubstantiated. We maintain that, on the basis of coherency and consistency of all the data obtained, as well as on independent published results, the most satisfactory interpretation for the thermal evolution of the Paris Basin is the one that we suggested in our publications.