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The character of parent material, organic matter and climatic conditions are the crucial factors of pedogenesis. They directly influence the intensity of weathering, transformation processes, elements release and geochemical cycles. The mineral transformation in a profile of the recent soil developed on loess (Haplic Luvisols, Siltic, Epidystric, Ochric) was studied. The land area Litovelske Pomoravi was chosen because of the stability of soil‐forming factors such as topography, relief, vegetation and climate. X‐ray diffraction (XRD) quantitative analysis of the fine earth (

Downhole nuclear magnetic resonance technology was applied in four boreholes intersecting glaciomarine sediments of the Ottawa Valley, Ontario. The study evaluated the ability of slim‐hole nuclear magnetic resonance tools to measure in situ volumetric water contents (porosities in saturated sediments) for geohazard and hydrogeological applications. The sediments are composed of clay‐ and silt‐sized grains of glacially eroded rock flour derived from the Precambrian Shield containing trace amounts of magnetic minerals, and porosities ranging from 40 to 74 porosity units (PU, 1% porosity = 1 PU). Two nuclear magnetic resonance instruments were deployed with echo times of 0.5 and 1.0 ms, and diameters of investigation ranging from 14.0 to 30.5 cm. Quantitative nuclear magnetic resonance porosities in the sediments were typically within ±5 PU (95% within ±10 PU) of core calibration data sets in the silty clays where threshold bulk magnetic susceptibility values were

International audience; Widespread anoxic events affected the Tethys Ocean during the Mesozoic. The Ocean Anoxic Event 1a (Early Aptian), expressed as the Selli Level or Goguel Level (GL) in European basins. The GL was deposited in the French Vocontian Basin, a semi-enclosed basin connected to the Tethys Ocean. This study presents an integrated approach (Rock Eval, clay minerals, grain-size, inorganic geochemistry and molecular biomarkers), applied to four sections in the basin distributed along a proximal-distal transect. This study shows that the GL was perturbed by turbidites. In particular, the results demonstrate: (a) a homogeneous redox status of the basin that experienced oxic to suboxic conditions, according to trace element distributions and (b) low organic matter contents (total organic carbon ca 1 wt%) in the three sections where turbiditic deposits are observed. The distal, condensed section exhibits the highest organic matter contents (total organic carbon >3 wt%). In addition, the presence of gammacerane and isorenieratene derivatives in the distal sections suggests that the water-column was intermittently stratified, with hypoxia developing in the photic zone. This stratification did not result from strong surface productivity but more likely from: (a) limited renewal of deep water in the basin; (b) reputedly high surface-water palaeotemperatures during the Early Aptian; and (c) the influx of waters, possibly depleted in free oxygen and in some dissolved trace elements, into the basin. The turbiditic inputs, in addition to organic matter dilution in the sediments and a brief rupture of the water-column stratification in the proximal areas of the basin, ventilated the sea floor and more specifically re-oxidized the sediment-water interface as well as underlying sediments. Such episodes of benthic re-ox-ygenation could have altered the long-term palaeoredox record, even in the distal sections where reducing conditions prevailed during deposition. In the area deprived of turbiditic input, sedimentary condensation, coupled with low oxygen conditions, furthered organic matter preservation and concentration.

Use of recycled concrete aggregate (RCA) as highway basecourse material conserves virgin aggregate, reduces energy consumption and CO2 emissions, and may also decrease costs during construction. However, concerns remain over possible negative environmental impacts associated with high pH (>11) effluent from RCA in contact with water. This study examines the reactive transport of high-pH and high-alkalinity water, modeled on RCA leachate, through model subgrade soils. By developing an understanding of the reactions controlling effluent neutralization, this study aims to quantify the change in pH from the discharge site through surrounding subgrade soils. Four types of subgrade soils with a range of mineral composition, Atterberg limits, and cation exchange capacities (CECs) are examined. They include a clayey sand (SC10), low-plasticity clays (M14, SC25), and a high-plasticity clay (CH38). Batch reaction experiments are used to develop kinetic parameters describing the neutralization of high-pH and -alkalinity leachate by clay minerals through mineral dissolution and reprecipitation. Given this information, a reactive transport model incorporating advection, diffusion, and reaction is used to model the change in pH as a function of distance traveled through model subgrade soils and is applied to laboratory-scale column experiments. The rate at which the high pH front travels is directly related to a soil's clay mineral content. Soils with high CECs effectively delay the propagation of hydroxide front by the dissolution of clay minerals. This study demonstrates that common subgrade soils with moderate clay content will effectively neutralize high pH leachate initially produced by RCA.

Limestone–marl alternations are commonly used for high‐resolution cyclostratigraphic studies and palaeoenvironmental reconstructions, but diagenetic studies indicate that not all limestone–marl alternations reflect genuine differences in the initial sediment composition driven by environmental changes. Differences in the ratios of diagenetically inert trace elements between limestones and marls indicate changes affecting the terrigenous fraction of the precursor sediment. Contrarily, limestone–marl alternations without these differences can be the product of: (i) variations in CaCO3 input (aragonite, calcite); (ii) distortion of the latter by diagenetic CaCO3 redistribution; or (iii) diagenetic CaCO3 redistribution in a homogeneous precursor sediment. The aim of this study is to provide a method to differentiate these cases and to identify variations in the proportion of calcite and aragonite in the precursor sediment composition. The model of differential diagenesis assumes that the concentration of diagenetically inert elements is inversely proportional to the amount of redistributed CaCO3. Consequently, the difference between ratios of diagenetically inert elements from two adjacent beds is a measure for CaCO3 redistribution. This is quantifiable by the vector length between ratios from two adjacent beds. The approach is illustrated here by evaluation of a case study from the Silurian of Gotland, Sweden. Trace elements were compared according to their solubility during diagenesis. All elements bound to clay minerals or calcite show similar patterns of vector length, while vector length of elements which fit into the aragonite lattice, and are diagenetically mobile, differ. The vector length approach provides a tool to test the diagenetic origin of limestone–marl alternations, to identify initial variations in CaCO3 input and to test a limestone–marl alternation’s suitability for cyclostratigraphic analyses., Deutsche Forschungsgemeinschaft http://dx.doi.org/10.13039/501100001659, Research Foundation of Flanders

Palaeogene Environmental evolution in East Asia remains ambiguous. Here we present integrative work including magnetostratigraphy, grain-size, geochemistry, and clay minerals from a 1609-m-thick fl...

The presence of smectite is critical for weakening the frictional strength of natural faults. The friction coefficient of smectite changes depending on water presence, chemical composition, and pre...

Clay minerals dominate the soil colloidal fraction and its specific surface area. Differences among clay mineral types significantly influence their effects on soil hydrological and mechanical behavior. Presently, the soil clay content is used to parameterize soil hydraulic and mechanical properties (SHMP) for land surface models while disregarding the type of clay mineral. This undifferentiated use of clay leads to inconsistent parameterization, particularly between tropical and temperate soils, as shown herein. We capitalize on recent global maps of clay minerals that exhibit strong climatic and spatial segregation of active and inactive clays to consider spatially resolved clay mineral types in SHMP estimation. Clay mineral-informed pedotransfer functions and machine learning algorithms trained with datasets including different clay types and soil structure formation processes improve SHMP representation regionally with broad implications for hydrological and geomechanical Earth surface processes., Geophysical Research Letters, 48 (20), ISSN:0094-8276, ISSN:1944-8007

The activation of landslides and shallow faults is related to the shear behavior of soft interlayers during groundwater infiltration. Regarding the water sensitivity of clay minerals, the shear beh...

This paper investigates the nano to core-scale geomechanical properties of a maturity series of organic-rich, calcareous shales buried to 100-180°C, with a focus on: (a) the mechanical properties of organic matter; (b) the elastic response and anisotropy of the shale composite at micro and core scale; and (c) the creep response. Atomic force microscopy was used to target kerogen at nanoscale resolution, and it was found that the elastic stiffness increased with thermal maturity from 5.8 GPa in an immature sample to 11.3 GPa in a mature sample. Nanoindentation testing of the shale matrix showed that diagenesis is a key factor in determining the bulk elasticity, with increasingly intense carbonate cementation at higher thermal maturities contributing to a stiffer response. A multiscale model was formulated to upscale the elastic properties from nanoscale solid clay minerals to a microcracked composite at core scale, with good predictions of the micro and core-scale stiffness in comparison to indentation and triaxial results. A negative correlation was found between the creep modulus and clay/kerogen content, with greater creep displacement observed in nanoindentation tests in the immature clay- and kerogen-rich sample compared to samples of higher thermal maturity.

Sorption of myo‐inositol hexakisphosphate (IHP), a common type of organic phosphorus in soils, largely controls its mobility and bioavailability. Research on the interaction between IHP and phyllosilicate minerals such as kaolinite, which is commonly present in highly weathered soils, has often been neglected, probably due to the common assumption that negatively charged phyllosilicate minerals have low sorption capacity and binding affinity to IHP and thus do not play any significant role in its fate. Here, the interaction between IHP and poorly crystallized kaolinite (KGa‐2) was investigated in batch experiments using Zeta (ζ) potential measurement and ³¹P nuclear magnetic resonance (NMR) spectroscopy. The results showed that dissolved Al(III) concentration at the adsorption initiation stage increased with increasing IHP concentration at pH 4.0. From pH 2.5 to 9.0, IHP presented a maximum sorption capacity (50 μmol g⁻¹) at pH 4.0 at 24 hr. With IHP sorption, the ζ potential of kaolinite first decreased sharply to a negative value, then gradually increased with resorption of Al(III) released from kaolinite dissolution at acidic pH, and finally approached the original value of the pure kaolinite. ³¹P NMR spectroscopy and ζ potential analyses revealed that IHP formed inner‐sphere surface complexes and aluminium phytate precipitated on kaolinite at low pH (2.5 and 4.0), whereas the formation of inner‐sphere surface complexes was the dominant sorption mechanism at pH ≥ 5.5. This study implies that various mechanisms, depending on ambient pH condition, can dominate the IHP sorption onto kaolinite, which impacts the mobility and bioavailability of phosphorus in highly weathered soils. HIGHLIGHTS: IHP promotes the dissolution of kaolinite mainly through the formation of aluminium phytate complex. IHP sorption presents a sharp maximum at pH 4.0. IHP forms inner‐sphere complexes at the surface of kaolinite. Formation of aluminium phytate surface precipitates is favourable at relatively low pH.

Although clay is composed of disconnected anisotropic clay platelets, many rock physics models treat the clay platelets in shale as interconnected. However, the clay matrix in shales can be modelled as anisotropic clay platelets embedded within a soft isotropic interplatelet region, allowing the influence of disconnected clay platelets on the elastic properties of the clay matrix to be analysed. In this model, properties of the interplatelet region are governed by its effective bulk and shear moduli, whereas the effective properties of the clay platelets are governed by their volume fraction, aspect ratio and elastic stiffness tensor. Together, these parameters implicitly account for variations in clay and fluid properties, as well as fluid saturation. Elastic stiffnesses of clay platelets are obtained from the literature, including both experimental measurements and first‐principles calculations of the full anisotropic (monoclinic or triclinic) elastic stiffness tensors of layered silicates. These published elastic stiffness tensors are used to compile a database of equivalent transverse isotropic elastic stiffness tensors, and other physical properties, for eight common varieties of layered silicates. Clay matrix anisotropy is then investigated by examining the influence of these different elastic stiffnesses, and of varying model parameters, upon the effective transverse isotropic elastic stiffness tensor of the clay matrix. The relationship between the different clay minerals and their associated anisotropy parameters is studied, and their impact on the resulting anisotropy of the clay matrix is analysed.

Soil mineral composition affects soil behavior, but field estimation of mineral composition has proved difficult. To investigate the potential of predicting soil mineral composition in situ, 15 soils representing diverse mineral composition from New South Wales, Australia, were scanned with visible near-infrared (VisNIR) and portable X-ray fluorescence (pXRF) spectrometers to a depth of 1 m at 2.5-cm scanning increments. The presence of phyllosilicate and Fe oxides was assessed using a pattern-matching algorithm with VisNIR spectra from mineral end-member libraries. Rule-based iterative partitioning was then applied on pXRF elemental compositions based on mineral stoichiometry to determine the abundance of kaolinite, smectite, illite, hematite, goethite, calcite, gypsum, and quartz. This fusion model correctly identified the most abundant mineral in a sample with 72% accuracy. Mineral predictions were stable under variable moisture and surface conditions, as experienced when scanning samples in situ and under air-dry and ground conditions in the laboratory. Relative changes in mineral composition within a profile and across horizon boundaries were accurately expressed. The fusion model accurately quantified the abundance of quartz (Cohen’s kappa coefficient, 0.67), and CaCO₃ (Cohen’s kappa coefficient, 0.76; Lin’s concordance correlation coefficient, 0.96; RMSE, 20.9 g kg⁻¹). The dominant phyllosilicate mineral was identified correctly with 86% accuracy, although accurate quantification of phyllosilicates and Fe oxides was not achieved. Conjoint use of VisNIR and pXRF spectroscopy as part of a fusion model approach showed great potential to provide comprehensive estimation of soil mineral composition in situ.

The laser diffraction method (LDM) has been increasingly applied for quantifying soil particle size distribution (PSD), owing to its advantages of rapid analysis, high reproducibility, and continuous PSD measurement for a wide range of size fractions. However, some ambiguities exist regarding the comparability of results with those obtained using other classical methods. The objective of the current study was to evaluate LDM-derived PSDs via comparisons with PSDs obtained with the standard sieve–pipette method (SPM) and from the absolute method of microscopy. A total of 277 soil samples were collected at different soil depths in a typical cropland in the northeast mountainous region of Beijing and analyzed with both SPM and LDM. Due to time and labor constraints, scanning electron microscopy (SEM) was performed on 100 samples randomly selected for the PSDs within the clay fraction withdrawn by SPM. The results manifested on the average 18.9% underestimation of clay content and 25.3% overestimation of silt content by LDM compared to SPM. These disagreements directly caused the shifts of soil texture class in 44.8% of the soil samples. Significant linear regression equations were generated to convert LDM–derived sand and silt contents to SPM–derived ones (p < 0.01). The linear conversions for the clay content were only significant for the calibration samples, but possessed negative coefficients of determination for the validation set. According to SEM, silt-sized particles were wrongly included in the clay fraction identified by SPM. Eliminating such particles, the clay contents corrected by SEM were significantly lower when assuming the shape of clay particles < 2 µm as plates or discs with constant thickness–diameter ratio of 1/10, and higher when considering the clay particles as spheres for volume calculation, in contrast to those measured by LDM (P < 0.01). Detailed volume-based PSDs within the clay fraction were further compared between SEM and LDM, revealing dissimilar PSD patterns but statistically similar median particle diameters. These findings suggest the effectiveness of LDM in soil PSD determination. Future work is needed to systematically quantify the impact of other possible factors such as clay mineralogy and refractive index on LDM-derived PSDs.

Due to initially high soil test K values, K soil test correlation and calibration for corn in North Dakota has previously not been intensely investigated. Potassium fertilizer rate experiments were conducted on 25 sites from 2014 to 2016. The previously published soil test K critical value of 150 mg kg⁻¹ predicted crop response correctly at 16 of the sites. Alternative soil test methods, including a resin-based extraction at two timings, sodium tetraphenylboron extractions at two timings, and 1 mol L⁻¹ NH₄OAc extraction using moist soil were conducted; however, the currently used 1 mol L⁻¹ ammonium acetate extraction using dry soil was most predictive. Mineral analysis of soil from all sites was determined for potassium feldspar content of whole soil, and clay species, particularly smectite, illite, and kaolinite, were determined on the clay fraction. Cluster analysis revealed that a smectite/illite ratio of 3.5 separated the sites into two unique K response data sets. Sites with a smectite/illite ratio >3.5 had a K critical level of ∼200 mg kg⁻¹, whereas sites with a smectite/illite ratio

Many studies have shown that the adsorption of ions like K and Cs on 2:1 clay minerals can prompt the collapse of their interlayers and render the adsorbing ions nonexchangeable. This study sought to better understand this unique adsorption mechanism through the generation of an adsorption envelope for Cs adsorption on vermiculite and the exploration of the kinetics of interlayer collapse. The collapse of the vermiculite interlayer was confirmed via X-ray diffraction (XRD), and the timing of interlayer collapse was determined by placing Cs in competition with K at different time intervals. The adsorption envelope for Cs on vermiculite showed that although H competition does affect the adsorption of Cs on vermiculite, the effect of this competition is quite limited, even at very low pH values. This hypothesis is supported by the fact that XRD demonstrated a significant decrease in interlayer dimension after Cs adsorption. Finally, kinetics experiments showed that the irreversible adsorption of K and the collapse of the interlayer may take place on a much longer time scale than previously considered.

Methanogenesis and iron reduction play major roles in determining global fluxes of greenhouse gases. Despite their importance, environmental factors that influence their interactions are poorly known. Here, we present evidence that pH significantly influences the balance between each reaction in anoxic environments that contain ferric (oxyhydr)oxide minerals. In sediment bioreactors that contained goethite as a source of ferric iron, both iron reduction and methanogenesis occurred but the balance between them varied significantly with pH. Compared to bioreactors receiving acidic media (pH 6), electron donor oxidation was 85% lower for iron reduction and 61% higher for methanogenesis in bioreactors receiving alkaline media (pH 7.5). Thus, methanogenesis displaced iron reduction considerably at alkaline pH. Geochemistry data collected from U.S. aquifers demonstrate that a similar pattern also exists on a broad spatial scale in natural settings. In contrast, in bioreactors that were not augmented with goethite, clay minerals served as the source of ferric iron and the balance between each reaction did not vary significantly with pH. We therefore conclude that pH can regulate the relative contributions of microbial iron reduction and methanogenesis to carbon fluxes from terrestrial environments. We further propose that the availability of ferric (oxyhydr)oxide minerals influences the extent to which the balance between each reaction is sensitive to pH. The results of this study advance our understanding of environmental controls on microbial methane generation and provide a basis for using pH and the occurrence of ferric minerals to refine predictions of greenhouse gas fluxes.

Previous studies have shown that Mt. Sharp has stratigraphic variation in mineralogy that may record a global transition from a climate more conducive to clay mineral formation to one marked by inc...