Lime Stabilization of Tropical Soil for Resilient Pavements: Mechanical, Microscopic, and Mineralogical Characteristics.

Lime stabilization is a sustainable technique due to its use of local materials, increased durability, reduced maintenance, and improved resistance to water action. This paper examines the impact of lime stabilization on the mechanical, microscopic, and mineralogical properties of a tropical soil. Two types of lime, calcitic and dolomitic, were tested at 3% and 5% by weight. Compressive, indirect tensile and flexural test results and statistical analysis revealed that calcitic lime mixtures had higher strength and stiffness, whereas dolomitic lime mixtures exhibited greater deformability with higher tensile strain at break. Scanning electron microscopy indicated that the soil's porous matrix closed within 7 days for both lime types due to flocculation, with increased matrix interlocking over time. The calcitic lime mixture developed a more closed matrix compared to the dolomitic lime, which showed weaker cementing. X-ray diffraction analysis indicated higher consumption of clay minerals and a notable reduction in calcium hydroxide peaks in the lime-treated soils. The study concludes that calcitic lime provides better pavement performance for stabilizing the soil, enhancing its engineering properties while also being sustainable by reducing the need for raw material extraction and improving resilience to climate-related issues such as floods.

Soil organic carbon sequestration potential explained by mineralogical and microbiological activity using spectral transfer functions.

The ability of soil to sequester carbon and reduce atmospheric CO2 concentrations is limited and depends on the soil minerals and their interaction with the microbiota. Microbial activities are closely associated with the types and amounts of soil organic matter (SOM) and clay minerals that have functional groups that interact with energy in Vis NIR-SWIR and Mid-IR wavelengths. The main objective of this research was to determine, based on these spectral ranges, the relation between mineralogical and organic compounds, as their sequestration and specialization in soils from Brazil. It was possible to map microbiological activity by spectral transfer functions and digital soil mapping reaching R2 from 0.77 to 0.85. Multiple regression equations were constructed to quantify enzymatic activity, microbial biomass carbon (MBC), particulate organic matter (POM), and resistant forms of carbon, and SOM associated with the mineral fraction (MAOM). All these properties were detected by specific bands obtained with the recursive feature elimination (RFE) algorithm, reaching correlations from 0.64 to 0.98 in specific ranges. The prediction model of the carbon sequestration potential was adjusted with microbiological and mineralogical variables from Vis-NIR-SWIR and the Mid-IR spectral range. A SARAR double autoregressive model was adjusted with r 0.61 and to a spatial error model (SEM) with r 0.7. The explanatory variables were associated with kaolinite, hematite, goethite, gibbsite, and the abundance of fungi, actinomycetes, vesico-arbuscular mycorrhizal fungi, enzymatic activity of beta-glucosidase, urease and phosphatase, and POM. Among the microbiological variables, the general abundance of fungi was the most important, in contrast to enzymatic activity that was the least important. The interaction between the different maps constructed and historical land use allowed the identification of areas that contribute to sequestering new carbon and could be the key to climate change mitigation strategies.

Characterization and detailed mapping of C by spectral sensor for soils of the Western Plateau of São Paulo.

Soil mineralogy and texture are directly related to soil carbon due to the physical properties of the clay surface. Traditional techniques for quantifying carbon in soil are time-consuming and expensive, making large-scale quantification for mapping unfeasible. The alternative is the use of soil sensors, such as diffuse reflectance spectroscopy (DRS), an economical, fast, and accurate technique for predicting carbon stocks. In this sense, this study aimed to (a) investigate the relationship of C with different soil mineralogical, chemical, and physical attributes for different geological and geomorphological compartments; (b) understand which spectral bands are most important for estimating C content; (c) estimate C content from diffuse reflectance spectroscopy using different mathematical techniques and indicate which one is the best for tropical soil conditions; and (d) map C contents in detail. The study area was the Western Plateau of São Paulo (WPSP), which covers approximately 13 million hectares (~ 48% of the State of São Paulo, Brazil). A total of 265 samples were collected in this area. The attributes clay, silt, sand, crystalline and non-crystalline iron, base saturation, soil density, total pore volume, total C, C stock, kaolinite/(kaolinite + gibbsite) and hematite/(hematite + goethite), hematite and goethite contents, and spectral curves were evaluated. The spectra were recorded at 0.5-nm intervals, with an integration time of 2.43 nm s-1 over the 350 to 2500-nm range (350-800 nm-visible-VIS and 801-2500 nm-near-infrared-NIR). The data were subjected to descriptive statistics, Spearman correlation, stepwise analysis, and cluster grouping for characterization purposes; partial least squares regression (PLSR) and random forest (RF) for estimation purposes; and geostatistics analysis for creation of spatial maps. Our results indicate that the highest C contents are associated with more clayey soils, oxidic mineralogy, higher total pore volume, and lower soil density in highly dissected basalt compartments. The random forest algorithm associated with the Vis-NIR spectral range is more efficient for estimating and mapping C contents. This suggests that integrating diffuse reflectance spectroscopy with machine learning techniques holds promise for shaping public policies related to land use, mitigating CO2 emissions, and facilitating the implementation of carbon credit policies in a rapid and economically efficient manner.

Magnetic signature and X-ray fluorescence for mapping trace elements in soils originating from basalt and sandstone.

The knowledge of the lithological context is necessary to interpret trace elements concentrations in the soil. Soil magnetic signature (χ) and soil X-ray fluorescence (XRF) are promising approaches in the study of the spatial variability of trace elements and the environmental monitoring of soil quality. This research aimed to assess the efficiency of measurements of χ and XRF sensors for spatial characterization of zinc (Zn), manganese (Mn), and copper (Cu) contents in soils of a sandstone-basalt transitional environment, using machine learning modeling. The studied area consisted of the Western Plateau of São Paulo (WPSP), with soils originating from sandstone and basalt. A total of 253 soil samples were collected at a depth of 0.0-0.2 m. The soils were characterized by particle size and chemical analysis: organic matter (OM), cation exchange capacity (CEC), ammonium oxalate-extracted iron (Feo), sodium dithionite-citrate-bicarbonate-extracted iron (Fed), and sulfuric acid-extracted iron (Fet). Hematite (Hm), goethite (Gt), kaolinite (Kt), and gibbsite (Gb) contents were obtained by X-ray diffraction (XRD). Magnetite (Mt) and maghemite (Mh) contents were obtained by soil χ, while trace elements contents were obtained by XRF and predicted by χ. Descriptive analysis, the test of means, and correlation were performed between attributes. Zn, Mn, and Cu contents were predicted using the machine learning algorithm random forest, and the spatial variability was obtained using the ordinary kriging interpolation technique. Landscape dissections influenced iron oxides, which had the highest contents in slightly dissected environments. Trace elements contents were not influenced by landscape dissections, demonstrating that lithological knowledge is necessary to characterize trace elements in soils. The prediction models developed through the machine learning algorithm random forest showed that χ can be used to characterize trace elements. The similar spatial pattern of trace elements obtained by XRF and χ measurements confirm the applicability of these sensors for mapping it under lithological and landscape transition, aiming for sustainable strategic planning of land use and occupation.

Rice husk ash-carbide lime as an alternative binder for waste foundry sand stabilization.

Rice husk ash (RHA) is an excellent pozzolana and associated with hydrated lime (HL), it becomes an alternative binder to Portland cement in soil stabilization. In the context of waste valorization, waste foundry sand (WFS) and carbide lime (CL) have been investigated in civil construction and environmental geotechnical applications. However, stabilizing WFS with alternative binders to Portland cement represents a large field of research to be explored. This study evaluated the stabilization of WFS with a binder based on RHA and CL, compared to the use of RHA-HL. An experimental design was carried out to evaluate the influence of different dry-specific weights (12.00, 12.75, and 13.50 kN/m3), RHA contents (10%, 20%, and 30%), and curing times (28, 60, and 90 days) under unconfined compressive strength (UCS). UCS results were submitted to statistical analysis and correlated to the porosity/binder content index (η/Biv). Healing capacity, mineralogy, microstructure, and leaching of metals from mixtures of interest were evaluated. The results showed that higher specific weights and higher percentages of RHA promoted better strength. The η/Biv0.28 index proved to be an adequate parameter to assess the UCS of WFS-RHA mixtures with different limes (CL and HL), lower porosity, and higher binder content leading to higher strengths. The mixture's mineralogy and microscopy showed the formation of cementing gels, corroborating the strength gains. WFS stabilized with both binders (RHA-CL and RHA-HL) presented satisfactory environmental performance, allowing the immobilization of metals in the waste compositions.

Soil mineralogy-controlled phosphorus availability in soils mixed with phosphate fertiliser and biochar.

The biochar amendment to soil proved to be beneficial to improve soil quality and provide nutrients. However, the effect of biochar on the availability of P is still controversial. We aim to study the effect of adding phosphate fertiliser and biochar on the P bioavailability in soils of different mineralogies. Eight biochars derived from biomass (rice husk and coffee husk), soil (sandy and clayey), and phosphate fertiliser (triple superphosphate) were produced. The biochar enrichment process with superphosphate was carried out before and after pyrolysis. Thus, we tested two biochar groups: (1) enriched biochars prior to pyrolysis; (2) enriched biochars after pyrolysis. These biochars were tested as P sources in soils of three mineralogies (kaolinite/oxide, kaolinite, and smectite). Batch sorption-desorption experiments were conducted. The sorbed P was fractionated to examine the factors controlling the retention of applied P. In the three soil mineralogies the use of enriched biochars prior to pyrolysis results in lower availability of P. In contrast, the enriched biochars after pyrolysis increase the bioavailability of P. The coffee husk biochar is more suitable than rice husk biochar to protect P from soil retention reactions. The use of sandy soil rather than clayey soil in enriched biochars compositions results in higher P content availability when applied to soils. The factor that controls the retention of P is the reaction between P, organic compounds, and Fe and Al compounds. The greater the relationship between biochar and soluble P in the fertiliser, the higher the increase of P retention.

Methodology for quantitative rock characterisation using multiple imaging systems and random particles generation.

The characterisation technologies have advanced rapidly in the last decade. From a qualitative observation of minerals with optical microscopy, more quantitative techniques have emerged. Examples are the SEM-based technologies that focus on mineralogical identification at the microscale and the X-ray microtomography systems that allow identifying rock features in three dimensions. Features such as rock texture and mineralogy have a degree of control on how the rock behaves in the processing plant and thus can affect the project's economic feasibility. None of the available measurement devices is currently capable of identifying all the aspects of rock characteristics that are of interest in linking mineralogy and texture to process response in a single measurement. However, through the integrated use of the techniques in a complementary approach is possible to generate the required suite of information about the mineralogical composition and mineral grain size and shape in a given sample. A multisource method for rock characterisation has been developed in this work. This method includes: • A multistage imaging process that uses 2D and 3D microscopes • An object-segmentation technique to separate mineral grains in the photomicrographs for the quantification of mineralogical and textural properties. • A segmentation technique was developed to create particles of different sizes from a larger image.

Analysis of the solubility of phosphate rock from Aipe (Colombia) via formation of 2Na-EDTA complex.

Phosphate rock (PR) is the main source of phosphorous used in fertilizers for Colombian soils. In many regions of Colombia, PR is applied directly to the soil, which affects eutrophication problems and phosphorus losses due to runoff, because to the low solubility of phosphorus in this georesource. In this article, phosphate rock samples from Colombia were treated with ethylenediamine tetra-acetic acid disodium salt dihydrate (2Na-EDTA) at different concentrations. PR obtained from the Media Luna Mine, located in Aipe, Huila (Colombia), was characterized using Infrared Spectroscopy, X-ray Diffraction and Scanning Electron Microscopy. Carbonate fluorapatite Ca9.74(PO4)5.45F2.05(CO3)0.53 (0.5%-61.5 %), hydroxyapatite - Ca5(PO4)3OH (26.6 %-84.0 %) and quartz- SiO2 (13.2 %) were the minerals found in the largest composition in the two samples of PR. The PR was crushed to powder (~125 µm) and it was treated with disodium EDTA dihydrate solutions at different concentrations [0.0025-0.1000 M]. Water-soluble phosphate was determined by UV-Vis spectrophotometry based on the ASTM -4500P method. The modified absolute solubility index (ASI*) was calculated for each EDTA treatment used in the phosphate rock, considering the total phosphorus solubilized in H2SO4 (40 % v/v) at 30 °C. The statistical analysis showed that there were significant differences between the treatments used, where (16.87 %) was presented highest ASI* for the treatment with 2Na-EDTA (0.353 M).

The "Table of mineral classification" by Oscar Nerval de Gouvêa: mineralogy and medicine in Brazil / A "Tabela de classificação mineral", de Oscar Nerval de Gouvêa: mineralogia e medicina no Brasil

Abstract Oscar Nerval de Gouvêa was a scientist and teacher in Rio de Janeiro, Brazil, whose work spanned engineering, medicine, the social sciences, and law. This paper presents and discusses a manuscript entitled "Table of mineral classification," which he appended to his dissertation Da receptividade mórbida , presented to the Faculty of Medicine in 1889. The foundations and features of the table provide a focus for understanding nineteenth-century mineralogy and its connections in Brazil at that time through this scientist. This text was Gouvêa's contribution to the various mineral classification systems which have emerged from different parts of the world.

Resumo Oscar Nerval de Gouvêa foi um cientista e professor no Rio de Janeiro, Brasil, cuja obra abrange engenharia, medicina, ciências sociais e direito. Este artigo apresenta e discute o texto intitulado "Tabela de classificação mineral", que ele anexou a sua tese Da receptividade mórbida, apresentada na Escola Superior de Medicina, em 1889. Os fundamentos e características da tabela propiciam a compreensão da mineralogia do século XIX e suas conexões no Brasil à época por intermédio desse cientista. O texto foi a contribuição de Gouvêa aos diversos sistemas de classificação de minerais originados de diferentes partes do mundo.

Long-term eutrophication and contamination of the central area of Sepetiba Bay (SW Brazil).

This work sheds light on the recent evolution (≈1915-2015 AD) of Sepetiba Bay (SB; SE Brazil), a subtropical coastal lagoon on the southwestern Brazilian coast, based on a multiproxy approach. Variations in geochemical proxies as well as textural, mineralogical and geochronological data allow us to reconstruct temporally constrained changes in the depositional environments along the SP3 sediment core collected from the central area of SB. At the beginning of the twentieth century, the substrate of the study site was composed of coarse-grained sediments, largely sourced from felsic rocks of proximal areas and deposited under moderate to strong shallow marine hydrodynamics. Since the 1930s, the study area has undergone silting and received high contributions of materials from mafic rocks sourced by river basins. The SP3 core reveals a shallowing-upward sequence due to human-induced silting with significant eutrophication since the middle of 1970, which was caused by significant enrichment of organic matter that was provided by not only marine productivity but also continental and human waste. In addition, the sediments deposited after 1980 exhibit significant enrichment and are moderately to strongly polluted by Cd and Zn. Metals were dispersed by hydrodynamics from the source areas, but diagenetic processes promoted their retention in the sediments. The potential ecological risk index (PERI) indicates that the level of high (considerable) ecological risk is in sediments deposited in ≈1995 (30-32 cm; subsurface). The applied methodology allowed us to understand the thickness of the bottom sediment affected by eutrophication processes and contaminants. Identical methodologies can be applied in other coastal zones, and can provide useful information to decision makers and stakeholders that manage those areas.

Respiratory bioaccessibility and solid phase partitioning of potentially harmful elements in urban environmental matrices.

Studies regarding the role of geochemical processes in urban environmental matrices (UEM) and their influence on respiratory bioaccessibility in humans are scarce in humid tropical regions, especially in Brazil. Contaminated UEM are potentially hazardous to humans if particles <10 µm in diameter are inhaled and reach the tracheobronchial region. In this study, we evaluated samples collected in Brazilian UEMs with a large environmental liability left by former mining industries and in a city with strong industrial expansion. UEM samples were classified into soil, sediment and mine tailings according to the characteristics of the collection sites. The respiratory bioaccessibility of potentially harmful elements (PHE) was evaluated using artificial lysosomal fluid (ALF, pH 4.5), and the BCR-sequential extraction was performed to evaluate how the respiratory bioaccessibility of the PHE was related to the solid phase partitioning. The bioaccessible fraction (BAF) ranged from 54 to 98% for Cd; 21-89% for Cu; 46-140% for Pb, 35-88% for Mn and; 41-84% for Zn. The average BAF of the elements decreased in the following order: Soil: Cd > Pb > Mn > Zn > Cu; Tailing: Pb > Cd > Zn > Mn > Cu; and Sediments: Pb > Mn > Cd > Zn > Cu. BCR-fractions were useful to predict the PHE bioaccessibility (R2 = 0.79-0.98), thus suggesting that particle geochemistry and mineralogy can influence PHE behaviour in the pulmonary fluid. Therefore, this approach provides a combination of quantitative and qualitative data, which allows us to carry out a more realistic assessment of the current situation of the potentially contaminated site and possible alternatives for decision making by the stakeholders.

Adsorption and desorption of arsenic and its immobilization in soils

Arsenic (As) is a naturally occurring chemical element considered toxic and carcinogenic by health and environmental protection agencies. Studies of As adsorption/desorption behavior in soils are important to predictions of As’ potential mobility in natural systems. The aim of this study was to assess the adsorption of As(V) in soils from Minas Gerais, Brazil, and determine its immobilization rate in order to identify soils with characteristics more favorable to its deployment as an As geochemical barrier. The adsorption experiment was performed using different As concentrations and the data pertaining to the maximum adsorption capacity of As(V) (MACAs) were determined by Langmuir and Freundlich isoterms. The Oxisols, due to their more oxidic mineralogy, especially more gibbsitic, and clayey texture, showed the highest MACAs, followed by Ultisols, Inceptisols, and Entisols. In terms of the desorption of As the Inceptisols were the soils that showed the most As desorption. Both As desorption and mobility was lower in the more oxidic and clayey soils. In all soils, the total amount of As was desorbed in due course, but the As release ratio tended to decrease with the passage of time. In general, soils with higher MACAs did not necessarily show less As desorption. For use as a geochemical barrier, as important as a high adsorption capacity of As by the soil is a low As desorption rate. The increase in As mobility may increase the risks of contaminating the supplies of water. To be a good As geochemical barrier the soil has to be a clayey Oxisol, with relatively high amounts of Fe and Al oxides, especially gibbsite.

Adsorption and desorption of arsenic and its immobilization in soils

Arsenic (As) is a naturally occurring chemical element considered toxic and carcinogenic by health and environmental protection agencies. Studies of As adsorption/desorption behavior in soils are important to predictions of As potential mobility in natural systems. The aim of this study was to assess the adsorption of As(V) in soils from Minas Gerais, Brazil, and determine its immobilization rate in order to identify soils with characteristics more favorable to its deployment as an As geochemical barrier. The adsorption experiment was performed using different As concentrations and the data pertaining to the maximum adsorption capacity of As(V) (MACAs) were determined by Langmuir and Freundlich isoterms. The Oxisols, due to their more oxidic mineralogy, especially more gibbsitic, and clayey texture, showed the highest MACAs, followed by Ultisols, Inceptisols, and Entisols. In terms of the desorption of As the Inceptisols were the soils that showed the most As desorption. Both As desorption and mobility was lower in the more oxidic and clayey soils. In all soils, the total amount of As was desorbed in due course, but the As release ratio tended to decrease with the passage of time. In general, soils with higher MACAs did not necessarily show less As desorption. For use as a geochemical barrier, as important as a high adsorption capacity of As by the soil is a low As desorption rate. The increase in As mobility may increase the risks of contaminating the supplies of water. To be a good As geochemical barrier the soil has to be a clayey Oxisol, with relatively high amounts of Fe and Al oxides, especially gibbsite.(AU)

Effects of acidic attack on chemical, mineralogical, and morphological properties of geomaterials.

Exposure of geomaterials to acidic leachates may compromise their structure and functionality due to changes in physicochemical, mineralogical, and hydraulic behavior. The literature identifies the need to evaluate changes in a pure state and in conditions of extreme acidity. This study aimed to evaluate changes in the chemical, mineralogical, and morphological properties of Osorio fine uniform sand (OFS), basalt residual soil (BRS), kaolin (KAO), and bentonite (BEN) exposed to sulfuric acid in concentrations of 0.00 mol/L (distilled water), 0.01 mol/L, and 1.00 mol/L. The tested samples were characterized using X-ray fluorescence spectrometry, X-ray diffraction, thermogravimetry, differential scanning calorimetry, and scanning electron microscopy. The acid attack on geomaterials by contact with the solution 1.00 mol/L has resulted in the solubilization of some constituent minerals, as well as the formation of sulfate minerals, changes in the water dehydration peak in the pores, and mass loss. The morphology of the sand and bentonite particles did not change with exposure to sulfuric acid. The acidic attack resulted in changes in the morphology of the particles for BRS and KAO. The results of this study are important for determining operational parameters of waste containment systems and contaminated areas, as well as for applying geomaterials as founding materials.

Modeling boron adsorption on five soils before and after removal of organic matter

Boron- B concentrations that cause deficiency and those that cause toxicity appear to be very similar, compared to other nutrients, which can complicate successful management of this element in soils. In this study, B adsorption onto two Oxisols from Brazil (Rhodic Eutroperox and Anionic Acroperox), two Alfisols (Natric Palexeralf and Aridic Paleustalf) and an Entisol (Xeric Torrifluvent) from the United States of America were evaluated. The samples were treated with sodium hypochlorite in order to remove soil organic matter. Both treated and untreated samples were used to determine B adsorption isotherms using different B concentrations (0-4.630 mmol L–1) and NaNO3 (0.05 M) as background electrolyte solution at pH 7. Boron adsorption envelopes were also measured using 0.463 mmol L–1 B at three ionic strengths (0.05, 0.1 and 1M) and NaNO3 as background electrolyte solutions at different pH values (3-12). The cation exchange capacity, specific surface area, free Al and Fe oxides, organic and inorganic carbon content, mineralogy and particle size distribution of the soils were also determined. The Langmuir isotherm and the constant capacitance model were fit to the B adsorption data and the parameters obtained were related to the chemical attributes by multiple linear regression equations. Boron maximum adsorption capacity (BMAC) and the complexation constant for the SH3BO4– inner-sphere complex (LogKB–) could be predicted under all experimental conditions. The Alc content was the main soil chemical attribute associated with the BMAC under the conditions evaluated and the LogKB–(int) in untreated and treated samples.

Modeling boron adsorption on five soils before and after removal of organic matter

Boron- B concentrations that cause deficiency and those that cause toxicity appear to be very similar, compared to other nutrients, which can complicate successful management of this element in soils. In this study, B adsorption onto two Oxisols from Brazil (Rhodic Eutroperox and Anionic Acroperox), two Alfisols (Natric Palexeralf and Aridic Paleustalf) and an Entisol (Xeric Torrifluvent) from the United States of America were evaluated. The samples were treated with sodium hypochlorite in order to remove soil organic matter. Both treated and untreated samples were used to determine B adsorption isotherms using different B concentrations (0-4.630 mmol L–1) and NaNO3 (0.05 M) as background electrolyte solution at pH 7. Boron adsorption envelopes were also measured using 0.463 mmol L–1 B at three ionic strengths (0.05, 0.1 and 1M) and NaNO3 as background electrolyte solutions at different pH values (3-12). The cation exchange capacity, specific surface area, free Al and Fe oxides, organic and inorganic carbon content, mineralogy and particle size distribution of the soils were also determined. The Langmuir isotherm and the constant capacitance model were fit to the B adsorption data and the parameters obtained were related to the chemical attributes by multiple linear regression equations. Boron maximum adsorption capacity (BMAC) and the complexation constant for the SH3BO4inner-sphere complex (LogKB–) could be predicted under all experimental conditions. The Alc content was the main soil chemical attribute associated with the BMAC under the conditions evaluated and the LogKB–(int) in untreated and treated samples.(AU)

Stream flow composition and sediment yield comparison between partially urbanized and undisturbed coastal watersheds-case study: St. John, US Virgin Islands.

In steep dry-tropical islands, rural and urban development can lead to accelerated soil erosion and the delivery of land-based materials into marine ecosystems. The objective of this paper was to compare stream water composition, clay minerology, and sediment yield between a partially urbanized (Coral Bay) and an undisturbed (Lameshur) coastal watersheds in St. John, US Virgin Islands (USVI). The saturation index of streamflow water samples was calculated using "The Geochemist's Workbench" software and most likely precipitated minerals from observed storm events was then compared with X-ray diffraction on soil clay mineralogy. The spatial distribution on both annual mean (2010) erosion rates and storm event-wise (Hurricane Otto) sediment yield among the two study watersheds were modeled using the revised and modified universal soil loss equations (RUSLE; MUSLE), respectively. Cations concentration in stream flow water samples and sediment yield were higher for the partially urbanized (Coral Bay) compared to the undisturbed (Lameshur) watershed. Our findings suggest that rural/urban development may increase stream water cations concentration and inputs of sediment to downstream ecosystems. Future studies evaluating the effect of management practices such as pavement or other stabilization of dirt roads and their impact on stream water quality and quantity and sediment yield are crucial for the proper sediment management in the study watersheds and potentially in other rural-urbanizing tropical watersheds.

Gastric/lung bioaccessibility and identification of arsenic-bearing phases and sources of fine surface dust in a gold mining district.

Bioaccessibility (BAC) of fine surface dust (FSD, particle size ≤10 µm) and surface dust samples (particle size ≤250 µm) collected from a gold mining district was used as a tool to determine the portion of arsenic that would be available via simulated lung and gastrointestinal (G.I) fluids. BAC was considered low for both tests (lung 2.7 ±â€¯1%, n = 5 and G.I 3.4 ±â€¯2%, n = 14 for residential surface dust samples). An analytical procedure was developed to further identify arsenic-bearing phases found in FSD samples and analyze the main components that regulate arsenic solubility. Up to five different arsenic-bearing phases were identified among a total of 35 minerals surveyed by scanning electron microscopy-based automated image analysis (Mineral Liberation Analyzer - MLA). Arsenic-bearing Fe oxy-hydroxides and mixed phases comprised the main arsenic phases encountered in FSD samples, thus likely being responsible for regulating arsenic bioaccessibility. Transmission electron microscopy showed that the mixed phases comprised a mix of oriented nanostructure aggregates formed by hematite and goethite entangled with phyllosilicates. The main As-bearing phases identified in FSD samples are similar to those reported in soil samples in the same region. The predominant arsenic-bearing phase encountered in the ore was arsenopyrite, mostly in large particles (>10 µm in size), and therefore unlikely to be found in residential dust. Arsenic intake from both inhalation and ingestion were minimal when compared to total arsenic intake (considering food and water ingestion), which itself was <7% of the value established by the Food and Agriculture Organization of the United Nations Benchmark Dose Lower Confidence Limit (BMDL0.5) of 3.0 µg per kg-1 body weight per day. These results indicated that the relative risks associated with arsenic exposure by inhalation and oral ingestion in this region are low.

Chemical, physical and mineralogical attributes of the soils of the Sertanejo pediplain in the sisal-growing areas of the semiarid Bahia / Atributos químicos, físicos e mineralógicos de solos do Pediplano Sertanejo cultivado com sisal no semiárido baiano

Information and available knowledge of the soils of the Sertanejo pediplain are relatively scarce and restricted to survey data. Researches about soil characterization and classification contributes to the knowledge of different soil orders within a region and allows information to be obtained systemically based on the physical, chemical, and mineralogical properties of the soil. This study aimed to evaluate the genesis of the Sertanejo pediplain soils, through the characterization of the chemical and mineralogical properties and classification of the soils of the sisal-growing region. Five soil profiles located in Araci, Retirolândia, St. Dominic, and Valente, cities located in the sisal-growing areas of the Bahia semiarid region, were studied, described morphologically, and analyzed for chemical (pH H2O and KCl, Ca2+, Mg2+, K+, Na+, Al3+, H+ + Al3+, P, and TOC) and mineralogical attributes. Most evaluated soil classes were formed by lithological discontinuity of material. The main processes involved in the formation of such soil classes were: cumulization, accretion, and lessivage. The mineralogy of the clay fraction observed was complex and included a variety of minerals, with a predominance of kaolinite and bayerite. In addition, we also found goethite and illite in most of the studied profiles, both in the sediment, horizons P1 C2, and in the crystalline horizon P1 Cr, P2 Bi, P3 2Cr, and P5 Bi. The soils were classified up to the fourth category level, as Entisol Eutrophic Inceptisol (RRE), Alfisols Haplic typical Eutrophic (SXE), and Inceptisols Ta Eutrophic vertissólico (CXve).(AU)

As informações e o conhecimento disponível sobre os solos presentes no Pediplano Sertanejo são relativamente escassas, restringindo-se a informações produzidas pelos levantamentos em nível exploratório ou de reconhecimento. Pesquisas pedológicas sobre caracterização, mineralogia e classificação de solos, contribuem para o conhecimento das diversas ordens de solo de uma região e permitem sistematizar informações sobre os atributos físicos, químicos e mineralógicos dos solos. Este estudo objetivou determinar as propriedades químicas e mineralógicas, bem como a classificação de solos do Pediplano Sertanejo, representativos da região sisaleira. Cinco perfis de solos localizados nos municípios de em Araci, Retirolândia, São Domingos e Valente pertencentes à região sisaleira, semiárido baiano, foram abertos, descritos morfologicamente e analisados nos seus atributos químicos (pH em água e KCl, Ca2+, Mg2+, K+, Na+, Al3+, H+ +Al3+, P e C) e mineralógicos. A maioria das classes de solos avaliadas são formadas por descontinuidade litológica. Os principais processos envolvidos na formação das classes de solos foram: cumulização, agradação e lessivagem. A mineralogia da fração argila observada é complexa e composta de uma variedade de minerais, com predomínio da caulinita e bayerita. Além destes, também foram encontrados goethita e ilita na maioria dos perfis estudados, tanto no sedimento, nos horizontes P1 C2, como no cristalino, horizontes P1 Cr, P2 Bi, P3 2Cr e P5 Bi. Os solos foram classificados, até o quarto nível categórico, como: Neossolo Regolítico Eutrófico léptico (RRe); Planossolo Háplico Eutrófico típico (SXe) e Cambissolo Háplico Ta Eutrófico vertissólico (CXve).(AU)

The role of soil mineralogy on oral bioaccessibility of lead: Implications for land use and risk assessment.

Understanding the oral bioaccessibility of lead (Pb) present in soils in urbanized areas is important for the human exposure risk assessment. In particular, the role of the soil-mineralogy in the oral bioaccessibility has not been extensively studied. To investigate bioaccessibility, five types of periurban soils were collected, samples were spiked with the same amount of lead-chromates from traffic paint, and subjected to the in vitro Physiological Based Extraction Test (PBET). Ten samples of urban topsoils were collected at elementary schools playgrounds, Pb-bioaccessibility was measured, and a prediction equation for bioaccessibility was constructed. Mineralogy, and metal content were identified with a combination of X-ray powder diffraction, scanning electron microscopy, and portable X-ray fluorescence techniques. Traffic paint sample is made of 15% quartz (SiO2), 13% crocoite (PbCrO4), 55% calcite (CaCO3), and 17% kaolinite (Al2Si2O5(OH)4) and it contains high metal content (Pb, Cr, Zn, and Ca). Studied soils are characterized by variable amounts of acid-neutralizing minerals (carbonates) and low metal content. Spiked soils contained almost equal concentration of Pb, Cr, and Zn, because the contribution of these metals is from the added paint. However, obtained Pb-bioaccessibility at gastric and intestinal conditions are variable (40 to 51% gastric, 24 to 70.5% intestinal). Carbonate content shows significant correlation (p < 0.05) with Cr, Ca, calcite, crocoite, and Pb-bioaccessible at gastric conditions. Correlation of Pb-bioaccessible at intestinal conditions is significant (p < 0.05) with kaolinite. Variability of Pb-bioaccesibility in urban environments is commonly associated to differences in Pb-sources, however, our results show that the bioaccessibility of the same pollutant behaves different for each soil type. This suggests that soil mineralogy may play a role in Pb-releasing at gastrointestinal conditions. Soil information about mineralogical characteristics from this study may help to reduce exposure to lead from urban sources if data are incorporated into urban planning.