The presence of Al-bearing goethites has been unequivocally established in Venezuelan laterite sediments by means of infrared spectroscopy (IR), chemical dissolution, and X-ray powder diffraction (XRD) methods. The composition of these samples ranges from [Fe0.89Al0.11]O(OH) to [Fe0.76Al0.24]O(OH). The data of dissolution experiments using a modified dithionite (CDB) treatment suggest a parallel behavior between Fe and Al; the gradual dissolution of Al is associated with the destruction of the Al-containing goethite. The interpretation of the CDB dissolution results for SiO2/Fe2O3 is different; silica was only slightly extracted from phases other than goethite. Substitution of Fe3+ by Al3+ in these goethites was represented on the XRD patterns by a lowering of the (110) and (111) reflections corresponding to a reduction in size of the unit cell of goethite. IR spectroscopy showed the formation of such solid solutions by a shift of the 405 cm−1 absorption band, assigned to v (Fe-O) in synthetic goethite, to >460 cm−1 in the spectrum of Al-bearing natural goethite. Moreover, this spectrum shows a shift of the 3140 cm−1 absorption, due to v (OH), to higher frequencies, indicating a H-bond weakening in [FexAl(1−x)]O(OH) compared to FeO(OH).

Sixty-five bauxite samples of different ages and origins were studied by scanning electron microscopy. Only broken surfaces of the specimens were investigated. Size and form of individual crystals and of grain aggregates were studied as were different types of microtextures and space-fillers.

Grain size varies from 0.05 μm to 1 mm. Smallest is the grain size of young karstic bauxite deposits that is explained by a physicochemical retardation effect of the carbonate environment. Significant differences were found by comparing the space-filling of karstic and lateritic bauxite deposits. High-level and low-level lateritic deposits show differences as well.

A combined use of macroscopic observations, petrographie microscopy, electron microprobe, SEM, and TЕM furnishes the best clues for any genetic interpretation of bauxites. SEM studies are useful in solving technological problems of bauxite processing.

Unheated natural mixtures of manganite and secondary pyrolusite, from the same lateritic manganiferous sequence, were studied in different orientations by high-resolution transmission electron microscopy (HRTEM), electron diffraction, and energy-dispersive X-ray analysis (EDX) to determine the fine structure of these phases, their possible crystallographic relations, and the genetic processes that led to the formation of the pyrolusite. Typical palisadic texture was observed for both minerals. Characteristic cracks parallel t. (010) of the pyrolusite structure and in particular <210> microfissures in manganite were noted as signs of structural accommodation accompanying the transformation phenomenon between these two minerals. A previously unreported manganese oxide of the spinel-type (γ-Mn2O3 or Mn3O4) was also identified in the original mixture. This oxide gave pure microdomains as intergrowths with pyrolusite adjacent to manganite. This is the first report of a natural occurrence of γ-Mn2O3. The manganite-pyrolusite transformation process and an unsuspected γ-Mn2O3 (Mn3O4)-pyrolusite transition were directly illustrated in detail for the first time. Interfaces between the concerned phases were not sharp or smooth, but exhibited strong strain contrasts and interferential periodicities. Lattice images and microdiffraction patterns proved that both transformations were oriented, suggestive of topotactic relations. In addition, the principal minerals in the matrix (illite, kaolinite, and goethite) were examined for a better understanding of their role in Mn-oxyhydroxides transformations.

An end-member natroalunite of composition (K0.04Na0.96)(Al2.98Fe0.02)(SO4)2(OH)6 occurs in saprolitic clays in a laterite profile developed over Deccan Trap basalts at Matanumad in the Kutch region of Gujarath state, India. Pseudocubic natroalunite crystals, ranging from 0.5 to 1 µm in size, have replaced pseudohexagonal, 2-µm-size platelets of kaolinite. The reverse reaction (kaolinization of natroalunite) has also been observed in the laterites and bauxites immediately adjacent to the saprolite. The kaolinite crystallites that replaced natroalunite occur as a mosaic of anhedral platelets that range in size from 0.1 to 0.3 µm. The formation of natroalunite at Matanumad postdates the laterization of the basalts. It is related to the post-diagenetic formation of sulfuric acid-rich solutions by the oxidation of pyrite in the Eocene-Oligocene black shales of the Matanumad basin. The kaolinitic clays at the top of the saprolite zone have been intensely altered by the acidic solutions, leading to a high concentration of natroalunite.

Pisolites from an iron crust in western Senegal were studied by conventional and high-resolution electron microscopy to determine their internal structure and the genetic processes that led to their formation. Each pisolite consisted of a concentric structure of hematite rimmed by goethite. Two types of goethite were distinguished: (1) large (≃ 0.6 μm long and 0.06 μm wide), euhedral laths arranged in fibrous aggregates of slightly misoriented grains devoid of internal defects as shown by their two-dimensional lattice images, and (2) a matrix of smaller (≃400 Å), anhedral grains surrounded by the larger laths. Based upon the crystal habit and the presence or absence of internal alveoles, the large goethite laths probably grew at the expense of the matrix goethite. Poorly crystalline kaolinite, presumably formed from well-crystalline precursor kaolinite, and clusters of partially dissolved quartz grains were also imaged. In addition, two uncommon phases were found—maghemite in topotactic relationship with hematite and a layered, Fe-rich, mica-like mineral with a 2M superstructure. Unlike kaolinite, this latter phase was likely in equilibrium with iron oxyhydroxides. Substituted Al probably was released during goethite recrystallization, and mass transfers probably took place through the heterogeneous porosity (i.e., large voids and cracks coupled with fine pores) revealed by transmission electron microscopy.

The first stage of lateritic weathering of pyroxenes in the Niquelandia area, Brazil, leads either to Fe-rich products or to a phyllosilicate clay. In relatively unfractured parent rock the phyllosilicate clay contains Ni-rich smectites, the atomic ratio of Ni: octahedral cations ranging from 0.3 to 0.5. These smectites were studied by polarized light microscopy, X-ray powder diffraction (XRD), transmission electron microscopy, and electron microprobe, and infrared, optical absorption, Mössbauer, and extended X-ray absorption fine-structure (EXAFS) spectroscopy. The chemical composition of the smectite is constant on the optical microscope scale even to the smallest analyzed particles (3000 A in diameter and about 75 Å thick). From XRD data the mineral is principally a swelling, trioctahedral smectite; however, some kerolite-pimelite-like layers are present, and a weak 06,33 reflection indicates the presence of a small amount of a dioctahedral phase. Mössbauer results show that all Fe cations are Fe3+ in octahedral sites. The structural formula of the smectite is: (Ca0.01K0.05)(Al0.17Fe0.5Mg0.48Ni1.47Cr0.02)(Si3.92Al0.08)O10(OH)2

The results obtained from all the above methods suggest that in the smectites Ni, and, perhaps, a small amount of Mg are clustered in pimelite-like domains (or layers), whereas Fe and some Al are clustered in nontronite-like domains (or layers). Most selected-area electron diffraction patterns exhibit continuous or punctuated (hk) rings, indicating that particles contain several stacked layers. The patterns of some thin particles, however, suggest dioctahedral layers having trans-octahedral vacancies, such as in the Garfield, Washington, nontronite. Thus, the Ni-Fe-Mg-smectite, which seemingly is homogeneous, actually consists of mixed trioctahedral and dioctahedral layers or domains.

In a lateritic pallid zone ilmenite crystals alter via pseudorutile to porous leucoxene grains composed of randomly oriented aggregates of ~0.06 μm anatase crystals. This style of alteration differs from that in beach sands where parallel oriented rutile crystals develop from pseudorutile. Increased Si and Al in the altered grains is due to the crystallization from soil solution of halloysite, kaolinite and gibbsite within pores rather than to the incorporation of these elements into anatase crystals. Manganese was a significant constituent (3.2% Mn2O3) of the original ilmenite but was not retained by the leucoxene grains. The minor constituents Ni, Zn, Cu, Mg, Co and Ca were also lost, but Cr and V were retained.

The upper 15−20 m of a 200 m thick lateritic weathering profile on Precambrian itabirites of Capanema, Brazil, reveals a genetic pathway for the formation of hematitic and goethitic nodules in the ferruginous crust through a very fine grain Al-hematite and Al-goethite mixture, called here the brick-red-material (brm). This evolution develops between the soft saprolite and a 10 m thick indurated ferruginous crust. The soft saprolite retains the original structures of the itabirite and is characterized by almost complete dissolution of quartz, the development of goethite septa, and the partial dissolution of primary hematite. Near the contact with the overlying ferruginous crust, the brm is gradually filling voids as well as replacing primary hematite and goethite in the saprolite. In the upper indurated crust, the brm transforms into coarse structureless ferruginous nodules (aluminous hematites and goethites) and is the precursor of the hematito-goethitic nodules of the crusts. Crystallization of newly-formed Al-goethite and Al-hematite within the brm occurs without detectable amounts of amorphous iron oxides of ferrihydrite precursors.

In the absence of the necessary valley topography, karst depressions are sometimes used to construct conventional impoundments in order to contain tailings. Leakage is a primary concern for such impoundments. The purpose of the current study was to determine the characteristics and barrier performance of laterite mantling karst depressions, using, as an example, the Wujiwatang (WJWT) tailings impoundment, located in the Gejiu mining area, southwestern China. The geotechnical-hydrogeological properties, geochemistry, mineral compositions, and particle shapes of the laterite were investigated by geotechnical techniques, chemical analysis, X-ray diffraction (XRD), and scanning electron microscopy (SEM). The results showed that the laterite contained poorly sorted particles that covered a wide spectrum of grain sizes (<5 mm to <50 nm), and was unexpectedly categorized as silty clay or silt with a high liquid limit. The continuous gradation and small D90 value helped the laterite achieve saturated hydraulic conductivities in the range of <10–6 cm/s required for impoundment liners. The laterite beneath the tailings impoundment was finer-grained and had a lower permeability than that of the laterite on the depression walls within the same depression. Geochemically and mineralogically, the laterite was classified as true laterite and its major mineralogical constituents were gibbsite and goethite with chlorite occurring in trace amounts. The laterite was dominated by subspherolitic–spherolitic cohesionless grains (concretions) made up of Al, Fe, Ti, and Mn oxides and hydroxides. The laterite did not have plasticity indices in the clay range. Fortunately, slopewash prior to tailings containment selectively transported the finer oxide concretions to the depression floor, creating a natural low-permeability barrier for the WJWT tailings impoundment. This is undoubtedly important for the planning and design of future karst depression-type tailings impoundments around the world.

Widespread lateritized ultramafic rocks in the southern part of the Muratdağı region of Turkey constitute a significant source of Ni-Cr-bearing ore with economic potential. However, no mineralogical or geochemical characterizations of these important materials have been performed previously. The aim of the present study was to describe the mineralogy, geochemistry, and genesis of Ni-Cr-bearing smectite in garnierite and ferruginous saprolite associated with the lateritized ophiolite-related ultramafic rocks. The lateritic zones are well developed over serpentinized harzburgitic mantle peridotites. The lateritized units and related bedrocks were examined using polarized-light microscopy, X-ray diffraction, scanning and transmission electron microscopies, and chemical and isotopic methods. The garnierite-containing saprolites are enriched in smectite, Fe-(oxyhydr)oxide phases, and opal-CT. Micromorphological images revealed that flaky smectite and, locally, Fe-rich particles, alunite, gypsum, gibbsite, and sulfur crystals developed along the fractures and dissolution voids. The development of saprolite demonstrates chemical weathering. The presence of silicified and Fe-(oxyhydr)oxide phases associated with gypsum, alunite, and local native sulfur in vertical and/or subvertical fractures and fault infillings are indicative of hydrothermal processes along the extensional, tectonically related fault systems. Chemical weathering and hydrothermal processes, which probably started during the Oligocene and Miocene, led to the formation of nontronite, Fe-bearing montmorillonite, and local Fe-rich kaolinite. Nickel and Cr are concentrated significantly in the saprolite zone and are positively correlated with Fe2O3 content, which is controlled by the formation of nontronite, montmorillonite, and Fe-(oxyhydr)oxide phases. Nickel-Cr-bearing nontronite and montmorillonite precipitated from alkaline water as a result of the increasing (Fe2O3+Al2O3+Cr2O5+Ni+Co)/(MgO+SiO2) ratio under the control of both chemical weathering and hydrothermal processes. The Fe and Mg (associated with Ni and Cr) required for the formation of smectite were supplied by solutions from both chemical weathering and hydrothermal alteration of Ni-Cr-bearing olivine and pyroxene in the harzburgitic bedrock; the Al was supplied by schists, granite, and volcanic units.

In spite of many studies of laterite origins in various parts of the world, the origin of laterite in the middle to lower reaches of the Yangtze River is still a topic of debate, thus leaving doubts about the prevailing environmental and climatic conditions at the time. The purpose of this study was to provide greater understanding of this subject by examining in more detail the associated mineralogical evolution, i.e. clay mineral composition, structural characteristics of clays in various beds with different degrees of weathering along the laterite profile, and the alteration mechanisms during the pedogenic process in tropical to semitropical climate conditions. High-resolution transmission electron microscopy (HTEM), X-ray diffraction, and wavelength dispersive X-ray fluorescence spectrometry were used to characterize the samples in order to link clay mineralogy in various beds with different degrees of weathering along the laterite profile to the formation and origin of laterites in the region. The laterite profile displayed a distinct layered structure and was divided into a saprolite (B4), a light colored net-like clay bed (B3), a brown-red gravelly clay bed (B2), and a dark-brown topsoil (B1), respectively, from bottom to top. The clay mineral assemblage of beds B1 and B2 was illite, kaolinite, and chlorite, while that of beds B3 and B4 was mainly kaolinite with minor illite. The bimodal particle-size distribution of clay minerals in the laterite profile indicated that fine-grained particles could have been produced by partial dissolution and decomposition of coarse-grained ones. Examination by HRTEM revealed that fine-grained particles usually occurred as X-ray amorphous materials in the upper soil beds, but with euhedral morphology in the lower portions, suggesting that the fine-grained particles in the lower soil beds might be partially neoformed during the weathering process. Amorphous spots occurred frequently in kaolinite crystals in the upper soil beds, while the structure of kaolinite was well preserved, with a well defined lattice-fringe image. The illite crystallinity index exhibited a trend of downward decrease, while the values of the chemical index of alteration (CIA = Al2O3/(Al2O3+ CaO+ K2O+ Na2O) × 100%) of the soil profile showed a trend of downward increase. Samples of the upper soil beds, B1 and B2, had comparable SiO2/Al2O3 ratios of 5.37–6.22, while those of the lower beds, B3 and B4, had significantly smaller SiO2/Al2O3 ratios of 1.92–3.98, suggesting that the latter had a greater degree of weathering than the former, in reasonable agreement with the results of the illite crystallinity and CIA index. In addition, samples from B1 and B2 had similar TiO2/Al2O3 ratios of 0.042–0.053, while those from B3 and B4 had comparable TiO2/Al2O3 ratios of 0.021–0.033, comparable to the value 0.020 of the bedrock, and were notably smaller than the upper soil beds, indicating that materials of the upper soil beds, B1 and B2, had a different origin from the lower soil beds. The upper bed was probably derived from eolian accumulation due to intensification of the winter monsoon and aridity in central Asia and was modified by intense chemical weathering since the late Pleistocene, while the lower bed originated from an in situ weathering of the underlying argillaceous limestone.

The tropical weathering of sedimentary kaolin deposits from the plateaux surrounding Manaus (Alter do Chao formation, Amazon basin, Brazil) leads to the in situ formation of thick kaolinitic soils. The structural changes of kaolinite have been investigated quantitatively by infrared spectroscopy and electron paramagnetic resonance. Both techniques consistently show that each sample contains two types of kaolinite in various proportions. The progressive decrease in kaolinite order from the bottom to the top of the profile results from the gradual replacement of an old population of well-ordered kaolinite, typical of the underlying sedimentary kaolin, by a more recent generation of poorly ordered soil kaolinite. The vertical pattern of kaolinite replacement differs from that of the transformation of Fe oxides and oxyhydroxides previously observed in the same profile. The inherited fraction of well-ordered kaolinite ranges from 60% at a depth of 9 m to 30% in the upper levels of the soil. The persistence of sedimentary kaolinite in the upper horizons suggests that the rate of kaolinite transformation is relatively slow at the time scale of lateritic soil formation. Kaolinite inheritance unlocks the lateritic record of past weathering conditions.

Interstratified serpentine-smectite was found in the fine-grained fraction of altered metasomatic contact biotite-schists developed between serpentinite and granite-type rocks (Lower Silesia ophiolite sequence, Poland). Ni-rich serpentine-smectite is R0-interstratified lizardite (0.80)-stevensite (0.15)-vermiculite-like (0.05), with a coherent scattering domain (csd) of 5 layers (mean value). The Mg-rich variety of serpentine-smectite is R1 lizardite (0.80)-stevensite (0.20) with a csd size of 7 layers (mean value). A transmission electron microscope study revealed complex layer relationships, with zones composed of various serpentine-smectite packets having lizardite/smectite ratios of 3:1, 2:1, 1:1, 4:1 and scarce serpentine segregations. In both cases, the serpentine-smectites appear to be late products of alteration of the parent biotite-schist.

Experimental and calculated positions and intensities of reflections of the ethylene glycol-saturated, heated (250°C, thermal stage), and air-dried samples are in good agreement. Calculated X-ray diffraction patterns for interstratified glycolated and anhydrous serpentine-smectite are included in the Appendix.

Morphological characterization and quantification of gold particles by optical image analysis (OIA) and by compositional analysis of microprobes using scanning electron microscope and electron microprobe analysis techniques were carried out on gold grains from the Minvoul area (Archean greenstone belt in Gabon). Large grains of almost pure gold were found throughout a weathering profile, which consisted of saprolite, mottled clay zone, iron duricrust, pisolitic gravels and yellow latosol. In the deeper horizons, gold was dissolved as shown by corrosion features on the surface of particles with average sizes of 2.6Φ and 2.35Φ in the saprolite and mottled clay zones, respectively. The occurrence of secondary gold in the duricrust was indicated by the larger size of the nuggets (average, 1.8Φ), the high fineness (> 995 in average) and the close textural relationship between gold and neoformed iron oxyhydroxides. The uppermost horizons composed of yellow latosol and pisolitic gravels were interpreted as transported materials based on their size distribution (average 0.85Φ and 1.34Φ), sorting and shape parameters. The best morphological parameter to describe the whole weathering profile was found to be the perimeter/area ratio. The highest ratios were recorded in the saprolite (average 0.192 μm−1), and decreased towards the surface (average 0.057 μm−1). The combination of the OIA technique and the microchemical analysis of gold grains allowed us to define specific morphological and compositional characteristics of the gold particles for each horizon. Both methods proved to be of great utility to understand gold concentration, dissolution and dispersion processes in supergene environments.

The clay mineralogy and chemical composition of the white veins, red matrix and both Fe- and Mn-bearing nodules occurring in a laterite profile in Hubei, south China were investigated using X-ray diffraction, scanning electron microscopy equipped with an energy-dispersive spectrometer, and high-resolution transmission electron microscopy. The results show that the mineral components of the red matrix are mainly quartz, kaolinite, halloysite, goethite and minor illite, whereas the white net-like veins contain mostly quartz, kaolinite, halloysite, and illite. In the net-like horizon, the chemical index of alteration (CIA, the ratio of Al2O3/(Al2O3+CaO+K2O+Na2O)) and the TiO2/Al2O3 ratio are 89.8% and 0.021 for the white vein and 90.7% and 0.025 for the red matrix, respectively. Both white-vein and red-matrix components have similar TiO2/Al2O3 ratios, and are similar to the ratio 0.027 of the unaltered bedrock. The similarity in TiO2/Al2O3 values indicates that all three portions of the laterite soil share the same origin. Also, although the white-vein and red-matrix components differ in Fe2O3 abundance, the similar CIA values do imply similar degrees of alteration. The Fe-bearing and Mn-bearing nodules were produced by the local accumulation of Fe2O3 and MnO, respectively. Halloysite in the weathering profile occurs in two different morphologies, tubular and platy crystals. Tubular halloysite occurs both in the red matrix and the Fe-bearing nodule whereas platy halloysite occurs only in the white vein and Mn-bearing nodule assemblages. Crystallization of small tubular halloysite from Si and Al concretions in the red matrix is observed, indicating that the morphology of these crystals in the weathering environment is mainly controlled by Fe3+ cations, whereas platy halloysite may be derived from the hydration of kaolinite.

The Linkuo terrace, situated to the west of the Taipei Basin in NW Taiwan, has thick red soils that have been little studied. This paper aims to interpret the development of these soils through chemical and micromorphological investigations, and relate the soils to their palaeo-environments. The soil samples were air dried, crushed and passed through a 2 mm sieve, and then subjected to conventional soil chemical and physical analyses, together with clay mineralogical and morphological characterization. Pedons I and II were clay with low base saturation (BS), cation-exchange capacity (CEC), and exchangeable cations. The pH of pedons I and II ranged from 3.80 to 5.26. The low magnetic susceptibility of these soils indicates that no magnetite (Fe3O4) or maghemite (γ-Fe2O3) are present. X-ray diffraction patterns of the magnetic clay fraction showed lepidocrocite, goethite and hematite, the amounts of which may relate to water fluctuation in the soil environments. Illite, kaolinite and quartz are major clay minerals in the red soil clay fractions. The micromorphology of all horizons showed a great accumulation of Fe-oxides. The upper horizon showed darkened isotropic Fe-oxide materials, and lower horizon showed a black to reddish dense plasma with soil matrix. The groundmass of the oxic horizon is generally characterized by a homogeneous distribution of the different coarse and fine constituents. The thick (4 m depth) and homogeneous red soils of the Linkuo terrace were developed from fine sediments after the gradual subsidence of the Taipei Basin. Alarge amount of gravel was flushed from the Xindian River before the Taipei Basin subsided. The Linkuo red soils can be classified as mesic, Typic Kandiudox. From the chemical compositions of clay fractions and the red soil features, these red soils can be considered as lateritic red earths or red earths that do not reach the criteria for laterite.

Fe-rich smectites from lateritic weathering profiles have previously been studied by XRD, ICP-AES, SEM-EDX and TEM-EDX analyses (Gaudin et al., 2004). These smectites exhibit intermediate chemistries between five end-members: Al-Fe beidellites, Al-Fe montmorillonites and Mg+Ni-saponite. The spectroscopic study by FTIR and XAS of these smectites reveals that: (1) tetrahedral Fe3+ is near or below the detection limit (0.05 cation for 4Si); (2) the large chemical variability is due to substitution of the three major cations (Fe, Al, Mg) within adjacent octahedra; (3) Ni is not concentrated in another clay phase such as Ni-kerolite and is located in the octahedral sheets of smectite; (4) octahedral cations are not randomly distributed but ordered in separated Fe, Al, Mg, Ni clusters; (5) the Mg-Ni saponite end-member actually appears as small trioctahedral clusters of Mg and Ni distributed within the dioctahedral smectite.

Processes of mineral alteration involving the mobilization and deposition of more than 30 chemical elements during bauxite formation and epigenesis have been studied on specimens from the Devonian Schugorsk bauxite deposit, Timan, Russia. Chemical analyses of the minerals were obtained by electron microprobe and element distribution in the minerals was studied by element mapping. Interpretation of these data also utilized high-resolution BSE and SE images.

The main rock-forming minerals of the Vendian parent rock are calcite, dolomite, feldspar, aegirine, riebeckite, mica, chlorite and quartz; accessory minerals are pyrite, galena, apatite, ilmenite, monazite, xenotime, zircon, columbite, pyrochlore, chromite, bastnaesite and some others. Typically, the grainsize of the accessory minerals in both parent rock and bauxite is from 1 to 40 µm. However, even within these rather small grains, the processes of crystal growth and alteration during weathering can be determined from the zonal distribution of the elements. The most widespread processes observed are: (1) Decomposition of Ti-bearing minerals such as ilmenite, aegirine and riebeckite with the formation of ‘leucoxene’, which is the main concentrator of Nb, Cr, V and W. Crystal growth can be traced from the zonal distribution of Nb (up to 16 wt.%). Vein-like ‘leucoxene’ is also observed in association with organics. (2) Weathering of columbite and pyrochlore: the source of Nb in ‘leucoxene’ is now strongly weathered columbite, while the alteration of pyrochlore is expressed in the growth of plumbopyrochlore rims around Ca-rich cores. (3) Dissolution of sulphide minerals and apatite and the formation of crandallite group minerals: ‘crandallite’ crystals of up to 40 µm size show a very clear zonation. From the core to the rim of a crystal, the following sequence of elements is observed: Ca → Ba → Ce → Pb → Sr → Nd. Sulphur also shows a zoned but more complicated distribution, while the distribution of Fe is rather variable. A possible source of REE is bastnaesite from the parent rock. More than twelve crandallite type cells can be identified in a single ‘crandallite’ grain. (4) Alteration of stoichiometric zircon and xenotime with the formation of metamict solid solution of zircon and xenotime: altered zircon rims also bear large amounts of Sc (up to 3.5 wt.%), Fe, Ca and Al in the form of as yet unidentified inclusions of 1–2 µm. Monazite seems to be the least altered mineral of the profile.

In the parent rock, an unknown mineral of the composition (wt.%): ThO2 – 54.8; FeO – 14.6; Y2O5 – 2.3; CaO – 2.0; REE – 1.8; SiO2 12.2; P2O5 – 2.8; total – 94.2 (average from ten analyses) was determined. In bauxite, another mineral was found, which has the composition (wt.%): ThO2 – 24.9; FeO – 20.5; Y2O5 – 6.7; CaO 2.0; – ZrO – 17.6; SiO2 – 8.8; P2O5 – 5.4; total – 89.3 (F was not analysed; average from nine analyses). Presumably, the second mineral is the result of weathering of the first one. Although the Th content is very high, the mineral is almost free of Pb. However, intergrowths of galena and pyrite are observed around the partially decomposed crystals of the mineral. Another generation of galena is enriched in chalcophile elements such as Cu, Cd, Bi etc., and is related to epigenetic alteration of the profile, as are secondary apatite and muscovite.

Synchrotron based μ-XRF, μ-XAS and μ-XRD have made a major impact in the field of environmental science in the last ten years. One of the first seven ‘day one’ beamlines on the Diamond Light Source is a microfocus spectroscopy beamline, beamline I18. Here the current status of the beamline and the opportunities it presents in the field of environmental science are described, with results from two of the first experiments also included. The first is based on the use of bonemeal to remediate soil. We used Zn K-edge and Pb L3-edge spectroscopy to characterize the speciation of these two elements on a soil after bonemeal treatment. The results are compared with bulk measurements taken on the whole soil and standard materials. The second experiment described here is a study of the speciation and association of Ni in a laterite from Moa Bay, Cuba. Here the differences in the Ni speciation associated with Mn oxides are examined and compared with Fe oxides phases.