Search Results (27)

Costa Rica is located along the narrow isthmus that connected South America to North America beginning in the mid-Cenozoic. The exchange of vertebrates between the two continents has received considerable study, but paleobotanical aspects are less known. The Pacific coast “ring of fire” volcanoes produced abundant hyaloclastic material that provided a source of silica for wood petrifaction, and the tropical forests contained diverse taxa. This combination resulted in the preservation of petrified wood at many sites in Costa Rica. Fossil wood ranges in age from Lower Miocene to Middle Pleistocene, but Miocene specimens are the most common. Our research involved the study of 54 specimens, with the goal of determining their mineral compositions and interpreting the fossilization processes. Data came from thin-section optical microscopy, SEM images, and X-ray diffraction. Two specimens were found to be mineralized with calcite, but most of the woods contained crystalline quartz and/or opal-CT. The preservation of anatomical detail is highly variable. Some specimens show evidence of decay or structural deformation that preceded mineralization, but other woods have well-preserved cell structures. This preliminary study demonstrates the abundance and botanical diversity of fossil wood in Costa Rica, hopefully opening a door into future studies that will consider the taxonomy and evolutionary aspects of the country’s fossil forests. Full article

In the northern part of the Niğde (Central Anatolian) Quaternary Bor Basin, stratigraphic sections P1 and P2 were sampled, reaching depths of 11 m and 25 m. The samples were analyzed with thin-section, XRD, and chemical analyses (ICP-MS) to determine their chemical and mineralogical properties. In the study area, partially lithified volcano-sedimentary rocks comprised paleosol, calcrete, gravel, sand, silt, mud, clay, and volcanoclastics such as pumice fall-out. Grain size analyses from the Zengen (P1) and Altunhisar (P2) regions showed very poor sorting and strong positive skewness. The Zengen-area (P1) samples contained rock fragments, calcite, quartz, opal-CT, feldspar, amphibole, pyroxene, biotite, and clay minerals such as smectite, chlorite, illite, palygorskite, and sepiolite. In calcrete zones, however, the amounts of CaO increased, whereas significant decreases in the amounts of SiO₂ were observed. Therefore, a negative correlation between SiO₂ and CaO was observed. The vertical distributions and behaviors of trace elements in the Zengen-area profile showed variation with the different levels of the P1 section. It is thought that in the Bor Plain, after 17,000 years ago, no lacustrine phase reached a level above the periglacial lake level in the region, reaching this level with the melting of the ice sheets in the area. During the late glacial period, shallow freshwater lacustrine phases and paleosols were identified from 12,500 to 11,000 yr BP in the basin. Full article

Agate veins and nodules occur in the Lece Volcanic Complex (Oligocene-Miocene) situated in the south of Serbia and occupying an area of 700 km². This volcanic complex is composed predominantly of andesites, with sporadic occurrences of andesite-basalts, dacites and latites, and features agate formations that have been very little investigated. This study focuses on five selected agate occurrences within the Lece Volcanic Complex, employing optical microscopy, scanning electron microscopy (SEM), X-ray powder diffraction analysis, inductively coupled plasma mass spectrometry (ICP-MS), and Fourier transform infrared spectroscopy (FTIR). In three localities (Rasovača, Mehane, and Ždraljevići), agate mineralization is directly related to distinct fault zones with strong local brecciation. In the other two localities (Vlasovo and Sokolov Vis), the agate is found in nodular form and does not show any connection with fracture zones. The silica phases of the Lece volcanic agates consist of cristobalite and tridymite, length-fast chalcedony, quartzine (length-slow chalcedony), and macrocrystalline quartz. Vein agates show a frequent alternation between length-fast chalcedony and quartz bands. Nodular agates consist primarily of length-fast chalcedony, occasionally containing notable quantities of opal-CT, absent in vein agates. Microtextures present in vein agates include crustiform, colloform, comb, mosaic, flamboyant, and pseudo-bladed. Jigsaw puzzle quartz microtexture supports the recrystallization of previously deposited silica in the form of opal or chalcedony from hydrothermal fluids. Growth lines in euhedral quartz (Bambauer quartz) point to agate formations in varying physicochemical conditions. These features indicate epithermal conditions during the formation of hydrothermal vein agates. Due to intense hydrothermal activity, vein agate host rocks are intensively silicified. Vein agates are also enriched with typical ore metallic elements (especially Pb, Co, As, Sb, and W), indicating genetic relation with the formation of polymetallic ore deposits of the Lece Volcanic Complex. In contrast, nodular agates have a higher content of major elements of host rocks (Al₂O₃, MgO, CaO, Na₂O, and K₂O), most probably mobilized from volcanic host rocks. Organic matter, present in both vein and nodular agate with filamentous forms found only in nodular agate, suggests formation in near-surface conditions. Full article

The migration of 32 elements from natural zeolitized tuffs from the Beli Plast and Golobradovo deposits (Bulgaria) was determined in ultrapure, tap, mineral, and coal mine waters in order to evaluate their desorption and adsorption properties. The tuffs are Ca-K-Na and contain clinoptilolite (90 and 78wt.%, respectively), plagioclase, sanidine, opal-CT, mica, quartz, montmorillonite, goethite, calcite, ankerite, apatite, and monazite. The desorption properties are best revealed during the treatment of ultrapure, tap, and mineral water, whereas the adsorption properties are best manifested in coal mine water treatment. The concentrations of Al, Si, Fe, Na, Mn, F, K, Pb, and U increase in the treated ultrapure, tap, and mineral water, while the content of K, Be, Pb, and F increase in the treated mine water. The tuffs show selective partial or complete adsorption of Na, Mg, Sr, Li, Be, Mn, Fe, Co, Ni, Cu, Zn, Al, Pb, U, and SO₄²⁻. They demonstrate the ability to neutralize acidic and alkaline pH. Sources of F are presumed to be clinoptilolite and montmorillonite. The usage of zeolitized tuffs for at-home drinking water treatment has to be performed with caution due to the migration of potentially toxic and toxic elements. Full article

Microscopic analysis of fossils from the Lightning Ridge district of northwestern New South Wales, Australia, shows that opal has been typically deposited in variable cavities left by the degradation of the original organic material. Fine-grained, clay-rich sediments have preserved the external morphology, and opalization has produced detailed casts with different modes of preservation of internal details. Plant remains include cones, cone scales, fruiting bodies, and seeds, but the most common specimens are twigs, stems, and wood fragments. These specimens commonly contain angular inclusions that represent small tissue fragments produced by the degradation of the original wood. Inclusions commonly have a “hollow box” structure where the organic material has decomposed after the initial opal filling of the mold. These spaces commonly contain traces of the cellular architecture, in the form of wood fiber textures imprinted on the cavity wall, degraded cellular material, and silicified tracheids. Opal casts of mollusk shells and crustacean bioliths preserve the shape but no calcium carbonate residue. Likewise, opal casts of vertebrate remains (bones, teeth, osteoderms) lack preservation of the original bioapatite. These compositions are evidence that burial in fine clays and silts, isolated from the effects of water and oxygen, caused protracted delays between the timing of burial, decomposition, and the development of vacuities in the claystones that became sites for opal precipitation. The length of time required for the dissolution of cellulosic/ligninitic plant remains, calcium carbonate items, and calcium phosphates in bones and teeth cannot be quantified, but evidence from opal-bearing formations worldwide reveals that these processes can be very slow. The timing of opalization can be inferred from previous studies that concluded that Cenozoic tectonism produced faults and fissures that allowed horizontal and lateral movement of silica-bearing groundwater. Comparisons of Australian opal-AG with opal from international localities suggest that opalization was a Neogene phenomenon. The transformation of Opal-AG → Opal-CT is well-documented for the diagenesis of siliceous biogenic sediments and siliceous sinter from geothermal areas. Likewise, precious and common opal from the late Miocene Virgin Valley Formation in northern Nevada, USA, shows the rapidity of the Opal-AG → Opal-CT transformation. Taken together, we consider this evidence to indicate a Neogene age for Lightning Ridge opalization and by inference for the opalization of the extensive opal deposits of the Great Artesian Basin in Australia. New paleontology discoveries include a surprising level of cellular detail in plant fossils, the preservation of individual tracheids as opal casts, evidence of opalized plant pith or vascular tissue (non-gymnosperm), and the first report of Early Cretaceous coprolites from New South Wales, Australia. Full article

For many decades, wood silicification has been viewed as a relatively simple process of permineralization that occurs when silica dissolved in groundwater precipitates to fill vacant spaces within the porous tissue. The presence of specific silica minerals is commonly ascribed to diagenetic changes. The possibility of rapid silicification is inferred from evidence from modern hot springs. Extensive examination of silicified wood from worldwide localities spanning long geologic time suggests that these generalizations are not dependable. Instead, wood silicification may occur via multiple pathways, permineralization being relatively rare. Mineralization commonly involves silica precipitation in successive episodes, where changes in the geochemical environment cause various polymorphs to coexist in a single specimen. Diagenetic changes may later change the mineral composition, but for many specimens diagenesis is not the dominant process that controls mineral distribution. Rates of silicification are primarily related to dissolved silica levels and permeability of sediment that encloses buried wood. Rapid silica deposition takes place on wood in modern hot springs, but these occurrences have dissimilar physical and chemical conditions compared to those that exist in most geologic environments. The times required for silicification are variable, and cannot be described by any generalization. Full article

The possibility of transforming a diatomite-rich waste from the brewing industry into synthetic zeolites has been investigated. After precalcination at 550 °C to eliminate the retained organic matter, the clean diatomite (Dt; with a Si/Al molar ratio of 17.4), was hydrothermally treated for 24 h with continuous stirring in a 3M NaOH solution at 80 °C. The results of mineralogical characterization by X-ray diffraction with Rietveld refinement have shown a crystallization of 55% of zeolite P, which was neoformed from the amorphous phase, opal-CT and quartz of the starting sample. The spectra obtained by Fourier Transform Infrared Spectrometry have corroborated such zeolitization. N₂ adsorption–desorption isotherms have shown that the zeolitized material (Dt-Z) is mesoporous, with almost 60% more specific surface area than Dt (62.6 m²/g vs. 39.4 m²/g), greater microporosity and 40% smaller average pore size than Dt (71 Å vs. 118 Å). This study is a first approximation to know the potential of diatomite wastes as zeolite precursors, for which additional research including an aluminum source will be required. Full article

After subjecting Zamora building stones to accelerated ageing tests, colour changes were studied, namely: (a) freezing/thawing and thermal shock (gelifraction and thermoclasty), and (b) combination of freezing/thawing plus thermal shock and salt crystallisation (sulphates or phosphates) (gelifraction, thermoclasty and haloclasty). Zamora building stones are silicified conglomerates (silcretes) from the Cretaceous that show marked colour changes due to the remobilisation of iron oxyhydroxides. In this work, four varieties were: white stone; ochreous stone; white and red stone; and purple stone Their micromorphological characterization (skeleton, weathering plasma and porosity/cutan) is formed of grains and fragments of quartz and quartzite as well as by accesory minerals muscovite and feldspar (more or less altered), and some opaque. Quartz, feldspar and illite/mica were part of the skeleton; kaolinite, iron oxyhydroxides, and CT opal were part of the weathering plasma or cutans; their porosity were 11.7–8.7%. Their chromatic data have been statistically analysed (MANOVA-Biplot). They showed higher variations in ΔE*, ΔL*, Δa* and Δb*on combined freezing/thawing plus thermal shock and sulphates crystallisation leading to rapid alteration of the building stones. Chromatic differences between the other two artificial ageing tests were less evident and were not detected in all samples. The global effect of ageing on the Zamora building stones darkened them and reduced their yellowing. The ochreous stone suffered the least variation and the purple stone the most. This study of the colour by statistical analyse may be of interest for the evaluation and monitoring of stone decay, which is an inexpensive, simple, easy and non-destructive technique. Full article

Diatomitic and clastic-volcanoclastic marly samples from the Paranisia area of Limnos Island, were studied mineralogically by X-ray diffraction (XRD), chemically by X-ray fluorescence spectroscopy (XRF) and morphologically by scanning electron microscopy (SEM-EDS), together with some physical properties such as the insulation block density, specific surface area and porosity. The diatomaceous samples were classified as porcelaneous or clayey (moler type) diatomite. Opal-CT forms microplates disseminated in the groundmass and are diagenetically formed in expense of opal-A dissolution. The purest diatomaceous beds have been transformed into opaline beds (opal-CT-rich rocks), whereas the clayey beds were not influenced by diagenetic transformations. The studied diatomites from Limnos Island are suitable materials for environmental uses, as an absorbent, for the production of insulation bricks or as lightweight aggregates. Full article

Single pulse, solid-state ²⁹Si nuclear magnetic resonance (NMR) spectroscopy offers an additional method of characterisation of opal-A and opal-CT through spin-lattice (T₁) relaxometry. Opal T₁ relaxation is characterised by stretched exponential (Weibull) function represented by scale (speed of relaxation) and shape (form of the curve) parameters. Relaxation is at least an order of magnitude faster than for silica glass and quartz, with Q₃ (silanol) usually faster than Q₄ (fully substituted silicates). 95% relaxation (Q₄) is achieved for some Australian seam opals after 50 s though other samples of opal-AG may take 4000 s, while some figures for opal-AN are over 10,000 s. Enhancement is probably mostly due to the presence of water/silanol though the presence of paramagnetic metal ions and molecular motion may also contribute. Shape factors for opal-AG (0.5) and opal-AN (0.7) are significantly different, consistent with varying water and silanol environments, possibly reflecting differences in formation conditions. Opal-CT samples show a trend of shape factors from 0.45 to 0.75 correlated to relaxation rate. Peak position, scale and shape parameter, and Q₃ to Q₄ ratios offer further differentiating feature to separate opal-AG and opal-AN from other forms of opaline silica. T₁ relaxation measurement may have a role for provenance verification. In addition, definitively determined Q₃/Q₄ ratios are in the range 0.1 to 0.4 for opal-AG but considerably lower for opal-AN and opal-CT. Full article

Silicified wood occurs abundantly in Middle Miocene flows and sedimentary interbeds of the Columbia River Basalt Group (CRBG) in central Washington State, USA. These fossil localities are well-dated based on radiometric ages determined for the host lava. Paleoenvironments include wood transported by lahars (Ginkgo Petrified Forest State Park), fluvial and palludal environments (Saddle Mountain and Yakima Canyon fossil localities), and standing forests engulfed by advancing lava (Yakima Ridge fossil forest). At all of these localities, the mineralogy of fossil wood is diverse, with silica minerals that include opal-A, opal-CT, chalcedony, and macrocrystalline quartz. Some specimens are composed of only a single form of silica; more commonly, specimens contain multiple phases. Opal-A and Opal-CT often coexist. Some woods are mineralized only with chalcedony; however, chalcedony and macrocrystalline quartz are common as minor constituents in opal wood. In these specimens, crystalline silica filling fractures, rot pockets, and cell lumen may occur. These occurrences are evidence that silicification occurred as a sequential process, where changes in the geochemical environment or anatomical structures affected the precipitation of silica. Fossilization typically began with precipitation of amorphous silica within cell walls, leaving cell lumen and conductive vessels open. Diagenetic transformation of opal-A to opal-CT in fossil wood has long been a widely accepted hypothesis; however, in opaline CRBG specimens, the two silica polymorphs usually appear to have formed independently, e.g., woods in which cell walls are mineralized with opal-A but in which lumen contain opal-CT. Similarly, opal-CT has been inferred to sometimes transform to chalcedony; however, in CRBG, these mixed assemblages commonly resulted from multiple mineralization episodes. Full article

Experimental studies increasingly often report low-temperature (200–800 °C) and low-pressure (0.05–3 kbar) hydrosilicate fluids with >40 wt.% of SiO₂ and >10 wt.% of H₂O. Compositionally similar fluids were long suggested to potentially exist in natural systems such as pegmatites and hydrothermal veins. However, they are rarely invoked in recent petrogenetic models, perhaps because of the scarcity of direct evidence for their natural occurrence. Here we review such evidence from previous works and add to this by documenting inclusions of hydrosilicate fluids in quartz and feldspar from Itrongay. The latter comprise opal-A, opal-CT, moganite and quartz inclusions that frequently contain H₂O and have negative crystal shapes. They coexist with inclusions of CO₂- and H₂O-rich fluids and complex polycrystalline inclusions containing chlorides, sulphates, carbonates, arsenates, oxides, hydroxides and silicates, which we interpret as remnants of saline liquids. Collectively, previous studies and our new results indicate that hydrosilicate fluids may be common in the Earth’s crust, although their tendency to transform into quartz upon cooling and exhumation renders them difficult to recognise. These data warrant more comprehensive research into the nature of such hydrosilicate fluids and their distribution across a wide range of pressure and temperature conditions and geological systems. Full article

Detailed mineralogical analyses in areas with surface hydrothermal alteration zones associated with recent volcanism (<1 Ma) in the Central Andean Volcanic Zone could provide key information to unravel the presence of hidden geothermal systems. In the Cordón de Inacaliri Volcanic Complex, a geothermal field with an estimated potential of ~1.08 MWe·km⁻² has been recently discovered. In this work, we focus on the hydrothermal alteration zones and discharge products of this area, with the aim to reconstruct the geological processes responsible for the space-time evolution leading to the geothermal records. We identified (1) discharge products associated with acid fluids that could be related to: (i) acid-sulfate alteration with alunite + kaolinite + opal CT + anatase, indicating the presence of a steam-heated blanket with massive fine-grained silica (opal-CT), likely accumulated in mud pots where the intersection of the paleowater table with the surface occurred; (ii) argillic alteration with kaolinite + hematite + halloysite + smectite + I/S + illite in the surrounding of the acid-sulfate alteration; and (2) discharge products associated with neutral-alkaline fluids such as: (i) discontinuous pinnacle-like silica and silica deposits with laterally developed coarse stratification which, together with remaining microorganisms, emphasize a sinter deposit associated with alkaline/freshwater/brackish alkaline-chlorine water bodies and laterally associated with (ii) calcite + aragonite deriving from bicarbonate waters. The scarce presence of relics of sinter deposits, with high degree crystallinity phases and diatom remnants, in addition to alunite + kaolinite + opal CT + anatase assemblages, is consistent with a superimposition of a steam-heated environment to a previous sinter deposit. These characters are also a distinguishing feature of paleosurface deposits associated with the geothermal system of the Cordón de Inacaliri Volcanic Complex. The presence of diatoms in heated freshwater bodies at 5100 m a.s.l. in the Atacama Desert environment could be related with the last documented deglaciation in the area (~20–10 ka), an important factor in the recharge of the hidden geothermal systems of the Pabelloncito graben. Full article

In order that the impact on the environment and human beings can be assessed, it may prove necessary for geochemical research work to entail determinations of concentrations of trace elements in building materials, and it is also likely that this will be a time-consuming and financially-demanding business. Additionally, once basic research has been carried out to determine the mineral composition and structural and textural features, it will then be important to determine concentrations of elements that affect the surrounding natural environment and the health of human beings. This paper thus describes mineralogical and geochemical analyses performed on the stone material that opoka rocks represent. Mineralogical studies have shown that the studied opoka rocks most often have cryptocrystalline silica dispersed among carbonate components. The texture of the rock is slightly porous. Silica in the form of type opal A and CT (cristobalite–tridymite) is the main mineral component of the opoka rocks. Carbonate minerals represented by calcite were an important component in the opoka rocks. Earlier geochemical studies focused on the concentration of Sr and Ba. However, the determination of the leachability of these elements as a function of time is a novelty in this study. Trace elements leached from the material matrix were made subject to determinations. The MATLAB program was used to assess leachability in the cases of both strontium and barium, by reference to the Mamdani–Assilian fuzzy algorithm. The presented work has thus sought to experiment with the use of statistical methods to monitor the effectiveness of geochemical processes taking place over time. Full article

Agates in Paleocene/Eocene tuffs from El Picado/Los Indios, Cuba were investigated to characterize the mineral composition of the agates and to provide data for the reconstruction of agate forming processes. The volcanic host rocks are strongly altered and fractured and contain numerous fissures and veins mineralized by quartz and chalcedony. These features indicate secondary alteration and silicification processes during tectonic activities that may have also resulted in the formation of massive agates. Local accumulation of manganese oxides/hydroxides, as well as uranium (uranyl-silicate complexes), in the agates confirm their contemporaneous supply with SiO₂ and the origin of the silica-bearing solutions from the alteration processes. The mineral composition of the agates is characterized by abnormal high bulk contents of opal-CT (>6 wt%) and moganite (>16 wt%) besides alpha-quartz. The presence of these elevated amounts of “immature” silica phases emphasize that agate formation runs through several structural states of SiO₂ with amorphous silica as the first solid phase. A remarkable feature of the agates is a heterogeneous distribution of moganite within the silica matrix revealed by micro-Raman mapping. The intensity ratio of the main symmetric stretching-bending vibrations (A₁ modes) of alpha-quartz at 465 cm⁻¹ and moganite at 502 cm⁻¹, respectively, was used to depict the abundance of moganite in the silica matrix. The zoned distribution of moganite and variations in the microtexture and porosity of the agates indicate a multi-phase deposition of SiO₂ under varying physico-chemical conditions and a discontinuous silica supply. Full article