Navegando por Assunto "Mineralogy"

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Acesso aberto (Open Access)
Caracterização mineralógica com espectroscopia de reflectância por infravermelho (SWIR): exemplo do Complexo máficocarbonatítico Santana, sul do Cráton Amazônico
(Universidade Federal do Pará, 2021-09-21) COSTA, Jhoseph Ricardo Costa e; FERNANDES, Carlos Marcello Dias; http://lattes.cnpq.br/0614680098407362; https://orcid.org/0000-0001-5799-2694
On the border of the Pará and Mato Grosso states, in the Amazonian Craton, municipality of Santana do Araguaia (PA), there is a volcano-plutonism named Santana mafic-carbonatitic complex. This set houses the Serra da Capivara phosphate deposit. A lower mafic-ultramafic member reveals plutono-volcanic lithofacies with pyroxenite, ijolite, apatitite, and alkaline basalt. Autoclastic lithofacies contains poorly selected deposits of massive polymictic breccia, lapilli-tuff, crystal tuff, and ash tuff. Volcanogenic epiclastics rocks cover these lithofacies. The upper carbonatite member contains plutonic lithofacies with coarse calcite-carbonatite (sövite). Fine carbonatite veins with pervasive carbonatic and apatitic alterations crosscut this lithotype. Minor thick apatitite occcurs associated to this member and represents the protore of the deposit. Effusive volcanic lithofacies reveals fine calcite-carbonatite (alvikite) with porphyritic, equigranular, or aphanitic textures. A poorly sorted lithofacies of crystals tuff, lapilli-tuff, and massive polymictic breccia completes this member. Stocks and syenitic dykes invade these lithofacies. Detailed mapping suggests that the complex is a volcanic caldera in which large zones of hydrothermal alterations occur with reddish, brownish red, and yellowish carbonatitic rocks. Petrographic observations reveal paragenesis of barite + fluorapatite + calcite + dolomite ± quartz ± rutile ± chalcopyrite ± pyrite ± monazite ± magnetite ± hematite. The application of short wave infrared spectroscopy (SWIR) revealed the chemical characteristics and their importance in the crystallinity of most of these hydrothermal minerals, such as radicals (OH- and CO3), H2O molecule, and cation-OH bonds such as Al-OH, Mg-OH, and Fe-OH. The main mineral phases identified were dolomite, calcite, serpentine, chlorite, muscovite with low, medium, and high aluminum, montmorillonite (Ca and Na), illite, nontronite (Na0.3Fe2((Si,Al)4O10) (OH)2·nH2O), and epidote. The data suggest a control by temperature, fluids composition, and fluid/rock ratio during the evolution of the Santana mafic-carbonatitic complex. This low-cost exploratory technique, which is applied in hand-held samples or drill holes on a large scale, is promising in characterization of volcano-plutonic centers in regions subjected to severe weathering conditions, as well as helping to develop models for prospecting mineral deposits of Rare Earth Elements (e.g. Nd, La) associated with alkaline-carbonatitic complexes. We can even combine this tool with artificial intelligence algorithms for more robust and faster results.
Acesso aberto (Open Access)
The ceramic artifacts in archaeological black earth (terra preta) from lower Amazon region, Brazil: Mineralogy
(Instituto Nacional de Pesquisas da Amazônia, 2004) COSTA, Marcondes Lima da; KERN, Dirse Clara; PINTO, Alice Helena Eleotério; SOUZA, Jorge Raimundo da Trindade
Several archaeological black earth (ABE) sites occur in the Amazon region. They contain fragments of ceramic artifacts, which are very important for the archaeological purpose. In order to improve the archaeological study in the region we carried out a detailed mineralogical and chemical study of the fragments of ceramic artifacts found in the two ABE sites of Cachoeira-Porteira, in the Lower Amazon Region. Their ceramics comprise the following tempers: cauixi, cariapé, sand, sand +feldspars, crushed ceramic and so on and are composed of quartz, clay equivalent material (mainly burned kaolinite), feldspars, hematite, goethite, maghemite, phosphates, anatase, and minerals of Mn and Ba. Cauixi and cariapé, siliceous organic compounds, were found too. The mineralogical composition and the morphology of their grains indicate a saprolite (clayey material rich on quartz) derived from fine-grained felsic igneous rocks or sedimentary rocks as source material for ceramic artifacts, where silica-rich components such cauixi, cariapé and/or sand (feldspar and rock fragments) were intentionally added to them. The high content of (Al,Fe)-phosphates, amorphous to low crystalline, must be product of the contact between the clayey matrix of pottery wall and the hot aqueous solution formed during the daily cooking of animal foods (main source of phosphor). The phosphate crystallization took place during the discharge of the potteries put together with waste of organic material from animal and vegetal origin, and leaving to the formation of the ABE-soil profile.
Acesso aberto (Open Access)
Efeitos das variações sazonais do clima tropical úmido sobre as águas e sedimentos de manguezais do estuário do rio Marapanim, costa nordeste do Estado do Pará
(Instituto Nacional de Pesquisas da Amazônia, 2008) SILVA, José Francisco Berrêdo Reis da; COSTA, Marcondes Lima da; VILHENA, Maria do Perpétuo Socorro Progene
To evaluate the short period climatic variations impact over Amazonic mangrove ecosystem, studies were carried out on the northeast coast of Para State. Sediments, surficial and interstitial waters were collected and examinated throughout salinity, pH and Eh (mV) measurements; mineralogical determination using X-ray diffraction and electronic microscopy. Chemical analysis of dissolved sulfides, sulfate and chloride, among others were made in samples collected seasonally, under spring and neap tides conditions. The seasonal chloride variations in the interstitial waters shows 20 g/l during the dry season and less of 10 g/l in the season; the concentration in surficial are higher at neap tides (rainy season) and spring tide (dry season). The dissolved sulfides were found only at 10 cm, indicating sediment exposure to the atmospheric oxygen advectives fluxes. The dissolved iron rates increases between 0-10 cm and the pH tends to neutrality. The saturation of interstitial waters at dry season is indicated by evaporitic minerals: gypsum and halite. The pluviometric variations are responsible by gradual changes in the nutrient and physical chemical properties of surficial and interstitial waters, into the saline equilibrium control at coastal waters, in the salinization and desalinization of sediments and the distribution of mangrove vegetation at the estuary. The prolonged exposure of sediments during the dry season and the morphological characteristics contribute to the total or partial oxidation of surficial sediments, modifying the mineralogy of sediments and the physical chemical characteristics of interstitial waters.
Acesso aberto (Open Access)
Evolução supergênica do depósito cuprífero Alvo 118 - Província Mineral de Carajás
(Universidade Federal do Pará, 2022-12-15) SANTOS, Pabllo Henrique Costa dos; COSTA, Marcondes Lima da; http://lattes.cnpq.br/1639498384851302; https://orcid.org/0000-0002-0134-0432
The Carajás Mineral Province is home to one of the most extensive cupriferous belts in the world, where hypogene mineralizations were partially transformed into gossans, later lateritized and/or truncated during landscape evolution. These covers represent an information source for mineral exploration and, in some cases, can be mined together with parental hypogene mineralizations. The plateaus of the South American Surface host complete and lateritized gossans, while the surrounding denuded areas, typical of the Velhas Surface, exhibit incomplete or immature gossans, with the Alvo 118 deposit as an example. In this orebody, the hypogene mineralization was converted into an immature gossan located at depth, while the host rocks were weathered near the surface, forming a mineralized saprolite. The gossan comprises an oxidation zone, which includes goethite, malachite, pseudomalachite, cuprite, tenorite, native copper, ramsbeckite, chrysocolla, and libethenite, with relics of a secondary sulfide zone, represented by chalcocite. These minerals are distributed in the goethite, malachite, cuprite, and libethenite zones, with their mineral successions reflecting the transition of mineralizing solutions from acidic to slightly alkaline conditions and an increase in oxidation potential. This environment was established from the interaction of acid solutions, derived from chalcopyrite dissolution, with the gangue minerals (calcite and apatite) and the host rocks, granodiorites and, secondarily, chloritites, which acted in buffering the system, favoring the formation of new copper-bearing minerals. The strong correlations of CuO with Ag, Te, Pb, Se, Bi, Au, In, Y, U, and Sn in the hypogene mineralization reflect the inclusions of petzite, altaite, galena, uraninite, cassiterite, and stannite in chalcopyrite. In the gossan, Ag, Te, Pb, Se, and Bi remained associated and were incorporated into neoformed copper minerals. On the other hand, Au, In, Y, U, and Sn exhibit greater affinity with iron oxyhydroxides, as well as Zn, As, Be, Ga, Mo and Ni. The δ65Cu values reinforce that the investigated gossan is immature and was not intensely affected by leaching processes. The main mineral phases identified in the saprolite are kaolinite (predominant), associated with chlorite, smectite, vermiculite, quartz, and iron oxyhydroxides. Iron oxyhydroxides are strongly correlated with Ga, Sc, Sn, V, Mn, Co, and Cr, partly derived from the weathering of parent rocks. Additionally, Mössbauer spectroscopy data point to the important role of ferrihydrite and goethite as copper-bearing phases. There is no evidence of copper incorporation by clay minerals. The δ56Fe values indicate a little contribution of primary mineralization to the Fe content of the saprolite, which is more influenced by chlorite weathering. The association Al2O3, Hf, Zr, Th, TiO2, Ce, La, Ba, and Sr represents the geochemical signature of the host rocks, which influence the chemical composition of the three types of mineralization. On the other hand, the association In, Y, Te, Pb, Bi, and Se comprise the main pathfinder elements of the hypogene mineralization. Detailed knowledge of the supergene mineral and geochemical fractionation makes the Alvo 118 deposit a reference guide for investigating immature gossans and mineralized saprolites in denuded areas of the Carajás Mineral Province or equivalent terrains.
Acesso aberto (Open Access)
Mineralogia e geoquímica de bauxitas de Barro Alto (Goiás): considerações genéticas
(Universidade Federal do Pará, 2019-10-01) MOURA, Vitor Hugo Santana; COSTA, Marcondes Lima da; http://lattes.cnpq.br/1639498384851302
In the municipality of Barro Alto, Goiás, a bauxite deposit was developed, mostly, on Neoproterozoic anorthosites. According to recent published data, the general mode of occurrence reinforces the lateritic origin, since bauxite follows the current topographic surface. However, the succession of the horizons is not corresponding to the others of the lateritic model, at least partially. The absence or restricted size of the clay horizon with kaolinite, or the presence of kaolinite bodies sectioning the bauxitic body, which locally reaches large thicknesses, overturn the simple lateritic model. This is reinforced by the absence of the classic leopard skin-like pattern or similar iron-aluminous crust and the absence of other coverage. For various authors the wide occurrence of extensive macrocrystalline, botrioidal gibbsite, apparently occupying venules and fracture walls suggests, along with the diversity of the way of occurrence of clays, a contribution of another process, not only lateritization. From this information a study was elaborated to deepen the knowledge about the formation of the Barro Alto bauxite, detailing the generations of gibbsite and kaolinite, as well as to try to identify the lateritic and hydrothermal contributions with these minerals. In the field, 5 mines explored by the company EDEM - Mineração LTDA were studied (Mining 1, Mining 2, Mining 5, Mining 6 and the SELA trench). From these mines, a greater detail was made in mines 1, 2, 5 and in SELA trench. Forty-eight samples were collected from which 22 most representative samples were selected for laboratory analysis involving mineralogical (X-ray Diffractometry), textural (Optical and Scanning Electron Microscopy), and chemistry (Inductively Coupled Plasma Mass and Optical Emission Spectrometry) characterization. In general, the bauxitic profile of Barro Alto comprises the anorthosite as substrate and possible source rock, on which a porous bauxite horizon (HBP) with stockworks and flint-type veins of kaolin (CF), and locally with subcentimeter corundum crystals (HBPC) was established. They converge to a bauxitic clay zone (ZAB) and then to a massive bauxite horizon (HBM). This in turn is superimposed by a capping formed by centimetric to decametric blocks and nodules of massive bauxite (HBANB), whose occurrence suggests a colluvial formation. In the profiles the horizons HBP, HBPC, HBM and HBANB consist essentially of gibbsite and kaolinite, sometimes containing accessory minerals such as corundum (HBPC), followed by hematite and goethite. In CF and in the bauxite clay zone (ZAB) the dominant mineral is kaolinite and/or halloysite, followed by gibbsite. The chemical composition of the bauxitic profile is basically composed of Al2O3, SiO2 and Fe2O3. CaO, MgO, K2O, MnO, Na2O and P2O5 concentrations are very low (generally <0.09), even below the analytical detection limit. TiO2 contents are also relatively low, generally <0.2%. Trace element concentrations when compared to the average values of the Earth's Upper Crust (EUC) are generally very low. The concentrations of elements such as Cr, Co, Cu, Zn, Rb, Sr, Y, Zr, Nb, Cs, Ba, Hf, Pb, Th and U are below EUC in all horizons. Only the element Mo has more concentrated values in all horizons. On the other hand, V, Ni, Cu, Cr, Ga, and Pb may eventually have higher values especially in some parts of CF and ZAB. Rare Earth Element (REE) concentrations are below the crustal average in all samples studied and also in the anorthosite. The higher concentrations are typically related to the clayey units such as CF and ZAB, and also to the presence of Fe oxides-hydroxides (HBPC). When normalized to the chondrites, the curves exhibit a slightly similar distribution pattern except for porous bauxite with corundum. There is a slight LREE enrichment and a HREE tendency, but only from Tm to Lu. This behavior resembles that of anorthosite, but with much lower concentrations, except for Tm. It is clear the negative anomalies in Ce and positive in Tm, anomalies linked to LREE depletion and a slight enrichment of HREE. From these mineralogical and chemical data, it was possible to distinguish three distinct generations of gibbsite and kaolinite: Gibbsite (I): of the porous bauxitic horizon, which appears to be that formed directly from the plagioclase and almandine; Gibbsite (II): associated with flint kaolin, along with kaolinite, halloysite and even locally hematite; Gibbsita (III): Cohesive and macrocrystalline, sometimes drusic and overlapping the thinner and more compact botryoidal gibbsite. It forms isolated bodies, apparently disconnected from the larger set of bauxites, in pockets of tens of meters wide and depths greater than 40 m; Kaolinite (I) at the gibbsite - anorthosite interface. This kaolinite makes up the halos of anorthosite alteration, when it does not go straight to gibbsite; Kaolinite (II) corresponds to that of flint kaolin, associated with halloysite and sometimes gibbsite. It occurs in the form of venules, veins and pockets, and vertical fractured zones, the stockworks in general. Kaolinite (III) corresponds to that found mainly in the clayey bauxite horizon with nodules, in which this mineral is yellowish, earthy, invading the bauxite mass and involves the centimetric to decametric nodules. The generations of gibbsite, I, II and III, especially II and III, are not compatible with lateritic evolution, likewise the kaolinite, I, II, and III generations, where I and II are not clearly lateritic, and the III seems to be current pedogenetic. Therefore, it is likely that Barro Alto bauxites are the product of the intense subsurface hydrothermal activity of anorthosites, due to the strong structural deformation in which these rocks were subjected in their final post-emplacement stages.
Acesso aberto (Open Access)
Mineralogia e geoquímica de perfis de solo com Terra Preta Arqueológica de Bom Jesus do Tocantins, sudeste da Amazônia
(Instituto Nacional de Pesquisas da Amazônia, 2012) SILVA, Any Kelly Terra da; GUIMARÃES, José Tasso Felix; LEMOS, Vanda Porpino; COSTA, Marcondes Lima da; KERN, Dirse Clara
The comparison of morphological, mineralogical and chemical data of a soil with anthropic horizons - Archeological Black Earth (ABE) and surrounding Argissolos (Typic Kandiudox or Ultisols) allowed the identification of the main process acting on the ABE formation from the town of Bom Jesus do Tocantins, southeastern Pará State. The similarity between the data in the subsurface horizons of ABE and surrounding soils indicates that the former was likely developed from Argissolos with later pedogenetic transformation by the input of organic and inorganic materials from ancient human settlements, which resulted in thickness of the surface horizon and higher concentrations of CaO and P2O5 (total content), Zn (trace content), available P and Zn (available content), and exchangeable Ca and Mg (exchangeable content) compared to surrounding Argissolos. Furthermore, such anthropic disturbance also resulted in changes in the subsurface horizon of Argissolos with ABE, such as high concentrations of P2O5 and available P. The Soil Taxonomy and Brazilian System of Soil Classification (BSSC) are suitable to identify soils with ABE, as they prioritize at the highest categorical level the main pedogenetic process acting on soil development and formation, related to the subsurface horizons, and later pedogenetic transformations in the surface horizon. However, this study proposes the addition of diagnostic properties such as ceramic and lithic artifacts, P2O5 and available P and Zn, organic C, Ca2++ Mg2+ (exchangeable content), CEC and base saturation in the surface horizon to classify and discriminate several kinds of anthropic soils in the Amazon region.
Acesso aberto (Open Access)
Mineralogical and geochemical influences on sediment color of Amazon wetlands analyzed by visible spectrophotometry
(Instituto Nacional de Pesquisas da Amazônia, 2013-09) GUIMARÃES, José Tasso Felix; COHEN, Marcelo Cancela Lisboa; FRANÇA, Marlon Carlos; SILVA, Any Kelly Terra da; RODRIGUES, Suyanne Flavia Santos
Based on sedimentological and geochemical data, this work relates spectrophotometric measurements with sediment composition and its application in palaeoecological studies of Amazon wetlands. The CIELAB values are directly related to mineralogical and chemical composition, mostly involving quartz, iron oxyhydroxides and sulfides (e.g. pyrite), and total organic carbon. Total organic carbon contents between 0.4-1%, 1-2%, 3-5% and 15-40% were related to L* (lightness) data of 27, 26-15, 7-10 and 7 or less, respectively. The CIELAB values of a deposit in Marabá, Pará, were proportional to variations in quartz and total organic carbon contents, but changes in zones of similar color, mainly in the +a* (red) and +b* (yellow) values of deposits in Calçoene, Amapá and Soure, Pará, indicate a close relationship between total organic carbon content and iron oxyhydroxides and sulfides. Furthermore, the Q7/4 diagram (ratio between the % re?ectance value at 700 nm to that at 400 nm, coupled with L*) indicated iron-rich sediments in the bioturbated mud facies of the Amapá deposit, bioturbated mud and bioturbated sand facies of Soure deposit, and cross-laminated sand and massive sand facies of the Marabá core. Also, organic-rich sediments were found in the bioturbated mud facies of the Amapá deposit, lenticular heterolithic and bioturbated mud facies of the Soure deposit, and laminated mud and peat facies of the Marabá deposit. At the Marabá site, the data suggest an autochthonous influence with peat formation. The coastal wetland sites at Marajó and Amapá represent the development of a typical tidal flat setting with sulfide and iron oxyhydroxides formation during alternated ?ooding and drying.
Acesso aberto (Open Access)
Resíduo mineral a partir de biomassas amazônicas como uma fonte alternativa de nutrientes para a agricultura
(Universidade Federal do Pará, 2021-06-25) ALBUQUERQUE, Alan Rodrigo Leal de; ANGÉLICA, Rômulo Simões; http://lattes.cnpq.br/7501959623721607; https://orcid.org/0000-0002-3026-5523; PAZ, Simone Patrícia Aranha da; http://lattes.cnpq.br/5376678084716817; https://orcid.org/0000-0002-5880-7638
The agrominerals and fertilizers deficiency in Brazil has acted as an obstacle to the country's consolidation plans as a world agricultural power and has placed damage on its trade balance. When we take the Amazon region as a reference, to which the expansion of the national agricultural border has been directed, this scenario has been even more unfavorable, since this region, in addition to having limited resources, also presents low developed technologies, which has increased the deforestation of large areas for low-yield agricultural production. In addition, in order to reduce dependence on fossil fuels, Brazil has been investing in modern biofuel production, mainly in the technological development of bioenergy conversion and production from lignocellulosic waste and energy forest plantations. Although the use of these bioenergy sources contributes to mitigating competition with food products and CO2 emissions problems, increase biomass uses, especially in the firewood and charcoal form, has caused an increase in the demand for fertilizers and has produced large quantities of mineral residues, which occur as biomass ashes. Therefore, one of the major challenges for the sustainable management of biomass residues as a source of renewable energy is the production of large quantities of ash, which are destined for disposal due to the lack of a recycling system. From an environmental and socio-economic aspect, ash recycling in agriculture and forestry soils can play an important role in facing the difficulty of integrating the use of renewable energy, fertilizers dearth, and organic and mineral residues management. Among the main advantages of the ash application in agricultural and forest soils are the ability to neutralize acidity and the ability to supply important nutrients to plants, such as Ca, Mg, P, and K. Although the agronomic effects of biomass ash are common knowledge, its application in the soil requires attention because textural and compositional variations can directly interfere in the solubility, availability, and absorption of nutrients. In addition, the response of the ash's fertilizing capacity depends on the properties of the soil, mainly pH, texture, and organic matter content. Thus, the applicability of biomass ash becomes more favorable after chemical, mineralogical, and agronomic tests. In this context, having as one of the biggest challenges of the Amazon region the residues management and the increased demand for fertilizer to attend the expansion of the agricultural border and the production of energy forests, the research aimed to evaluate the yield and composition of ash from Amazonian biomasses, as well as carrying out a first evaluation of the effects of these residues on the fertility of acid soils, with special attention to the P dynamics and the plant nutrition and yield. To this end, the mineral residue, generated by the açaí seeds and wood chips combustion and co-produced by a calcined phosphate fertilizer industry, was subjected to chemical and mineralogical analyzes, and to incubation tests with soils and plant. The results were used to estimate that the fertilizer industry produces ~ 4.7 – 9.9 tons/day of ash, which occurs as bottom ash and has a relatively low compositional variability throughout the year. Ash from Amazonian biomasses is mineralogically composed of amorphous phases, silicates, and oxides and chemically composed of SiO2, Al2O3, CaO, Fe2O3, P2O5, K2O, and MgO. The highest quantities of SiO2 and Al2O3 mainly result from quartz and kaolinite incorporated in the biomasses. By contrast, CaO and MgO originate from wood chips, whereas K2O and P2O5 originate from açaí seeds. According to the results of the soils incubations and the Avena sativa cultivation, the applications of ash from Amazonian biomasses promoted moderate effects in the correction of acidity in soils, produced increases in the availability of macronutrients (P, Ca, Mg, and K) and micronutrients (B, Cu, Fe, and Mo), and favored plant production and nutrition. In soils rich in organic matter content, the applications of biomass ash also positively affected the transformation of inorganic P into organic P. Even in high amounts, the biomass ash supply offered no risk salinity, nutrient immobilization, Al and Mn toxicity, and contamination by As, Cd, Cr, Hg, and Pb soil and plants. Therefore, the recycling of mineral residue co-produced by the combustion of Amazonian biomass in agricultural or forest soils may represent a sustainable and strategic alternative for the management of industrial waste and for the maintenance of the fertility of the dystrophic soils of the Amazon region. In addition, the application of biomass ash can be a great ally in reducing losses due to P precipitation in acidic soils in the region.
Acesso aberto (Open Access)
The Belterra Clay On The Bauxite Deposits Of Rondon Do Pará, Eastern Amazon
(Sociedade Brasileira de Geologia, 2018-09) NEGRÃO, Leonardo Boiadeiro Ayres; COSTA, Marcondes Lima da; POELLMANN, Herbert
Bauxite deposits in the Amazon region are commonly covered by yellowish clays which can reach up to 25m thick, known as Belterra Clay (BTC). In Rondon do Pará, Eastern Amazon, BTC is 13m thick and covers world-class bauxite reserves. Three pilot bauxite mines were investigated in Rondon do Pará for an initial characterization of the local BTC. In discordant contact with the lateritic profile, the BTC has reddish brown colors at its base to ocher tones towards the top. It has a massive structure with silt-clayey texture and nodular bauxitic fragments at its base. Rietveld mineral quantification of the material attests that it is dominated by kaolinite, with goethite, gibbsite, hematite, anatase and residual quartz. The thermal behavior of the material also confirms its mineralogical composition. Kaolinite is of low structural order, which was considered the main difficulty in the application of the Rietveld method. Goethite has up to 33 mol% of Al. As observed by scanning electron microscopy (SEM), the minerals represent pseudo-hexagonal crystals measuring from 150 to 700 nm. The BTC in the studied area is correlated to BTC on others bauxitic deposits of the Amazon region, suggesting this material experienced the same genesis and geological evolution, probably during the Pliocene.