Mapeamento geológico e petrografia do alvo T-578 - Greenstone Belt Pilar de Goiás (Pilar de Goiás - GO)

The study area is located in the geological parameters of the Pilar de Goiás Greenstone Belt (GO), it is part of the Pilar de Goias Group’s meta-volcano-sedimentary sequence. This is a homoclinal package constituted by terrigenous metassediments containing intercalations of meta-ultramafic rocks and iron formations. The units that were informally named in this work, are interpreted as belongs to the Serra do Moinho Formation. Through mineralogical associations the area’s metamorphism were classified as high greenschist facies garnet zone. Prior to this work were detected in the area, through soil samples, some auriferous anomalies. One of the objectives of this work is the detection of possibles hidrotermal alterations related to these anomalies presents in the study area

Caracterização petrográfica dos alvos Hidrotermalitos Norte e Sul, Suruca e porção NW da Mina de Chapada - Alto Horizonte, GO

Main occurrence of Cu-Au in Goias Magmatic Arc, the Chapada mine fits into the geological context of the Brasilia Fold Belt, specifically in the Mara Rosa Magmatic Arc. Four targets, named Hidrotermalito Norte and Sul, NW Chapada Mine Portion and Suruca, are situated in this context, which includes ortogneisses and rocks from the Mara Rosa volcanic-sedimentary sequence. All these targets have been studied due to the possibility of presenting a great potential in Cu-Au, as well as the Chapada mine. Hidrotermalitos Norte and Sul targets presents four lithological sequences, which were identified as: quartz-muscovite schist; muscovite quartzites and kyanite quartzites; quartz-biotite-amphibole schist with pyrite and epidote-amphibole-biotite gneisses with muscovite; muscovite-biotite gneisses. They are metamorphosed to amphibolites facies and retrogressive greenschist facies. Sulfetation represented mainly by pyrite. In the NW Chapada Mine Portion, three main lithological groups were identified and classified as biotite gneisses; honblende-quartz-biotite-schist; amphibolites, with the first group metamorphosed in greenschist facies (low grade), and the other two groups metamorphosed in amphibolites facies, with subsequent retrogressive metamorphism in greenschist facies. Sulfetation is represented by chalcopyrite and pyrite. Finally, also three main lithological groups were identified in the Suruca target, classified as garnet-chlorite-epidote-eiotite gneiss; biotite gneiss and chlorite-biotite gneiss with epidote and muscovite; muscovite-quartz schist, all them metamorphised in amphibolites, with retrometamorphism in greenschist facies. Sulfetation represented by pyrite and sphalerite

Grãos em carbonatos marinhos cretácicos da Bacia Potiguar: formações Ponta do Mel e Jandaíra

This work aims to identify and photograph grains that compose important Cretaceous carbonate units of the Potiguar Basin, represented by the Ponta do Mel and Jandaíra formations (Albian-Campanian). Petrographic investigation of thin sections was essential. The samples studied come from wells and surface samples from the collection UNESPetro – UNESP, Rio Claro. In the Ponta do Mel Formation, the grains consist of ooids, oncoids, peloids and bioclasts. Regarding to the identified bioclasts, the solenoporacean red algae, mollusks (bivalves and gastropods), echinoids, foraminifera, ostracods and worms were the dominant elements. In the Jandaíra Formation, the grains are composed by ooids, peloids and bioclasts, which are represented by green algae, mollusks (bivalves and gastropods), benthic foraminifera miliolids, worms, echinoderms and ostracods. The grains found in the Ponta do Mel Formation are somewhat similar to those found in the Jandaíra Formation, with the exception of calcareous algae. The subsurface material from the Ponta do Mel Formation is derived from the upper part of the unit, representing marine high-energy carbonates, which also contains ooids and Trocholina. The samples of Jandaíra Formation, collected in outcrops, often contain green algae, mollusks and miliolids, and come from inner shelf and lagoon facies previously described

Mapeamento geológico, caracterização litoquímica e potencial econômico do corpo de cromitito de Cedrolina, Santa Terezinha de Goiás - GO

Studies of mafic-ultramafic bodies have been carried out through the years due to their great use on the interpretation of geochemical and geotectonic processes that took place in Earth's history. Amongst them, chromitites are notably recognized for being excellent indicators of their parental magma chemistry and of different geotectonic environments, as well for frequently containing associated noble metals mineralization. Thus the investigation of one of this ultramafic bodies that occurs inside the Pilar de Goiás Greenstone Belt was proposed, resulting in a detailed map of the chromitites and country rocks, as well as innumerous new data on the chemistry of chromite and associated matrix and accessory minerals. These studies were based upon geological field observations, optic and Scanning Electron Microscope (SEM), besides electron microprobe and cathodoluminescence analysis performed at the “Eugen F. Stumpfl Laboratory” of the Montanuniversität Institute of Resource Mineralogy, University of Leoben - Leoben, Austria. The chromitites are composed of 40-70% in volume of chromite (~50% on average), 14-55% of talc (~30% on average), 3-60% of chromium rich chlorite (~20% on average), traces to 4% of iron hydroxides and traces to 3% of rutile (1,5% on average). The chromite occurs as large spherical aggregates or as fine grained subhedral crystals disseminated in the matrix. This aggregates have diameters of 0.3-1.5 cm (1 cm on average) and are extremely well rounded, massive to intensively fractured, and commonly deformed to ellipsoids. When observed under the microscope, these aggregates show well rounded to slightly irregular borders, but on their interiors, these structures are represented by fine to medium grained euhedral to subhedral chromite crystals that have sharp contacts between themselves. The rock's matrix is basically made of chlorite and talc that define a metamorphic foliation (Sn), being the talc an alteration product ...

Corpos intrusivos básicos na coluna sedimentar Permo-Carbonífera no vale do rio Corumbataí

As rochas intrusivas básicas associadas a Formação Serra Geral na porção sul do município de Rio Claro e norte de Piracicaba configuram geometrias na forma de diques e soleiras. Estes corpos estão associados à uma parte da Bacia Sedimentar do Paraná que foi deformada por eventos tectônico que resultaram em trends preferencias NW-SE, condicionando a estratigrafia, a intrusão e geometria dos corpos de diabásio e formação da estrutura domática do alto de Pitanga. Os corpos intrusivos tem em sua maioria a forma de soleiras e em menor quantidade a forma de diques. A compreensão destes corpos é importante para o entendimento da estratigrafia da área conhecida como domo de Pitanga na região de Rio e Piracicaba

Quimioestratigrafia do vulcanismo ácido mesozóico da província magmática do Paraná: porção SE do estado de Santa Catarina

The Mesozoic acid volcanism of the Paraná-Etendeka Province can be considered as one of the biggest events of its kind in the Earth's surface, and its study have attracted special interest in characterizing the end of magmatism that preceded the rupture process and the formation of continental Africa and South America Although significant, the acid volcanism featuring Members Chapecó Palmas and Serra Geral Formation represents only 2.5% of the total generated by the magmatic rocks and perhaps therefore the existing literature on these rocks is well less significant than that on the basalts. However, there are still aspects still unclear about the origin and evolution of these rocks in relation to the associated basalts. Thus, two profiles were selected, called RA and TA, which be a systematic collection of samples from the base where the Botucatu Formation sandstones occur at the top, where they observe Palmas acid rock type. These samples should be analyzed for major, minor and trace elements and treated in specific diagrams to define the vertical variation lithochemistry and their possible relationships with the associated basalts

Ultramafic complexes and associated mineral deposits in the Precambrian of eastern Minas Gerais, Brazil

Based on field work, prospection and petrographic studies ultramafic complexes and their mineral deposits from eastern Minas Gerais in southeastern Brazil are generally outlined to form a basis for future investigations in this region. The bodies dealt with occur at Ipanema, Córrego Novo, Bela Vista de Minas, Rio Pomba and Liberdade. These ultramafic bodies are generally enclosed in high-grade gneisses and consist of serpentinized peridotites and harzburgites which were metamorphosed together with their country rocks in upper amphibolite to granulite facies. Weathering of these rocks gives rise to nickeliferous laterite, while metamorphism has resulted in anthophyllite asbestos and talc deposits. © 1985 Springer-Verlag.

Gravimetria no estudo da extremidade sudeste da faixa de dobramentos Brasília

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Laminitos microbiais no membro Crato (Neoaptiano), bacia do Araripe, nordeste do Brasil

Pós-graduação em Geociências e Meio Ambiente - IGCE

Laminitos microbiais no membro Crato (Neoaptiano), bacia do Araripe, nordeste do Brasil

Pós-graduação em Geociências e Meio Ambiente - IGCE

Magmatism and fenitization in the Cretaceous potassium-alkaline-carbonatitic complex of Ipanema So Paulo State, Brazil

The Ipanema alkaline-carbonatitic complex is part of the Meso-Cenozoic alkaline magmatism located within the southeastern part of the Brazilian Platform. Drill-core and field sampling have indicated the occurrence of glimmerites, with subordinate shonkinites (mela-syenites), clinopyroxene-bearing glimmerites, diorites and syenites. The glimmerites are cross-cut by lamprophyric dykes and calciocarbonatites. Fenitization has deeply affected the country rocks, originating dioritic and syenitic rocks. The Ipanema rocks show a distinct potassic affinity. The initial Sr-Nd- isotopic composition of the Ipanema rocks ((87)Sr/(86)Sr = 0.70661-0.70754 and (143)Nd/(144)Nd = 0.51169-0.51181) is similar to that of tholeiitic and potassium-rich-alkaline rocks of the Eastern Paraguay. Stable isotope data for the Ipanema calciocarbonatite suggest interaction with fluids at temperatures typical of hydrothermal stages, as hypothesized for other carbonatite complexes from southeastern Brazil. The chemical differences between the lamprophyre, glimmerites, carbonatites, apatitites and magnetitites, and the absence of marked REE enrichment in the evolved lithologies, all indicate that fractional crystallization and accumulus of liquidus phases in a magma reservoir, likely coupled with liquid immiscibility processes, may have played an important role in the genesis of the Ipanema rocks.

The Banhado Alkaline Complex, Southeastern Brazil: source and evolution of potassic SiO2-undersaturated high-Ca and low-Ca magmatic series

The Cretaceous Banhado alkaline complex in southeastern Brazil presents two potassic SiO2-undersaturated series. The high-Ca magmatic series consist of initially fractionated olivine (Fo(92-91)) + diopside (Wo(48-43)En(49-35)Ae(0-7)), as evidenced by the presence of xenocrysts and xenoliths. In that sequence, diopside (Wo(47-38)En(46-37)Ae(0-8)) + phlogopite + apatite + perovskite (Prv(> 92)) crystallized to form the phlogopite melteigite and led to the Ca enrichment of the magma. Diopside (Wo(47-41)En(32-24) Ae(3-14)) continued to crystallize as an early mafic mineral, followed by nepheline (Ne(74.8-70.1)Ks(26.3-21.2)Qz(7.6-0.9)) and leucite (Lc(65-56)) and subsequently by melanite and potassic feldspar (Or(85-99)Ab(1-7)) to form melanite ijolites, wollastonite-melanite urtites and melanite-nepheline syenites. Melanite-pseudoleucite-nepheline syenites are interpreted to be a leucite accumulation. Melanite nephelinite dykes are believed to represent some of the magmatic differentiation steps. The low-Ca magmatic series is representative of a typical fractionation of aegirine-augite (Wo(36-29)En(25-4)Ae(39-18)) + alkali feldspar (Or(57-96)Ab(3-43)) + nepheline (Ne(76.5-69.0)Ks(19.9-14.4)Qz(15.1-7.7)) + titanite from phonolite magma. The evolution of this series from potassic nepheline syenites to sodic sodalite syenites and sodalitolites is attributed to an extensive fractionation of potassic feldspar, which led to an increase of the NaCl activity in the melt during the final stages forming sodalite-rich rocks. Phonolite dykes followed a similar evolutionary process and also registered some crustal assimilation. The mesocratic nepheline syenites showed interactions with phlogopite melteigites, such as compatible trace element enrichments and the presence of diopside xenocrysts, which were interpreted to be due to a mixing/mingling process of phonolite and nephelinite magmas. The geochemical data show higher TiO2 and P2O5 contents and lower SiO2 contents for the high-Ca series and different LILE evolution trends and REE chondrite-normalized patterns as compared to the low-Ca series. The Sr-87/Sr-86, Nd-143/Nd-144, Pb-206/Pb-204 and Pb-208/Pb-204 initial ratios for the high-Ca series (0.70407-0.70526, 0.51242-0.51251, 17.782-19.266 and 38.051-39.521, respectively) were slightly different from those of the low-Ca series (0.70542-0.70583, 0.51232-0.51240, 17.758-17.772 and 38.021-38.061, respectively). For both series, a CO2-rich potassic metasomatized lithospheric mantle enriched the source with rutile-bearing phlogopite clinopyroxenite veins. Kamafugite-like parental magma is attributed to the high-Ca series with major contributions from the melting of the veins. Potassic nephelinite-like parental magma is assigned to the low-Ca series, where the metasomatized wall-rock played a more significant role in the melting process.

Application of reactive fluid transport modeling to hydrothermal systems

A one-dimensional multi-component reactive fluid transport algorithm, 1DREACT (Steefel, 1993) was used to investigate different fluid-rock interaction systems. A major short coming of mass transport calculations which include mineral reactions is that solid solutions occurring in many minerals are not treated adequately. Since many thermodynamic models of solid solutions are highly non-linear, this can seriously impact on the stability and efficiency of the solution algorithms used. Phase petrology community saw itself faced with a similar predicament 10 years ago. To improve performance and reliability, phase equilibrium calculations have been using pseudo compounds. The same approach is used here in the first, using the complex plagioclase solid solution as an example. Thermodynamic properties of a varying number of intermediate plagioclase phases were calculated using ideal molecular, Al-avoidance, and non-ideal mixing models. These different mixing models can easily be incorporated into the simulations without modification of the transport code. Simulation results show that as few as nine intermediate compositions are sufficient to characterize the diffusional profile between albite and anorthite. Hence this approach is very efficient, and can be used with little effort. A subsequent chapter reports the results of reactive fluid transport modeling designed to constrain the hydrothermal alteration of Paleoproterozoic sediments of the Southern Lake Superior region. Field observations reveal that quartz-pyrophyllite (or kaolinite) bearing assemblages have been transformed into muscovite-pyrophyllite-diaspore bearing assemblages due to action of fluids migrating along permeable flow channels. Fluid-rock interaction modeling with an initial qtz-prl assemblage and a K-rich fluid simulates the formation of observed mineralogical transformation. The bulk composition of the system evolves from an SiO2-rich one to an Al2O3+K2O-rich one. Simulations show that the fluid flow was up-temperature (e.g. recharge) and that fluid was K-rich. Pseudo compound approach to include solid solutions in reactive transport models was tested in modeling hydrothermal alteration of Icelandic basalts. Solid solutions of chlorites, amphiboles and plagioclase were included as the secondary mineral phases. Saline and fresh water compositions of geothermal fluids were used to investigate the effect of salinity on alteration. Fluid-rock interaction simulations produce the observed mineral transformations. They show that roughly the same alteration minerals are formed due to reactions with both types of fluid which is in agreement with the field observations. A final application is directed towards the remediation of nitrate rich groundwaters. Removal of excess nitrate from groundwater by pyrite oxidation was modeled using the reactive fluid transport algorithm. Model results show that, when a pyrite-bearing, permeable zone is placed in the flow path, nitrate concentration in infiltrating water can be significantly lowered, in agreement with proposals from the literature. This is due to nitrogen reduction. Several simulations investigate the efficiency of systems with different mineral reactive surface areas, reactive barrier zone widths, and flow rates to identify the optimum setup.

Nature and origin of ultramafic lamprophyres and carbonatites from the borders of the Labrador Sea

Die Ränder des Labrador Meeres wurden während des späten Neoproterozoikums intensiv von karbonatreichen silikatischen Schmelzen durchsetzt. Diese Schmelzen bildeted sich bei Drucken zwischen ca. 4-6 GPa (ca. 120-180 km Tiefe) an der Basis der kontinentalen Mantel-Lithosphäre. Diese Magmengenerierung steht in zeitlichem und räumlichem Zusammenhang mit kontinentalen Extensionsprozessen, welche zu beiden Seiten des sich öffnenden Iapetus-Ozeans auftraten.

Ophiolites of the eastern Vardar Zone, N. Greece

In the present thesis, the geochemistry, petrology and geochronology of ophiolite complexes from central northern Greece were studied in detail in order to gain insights on the petrogenetic pathways and geodynamic processes that lead to their formation and evolution. The major- and trace-element content of minerals and whole rocks from all four ophiolite complexes was determined using high-precision analytical equipment. These results were then coupled with Nd and Sr isotopic measurements. In order to precisely place the evolution of these ophiolites in time, U-Pb geochronology on zircons was conducted using a SHRIMP-II. The data obtained suggest that the ophiolites studied invariably show typical characteristics of subduction-zone magmatism (e.g. negative Nb anomalies, Th enrichment). In N-MORB-normalised multielement profiles the high field-strength elements display patterns that vary from depleted to N-MORB-like. Chondrite-normalised rare-earth element (REE) profiles show flat heavy-REE patterns suggesting a shallow regime of source melting for all the ophiolites, well within the stability field of spinel lherzolite. The majority of the samples have light-REE depleted patterns. 87Sr/86Sr isotopic ratios range from 0.703184 to 0.715853 and are in cases influenced by alteration. The εNd values are positive (the majority of the mafic samples is typically 7.1-3.1) but lower than N-MORB and depleted mantle. With the exception of the Thessaloniki ophiolite that has uniform island-arc tholeiitic chemical characteristics, the rest of the ophiolites show dual chemistry consisting of rocks with minor subduction-zone characteristics that resemble chemically back-arc basin basalts (BABB) and rocks with more pronounced subduction-zone characteristics. Tectonomagmatic discrimination schemes classify the samples as island-arc tholeiites and back-arc basin basalts or N-MORB. Melting modelling carried out to evaluate source properties and degree of melting verifies the dual nature of the ophiolites. The samples that resemble back-arc basin basalts require very small degrees of melting (<10%) of fertile sources, whereas the rest of the samples require higher degrees (25-15%) of melting. As deduced from the present geochemical and petrological investigation, the ophiolites from Guevguely, Oraeokastro, Thessaloniki, and Chalkidiki represent relics of supra-subduction zone crust that formed in succeeding stages of island-arc rifting and back-arc spreading as well as in a fore arc setting. The geochronological results have provided precise determination of the timing of formation of these complexes. The age of the Guevguely ophiolite has been determined as 167±1.2 Ma, that of Thessaloniki as 169±1.4 Ma, that of Kassandra as 167±2.2 Ma and that of Sithonia as 160±1.2 Ma.