97 resultados para Porphyry


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Samples from carbonate wall-rocks, skarn, ore of skarn type, later calcite vein, and ore of porphyry type in Shouwangfen copper deposit district were collected. Systematic study was carried out on carbon, oxygen, rubidium, strontium and sulfur isotope compositions of carbonates and sulfides in these samples. The first Isochron dating by the Rb-Sr isotopes in chalcopyrite of ore sub-sample was done as well. The following conclusions were obtained. The age (113.6±4.3Ma), obtained by Rb-Sr isotope isochron dating of chalcopyrite and pyrite from sub-sample of skarn ores, probably represents the true mineralization age of skarn ores. That demonstrates the genetic relationship between granodiorite in Shouwangfen complex and skarn copper ores. On the other hand, the Rb-Sr isochron age (73±15Ma) of chalcopyrite from porphyry ores is a little incredible because of bad synthesizing evaluation. But combined with other age data of igneous rocks, it implies the possibility of hydrothermal mineralization in connection with magma activity during the fourth period of Yanshanian in Hebei Province, even in the whole northern edge of Huabei continental block. Together from structure analysis of sulfide sub-samples, from pretreating preccedure of Rb-Sr isotope isochron and its' valuating, we found out that Rb-Sr isotope isochron of sulfide sub-samples is influenced by the crystal structure of sulfides. That is, sulfide ores with very big crystals are not suitable for sub-sample isochron. Carbon, oxygen, sulfur and strontium compositions, of different minerals in these two kinds of ores, imply that the ore-forming hydrothermal fluids were probably derived from magma deep under the crust. The calcite ~(87)Sr/~(86)Sr ratios from the porphyry are consistent to the initial 87Sr/86Sr ratio of the Rb-Sr isochron of chalcopyrite and pyrite in the skarn ore, indicating that these two kinds of ores have the same source characteristic, although the porphyry deposit was formed probably 40 million years later than the skarn one according to our dating results. Skarn and skarn ores are usually considered as interaction product between carbonate wall-rocks and magmatic fluids, but the carbon of the sedimentary carbonate seems not involved in the skarn ores. Considering the connection of magmatic processes and hydrothermal ore formation in the Shouwangfen district, particularly, the spatial distribution of skarn-type and porphyry-type ores, it is possible that the Shouwangfen ore district corresponds to a hydrothermal ore-forming system, which was promoted by high-intruding magmatic rocks. Systematic stable isotopic research can help to reveal the upper part of this hydrothermal ore-forming system, which mainly related to heated and circulating meteoric water, and the lower part principally related to ascending magmatic fluids. Both skarn and porphyry ore-bodies are formed by up-intruding magmatic fluids (even more deep mantle-derived fluids).

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This paper deals with the relations between the Machangqing rockbody which corresponds to the A-type granites and porphyry copper mineralization in terms of petrochemistry, trace element geochemistry, fluid inclusion geochemistry and isotope geochemistry. The results show that the Machangqing porphyry copper deposit was formed from the fluid predominated by mag-matic fluid. This kind of ore-forming fluid was just differentiated from the magma responsible for the A-type granites. therefore,as viewed from whereer they contain water or not,the A-type granites can,at least,be divided into two types: water-bearing and water-free.The water-bearing A-type granites can serve as the host ofporphyry copper deposits under certain geological conditions.

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中甸格咱地区是在晚三叠世甘孜-理塘洋盆向西俯冲过程中所形成的中甸弧的主弧带,区内岛弧火山活动和岩浆侵入活动均非常强烈,广泛分布有印支期斑岩体,同时发育有众多的与其有关的斑岩型和矽卡岩型矿床或矿点。普朗斑岩铜矿就是近年来在该区发现的一个大型乃至超大型矿床,目前已圈定5个矿化体,7个工业矿体,其中,主矿体探明铜资源量436.5万吨。 本论文主要从区域地质背景、矿床地质特征、元素地球化学、同位素地球化学、流体包裹体地球化学、矿床年代学及成矿机理等角度对普朗斑岩铜矿进行了较为系统的研究,主要获得如下认识: 普朗复式岩体具明显的多次脉动侵入特征,可分为三期:第一期为大面积分布的石英闪长玢岩(部分为二长闪长玢岩),第二期为岩体中心的石英二长斑岩和花岗闪长斑岩,第三期为岩脉状闪长玢岩。岩体具有典型的斑岩铜矿蚀变分带特征,由内向外依次为强硅化带(局部)→钾化硅化带→绢英岩化带→青磐岩化带。 矿化石英二长斑岩的锆石离子探针U-Pb年龄约为226~228Ma;钾化硅化带中黑云母的40Ar-39Ar坪年龄约为210~216Ma;含矿石英脉中辉钼矿Re-Os等时线年龄约为214Ma。 普朗岩体总体显示I型花岗岩类特征,属典型的钙碱性系列岩石。锶、钕、铅同位素特征显示其岩浆源区具有幔源物质(占主要地位)与壳源物质较为均匀混合的特征。金属硫化物的硫、铅同位素特征显示成矿元素与岩体具有密切的亲缘关系。脉石矿物的氢、氧、碳同位素特征和流体包裹体特征显示成矿流体自钾化阶段至网脉状矿化阶段均具岩浆流体特征。 根据不同期次的含矿石英脉中的流体包裹体特征,主要发现有四种流体:高盐度岩浆流体(盐度:34~54wt%NaCl)、含CO2低盐度流体(盐度:2.7~6.4wt%NaCl,XCO2:0.04~0.25)、中等盐度流体(盐度:19~25wt%NaCl)以及低盐度水溶液(盐度:<10wt%NaCl)。这些流体可能主要是原始岩浆流体演化至不同阶段的产物。 原始岩浆流体可能有两种来源:其一是斑岩侵入过程中自身分异的流体,其二是岩浆房中分异的流体。其中,岩浆房来源的岩浆流体对普朗岩体的蚀变及矿化作用起到了主导性作用。主成矿期金属硫化物的沉淀主要与流体系统开放后因其物理化学条件的变化而产生的流体相分离作用及流体对围岩的蚀变作用有关。

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矿化剂在热液矿床成矿过程中的重要作用一直为人们所关注,矿化剂地球化学行为直接影响成矿元素的富集成矿,不同的矿化剂元素可能对金属成矿具有一定的专属性。本文以著名的江西德兴铜厂超大型斑岩铜矿床和大吉山钨矿床作为研究对象,研究F、Cl与W、Cu成矿的关系。主要的认识如下:(1)F在花岗质岩浆中,可以降低岩浆的粘度、密度、固液相线温度、改变熔体结构,而Cl对熔体结构没有多大的影响。F在流体一花岗质熔体相间,绝大多数配分系数小于1.0,趋向于熔体相中配分,DF随体系中F浓度的升高而增加。Cl在流体一花岗质熔体相间的配分系数均大于1.0,且Dc1 随体系中Cl浓度的升高而增大·Cl强烈地趋向富集于流体相中。(2)Cu在流体一花岗质熔体作用过程中,铜总趋向于流体相中分布(DCu都大于1)。特别是在富Cl流体中Cu浓度较高,说明在富含Cl的热液流体能够从共存的熔体中活化迁移出大量的 Cu,S的加入DCu有降低的趋势。钨趋向于熔体相中富集,其配分系数大多小于1.0。(3)德兴铜厂花岗闪长斑岩属钙碱性系列岩石属I型花岗岩类,具有埃达克岩的特征。岩浆来源于深部,在结晶演化过程中发生了围岩物质的混染,这种高铜含量围岩的混染使成矿物质在岩浆中得到富集,有利于铜的活化、迁移。在铜厂岩体不同的蚀变带中,SiO2、K2O、Cu、Mo等从新鲜斑岩甚至弱蚀变带中带出,而在强蚀变带强烈富集,Cl同样有在强蚀变岩石中富集的趋势;而Na2O、Fe从斑岩体中带出,进入流体相中,流体中大量Fe的存在,有利于铜的沉淀、富集成矿。(4)德兴铜厂斑岩体微量元素和稀土元素地球化学特征表明,该岩体发生了流体一熔体作用,分异出来的流体是一种相对富氯的流体,同时成矿流体的流向是从岩体中心向接触带方向流动。(5)大吉山花岗岩具有高SiO2、A/CNK值,显示过铝质特点。黑云母花岗岩是壳源花岗岩但又受到慢源岩浆或慢源流体的影响。随着花岗岩的演化(从I→II→III)SiO2、K2O+Na2O逐渐增加,ΣFe、Al2O3、CaO、F含量降低,为成矿提供了大量的矿化剂(F)和沉淀剂(Fe、Ca)。Eu负异常从I至III阶段花岗岩逐渐加强,表明该岩浆经历了高度的分异演化。(6)大吉山花岗岩类稀土元素具有“四重效应”配分的特点以及微量元素对玲Rb、Y/Ho、Zr/Hf以及Nb/Ta发生明显分异,暗示在花岗岩岩浆的演化过程中,经历了充分的流体一熔体作用,同时分异出大量富含F、W等矿化剂元素和成矿元素的热液流体,致使钨矿的形成。大吉山石英脉型钨矿的成矿年龄大约在155 Ma。(7)通过对成矿流体和花岗质岩石黑云母、白云母中卤素相对逸度的研究(log(H2O/fHCl)fluid、log(fHF/fHCl)fluid)发现,铜厂斑岩型铜矿床的成矿体系是相对富氯体系,而大吉山石英脉型钨矿床成矿体系相对富氟,同时氟可能主要迁移W、Sn、Nb、Ta等金属元素。(8)结合斑岩型铜矿床成矿流体特征,铜主要以C1的络合物形式存在和迁移,迁移形式主要是CuCl0、CuCl2等。石英脉型钨矿床中,钨主要以钨酸、钨酸盐及其离解形式存在和迁移,如WO42-、HWO4-、NaHWO4、Naw伍.等;在高度富氟的成矿流体中,钨的氟氧络合物(如WO3F-,WO2F42-等)对钨迁移也具有重要的作用。因此,不同矿化剂类型具有一定的成矿专属性,热液铜矿床主要与Cl、S有 关,而热液钨矿床大多与F有关。

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There is almost not a case in exploration geology, where the studied data doesn’t includes below detection limits and/or zero values, and since most of the geological data responds to lognormal distributions, these “zero data” represent a mathematical challenge for the interpretation. We need to start by recognizing that there are zero values in geology. For example the amount of quartz in a foyaite (nepheline syenite) is zero, since quartz cannot co-exists with nepheline. Another common essential zero is a North azimuth, however we can always change that zero for the value of 360°. These are known as “Essential zeros”, but what can we do with “Rounded zeros” that are the result of below the detection limit of the equipment? Amalgamation, e.g. adding Na2O and K2O, as total alkalis is a solution, but sometimes we need to differentiate between a sodic and a potassic alteration. Pre-classification into groups requires a good knowledge of the distribution of the data and the geochemical characteristics of the groups which is not always available. Considering the zero values equal to the limit of detection of the used equipment will generate spurious distributions, especially in ternary diagrams. Same situation will occur if we replace the zero values by a small amount using non-parametric or parametric techniques (imputation). The method that we are proposing takes into consideration the well known relationships between some elements. For example, in copper porphyry deposits, there is always a good direct correlation between the copper values and the molybdenum ones, but while copper will always be above the limit of detection, many of the molybdenum values will be “rounded zeros”. So, we will take the lower quartile of the real molybdenum values and establish a regression equation with copper, and then we will estimate the “rounded” zero values of molybdenum by their corresponding copper values. The method could be applied to any type of data, provided we establish first their correlation dependency. One of the main advantages of this method is that we do not obtain a fixed value for the “rounded zeros”, but one that depends on the value of the other variable. Key words: compositional data analysis, treatment of zeros, essential zeros, rounded zeros, correlation dependency

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New data show that island arc rocks have (Pb-210/Ra-226)(o) ratios which range from as low as 0.24 up to 2.88. In contrast, (Ra-22S/Th-232) appears always within error of I suggesting that the large Ra-226-excesses observed in arc rocks were generated more than 30 years ago. This places a maximum estimate on melt ascent velocities of around 4000 m/year and provides further confidence that the Ra-226 excesses reflect deep (source) processes rather than shallow level alteration or seawater contamination. Conversely, partial melting must have occurred more than 30 years prior to eruption. The Pb-210 deficits are most readily explained by protracted magma degassing. Using published numerical models, the data suggest that degassing occurred continuously for periods up to several decades just prior to eruption but no link with eruption periodicity was found. Longer periods are required if degassing is discontinuous, less than 100% efficient or if magma is recharged or stored after degassing. The long durations suggest much of this degassing occurs at depth with implications for the formation of hydrothermal and copper-porphyry systems. A suite of lavas erupted in 1985-1986 from Sangeang Api volcano in the Sunda arc are characterised by deficits of Pb-210 relative to Ra-226 from which 6-8 years of continuous Rn-222 degassing would be inferred from recent numerical models. These data also form a linear (Pb-210)/Pb-(Ra-226)/Pb array which might be interpreted as a 71-year isochron. However, the array passes through the origin suggesting displacement downwards from the equiline in response to degassing and so the slope of the array is inferred not to have any age significance. Simple modelling shows that the range of (Ra-226)/Pb ratios requires thousands of years to develop consistent with differentiation occurring in response to cooling at the base of the crust. Thus, degassing post-dated, and was not responsible for magma differentiation. The formation, migration and extraction of gas bubbles must be extremely efficient in mafic magma whereas the higher viscosity of more siliceous magmas retards the process and can lead to Pb-210 excesses. A possible negative correlation between (Pb-210/Ra-226)(o) and SO2 emission rate requires further testing but may have implications for future eruptions. (C) 2004 Elsevier B.V. All rights reserved.

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New data show that island arc rocks have (Pb-210/Ra-226)(o) ratios which range from as low as 0.24 up to 2.88. In contrast, (Ra-22S/Th-232) appears always within error of I suggesting that the large Ra-226-excesses observed in arc rocks were generated more than 30 years ago. This places a maximum estimate on melt ascent velocities of around 4000 m/year and provides further confidence that the Ra-226 excesses reflect deep (source) processes rather than shallow level alteration or seawater contamination. Conversely, partial melting must have occurred more than 30 years prior to eruption. The Pb-210 deficits are most readily explained by protracted magma degassing. Using published numerical models, the data suggest that degassing occurred continuously for periods up to several decades just prior to eruption but no link with eruption periodicity was found. Longer periods are required if degassing is discontinuous, less than 100% efficient or if magma is recharged or stored after degassing. The long durations suggest much of this degassing occurs at depth with implications for the formation of hydrothermal and copper-porphyry systems. A suite of lavas erupted in 1985-1986 from Sangeang Api volcano in the Sunda arc are characterised by deficits of Pb-210 relative to Ra-226 from which 6-8 years of continuous Rn-222 degassing would be inferred from recent numerical models. These data also form a linear (Pb-210)/Pb-(Ra-226)/Pb array which might be interpreted as a 71-year isochron. However, the array passes through the origin suggesting displacement downwards from the equiline in response to degassing and so the slope of the array is inferred not to have any age significance. Simple modelling shows that the range of (Ra-226)/Pb ratios requires thousands of years to develop consistent with differentiation occurring in response to cooling at the base of the crust. Thus, degassing post-dated, and was not responsible for magma differentiation. The formation, migration and extraction of gas bubbles must be extremely efficient in mafic magma whereas the higher viscosity of more siliceous magmas retards the process and can lead to Pb-210 excesses. A possible negative correlation between (Pb-210/Ra-226)(o) and SO2 emission rate requires further testing but may have implications for future eruptions. (C) 2004 Elsevier B.V. All rights reserved.

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The basement in the `Altiplano` high plateau of the Andes of northern Chile mostly consists of late Paleozoic to Early Triassic felsic igneous rocks (Collahuasi Group) that were emplaced and extruded along the western margin of the Gondwana supercontinent. This igneous Suite crops out in the Collalluasi area and forms the backbone of most of the high Andes from latitude 20 degrees to 22 degrees S. Rocks of the Collahuasi Group and correlative formations form art extensive belt of volcanic and subvolcanic rocks throughout the main Andes of Chile, the Frontal Cordillera of Argentina (Choiyoi Group or Choiyoi Granite-Rhyolite Province), and the Eastern Cordillera of Peru. Thirteen new SHRIMP U-Pb zircon ages from the Collahuasi area document a bimodal timing for magnatism, with a dominant peak at about 300 Ma and a less significant one at 244 Ma. Copper-Mo porphyry mineralization is related to the younger igneous event. Initial Hf isotopic ratios for the similar to 300 Ma zircons range from about -2 to +6 indicating that the magmas incorporated components with a significant crustal residence time. The 244 Ma magmas were derived from a less enriched source, with the initial HT values ranging from +2 to +6, suggestive of a mixture with a more depleted component. Limited whole rock (144)Nd/(143)Nd and (87)Sr/(86)Sr isotopic ratios further support the likelihood that the Collahuasi Group magmatism incorporated significant older crustal components, or at least a mixture of crustal sources with more and less evolved isotopic signatures. (C) 2007 International Association for Gondwana Research. Published by Elsevier B.V. All rights reserved.

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This dissertation focuses on rock thermal conductivity and its correlations with petrographic, textural, and geochemical aspects, especially in granite rocks. It aims at demonstrating the relations of these variables in an attempt to enlighten the behavior of thermal effect on rocks. Results can be useful for several applications, such as understanding and conferring regional thermal flow results, predicting the behavior of thermal effect on rocks based upon macroscopic evaluation (texture and mineralogy), in the building construction field in order to provide more precise information on data refinement on thermal properties emphasizing a rocky material thermal conductivity, and especially in the dimension stone industry in order to open a discussion on the use of these variables as a new technological parameter directly related to thermal comfort. Thermal conductivity data were obtained by using Anter Corporation s QuicklineTM -30 a thermal property measuring equipment. Measurements were conducted at temperatures ranging between 25 to 38 OC in samples with 2cm in length and an area of at least 6cm of diameter. As to petrography data, results demonstrated good correlations with quartz and mafics. Linear correlation between mineralogy and thermal conductivity revealed a positive relation of a quartz percentage increase in relation to a thermal conductivity increase and its decrease with mafic minerals increase. As to feldspates (K-feldspate and plagioclase) they show dispersion. Quartz relation gets more evident when compared to sample sets with >20% and <20%. Sets with more than 20% quartz (sienogranites, monzogranites, granodiorites, etc.), exhibit to a great extent conductivity values which vary from 2,5 W/mK and the set with less than 20% (sienites, monzonites, gabbros, diorites, etc.) have an average thermal conductivity below 2,5 W/mK. As to textures it has been verified that rocks considered thick/porphyry demonstrated in general better correlations when compared to rocks considered thin/medium. In the case of quartz, thick rocks/porphyry showed greater correlation factors when compared to the thin/medium ones. As to feldspates (K-feldspate and plagioclase) again there was dispersion. As to mafics, both thick/porphyry and thin/medium showed negative correlations with correlation factor smaller than those obtained in relation to the quartz. As to rocks related to the Streckeisen s QAP diagram (1976), they tend to fall from alcali-feldspates granites to tonalites, and from sienites to gabbros, diorites, etc. Thermal conductivity data correlation with geochemistry confirmed to a great extent mineralogy results. It has been seen that correlation is linear if there is any. Such behavior could be seen especially with the SiO2. In this case similar correlation can be observed with the quartz, that is, thermal conductivity increases as SiO2 is incremented. Another aspect observed is that basic to intermediate rocks presented values always below 2,5 W/mK, a similar behavior to that observed in rocks with quartz <20%. Acid rocks presented values above 2,5 W/mK, a similar behavior to that observed in rocks with quartz >20% (granites). For all the other cases, correlation factors are always low and present opposite behavior to Fe2O3, CaO, MgO, and TiO2. As to Al2O3, K2O, and Na2O results are not conclusive and are statistically disperse. Thermal property knowledge especially thermal conductivity and its application in the building construction field appeared to be very satisfactory for it involves both technological and thermal comfort aspects, which favored in all cases fast, cheap, and precise results. The relation between thermal conductivity and linear thermal dilatation have also shown satisfactory results especially when it comes to the quartz role as a common, determining phase between the two variables. Thermal conductivity studies together with rocky material density can function as an additional tool for choosing materials when considering structural calculation aspects and thermal comfort, for in the dimension stone case there is a small density variation in relation to a thermal conductivity considerable variation

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Estudos de pesquisa mineral são fundamentais para o reconhecimento e a incorporação de novas reservas. Esse trabalho apresenta os resultados de aplicação do método geofísico da eletrorresistividade numa ocorrência mineralizada em carbonatos de cobre, por meio da técnica de caminhamento elétrico em arranjo azimutal. A área de estudos está inserida na bacia sedimentar do Camaquã, formada por um conjunto de unidades estratigráficas sedimentares e vulcanogênicas, onde são descritas diversas ocorrências cupríferas. A presença de azurita e malaquita em fraturas e zonas de maior porosidade em arenito encaixante define a geologia local. Os modelos de inversão revelam anomalias circulares de resistividade moderada para até 25m abaixo da ocorrência aflorante e anomalias de baixa resistividade em profundidades abaixo de 25m, além de áreas adjacentes com alta resistividade. Indicadores de mineralização descritos para ocorrências de cobre estudadas, no âmbito da bacia sedimentar do Camaquã, ocorrem na área de estudos e permitem caracterização em termos de resistividade elétrica. Áreas com silicificação apresentam alta resistividade, enquanto que valores intermediários são atribuídos a zonas com carbonatação e, finalmente, áreas de baixa resistividade, provavelmente, indicam concentrações de sulfetos disseminados.

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The Rio Branco Rapakivi Batholith belongs to the Cachoeirinha Tectonic Domain, part of the Rio Negro-Juruena Geochronological Province located on the southwestern portion of the Amazonian Craton in Mato Grosso, Central Brasil. A systematic geological mapping on a 1:100.000 scale, coupled with petrographic and geochemical studies allowed to redefine this batholithic unit, to recognize faciological variations and to characterize the geochemical features of this rapakivi magmatism. The batholith is constituted by two major plutonic suites, the first forming a basic suite of fine-grained, equigranular, mesoto melanocratic gray to black lithotypes, with usually discontinuous porphyritic varieties located near the margins of the intrusion. The second one is characterized by acid to intermediate rocks constituted by porphyritic granites, in part granophyric, with rapakivi textures. They have K-feldspar phenocrysts of up to 4cm. Three distinct petrographic facies are recognized in this suite: 1. equigranular to pegmatitic monzogranites; 2. red rapakivi leuco-monzogranites; 3. dark red rapakivi monzogranites to quartz-monzonites. Rocks present SiO2 contents from 67% to 73%, show peraluminous to metaluminous compositions and define a high-K calc-alkaline to shoshonitic magmatism in an I- and A-type, post-orogenic to anorogenic intraplate environment. The magmatic processes are associated with the end of the collisional event that consolidated and stabilized the SW part of the Amazonian Craton.

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Sararé Massif occurs in the southwest Mato Grosso state intruded into Mesoproterozoic units of the Jauru Block inside the Amazonian Craton. It presents an extension of approximately 80 km2 and NW-SE tectonic structures control the elongated shape. It is constituted by three major monzogranitic petrographic facies, represented by leucocratic, reddish, isotropic, equi-inequigranular to locally porphyritic rocks. The composition indicates S-type, peraluminous, with indicatives of late- to post-kinematic magmatism. Geochronological studies with 40Ar/39Ar in biotites and muscovites resulted in ages of 903 to 906 Ma was interpreted as massif rocks cooling period and U-PB 917 ± 18 Ma. ages points to the crystallization of the intrusive body. The massif is formed by melting of material of the upper crust, in an environment of continental collision and/or of post-collisional decompression at the ending of the Aguapeí-Sunsás event, in more stable environments of consolidation and tectonic stabilization of the Amazonian Craton.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

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O Granito Seringa, com cerca de 2250 km2 de superfície afl orante, representa o maior batólito da Província Carajás. É intrusivo em unidades arqueanas do Terreno Granito-Greenstone de Rio Maria, sudeste do Cráton Amazônico. É constituído por dois grandes conjuntos petrográficos: a) rochas monzograníticas, representadas por bitotita-anfibólio monzogranito grosso (BAMGrG) e anfibólio-bitotita monzogranito grosso (ABMGrG); b) rochas sienograníticas, representadas por anfibólio-biotita sienogranito porfirítico (ABSGrP), leucosienogranito heterogranular (LSGrH), leucomicrosienogranito (LMSGr) e anfibólio-biotita sienogranito heterogranular (ABSGrH). Biotita e anfibólio são os minerais varietais e zircão, apatita, minerais opacos e allanita, os acessórios. O Granito Seringa mostra caráter subalcalino, metaluminoso a fracamente peraluminoso e possui altas razões FeOt/FeOt+MgO (0,86 a 0,97) e K2O/Na2O (1 a 2). Os ETR mostram padrão de fracionamento moderado para os ETRL e sub-horizontalizado para os ETRP. As anomalias negativas de Eu são fracas nas rochas monzograníticas e moderadas a acentuadas nas sienograníticas e leucomonzograníticas, respectivamente, com exceção dos ABSGrP. Mostra afinidades geoquímicas com granitos intraplacas ricos em ferro, do subtipo A2 e do tipo A oxidados. As relações de campo e os aspectos petrográficos e geoquímicos não são coerentes com a evolução das fácies do Granito Seringa a partir da cristalização fracionada de um mesmo pulso magmático. O Granito Seringa apresenta maiores semelhanças petrográficas, geoquímicas e de suscetibilidade magnética com as rochas da Suíte Serra dos Carajás, podendo ser enquadrado nesta importante suíte granitoide.

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O depósito de ouro São Jorge, de idade paleoproterozóica, está situado na Província Aurífera do Tapajós, Cráton Amazônico. Ele está hospedado em um anfibólio-biotita-monzogranito constituído por quartzo, feldspato potássico, plagioclásio, anfibólio, biotita, titanita e opacos. Quatro associações minerais foram reconhecidas no depósito. A associação 1, formada durante o estágio magmático, é caracterizada pela presença de anfibólio e andesina-oligoclásio. A associação 2 mostra substituição total do anfibólio e intensa saussuritização do plagioclásio primário; o epidoto é uma fase marcante e a biotita é parcialmente cloritizada. As associações 3 e 4 estão relacionadas aos processos hidrotermais que geraram a mineralização de sulfeto e ouro. A assembléia 3 é dominada por clorita e plagioclásio albítico, com quantidade subordinada de mica branca e, por vezes, biotita. A associação 4 é dominada por mica branca, pirita e carbonatos sendo o resultado de uma alteração fílica com carbonatação associada. O geotermômetro da clorita sugere temperaturas de 300±40 °C para as associações 3 e 4. O geobarômetro do Al na hornblenda indica pressões em torno de 1 kbar para a cristalização dos granitos mineralizados. Condições oxidantes, acima do tampão NNO, prevaleceram durante a gênese dos depósitos. As associações hidrotermais de São Jorge diferem daquelas descritas nos garimpos Joel e Davi e não são dominadas por epidoto, como sugerido em outras áreas da Província Tapajós. Um modelo pórfiro ou intrusion-related são melhor adaptados para o depósito São Jorge. Este último tem similaridades com o depósito Serrinha da Província Juruena e Batalha, na Província Tapajós, e fortes analogias com o sistema hidrotermal Volta Grande no sul do Brasil.