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1.
The geochemical and isotopic compositions of river water are controlled by different factors. The seasonal and spatial variations in the geochemical composition, δD, δ18O, and δ15N–NO3 of the Kumho River were investigated to reveal the geochemical processes occurring at different seasons. The Kumho River, which runs through different geologic terrains with different land use characteristics, is the largest tributary of the Nakdong River, the longest river in South Korea. The data varied significantly according to the land use and the season. Each monitoring station showed the lowest concentrations of various ions during July, the rainy season, due to the increase of precipitation rate. The ionic concentrations gradually increased downstream by the mineral weathering and anthropogenic activity. At the upper regions of the river, Ca and HCO3, which are closely associated with mineral weathering, were the most dominant cation and anion, respectively. The relatively high Si concentration of the headwater samples, caused by the weathering of volcanic rocks, also showed the importance of weathering in the upper regions mainly composed of volcanic rocks. The downstream regions of the Kumho River are mainly influenced by sedimentary rocks. At the lower reaches of the river, especially near the industrial complexes in Daegu, the third largest city in Korea, Na, Cl, and SO4 became the dominant ions, indicating that the anthropogenic pollution became more important in regulating the chemical composition of the river. The increasing (Ca + Mg + Na + K)/HCO3 ratio downstream also indicates that the anthropogenic effects became more important as the river flows downstream. The isotopic compositions of δD and δ18O indicate that the river waters were significantly affected by evaporation during May and July, but the evaporation effect was relatively low during October. The isotopic composition of δ15N–NO3 increased downstream, also confirming that anthropogenic effects became more significant at the lower reach of the river and near Daegu. 相似文献
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《地学前缘(英文版)》2023,14(2):101517
We present in situ trace element and Nd isotopic data of apatites from metamorphosed and metasomatized (i.e., altered) and unaltered granitoids in the Songnen and Jiamusi massifs in the eastern Central Asian Orogenic Belt, with the aim of fingerprinting granitoid petrogenesis, including both the magmatic and post-magmatic evolution processes. Apatites from altered granitoids (AG) and unaltered granitoids (UG) are characterized by distinct textures and geochemical compositions. Apatites from AG have irregular rim overgrowths and complex internal textures, along with low contents of rare earth elements (REEs), suggesting the re-precipitation of apatite during epidote crystallization and/or leaching of REEs from apatite by metasomatic fluids. εNd(t) values of the these apatites are decoupled from zircon εHf(t) values for most samples, which can be attributed to the higher mobility of Nd as compared to Sm in certain fluids. Apatites from UG are of igneous origin based on their homogeneous or concentric zoned textures and coupled Nd-Hf isotopic compositions. Trace element variations in igneous apatite are controlled primarily by the geochemical composition of the parental melt, fractional crystallization of other REE-bearing minerals, and changes in partition coefficients. Sr contents and Eu/Eu* values of apatites from UG correlate with whole-rock Sr and SiO2 contents, highlighting the effects of plagioclase fractionation during magma evolution. Apatites from UG can be subdivided into four groups based on REE contents. Group 1 apatites have REE patterns similar to the host granitoids, but are slightly enriched in middle REEs, reflecting the influence of the parental melt composition and REE partitioning. Group 2 apatites exhibit strong light REE depletions, whereas Group 3 apatites are depleted in middle and heavy REEs, indicative of the crystallization of epidote-group minerals and hornblende before and/or during apatite crystallization, respectively. Group 4 apatites are depleted in heavy REEs, but enriched in Sr, which are features of adakites. Some unusual geochemical features of the apatites, including the REE patterns, Sr contents, Eu anomalies, and Nd isotopic compositions, indicate that inherited apatites are likely to retain the geochemical features of their parental magmas, and thus provide a record of small-scale crustal assimilation during magma evolution that is not evident from the whole-rock geochemistry. 相似文献
4.
成矿热液的氢、氧同位素组成与其水的类型、水/岩交换的岩石成分和同位素组成、水/岩交换时的温度及水/岩交换程度(W/R比值大小)等诸多因素有关,微生物和有机质也对其有一定的影响。因此,仅通过简单投影的方法将成矿热液的氢、氧同位素值与一些所谓的标准值进行类比,由此就推断出热液中水的来源,这种方法是不可取的;尤其当成矿热液的氢、氧同位素值介于大气降水和岩浆水的值之间时,切忌滥用两种水混合成矿模式,因为实际情况往往并不是这样。本文以胶东乳山金矿床为例,展开了这方面的讨论。 相似文献
5.
Elisa Sacchi Gian Maria Zuppi Luca Pizzino Fedora Quattrocchi Salvatore Lombardi 《Aquatic Geochemistry》2008,14(4):301-319
The EC funded Geochemical Seismic Zonation program (EEC GSZ Project 1996–1998) chose Sardinia as a low-seismicity site, in which the relationships between fluid geochemistry and seismo-tectonics
had to be investigated and results compared with outcomes from other selected high-seismicity sites. A first article, examining
the role of fault segmentation and seismic quiescence on the geochemical composition of groundwaters and gases, has already
been presented (Angelone et al. 2005). This article deals with environmental isotopes which, together with selected hydrochemical data, give hints on tectonically-related
fluid circulations. Four water-dominated hydrothermal systems were considered, all located along regional fault systems and
discharging groundwaters belonging to the Na–HCO3 and Na–Cl facies. In the considered systems, groundwater circulation takes place, principally, in the Palaeozoic Crystalline
Basement (PCB), with the exception of the Logudoro system, where hydrological circuits develop in the Mesozoic Carbonate Platform
(MCP). The high CO2 contents, the non-attainment of fluid-rock equilibrium and the large lithological variability prevent the construction of
a unique hydrogeological–geochemical conceptual model. In this case, stable isotopes provide a useful tool to describe the
origin of fluids and their subterranean movements. Stable isotopes of water, integrated with hydrochemical data, indicate
that fluids are derived from three main end members. The dominant component is a relatively recent local meteoric water; the
second one is marine water; and the third one is a fossil freshwater, depleted in heavy isotopes with respect to modern rains.
The latter end member entered the aquifer system in the past, when climatic conditions were greatly different from today.
At least two circulation systems can be recognised, namely a shallow cold system and a deep hydrothermal system, as well as
two distinct hydrological processes: (1) gravity-controlled descent of cold water towards greater depths and (2) convection
linked to a thermal gradient, causing deep fluids to rise up from the hydrothermal reservoir towards the surface. The highly
variable δ13CTDIC values suggest the presence of two distinct CO2 sources, namely, a biogenic one and a thermogenic one. The relation between the isotopic compositions of CO2 and He indicates an increased mantle signature in uprising CO2-rich fluids. 相似文献
6.
Niutuozhen geothermal field is located in the Jizhong graben, belonging to the northern part of Bohai Bay Basin in North China. Chemical and isotopic analyses were carried out on 14 samples of the geothermal fluids discharged from Neogene Minghuazhen (Nm), Guantao (Ng), and Jixianian Wumishan (Jxw) formations. The δ2H and δ18O in water, δ13C in CH4, δ13C in CO2, and 3He/4He ratio in the gases were analyzed in combination with chemical analyses on the fluids in the Niutuozhen geothermal field. The chemical and isotopic compositions indicate a meteoric origin of the thermal waters. The reservoir temperatures estimated by chemical geothermometry are in the range between 60 and 108 °C. The results show that the gases are made up mainly by N2 (18.20–97.42 vol%), CH4 (0.02–60.95 vol%), and CO2 (0.17–25.14 vol%), with relatively high He composition (up to 0.52 vol%). The chemical and isotopic compositions of the gas samples suggest the meteoric origin of N2, predominant crustal origins of CH4, CO2, and He. The mantle-derived He contributions are calculated to be from 5 to 8% based on a crust–mantle binary mixing model. The deep temperatures in the Jxw reservoir were evaluated based on gas isotope geothermometry to be in the range from 141 to 165 °C. The mantle-derived heat fraction in the surface heat flow is estimated to be in the range of 48–51% based on 3He/4He ratios. 相似文献
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《International Geology Review》2012,54(4):411-429
The Bairendaba vein-type Ag–Pb–Zn deposit, hosted in a Carboniferous quartz diorite, is one of the largest polymetallic deposits in the southern Great Xing'an Range. Reserves exceeding 8000 tonnes of Ag and 3 million tonnes of Pb?+?Zn with grades of 30 g/t and 4.5% have been estimated. We identify three distinct mineralization stages in this deposit: a barren pre-ore stage (stage 1), a main-ore stage with economic Ag–Pb–Zn mineralization (stage 2), and a post-ore stage with barren mineralization (stage 3). Stage 1 is characterized by abundant arsenopyrite?+?quartz and minor pyrite. Stage 2 is represented by abundant Fe–Zn–Pb–Ag sulphides and is further subdivided into three substages comprising the calcite–polymetallic sulphide stage (substage 1), the fluorite–polymetallic sulphide stage (substage 2), and the quartz–polymetallic sulphide stage (substage 3). Stage 3 involves an assemblage dominated by calcite with variable pyrite, galena, quartz, fluorite, illite, and chlorite. Fluid inclusion analysis and mineral thermometry indicate that the three stages of mineralization were formed at temperatures of 320–350°C, 200–340°C, and 180–240°C, respectively. Stage 1 early mineralization is characterized by low-salinity fluids (5.86–8.81 wt.% NaCl equiv.) with an isotopic signature of magmatic origin (δ18Ofluid = 10.45–10.65‰). The main ore minerals of stage 2 precipitated from aqueous–carbonic fluids (4.34–8.81 wt.% NaCl equiv.). The calculated and measured oxygen and hydrogen isotopic compositions of the ore-forming aqueous fluids (δ18Ofluid = 3.31–8.59‰, δDfluid?=??132.00‰ to??104.00‰) indicate that they were derived from a magmatic source and mixed with meteoric water. Measured and calculated sulphur isotope compositions of hydrothermal fluids (δ34S∑S?=??1.2–3.8‰) indicate that the ore sulphur was derived mainly from a magmatic source. The calculated carbon isotope compositions of hydrothermal fluids (δ13Cfluid?=??26.52‰ to??25.82‰) suggest a possible contribution of carbon sourced from the basement gneisses. The stage 3 late mineralization is dominated (1.40–8.81 wt.% NaCl equiv.) by aqueous fluids. The fluids show lower δ18Ofluid (?16.06‰ to??0.70‰) and higher δDfluid (?90.10‰ to??74.50‰) values, indicating a heated meteoric water signature. The calculated carbon isotope compositions (δ13Cfluid?=??12.82‰ to??6.62‰) of the hydrothermal fluids in stage 3 also suggest a possible contribution of gneiss-sourced carbon. The isotopic compositions and fluid chemistry indicate that the ore mineralization in the Bairendaba deposit was related to Early Cretaceous magmatism. 相似文献
9.
《Resource Geology》2018,68(3):227-243
As a newly discovered medium‐sized deposit (proven Pb + Zn resources of 0.23 Mt, 9.43% Pb and 8.73% Zn), the Dongzhongla skarn Pb–Zn deposit is located in the northern margin of the eastern Gangdese, central Lhasa block. Based on the geological conditions in this deposit of ore‐forming fluids, H, O, C, S, Pb, Sr, and noble gas isotopic compositions were analyzed. Results show that δ18OSMOW of quartz and calcite ranged from −9.85 to 4.17‰, and δDSMOW ranged from −124.7 to −99.6‰ (where SMOW is the standard mean ocean water), indicating magma fluids mixed with meteoric water in ore‐forming fluids. The δ13CPDB and δ18OSMOW values of calcite range from −1.4 to −1.1‰ and from 5.3 to 15.90‰, respectively, show compositions consistent with the carbonate limestone in the surrounding rocks, implying that the carbon was primarily sourced from the dissolution of carbonate strata in the Luobadui Formation. The ore δ34S composition varied in a narrow range of 2.8 to 5.7‰, mostly between 4‰ and 5‰. The total sulfur isotopic value δ34S was 4.7‰ with characteristics of magmatic sulfur. The 3He/4He values of pyrite and galena ranged from 0.101 to 5.7 Ra, lower than those of mantle‐derived fluids (6 ± 1 Ra), but higher than those of the crust (0.01–0.05 Ra), and therefore classified as a crust–mantle mixed source. The Pb isotopic composition for 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb values of the ores were in the ranges of 18.628–18.746, 15.698–15.802, and 39.077–39.430, respectively, consistent with the Pb isotopic composition of magmatic rocks in the deposit, classified as upper‐crust lead. The ore lead was likely sourced partially from the crustal basement of the Lhasa Terrane. The initial (87Sr/86Sr)i value from five sulfide samples ranged from 0.71732 to 0.72767, and associated ore‐forming fluids were mainly sourced from the partial melting of the upper‐crust materials. Pb isotopic compositions of ore sulfides from the Dongzhongla deposit are similar to that of the Yuiguila and Mengya'a deposit, indicating that they have similar sources of metal‐rich ore‐forming solution. According to basic skarn mineralogy, the economic metals, and the origin of the ore‐forming fluids, the Dongzhongla deposit was classified as a skarn‐type Pb–Zn deposit. 相似文献
10.
There has been little research on geochemistry and isotopic compositions in tholeiites of the Northern region from the Paraná Continental Flood Basalts (PCFB), one of the largest continental provinces of the world. In order to examine the mantle sources involved in the high-Ti (Pitanga and Paranapanema) basalt genesis, we studied Sr, Nd, and Pb isotopic systematics, and major, minor and incompatible trace element abundances. The REE patterns of the investigated samples (Pitanga and Paranapanema magma type) are similar (parallel to) to those of Island Arc Basalts' REE patterns. The high-Ti basalts investigated in this study have initial (133 Ma) 87Sr/86Sr ratios of 0.70538–0.70642, 143Nd/144Nd of 0.51233–0.51218, 206Pb/204Pb of 17.74–18.25, 207Pb/204Pb of 15.51–15.57, and 208Pb/204Pb of 38.18–38.45. These isotopic compositions do not display any correlation with Nb/Th, Nb/La or P2O5/K2O ratios, which also reflect that these rocks were not significantly affected by low-pressure crustal contamination. The incompatible trace element ratios and Sr–Nd–Pb isotopic compositions of the PCFB tholeiites are different to those found in Tristan da Cunha ocean island rocks, showing that this plume did not play a substantial role in the PCFB genesis. This interpretation is corroborated by previously published osmium isotopic data (initial γOs values range from +1.0 to +2.0 for high-Ti basalts), which also preclude basalt generation by melting of ancient subcontinental lithospheric mantle. The geochemical composition of the northern PCFB may be explained through the involvement of fluids and/or small volume melts related to metasomatic processes. In this context, we propose that the source of these magmas is a mixture of sublithospheric peridotite veined and/or interlayered with mafic components (e.g., pyroxenites or eclogites). The sublithospheric mantle (dominating the osmium isotopic compositions) was very probably enriched by fluids and/or magmas related to the Neoproterozoic subduction processes. This sublithospheric mantle region may have been frozen and coupled to the base of the Parana basin lithospheric plate above which the Paleozoic subsidence and subsequent Early Cretaceous magmatism occurred. 相似文献
11.
Huang Jizhong 《中国地球化学学报》1991,10(1):45-57
This paper is the continuation of the paper published in 1985, with the emphasis on the irregular components of natural gases from the Sichuan Basin—the isotopic compositions of C,H and S, the n-and iso-alkane predominance (C6-C13) of methane homologues, the compositional characteristics of benzene and methylbenzene, and the distribution and geochemical characteristics of organic sulfur-bearing compounds including thiophen, thio-alcohol, etc. It is considered that natural gases from the Sichuan Basin have different distributional characteristics in different layers and locations, suggesting that they are controlled by a combination of factors such as kerogen type, maturity of organic matter and wall-rock assemblage.
- The type of source material (or precursor) is a main factor affecting the geochemical characteristics of natural gases. T3x-h and P2l produce coal-series gases with type-III source material dominant. The C and H isotopic compositions of natural gases are heavier, the contents of C6H6 and C7H8 are high, C7H8/C6H6 < 1. the content of C4H4S is low, and the predominance in isoalkane (C6C13) is obvious. J1t. P1y. Z2b. etc. produce oil-series gases with type-I and -II kerogens dominant, indicating that the geochemical characteristics of natural gases are different from those described above.
- The maturity of organic matter is an important factor affecting the composition of natural gases.With increasing maturity of organic matter, the C and H isotopic compositions tend to become light. C1 and C2 isotopic values are nearly equal or even inverse, and C4H4S decreases in content.
- Wall-rock assemblage has apparent influence on the S isotopic composition. The Middle-Lower Triassic series belongs to sulfate-carbonate formations enriched in gypsum. Therefore, the (δ34S values of natural gases are relatively high (< 20 %.) against the lower values for other layers due to the absence of gypsum layers.
12.
《Applied Geochemistry》2000,15(2):211-234
Fluid chemistry and the hydraulic regime in a marl formation of the Swiss Alps were studied by a number of techniques. Fluid inclusions record the conditions of maximum burial and regional low-temperature metamorphism, whereas fluid samples and hydraulic tests derived from deep boreholes reflect present-day, near-surface conditions. The characterization of the different types of fluids places constraints on the geochemical and hydraulic evolution of low-permeability argillaceous rocks during uplift and exhumation.Fluid inclusions were studied by microthermometry and sampled directly by decrepitation techniques. They contain a two-phase system consisting of an aqueous fluid and a coexisting CH4-rich gas (T=190–250°C, Plith≈2500 bar). Bulk and isotopic compositions of aqueous fluid inclusions are consistent with a mixture of connate seawater and water derived from the dehydration of clay minerals. Methane was generated in situ by thermal cracking of kerogen. Textural evidence and stable isotopic signatures of carbonates in veins and in the rock matrix indicate local buffering of fluid compositions and very low water/rock ratios. Free fluids residing in the present-day fracture and matrix porosity consist of CH4-saturated Na–Cl groundwater with minute amounts of free CH4 gas which occurs in druses. Their chemical and isotopic compositions are very similar to those of the fluid inclusions, suggesting a common origin. Post-metamorphic admixtures of externally derived waters cannot be identified, and it is suggested that present-day Na–Cl groundwaters that occur in the central parts of the marl have resided in the formation since the time of metamorphism some 20 Ma b.p. The only major change in the fluid composition has been the outgassing of CH4 from the formation, most probably by diffusion.The hydraulic regime during metamorphism was characterized by localized fluid underpressures in open veins because widely scattered, sub-hydrostatic pressures were often identified in fluid inclusions. The central part of the argillaceous rock body, approximately coinciding with the region where Na–Cl groundwaters occur, has sub-hydrostatic pressures today, as indicated by hydraulic tests in deep boreholes.Both the closed-system behavior derived from the chemical and isotopic characteristics of the fluids and the (recurrent or continuous) existence of hydraulic underpressures suggest very low permeabilities of argillaceous rocks during metamorphism and throughout subsequent uplift and exhumation. All fluids present in the central parts of the formation are either connate or produced in situ. Even though major events of brittle faulting and unloading due to uplift occurred since the peak of metamorphism, fluid flow through the formation has been negligible. 相似文献
13.
Yan Shuang Xian-Wu Bi Rui-Zhong Hu Jian-Tang Peng Hang Li Da-Hua Li Chang-Sheng Zhu 《Resource Geology》2010,60(1):18-34
The Furong tin deposit in the central Nanling region, South China, consists of three main types of mineralization ores, i.e. skarn-, altered granite- and greisen-type ores, hosted in Carboniferous and Permian strata and Mesozoic granitic intrusions. Calcite is the dominant gangue mineral intergrown with ore bodies in the orefield. We have carried out REE, Mn, Fe, and Mg geochemical and C, and O isotopic studies on calcites to constrain the source and evolution of the ore-forming fluids. The calcites from the Furong deposit exhibit middle negative Eu anomaly (Eu/Eu*= 0.311–0.921), except for one which has an Eu/Eu* of 1.10, with the total REE content of 5.49–133 ppm. The results show that the calcites are characterized by two types of REE distribution patterns: a LREE-enriched pattern and a flat REE pattern. The LREE-enriched pattern of calcites accompanying greisen-type ore and skarn-type ore are similar to those of Qitianling granite. The REE, Mn, Fe, and Mg abundances of calcites exhibit a decreasing tendency from granite rock mass to wall rock, i.e. these abundances of calcites associated with altered granite-type and greisen-type ores are higher than those associated with skarn-type ores. The calcites from primary ores in the Furong deposit show large variation in carbon and oxygen isotopic compositions. The δ13C and δ18O of calcites are −0.4 to −12.7‰ and 2.8 to 16.4‰, respectively, and mainly fall within the range between mantle or magmatic carbon and marine carbonate. The calcites from greisen and altered granite ores in the Furong deposit display a negative correlation in the diagram of δ13C versus δ18O, probably owing to the CO2-degassing of the ore-forming fluids. From the intrusion to wall-rock, the calcites display an increasing tendency with respect to δ13C values. This implies that the carbon isotopic compositions of the ore-bearing fluids have progressively changed from domination by magmatic carbon to sedimentary carbonate carbon. In combination with other geological and geochemical data, we suggest that the ore-forming fluids represent magmatic origin. We believe that the fluids exsolved from fractionation of the granitic magma, accompanying magmatism of the Qitianling granite complex, were involved in the mineralization of the Furong tin polymetallic deposit. 相似文献
14.
He-Ar Isotopic Systematics of Fluid Inclusions in Pyrites from PGEpolymetallic Deposits in Lower Cambrian Black Rock Series, South China 总被引：6，自引：1，他引：5
SUN Xiaoming WANG Min XUE Ting MA Mingyang LI YinheDepartment of Earth Sciences Sun Yat-sen University Guangzhou Guangdong State Key Laboratory for Mineral Deposits Research Nanjing University Nanjing Jiangsu Institute of Mineral Resources Chinese Academy of Geological Sciences Beijing 《《地质学报》英文版》2004,78(2):471-475
He-Ar isotopic compositions of fluid inclusions trapped in pyrites from some representative PGE-polymetallic deposits in Lower Cambrian black rock series in South China were analyzed by using an inert gas isotopic mass spectrometer. The results show that the ore-forming fluids possess a low 3He/4He ratio, varying from 0.43×10-8 to 26.39×10-8, with corresponding R/Ra value of 0.003-0.189. The 40Ar/36Ar ratios are 258-287, close to those of air saturated water (ASW). He-Ar isotopic indicator studies show that the ore-forming fluids were mainly derived from the formation water or basinal hot brine and sea water, while the content of mantle-derived fluid or deep-derived magmatic water might be negligible. The PGE-polymetallic mineralization might be related to the evolution of the Caledonian miogeosynclines distributed along the southern margin of the Yangtze Craton. During the Early Cambrian, the formation water or basinal hot brine trapped in Caledonian basins which accumulated giant thick sediments was 相似文献
15.
弧后盆地玄武岩(BABB)是弧后盆地扩张过程中岩浆作用的主要产物,其地球化学组成是认识弧后盆地演化的关键。现今弧后盆地主要集中在西太平洋地区。本文总结了该地区弧后盆地玄武岩的元素地球化学和同位素组成特征。总体而言,相对于开阔大洋洋中脊玄武岩(MORB),弧后盆地玄武岩的主量元素成分变化范围很大,在Al_2O_3-Mg O、Ti O_2-Mg O相关图上偏离了MORB的演化趋势,在Mg O相同的情况下表现出更高的Al_2O_3含量和更低的Ti O_2含量。弧后盆地玄武岩的微量元素特征一般介于MORB和弧玄武岩之间。一方面,它们与MORB一样在中、重稀土元素之间没有明显分馏;另一方面,与弧玄武岩一样富集大离子亲石元素Rb、Ba、Th、U、K,具有Pb的正异常和Nb、Ta的负异常等。其中,劳海盆、日本海海盆和冲绳海槽有部分样品具有Nb、Ta的正异常,表现出类似于E-MORB的微量元素特征。西太平洋地区弧后盆地玄武岩的Sr-Nd-Pb同位素组成变化范围较大,相对于MORB,其富集组分更常见,总体介于亏损地幔端元(DMM)、1型富集地幔(EM1)和2型富集地幔(EM2)三者之间。不同基底属性(大陆基底和大洋基底)和不同阶段的弧后盆地玄武岩的地球化学组成也有明显区别。弧后盆地玄武岩地球化学成分上的多样性主要受控于源区(地幔楔)的物质组成、熔融程度和岩浆上升过程中的变化等因素。地幔源区的不均一性主要体现在地幔楔自身的化学性质和俯冲板片的物质贡献差异。部分弧后盆地玄武岩具有异常高的地幔潜能温度、高的3He/4He比值以及E-MORB型的微量元素特征,说明其地幔源区还可能受到了地幔柱的影响。地幔潜能温度越高,俯冲流体贡献越多,地幔楔的熔融程度越大。此外,岩浆上升过程中发生的地壳混染、岩石圈中的熔体-岩石反应以及矿物的结晶分离都会改造岩浆的成分。 相似文献
16.
Whole rock trace element and isotopic compositions of different HP–LT metamorphic rocks of the Ile de Groix were analysed to characterise geochemical fingerprints during subduction and exhumation in a late Palaeozoic HP metamorphic terrain. Massive metabasites of hydrothermally altered enriched mid-ocean ridge basalt (E-MORB) origin are in association with banded metabasic rocks of volcano-sedimentary origin and metapelites. Fluid-rock interactions that likely occurred during seafloor hydrothermal alteration and early subduction metasomatism increased δ18O values, as well as K2O, Na2O, MgO, and LILE contents and decreased CaO contents of metabasites. Most metabasites have retained their early-subduction and pre-HP trace element and isotopic composition, even for rocks metamorphosed to lower eclogite-facies P–T conditions. Micaschists also preserved apparent pelitic protolith trace element values and oxygen isotopic compositions. During retrograde metamorphism related to the exhumation, metabasites were rehydrated by fluids in equilibrium with the host rock compositions, which were likely derived from the basic rocks. This style of fluid–rock interaction formed a greenschist facies mineral assemblage. Metabasites that underwent pervasive alteration by seafloor hydrothermal and metasomatism processes prior to peak metamorphism, show greater effects of retrogression and albitisation, probably because they were richer in H2O and Na2O. The variety of metamorphic assemblages on the Ile de Groix is thus directly related to the pre-HP rock composition. The extent of retrogression in the western part of the Ile de Groix primarily reflects stronger metasomatic intensities than in the eastern part. 相似文献
17.
Li Songtao Xia Yong Liu Jianzhong Xie Zhuojun Tan Qinping Zhao Yimeng Meng Minghua Tan Lijin Nie Rong Wang Zepeng Zhou Guanghong Guo Haiyan 《中国地球化学学报》2019,38(4):587-609
The newly discovered Baogudi gold district is located in the southwestern Guizhou Province, China, where there are numerous Carlin-type gold deposits. To better understand the geological and geochemical characteristics of the Baogudi gold district, we carried out petrographic observations, elemental analyses, and fluid inclusion and isotopic composition studies. We also compared the results with those of typical Carlin-type gold deposits in southwestern Guizhou. Three mineralization stages, namely, the sedimentation diagenesis, hydrothermal (main-ore and late-ore substages), and supergene stages, were identified based on field and petrographic observations. The main-ore and late-ore stages correspond to Au and Sb mineralization, respectively, which are similar to typical Carlin-type mineralization. The mass transfer associated with alteration and mineralization shows that a significant amount of Au, As, Sb, Hg, Tl, Mo, and S were added to mineralized rocks during the main-ore stage. Remarkably, arsenic, Sb, and S were added to the mineralized rocks during the late-ore stage. Element migration indicates that the sulfidation process was responsible for ore formation. Four types of fluid inclusions were identified in ore-related quartz and fluorite. The main-ore stage fluids are characterized by an H2O–NaCl–CO2–CH4 ± N2 system, with medium to low temperatures (180–260 °C) and low salinity (0–9.08% NaCl equivalent). The late-ore stage fluids featured H2O–NaCl ± CO2 ± CH4, with low temperature (120–200 °C) and low salinity (0–7.48% NaCl equivalent). The temperature, salinity, and CO2 and CH4 concentrations of ore-forming fluids decreased from the main-ore stage to the late-ore stage. The calculated δ13C, δD, and δ18O values of the ore-forming fluids range from − 14.3 to − 7.0‰, −76 to −55.7‰, and 4.5–15.0‰, respectively. Late-ore-stage stibnite had δ34S values ranging from − 0.6 to 1.9‰. These stable isotopic compositions indicate that the ore-forming fluids originated mainly from deep magmatic hydrothermal fluids, with minor contributions from strata. Collectively, the Baogudi metallogenic district has geological and geochemical characteristics that are typical of Carlin-type gold deposits in southwest Guizhou. It is likely that the Baogudi gold district, together with other Carlin-type gold deposits in southwestern Guizhou, was formed in response to a single widespread metallogenic event.
相似文献18.
The Tiemurt Pb-Zn-Cu deposit (metal reserve: 0.29 Mt (Pb + Zn) and 0.14 Mt Cu) is hosted in the Kangbutiebao Formation volcanic-sedimentary rocks in the Chinese Altay Orogen, NW China. Although some geological and geochemical characteristics of primary seafloor sedimentary mineralization are preserved, major fault-controlled Pb-Zn-Cu orebodies are adjacent to the Sarekbuobu orogenic gold deposit, and therefore it is also interpreted to be closely related to regional deformational-metamorphic processes. The seafloor sedimentary mineralization is evidenced by the occurrence of the banded ores and marine sulfate-originated sulfur isotopic compositions of the sulfides (bimodal δ34S values of 17.29–18.67‰ and −25.03 to −17.58‰). The lead isotope compositions accord with the evolution line of mantle, implying that the Pb were chiefly sourced from the mantle-reservoir. The later deformational and metamorphic overprinting are recorded by the fault-controlled lodes with ore textures of epigenetic infilling and replacement. Besides well-developed CO2-rich fluid inclusions, the D-O isotopic data of the overprinting fluids fall into the area between metamorphic fluids and meteoric water line, indicative of metamorphic fluids origin with meteoric water involvement. To further trace the Pb-Zn-Cu accumulation and remobilization processes, systematic in-situ trace elements in sulfides of different generations are analyzed using LA-ICP-MS. Ti-Mn-Cu-Pb-Zn-Bi concentrations in pyrite show a trend of progressive decrease from early to late generations. Similar decreasing trends of trace element concentrations are also present in sphalerite, galena, chalcopyrite and pyrrhotite, although the combinations of trace element are slightly different. This indicates that the ore-forming metals (esp. Cu, Pb and Zn) were initially locked up in the crystal lattice of the VMS sulfides (especially pyrite). Deformational and metamorphic processes of the primary ores during the Permian-Triassic collisional orogeny have likely led to trace element remobilization and sulfides purification, which redistributed the metals and upgraded the ores. Combined with previous studies, we proposed that the Pb-Zn-Cu of Tiemurt had been accumulated from seafloor sedimentation (ca. 400 Ma) to deformation-metamorphism processes (ca. 240 Ma). 相似文献
19.
Samuel Y. Ganyaglo Shiloh Osae Samuel B. Dampare Joseph R. Fianko Mohammad A. H. Bhuiyan Abass Gibrilla Edward Bam Elikem Ahialey Juliet Osei 《Environmental Earth Sciences》2012,66(2):573-587
Insufficient knowledge of the hydrogeochemistry of aquifers in the Central Region of Ghana has necessitated a preliminary water quality assessment in some parts of the region. Major and minor ions, and trace metal compositions of groundwater have been studied with the aim of evaluating hydrogeochemical processes that are likely to impair the quality of water in the study area. The results show that groundwater in the area is weakly acidic with mean acidity being 5.83 pH units. The dominant cation in the area is Na, followed by K, Ca, and Mg, and the dominant anion is Cl?, followed by HCO3 ? and SO4 2?. Two major hydrochemical facies have been identified as Na–Cl and Na–HCO3, water types. Multivariate statistical techniques such as cluster analysis (CA) and factor analysis/principal component analysis (PCA), in R mode, were employed to examine the chemical compositions of groundwater and to identify factors that influenced each. Q-mode CA analysis resulted in two distinct water types as established by the hydrochemical facies. Cluster 1 waters contain predominantly Na–Cl. Cluster 2 waters contain Na–HCO3 and Na–Cl. Cluster 2 waters are fresher and of good quality than cluster 1. Factor analysis yielded five significant factors, explaining 86.56% of the total variance. PC1 explains 41.95% of the variance and is contributed by temperature, electrical conductivity, TDS, turbidity, SO4 2?, Cl?, Na, K, Ca, Mg, and Mn and influenced by geochemical processes such as weathering, mineral dissolution, cation exchange, and oxidation–reduction reactions. PC2 explains 16.43% of the total variance and is characterized by high positive loadings of pH and HCO3 ?. This results from biogenic activities taking place to generate gaseous carbon dioxide that reacts with infiltrating water to generate HCO3 ?, which intend affect the pH. PC3 explains 11.17% of the total variance and is negatively loaded on PO4 3? and NO3 ? indicating anthropogenic influence. The R-mode PCA, supported by R-mode CA, have revealed hydrogeochemical processes as the major sources of ions in the groundwater. Factor score plot revealed a possible flow direction from the northern sections of the study area, marked by higher topography, to the south. Compositional relations confirmed the predominant geochemical process responsible for the various ions in the groundwater as mineral dissolution and thus agree with the multivariate analysis. 相似文献
20.
This paper investigates the isotopic composition (O, D, Sr, OSO4, SSO4, Cl, He) of a present saline fluid sample collected at the sediment/basement interface in the Permian continental formation at 634 m depth in the SE margin of the Massif Central shield (Ardèche margin of the Southeast basin of France). The fluid sample shows clear water–rock interaction processes, such as feldspar dissolution and kaolinite precipitation, which have led to high Na concentrations and water stable isotopes above the local meteoric water line. The geological formations of the SE margin of the Massif Central shield show that intensive fluid circulation phases occurred across the margin from the late Triassic to the middle Jurassic. The fluids most probably originated from fluid expulsion during burial of the thick Permo-Carboniferous sedimentary succession. These circulation phases were responsible for cementation of the margin and for the solutes in the matrix microporosity which were extracted by leaching core samples.The chemical and isotopic composition of the saline fluid sample at 634 m in the Permian rock is very similar to that of fluids in the microporosity of the rock matrix. Their SSO4, OSO4 and Sr isotopic compositions are close to those of cements investigated in fracture fillings in the same geological formations. Simple diffusion computations and comparison of the chemical composition of the present free fluid sample with matrix porosity fluids indicate that the solutes in the present free fluid sample are related to solutes originating from fluid circulation events which occurred 160–200 Ma ago through their diffusion from the matrix microporosity.A two-stage fluid flow regime is proposed to interpret the chemistry of present and paleo-fluids. (1) During the extensional context (Permian to Cretaceous), basinal brines migrated along the basement/sediment interface after expulsion from the subsiding basin. This fluid migration would be responsible for the solutes in the rock matrix microporosity and the solutes in the present free fluid sample. (2) Following the Alpine and Pyrenean compressive phases, gravity-driven meteoritic fluids slowly migrated from the surface down to the basement along major faults. This fluid regime would be responsible for the meteoric water collected in the present free fluid sample. Several investigations in Europe have shown that the existence of other saline fluids sampled elsewhere could be explained by these phases of fluid circulation related to specific geodynamic events. 相似文献