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1.
Abundant iron oxide deposits including banded iron formations, apatite iron oxide ores, and enigmatic marble/skarn-hosted magnetite deposits occur in the Palaeoproterozoic Bergslagen region, southern Sweden. During the last 100 years, the latter deposit class has been interpreted as contact metasomatic skarn deposits, metamorphosed iron formations, or metamorphosed carbonate replacement deposits. Their origin is still incompletely understood. At the Smältarmossen mine, magnetite was mined from a ca. 50-m-thick calcic skarn zone at the contact between rhyolite and stratigraphically overlying limestone. A syn-volcanic dacite porphyry which intruded the footwall has numerous apophyses that extend into the mineralized zone. Whole-rock lithogeochemical and mineral chemical analyses combined with textural analysis suggests that the skarns formed by veining and replacement of the dacite porphyry and rhyolite. These rocks were added substantial Ca and Fe, minor Mg, Mn, and LREE, as well as trace Co, Sn, U, As, and Sr. In contrast, massive magnetite formed by pervasive replacement of limestone. Tectonic fabrics in magnetite and skarn are consistent with ore formation before or early during Svecokarelian ductile deformation. Whereas a syngenetic–exhalative model has previously been suggested, our results are more compatible with magnetite formation at ca. 1.89 Ga in a contact metasomatic skarn setting associated with the dacite porphyry.  相似文献   

2.
The Chilpi Group (2050–1850 Ma) in the Bastar Craton contains Banded Iron Formation (BIF) deposited immediately after the Great Oxidation Event but before the “Proterozoic iron ore gap”. Baseline geochemical data generated from this crucial period of Earth's history representing the transition from an initial high productivity period followed by productivity collapse, thereby delaying the evolution of biota, are interpreted in terms of the redox state of the ocean and atmospheric oxygen content. Presence of chamosite, greenalite and siderite in the ironstones of the Chilpi Group, identified during present analysis, provide valuable information regarding the redox state of the shallow sea. Geochemical analyses reveal high concentrations of Fe2O3total and SiO2 (average ~ 87.85 wt%) in iron-rich bands. Trace elements commonly enriched in detrital phases (e.g. Sc, Hf, Nb, Th and Zr) show good correlation with total REE concentration, but these have concentration below the cut-off limit defined for detrital sediments (except 3 samples). Higher concentration of these elements in greenalite/chamosite-rich samples indicates accumulation of these elements in greenalite/chamosite during primary precipitation. Most of the samples have low concentrations of Al2O3 (<5 wt%) and TiO2 (<0.5 wt%), but some chamosite-bearing samples show enrichments of Al2O3 (up to ~20 wt%). Post-Archean Australian Shale normalised rare earth elements with Y (REEY) patterns, showing a superchondritic Y/Ho ratio (average 32.15) and positive La, Gd and Y anomalies, indicate the preservation of seawater like signatures. Though a low positive Eu-anomaly, and Al/(Al + Fe + Mn) versus Fe/Ti plot suggest seawater signature with possible mixing of hydrothermal fluids and/or <10 % detrital components, preservation of seawater signatures and no involvement of high-temperature hydrothermal fluids are deduced from Eu/Sm versus Sm/Yb and Eu/Sm versus Y/Ho patterns. The Eu/Sm and Y/Ho ratios lower than the seawater and a mixing trend away from oceanic hydrothermal solution indicate possible mixing of freshwater with seawater for the observed REEY patterns. Redox-sensitive trace element ratios indicate a dysoxic to suboxic-anoxic condition in the depositional basin. Presence of oolitic textures and occurrence of chamosite support the shallow water (<60 m water depth) and anoxic condition in the depositional basin. The oxygen content of 10−3–10−5 times the present atmospheric level in the atmosphere is inferred for the period during the deposition of the BIF.  相似文献   

3.
Although nitrogen in the Earth’s interior has attracted significant attention recently,it remains the most enigmatic of the light elements in the Earth’s core.In this work,synchrotron X-ray diffraction(XRD)and electrical conductivity experiments were conducted on iron nitrides(Fe2N and Fe4N)in diamond anvil cells(DACs)up to about 70 GPa at ambient temperature.These results show that iron nitrides are stable up to at least 70 GPa.From the equation of state(EOS)parameters,iron nitrides are more compressible than iron carbides.Moreover,using the van der Pauw method and Wiedemann-Franz law,the electrical and thermal conductivity of samples were determined to be much lower than that of iron carbides.The conductivities of Fe2N and Fe4N were similar at 20–70 GPa,suggesting no evident effects by varying the N stoichiometries in iron nitrides.Iron nitrides are less dense and conductive but more compressible than carbides at 0–70 GPa.This study indicates that less nitrogen than carbon can explain geophysical phenomena in the deep Earth,such as the density deficit.  相似文献   

4.
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5.
Banded iron formations (BIFs) within the Lvliang region of Shanxi Province, China, are hosted by sediments of the Yuanjiacun Formation, part of the Paleoproterozoic Lvliang Group. These BIFs are located in a zone where sedimentation changed from clastic to chemical deposition, indicating that these are Superior-type BIFs. Here, we present new major, trace, and rare earth element (REE) data, along with Fe, Si, and O isotope data for the BIFs in the Yuanjiacun within the Fe deposits at Yuanjiacun, Jianshan, and Hugushan. When compared with Post Archean Australian Shale (PAAS), these BIFs are dominated by iron oxides and quartz, contain low concentrations of Al2O3, TiO2, trace elements, and the REE, and are light rare earth element (LREE) depleted and heavy rare earth element (HREE) enriched. The BIFs also display positive La, Y, and Eu anomalies, high Y/Ho ratios, and contain 30Si depleted quartz, with high δ18O values that are similar to quartz within siliceous units formed during hydrothermal activity. These data indicate that the BIFs within the Yuanjiacun Formation were precipitated from submarine hydrothermal fluids, with only negligible detrital contribution. None of the BIF samples analyzed during this study have negative Ce anomalies, although a few have a positive Ce anomaly that may indicate that the BIFs within the Yuanjiacun Formation formed during the Great Oxidation Event (GOE) within a redox stratified ocean. The positive Ce anomalies associated with some of these BIFs are a consequence of oxidization and the formation of surficial manganese oxide that have preferentially adsorbed Ho, LREE, and Ce4 +; these deposits formed during reductive dissolution at the oxidation–reduction transition zone or in deeper-level reducing seawater. The loss of Ce, LREE, and Ho to seawater and the deposition of these elements with iron hydroxides caused the positive Ce anomalies observed in some of the BIF samples, although the limited oxidizing ability of surface seawater at this time meant that Y/Ho and LREE/HREE ratios were not substantially modified, unlike similar situations within stratified ocean water during the Late Paleoproterozoic. Magnetite and hematite within the BIFs in the study area contain heavy Fe isotopes (56Fe values of 0.24–1.27‰) resulting from the partial oxidation and precipitation of Fe2 + to Fe3 + in seawater. In addition, mass-independent fractionation of sulfur isotopes within pyrite indicates that these BIFs were deposited within an oxygen-deficient ocean associated with a similarly oxygen-deficient atmosphere, even though the BIFs within the Yuanjiacun Formation formed after initiation of the GOE.  相似文献   

6.
Biological iron and manganese removal utilizing indigenous iron and manganese oxidizing bacteria （IRB hereafter） in groundwater can also be applied to arsenic removal according to our pilot-scale test. The arsenic removal probably occurred through sorption and complexation of arsenic to iron and manganese oxides formed by enzymic action of IRB. We investigated the chemical properties of iron and manganese oxides in IRB floc and the valence state of arsenic sorbed to the floc to clarify the mechanisms of the arsenic [especially As （Ⅲ）] removal. The floc samples were collected from two drinking water plants using IRB （Jyoyo and Yamatokoriyama, Japan）, and our pilot - scale test site where arsenic and iron removal using IRB is under way （Mukoh, Japan）. The Jyoyo and Yamatokoriyama IRB floc samples were subjected to As （Ⅲ） and As（Ⅴ） sorption experiments. The elemental composition of the floc samples was measured. XANES spectra were collected on As, Fe and Mn K-edges at synchrotron radiation facility Spring 8 （Hyogo, Japan）. FT-IR and the X-ray diffraction spectra of the samples were also obtained. The IRB floc contained ca. 35 % Fe, 0.3%-3.5% Mn and 2%-6% P. The samples were highly amorphous and contained ferrihidrites and hydrated iron phosphate. According to XANES analyses of IRB, As associated with IRB was in ＋5 valence state when As （Ⅲ） （or As （Ⅴ）） was added in laboratory sorption test, Fe in ＋3 valence state, and Mn a mixture of＋3 and ＋4 valence states. Small shift was observed in the XANES spectra of IRB on As K-edge as the equilibration time of the sorption experiment was increased. Gradual oxidation of a small amount of As （Ⅲ） associated with IRB or change in arsenic binding with sorption site were the probable mechanism.  相似文献   

7.
The thermal characteristics of magnetic susceptibilities and their anisotropies of single crystal of ilvaite, a mixed valence iron sorosilicate, have been analysed in the light of Ligand Field (LF) theory using a minimum number of approximations. The electronic energy pattern and the corresponding wavefunctions were obtained from best fitting of these experimental results with the corresponding theoretical values. These results were next used to calculate the thermal characteristic of the quadrupole splitting E Q in ilvaite. It was found that the values of E Q are reasonably close to those reported from Mössbauer studies. The present analysis suggest appreciable molecular overlap between the orbits of the ligand electrons and those of the Fe2+ atoms, the overlap being prominent along the chain direction as also observed from electrical conductivity measurements.  相似文献   

8.
《Sedimentary Geology》1999,123(1-2):63-80
On the Baltic platform a lower Llanvirn (Ordovician) iron oolite can be traced for a distance of 1200 km from Norway to the east of Lake Ladoga in Russia. This oolite is usually thin (seldom exceeding 0.5 m) and is dominated by goethite (limonite) type ooids. The easternmost part of the oolite, from Tallinn to Ladoga, is examined here. The oolitic limestone is intercalated with oolitic clay beds. The mineralogical, chemical and isotopic composition and other indicators point to volcanic ash being the source for the clay. Similarities in REE distribution patterns and immobile element contents between ooids and the oolitic clay suggest that the ooids were also formed from volcanic ash.  相似文献   

9.
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10.
The Serra da Serpentina and the Serra de São José groups are two distinct banded iron formation-bearing metasedimentary sequences along the eastern border of the southern Espinhaço Range that were deposited on the boundary between the Orosirian and Statherian periods.The Serra da Serpentina Group (SSG) has an Orosirian maximum depositional age (youngest detrital zircon grain age = 1990 ± 16 Ma) and consists of fine clastic metasediments at the base and chemical sediments, including banded iron formations (BIFs), on the top, corresponding to the Meloso and Serra do Sapo formations, respectively, and correlating with the pre-Espinhaço Costa Sena Group. The SSG represents sedimentary deposition on an epicontinental-epeiric, slow downwarping sag basin with little tectonic activity.The younger Serra de São José Group (SJG) is separated from the older SSG by an erosional unconformity and was deposited in a tectonically active continental rift-basin in the early stages of the opening of the Espinhaço Trough. The Serra do São José sediments stretch along the north-south axis of the rift and comprise a complete cycle of transgressive sedimentary deposits, which were subdivided, from base to top, into the Lapão, Itapanhoacanga, Jacém and Canjica formations. The Itapanhoacanga Formation has a maximum depositional age of 1666 ± 32 Ma (Statherian), which coincides with the maximum depositional age (i.e., 1683 ± 11 Ma) of the São João da Chapada Formation, one of the Espinhaço Supergroup's basal units. The Serra de São José Rift and the Espinhaço Rift likely represent the same system, with basal units that are facies variations of the same sequence.The supracrustal rocks have undergone two stages of deformation during the west-verging Brasiliano orogeny that affected the eastern margin of the São Francisco Craton and generated a regional-scale, foreland N–S trending fold-thrust belt, which partially involved the crystalline basement. Thrust faults have segmented the terrain into a large number of tectonic blocks, where the stratigraphic sequence was nevertheless well preserved.  相似文献   

11.
The paper presents original authors' data on the O, H, C, S, and Sr isotopic composition of water and sediments from the basins into which the Aral Sea split after its catastrophic shoaling: Chernyshev Bay (CB), the basin of the Great Aral in the north, Lake Tshchebas (LT), and Minor Sea (MS). The data indicate that the δ18О, δD, δ13C, and δ34S of the water correlate with the mineralization (S) of the basins (as of 2014): for CB, S = 135.6‰, δ18О = 4.8 ± 0.1‰, δD = 5 ± 2‰, δ13C (dissolved inorganic carbon, DIC) = 3.5 ± 0.1‰, δ34S = 14.5‰; for LT, S = 83.8‰, δ18О = 2.0 ± 0.1‰, δD =–13.5 ± 1.5‰, δ13C = 2.0 ± 0.1‰, δ34S = 14.2‰; and for MS, S = 9.2‰, δ18О =–2.0 ± 0.1‰, δD =–29 ± 1‰, δ13C =–0.5 ± 0.5‰, δ34S = 13.1‰. The oxygen and hydrogen isotopic composition of the groundwaters are similar to those in MS and principally different from the artesian waters fed by atmospheric precipitation. The mineralization, δ13С, and δ34S of the groundwaters broadly vary, reflecting interaction with the host rocks. The average δ13С values of the shell and detrital carbonates sampled at the modern dried off zones of the basins are similar: 0.8 ± 0.8‰ for CB, 0.8 ± 1.4‰ for LT, and –0.4 ± 0.3‰ for MS. The oxygen isotopic composition of the carbonates varies much more broadly, and the average values are as follows: 34.2 ± 0.2‰ for CB, 32.0 ± 2.2‰ for LT, and 28.2 ± 0.9‰ for MS. These values correlate with the δ18O of the water of the corresponding basins. The carbonate cement of the Late Eocene sandstone of the Chengan Formation, which makes up the wave-cut terrace at CB, has anomalously low δ13С up to –38.5‰, suggesting origin near a submarine methane seep. The δ34S of the mirabilite and gypsum (11.0 to 16.6‰) from the bottom sediments and young dried off zone also decrease from CB to MS in response to increasing content of sulfates brought by the Syr-Darya River (δ34S = 9.1 to 9.9‰) and weakening sulfate reduction. The 87Sr/86Sr ratio in the water and carbonates of the Aral basins do not differ, within the analytical error, and is 0.70914 ± 0.00003 on average. This value indicate that the dominant Sr source of the Aral Sea is Mesozoic–Cenozoic carbonate rocks. The Rb–Sr systems of the silicate component of the bottom silt (which is likely dominated by eolian sediments) of MS and LT plot on the Т = 160 ± 5 Ma, I0 = 0.7091 ± 0.0001, pseudochron. The Rb–Sr systems of CB are less ordered, and the silt is likely a mixture of eolian and alluvial sediments.  相似文献   

12.
Adsorption of arsenate on hydrous iron oxide is an important process controlling geochemical cycling of arsenic in environment as well as the fate of arsenic-bearing mining wastes. The widely accepted view on the mechanism of adsorption is that arsenate is adsorbed via bidentate binuclear inner-sphere complexation. In this study, we characterized the arsenate-hydrous iron oxide sorption solids synthesized at pH=3-8 using Fourier transformed infrared spectroscopy （FTIR） and X-ray diffraction （XRD）. It has been determined that poorly crystalline ferric arsenate developed on the surface of iron oxide when arsenate was sorbed at acidic pH, while at alkaline pH the adsorption of arsenate was via bidentate complexation.  相似文献   

13.
The Makeng iron deposit is located in the Yong’an-Meizhou depression belt in Fujian Province, eastern China. Both skarn alteration and iron mineralization are mainly hosted within middle Carboniferous-lower Permian limestone. Five paragenetic stages of skarn formation and ore deposition have been recognized: Stage 1, early skarn (andradite–grossular assemblage); Stage 2, magnetite mineralization (diopside–magnetite assemblage); Stage 3, late skarn (amphibole–chlorite–epidote–johannsenite–hedenbergite–magnetite assemblage); Stage 4, sulfide mineralization (quartz–calcite–fluorite–chlorite–pyrite–galena–sphalerite assemblage); and Stage 5, carbonate (quartz–calcite assemblage). Fluid inclusion studies were carried out on inclusions in diopside from Stage 2 and in quartz, calcite, and fluorite from Stage 4.Halite-bearing (Type 1) and coexisting two-phase vapor-rich aqueous (Type 3) inclusions in the magnetite stage display homogenization temperatures of 448–564 °C and 501–594 °C, respectively. Salinities range from 26.5 to 48.4 and 2.4 to 6.9 wt% NaCl equivalent, respectively. Two-phase liquid-rich aqueous (Type 2b) inclusions in the sulfide stage yield homogenization temperatures and salinities of 182–343 °C and 1.9–20.1 wt% NaCl equivalent. These fluid inclusion data indicate that fluid boiling occurred during the magnetite stage and that fluid mixing took place during the sulfide stage. The former triggered the precipitation of magnetite, and the latter resulted in the deposition of Pb, Zn, and Fe sulfides. The fluids related to magnetite mineralization have δ18Ofluid-VSMOW of 6.7–9.6‰ and δD of −96 to −128‰, which are interpreted to indicate residual magmatic water from magma degassing. In contrast, the fluids related to the sulfide mineralization show δ18Ofluid-VSMOW of −0.85 to −1.04‰ and δD of −110 to −124‰, indicating that they were generated by the mixing of magmatic water with meteoric water. Magnetite grains from Stage 2 exhibit oscillatory zoning with compositional variations in major elements (e.g., SiO2, Al2O3, CaO, MgO, and MnO) from core to rim, which is interpreted as a self-organizing process rather than a dissolution-reprecipitation process. Magnetite from Stage 3 replaces or crosscuts early magnetite, suggesting that later hydrothermal fluid overprinted and caused dissolution and reprecipitation of Stage 2 magnetite. Trace element data (e.g., Ti, V, Ca, Al, and Mn) of magnetite from Stages 2 and 3 indicate a typical skarn origin.  相似文献   

14.
According to differences of the protolith formations, the early Precambrian strata in the northern part ofthe North China platform may be divided into the stable stratigraphic region in the west and the mobilestratigraphic region in the east. Based on unconformities, either stratiragphic or tectonic, as well as significantmetamorphic thermal events, the two regions may be stratigraphically defined as follows: 1) the middleArchaean Fuping Supergroup composed of the Chenzhuang and Wanzi Groups (stable areas), and the middleArchaean Qianxi Group (mobile area), whose upper limits are all dated at 2800 Ma; and 2) the upper ArchaeanWutai Supergroup composed of the Longquanguan, Shizui and Taihuai Groups (stable areas), and the upperArchaean Zunhua, Dantazi and Zhuzhangzi Groups (mobile areas). whose upper limits are all dated at 2500Ma. A correlation of the above-mentioned units is also made. The lower Proterozoic Hutuo Group of the sta-ble region is adjusted to comprise the Gaofan, Doucun, Dongye and Guojiazhai Groups. The upper limit of theGaofan Group is placed at 2350 Ma, Dongye 1850 Ma and Guojiazhai (the lower limit of the Changcheng Sys-tem) 1700 Ma.  相似文献   

15.
The role of siderite in Phanerozoic and Precambrian iron formations is discussed. Various types of iron formations are characterized, and their place in the evolution of sedimentary iron ore deposition is outlined. In Precambrian iron ore deposition, siderite is a primary mineral, whereas in Phanerozoic iron formations it becomes a secondary mineral and is commonly related to diagenetic and catagenetic processes.  相似文献   

16.
Uranium processing and mining activities that generate many contaminants, such as high concentrations of U （VI）, sulfate and heavy metals （Zn, Cu, Ni, etc）, may pose a serious threat to the groundwater resources. In recent years, considerable research has been conducted respectively on two kinds of permeable reactive barriers （PRB）, including zerovalent iron （ZVI） and sulfate reducing bacteria （SRB）, for in-situ removal of these pollutants from groundwater. However, little investigation has been carried out on the potential benefits of bioaugmenting ZVI barriers to enhance the elimination of the pollutants by combining ZVI with SRB systems. The main goal of this study was to conduct batch and column experiments to determine whether the combination of SRB and ZVI can function synergistically and accelerate the rate of pollutant removal. The results of anaerobic batch experiments demonstrated that although the integrated ZVI/PRB system itself has no ability to reduce and remove sulfate directly, SRB can utilize hydrogen gas produced during the slow process of ZVI corrosion as an electron donor to raise biomass yields significantly and accelerate reductive sulfate removal. In particular, ferrous cations produced as the byproduct of ZVI corrosion process reacted with hydrogen sulfide from sulfate reduction and formed iron-bearing sulfide precipitates, which can stimulate the growth of SRB and promote sulfate removal activity by eliminating the biotoxicity of hydrogen sulfide. It was also shown that secondary mineral products （pyrite/ferrous sulfide） formed as a consequence of microbial sulfate reduction and ZVI corrosion process can enhance the microbial precipitation of soluble U （VI） as insoluble uraninite（uranium dioxide）.  相似文献   

17.
Iron oxide–apatite (IOA) deposits, often referred to as Kiruna-type iron ore deposits, are known to have formed from the Proterozoic to the Tertiary. They are commonly associated with calc–alkaline volcanic rocks and regional- to deposit-scale metasomatic alteration. In the Bafq District in east Central Iran, economic iron oxide–apatite deposits occur within felsic volcanic tuffs and volcanosedimentary sequences of Early Cambrian age. In order to constrain the age of formation of these ores and their relationship with the Early Cambrian magmatic event, we have determined the U–Pb apatite age for five occurrences in the Bafq District. In a 206Pb/238U vs. 207Pb/235U diagram, apatite free of or poor in inclusions of other minerals plots along the Concordia between 539 and 527 Ma with four out of five samples from one deposit clustering at the upper end of this range. For this deposit, we interpret this cluster to represent the age of apatite formation, whereas the spread towards younger ages may reflect either minor Pb loss or several events of IOA formation. Apatite with inclusions of monazite (±xenotime) yields disturbed systems with inclusions having developed after formation of the iron ore–apatite deposits, possibly as late as 130–140 Ma ago. Obtained apatite ages confirms that (IOA) and the apatite-rich rocks (apatites) of the Bafq district formed coevally with the Early Cambrian magmatic (-metasomatic) events.  相似文献   

18.
《Precambrian Research》2004,128(1-2):167-188
Thirty-nine oriented block samples of iron-formation were collected at 13 sites, including opposite limbs of major folds, from the 1.88-Ga Sokoman Formation (Knob Lake Group) in the Schefferville–Knob Lake area of the central New Québec Orogen, northern Québec. The samples assayed up to 80.24% Fe2O3T (54.08% Fe), implying Fe-enrichment of the iron-formation up to ore grade. Anisotropy of magnetic susceptibility measurements on 245 standard specimens indicate a well preserved bedding-parallel fabric in the iron-formation, suggesting minimal alteration of the magnetic mineralogy since deposition and/or a mimetic secondary magnetic mineralogy. The iron-formation has not been internally deformed since the magnetic mineralogy was established. Analyses by variable-field translation balance and X-ray diffraction showed that the predominant magnetic mineral is hematite but a small amount of magnetite also is present in most samples. Following low-temperature pre-treatment as appropriate, stepwise thermal and alternating-field demagnetization of 218 specimens revealed a low-temperature, post-folding component (maximum Tub≈400 °C, D=27.1°, I=20.1°, α95=10.9°, from seven sites; pole position of 40.6°S, 257.0°E), and components carried by magnetite (maximum Tub≈580 °C, D=35.8°, I=3.9°, α95=9.1°, from 10 sites; pole position of 29.6°S, 250.9°E) and hematite (maximum Tub≈680 °C, D=40.0°, I=1.6°, α95=18.6°, from seven sites; pole position of 26.8°S, 247.0°E). The components carried by magnetite and hematite are pre-, syn- and post-folding depending on the sampling site, indicating that the magnetization was acquired continuously with deformation in the New Québec Orogen at 1.84–1.83 Ga. No evidence was found for acquisition of magnetization during the Mesozoic, when many of the iron oxide orebodies in the Schefferville–Knob Lake area are thought to have formed. Our findings imply that an episode of Fe-enrichment of iron-formation in the Sokoman Formation involved the circulation of hydrothermal fluids related to late Paleoproterozoic orogenesis. Such orogenic circulation of fluids may have contributed to the development of hematitic orebodies in the central New Québec Orogen.  相似文献   

19.
K-Ar ages of illite-muscovite and fission track ages of zircon and apatite were determined from various lithotypes of the Bükkium, which forms the innermost segment of the Western Carpathians. The stratigraphic ages of these Dinaric type formations cover a wide range from the Late Ordovician up to the Late Jurassic. The grade of the orogenic dynamo-thermal metamorphism varies from the late diagenetic zone through the anchizone up to the epizone (chlorite, maximally biotite isograd of the greenschist facies). The K-Ar system of the illite-muscovite in the < 2 m grain-size fraction approached equilibrium only in epizonal and high-temperature anchizonal conditions. The orogenic metamorphism culminated between the eo-Hellenic (160-120 Ma) phase connected to the beginning of the subduction in the Dinarides, and the Austrian (100-95 Ma) phase characterized by compressional crustal thickening. No isotope geochronological evidence was found for proving any Hercynian recrystallization. The stability field of fission tracks in zircon was approached using the thermal histories of the different tectonic units. A temperature less than 250°C and effective heating time of 20–30 Ma had only negligible effects on the tracks, whereas total annealing was reached between 250 and 300°C. Apatite fission track ages from the Paleozoic and Mesozoic formations show that the uplift of the Bükk Mountains occurred only in the Tertiary (not earlier than ca. 40 Ma ago). Thermal modeling based on apatite fission track length spectra and preserved Paleogene sediment thickness data proved that the Late Neogene burial of the recently exhumed plateau of the Bükk Mountains exceeded 1 km.  相似文献   

20.
This paper models the physico-chemical conditions of a Neoarchæan to Palæoproterozoic marine basin in which the sedimentary sequence of BIF, Fe and Mn ores of the Lake Superior-type formed. The model is based on Eh-pH diagram stability fields for Fe, silica and Mn solubilities (taken from the literature) and on field observations of the lithological sequences. BIF formation took place in epicontinental marine basins with free access to the ocean. The main Fe source for BIF formation was ocean enriched with about 6–10 ppm ferrous Fe of hydrothermal geochemical affinity. Land-derived Fe influxes into the BIF-forming basins certainly contributed, but the lack of clastic sedimentation precludes estimation of element budgets. The main silica source for formation of chert layers is sea water. If silica was precipitated by evaporation, the silica concentration of the BIF-forming sea must have been close to saturation (15–20 ppm). Biogenic silica concentration from a possible silica undersaturated sea may not be excluded. These inferred BIF-forming conditions fit the global occurrence of Lake Superior-type BIF in general, whereas special sedimentary environments were probably responsible for the formation of highly enriched laminated Fe ore at the Maremane Dome and in the Sishen-Kathu mining district in Griqualand West, and for the FeMn ores in the Kalahari field. Formation of laminated Fe ore in the Maremane Dome and in the Sishen-Kathu areas were restricted to local deeps within the BIF basins, caused by karst collapse in the underlying Campbellrand dolomites. In such deeps, increased pH values relative to the normal BIF-forming sea caused sufficiently increased silica solubility, resulting in the almost exclusive sedimentation of colloidal Fe precipitates.In the Kalahari field, the BIF sedimentation pile became silica-depleted when approaching the Mn layers. This was genetically controlled by the increased pH of sea water and increased silica solubility. Under such increased pH conditions, Mn oxides become stable for precipitation if minimum Mn activity is achieved in the sedimentary basin. The sedimentation sequence of low silica BIF - kutnahoritic BIF - jacobsitic BIF - braunitic Mn ore can be explained, using combined Eh-pH diagrams, as reflecting a precipitation path of increasing redox potential in a pH environment slightly above 9. These conditions were achieved by closing the access of the basin to the open ocean, resulting in the reduction of water level by evaporation and thereby increasing salinity and pH. Precipitation of low silica BIF followed and, in the presence of sufficient Mn activity with increasing Eh in the precipitating water stratum, deposition of the Mn mineral associations occurred.  相似文献   

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