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1.
Boehmite-rich coal of Pennsylvanian age was discovered earlier at the Heidaigou Surface Mine, Jungar Coalfield, Inner Mongolia, China. This paper reports new results on 29 bench samples of the no. 6 coal from a drill core from the adjacent Haerwusu Surface Mine, and provides new insights into the origin of the minerals and elements present. The results show that the proportion of inertinite in the no. 6 coal is higher than in other Late Paleozoic coals in northern China. Based on mineral proportions (boehmite to kaolinite ratio) and major element concentrations in the coal benches of the drill core, the no. 6 coal may be divided into five sections (I to V). Major minerals in Sections I and V are kaolinite. Sections II and IV are mainly kaolinite with a trace of boehmite, and Section III is high in boehmite. The boehmite is derived from bauxite in the weathered surface (Benxi Formation) in the sediment-source region. The no. 6 coal is rich in Al2O3 (8.89%), TiO2 (0.47%), Li (116 μg/g), F (286 μg/g), Ga (18 μg/g), Se (6.1 μg/g), Sr (350 μg/g), Zr (268 μg/g), REEs (172 μg/g), Pb (30 μg/g), and Th (17 μg/g). The elements are classified into five associations by cluster analysis, i.e. Groups A, B, C, D, and E. Group A (ash–SiO2–Al2O3–Na2O–Li) and Group B (REE–Sc–In–Y–K2O–Rb–Zr–Hf–Cs–U–P2O5–Sr–Ba–Ge) are strongly correlated with ash yield and mainly have an inorganic affinity. The elements that are negatively or less strongly correlated with ash yield (with exceptions of Fe2O3, Be, V, and Ni) are grouped in the remaining three associations: Group C, Se–Pb–Hg–Th–TiO2–Bi–Nb–Ta–Cd–Sn; Group D, Co–Mo–Tl–Be–Ni–Sb–MgO–Re–Ga–W–Zn–V–Cr–F–Cu; and Group E, S–As–CaO–MnO–Fe2O3. Aluminum is mainly distributed in boehmite, followed by kaolinite. The high correlation coefficients of the Li–ash, Li–Al2O3, and Li–SiO2 pairs indicate that Li is related to the aluminosilicates in the coal. The boehmite-rich coal is high in gallium and F, which occur in boehmite and the organic matter. Selenium and Pb are mainly in epigenetic clausthalite fillings in fractures. The abundant rare earth elements in the coal benches were supplied from two sources: the bauxite on the weathered surface of the Benxi Formation and from adjacent partings by groundwater leaching during diagenesis. The light rare earth elements (LREEs) are more easily leached from the partings and incorporated into the organic matter than the heavy REEs, leading to a higher ratio of LREEs to HREEs in the coal benches than in the overlying partings.  相似文献   

2.
Phase equilibria in the system CaO–MgO–SiO2–CO2–H2O–NaCl are calculated to illustrate phase relations in metacarbonates over a wide-range of P–T–X[H2O–CO2–NaCl] conditions. Calculations are performed using the equation of state of Duan et al. (Geochim Cosmochim Acta 59:2869–2882, 1995) for H2O–CO2–NaCl fluids and the internally consistent data set of Gottschalk (Eur J Mineral 9:175–223, 1997) for thermodynamic properties of solids. Results are presented in isothermal-isobarical plots showing stable mineral assemblages as a function of fluid composition. It is shown that in contact-metamorphic P–T regimes the presence of very small concentrations of NaCl in the fluid causes almost all decarbonation reactions to proceed within the two fluid solvus of the H2O–CO2–NaCl system. Substantial flow of magma-derived fluids into marbles has been documented for many contact aureoles by shifts in stable isotope geochemistry of the host rocks and by the progress of volatile-producing mineral reactions controlled by fluid compositions. Time-integrated fluid fluxes have been estimated by combining fluid advection/dispersion models with the spatial arrangement of mineral reactions and isotopic resetting. All existing models assume that minerals react in the presence of a single phase H2O–CO2 fluid and do not allow for the effect that fluid immiscibility has on the flow patterns. It is shown that fluids emanating from calc-alkaline melts that crystallize at shallow depths are brines. Their salinity may vary depending mainly on pressure and fraction of crystallized melt. Infiltration-driven decarbonation reactions in the host rocks inevitably proceed at the boundaries of the two fluid solvus where the produced CO2 is immiscible and may separate from the brine as a low salinity, low density H2O–CO2 fluid. Most parameters of fluid–rock interaction in contact aureoles that are derived from progress of mineral reactions and stable isotope resetting are probably incorrect because fluid phase separation is disregarded.  相似文献   

3.
The giant Bayan Obo REE–Nb–Fe deposit consists of replacement bodies hosted in dolomite marble made up of magnetite, REE fluorocarbonates, fluorite, aegirine, amphibole, calcite and barite. Two or three phase CO2-rich, three phase hypersaline liquid–vapor–solid, and two phase liquid-rich inclusions have been recognized in mineralized fluorite and quartz samples. Microthermometry measurements indicate that the carbonic phase in CO2-rich inclusions is nearly pure CO2. Fluids involving in REE–Nb–Fe mineralization at Bayan Obo might be mainly of H2O–CO2–NaCl–(F–REE) system. Coexistences of brine inclusions and CO2-rich inclusions with similar homogenization temperatures give evidence that immiscibility happened during REE mineralization. An unmixing of an original H2O–CO2–NaCl fluid probably derived from carbonatitic magma. The presence of REE-carbonates as an abundant solid in fluid inclusions shows that the original ore-forming fluids are very rich in REE, and therefore, have the potential to produce economic REE ores at Bayan Obo.  相似文献   

4.
The changing XCO2 in fluids during the progressive metamorphism in Sanbagawa belt of the Cretaceous subduction zone, Japan, was estimated by a newly proposed method. The subduction zone meta-sediments are characterized commonly by four-phase assemblages in the CaO–NaAlO2–KAlO2–Al2O3 system with excess quartz and a CO2–H2O binary fluid phase. Using the common assemblage of calcite–albite–muscovite–clinozoisite, XCO2 of the fluid was estimated to be from about 0.0001–0.0005 (the lowest grade chlorite zone), through 0.004–0.01 (garnet zone), 0.01–0.05 (albite–biotite zone) to 0.06–0.2 (oligoclase–biotite zone).The paragenetic relationship of meta-sediments from the subduction zones was compared in a wide P–T range to cover the stability fields of aragonite and jadeite. As a result, an excellent P–T–XCO2 relationship was delineated to serve as a quantitative monitor for the evolving fluid composition during the progressive metamorphism in subduction zones.  相似文献   

5.
Fluid inclusion microthermometry and structural data are presented for quartz vein systems of a major dextral transcurrent shear zone of Neoproterozoic–Cambrian age in the Ribeira River Valley area, southeastern Brazil. Geometric and microstructural constraints indicate that foliation–parallel and extensional veins were formed during dextral strike–slip faulting. Both vein systems are formed essentially by quartz and lesser contents of sulfides and carbonates, and were crystallized in the presence of CO2–CH4 and H2O–CO2–CH4–NaCl immiscible fluids following unmixing from a homogeneous parental fluid. Contrasting fluid entrapment conditions indicate that the two vein systems were formed in different structural levels. Foliation–parallel veins were precipitated beneath the seismogenic zone under pressure fluctuating from moderately sublithostatic to moderately subhydrostatic values (319–397 °C and 47–215 MPa), which is compatible with predicted fluid pressure cycle curves derived from fault–valve action. Growth of extensional veins occurred in shallower structural levels, under pressure fluctuating from near hydrostatic to moderately subhydrostatic values (207–218 °C and 18–74 MPa), which indicate that precipitation occurred within the near surface hydrostatically pressured seismogenic zone. Fluid immiscibility and precipitation of quartz in foliation–parallel veins resulted from fluid pressure drop immediately after earthquake rupture. Fluid immiscibility following a local pressure drop during extensional veining occurred in pre-seismic stages in response to the development of fracture porosity in the dilatant zone. Late stages of fluid circulation within the fault zone are represented dominantly by low to high salinity (0.2 to 44 wt.% equivalent NaCl) H2O–NaCl–CaCl2 fluid inclusions trapped in healed fractures mainly in foliation–parallel veins, which also exhibit subordinate H2O–NaCl–CaCl2, CO2–(CH4) and H2O–CO2–(CH4)–NaCl fluid inclusions trapped under subsolvus conditions in single healed microcracks. Recurrent circulation of aqueous–carbonic fluids and aqueous fluids of highly contrasting salinities during veining and post-veining stages suggests that fluids of different reservoirs were pumped to the ruptured fault zone during faulting episodes. A fluid evolution trending toward CH4 depletion for CO2–CH4–bearing fluids and salinity depletion and dilution (approximation of the system H2O–NaCl) for aqueous–saline fluids occurred concomitantly with decrease in temperature and pressure related to fluid entrapment in progressively shallower structural levels reflecting the shear zone exhumation history.  相似文献   

6.
Hydrochemistry of groundwater in Chithar Basin, Tamil Nadu, India was used to assess the quality of groundwater for determining its suitability for drinking and agricultural purposes. Physical and chemical parameters of groundwater such as electrical conductivity, pH, total dissolved solids (TDS), Na+, K+, Ca2+, Mg2+, Cl–, HCO3–, CO32–, SO42–, NO–3, F–, B– and SiO2 were determined. Concentrations of the chemical constituents in groundwater vary spatially and temporarily. Interpretation of analytical data shows that mixed Ca–Mg–Cl, Ca–Cl and Na–Cl are the dominant hydrochemical facies in the study area. Alkali earths (Ca2+, Mg2+) and strong acids (Cl–, SO42–) are slightly dominating over alkalis (Na+, K+) and weak acids (HCO3–, CO32–). The abundance of the major ions is as follows: Na+ Ca2+ Mg2+ > K+ = Cl– > HCO3–> SO42– > NO3– > CO32– . Groundwater in the area is generally hard, fresh to brackish, high to very high saline and low alkaline in nature. High total hardness and TDS in a few places identify the unsuitability of groundwater for drinking and irrigation. Such areas require special care to provide adequate drainage and introduce alternative salt tolerance cropping. Fluoride and boron are within the permissible limits for human consumption and crops as per the international standards.  相似文献   

7.
Using the Chiller computer program, we performed modeling of the mechanisms of the joint transport and deposition of Au and Sb from various ore-forming solutions during the formation of Au-Sb deposits. Three models are considered by the example of the Uderei Au-Sb deposit in the Yenisei Ridge: (1) simple cooling (cooling only), (2) iso-enthalpy boiling (P = f(T)), and (3) solution–rock interaction (rock titration model). The behavior of Sb(III) and Au(I) in the system Au–Sb–Fe–Cu–Pb–Zn–As–H2O–Cl–H2S–CO2 under hydrothermal conditions was studied. It is shown that both weakly alkaline (near-neutral) and reduced acidic Feaq2+-enriched low-chloride high-CO2 and high-chloride hydrothermal solutions play a crucial role in the formation of gold parageneses of Au-Sb ores.  相似文献   

8.
The mineral and chemical compositions and physical properties of diatomaceous clayey–siliceous sediments in the Sea of Okhotsk are studied. Absolute masses of silica accumulation are determined. Their compositional model based on the silica content is similar to that of Late Jurassic and Olenekian–middle Anisian cherts of the Sikhote Alin region. The thickness of the Holocene siliceous unit and the absolute mass of siliceous deposits depended on bioproductivity in the upper water column and the seafloor topography. Absolute masses of SiO2 am (0.05–5.7 g cm–2 ka–1) and SiO2 fr (0.5–11.6 g cm–2 ka–1) are minimal on seamounts and maximal in depressions near foothills. These values match absolute masses of SiO2 fr accumulations in Triassic and Late Jurassic basins of the Sikhote Alin region (0.33–3 g cm–2 ka–1). Comparison of the composition and absolute masses of silica shows that Triassic and Late Jurassic siliceous sequences of Sikhote Alin could be accumulated in the marginal marine basin near a continent.  相似文献   

9.
The Gemericum is a segment of the Variscan orogen subsequently deformed by the Alpine–Carpathian orogeny. The unit contains abundant siderite–sulphide and quartz–antimony veins together with stratabound siderite replacement deposits in limestones and stratiform sulphide mineralization in volcano-sedimentary sequences. The siderite–sulphide veins and siderite replacement deposits of the Gemericum represent one of the largest accumulations of siderite in the world, with about 160 million tonnes of mineable FeCO3. More than 1200 steeply dipping hydrothermal veins are arranged in a regional tectonic and compositional pattern, reflecting the distribution of regional metamorphic zones. Siderite–sulphide veins are typically contained in low-grade (chlorite zone) sedimentary, volcano-sedimentary or volcanic Lower and Upper Paleozoic rocks. Quartz–antimony veins are hosted by higher-grade units (biotite zone). Siderite–sulphide veins are dominated by early siderite followed by a complex set of stages, including quartz–sulphide (chalcopyrite, tetrahedrite), barite, tourmaline–quartz, and sulphide-remobilization stages. The temporal evolution of these stages is difficult to study because of the widespread and repeated tectonic processes, within-vein replacement and recrystallization. Siderite–sulphide veins show considerable vertical (up to 1200 m) and lateral (up to 15 km) extent, and a thickness typically reaching several metres. Carbonate-replacement siderite deposits of the Gemericum are hosted by a Silurian limestone belt and are similar to stratabound siderite deposits of the Eastern Alps (e.g., Erzberg, Austria).Based on a review of geological, petrological and geochronological data for the Gemericum, and extensive stable and radiogenic isotope data and fluid inclusion data on hydrothermal minerals, the siderite–sulphide veins and siderite replacement deposits are classified as metamorphogenic in a broad sense. The deposits were formed during several stages of regional crustal-scale fluid flow. Isotope (S, C, Sr, Pb) fingerprinting identifies the metamorphosed rock complexes of the Gemericum as a source of most components of hydrothermal fluids. Fluid inclusion and stable isotope data evidence the participation of several contrasting fluid types, and the existence of contrasting P–T conditions during vein evolution. A high-δ18O, medium- to high-salinity, H2O-type fluid is the most important component during siderite deposition, whereas H2O–CO2-type fluid inclusion containing dense liquid CO2 and corresponding to minimal pressures between 1 and 3 kbar were found in a younger tourmaline–quartz stage. Younger quartz–ankerite(±siderite)–sulphide stages are characterized by high-salinity (17 to 35 wt.% NaCl equivalent) and low-temperature (Th=90 to 180 °C) H2O-type fluids.The vein deposits are interpreted as a result of multistage hydrothermal circulation, with Variscan and Alpine mineralization phases. Based on available indirect data, the most important mineralization phase was related to regional fluid flow during the uplift of a Variscan metamorphic core complex, producing siderite–sulphide (±barite) mineralization, while tourmaline–quartz stage and sulphide remobilization stages are related to Alpine processes. Two phases of vein evolution are evident from two groups of 87Sr/86Sr isotope ratios of Sr-rich, Rb-poor hydrothermal minerals: 0.71042–0.71541 in older barite and 0.7190–0.7220 in late-stage celestine and strontianite.  相似文献   

10.
Birimian supracrustal sequences in NE Burkina Faso are dominated by meta-volcaniclastic greywacke, intercalated meta-conglomerate, siltstone and shale. The sequences where subjected to two phases of deformation and contact metamorphosed to hornblende–hornfels facies during emplacement of pyroxenite–gabbro–norite (Yacouba Mafic complex), granodiorite–tonalite (Tin Taradat granodiorite–tonalite) and dolerite dykes.Structural studies indicated that the NE-trending, first-order crustal-scale Markoye Shear Zone (MSZ; Markoye Fault of [Jeambrun, M., Delfour, J., Gravost, M., 1970. Carte géologique de L’Oudalan. Bureau De Recherches Geologiques et Miniéres, Burkina Faso.]) has undergone at least two phases of reactivation concomitant to two phases of regional deformation. The first phase of deformation, D1, resulted in the formation of NNW-NW trending folds and thrusts during dextral-reverse displacement on the MSZ. The deformation is termed the Tangaean Event and predates the Eburnean Orogeny. D2 phase involved a period of SE–NW crustal shortening and sinistral-reverse displacement on the MSZ, and is correlated to the Eburnean Orogeny 2.1 Ga. Deformation in D2 is characterised by NE-trending regional folds (F2) and a pervasive NE-trending foliation (S2-C to S2). Within the MSZ, deformation is characterised by NNE-trending zones of mylonite that are bordered in the hangingwall and footwall by pseudotachylite veins. Buck quartz-carbonate veins and quartz cataclasite veins crosscut the mylonite zones and are, in turn, crosscut by quartz–chlorite–(muscovite) shears that formed during reactivation of the MSZ late in D2. Several generations of veins are recognised at the Essakane main deposit (EMZ): Arsenopyrite–pyrite–gold mineralization in quartz veins formed in D1 during metasomatic alteration of the host rocks; Vein-stockwork gold mineralization is interpreted to have formed late in D2.  相似文献   

11.
Global tracing of the key surfaces of Triassic deposits may contribute significantly to the understanding of the common patterns in their accumulation. We attempt to define synthems – disconformity-bounded sedimentary complexes – in the Triassic successions of southern South America (southwestern Gondwana, Brazil and Argentina) and the Western Caucasus (the northern Neotethys, Russia), and then to trace their boundaries in the adjacent regions and globally. In southern South America, a number of synthems have been recognized – the Cuyo Basin: the Río Mendoza–Cerro de las Cabras Synthem (Olenekian–Ladinian) and the Potrerillos–Cacheuta–Río Blanco Synthem (Carnian–Rhaetian); the Ischigualasto Basin: the Ischichuca-Los Rastros Synthem (Anisian–Ladinian) and the Ischigualasto–Los Colorados Synthem (Carnian–Rhaetian); the Chaco–Paraná Basin: the Sanga do Cabral Synthem (Induan), the Santa Maria 1 Synthem (Ladinian), the Santa Maria 2 Synthem (Carnian), and the Caturrita Synthem (Norian); western Argentina: the Talampaya Synthem (Lower Triassic) and the Tarjados Synthem (Olenekian?). In the Western Caucasus, three common synthems have been distinguished: WC-1 (Induan–Anisian), WC-2 (uppermost Anisian–Carnian), and WC-3 (Norian–lower Rhaetian). The lower boundary of WC-1 corresponds to a hiatus whose duration seems to be shorter than that previously postulated. The synthem boundaries that are common to southwestern Gondwana and the Western Caucasus lie close to the base and top of the Triassic. The Lower Triassic, Ladinian, and Upper Triassic disconformities are traced within the studied basins of southern South America, and the first two are also established in South Africa. The Upper Triassic disconformity is only traced within the entire Caucasus, whereas all synthem boundaries established in the Western Caucasus are traced partly within Europe. In general, the synthem boundaries recognized in southern South America and the Western Caucasus are correlated to the global Triassic sequence boundaries and sea-level falls. Although regional peculiarities are superimposed on the appearance of global events in the Triassic synthem architecture, the successful global tracing suggests that planetary-scale mechanisms of synthem formation existed and that they were active in regions dominated by both marine and non-marine sedimentation.  相似文献   

12.
Raman spectroscopy was used to analyze quantitatively water in silicate glasses and melt inclusions and to monitor H2O–OH speciation. Calibration is based on synthetic glasses with various water contents (0.02–7.67% H2O); water determination and OH–H2O differentiation on the area of the Si–O broad band at 468 cm–1 and the asymmetric O–H band at 3,550 cm–1. Each Raman spectrum has been decomposed into four Gaussian + Lorentzian components centered at 3,330, 3,458, 3,560, and 3,626 cm–1 using the Levenberg–Marquardt algorithm. These components are interpreted to be two different types of H2O molecule sites. The influence of the temperature on the loss of water is more important for molecular water than for the hydroxyl groups. The H2O–OH partition confirms the typical evolution of water speciation in rhyolitic glasses as a function of the bulk water content. Method limitations have been studied for the application to natural melt inclusions.Editorial responsibility: T.L Grove  相似文献   

13.
The mineralized Proterozoic metasediments of Bushmanland are characterized by the presence of ferriferous rocks. This includes banded and unbanded iron formations and various types of gossans. These units are not laterally extensive and occur in different stratigraphic levels. The prevalent minerals in the ferriferous rocks are hematite, magnetite, quartz, garnet, muscovite, biotite and sillimanite, but less common occurrences of graphite, alunite, plumbojarosite, gahnite and dufrenite have been noted. The chemical variation (wt%) is extensive: total Fe2O3 (1.3–93.5), SiO2 (4–93), Al2O3 (0.2–14.0), CaO (0.02–20.7), MnO (0.0–14.3), MgO (0.0–5.7), TiO2 (0.0–4.4), Na2O (0.0–2.0), K2O (0.0–1.5) and P2O5 (0.1–7.0). The preliminary nature of the data set precludes, however, firm conclusions regarding stratigraphic control of the chemical composition. The trace-element contents (ppm) extend over several orders of magnitude: Zn (0–7,000), Ba (0–5,200), Cu (0–1,400), Pb (0–1,070) and Ni (6–540). Collectively, the data indicate that most of the ferriferous rocks represent highly metamorphosed sediments.  相似文献   

14.
Two mineralogically different rare metal granites located in two distinct terranes from the Tuareg area are compared: the Tin-Amzi granite in the north of the Laouni Terrane and the Ebelekan granite in the Assodé–Issalane Terrane.The Tin-Amzi granite is enclosed within Eburnean granulitic gneisses, and consists of albite, quartz, protolithionite, K-feldspar and topaz granite (PG). The accessory minerals include columbite tantalite, U- and Hf-rich zircon, Th-uraninite, wolframoixiolite and wolframite. This facies is characterised by a mineralogical evolution from the bottom to the top underlined by a strong resorption of K-feldspar and albite and the crystalliK-feldspar of more abundant topaz and protolithionite II which is further altered in muscovite and Mn-siderite. It is underlain by an albite, K-feldspar, F-rich topaz, quartz and muscovite granite (MG), with W–Nb–Ta oxides, wolframite, Nb-rutile, zircon and scarce uranothorite as accessories.The Ebelekan granite intrudes into a coarse-grained biotite granite enclosed within upper amphibolite-facies metasediments. It comprises a zinnwaldite, albite, topaz porphyritic granite (ZG) with “snow ball” quartz and K-feldspar. The accessories are zircon, monazite, uranothorite, Ta bearing cassiterite, columbite tantalite and wodginite. It is capped by a banded aplite-pegmatite (AP).The geochemistry of Tin-Amzi and Ebelekan granites is nearly comparable. Both are peraluminous (A/CNK=1.10–1.29; ASI=1.17–1.31), sodolithic and fluorine rich with high SiO2, Al2O3, Na2O+K2O, Rb, Ga, Li, Ta, Nb, Sn and low FeO, MgO, TiO2, Ba, Sr, Y, Zr and REE contents. These rare metal Ta bearing granites belong to the P-poor subclass, relating to their P2O5 content ( 0.03–0.15 wt.%). Nevertheless, they are distinguished by their concentration of W, Sn and Ta. The Tin-Amzi granite is W–Ta bearing with high W/Sn ratio whereas the Ebelekan granite is Ta–Sn bearing with insignificant W content.At Tin-Amzi the W–Nb–Ta minerals define a sequence formed by W-columbite tantalite followed by wolframoixiolite and finally wolframite showing the effect of hydrothermal overprinting with an extreme W enrichment of the fluids. At Ebelekan, the Sn–Nb–Ta oxides follow a Mn sequence: manganocolumbite→manganotantalite→wodginite+titanowodginite→cassiterite that represents a trend of primary crystallisation resulting from progressive substitution Fe→Mn and Nb→Ta during the magmatic fractionation.  相似文献   

15.
N. Hald  C. Tegner   《Lithos》2000,54(3-4):207-233
The Paleozoic–Mesozoic Jameson Land Basin (East Greenland) is intruded by a sill complex and by a swarm of ESE trending dykes. Together with dykes of the inner Scoresby Sund fjord, they form a regional Early Tertiary intrusive complex located 200–400 km inland of the East Greenland rifted continental margin. Most of the intrusive rocks in the Jameson Land Basin are geochemically coherent and consist of evolved plagioclase–augite–olivine saturated, uncontaminated high-Ti basalt with 48.5–50.2 wt.% SiO2, 2.2–3.2 wt.% TiO2, 5.1–7.4 wt.% MgO, 9–17 ppm Nb and La/YbN=2.8–3.6. Minor tholeiitic rock types are: (a) low-Ti basalt (49.7 wt.% SiO2, 1.7 wt.% TiO2, 6.8 wt.% MgO, 2.6 ppm Nb and La/YbN=0.5) akin to oceanic basalts; (b) very-high-Ti basalt (48.6 wt.% SiO2, 4.1 wt.% TiO2, 5.1 wt.% MgO and 21 ppm Nb); and (c) plagioclase ultraphyric basalt. The tholeiitic dolerites are cut by alkali basalt (43.7–47.3 wt.% SiO2, 4.1–5.1 wt.% TiO2, 4.9–6.2 wt.% MgO, 29–46 ppm Nb and La/YbN=16–17) sills and dykes.Modelling of high-field-strength and rare-earth elements indicate that the high-Ti basalts formed from 6–10% melting of approximately equal proportions of garnet- and spinel-bearing mantle of slightly depleted composition beneath thick continental lithosphere. Conversely, dolerite intrusions and flood basalts of similar compositional kindred from adjacent but more rift-proximal occurrences in Northeast Greenland formed from shallower melting of dominantly spinel-bearing mantle beneath extended and thinned continental lithosphere. These variations in lithospheric thickness suggest the continent–ocean transition of the East Greenland rifted volcanic margin is sharp and narrow.40Ar–39Ar dating and paleomagnetism show that the high-Ti dolerites were emplaced at 53–52 Ma (most likely during C23r) and hence surprisingly postdate the main flood volcanism by 2–5 Ma and the inception of seafloor spreading between Greenland and Europe by 1–2 Ma. The formation of tholeiitic and alkaline magmas emplaced into the Jameson Land Basin corroborates to the importance of post-breakup magmatism along the East Greenland volcanic rifted margin. Upwelling of the ancestral Iceland mantle plume under central Greenland at 53–52 Ma (rather than under the active rift), perhaps accompanied by a failed attempt to shift the rift zone westward towards the plume axis, may have triggered post-breakup continental magmatism of the Jameson Land Basin and the inner Scoresby Sund region, along preexisting structural lineaments.  相似文献   

16.
Two kimberlite pipes in Elliott County contain rare ultramafic xenoliths and abundant megacrysts of olivine (Fo85–93), garnet (0.21–9.07% Cr2O3), picroilmenite, phlogopite, Cr-poor clinopyroxene (0.56–0.88% Cr2O3), and Cr-poor orthopyroxene (<0.03–0.34% Cr2O3) in a matrix of olivine (Fo88–92), picroilmenite, Cr-spinel, magnetite, perovskite, pyrrhotite, calcite, and hydrous silicates. Rare clinopyroxene-ilmenite intergrowths also occur. Garnets show correlation of mg (0.79–0.86) and CaO (4.54–7.10%) with Cr2O3 content; the more Mg-rich garnets have more uvarovite in solution. Clinopyroxene megacrysts show a general decrease in Cr2O3 and increase in TiO2 (0.38–0.56%) with decreasing mg (0.87–0.91). Clinopyroxene megacrysts are more Cr-rich than clinopyroxene in clinopyroxene-ilmenite intergrowths (0.06–0.38% Cr2O3) and less Cr-rich than peridotite clinopyroxenes (1.39–1.46% Cr2O3). Orthopyroxene megacrysts and orthopyroxene inclusions in olivine megacrysts form two populations: high-Ca, high-Al (1.09–1.16% CaO and 1.16–1.18% Al2O3) and low-Ca, low-Al (0.35–0.46% CaO and 0.67–0.74% Al2O3). Three orthopyroxenes belonging to a low-Ca subgroup of the high-Ca, high-Al group were also identified (0.86–0.98% CaO and 0.95–1.01% Al2O3). The high-Ca, high-Al group (Group I) has lower mg (0.88–0.90) than low-Ca, low-Al group (Group II) with mg=0.92–0.93; low mg orthopyroxenes (Group Ia) have lower Cr2O3 and higher TiO2 than high mg orthopyroxenes (Group II). The orthopyroxene megacrysts have lower Cr2O3 than peridotite orthopyroxenes (0.46–0.57% Cr2O3). Diopside solvus temperatures indicate equilibration of clinopyroxene megacrysts at 1,165°–1,390° C and 1,295°–1,335° C for clinopyroxene in clinopyroxene-ilmenite intergrowths. P-T estimates for orthopyroxene megacrysts are bimodal: high-Ca, high-Al (Group I) orthopyroxenes equilibrated at 1,165°–1,255° C and 51–53 kb (± 5kb) and the low-Ca, low-Al (Group II) orthopyroxenes equilibrated at 970°–1,020°C and 46–56 kb (± 5kb). Garnet peridotites equilibrated at 1,240°–1,360° C and 47–49 kb. Spinel peridotites have discordant temperatures of 720°–835° C (using spinel-olivine Fe/Mg) and 865°–1,125° C (Al in orthopyroxene).Megacrysts probably precipitated from a fractionating liquid at >150 km depth. They are not disaggregated peridotite because: (1) of large crystal size (up to 1.5 cm), (2) compositions are distinctly different from peridotite phases, and (3) they display fractionation trends. The high mg, low T orthopyroxenes and the clustering of olivine rims near Fo89–90 reflect liquid changes to higher MgO contents due to (1) assimilation of wall-rock and/or (2) an increase in Fe3+/Fe2+ and subsequently MgO/FeO as a result of an increase in f o.  相似文献   

17.
The occurrence of synkinematic and authigenic clay minerals is a common feature in fault gouges. Few attempts have been made to date fault gouges. We present the first age data in Australia for synkinematic illite–smectite growth in two fault zones of the northern Sydney Basin, NSW. The faults occur at Burwood Beach, NSW in the northern part of the Sydney Basin and are hosted by Early Permian siltstones, tuffs and coals of the Lambton Formation, Newcastle Coal Measures. The faults are 1.5 m apart, show normal displacement and trend N–S with steep easterly dips. Foliated gouge zones, comminution and dilational breccias are developed along both fault surfaces. K–Ar ages extracted from samples in the gouge and tuffs in the damage zones are 172 (6–10 μm) to 119 Ma (<0.4 μm), respectively. Older ages of 272–281 Ma for the coarse fractions (>2 μm), 237–245 Ma for the <2 μm fraction, 218 Ma for the <0.4 μm fraction and 196 Ma for the <0.1 μm fraction have been obtained from siltstones within and outside the damage zone. We believe the younger ages of 196–237 Ma indicate the time at which diagenetic illite–smectite formed and the 122–150 Ma dates from the <2 μm fraction represent the maximum age of gouge formation. The younger ages are thought to reflect the last slip event occurring on the faults, which is related to the rifting and dispersal of the eastern margin of the Australian continent.  相似文献   

18.
In order to determine time-dependent changes in estuarine pore-water chemistry and flux variations across the sediment-water interface, sediment cores of an intertidal mud flat in the Weser Estuary were taken monthly over a one-year period. Sediment temperature, pH, Eh, Cl–, O2, NO 3 – , and SO 4 2– pore-water concentrations were measured and showed variations that relate to the changes of surface temperature and estuarine water composition. Fick's first law was applied to quantify diffusive fluxes from concentration gradients in the diffusive boundary layer and in the pore water. Total nitrate fluxes were calculated from flux chamber experiments. Diffusive oxygen fluxes increased from 5 mmol m–2 d–1 in winter to 18 mmol m–2 d–1 in early summer, while nitrate fluxes into the sediment increased from 3 mmol m–2 d–1 in winter to 60 mmol m–2 d–1 in early summer. Oxygen and nitrate fluxes into the sediment correlated linearly to sediment temperature. Sulfate fluxes increased from 0.5 mmol m–2 d–1 in winter to 10 mmol m–2 d–1 in August and September. Converted into carbon fluxes, the sum of these oxidants ranged from 10 mmol m–2 d–1 in winter to 80 mmol m–2 d–1 in summer. An estimation of the upper limit of the annual nitrate flux into the sediment showed that about 10% of the 250,000 t of nitrate discharged annually by the river may be decomposed within the inner Weser Estuary.  相似文献   

19.
The dissolution of water does not stop at the OH– stage but may proceed further towards H2 plus O– formation. The discovery of atomic carbon dissolved in minerals suggests that, if CO2 enters oxides and silicates at high pressures and temperatures, not only [CO3]2– ions but also [CO 4 . ]4– complexes are formed via a charge transfer which produces O– and essentially zero-valent, atomic carbon. Under P —T-conditions of the mantle, where the solubility for water and CO2 is high, the silicate phases formed may therefore consist to a large volume fraction of O– ions which are much smaller than O2–ions and strongly cova-lently bonding. The implications for the crystal chemistry of high pressure phases, for the petrology of mantle rocks are outlined.  相似文献   

20.
The Mozambique Belt (MB) of the East Africa Orogen contains large areas of granulite-facies migmatitic gneisses with Archaean and Palaeoproterozoic protolith ages and that were recycled during the Neoproterozoic Pan-African orogeny. The study area is situated along the Great Ruaha River and within the Mikumi National Park in central Tanzania where migmatitic gneisses and mafic to intermediate granulites are interlayered with Neoproterozoic granulite-facies migmatitic metapelites. Mineral textures suggest isothermal decompression, with the peak mineral assemblage comprising Grt–Bt–Ky–Kfs–Pl–Qtz ± Phn ± Ti-Oxide ± melt and amphibolite-facies retrograde assemblage Grt–Bt–Sil–Ms–Kfs–Pl–Qtz ± Fe–Ti-Oxide. The near isothermal retrograde overprint is seen in well-developed formation of pseudomorphs after garnet. The HP granulite-facies assemblages record P–T conditions of 13–14 kbar at 760–800 °C. Retrogression and the release of fluids from crystallizing melts occurred at 7 kbar and 650–700 °C. A fluid inclusion study shows three types of fluid inclusion consisting of nearly pure CO2, as well as H2O–NaCl and H2O–CO2 mixtures. We suggest that a immiscible CO2-bearing brine represents the fluid composition during high-grade peak metamorphism, and that the fluid inclusions containing H2O–NaCl or nearly pure CO2 represent trapped fluids from in situ crystallised melt. The results suggest strong isothermal decompression, which is probably related to a fast exhumation after crustal thickening in the central part of the Mozambique Belt in Tanzania.  相似文献   

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