Stratiform and vein U,Mo and Cu mineralization in the Novoveská Huta area,CSFR     

I. Rojkovič  L. Novotny  M. Háber 《Mineralium Deposita》1993,28(1):58-65

U-Mo and Cu mineralization occurs in horizons as well as in veins in the Permian formations near Novoveská Huta. Ore mineralization is represented by uraninite, U-Ti oxides, coffinite, molybdenite, chalcopyrite, tennantite and pyrite. The isotopic composition of S and C displays a larger variability in the stratiform ores (³⁴S from –32.7 to +2.7 and ¹³C from –27.1 to — 0.5) These data suggest mixing of meteoric solutions with fluids of volcanic origin and a complex history. There is a narrower range of ³⁴S from –18.8 to –4.6 and ¹³C from –6.3 to –2.5% in quartz-carbonate veins with Cu mineralization suggesting a deep source of ore-bearing solutions. The Permian volcanics were a significant source of ore elements.Their contents of U, Mo, Cu and Y are from two to eight times higher than in sedimentary rocks. Accumulations of ore elements in the horizons were formed by the reduction and adsorption processes 240 ± 30 Ma ago according to U-Pb isotopic dating. Due to Alpine tectonism, these low-grade ores (U<0.1 wt%) were remobilized and higher-grade U-Mo ores (U>0.1 wt%) were formed 130 ± 20 Ma ago at temperatures ranging from 110 to 120° C, according to fluid inclusions. Younger veins with Cu mineralization were formed 115 ± 10 Ma according to the model age of Pb at temperatures ranging from 95 to 190°C.  相似文献   

Recreation on public lands in New Zealand — past,present and future     

Kay L. Booth 《GeoJournal》1993,29(3):299-305

Since the turn of the century, recreation has grown as a motivating force in public land administration. Today, the Department of Conservation manages approximately one third of New Zealand's outdoor recreation resources and has the mandate to foster the use of natural and historic resources for recreation, and to allow their use for tourism (Conservation Act 1987:8). This paper traces the emergence of a recreation perspective within public land administration and examines the development of a recreation philosophy and policy within the Department of Conservation. It suggests future directions for outdoor recreation management in New Zealand.  相似文献   

Electron paramagnetic resonance of Sc3+-stabilized CO 3 3− molecule-ion in natural calcite     

R. M. Mineyeva  L. V. Bershov  A. V. Speranskiy 《Physics and Chemistry of Minerals》1993,20(2):136-140

Electron paramagnetic resonance (EPR) spectra of CO ₃ ^3– molecule-ions stabilized by Sc³⁺ in natural calcite were identified and studied at X-band frequencies and room temperature. The principal values of the g-tensor (g _xx= 1.9997, g _yy = 2.0030, g _zz = 1.9972) and the direction cosines of the g and A tensors for CO ₃ ^3– -Sc³⁺ center were found to be close to that for the well-known CO ₃ ^3– -Y³⁺ center. A quantitative comparison of different impurity contents in calcite samples and analysis of the intensities of forbidden transitions were used to identify Sc³⁺. An estimation of the unpaired electron spin density on the nuclei of paramagnetic centers confirms that both centers, CO ₃ ^3– -Sc³⁺ and CO ₃ ^3– -Y³⁺, have the same nature.  相似文献   

Magnetic properties,self-reversal remanence and thermal alteration products of smythite     

Miroslav Krs  František Novák  Marta Krsová  Petr Pruner  Jiří Jansa 《Studia Geophysica et Geodaetica》1993,37(4):382-400

Summary This study is a follow up of the investigation of some magnetic properties and metastability of greigite in samples obtained from Miocene claystones in the Kruné hory (Erzgebirge) Piedmont basins (Bohemia). Three different methods of upgrading the smythite were applied; the magnetic properties of the concentrates are compared. The thermal conversion of smythite sets in at 200°C while greigite converts at 250°C. The first intermediate products to be formed are iron sulphides, marcasite clearly dominating over pyrite and pyrrhotite. Apart from a Fe³⁺ sulphate with a composition of Fe₂(SO₄)₃, oxidation of these sulphides gives rise to -Fe₂O₃. The result of the subsequent decomposition of the mentioned sulphate is the formation of -Fe₂O₃, which retains the sulphate structure. The final product of the thermal decomposition at 800°C is -Fe₂O₃. In the smythite concentrate the conversion to Fe³⁺ sulphate and -Fe₂O₃ is about twice as intensive as in greigite. No direct conversion to -Fe₂O₃ was found. During the thermal process self-reversals of remanence were observed, in various samples as many as four reversals in the temperature interval from 340 to 590°C. The occurrences of self-reversals of remanence were only observed at high degrees of thermal demagnetization, of the order of 10^–2 down to 10^–3 in the temperature interval of sulphide origin (below 400°C), and of the order of 10^–4 down to 10^–6 in the temperature interval of Fe-oxides origin (above 400°C).Presented at the 3rd Conference on New Trends in Geomagnetism, Castle of Smolenice, Czechoslovakia, June 22–29, 1992  相似文献   

极性转换期间地球磁场形态学研究   总被引：3，自引：1，他引：2  

朱日祥  丁仲礼 《地球物理学报》1993,36(3):347-359

本文对采自中国黄土高原西峰（35.7°N,107.6°E）和段家坡（34.2°N,109.2°E）两个剖面中黄土层L8和古土壤层S8的1281块定向古地磁样品做了详细的岩石磁学和古地磁学研究.证实了Matuyama-Brunhes（M-B）极性转换带位于L8的中下部.提出了下列观点:1.M-B极性转换过程与地球磁场方向变化相联系的持续时间为3600-4500a,而与地球磁场强度变化相联系的持续时间则为8000-9000a,即强度变化存在“超前和滞后” 效应;2.M-B转换场的形态是由三次快速倒转和一次不成功的倒转构成,或者说,转换场具有快速变换极性的振荡特征;3.M-B转换过程中地球磁场并不是以轴对称的非偶极子场为主,而是偶极子场至少与非偶极子场相当;4.中国黄土-古土壤沉积物所含磁性矿物的主要成分是磁铁矿,它是研究极性转换期间地球磁场详细结构的良好物质.  相似文献   

Isotope and trace element evidence for three component mixing in the genesis of the North Luzon arc lavas (Philippines)   总被引：5，自引：0，他引：5  

F. McDermott  M. J. Defant  C. J. Hawkesworth  R. C. Maury  J. L. Joron 《Contributions to Mineralogy and Petrology》1993,113(1):9-23

Post-3Ma volcanics from the N Luzon arc exhibit systematic variations in ⁸⁷Sr/⁸⁶Sr (0.70327–0.70610), ¹⁴³Nd/¹⁴⁴Nd (0.51302–0.51229) and ²⁰⁸Pb^*/²⁰⁶Pb^* (0.981–1.035) along the arc over a distance of about 500 km. Sediments from the South China Sea west of the Manila Trench also exhibit striking latitudinal variations in radiogenic isotope ratios, and much of the isotopic range in the volcanics is attributed to variations in the sediment added to the mantle wedge during subduction. However, Pb-Pb isotope plots reveal that prior to subduction, the mantle end-member had high 8/4, and to a lesser extent high 7/4, similar to that in MORB from the Indian Ocean and the Philippine Sea Plate. Th isotope data on selected Holocene lavas indicate a source with unusually high Th/U ratios (4.5–5.5). Combined trace element and isotope data require that three end-members were implicated in the genesis of the N Luzon lavas: (1) a mantle wedge end-member with a Dupal-type Pb isotope signature, (2) a high LIL/HFS subduction component interpreted to be a slab-derived hydrous fluid, and (3) an isotopically enriched end-member which reflects bulk addition (<5%) of subducted S China Sea terrigenous sediment. The ⁸⁷Sr/⁸⁶Sr ratios in the volcanics show a restricted range compared with that in the sediments, and this contrasts with ¹⁴³Nd/¹⁴⁴Nd and ²⁰⁸Pb^*/²⁰⁶Pb^*, both of which have similar ranges in the volcanics and sediments. Such differences imply that whereas the isotope ratios of Nd, Pb and Th are dominated by the component from subducted sediment, those of Sr reflect a larger relative contribution from the slab-derived fluid.  相似文献   

Fractional crystallization and zoning in igneous feldspars: ideal water-buffered liquid fractionation lines and feldspar zoning paths     

William L. Brown 《Contributions to Mineralogy and Petrology》1993,113(1):115-125

Diagrams giving plagioclase and sanidine fractionation paths and liquid fractionation lines under conditions of ideal water-buffered fractional crystallization in the ternary feldspar system were constructed graphically using topological reasoning, and experimental data and calculated phase relationships from the literature. The liquidus lines and solidus or solvus paths are unique at constant P and a _{H 2}O. The composition of a liquid evolves with time and moves along a fractionation line by removal of successive crystal fractions, whereas the compositions of each of the crystal fractions lie on and define a solidus or solvus path. Most but not all such water-buffered lines and paths differ only slightly from those in which water is free to build up during crystallization and a _{H 2}O to increase, as in many rocks. Liquid compositions lying along liquidus fractionation lines are not normally preserved, unless erupted as aphyric lavas. The solidus or solvus paths may be preserved either as overgrowth zones in crystals (zoning paths) or as a series of crystal fractions in layered intrusions. The topologies of the lines and paths depend mainly on the nature of the two-feldspar boundary line separating the plagioclase and sanidine fields which is a function of P _{H 2}O or a _{H 2}O at constant P; increases in either progressively lower the liquidi and solidi and cause larger intersections of the solidi with the solvus. One-feldspar solidus paths at high P and a _{H 2}O are simple, whereas they are complex and may bend back on themselves at low P _{H 2}O or low a _{H 2}O at high P. Two-feldspar paths may be simultaneous (cotectic) or sequential (peritectic). The former are simple and do not meet at high P and a _{H 2}O, the critical solution line lying in the gap; they are complex and may bend back or overlap at low P _{H 2}O or low a _{H 2}O at high P, the position of the critical solution line being hard to determine. Liquids which have simultaneously fractionated two feldspars may fractionate only one towards the end, crystallization changing from subsolvus to hypersolvus. Sequential paths may involve overgrowth of an early feldspar by a later one, usually sanidine overgrowths on plagioclase, but plagioclase overgrowths on sanidine occur. These complexities explain in part the difficulties of unravelling the textural and compositional relationships of ternary feldspars in water-poor felsic igneous rocks (even in the absence of alteration or complex magma dynamics) and of trying to deduce phase relationships from natural occurrences of feldspars.C.R.P.G. contribution number 948  相似文献   

Alkaline and ultramafic carbonate lamprophyres in Central Bohemian carboniferous basins,Czech Republic     

Dr. J. Ulrych  Dr. E. Pivec  Dr. K. Zák  Dr. J. Bendl  Dr. P. Bosák 《Mineralogy and Petrology》1993,48(1):65-81

Summary Dykes of alkaline and ultramafic carbonate lamprophyres (monchiquite-ouachitite and aillikite) intrude the Carboniferous sediments of Central Bohemia. Their characteristic feature is the presence of substantial amounts of a sodalite group mineral (presumably haüyne), carbonate and barite. Isotopic compositions of ¹³C (–3.4 to –6.2) and ¹⁸O ( + 13.5 to + 15.9) indicate that the carbonate is of primary magmatic origin and that fluids were formed at temperatures of 500 to 350°C. High contents of CO₂ (3.6 to 17.6 wt.%) and incompatible elements, high LREE/HREE ratios (30.0 to 57.7), and low Rb/Sr (0.025 to 0.078) and⁸⁷Sr/⁸⁶Sr (0.7038 to 0.7042) ratios suggest the ultramafic lamprophyres are related to deep-seated carbonated magmas of mantle origin. Low degree of partial melting ( < 1%) of the mantle peridotite is envisaged, with additional transport of fluids rich in incompatible elements into the crustal chamber. Alkaline lamprophyres are fractionated derivatives which originated from the same source. Magma intrusion from different levels of a magma chamber into fracture zones under horizontal tension without a central intrusion could result in variability in lamprophyre composition (cumulates or evolved derivatives).

---

Alkalische und ultramafische Karbonat-Lamprophyre der zentralen böhmischen Karbonbecken, Tschische Republik

Zusammenfassung Alkalische und ultramafische Karbonat-Lamprophyrgänge (Monchiquit-Ouachitit und Aillikit) intrudieren in karbonische Sedimente Zentralböhmens. Sie sind charakterisiert durch das Auftreten von beträchtlichen Mengen an Mineralen der Sodalith-Gruppe (v.a. Haüyn), Karbonaten und Baryt. Ihre Isotopenzusammensetzung von ¹³C (–3.4 bis –6.2) und ¹⁸O (13.5 bis 15.9) zeigt, daß die Karbonate primär magmatischen Ursprungs sind und daß assoziierte Fluide in einem Temperaturbereich von 350 bis 500°C gebildet wurden. Hohe Gehalte an CO₂ (3.6 bis 17.6 Gew. %), inkompatiblen Elementen, hohe LREE/HREE-Verhältnisse (30.0 bis 57.7), sowie niedrige Rb/Sr—(0.025 bis 0.078) und⁸⁷Sr/⁸⁶Sr-(0.7038 bis 0.7042) Verhältnisse lassen vermuten, daß die ultramafischen Lamprophyre mit karbonatischen Magmen des Mantels in Beziehung stehen. Eine niedrige Aufschmelzungsrate ( < 1%) von Mantelperidotit mit zusätzlichem Transport von, an inkompatiblen Elementen angereicherten Fluiden, in die krustale Magmenkammer wird diskutiert. Alkalische Lamprophyre sind als stärker fraktionierte Magmen, die derselben Quelle entstammen, zu verstehen. Die Intrusion der aus verschiedenen Bereichen der Magmenkammer stammenden Magmen in durch horizontale Dehnung verursachte Störungszonen könnte das Fehlen eines zentralen Intrusionskörpers und die unterschiedliche Zusammensetzung der Lamprophyre (Kumulate oder entwickelte Derivate) erklären.

---

---

With 8 Figures  相似文献   

On the tidal variation of the geopotential     

José M. Ferrándiz  Juan Getino 《Celestial Mechanics and Dynamical Astronomy》1993,57(1-2):279-292

In this paper analytical expressions are derived for the temporal variations ofJ ₂ andJ ₂₂ due to the tides of the solid Earth, taking into account only the deformation of the mantle, and employing a procedure already used by the authors in their Hamiltonian theory of the Earth's rotation, which obtain the necessary parameters in a direct way by integration of those provided by a selected model of Earth interior.Numerical tables giving the periodic variation of coefficients are given, as well as a new prediction for UT1. For J ₂ and J ₂₂ the amplitudes reach such a magnitude that both two variations should not be ignored in studies involving the analysis of highly precise satellite tracking data. Moreover, the possibility of improving our knowledge of the value of those harmonic coefficients in only a more exact digit appears as to be strongly dependent on the limitations in the theoretical modeling of the variations of the inertia tensor due to solid tides.  相似文献   

H2 in interstellar and extragalactic ices: infrared characteristics, ultraviolet production, and implications     

Sandford SA  Allamandola LJ 《The Astrophysical journal》1993,409(2):L65-L68

H2 is the most abundant molecule in the universe. We demonstrate that this molecule may be an important component of interstellar and possibly intergalactic ices, both because it can be formed in situ, within the ices, and because gas phase H2 can freeze out onto dust grains in some astrophysical environments. The condensation-sublimation and infrared spectral properties of ices containing H2 are presented. We show that solid H2 in H20-rich ices can be detected by an infrared absorption band at 4137 cm-1 (2.417 micrometers). The surface binding energy of H2 to H2O ice was measured to the delta Hs/k = 555 +/- 35 K. Surface binding energies can be used to calculate the residence times of H2 on grain surfaces as a function of temperature. Some of the implications of these results are considered.  相似文献