High-T, low-P metamorphism in the Palaeoproterozoic Halls Creek Orogen, northern Australia: the middle crustal response to a mantle-related transient thermal pulse   总被引：1，自引：1，他引：1  

S. Bodorkos  M. Sandiford  N. H. S. Oliver  P. A. Cawood 《Journal of Metamorphic Geology》2002,20(2):217-237

High‐T, low‐P metamorphic rocks of the Palaeoproterozoic central Halls Creek Orogen in northern Australia are characterised by low radiogenic heat production, high upper crustal thermal gradients (locally exceeding 40 °C km^?1) sustained for over 30 Myr, and a large number of layered mafic‐ultramafic intrusions with mantle‐related geochemical signatures. In order to account for this combination of geological and thermal characteristics, we model the middle crustal response to a transient mantle‐related heat pulse resulting from a temporary reduction in the thickness of the mantle lithosphere. This mechanism has the potential to raise mid‐crustal temperatures by 150–400 °C within 10–20 Myr following initiation of the mantle temperature anomaly, via conductive dissipation through the crust. The magnitude and timing of maximum temperatures attained depend strongly on the proximity, duration and lateral extent of the thermal anomaly in the mantle lithosphere, and decrease sharply in response to anomalies that are seated deeper than 50–60 km, maintained for <5 Myr in duration and/or have half‐widths <100 km. Maximum temperatures are also intimately linked to the thermal properties of the model crust, primarily due to their influence on the steady‐state (background) thermal gradient. The amplitudes of temperature increases in the crust are principally a function of depth, and are broadly independent of crustal thermal parameters. Mid‐crustal felsic and mafic plutonism is a predictable consequence of perturbed thermal regimes in the mantle and the lowermost crust, and the advection of voluminous magmas has the potential to raise temperatures in the middle crust very quickly. Although pluton‐related thermal signatures significantly dissipate within <10 Myr (even for very large, high‐temperature intrusive bodies), the interaction of pluton‐ and mantle‐related thermal effects has the potential to maintain host rock temperatures in excess of 400–450 °C for up to 30 Myr in some parts of the mid‐crust. The numerical models presented here support the notion that transient mantle‐related heat sources have the capacity to contribute significantly to the thermal budget of metamorphism in high‐T, low‐P metamorphic belts, especially in those characterised by low surface heat flow, very high peak metamorphic geothermal gradients and abundant mafic intrusions.  相似文献   

Small-Mammal Data on Early and Middle Holocene Climates and Biotic Communities in the Bonneville Basin, USA     

Dave N. Schmitt  David B. Madsen  Karen D. Lupo 《Quaternary Research》2002,58(3):255

Archaeological investigations in Camels Back Cave, western Utah, recovered a series of small-mammal bone assemblages from stratified deposits dating between ca. 12,000 and 500 ¹⁴C yr B.P. The cave's early Holocene fauna includes a number of species adapted to montane or mesic habitats containing grasses and/or sagebrush (e.g., Lepus townsendii, Marmota flaviventris, Reithrodontomys megalotis, and Brachylagus idahoensis) which suggest that the region was relatively cool and moist until after 8800 ¹⁴C yr B.P. Between ca. 8600 and 8100 ¹⁴C yr B.P. these mammals became locally extinct, taxonomic diversity declined, and there was an increase in species well-adapted to xeric, low-elevation habitats, including ground squirrels, Lepus californicus and Neotoma lepida. The early small-mammal record from Camels Back Cave is similar to the 11,300–6000 ¹⁴C yr B.P. mammalian sequence from Homestead Cave, northwestern Utah, and provides corroborative data on Bonneville Basin paleoenvironments and mammalian responses to middle Holocene desertification.  相似文献   

Cation distribution in amphiboles synthesized along the Ga analogue of the tremolite–aluminotschermakite join     

D. M. Jenkins  K. Ishida  V. Liogys  D. Ghosh 《Physics and Chemistry of Minerals》2002,29(2):87-97

 Amphiboles were synthesized from bulk compositions prepared along the join Ca_1.8Mg_5.2Si₈O₂₂(OH)₂–Ca_1.8Mg₃Ga₄Si₆O₂₂(OH)₂ hydrothermally at 750–850 °C and 1.0–1.8 GPa, and along the join Ca₂Mg₅Si₈O₂₂F₂–Ca₂Mg₃Ga₄Si₆O₂₂F₂, anhydrously at 1000 °C and 0.7 GPa to document how closely the tschermak-type substitution is obeyed in these analogues of aluminous amphiboles. Electron-microprobe analyses and Rietveld X-ray diffraction structure refinements were performed to determine cation site occupancies. The extent of Ga substitution was found to be limited in both joins, but with the fluorine series having about twice the Ga content (0.6 atoms per formula unit, apfu) of the hydroxyl-series amphiboles (0.3 apfu). The tschermak-type substitution was followed very closely in the hydroxyl series with essentially equal partitioning of Ga between tetrahedral and octahedral sites. The fluorine-series amphiboles deviated significantly from the tschermak-type substitution and, instead, appeared to follow a substitution that is close to a Ca-pargasite substitution of the type: ^[6]Ga³⁺+2^[4]Ga³⁺+1/2^[A] Ca²⁺ = ^[6]Mg²⁺+2^[4]Si⁴⁺+1/2^[A]□. Infrared spectroscopy revealed an inverse correlation between the intensity of the OH-stretching bands and the Ga content for the hydroxyl- and fluorine-series amphiboles. The direct correlation between the Ga and F content and inverse relationship between the Ga and OH content may be a general phenomenon present in other minerals and suggests, for example, that high F contents in titanite are controlled by the Al content of the host rock and that there may be similar direct Al–F correlations in tschermakitic amphiboles. Evidence for the possibility that Al (Ga) might substitute onto only a subset of the tetrahedral sites in tschermakitic amphiboles was sought but not observed in this study. Received: 5 March 2001 / Accepted: 31 July 2001  相似文献   

Formation of hydroxyl radicals catalyzed by clay surfaces     

D. Gournis  M. A. Karakassides  D. Petridis 《Physics and Chemistry of Minerals》2002,29(2):155-158

 The formation of superoxide and hydroxyl radicals at the surface of smectite clays due to oxygen reduction is demonstrated by electron paramagnetic resonance spectroscopy. The yield of hydroxyl radicals is mainly a function of particle size of the clays and depends, to a lesser extent, on the clay lattice iron. Synthetic laponite clay with small platelet size (∼20 nm) and without lattice iron is leading in the formation of hydroxyl radicals followed by montmorillonite (∼200 nm). Fluorohectorite (∼2000 nm) was inactive to hydroxyl radical formation by oxygen reduction. Received: 20 January 2001 / Accepted: 7 August 2001  相似文献   

Incorporation of Cr<Superscript>3+</Superscript> in dickite: a spectroscopic study     

E. Balan  T. Allard  G. Morin  G. Calas 《Physics and Chemistry of Minerals》2002,29(4):273-279

 We have investigated a well-ordered sample of natural Cr-bearing dickite from Nowa Ruda (Lower Silesia, Poland) using electron paramagnetic resonance (EPR) at X- and Q-band frequencies (9.42 and 33.97 GHz, respectively) and optical diffuse reflectance spectroscopy. The observation of the spin-forbidden transitions at 15500 and 14690 cm⁻¹ allows us to unambiguously identify the major contribution of octahedrally coordinated Cr³⁺ ions in the optical spectrum. The X- and Q-band EPR spectra show two superposed Cr³⁺ signals. The corresponding fine-structure parameters were determined at room temperature and 145 K. These results suggest the substitution of Cr³⁺ for Al³⁺ in equal proportions in the two unequivalent octahedral sites of the dickite structure. In kaolin group minerals, the distortion around Cr³⁺ ions (λ≈ 0.2–0.4) in Al sites is significantly less rhombic than that observed around Fe³⁺ ions (λ≈ 0.6–0.8). Received: 29 June 2001 / Accepted: 22 October 2001  相似文献   

Low-temperature thermodynamic properties of disordered zeolites of the natrolite group     

I. E. Paukov  N. K. Moroz  Yu. A. Kovalevskaya  I. A. Belitsky 《Physics and Chemistry of Minerals》2002,29(4):300-306

 The heat capacity of paranatrolite and tetranatrolite with a disordered distribution of Al and Si atoms has been measured in the temperature range of 6–309 K using the adiabatic calorimetry technique. The composition of the samples is represented with the formula (Na_1.90K_0.22Ca_0.06)[Al_2.24Si_2.76O₁₀]·nH₂O, where n=3.10 for paranatrolite and n=2.31 for tetranatrolite. For both zeolites, thermodynamic functions (vibrational entropy, enthalpy, and free energy function) have been calculated. At T=298.15 K, the values of the heat capacity and entropy are 425.1 ± 0.8 and 419.1 ±0.8 J K⁻¹ mol⁻¹ for paranatrolite and 381.0 ± 0.7 and 383.2 ± 0.7 J K⁻¹ mol⁻¹ for tetranatrolite. Thermodynamic functions for tetranatrolite and paranatrolite with compositions corrected for the amount of extraframework cations and water molecules have also been calculated. The calculation for tetranatrolite with two water molecules and two extraframework cations per formula yields: C _p (298.15)=359.1 J K⁻¹ mol⁻¹, S(298.15) −S(0)=362.8 J K⁻¹ mol⁻¹. Comparing these values with the literature data for the (Al,Si)-ordered natrolite, we can conclude that the order in tetrahedral atoms does not affect the heat capacity. The analysis of derivatives dC/dT for natrolite, paranatrolite, and tetranatrolite has indicated that the water- cations subsystem within the highly hydrated zeolite may become unstable at temperatures above 200 K. Received: 30 July 2001 / Accepted: 15 November 2001  相似文献   

Electrons in feldspar II: a consideration of the influence of conduction band-tail states on luminescence processes     

N. R. J. Poolton  K. B. Ozanyan  J. Wallinga  A. S. Murray  L. Bøtter-Jensen 《Physics and Chemistry of Minerals》2002,29(3):217-225

 Most natural feldspars contain many charged impurities, and display a range of bond angles, distributed about the ideal. These effects can lead to complications in the structure of the conduction band, giving rise to a tail of energy states (below the high-mobility conduction band) through which electrons can travel, but with reduced mobility: transport through these states is expected to be thermally activated. The purpose of this article is twofold. Firstly, we consider what kind of lattice perturbations could give rise to both localized and extended conduction band-tail states. Secondly, we consider what influence the band tails have on the luminescence properties of feldspar, where electrons travel through the sample prior to recombination. The work highlights the dominant role that 0.04–0.05-eV phonons play in both the luminescence excitation and emission processes of these materials. It also has relevance in the dating of feldspar sediments at elevated temperatures. Received: 11 May 2001 / Accepted: 6 September 2001  相似文献   

Fluid-bearing alkaline carbonate melts as the medium for the formation of diamonds in the Earth''s mantle: an experimental study     

N. Pal''yanov  A. G. Sokol  M. Borzdov  A. F. Khokhryakov 《Lithos》2002,60(3-4):145-159

We have experimentally studied the formation of diamonds in alkaline carbonate–carbon and carbonate–fluid–carbon systems at 5.7–7.0 GPa and 1150–1700 °C, using a split-sphere multi-anvil apparatus (BARS). The starting carbonate and fluid-generating materials were placed into Pt and Au ampoules. The main specific feature of the studied systems is a long period of induction, which precedes the nucleation and growth of diamonds. The period of induction considerably increases with decreasing P and T, but decreases when adding a C–O–H fluid to the system. In the range of P and T corresponding to the formation of diamonds in nature, this period lasts for tens of hours. The reactivity of the studied systems with respect to the diamond nucleation and growth decreases in this sequence: Na₂CO₃–H₂C₂O₄·2H₂O–C>K₂CO₃–H₂C₂O₄·2H₂O–C>>Na₂CO₃–C>K₂CO₃–C. The diamond morphology is independent of P and T, and is mainly governed by the composition of the crystallization medium. The stable growth form is a cubo-octahedron in the Na₂CO₃ melt, and an octahedron in the K₂CO₃ melt. Regardless of the composition of the carbonate melt, only octahedral diamond crystals formed in the presence of the C–O–H fluid. The growth rates of diamond varied in the range from 1.7 μm/h at 1420 °C to 0.1–0.01 μm/h at 1150 °C, and were used to estimate, for the first time, the possible duration of the crystallization of natural diamonds. From the analysis of the experimental results and the petrological evidence for the formation of diamonds in nature, we suggest that fluid-bearing alkaline carbonate melts are, most likely, the medium for the nucleation and growth of diamonds in the Earth's upper mantle.  相似文献   

Environmental response to a large, explosive rhyolite eruption: sedimentology of post-1.8 ka pumice-rich Taupo volcaniclastics in the Hawke''s Bay region, New Zealand     

B. Segschneider  C. A. Landis  V. Manville  J. D. L. White  C. J. N. Wilson 《Sedimentary Geology》2002,150(3-4):275-299

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The role of an H<Subscript>2</Subscript>O-rich fluid component in the generation of primitive basaltic andesites and andesites from the Mt. Shasta region,N California   总被引：2，自引：1，他引：2  

T. Grove  S. Parman  S. Bowring  R. Price  M. Baker 《Contributions to Mineralogy and Petrology》2002,142(4):375-396

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