Tectono-metamorphic evolution of a nappe stack: A case study of the Swiss Alps   总被引：1，自引：1，他引：1  

M. Herwegh  O.A. Pfiffner 《Tectonophysics》2005,404(1-2):55-76

Fold-and-thrust belts are prominent structures that occur at the front of compressional orogens. To unravel the tectonic and metamorphic evolution of such complexes, kinematic investigations, quantitative microstructural analysis and geothermometry (calcite–graphite, calcite–dolomite) were performed on carbonate mylonites from thrust faults of the Helvetic nappe stack in Central Switzerland. Paleo-isotherms of peak temperature conditions and cooling stages (fission track) of the nappe pile were reconstructed in a vertical section and linked with the microstructural and kinematic evolution. Mylonitic microstructures suggest that under metamorphic conditions close to peak temperature, strain was highly localized within thrust faults where deformation temperatures spatially continuously increased in both directions, from N to S within each nappe and from top–down in the nappe stack, covering a temperature range of 180–380 °C. Due to the higher metamorphic conditions, thrusting of the lowermost nappe, the Doldenhorn nappe, was accompanied by a much more pronounced nappe internal ductile deformation of carbonaceous rock types than was the case for the overlying Wildhorn- and Gellihorn nappes. Ongoing thrusting brought the Doldenhorn nappe closer to the surface. The associated cooling resulted in a freezing in of the paleo-isotherms of peak metamorphic conditions. Contemporaneous shearing localized in the basal thrust, initially still in the ductile deformation regime and finally as brittle faulting and cataclasis inducing ultimately an inverse metamorphic zonation. With ongoing exhumation and the formation of the Helvetic antiformal nappe stack, a bending of large-scale tectonic structures (thrusts, folds), peak temperature isotherms and cooling isotherms occurred. While this local bending can directly be attributed to active deformation underneath the section investigated up to times of 2–3 ma, a more homogeneous uplift of the entire region is suggested for the very late and still active exhumation stage.  相似文献   

An unusual modern silica–carbonate sinter from Pavlova spring, Ngatamariki, New Zealand     

Kathleen A. Campbell†  K. A. Rodgers‡  Jane M. A. Brotheridge  P. R. L. Browne§ 《Sedimentology》2002,49(4):835-854

ABSTRACT A silica–carbonate deposit is forming from the dilute alkali chloride waters of Pavlova spring, a small thermal pool and outflow channel (85 to <40 °C), situated at the northern extent of the South Orakonui area of the Ngatamariki geothermal field, Taupo Volcanic Zone (TVZ), New Zealand. It is one of a small but growing number of thermal spring features known to yield deposits of mixed mineralogy. At Pavlova, a distinctive, crustose, chalk‐white, meringue‐like sinter, comprising non‐crystalline opal‐A silica with subordinate calcite, is actively precipitating both around the margins of and as small islets within the spring, with an average accumulation rate of ≈ 2 mm year^?1. Both emergent and partly submerged substrates host the sinter, including fallen pine branches, twigs, needles and cones, gum leaves, grass blades, bracken fronds, pumice, sediment and microbial mats. The sinter is thin (25–35 mm thickness), finely laminated and contains three distinct types of stacked horizons. Submerged basal layers constitute stratiform to undulatory microstromatolites with pseudocolumns, which grew outwards and upwards on narrow twig nuclei. Emergent middle layers comprise discontinuous, spicular microstromatolites (to 10 mm height), with prostrate and erect microbial filaments, silica spheres and silicified mucus, overlain by silicified structures of probable fungal origin. In places, lower and middle sinter layers are capped by white, smooth, convex surfaces that coalesce into subdued, curved ridges, resembling laterally continuous peaks of egg‐white meringue. The meringue is internally laminated, with fossilized microbes preserved in thin horizons. Small lensoid masses of calcite crystals nestle between silica laminae throughout the sinter. The near‐neutral (pH ≈ 7·2) spring water is a dilute chloride‐carbonate type (HCO≈ 470 µg g^?1, Cl^–≈ 600 µg g^?1) with low (≈ 50 µg g^?1), typical of TVZ thermal fields where deep chloride fluid mixes with CO₂‐rich, steam‐heated shallow waters before discharge. The hot water changed little in composition from 1993 to 1999 and, despite dilution by meteoric waters, contains sufficient SiO₂ (≈ 220 µg g^?1) for opal‐A to deposit at the surface upon cooling. However, the concentration of Ca²⁺ (≈ 6 µg g^?1) is such that the precipitation of calcite is not expected without modification of spring waters. Precipitation occurs by evaporation of thin water films at exposed substrate surfaces, via meniscoid as well as capillary creep (wicking), through porous sinter horizons and across emergent vegetative surfaces in contact with spring water or steam. The height of the deposit above the water surface is restricted by the upper limit of moisture bathing these substrates. Splash and spray are not involved in the formation of Pavlova spicular microstromatolites, as is the case for other texturally similar deposits from hotsprings elsewhere. This young (< 15 years), mineralogically and morphologically complex hot‐spring deposit exhibits > 10 times lower accumulation rates than typical siliceous sinters in the TVZ, and deposition of both silica and calcite is controlled by microchemical conditions and local temperature gradients, rather than by bulk spring water chemistry.  相似文献   

Transfer zones and fault reactivation in inverted rift basins: Insights from physical modelling   总被引：2，自引：0，他引：2  

Elena A. Konstantinovskaya  Lyal B. Harris  Jimmy Poulin  Gennady M. Ivanov 《Tectonophysics》2007,441(1-4):1-26

Carbonate mylonites with varying proportions of second-phase minerals were collected at positions of increasing metamorphic grade along the basal thrust of the Morcles nappe (Helvetic nappes, Switzerland). Variations of temperature, stress, and strain rate, changes in chemistry of solid and fluid phases, and differing degrees of strain localization and annealing were tracked by measuring the shapes, mean sizes, and size distributions of both matrix and second-phase grains, as well as crystal preferred orientation (CPO) of the matrix. Field structures suggest that strain rate was constant along the fault. The mean and distribution of the calcite grain sizes were affected most profoundly by temperature: Increased temperature, presumably accompanied by decreased stress, correlated with larger mean sizes and wider size distributions. At a given location, the matrix grains in mylonites with more second-phase particles are, on average, smaller, have narrower size distributions, and have more elongate shapes. For example, mylonites with 50 vol.% of second phases have matrix grain sizes half that of pure mylonites. Changes in calcite chemistry and the presence of synkinematic fluids seemed to influence microfabric only weakly. Temporal variations in conditions, such as exhumation-induced cooling, apparently provoke changes in temperature, stress, and strain rate along the nappe. These changes result in further strain localization during retrograde conditions and cause the grain size to be reduced by an additional 50%. The matrix CPO strengthens with increasing temperature or strain, but weakens and rotates with increasing second-phase content. These fabric changes suggest differing rates of grain growth, grain size reduction, and development of CPO owing to variations in the deformation conditions and, perhaps, mechanisms. To interpret natural mylonite structures or to extrapolate mechanical data to natural situations requires careful characterization of the microfabric, and, in particular, second-phase minerals.  相似文献   

Magmatic anhydrite and calcite in the ore-forming quartz-monzodiorite magma at Santa Rita, New Mexico (USA): genetic constraints on porphyry-Cu mineralization   总被引：6，自引：0，他引：6  

A. Audtat  T. Pettke  D. Dolej 《Lithos》2004,72(3-4):147-161

A quartz-monzodioritic dike associated with the porphyry-Cu mineralized stock at Santa Rita, NM, has been studied to constrain physico-chemical factors (P, T, f_O2, and volatile content) responsible for mineralization. The dike contains a low-variance mineral assemblage of amphibole, plagioclase (An_30–50), quartz, biotite, sphene, magnetite, and apatite, plus anhydrite and calcite preserved as primary inclusions within the major phenocryst phases. Petrographic relationships demonstrate that anhydrite originally was abundant in the form of phenocrysts (1–2 vol.%), but later was replaced by either quartz or calcite. Hornblende–plagioclase thermobarometry suggests that several magmas were involved in the formation of the quartz-monzodiorite, with one magma having ascended directly from ≥14 km depth. Rapid magma ascent is supported by the presence of intact calcite inclusions within quartz phenocrysts.

The assemblage quartz+sphene+magnetite+Mg-rich amphibole in the quartz-monzodiorite constrains magmatic oxygen fugacity at logf_O2>NNO+1, in agreement with the presence of magmatic anhydrite and a lack of magmatic sulfides. The same reasoning generally applies for rocks hosting porphyry-Cu deposits, seemingly speaking against a major role of magmatic sulfides in the formation of such mineralizations. There is increasing evidence, however, that magmatic sulfides play an important role in earlier stages of porphyry-Cu evolution, the record of which is often obliterated by later processes.  相似文献   

An experimental study of calcite dissolution rates at acidic conditions and 25 °C in the presence of NaPO₃ and MgCl₂     

Marwan Alkattan  Eric H. Oelkers  Jean-Louis Dandurand  Jacques Schott 《Chemical Geology》2002,190(1-4):291-302

Dissolution rates of single calcite crystals were determined from sample weight loss using free-drift rotating disk techniques. Experiments were performed at 25 °C in aqueous HCl solutions over the bulk solution pH range −1 to 3 and in the presence of trace concentrations of aqueous NaPO₃ and MgCl₂. These salts were chosen for this study because aqueous magnesium and phosphate are known to strongly inhibit calcite dissolution at neutral to basic pH. Reactive solutions were undersaturated with respect to possible secondary phases. Neither an inhibition or enhancement of calcite dissolution rates was observed in the presence of aqueous MgCl₂ at pH 1 and 3. The presence of trace quantities of NaPO₃, which dissociates in solution to Na⁺ and H₂PO₄⁻, decreased the overall calcite dissolution rate at pH≤2. This contrasting behavior could be attributed to the different adsorption behavior of these dissolved species. As calcite surfaces are positively charged in acidic solutions, aqueous Mg²⁺ may not adsorb, whereas aqueous phosphate, present as either the anion H₂PO₄⁻ or the neutral species H₃PO₄⁰, readily adsorbs on calcite surfaces leading to significant dissolution inhibition.  相似文献   

Calcite formation in microbial mats: modeling and quantification of inhomogeneous distribution patterns by a cellular automaton model and multifractal measures     

Jürgen Kropp  Werner von Blob  Thomas Klenke 《International Journal of Earth Sciences》1996,85(4):857-863

The evolution of early diagenetic calcite cements in microbial mats of recent supratidal sediments of the southern North Sea is modeled in a two-dimensional microscale approach by a cellular automaton model (CAM). Calcite is traced out in the model by virtual calcium distribution patterns obtained from runs under different assumptions concerning sediment-intrinsic conditions. For justification of the CAM, real calcium distribution patterns, documented by scanning electron microscopy coupled with energy-dispersive X-ray spectrometry (SEM/EDX), are quantitatively compared with the virtual patterns on the basis of multifractal analyses. The formation of high magnesian calcite as a consequence of biogenic anaerobic decomposition of organic matter starts at certain initial calcite domains. In this stage an inhomogeneous and multifractal calcium distribution is characteristic. Nearly complete remineralization of organic matter leads to monofractal behavior of generalized fractal dimensions (D_B(q) ±1.84). The CAM results confirm that calcite formation is a self-determining morphogenetical process and diffusive transport processes of reactants within the mat affect the biogenic calcite formation.  相似文献   

锡铁山铅锌矿中石英,方解石的热发光研究     

陈振强 《矿产与地质》1996,10(6):412-416

在测试锡铁山铅锌矿中石英、方解石热发光的基础上，结合石英、方解石中微量元素特征，研究其热发光曲线特征和参数特征，并对比其它铅锌矿区石英、方解石热发光的资料，认为锡铁山铅锌矿中石英的热发光强度愈大，反映的含矿性愈差；方解石的热发光受其方解石中Ｍｎ＾２＋（Ｆｅ＾２＋）和ＲＥＥ＾３＋的影响，靠近矿体的方解石热发光强度降低，为进一步扩大矿区找矿工作提供了石英、方解石热发光的科学依据。  相似文献   

Geochemische und 13C/12C-isotopenchemische Untersuchung zur Herkunft der Kohlensäure in mineralhaltigen Wässern Nordhessens (Deutschland)     

M. Dietzel  H. Schwecke  A. Hirschfeld  M. Rhring  M. E. Bttcher 《洁净——土壤、空气、水》1997,25(4):191-201

Geochemical and ¹³C/¹²C-isotopical Investigation of Mineral Waters in Northern Hessia (Germany) and the Origin of their CO₂ Content The dissolved carbonate originates from three sources: 1. biogenetic soil-CO₂, 2. volcanic CO₂ related to the evaporites of the Zechstein formation, and 3. carbonate derived from the dissolution of limestones and dolomites. Miocenic basaltic melts penetrated the evaporites of the Zechstein, and the related CO₂ was trapped in the intra- and intergranulars of the salt minerals. Circulating meteoric waters dissolve the salt minerals releasing CO₂ gas. Thus, the occurrence of basalt is related to the CO₂ contents of the evaporites, and the dissolution of only small amounts of salts rich in CO₂ may result in a high concentration of carbonic acid. In waters rich in carbonate, where volcanic CO₂ dominates over the other two sources of carbon, a δ¹³C-value of “salt-CO₂” of about –1‰ (PDB) is obtained. Water with less dissolved carbonate species have smaller quantities of salt-CO₂ down to about 20%.  相似文献   

Effect of Iron and Manganese Ions on the Crystal Growth of Calcium Carbonate     

K. Johannsen  T. Alex  H. Burwieck  T. Dorsch  K. Wichmann 《洁净——土壤、空气、水》1997,25(4):202-207

The present study describes examinations of growth rate of calcium carbonate using seed crystals of different sizes in the range of 10 to 50 μm at concentrations in the range of 5 to 50 g·L^?1. The rate constant related to the crystal surface per volume was found to be independend of the crystal size. The effect of temperature on the rate constant was described using the Arrhenius equation. The use of suspension of lime as precipitating agent leads to decrease of the rate constant compared to lime water. This effect can be explained by the dissolution of suspended calcium hydroxide particles. Using the presented conditions (SI₀ = 2.8), no impact of iron and manganese ions was observed.  相似文献   

Overview of calcite/opal deposits at or near the proposed high-level nuclear waste site,Yucca Mountain,Nevada, USA: Pedogenic,hypogene, or both?     

C. A. Hill  Y. V. Dublyansky  R. S. Harmon  C. M. Schluter 《Environmental Geology》1995,26(2):69-88

Calcite/opal deposits (COD) at Yucca Mountain were studied with respect to their regional and field geology, petrology and petrography, chemistry and isotopic geochemistry, and fluid inclusions. They were also compared with true pedogenic deposits (TPD), groundwater spring deposits (GSD), and calcite vein deposits (CVD) in the subsurface. Some of the data are equivocal and can support either a hypogene or pedogenic origin for these deposits. However, Sr-, C-, and O-isotope, fluid inclusion, and other data favor a hypogene interpretation. A hypothesis that may account for all currently available data is that the COD precipitated from warm, CO₂-rich water that episodically upwelled along faults during the Pleistocene, and which, upon reaching the surface, flowed downslope within existing alluvial, colluvial, eluvial, or soil deposits. Being formed near, or on, the topographic surface, the COD acquired characteristics of pedogenic deposits. This subject relates to the suitability of Yucca Mountain as a high-level nuclear waste site.  相似文献