Interplay between equilibrium and kinetics in prograde metamorphism of pelites: an example from the Nelson aureole, British Columbia

The distribution of metapelitic mineral assemblages in the Nelson aureole, British Columbia, generally conforms to what is predicted from phase equilibria. However, in detail, the sequence and spacing of isograds, mineral textures and mineral compositions and mineral chemical zoning do not. Two of the main disequilibrium features in the aureole are: (i) delay in the onset and progress of several reactions, i.e. overstepping in temperature; and (ii) unreactivity of staurolite and especially garnet porphyroblasts when they are reactants in prograde reactions. The thermal overstepping is ascribed to difficulty of nucleation of the product porphyroblasts and sluggishness of dissolution of porphyroblasts when they are reactants. The extent to which these kinetic barriers delay the onset of reaction is related to the reaction affinity of each reaction, defined herein as the Gibbs free‐energy difference between the thermodynamically stable, but not‐yet‐crystallized, products and the metastable reactants. For oversteps in temperature (ΔT), reaction affinity is, in turn, related to the difference in entropy (ΔS) between these two states through the relation A = ΔT * ΔS. Mineral reactions which release large quantities of H₂O, such as chlorite‐consuming reactions, have a higher entropy change per unit of temperature overstep, and therefore a higher reaction affinity, than those which release little or no H₂O, such as the chlorite‐free staurolite‐consuming reaction. Thermal overstepping is consequently expected to be less for the former than for the latter, as was estimated in the aureole where 0 to 30 °C overstepping was required for garnet, staurolite and andalusite growth from a muscovite + chlorite‐bearing precursor rock and ～70 °C overstepping was required for the growth of Al₂SiO₅ from a staurolite‐bearing, chlorite‐free precursor. In all cases, reaction progress was strongly influenced by the presence or absence of fluid, with presence of fluid lowering kinetic barriers to nucleation and growth and therefore the degree of thermal overstepping. Textural features of rocks from the nearly coincident garnet, staurolite and andalusite isograds are suggestive of a fluid‐catalysed ‘cascade effect’ in which reaction took place in a narrow temperature interval; several competing muscovite + chlorite‐consuming reactions, some metastable, appear to have occurred in parallel. Metamorphic reaction, fluid release and possibly fluid presence in general in the aureole were episodic rather than continuous, and in several cases well removed from equilibrium conditions. The extent to which these findings apply to regional metamorphism depends on several factors, a major one being enhanced deformation, which is expected to lower kinetic barriers to nucleation and growth.     

Reaction localization and softening of texturally hardened mylonites in a reactivated fault zone, central Argentina

The Tres Arboles ductile fault zone in the Eastern Sierras Pampeanas, central Argentina, experienced multiple ductile deformation and faulting events that involved a variety of textural and reaction hardening and softening processes. Much of the fault zone is characterized by a (D2) ultramylonite, composed of fine‐grained biotite + plagioclase, that lacks a well‐defined preferred orientation. The D2 fabric consists of a strong network of intergrown and interlocking grains that show little textural evidence for dislocation or dissolution creep. These ultramylonites contain gneissic rock fragments and porphyroclasts of plagioclase, sillimanite and garnet inherited from the gneissic and migmatitic protolith (D1) of the hangingwall. The assemblage of garnet + sillimanite + biotite suggests that D1‐related fabrics developed under upper amphibolite facies conditions, and the persistence of biotite + garnet + sillimanite + plagioclase suggests that the ultramylonite of D2 developed under middle amphibolite facies conditions. Greenschist facies, mylonitic shear bands (D3) locally overprint D2 ultramylonites. Fine‐grained folia of muscovite + chlorite ± biotite truncate earlier biotite + plagioclase textures, and coarser‐grained muscovite partially replaces relic sillimanite grains. Anorthite content of shear band (D3) plagioclase is c. An30, distinct from D1 and D2 plagioclase (c. An35). The anorthite content of D3 plagioclase is consistent with a pervasive grain boundary fluid that facilitated partial replacement of plagioclase by muscovite. Biotite is partially replaced by muscovite and/or chlorite, particularly in areas of inferred high strain. Quartz precipitated in porphyroclast pressure shadows and ribbons that help define the mylonitic fabric. All D3 reactions require the introduction of H⁺ and/or H₂O, indicating an open system, and typically result in a volume decrease. Syntectonic D3 muscovite + quartz + chlorite preferentially grew in an orientation favourable for strain localization, which produced a strong textural softening. Strain localization occurred only where reactions progressed with the infiltration of aqueous fluids, on a scale of hundreds of micrometre. Local fracturing and microseismicity may have induced reactivation of the fault zone and the initial introduction of fluids. However, the predominant greenschist facies deformation (D3) along discrete shear bands was primarily a consequence of the localization of replacement reactions in a partially open system.     

岩盐及芒硝中各种化合物质量分数的计算

本文以等物质的量的反应规则建立了岩盐、芒硝中各种化合物的质量分数的计算公式。这些公式既符合法定计量单位的要求，又方便计算。     

高温超高压下Ni40Mn30Fe30与叶蜡石反应的研究

本文对Ｎｉ４０Ｍｎ３０Ｆｅ３０合金与在不同焙烧温度下得到的含水叶蜡，在高温超高压下的反应进行了实验研究，温度测至１４２０℃，压是至５．５ＧＰａ，研究了该反应的物质－化学机制，以及反应速率与温度，压力，含水量等参数的关系，对高压下物质迁移运动的固有特征进行了探讨。     

Geothermobarometry of mafic granulites and metapelite from the Palghat Gap, South India: petrological evidence for isothermal uplift and rapid cooling

The Palghat Gap region is located near the centre of the large southern Indian granulite terrane. at the northern edge of the Kodaikanal charnockite massif. The dominant rock types in the region are hornblende-biotite ± orthopyroxene gneisses and charnockites along with minor amounts of intercalated mafic granulite, metapelite and calc-silicate. The P-T estimates from garnetiferous mafic granulites and metapelite samples are generally in the range 9-10 kbar and 800-900 C using both conventional thermobarometric methods and the TWEEQU thermobarometry program. These P-T estimates, which should be taken as minimum values, are among the highest yet reported for South Indian and Sri Lankan granulites. The occurrence of orthopyroxene + plagioclase symplectites around embayed garnet grains in the mafic granulites and cordierite rims around garnet grains in metapelite suggest an isothermal decompression-type path. Similarly, a core-rim P-T trajectory indicates c. 3 and 7 kbar decompression at high temperature in the mafic granulites and metapelite, respectively. In both rock types, the key to the determination of the retrograde P-T path was the recognition of small amounts of second generation plagioclase with a more anorthitic composition than the matrix plagioclase. The preservation of high garnet-pyroxene temperatures in the mafic granulites (despite small garnet grain size) suggests rapid cooling of the terrane. Calculated minimum cooling rates range from 8 to 80 C Ma^-1. Such cooling rates are more rapid than those associated with normal isostatic processes and suggest that the terrane was tectonically exhumed at high temperature.     

凹凸棒石与Zn^2＋的长期作用研究

以凹凸棒石与Zn2＋为例研究粘土矿物与重金属离子长期作用过程,并运用高分辨透射电镜和X射线衍射分析粘土矿物与重金属离子长期作用的次生物相。结果表明：Zn2＋与凹凸棒石的长期作用是一个二阶段的过程,初始阶段为快速吸附作用,其后表现为慢速沉淀反应。高分辨透射电镜和X射线衍射分析表明,凹凸棒石与Zn2＋的长期作用过程中,具有纳米矿物特性的凹凸棒石表面快速水化,提高了悬浮液的pH值,诱导Zn2＋水解沉淀。而后,凹凸棒石缓慢溶解释放Al3＋和SiO44-与Zn（OH）2沉淀反应,形成Zn-A1双氢氧化物和异极矿。这一结果对认识土壤环境中重金属与粘土矿物的作用及重金属的归宿具有重要意义。     

A garnet population in Yellowknife schist, Canada

Abstract Data are presented on a garnet population in a specimen of garnet-biotite-plagioclase-quartz schist from the cordierite zone of an Archaean thermal dome in the Southern Slave Province of the Canadian Shield. Garnet crystals are bounded by planar dodecahedral faces and by trapezohedral faces which on the 10-μm scale are corrugated. Crystal distribution, as revealed by dissection of a small cubic volume of rock, is random. The size distribution is normal, with a mean diameter of 0.81 mm and a standard deviation of 0.32 mm. In the largest crystal of the population (mean radius 0.83 mm), [Mn] = 100 Mn/(Fe + Mg + Mn + Ca) decreases from 14.5 at the centre to 7.5 and then increases in the outer margin to 8.5; [Fe] increases continuously from 67 at the centre to 77 at the surface; [Mg] increases from 12.5 to 13.5 and then falls sharply to 11; [Ca] remains unchanged at 4.0 and then drops to 3.3. Progressively smaller crystals have progressively lower [Mn] and higher [Fe] concentrations at their centres, while all crystals have the same margin composition. Growth vectors extending from given concentration contours to crystal surfaces are of equal length regardless of the size of the crystal in which the vector is located. A garnet-forming model is presented in which reaction was initiated by a rise in temperature. Nucleation sites were randomly selected. The nucleation rate increased with time and then declined. Crystal faces advanced at a constant linear rate, which implies an increase in volume proportional to surface area. Initially, the composition of garnet deposited on crystal surfaces was determined by van Laar equations of equilibrium, which demanded the withdrawal of Mn and Fe from within chlorite crystals. This transfer reaction was then accompanied by an ion exchange reaction which moved Mn and Fe to garnet surfaces from biotite, in exchange for Mg. The exchange reaction provides an explanation for the high overall concentration of Mn and Fe in garnet and for the observed Mn and Mg reversals in the margins of crystals. The increase of garnet volume in the garnet population is found to be parabolic, i.e. Vαα⁵.     

Hydrothermal Alteration Zoning and Kinetic Process of Mineral-Water Interactions

This study reports the kinetic experimental results of albite in water and in KCI solution at 22 MPa in the temperature range of 25 to 400℃. Kinetic experiments have been carried out in an open flow-through reaction system (packed bed reactor). Albite dissolution is always incongruent in water at most temperatures, but becomes congruent at 300℃ (close to the critical point 374℃). At temperatures from 25 to 300℃, the incongruent dissolution of albite is reflected by the fact that sodium and aluminum are easily dissolved into water; from 300 to 400℃ it is reflected by silicon being more easily dissolved in water than Al and Na. Maximum albite dissolution rates in the flow hydrothermal systems have been repeatedly observed at 300℃, independent of flow rates.The kinetic experiments of albite dissolution in a KCl aqueous solution (0.1 mol KCl) indicate that the dissolution rate of albite increases with increasing temperature. Maximum silicon release rates of albite have been observed at 400℃, while ma     

An experimental study of the grain-scale processes of peridotite melting: implications for major and trace element distribution during equilibrium and disequilibrium melting

The grain-scale processes of peridotite melting were examined at 1,340°C and 1.5 GPa using reaction couples formed by juxtaposing pre-synthesized clinopyroxenite against pre-synthesized orthopyroxenite or harzburgite in graphite and platinum-lined molybdenum capsules. Reaction between the clinopyroxene and orthopyroxene-rich aggregates produces a melt-enriched, orthopyroxene-free, olivine + clinopyroxene reactive boundary layer. Major and trace element abundance in clinopyroxene vary systematically across the reactive boundary layer with compositional trends similar to the published clinopyroxene core-to-rim compositional variations in the bulk lherzolite partial melting studies conducted at similar P–T conditions. The growth of the reactive boundary layer takes place at the expense of the orthopyroxenite or harzburgite and is consistent with grain-scale processes that involve dissolution, precipitation, reprecipitation, and diffusive exchange between the interstitial melt and surrounding crystals. An important consequence of dissolution–reprecipitation during crystal-melt interaction is the dramatic decrease in diffusive reequilibration time between coexisting minerals and melt. This effect is especially important for high charged, slow diffusing cations during peridotite melting and melt-rock reaction. Apparent clinopyroxene-melt partition coefficients for REE, Sr, Y, Ti, and Zr, measured from reprecipitated clinopyroxene and coexisting melt in the reactive boundary layer, approach their equilibrium values reported in the literature. Disequilibrium melting models based on volume diffusion in solid limited mechanism are likely to significantly underestimate the rates at which major and trace elements in residual minerals reequilibrate with their surrounding melt. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Glacier fluctuations in the southern Peruvian Andes during the late‐glacial period,constrained with cosmogenic 3He

The occurrence of pronounced climate reversals during the last glacial termination has long been recognised in palaeoclimate records from both hemispheres and from high to low latitudes. Accurate constraint of both the timing and magnitude of events, such as the Younger Dryas and Antarctic Cold Reversal, is vital in order to test different hypotheses for the causes and propagation of abrupt climate change. However, in contrast to higher‐latitude regions, well‐dated records from the Tropics are rare and the structure of late‐glacial tropical climate remains uncertain. As a step toward addressing this problem, we present an in situ cosmogenic ³He surface exposure chronology from Nevado Coropuna, southern Peru, documenting a significant fluctuation of the ice margin during the late‐glacial period. Ten tightly clustered ages from a pair of moraines located halfway between the modern glacier and the Last Glacial Maximum terminus range from 11.9 to 13.9 ka and give an arithmetic mean age of 12.8 ± 0.7 ka (1σ). These data constitute direct evidence for a readvance, or prolonged stillstand, of glaciers in the arid Andes of southwestern Peru. Copyright © 2011 John Wiley & Sons, Ltd.