The importance of local‐scale openness within regions dominated by closed woodland

New and existing pollen data from Wales, UK, are used to assess the level of landscape openness at the regional and local scale. At the regional scale, the existing pollen data support the high‐forest model of vegetation structure by 6000 cal. yr. BC prior to any palynological signal for anthropogenic impact in the region. New data from two sites in southwest Wales follow the general regional pattern of early to middle Holocene vegetation succession, but are striking owing to maintenance of high non‐arboreal pollen percentages (NAPs) throughout the mid‐Holocene. It is argued that these NAPs indicate that a significant degree of openness can be found at the local level (and beyond the confines of the peat‐forming site) within regions characterised by closed woodland. It is possible that woodland development in these areas may have been suppressed by reduced drainage, although the role of grazing animals in maintenance of clearings cannot be assessed. Implications for this local degree of openness are discussed, in particular the significance of vegetation heterogeneity at the local scale for the construction of place or locale for prehistoric communities. Copyright © 2006 John Wiley & Sons, Ltd.     

Experimental studies on three potassium-rich ultramafic rocks from Damodar Valley, East India

Summary An experimental study on the phase relationships of three potassium-rich ultramafic rocks from the Damodar Valley, Gondawana basins, has been performed under upper mantle P–T conditions (1.0–2.5 GPa, 700–1200 °C). The Mohanpur lamproite and Satyanarayanpur minette, both from the Raniganj basins, have been investigated with the addition of 15 wt% H₂O. No water was added in the experiments done on an olivine minette from the Jarangdih coal mine, Bokaro Basin, which originally contains 15 wt% CO₂ and 2.86 wt% H₂O. In all cases, olivine is the liquidus phase followed by phlogopite. The subsolidus assemblage for the three rocks is a phlogopite-bearing harzburgite, associated with apatite, Mg-ilmenite and carbonates for the Jarangdih rock; apatite, chromian spinel and carbonates and priderite (only between 1.0 and 1.2 GPa) in the case of the Mohanpur lamproite, and finally apatite, chromian spinel, rutile, and carbonate in the Satyanarayanpur sample. Although orthopyroxene is absent in the natural potassium-rich ultramafic rocks, its presence in the run products of the Jarangdih rock is possibly related to a reaction between olivine and a CO₂-bearing fluid phase. The presence of orthopyroxene in the run products of Mohanpur and Satyanarayanpur rocks may be due to a reaction between K-feldspar, olivine and a vapour phase to produce phlogopite and orthopyroxene. On the basis of present experimental investigation and isotopic studies made by previous investigators, it has been suggested that these K-rich rocks have crystallized from melts derived by vein-plus-wall-rock melting of a phlogopite-bearing harzburgite source rock. Received December 15, 1999; revised version accepted June 17, 2001     

On the growth of disturbances to forced and dissipated barotropic flows

Abstract

We consider the growth of disturbances to large-scale zonally-asymmetric steady states in a truncated spectral model for forced and dissipated barotropic flow. A variant of the energy method is developed to optimize the instantaneous disturbance energy growth rate. The method involves solving a matrix eigenvalue problem amenable to standard numerical techniques. Two applications are discussed. (1) The global stability of a family of steady states is assessed in terms of the Ekman damping coefficient r. It is shown that monotonic global stability (i.e., every disturbances energy monotonically decays to zero) prevails when r≥r_c . (2) Initially fastest-growing disturbances are constructed in the r<r_c regime. Particular attention is paid to a subregion of the r<r_c regime where initially-growing disturbances exist despite stability with respect to normal modes. Nonlinear time-dependent simulations are performed in order to appraise the time evolution of various disturbances.     

红土型金矿床综述(英文)

近二十年来 ,热带地区普遍存在的红土型风化作用及其对矿床与矿化带的影响引起了普遍的关注。红土型风化壳的主要矿物成分是以铁铝的氧化物及氢氧化物和粘土矿物为主 ,如针铁矿、赤铁矿、铝土矿、高岭石及石英等 ,与其未风化的母岩相比 ,含有相当高的铁和铝。红土型风化过程中 ,易溶元素均不同程度地被淋滤 ,而难溶元素则相对富集。红土型金矿床就是在这样强烈的风化作用中由原生的金矿化带进一步富集而成 ,并可形成极富的矿体。金矿体常常赋存于风化壳的上部 ,易于露天开采。目前 ,在澳大利亚、巴西、巴布亚新几内亚、印度以及非洲的一些国家均发现了红土型金矿床。红土型风化剖面一般可分为 5个特征带 ,由上而下为 :表土带、铁质带、斑点带、浅色带、腐岩带 ,下面即为未风化的母岩 ,金矿体主要赋存于铁质带和斑点带中。红土型风化壳厚度变化很大 ,薄则几米 ,厚可达数百米。金在风化过程中往往向矿化带两侧运移 ,矿体常呈上宽下窄状。次生金常呈自形晶、树枝晶、浑圆状及不规则状产出 ,并常常与铁质结核共生。一般地说 ,次生金的成色很高 ,因为红土型风化作用常常是在氧化并且酸性的地球化学环境中进行 ,金和银主要以氯化物的形式运移 ,局部地球化学环境的变化可导致金的沉淀 ,而银的氯化物则较稳定 ,?     

Stable and Sr-isotope evidence for fluid advection during thrusting of the glarus nappe (swiss alps)

At the Glarus thrust in the Swiss Helvetic Alps, Permian Verrucano siltstones are allochthonously superimposed over Tertiary Flysch with an intermediate, about 1 metre thin layer of intensively deformed calcmylonite of probable Mesozoic provenance. The H–O–C- and Sr-isotope compositions of minerals from the calc-mylonite and strongly mylonitized Verrucano siltstones were determined in order to assess: (1) equilibrium-disequilibrium relationships; (2) isotopic composition of the fluid phase, its provenance and water/rock ratios; (3) sources of Sr in the calc-mylonite; (4) deformation temperatures. The isotopic composition of cale-mylonite micro-samples from five sites along the thrust varies from 22 to 12 and 2 to-10 for ¹⁸O and ¹³C respectively. All samples are ¹⁸O depleted by up to 14 relative to the presumed marine Helvetic carbonate protoliths (¹⁸O=25.4±2). A pronounced geographic trend of ¹⁸O depletion from 22 in the north to 12 in the south is observed. In calc-mylonites, ⁸⁷Sr/⁸⁶Sr ratios range from typical Mesozoic marine carbonate protolith signatures (0.708±0.005) to more radiogenic values as high as 0.722. A variable contribution of radiogenic ⁸⁷Sr to the calc-mylonite is though to reflect interaction with fluids that aquired their Sr from the Hercynian granitic basement. Chlorites and muscovites from the calc-mylonite and Verrucano have uniform ¹⁸O values but display D values from-40 to-147%: the D-enriched values correspond to the primary metamorphic or formational fluids expelled during thrusting, whereas the D-depleted samples reflect selective H-isotope exchange with meteoric fluids during uplift of the Alpine belt. The isotopic composition of the calc-mylonites requires exchange with ¹⁸O—depleted, ⁸⁷Sr—enriched fluids at very high water/rock ratios. Possible sources for these are dewatering of the underlying Flysch and/or metamorphic fluids, or formation brines expelled along the thrust from greater depth. These could be derived from compaction and dewatering of the Flysch in the northern part of the thrust; in the south, however, where Verrucano is thrust over ¹⁸O-rich Mesozoic carbonates, the extreme ¹⁸O depletion of the calc-mylonite has to be explained either by fluid advection within the Verrucano hanging wall and thrust zone or alternatively by exchange with metamorphic fluids from greater depth, expelled along the thrust. Microstructural evidence (abundant veins, stylolites, breccias) suggests that fluids played an important role in deformation and strain localization. Excepting albite all major components (quartz, chlorite, muscovite, calcite) are both dynamically recrystallized and crystallized as secondary minerals in pressure shadows and syn-mylonitic veins, indicating that these minerals were potentially open to oxygen isotopic exchange during alpine metamorphism and thrust deformation. Within the mylonitized Verrucano silstones, isolated quartz-chlorite and quartz-calcite fractionations yield temperatures of around 320°C close to values obtained from calcite-dolomite thermometry (355°C±30) and in agreement with the regional lower greenschist facies metamorphism. Quartz-calcite and quartz-albite fractionations indicate slightly lower temperatures around 250°C, owing to selective lower temperature re-equilibration of the calcite and albite during post peak metamorphism.     

Sub-sea-floor metamorphism,heat and mass transfer

The ophiolitic rocks of E. Liguria, Italy contain a spilitic metamorphic assemblage sequence, cross-cut by hydrothermal veins, which developed in the oceanic environment. Metamorphic parageneses indicate that temperatures as high as 400°C were realised at depths as shallow as 300 m below the original rock/water interface. The inferred temperature interval was equivalent to a geothermal gradient of 1300°C/km.It is suggested that metamorphism took place in a sub-sea-floor geothermal system, and that such systems are an integral part of the sea-floor spreading process. Modern evidence is provided to support this hypothesis, and to suggest that heavy metal rich solutions discharged from such systems are responsible for the formation of a metal enriched sedimentary component. A unified model of sub-sea-floor metamorphism and mass transfer is proposed, and possible differences between sub-sea-floor and terrestial geothermal systems are discussed. In the light of the model, the origins of certain aspects of bedded cherts found associated with ophiolitic rocks, of ophiolitic massive sulphide deposits and of certain trace element patterns are considered.     

The crystallization of magnesite from aqueous solution

It has been suggested that the highly hydrated character of the Mg²⁺ ion in aqueous solution is responsible for the often encountered difficulty of precipitating stable, anhydrous phases of magnesium carbonate and calcium-magnesium carbonate. In an effort to investigate this, a study of magnesite crystallization kinetics was undertaken, utilizing the reaction of hydromagnesite plus CO₂ to yield magnesite at 126°C. The reactions were characterized by prolonged initial quiescent periods prior to the onset of detectable crystallization. The length of the initial period was found to vary with Mg concentration, pCO₂ and ionic strength. Contrary to classical kinetics, the reaction studied was inhibited by increased Mg concentration. Ionic strength and pCO₂ acted as positive catalysts.