A thermochemical study of glasses and crystals along the joins silica-calcium aluminate and silica-sodium aluminate

Enthalpies of solution in molten 2PbO · B₂O₃ at 985 K are reported for series of glasses xCa_0.5AlO₂-(1?x)SiO₂ (O ≤ x ≤ 0.99) and xNaAlO₂-(1?x)SiO₂ (0 ≤ x ≤ 0.56). The data are compared to values for the corresponding crystalline aluminosilicates and to preliminary data for systems containing KAlO₂ and Mg_0.5AlO₂. The enthalpies of mixing of glasses become more exothermic with increasing basicity of the mono- or divalent oxide. The tendency toward immiscibility on the silica-rich side, indicated by the shape of the heat of mixing curve between x = 0 and x = 0.4, is pronounced in the calcium aluminate system, but not in the sodium aluminate system. The shape of the heat of mixing curve, which is roughly symmetrical about x = 0.5, can be rationalized in terms of glass structure by considering essentially random substitution of Si and Al on a continuous three dimensional tetrahedral framework, with stabilization arising from electrostatic interactions between aluminum and the nonframework cation balancing the destabilizing effects arising from perturbation of the aluminosilicate framework by the nonframework cation. These trends are consistent with the variation of physical properties of aluminosilicate melts.     

Late Pleistocene paleo-oceanography of the Norwegian-Greenland Sea: Benthic foraminiferal evidence

Fluctuations in benthic foraminiferal faunas over the last 130,000 yr in four piston cores from the Norwegian Sea are correlated with the standard worldwide oxygen-isotope stratigraphy. One species, Cibicides wuellerstorfi, dominates in the Holocene section of each core, but alternates downcore with Oridorsalis tener, a species dominant today only in the deepest part of the basin. O. tener is the most abundant species throughout the entire basin during periods of particularly cold climate when the Norwegian Sea presumably was ice covered year round and surface productivity lowered. Portions of isotope Stages 6, 3, and 2 are barren of benthic foraminifera; this is probably due to lowered benthic productivity, perhaps combined with dilution by ice-rafted sediment; there is no evidence that the Norwegian Sea became azoic. The Holocene and Substage 5e (the last interglacial) are similar faunally. This similarity, combined with other evidence, supports the presumption that the Norwegian Sea was a source of dense overflows into the North Atlantic during Substage 5e as it is today. Oxygen-isotope analyses of benthic foraminifera indicate that Norwegian Sea bottom waters warmer than they are today from Substage 5d to Stage 2, with the possible exception of Substage 5a. These data show that the glacial Norwegian Sea was not a sink for dense surface water, as it is now, and thus it was not a source of deep-water overflows. The benthic foraminiferal populations of the deep Norwegian Sea seem at least as responsive to near-surface conditions, such as sea-ice cover, as they are to fluctuations in the hydrography of the deep water. Benthic foraminiferal evidence from the Norwegian Sea is insufficient in itself to establish whether or not the basin was a source of overflows into the North Atlantic at any time between the Substage 5e/5d boundary at 115,000 yr B.P. and the Holocene.     

Texture and structural interpretation of the alteration of pyroxene to other biopyriboles

In a metamorphosed gabbro from Hokkaido, Japan, augite containing exsolved orthohypersthene and minor pigeonite has been altered to a variety of biopyriboles. High resolution transmission electron microscopy of slightly altered augite shows only narrow (010) lamellae of clinoamphibole which always contain even numbers of double chains. In more highly altered regions, all three pyroxenes are changed to double-, triple- and more highly polymerized multiple-chain biopyriboles, with chlorite d ₀₀₁ 14.5 Å) found only in orthopyroxene. Several (010) lamellae containing only one double chain have been observed, and their textural relationship to the surrounding single-chain host may explain how the rotated domains of biopyribole initially attain their orientation in the host pyroxene.A structural model is proposed for the polymerization of single chains in the tetrahedral layers of pyroxene which involves small movements of oxygens and tetrahedral atoms (Si, Al) with a minimum of bond breaking and re-forming, concommitant with hydroxylization of certain oxygens and the diffusion of Mg, Fe and/or Ca along the rift in the octahedral layer.     

Reaction relationships of chrome-spinels in igneous rocks — further evidence from the layered intrusions of Rhum and Mull,Inner Hebrides,Scotland

Compositions of chrome-spinels in peridotites from the layered igneous rocks of Rhum and of the Ben Buie intrusion, Mull, show evidence of post-depositional reaction relationships with the cumulus olivine and/or the intercumulus liquid. Some seam-forming spinels in the Ben Buie intrusion are highly aluminous, more so than those in the Rhum intrusion. Occasional zoned spinels, in both intrusions, show enrichment in Al towards their rims. The evidence suggests that the spinel reaction trend involving Cr-Al exchange proceeds in the direction of Al-enrichment. Equilibrium between chrome-spinel and cumulus olivine appears to have been attained rarely, thus limiting the application of the olivine-spinel geothermometer.     

Seismic risk of circum-pacific earthquakes I. Strain energy release

Commonly used earthquake “whole process” frequency - magnitude and strain energy - magnitude laws are merged to obtain an analytic expression for an upper bound magnitude to regional earthquake occurrenceM ₃, which is expressed primarily in terms of the annual maximum magnitudeM ₁ and the magnitude equivalent of the annual average total strain energy releaseM ₂. Values ofM ₃ are also estimated graphically from cumulative strain energy release diagrams. Both methods are illustrated by application to the high seismicity of the circum-Pacific belt, using Duda’s (1965) data and regionalisation. Values ofM ₃ obtained analytically, with their uncertainties, are in agreement with those obtained graphically. Empirical relations are then obtained betweenM ₁,M ₂, andM ₃, which could be of general assistance in regional seismic risk considerations if they are found to be of a universal nature. For instance.M ₃ andM ₂ differ by one magnitude unit in subregions of the circum-Pacific.     

X-Ray Fluorescence Determination of Trace Elements in 6 B.C.S. and 5 P.R.E. Reference Materials

The concentrations of 20 trace elements in 6 British Chemical Standards (BCS) reference materials and 5 European Federation of Refractories Producers (PRE) reference materials have been determined by X-ray fluorescence spectrometry.     

Stepwise fluorination—a useful approach for the isotopic analysis of hydrous minerals

Analytical uncertainties in oxygen isotopic studies of hydrous silica have been investigated using a partial fluorination procedure in which fractional oxygen yields are achieved by reducing the amount of fluorine. Stepwise reaction of opaline silica results in a set of sequential oxygen fractions which show a wide range of δ¹⁸O values due to variable amounts of water, organic matter, and other impurities, δ-values for successive fractions in non-biogenic opal systematically increase as water is reacted away and then remain constant to within ±0.2%. as the remaining silica reacts, δ-values in biogenic silica increase similarly but then decrease when low ¹⁸O oxide(?) impurities begin to react.The troublesome water component in opal is readily removed by Stepwise fluorination. This technique allows more precise oxygen isotope analysis of non-biogenic opal-A, and may improve the analytical precision for biogenic silica and any silicate mineral containing a significant water component.     

Further Studies Of Atmospheric Turbulence In Layers Near The Surface: Scaling The Tke Budget Above The Roughness Sublayer

The second of two experimental studies of the TKE budget conducted on sites of different roughness is described, and results are compared. The first took place within a shallow layer above a small field of mostly bare, cultivated soil; the second was carried out above a roughness sublayer of significant depth on an extensive plain of tall dry grass. Budget terms observed in the second study were scaled with a modified u which compensated for effects of an unusually large stress gradient and ensured that the _m functions would be collinear. By showing that the modification becomes negligible in smaller gradients, it is demonstrated that in normal conditions, budgets observed above significant roughness sublayers should be normalized by scaling in terms of the unreduced Reynolds stress at the sublayer's upper surface. This procedure is shown to be consistent with the expectation that TKE budgets in layers near the surface all scale in fundamentally the same way.Other findings include: (1) the fact that most _m functions previously reported are not quite collinear is attributed to a type of overspeeding known to affect three-cup anemometers; (2) revised _m functions, collinear and largely free of the effects of overspeeding, are determined from a well-established characteristic of the linear _m relation for the stable case; (3) data that define collinear _m functions can also be represented with single hyperbolic curves; (4) dissipation is found to be 10 to 15% too small to balance total TKE production in unstable and neutral conditions and to decrease with increasing z/L in thestable regime; and (5) new relations for based on the observed behaviour of the dissipation deficit provide an improved closure for the set of equations that express the budget terms as functions of _m and z/L.     

Regional Energy Demand Responses To Climate Change: Methodology And Application To The Commonwealth Of Massachusetts

Climate is a major determinant of energy demand. Changes in climate may alter energy demand as well as energy demand patterns. This study investigates the implications of climate change for energy demand under the hypothesis that impacts are scale dependent due to region-specific climatic variables, infrastructure, socioeconomic, and energy use profiles. In this analysis we explore regional energy demand responses to climate change by assessing temperature-sensitive energy demand in the Commonwealth of Massachusetts. The study employs a two-step estimation and modeling procedure. The first step evaluates the historic temperature sensitivity of residential and commercial demand for electricity and heating fuels, using a degree-day methodology. We find that when controlling for socioeconomic factors, degree-day variables have significant explanatory power in describing historic changes in residential and commercial energy demands. In the second step, we assess potential future energy demand responses to scenarios of climate change. Model results are based on alternative climate scenarios that were specifically derived for the region on the basis of local climatological data, coupled with regional information from available global climate models. We find notable changes with respect to overall energy consumption by, and energy mix of the residential and commercial sectors in the region. On the basis of our findings, we identify several methodological issues relevant to the development of climate change impact assessments of energy demand.