The impact of binary-star yields on the spectra of galaxies

One of the complexities in modelling integrated spectra of stellar populations is the effect of interacting binary stars besides Type Ia supernovae (SNeIa). These include common envelope systems, cataclysmic variables, novae, and are usually ignored in models predicting the chemistry and spectral absorption line strengths in galaxies. In this paper, predictions of chemical yields from populations of single and binary stars are incorporated into a galactic chemical evolution model to explore the significance of the effects of these other binary yields. Effects on spectral line strengths from different progenitor channels of SNeIa are also explored. Small systematic effects are found when the yields from binaries, other than SNeIa, are included, for a given star formation history. These effects are, at present, within the observational uncertainties on the line strengths. More serious differences can arise in considering different types of SNIa models, their rates and contributions.     

Structural elements in southeastern Quebec,northwestern Appalachians,Canada

An attempt is made to correlate and separate in terms of style and time two contrasting sets of structural elements in the northwestern part of the Appalachian Uplands in the Province of Quebec, Canada. There is sufficient evidence to indicate that a fold system with north-south trending axes is superimposed on a fold system with east-west axes. It is suggested that the two sets of structures represent pulses of one long-continued deformation accompanied by corresponding early and late phases of metamorphism.

---

Zusammenfassung Es wurde versucht, in den Appalachen des südöstlichen Teiles der Provinz Quebec, Kanada, zwei ungleichzeitige tektonische Systeme verschiedenen Baustils zu trennen. Die komplexen Kleinstrukturen zeigen, da\ Ost-West streichende Faltenachsen von einer jüngeren Nord-Süd-Faltung überprägt worden sind. Der Autor ist der Meinung, da\ die zwei tektonischen Systeme, die von einer frühen und späten Phase der Metamorphose begleitet werden, den zeitlich getrennten Verformungsstadien einer Orogenese entsprechen.

     

Schorlomite: a discussion of the crystal chemistry, formula, and inter-species boundaries

Examination of schorlomite from ijolite at Magnet Cove (USA) and silicocarbonatite at Afrikanda (Russia), using electron-microprobe and hydrogen analyses, X-ray diffraction and Mössbauer spectroscopy, shows the complexity of substitution mechanisms operating in Ti-rich garnets. These substitutions involve incorporation of Na in the eightfold-coordinated X site, Fe²⁺ and Mg in the octahedrally coordinated Y site, and Fe³⁺, Al and Fe²⁺ in the tetrahedrally coordinated Z site. Substitutions Ti⁴⁺Fe³⁺Fe³⁺_–1Si_–1 and Ti⁴⁺Al³⁺Fe³⁺_–1Si_–1 are of major significance to the crystal chemistry of schorlomite, whereas Fe²⁺ enters the Z site in relatively minor quantities (<3% Fe). There is no evidence (either structural or indirect, such as discrepancies between the measured and calculated Fe²⁺ contents) for the presence of ^[6]Ti³⁺ or ^[4]Ti⁴⁺ in schorlomite. The simplified general formula of schorlomite can be written as Ca₃Ti⁴⁺₂[Si_3-x(Fe³⁺,Al,Fe²⁺)_xO₁₂], keeping in mind that the notion of end-member composition is inapplicable to this mineral. In the published analyses of schorlomite with low to moderate Zr contents, x ranges from 0.6 to 1.0, i.e. Ti⁴⁺ in the Y site is <2 and accompanied by appreciable amounts of lower-charged cations (in particular, Fe³⁺, Fe²⁺ and Mg). For classification purposes, the mole percentage of schorlomite can be determined as the amount of ^[6]Ti⁴⁺, balanced by substitutions in the Z site, relative to the total occupancy in the Y site: (^[6]Ti⁴⁺–^[6]Fe²⁺–^[6]Mg²⁺– ^[8]Na⁺)/2. In addition to the predominant schorlomite component, the crystals examined in this work contain significant (>15 mol.%) proportions of andradite (Ca₃Fe³⁺₂Si₃O₁₂), morimotoite (Ca₃Fe²⁺TiSi₃O₁₂), and Ca₃MgTiSi₃O₁₂. The importance of accurate quantitative determination and assignment of Fe, Ti and other cations to the crystallographic sites for petrogenetic studies is discussed.

A STUDY OF THE SEISMIC SIGNATURES OF SEDIMENTATION MODELS USING SYNTHETIC SEISMOGRAMS*

In modern exploration for hydrocarbons there is a great emphasis on the location of stratigraphic traps and estimation of lithologic information like sand-shale ratios from seismic data. In order to investigate the possibilities of success in this endeavour we have studied the synthetic seismograms for wave form and spectral characteristic for four basic sedimentation models: (I) interbedded sand-shale model representing the sediments of generally fluviatile origin, (2) interbedded coal-shale model representing deltaic deposits, (3) sedimentary models representing transgression and regression of shore lines, and (4) a basal sand model. The results have shown that for the first two models a change in the sand-shale or coal-shale ratio results in a characteristically different seismogram. The nature of the seismogram, however, is also strongly dependent on how the sand-shale or coal shale layers are arranged to ultimately give the same number of total layers, thus implying the same coal-shale or sand-shale ratios. The transgression, regression, and basal sand models also produce characteristically different seismic signatures. The spectra of these seismograms show attendant characteristic changes. However, it seems that in the case of real data which are disturbed by noise and the effects of overlying layers these characteristic features may not always be distinguishable.     

Principles of tabling

The mechanism of concentration on the shaking table is discussed and a fresh attempt is made to obtain the theoretical model describing the velocity of a fluid in depth and time when in contact with a symmetrically reciprocating surface.The significance of the many design and operational variables and their interrelationships are examined. The various areas where the shaking table plays its role are then considered.The relevant features of micropanner, superpanner and the subsequent macropanner and pulsepanner are also treated since they all, like the shaking table, have the differential motion in common.     

X-ray transient sources

The galactic distribution and physical nature of X-ray transient sources is investigated. Two types of transients are considered. The observational data on 41 X-ray transient sources are given, and the average parameters of hard and soft X-ray transients are estimated.     

Power spectrum of brightness temperature fluctuations derived from solar eclipse observations at 2.8 GHz

In this paper we report on the MEM power spectrum analysis of brightness temperature fluctuations observed at 2.8 GHz during the total solar eclipse of 16 February 1980. The observed periodicities range from 3.5 min to 64 min. These periodicities may arise due to spatial and/or temporal variations in the solar radio emission. The observed periodicities imply presence of scale sizes ranging from 70,000 to 600,000 km assuming that the brightness fluctuations arise because of spatial variation only. On the other hand, if these fluctuations are due to temporal variation, the observed periodicities correspond well to predicted modes of solar global oscillations.     

Evidence for focused hot fluid flow within the Britannia Field, offshore Scotland, UK

Fluid inclusion and scanning electron microscope‐cathodoluminescence evidence indicates focused hot, saline, diagenetic fluid flow within the Eastern Flank of the Britannia Field, offshore Scotland, UK. The fluid was sourced from the Andrew Salt Dome, 10 km to the east. The fluids, which promoted quartz cementation of the upper zones within the field, were up to ～30°C hotter and had salinities up to ～10 wt% NaCl equivalent higher than fluids from lower in the reservoir section. During diagenesis hot saline fluids migrated westwards as part of a radiating ‘diagenetic front’ from the Andrew Salt Dome. Structural dip associated with the Eastern Flank of the Fladen Ground Spur impeded the westward movement of the diagenetic fluid. The quartz cements from the upper and lower reservoir zones can be distinguished by morphology. In the upper zones the quartz cements have well‐developed macro‐crystalline zoning and heterogeneous luminescence across the grain. In the lower zones, the cements are much less developed, unzoned and very weakly luminescent. The diagenetic fluids were primarily focused into Zone 45 within the upper reservoir. Furthermore, within the Main Platform Area the most prolific producing zone is Zone 45, indicating the importance of this interval as a permeable flow unit during both diagenetic and production timescales. Within the Eastern Flank, the quartz overgrowths have a major impact on reservoir permeability and thus well productivity. The overgrowths are most extensive in the originally clean sandstones with low clay content. Clay in optimum volumes (5–10%) can inhibit nucleation of the damaging quartz overgrowths without having a detrimental effect on pore connectivity. These observations provide a predictive concept for use in the search for relative reservoir sweetspots within the degraded Eastern Flank.     

Trace-element composition and zoning in clinopyroxene- and amphibole-group minerals: Implications for element partitioning and evolution of carbonatites

The present work is a first comprehensive study of the trace-element composition and zoning in clinopyroxene- and amphibole-group minerals from carbonatites, incorporating samples from 14 localities worldwide (Afrikanda, Aley, Alnö, Blue River, Eden Lake, Huayangchuan, Murun, Oka, Ozernaya Varaka, Ozernyi, Paint Lake, Pinghe, Prairie Lake, Turiy Mys). The new electron-microprobe data presented here significantly extend the known compositional range of clinopyroxenes and amphiboles from carbonatites. These data confirm that calcic and sodic clinopyroxenes from carbonatites are not separated by a compositional gap, instead forming an arcuate trend from nearly pure diopside through intermediate aegirine–augite compositions confined to a limited range of CaFeSi₂O₆ contents (15–45 mol%) to aegirine with < 25 mol% of CaMgSi₂O₆ and a negligible proportion of CaFeSi₂O₆. A large set of LA-ICPMS data shows that the clinopyroxenes of different composition are characterized by relatively low levels of Cr, Co and Ni (≤ 40 ppm) and manifold variations in the concentration of trivalent lithophile and some incompatible elements (1–150 ppm Sc, 26–6870 ppm V, 5–550 ppm Sr, 90–2360 ppm Zr, and nil to 150 ppm REE), recorded in some cases within a single crystal. The relative contribution of clinopyroxenes to the whole-rock Rb, Nb, Ta, Th and U budget is negligible. The major-element compositional range of amphiboles spans from alkali- and Al-poor members (tremolite) to Na–Al-rich Mg- or, less commonly, Fe-dominant members (magnesiohastingsite, hastingsite and pargasite), to calcic–sodic, sodic and potassic–sodic compositions intermediate between magnesio-ferrikatophorite, richterite, magnesioriebeckite, ferri-nyböite and (potassic-)magnesio-arfvedsonite. In comparison with the clinopyroxenes, the amphiboles contain similar levels of tetravalent high-field-strength elements (Ti, Zr and Hf) and compatible transition elements (Cr, Co and Ni), but are capable of incorporating much higher concentrations of Sc and incompatible elements (up to 500 ppm Sc, 43 ppm Rb, 1470 ppm Sr, 1230 ppm Ba, 80 ppm Pb, 1070 ppm REE, 140 ppm Y, and 180 ppm Nb). In some carbonatites, amphiboles contribute as much as 25% of the Zr + Hf, 15% of the Sr and 35% of the Rb + Ba whole-rock budget. Both clinopyroxenes and amphiboles may also host a significant share (~ 10%) of the bulk heavy-REE content. Our trace-element data show that the partitioning of REE between clinopyroxene (and, in some samples, amphibole) and the melt is clearly bimodal and requires a revision of the existing models assuming single-site REE partitioning. Clinopyroxenes and amphiboles from carbonatites exhibit a diversity of zoning patterns that cannot be explained exclusively on the basis of crystal chemistry and relative compatibility of different trace-element in these minerals. Paragenetic analysis indicates that in most cases, the observed zoning patterns develop in response to removal of selected trace elements by phases co-precipitating with clinopyroxene and amphibole (especially magnetite, fluorapatite, phlogopite and pyrochlore). With the exception of magnesiohastingsite–richterite sample from Afrikanda, the invariability of trace-element ratios in the majority of zoned clinopyroxene and amphibole crystals implies that fluids are not involved in the development of zoning in these minerals. The implications of the new trace-element data for mineral exploration targeting REE, Nb and other types of carbonatite-hosted rare-metal mineralization are discussed.