A filament eruption and accompanying coronal field changes on November 5, 1992

An H filament eruption on November 5, 1992 was fully observed in H with the Hida Flare Monitoring Telescope, while Yohkoh's Soft X-ray Telescope observed the pre- and post-eruption evolution of the coronal magnetic fields. From the H data, including the red and blue wings, we have reconstructed the rise of the filament, including trajectory, velocity, and acceleration. In combination with the Yohkoh data this reconstruction suggests that the filament had several interactions with other coronal magnetic fields during the eruption. The Yohkoh data also shows pre-eruption changes in the coronal fields and several post-eruption bright coronal structures. The pre-eruption changes are interpreted as a partial opening of the corona, indicating that it is not necessary to have a complete opening of the corona in order for a filament to erupt and we discuss the several possible contributions from emerging flux. The post-event bright coronal structures are compared with theory and with a cleaner filament eruption event on July 31, 1992. These comparisons suggest that, although there are many similarities, it is hard to completely reconcile the observations with the existing theory.     

Imaging coronal emission lines under high sky-background conditions

We have obtained images in solar coronal emission lines under high sky-background conditions by making precise differential measurements between the coronal emission line and the near-by continuum, which is primarily due to scattered light from the solar disk. Chopping between the two wavelengths was performed at 100 kHz to avoid artifacts from fast-flying dust particles and other aerosols, and also from seeing effects. The differential signal was detected with a novel CCD camera that demodulates signals up to 100 kHz. These preliminary observations show coronal emission at the 0.2% level of the scattered-light background and pave the way to efficient and precise imaging of coronal emission features under less than ideal coronal-sky conditions.Operated by the Association of Universities for Research in Astronomy, Inc. (AURA) under cooperative agreement with the National Science Foundation.     

Spectroscopic observations of parsamian 21

This work presents spectroscopic observations of Parsamian 21, which has been shown recently by Staude and Neckel to be a fuor-type star. A list of identified absorption lines is given. The results are compared with previous spectroscopic observations over the period 1966–1990. It is shown that the H line profile changed during this period; according to the observations of 1986, the center of the H absorption line was shifted by –140 km/sec from ₀ and reached –600 km/sec at the line edge. It follows from the presented lightcurve that the star has undergone brightness variations of nearly three magnitudes and most likely became a fuor before 1902.Translated fromAstrofizika, Vol. 39, No. 2, pp. 227–235, April–June, 1996.     

Nd,Sr, and Pb isotopic characteristics of Cretaceous intrusive rocks from deep levels of the Sierra Nevada batholith,Tehachapi Mountains,California

The Cretaceous gabbroic to granitic intrusive rocks of the Tehachapi Mountains were emplaced at depths of 25–30 km and thus afford a view of deep processes in the Sierra Nevada batholith. They consist of the 115 Ma Tehachapi suite and the 100 Ma Bear Valley suite; new zircon U-Pb age data reveal the presence of the latter as far west as Grapevine Canyon. The Nd, Sr, Pb, and O isotopic whole-rock data and zircon Pb inheritance patterns for the bulk of the suites suggest an origin by mixing between depleted mantlederived magmas and metasedimentary material with a substantial component of old continental material. However, this mixing is not evident in variations between isotopic ratios and chemical and lithologic parameters. This implies that isotopic hybridization of magmas took place deeper than 30 km, and that fractionation processes are likely responsible for the bulk of the chemical variation in this part of the Sierra Nevada batholith. Consideration of the isotopic data in the context of the Sierra Nevada batholith as a whole suggests that the well-known east-to-west isotopic gradients in the batholith may reflect a change in the average isotopic character of the preintrusive frame-work rather than a change in amount of crustal component. On the other hand, the lack of areal gradients in Sr and Nd isotopic ratios in the main study area may indicate a lack of pronounced gradation at deep levels, at least within the western batholith.     

Compressibility of titanosilicate melts

The effect of composition on the relaxed adiabatic bulk modulus (K₀) of a range of alkali- and alkaline earth-titanosilicate [X ₂ ^n/n+ TiSiO₅ (X=Li, Na, K, Rb, Cs, Ca, Sr, Ba)] melts has been investigated. The relaxed bulk moduli of these melts have been measured using ultrasonic interferometric methods at frequencies of 3, 5 and 7 MHz in the temperature range of 950 to 1600°C (0.02 Pa s < _s < 5 Pa s). The bulk moduli of these melts decrease with increasing cation size from Li to Cs and Ca to Ba, and with increasing temperature. The bulk moduli of the Li-, Na-, Ca- and Ba-bearing metasilicate melts decrease with the addition of both TiO₂ and SiO₂ whereas those of the K-, Rb- and Cs-bearing melts increase. Linear fits to the bulk modulus versus volume fraction of TiO₂ do not converge to a common compressibility of the TiO₂ component, indicating that the structural role of TiO₂ in these melts is dependent on the identity of the cation. This proposition is supported by a number of other property data for these and related melt compositions including heat capacity and density, as well as structural inferences from X-ray absorption spectroscopy (XANES). The compositional dependence of the compressibility of the TiO₂ component in these melts explains the difficulty incurred in previous attempts to incorporate TiO₂ in calculation schemes for melt compressibility. The empirical relationship KV^-4/3 for isostructural materials has been used to evaluate the compressibility-related structural changes occurring in these melts. The alkali metasilicate and disilicate melts are isostructural, independent of the cation. The addition of Ti to the metasilicate composition (i.e. X₂TiSiO₅), however, results in a series of melts which are not isostructural. The alkaline-earth metasilicate and disilicate compositions are not isostructural, but the addition of Ti to the metasilicate compositions (i.e. XTiSiO₅) would appear, on the basis of modulus-volume systematics, to result in the melts becoming isostructural with respect to compressibility.     

Stable isotope study of antimony deposits in the Muratdagi region,western Turkey

The Muratdagi region is rich in antimony deposits having the following common characteristics: post Miocene age, location on the down-thrown blocks next to normal faults, in the vicinity of active or fossil thermal springs, and in contact with carbonate rocks. The isotopic composition of — 7. SMOW of the mineralizing fluid calculated from the measured ° ¹⁸O of quartz and the fluid inclusion microthermometry, is indicative of meteoric water origin. The ° ¹³C of the inclusion CO₂ of — 19.1 to — 25.4 PDB is indicative of interaction with organic material-graphite. The ° ³⁴S of stibnite — 3.6 to — 0.7 is, in view of the mineral assemblage, indicative of magmatic origin of the sulphur. A tightly confined set of structural, lithological, hydrological and geochemical features define a sequence of geochemical processes; formation of acid and reducing fluid, leaching and transport of antimony complexes and precipitation of stibnite within defined lithological units. The set of processes seems to have taken place within a space of 5000 m lateral and 1000 m vertical extension.     

Optical absorption investigation of Cr3+ ion-bearing minerals in the temperature range 77–797 K

The effect of raising temperature on spin-allowed dd-transitions of octahedral Cr³⁺ was studied for various point symmetries of the Cr³⁺-bearing structural sites, i.e. 3 m and 3 with inversion center in spinel and garnets, respectively, or 32, 3, 2 and 1, lacking the inversion centre, in beryl, corundum, diopside and topaz, respectively. For this purpose, crystals of Cr³⁺-bearing spinel, pyrope, andradite, grossular, uvarovite, emerald, ruby, diopside and topaz were analyzed by microprobe, oriented, and measured in polarized radiation (except for the cubic minerals) in the spectral range 30 000 to 11 100 cm^-1 and at temperatures between 77 and 797 K. The evaluation of the intensities, half widths, and energy positions of bands due to Cr³⁺-transitions derived from ⁴ A _2g ⁴ T _2g (F) and ⁴ T _1g (F) as well as of Dq- and B-values derived, had the following results:In all cases, red shift of the above bands and, hence, independent on the site symmetry of Cr³⁺, decreases in the Dq-values were obtained. The dependcies of Dq on T are nearly linear above room temperature and amount between -1.6% in topaz and -5.1% in pyrope in the temperature range studied. From this, values for the local thermal expansion of the Cr³⁺-centered octahedra, _loc, were derived on the basis of the R _M-0 ^-5 -proportionality of 10Dq. Such values are consistently higher than those obtained from X-ray refinements, a method averaging r_m-o for all the respective octahedral positions.     

Silicate melts at magmatic temperatures: in-situ structure determination to 1651°C and effect of temperature and bulk composition on the mixing behavior of structural units

The abundance of coexisting structural units in K-, Na-, and Li-silicate melts and glasses from 25° to 1654°C has been determined with in-situ micro-Raman spectroscopy. From these data an equilibrium constant, K_x, for the disproportionation reaction among the structural units coexisting in the melts, Si₂O₅(2Q³)SiO₃(Q²)+SiO₂(Q⁴), was calculated (K_x is the equilibrium constant derived by using mol fractions rather than activities of the structural units). From ln K_x vs l/T relationships the enthalpy (H_x) for the disproportionation reaction is in the range of-30 to 30 kJ/mol with systematic compositional dependence. In the potassium and sodium systems, where the disproportionation reaction shifts to the right with increasing temperature, the H_x increases with silica content (M/Si decreases, M=Na, K). For melts and supercooled liquids of composition Li₂O·2SiO₂ (Li/Si=1), the H_x is indistinguishable from 0. By decreasing the Li/Si to 0.667 (composition LS3) and beyond (e.g., LS4), the disproportionation reaction shifts to the left as the temperature is increased. For a given ratio of M/Si (M=K, Na, Li), there is a positive, near linear correlation between the H_x and the Z/r² of the metal cation. The slope of the H_x vs Z/r² regression lines increases as the system becomes more silica rich (i.e., M/Si is decreased). Activity coefficients for the individual structural units, _i, were calculated from the structural data combined with liquidus phase relations. These coefficients are linear functions of their mol fraction of the form _i=a lnX _i+b, where a is between 0.6 and 0.87, and X _i is the mol fraction of the unit. The value of the intercept, b, is near 0. The relationship between activity coefficients and abundance of individual structural units is not affected by temperature or the electronic properties of the alkali metal. The activity of the structural units, however, depend on their concentration, type of metal cation, and on temperature.     

Correlation by Rb-Sr geochronology of garnet growth histories from different structural levels within the Tauern Window,Eastern Alps

In order to evaluate rates of tectonometamorphic processes, growth rates of garnets from metamorphic rocks of the Tauern Window, Eastern Alps were measured using Rb-Sr isotopes. The garnet growth rates were determined from Rb-Sr isotopic zonation of single garnet crystals and the Rb-Sr isotopic compositions of their associated rock matrices. Garnets were analyzed from the Upper Schieferhülle (USH) and Lower Schieferhülle, (LSH) within the Tauern Window. Two garnets from the USH grew at rates of 0.67 _–0.13 ^+0.19 mm/million years and 0.88 _–0.19 ^+0.34 mm/million years, respectively, indicating an average growth duration of 5.4±1.7 million years. The duration of growth coupled with the amount of rotation recorded by inclusion trails in the USH garnets yields an average shear-strain rate during garnet growth of 2.7 _–0.7 ^+1.2 ×10^-14 s^-1. Garnet growth in the sample from the USH occurred between 35.4±0.6 and 30±0.8 Ma. The garnet from the LSH grew at a rate of 0.23±0.015 mm/million years between 62±1.5 Ma and 30.2±1.5 Ma. Contemporaneous cessation of garnet growth in both units at 30 Ma is in accord with previous dating of the thermal peak of metamorphism in the Tauern Window. Correlation with previously published pressure-temperature paths for garnets from the USH and LSH yields approximate rates of burial, exhumation and heating during garnet growth. Assuming that theseP — T paths are applicable to the garnets in this study, the contemporaneous exhumation rates recorded by garnet in the USH and LSH were approximately 4 _–2 ⁺³ mm/year and 2±1 mm/year, respectively.     

Aqueous alteration of the Bali CV3 chondrite: evidence from mineralogy, mineral chemistry, and oxygen isotopic compositions

A petrographic, geochemical, and oxygen isotopic study of the Bali CV3 carbonaceous chondrite revealed that the meteorite has undergone extensive deformation and aqueous alteration on its parent body. Deformation textures are common and include flattened chondrules, a well-developed foliation, and the presence of distinctive (100) planar defects in olivine. The occurrence of alteration products associated with the planar defects indicates that the deformation features formed prior to the episode of aqueous alteration. The secondary minerals produced during the alteration event include well-crystallized Mg-rich saponite, framboidal magnetite, and Ca-phosphates. The alteration products are not homogeneously distributed throughout the meteorite, but occur in regions adjacent to relatively unaltered material, such as veins of altered material following the foliation. The alteration assemblage formed under oxidizing conditions at relatively low temperatures (<100 degrees C). Altered regions in Bali have higher Na, Ca, and P contents than unaltered regions which suggests that the fluid phase carried significant dissolved solids. Oxygen isotopic compositions for unaltered regions in Bali fall within the field for other CV3 whole-rocks, however, the oxygen isotopic compositions of the heavily altered material lie in the region for the CM and CR chondrites. The heavy-isotope enrichment of the altered regions in Bali suggest alteration conditions similar to those for the petrographic type-2 carbonaceous chondrites.