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.     

Dynamics of the plasmasphere in the dusk sector as observed in the outer ionosphere

Summary Direct measurements of the thermal plasma parameters in the topside ionosphere reveal variations of the plasmasphere boundary in the dusk sector. The ACTIVE satellite's near-polar orbits at altitudes of 500 – 1800 km around winter solstice 1989 were used to study the bulge region of the plasmasphere during intervals with different levels of geomagnetic agitation. The narrow, sharply defined trough in electron concentration corresponding to the plasmapause under quiet conditions situated at L = 6 – 7 moved to lower L-values with increasing geomagnetic activity. This narrow trough can be found in all main ion constituents. During periods of moderate geomagnetic activity, following the onset of a weak magnetic storm, a portion of the plasmaspheric bulge region was separated from the main plasmaspheric body. This can be seen in the outer ionosphere as an inner narrow trough at lower L-value. Troughs in light ions need no longer coincide with this in electron concentration. He⁺ is the most sensitive constituent reflecting the dusk sector plasmaspheric situation at this altitude.Dedicated to the Memory of Professor Karel P     

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.     

About the specification of erosion flux for soft stratified cohesive sediments

The present paper deals with the specification of bed erosion flux that accounts for the effects of sediment-induced stratification in the water column. Owing to difficulties in measuring the bed shear stress _b and the erosive shear strength _s, we suggest a series of methods that combine laboratory and numerical experiments. A simplified turbulent transport model that includes these effects helps to quantify _b and _s. Focusing on soft stratified beds, the present study considers erosion rate formulas of the form =_f exp {[T_b-T_s]} where is a model constant (=1 for Gularte's (1978) formula and =1/2 for Parchure's (1984) formula). First, the bed erosive strength profile _s(Z) is adjusted by forcing the turbulent transport model with measured erosion rates. Second, three procedures are suggested to determine the erosion rate formula coefficients _f and : a global procedure and two different layer-by-layer procedures. Each procedure is applied to an erosion experiment conducted in a rotating annular flume by Villaret and Paulic (1986). The use of the layer-by-layer procedure based on a least squares fitting technique provides a closer fit than the global procedure. The present study points out the complementarity of experimental and numerical approaches and also suggests possible improvements in laboratory test procedures.     

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.     

Pb−Sr−Nd−O isotopic constraints on the origin of rhyolites from the Taupo Volcanic Zone of New Zealand: evidence for assimilation followed by fractionation from basalt

A comprehensive Sr–Nd–Pb–O isotopic study is reported for rhyolites from the Maroa Volcanic Centre in the Taupo Volcanic Zone (TVZ) of New Zealand. The Sr–Nd isotopic compositions of the rhyolites (⁸⁷Sr/⁸⁶Sr=0.705236 to 0.705660 and _Nd = 2.0 to 0.2) are intermediate between those of primitive basalts (⁸⁷Sr/⁸⁶Sr=0.70387 and _Nd = 5.3) and the Torlesse basement (⁸⁷Sr/⁸⁶Sr=0.709 and _Nd = -4.5). The relatively low mantle-like oxygen isotopic compositions of ¹⁸ O = 7 ± 0.5 are consistent with the Nd-Sr isotopic constraints in that they can be accounted for by 15% to 25% crustal contamination of a basaltic parent by relatively ¹⁸ O-rich Torlesse metasediment. High precision Pb isotopic analyses of plagioclase separates from the Maroa rhyolites show that they have essentially the same compositions as the Torlesse metasedimentary terrane which is itself distinctive from the Western or Waipapa metasediments. Due to the high concentration of Pb in the Torlesse metasediments (>20 ppm) compared to the basalts (<2 ppm), the Pb isotopic composition of the volcanics may be controlled by relatively small amounts (>10%) of crustal contamination. All these results are shown to be consistent with derivation of the rhyolites by 15% to 25% contamination of relatively primitive basaltic magmas with Torlesse metasedimentary crust, followed by extensive, essentially closed system fractionation of the basalt to a magma of rhyolite composition. It is argued that the processes of assimilation and fractionation are separated in both space and time. The voluminous high silica rhyolites, which make up >97% of the exposed volcanism in the continental margin back-are basin environment of the TVZ, therefore appear to be a product of predominantly new additions to the crust with assimilation-recycling of pre-existing crust being of secondary importance.     

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.     

Geochemistry and origin of the Proterozoic ultrapotassic rocks of the Churchill Province,Canada

Summary Early Proterozoic ultrapotassic dikes, lava flows, and pyroclastic rocks of the Christopher Island Formation (CIF) erupted throughout an area 600 × 300 km within the Churchill Province of the Canadian Shield at 1.84 Ga. The rocks range from mafic lamprophyres (mg # 60; SiO₂ 47–54%, mean K₂O/Na₂O > 4) with phenocrysts of phlogopite + diopside + apatite ± olivine ± magnetite, to phenocryst-poor felsic rocks and sanidine porphyries (SiO₂55–69%). All samples have high incompatible element contents and display large depletions of high field strength elements relative to K, Rb, Sr, Ba, and Th. The CIF has geochemical and petrographic characteristics of both minettes and lamproites, but overall most closely resembles young Mediterranean lamproites. Felsic rocks of the CIF were produced by crystal fractionation and crustal contamination of mafic ultrapotassic magma, and include both high-silica lamproites strongly enriched in Zr, U, and Th, and weakly potassic to sodic rocks of trachytic composition. Flows and feeder dikes have relatively homogeneous _{Nd, 1840 Ma} (–6 to –11) but highly variable ES., 1840 Ma (–40 to + 100); samples classified as lamproites have higher average _Sr. Dike samples have highly variable present-day Pb isotope compositions, ranging from moderately to strongly nonradiogenic. Geochemical and isotopic data are consistent with contributions from depleted Archean lithospheric mantle, and OIB-type convecting mantle, both metasomatized by subduction-related processes during the Early Proterozoic. The lithospheric mantle probably contained Archean enriched domains as well. Proterozoic enrichment may have accompanied shallow underplating of subducted oceanic lithosphere beneath the Churchill Province during amalgamation of the Laurentian supercontinent. There are strong analogies in isotopic composition, and interpreted source region history, between the CIF and lamproites and minettes of the Wyoming Province and western Greenland, which suggest the existence of a Laurentian ultrapotassic superprovince.

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Geochemie und Entstehung der Proterozoischen ultrapotassischen Gesteine der Churchill Provinz, Kanada

Zusammenfassung Altproterozoische, ultrapotassische Gänge, Lavaströme und pyroklastische Gesteine der Christopher Island Formation (CIF), eruptierten in einem Gebiet von 600 × 300 km in der Churchill Provinz des Kanadischen Schildes vor 1.84 Ga. Die Zusammensetzung dieser Gesteine variiert von mafischen Lamprophyren (mg > 60; SiO₂ = 47–54%, durchschnittliches K₂O/Na₂O > 4) mit Phänokristallent von Phlogopit + Diopsid + Apatit + Olivin + Magnetit, bis zu phänokristallarmen felsischen Gesteinen und Sanidinporphyren (SiO₂ = 55–69%). Alle Proben zeigen hohe Gehalte an inkompatiblen Elementen und zeigen beträchtliche Verarmung an high field strength Elementen relativ zu K, Rb, Sr, Ba und Th. Die CIF hat geochemische und petrographische Eigenschaften sowohl von Minetten wie von Lamproiten, aber im allgemeinen ähnelt sie am stärksten jungen mediterranen Lamproiten. Felsische Gesteine der CIF wurden durch Fraktionierung und Krustenkontamination aus mafischen ultrapotassischen Magmen gebildet. Letztere umfassen sowohl siliziumreiche Lamproite, die deutlich an Zr, U und Th angereichert sind und schwach potassische bis sodische Gesteine von trachytischer Zusammensetzung. Lavenergüsse und zufuhrgänge zeigent ein relativ homogenes _{Nd, 1840 Ma} (–6 bis –11) aber ein sehr variables _{Sr, 1840 Ma} (-40 bis + 100); Proben die als Lamproite klassifiziert wurden, zeigent höhere durchschnittliche _Sr-Werte. Proben von Gängen haben sehr variable Bleiisotopen-Zusammensetzungen, die von mäßig bis stark nichtradiogen variieren. Geochemische und Isotopendaten weisen auf Beiträge aus verarmtem archaischen lithosphärischen Mantel und aus konvektierendem OIB-Typ Mantel hin, die beide während des Alproterozoikums durch Subduktions-Vorgänge metasomatisiert wurden. Der lithosphärische Mantel enthielt wahrscheinlich auch angereicherte archaische Domänen. Proterozoische Anreicherungsvorgänge dürften seichtes Underplating subduzierter ozeanischer Lithosphäre unter der Churchill Provinz während der Amalgamation des laurentischen Superkontinentes begleitet haben. Es gibt starke Analogien in der Isotopenzusammensetzung und in der interpretierten Geschichte der Ursprungsregion, zwischen den CIF und Lamproiten und Minetten der Wyoming Provinz, und des westlichen Grönland. Diese weisen auf die Existenz einer laurentischen ultrapotassischen Superprovinz hin.

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With 7 Figures