Volatiles in glasses from Mauna Loa Volcano,Hawai'i: implications for magma degassing and contamination,and growth of Hawaiian volcanoes

Glasses from Mauna Loa pillow basalts, recent subaerial vents, and inclusions in olivine were analyzed for S, Cl, F, and major elements by electron microprobe. Select submarine glasses were also analyzed for H₂O and CO₂ by infrared spectroscopy. The compositional variation of these tholeiitic glasses is dominantly controlled by crystal fractionation and they indicate quenching temperatures of 1,115-1,196 °C. Submarine rift zone glasses have higher volatile abundances (except F) than nearly all other submarine and subaerial glasses with the maximum concentrations increasing with water depth. The overwhelming dominance of degassed glasses on the submarine flanks of Mauna Loa implies that much of volcano's recent submarine growth involved subaerially erupted lava that reached great water depths (up to 3.1 km) via lava tubes. Anomalously high F and Cl in some submarine glasses and glass inclusions indicate contamination possibly by fumarolic deposits in ephemeral rift zone magma chambers. The relatively high CO₂ but variable H₂O/K₂O and S/K₂O in some submarine rift zone glasses indicates pre-eruptive mixing between degassed and undegassed magma within Mauna Loa's rift system. Volatile compositions for Mauna Loa magmas are similar to other active Hawaiian volcanoes in S and F, but are less Cl-rich than Ll'ihi glasses. However, Cl/K2O ratios are similar. Mauna Loa and Ll'ihi magmas have comparable, but lower H₂O than those from Kilauea. Thus, Kilauea's source may be more H₂O-rich. The dissimilar volatile distribution in glasses from active Hawaiian volcanoes is inconsistent with predictions for a simple, concentrically zoned plume model.     

Radio identification and continuum spectra of decameter-wavelength sources

The paper describes a method for the radio identification of decameter-wavelength sources based on their continuum spectra and analysis of their coordinates in relatively large error boxes surrounding a specified position on the sky. The distribution of continuum spectra and identifications in other wavelength ranges are analyzed for the resulting radio catalog. Using identifications with the FIRST and NVSS surveys, the statistics of the spectral index-size and spectral index-flux density distributions for steep-spectrum sources have been studied, and a catalog of ultrasteep-spectrum (α相似文献   

The chemically distinct nucleus and structure of the S0 galaxy NGC 80

The giant lenticular galaxy NGC 80, which is the brightest member of a rich group, possesses a central evolutionarily-distinct region: the stars in the nucleus and in a circumnuclear ring of radius 5″t–7″ have a mean age of only 7 Gyr, whereas the stellar population of the bulge is older than 10 Gyr. The nucleus of NGC 80 is also chemically distinct: it is a factor of 2–2.5 richer in metals than its immediate neighborhood and is characterized by a high magnesium-to-iron abundance ratio [Mg/Fe]≈+0.3. The global stellar disk of NGC 80 has a two-tiered structure: its outer part has an exponential scale length of 11 kpc and normal surface density, while the inner disk, which is also exponential and axisymmetric, is more compact and brighter. Although the two-tiered structure and the chemically distinct nucleus obviously have a common origin and owe their existence to some catastrophic restructuring of the protogalactic gaseous disk, the origin of this remains unclear, since the galaxy lacks any manifestations of perturbed morphology or triaxiality.     

A Linear Programming Approach to Determine the Normative Composition of Sedimentary Rocks

The analysis of modal and normative composition of sedimentary rocks is widely used for studying their sources and tectonic settings. The normative calculation of the mineral composition of rocks in this study is formulated as a linear programming problem and is solved by means of the simplex method. This enables both simultaneous and successive subtraction of a set of basic minerals from a rock sample represented by its chemical composition {SiO₂...LOI}. Such an approach provides a more exact calculation of the contribution of basic minerals in the rock. This mathematical approach is used to study two representative sets of sandstones and fine-grained rocks from a Meso- to Neoproterozoic marginal basin of southeastern Siberia (Uchur–Maya region, Yakutia) and a Pennsylvanian-Lower Permian uplifted continental block in Colorado, USA. The calculated normative mineral compositions of the Siberian sandstones are consistent with the observed modal compositions. These sandstones vary from K- Feldspar rich arkoses at the base of the sequence (the Uchur Group, lower Riphean) to quartz arenites or lithic sandstones and wacke in transgressive successions of the middle-upper Riphean. Arkoses and quartz arenites are dominant in Meso- to Neoproterozoic Siberia. These samples represent craton interior uplifted basement and quartzose, recycled orogen provenance of a stable craton in Rodinia. There are higher but consistent discrepancies between the calculated and observed compositions for the Pennsylvanian to Lower-Permian arkoses and quartz arenites (Sangre de Cristo, Belden, and Maroon Formations). The differences between the predicted and observed mineralogy may be due to uncertainties in the modes in the matrix and cement of the sandstones. This normative program should supplement modal calculations and provide better genetic constructions, especially in case of matrix-rich sandstones.     

The Quantitative Mineral Composition of Sedimentary Rocks: Calculation from Chemical Analyses and Assessment of Adequacy (MINLITH Computer Program)

The MINLITH program provides for calculating the first approximation mineral composition of sedimentary rocks and their metamorphic counterparts from the bulk chemical compositions. The method is universal and can be applied to most types of clastic, pelitic, and carbonate sedimentary rocks based on a limited set of minerals and their simplified compositions. The program comprises a great number of arithmetic operations making up an algorithm. Each operation solves the equations allocating the major oxides to possible (expected) normative minerals. The operation sequence is determined from empirical relationships based on the study of numerous reference samples. The accuracy of MINLITH calculations was statistically estimated from comparison with results of the high-precision study of modal mineral compositions. Uncertainty is commonly within a range of 5–15 rel % and attains 60–70 rel % if the mineral content is below 5 wt %. It is evident that the program is a rather simple, convenient, and useful tool for the approximate estimation of mineral compositions of sedimentary rocks for lithological purposes.     

A Petrologic Perspective of Kilauea Volcano's Summit Magma Reservoir

Two hundred years of magmatic history are documented by thelavas and tephra sampled from K     

Eastern Laurentia in Rodinia: constraints from whole-rock Pb and U/Pb geochronology

Whole-rock Pb isotopic signatures and U/Pb geochronology refute a Rodinian correlation of northeastern Laurentia and proto-Andean Amazonia. According to this previously proposed model, the Labrador–Scotland–Greenland Promontory (LSGP) of northeastern Laurentia collided with the proto-Andean margin of Amazonia, at the Arica Embayment, during the Grenville/Sunsás Orogeny (ca. 1.0 Ga). Links between the two margins were based upon the correlation of the LSGP with Arequipa-Antofalla Basement (AAB), a Proterozoic block along the proto-Andean margin of Amazonia adjacent to the Arica Embayment. Specifically, similarities in 1.8–1.0 Ga basement rocks in both regions suggested that the AAB was originally a piece of the LSGP. Furthermore, similarities in unique, post-collisional, but pre-rift, glacial sedimentary sequences also supported a link between the AAB and LSGP.Tests of these apparent similarities fail to support correlation of the AAB and the LSGP and, thus, eliminate a direct link between northeastern Laurentia and southwestern Amazonia in Rodinia. However, Pb isotopic compositions and U/Pb geochronology provide the basis for two new correlations, namely, (1) the ca. 1.3–1.0 Ga basement in the central and southern Appalachians may be an allochthonous block that was transferred to Laurentia from Amazonia at ca. 1.0 Ga, and (2) an allochthonous AAB may be a piece of the Kalahari Craton that was transferred to Amazonia at ca. 1.0 Ga. Based on these new correlations and a previously proposed Grenvillian connection between southern Laurentia (Llano) and Kalahari, we propose that Amazonia may have collided with a contiguous southeastern Laurentia/Kalahari margin at ca. 1.0 Ga.     

Petrographic of Northwestern Sudan

The sedimentology of the Northwestern Sudan consists of lower, middle and upper cycles. The lower and upper cycles are composed of intercalated fluvial and shallow marine facies, whereas the middle cycle consists entirely of fluvial and glaciofluvial facies. The petrographic analysis shows that the lower and upper cydes consist of quartz and lithic arenite sandstones, whereas the middle cycle consists of arkosic and lithic arenite sandstones. The lower and upper cycle sandstones reflect derivation mainly from recycled orogens with minor contribution from craton interior provenances. However, the middle cycle sandstones indicate derivation from basement uplift, transitional and mainly recycled orogens provenances.     

Ion microprobe measurements of O/O ratios of phosphate minerals in the Martian meteorites ALH84001 and Los Angeles

Oxygen isotope ratios of merrillite and chlorapatite in the Martian meteorites ALH84001 and Los Angeles have been measured by ion microprobe in multicollector mode. δ¹⁸O values of phosphate minerals measured in situ range from ∼3 to 6‰, and are similar to Martian meteorite whole-rock values, as well as the δ¹⁸O of igneous phosphate on Earth. These results suggest that the primary, abiotic, igneous phosphate reservoir on Mars is similar in oxygen isotopic composition to the basaltic phosphate reservoir on Earth. This is an important first step in the characterization of Martian phosphate reservoirs for the use of δ¹⁸O of phosphate minerals as a biomarker for life on Mars. Cumulative textural, major-element, and isotopic evidence presented here suggest a primary, igneous origin for the phosphates in Los Angeles and ALH84001; textural and chemical evidence suggests that phosphates in ALH84001 were subsequently shock-melted in a later event.