Shock effects on hydrous minerals and implications for carbonaceous meteorites

New infrared absorption spectra, thermo-gravimetric analyses and optical-and scanning electron microscopy of shock-recovered specimens of antigorite serpentine (Mg₃Si₂O₅(OH)₄) from the pressure range between 25 to 59 GPa are reported. The infrared spectra show systematic changes in absorption peaks related to structural and molecular surface absorbed water. H₂O absorption peaks increase at the expense of OH peaks with increasing shock pressure. Changes in SiO bond vibrational modes with increasing shock pressure parallel those seen for other, non-hydrous minerals. Thermogravimetric analyses of shock-recovered samples determine the amount of shock-induced water loss. For samples shocked in vented assemblies, the data define a relation between shock-induced water loss versus shock pressure. Results for samples shocked in sealed assemblies demonstrate a dependence of water loss on shock pressure and target confinement. For the vented assembly samples, a linear relation between shock pressure and both the length of dehydration interval and the effective activation energy for releasing post-shock structural water in antigorite is found. Optical and scanning electron miscroscopy of shocked antigorite reveal a number of textures thought to be unique to shock loading of volatile-bearing minerals. Gas bubbles, which probably are the result of shock-released H₂O appear to be injected into zones of partial melting. This process may produce the vesicular dark veins which are distributed throughout heavily shocked samples. The present observations suggest several criteria which may constrain possible shock histories of the hydrous matrix phases of carbonaceous condrites. A model is proposed for explaining hydrous alteration processes occurring on carbonaceous chondrite parent bodies in the course of their accretion. We speculate that shock loading of hydrous minerals would release and redistribute free water in the regoliths of carbonaceous chondrite parent bodies giving rise to the observed hydrous alterations.     

Melting and subsolidus reactions in the system K2O-CaO-Al2O3-SiO2-H2O: corrections and additional experimental data

Melting relationships in the system K₂O-CaO-Al₂O₃-SiO₂-H₂O have been reinvestigated using Schreinemakers analysis and hydrothermal experiments. The reaction sanidine+muscovite+zoisite+quartz+vapor =melt has been bracketed at 10, 15, and 20 kbars and 670–680, 680–690, and 690–700° C, respectively and it marks the lowest solidus temperatures in the system investigated.Below 10 kbars, experimental data on the beginning of melting in zoisite- or muscovite-bearing anorthite+sanidine assemblages have been obtained, which are not showing any differences and therefore point to melt compositions close to the feldspar-quartz join.     

Whole-bird models for the magnetic cleansing of oiled feathers

Iron powder, a promising dry-cleansing agent for oiled feathers where both the contaminant and the cleansing agent may be harvested magnetically, has been tested on the plumage of whole-bird models. The breast and back plumage of Mallard Duck (Anas platyrhynchos) and Little Penguin (Eudyptula minor) carcasses were patch-contaminated with commercial-grade engine oil, three different crude oils, and an oil/seawater emulsion. The plumage was then subjected to a magnetic cleansing protocol. The contaminant removal was assessed gravimetrically and was found to reflect the outcomes for a previously reported in vitro study using feather clusters. Between 92-98% of the contaminants, and effectively all of the cleansing agent, were removed from the feathers.     

Seismostratigraphy and structural framework of the SW Baltic Sea

The SW part of the Baltic Sea between Scania, Rügen, Bornholm and Mön constitutes a complex crustal transition between the Baltic Shield and the accreted Phanerozoic provinces of the West European Platform. An integrated interpretation of marine reflection seismic data sets from the BABEL AC line and two commercial surveys offshore NE Germany and S Sweden have resulted in a complete view of the structural framework in the area. The general seismic picture can best be detected by two characteristic sets of reflection phases. The lower set is dominated by slightly dipping and vertically displaced prominent reflectors corresponding to downfaulted Lower Palaeozoic strata on top of the Precambrian basement. The upper set represents Mesozoic and Cenozoic coherent reflection phases including a thick Upper Cretaceous unit. The Caledonian deformation front is identified in the southern part of the investigated area as the border against which basement rocks have been affected by Caledonian metamorphism and deformation. Major structural elements also include the N–S trending Agricola–Svedala Fault and North Rügen-Skurup Fault. Several NW–SE trending faults are also identified including the Nordadler–Kamien Fault, Jutland–Mön Fault, Carlsberg Fault, Romeleåsen Fault Zone and the Fyledalen Fault Zone. The sedimentary record from NE German offshore wells and Scanian boreholes is compared with the seismic data. The Cambro-Silurian strata are composed mainly of quartzitic sandstones, shales and biomicritic limestones. The Silurian is dominated by grey, micaceous shale and micaceous siltstone deposited in a marginal basin. Upper Palaeozoic strata are merely encountered in the southernmost part of the investigated area. These include Zechstein strata. The Mesozoic deposits are dominated by a thick Cretaceous sequence of mainly limestones with interbedded sandstones.     

Studies of the motion of equatorial 630.0 nm airglow depletions

An all-sky-mapping filter photometeer has been used to study equatorial 630.0 nm nightglow intensity depletions. A generally eastward drift of the ～ 0m/sec. At times two airglow depletions moving at different velocities were observed simultaneously; in one case they merged. Simultaneous interferometric determinations of doppler shifts in the 630.0 nm line indicated that the velocity of the neutral atmosphere does not appear to be correlated with the drift of the airglow depletions. The results are compared with other observations.     

(Na,Ca)(Ti3+,Mg)Si2O6-clinopyroxenes at high pressure: influence of cation substitution on elastic behavior and phase transition

A compressional study of (Na,Ca)(Ti³⁺,Mg)Si₂O₆-clinopyroxenes was carried out at high pressures between 10⁻⁴ and 10.2 GPa using in situ single-crystal X-ray diffraction, Raman spectroscopy and optical absorption spectroscopy. Compressional discontinuities accompanied by structural changes, in particular, the appearance of two distinct Ti³⁺–Ti³⁺ distances within the octahedral chains at 4.37 GPa, provide evidence for the occurrence of a phase transition in NaTi³⁺Si₂O₆. Equation-of-state parameters are K ₀ = 115.9(7) GPa with K′ = −0.9(3) and K ₀ = 102.7(8) GPa with K′ = 4.08(5) for the low- and high-pressure range, respectively. The transition involves a C2/c–P [`1] \overline{1} symmetry change, which can be confirmed by the occurrence of new modes in Raman spectra. Since no significant discontinuity in the evolution of the unit-cell volume with pressure has been observed, the transition appears to be second-order in character. The influence of the coupled substitution Na⁺Ti³⁺↔Ca²⁺Mg²⁺ on the static compression behavior and the structural stability has been investigated using a sample of the intermediate composition (Na_0.54Ca_0.46)(Mg_0.46Ti_0.54)Si₂O₆. No evidence for a deviation from continuous compression behavior has been found, neither in lattice parameter nor in structural data and the fit of a third-order Birch–Murnaghan equation-of-state to the pressure–volume data yields a bulk modulus of K ₀ = 109.1(5) GPa and K′ = 5.02(13). Raman and polarized absorption spectra have been compared to NaTiSi₂O₆ and reveal major similarities. The main driving force for the phase transition in NaTi³⁺Si₂O₆ is the localization of the Ti³⁺ d-electron and the accompanying distortion, which is suppressed in the (Na,Ca)(Ti³⁺,Mg)Si₂O₆-clinopyroxene.     

Geochemical and petrological characteristics of Eppawala phosphate deposits,Sri Lanka

The apatite-bearing carbonate rocks at Eppawala, Sri Lanka occur as massive, discontinuous bodies in a Precambrian, high-grade metamorphic terrain, which weather to form economically important phosphate deposits. The ore bodies at Eppawala contain =42% P ₂O ₅, and citric acid solubility of different components varies from 4 to 6%. The parent rocks are mainly made up of calcite, dolomite and apatite, with lesser amounts of ilmenite, magnetite, pyrite, forsterite, phlogopite, enstatite, magnesite, diopside, tremolite and spinel. Most of minerals show an euhedral habit, with a wide range of crystal sizes (from a few millimetres to several decimetres). The Eppawala rocks are characterised by low silica (=0.41%), high phosphorous (=10.58%) and high strontium content (2,960–6,819 ppm). Concentrations of light rare-earth elements in these rocks are comparably higher than those of marbles. The REE fractionation of these rocks is pronounced, and La/Yb ratios vary between 14 and 43. Both apatite and calcite show markedly elevated strontium levels (=0.6%). The d ¹³C _PDB and d ¹⁸O _SMOW values of the carbonates are in the range of –3.4 to –2.2 and 7.7 to 16.4‰ respectively. The euhedral habit, as well as the presence of major quantities of apatite and considerable amounts of iron-bearing minerals suggest that the ore host rock has genetic links to an igneous source rather than to an intensely metamorphosed limestone. The higher light REE contents of the rocks, compared to marbles, also argue against a metamorphic or sedimentary origin. The Sr/Mn and Ce/La ratios in the apatite are ~40 and ~2 respectively, suggesting that they were formed in a carbonatite magma. The markedly increased REE concentrations in the bulk chemistry of the rocks have been shown to be mainly controlled by the content of phosphate minerals. Compared to most carbonatites, the Eppawala rocks are generally depleted in selected trace elements, particularly Ba, Nb, Th, V, U and Zr. This depletion may be due to either a primary infertility of the parent magma with regard to such trace elements, or it is a result of fractional crystallisation during the rock formation. The stable isotope ratios do not plot within the defined "mantle carbonatite box", but still lie within the broader range of carbonatitic rocks. With these data at hand, it can be readily argued that the mode of occurrence, petrography and geochemistry of the Eppawala apatite-bearing carbonates provide conclusive evidence of their carbonatitic origin.     

On changes of the rotation velocities of stable,recurrent sunspots and their interpretation with a flux tube model

The angular rotation velocities of stable, recurrent sunspots were investigated using data from the Greenwich Photoheliographic Results 1940 until 1968. We found constant rotation velocities during the passages on the solar disk with errors of about ±4 m s^–1. During their lifetime these spots show a decreasing braking of their rotation velocities from 0.8 to 0.3 m s^–1 per day. A plausible interpretation is found by assuming the spots to be coupled to a slowly rising subsurface flux tube and a rotation velocity which increases with depth.Mitteilungen aus dem Kiepenheuer-Institut Nr. 201.     

Major and trace elements in German bottled water,their regional distribution,and accordance with national and international standards

The market for mineral water has been growing steadily over the last few years. Germany is the country with the highest number of bottled mineral water brands (908 bottled water samples from 502 wells/brands were analyzed). The per capita consumption of mineral water in Germany in 2003 was 129 L. A wide range of values of one to seven orders of magnitude was determined for 71 elements in the bottled water samples analyzed by ICP-QMS, ICP-AES, IC, titration, photometric, conductometric and potentiometric methods. A comparison of the element concentrations and the legal limits for both bottled and tap water (EU, Germany, US EPA, WHO) shows that only 70% of the 908 mineral water samples fulfill the German and EU drinking water (i.e., tap water) regulations for all parameters (not including pH) for which action levels are defined. Nearly 5% of the bottled water samples not fulfill the German and EU regulations for mineral and table water. Comparison of our results with the current German and European action levels for mineral and table water shows that only 42 of the bottled water samples exceed the limits for one or more of the following elements: arsenic, nitrate, nitrite, manganese, nickel and barium concentrations. Ten of the bottled water samples contain uranium concentrations above the 10 μg/L recommended limit.