Erratum: the 2.27 day period of WR-134 (HD 191765)

The original temporal analysis of a 12 night spectral timeseries of WR-134 has been found to be flawed and a re-analysis shows that the line profile variations are indeed periodic. When combined with a 4 night timeseries taken 45 days earlier, a period near 2.27 d is found in periodograms of the Heii 5412 line centroid,rms line width, and line skew variations. When the emission line residuals are ordered as a function of phase, a sinuous feature appears to snake about the line center with an amplitude of ± 500 km s^–1. This is 20 larger than the line centroid amplitude; the calculation of which is heavily weighted by static portions of the line profile. In addition to the snake, emission residuals appear that move away from line center on unbound trajectories and are thought to result from the interaction of a periodic driver with the unstable flow of the radiation driven wind. The nature of the periodic driver is a topic for discussion.     

In situ Sr/Sr investigation of igneous apatites and carbonates using laser-ablation MC-ICP-MS

In situ Sr isotopic compositions of coexisting apatite and carbonate for carbonatites from the Sarfartoq alkaline complex, Greenland, have been determined by laser-ablation multicollector inductively coupled plasma mass spectrometry. This study is the first to examine the extent of Sr isotopic homogeneity among coexisting igneous minerals containing high Sr (>3000 ppm) and low Rb (?1 ppm) contents within a single ∼50-μm-thick thin-section mount. This technique is capable of producing measured ⁸⁷Sr/⁸⁶Sr values with analytical precision (∼0.005%, 2σ) approaching those obtained by thermal ionization mass spectrometry but in a much shorter interval of time (100 s vs. >1 h, respectively). The combined total analyses (n = 107) of apatite and carbonate yield ⁸⁷Sr/⁸⁶Sr compositions ranging from ∼0.7025 to ∼0.7031. This relatively large variation in Sr isotopic compositions (∼0.0006) is ∼1 order of magnitude larger than the estimated external reproducibility (∼0.00005, 2σ) of the method. The large range in ⁸⁷Sr/⁸⁶Sr values suggests that apatite and carbonate precipitated predominantly under nonequilibrium conditions. The isotopic variations observed within individual hand specimens may therefore reflect larger (regional) scale open-system processes, possibly involving mixing of carbonatitic melts derived from distinct mantle sources or from a common isotopically heterogeneous mantle.     

Origin, age and stratigraphic significance of distal fallout ash tuffs from the Carboniferous–Permian continental Saar–Nahe Basin (SW Germany)

Thin, widespread, fallout tuff layers interbedded within fluvio-lacustrine successions of the Carboniferous-Permian Saar-Nahe Basin provide important tephrostratigraphic markers. In addition, radiogeochronometric data derived from the tuffs serve as calibration points for the adjustment to regional chronostratigraphy and to numerical time scales. The Pappelberg-Tuff in the Meisenheim Formation (Glan Group) has been dated by U/Pb zircon SHRIMP technique at 297.0Dž.2 Ma. Taking the Carboniferous/Permian boundary at 296 Ma, the Meisenheim Formation coincides approximately with this boundary. Consequently, underlying strata, lithostratigraphically regarded as the basal part of the 'Rotliegend', chronostratigraphically belong to the Upper Carboniferous. Bed thicknesses, grain size and sorting characteristics of the tuffs and the absence of contemporaneously emplaced volcanics within the Saar-Nahe Basin point to an extrabasinal derivation of the wind-drifted volcanic ash. Decreasing grain sizes of juvenile pyroclastic particles towards the north suggest source areas south of the basin within 300 km distance. The majority of the tuffs are rhyolitic to rhyodacitic and indicate petrographic and geochemical affinities to Moldanubian S-type granitoids, in particular to highly differentiated two-mica granites, and related volcanic effusives. Within the time frame considered here, such potential source rocks were emplaced in the northern and central Black Forest (SW Germany) and the northern Vosges (E France) at 100-150 km distance south of the Saar-Nahe Basin.     

3‐D elemental and isotopic composition of presolar silicon carbides

Abstract— Thirteen presolar silicon carbide grains—three of supernova (SN) origin and ten of asymptotic giant branch (AGB) star origin—were examined with time‐of‐flight‐secondary ion mass spectrometry (TOF‐SIMS). The grains had been extracted from two different meteorites—Murchison and Tieschitz—using different acid residue methods. At high lateral resolution of ～300 nm, isotopic and elemental heterogeneities within the micrometer‐sized grains were detected. The trace elemental abundances, when displayed in two‐element correlation plots, of Li, Mg, K, and Ca show a clear distinction between the two different meteoritic sources. The different concentrations might be attributed to differences of the host meteorites and/or of extraction methods whereas the stellar source seems to be less decisive. In one SN grain with ²⁶Mg‐enrichment from extinct ²⁶Al, the acid treatment, as part of the grain separation procedure, affected the Mg/Al ratio in the outer rim and therefore the inferred initial ²⁶Al/²⁷Al ratio. A second SN grain exhibits a lateral heterogeneity in ²⁶Al/²⁷Al, which either is due to residual Al‐rich contamination on the grain surface or to the condensation chemistry in the SN ejecta.     

Hubble Space Telescope observations of Comet 9P/Tempel 1 during the Deep Impact encounter

We report on the Hubble Space Telescope program to observe periodic Comet 9P/Tempel 1 in conjunction with NASA's Deep Impact Mission. Our objectives were to study the generation and evolution of the coma resulting from the impact and to obtain wide-band images of the visual outburst generated by the impact. Two observing campaigns utilizing a total of 17 HST orbits were carried out: the first occurred on 2005 June 13-14 and fortuitously recorded the appearance of a new, short-lived fan in the sunward direction on June 14. The principal campaign began two days before impact and was followed by contiguous orbits through impact plus several hours and then snapshots one, seven, and twelve days later. All of the observations were made using the Advanced Camera for Surveys (ACS). For imaging, the ACS High Resolution Channel (HRC) provides a spatial resolution of 36 km (16 km pixel⁻¹) at the comet at the time of impact. Baseline images of the comet, made prior to impact, photometrically resolved the comet's nucleus. The derived diameter, 6.1 km, is in excellent agreement with the 6.0±0.2 km diameter derived from the spacecraft imagers. Following the impact, the HRC images illustrate the temporal and spatial evolution of the ejecta cloud and allow for a determination of its expansion velocity distribution. One day after impact the ejecta cloud had passed out of the field-of-view of the HRC.     

Climatic forcing before,during, and after the 8.2 Kyr B.P. global cooling event

This paper attempts at full characterization of the unique global 8.2 Kyr B.P. cooling event. Significant atmospheric cooling started during 9.5–8.5 Kyr B.P. when the Sun was extremely quiet during three periods of ∼ 50–100 years. The flood of melt water in the N. Atlantic from glacial lakes during the demise of the Laurentide ice sheet, starting at ∼ 8.5 Kyr B.P., adds to the atmospheric cooling. Climatic forcing events occurred at 8.5 Kyr B.P., at 8.2 Kyr B.P. and finally at 8.06 Kyr B.P., leading to concurrent increases or decreases in the atmospheric Δ¹⁴C levels, completely consistent with the climatic forcing proposed here.     

Field experiments yield new insights into gas exchange and excess air formation in natural porous media

Gas exchange between seepage water and soil air within the unsaturated and quasi-saturated zones is fundamentally different from gas exchange between water and gas across a free boundary layer, e.g., in lakes or rivers. In addition to the atmospheric equilibrium fraction, most groundwater samples contain an excess of dissolved atmospheric gases which is called “excess air”. Excess air in groundwater is not only of crucial importance for the interpretation of gaseous environmental tracer data, but also for other aspects of groundwater hydrology, e.g., for oxygen availability in bio-remediation and in connection with changes in transport dynamics caused by the presence of entrapped air bubbles. Whereas atmospheric solubility equilibrium is controlled mainly by local soil temperature, the excess air component is characterized by the (hydrostatic) pressure acting on entrapped air bubbles within the quasi-saturated zone. Here we present the results of preliminary field experiments in which we investigated gas exchange and excess air formation in natural porous media. The experimental data suggest that the formation of excess air depends significantly on soil properties and on infiltration mechanisms. Excess air was produced by the partial dissolution of entrapped air bubbles during a sprinkling experiment in fine-grained sediments, whereas similar experiments conducted in coarse sand and gravel did not lead to the formation of excess air in the infiltrating water. Furthermore, the experiments revealed that the noble gas temperatures determined from noble gases dissolved in seepage water at different depths are identical to the corresponding in situ soil temperatures. This finding is important for all applications of noble gases as a paleotemperature indicator in groundwater since these applications are always based on the assumption that the noble gas temperature is identical to the (past) soil temperature.     

Laboratory studies about the interaction of ammonia with ice crystals at temperatures between 0 and −20°C

In laboratory experiments the interactions of ammonia with ice crystals were studied within the temperature range between 0 and −20°C. In a first series of experiments dendritic ice crystals were grown from water vapor in presence of ammonia gas in various concentrations between 4 and 400 ppbv. In a second series of experiments pure ice crystals were exposed to a humidified ammonia–air mixture inside a horizontal flow tube. The influence of temperature, ammonia gas concentration (0.6, 1.5, and 10 ppmv), exposure time, and the presence of impurities such as sulfate on the ammonia uptake by the ice surface was investigated by determining the ammonium content in the melt water of the ice crystals by ion chromatography. During the growth of ice crystals significant amounts of ammonia (around 200 μg/l) were taken up even at small gas concentrations. In contrast, even at high gas concentrations the uptake of ammonia by non-growing ice crystals was lower by approximately one order of magnitude. The presence of sulfate on the ice surface affected an enhanced uptake of ammonia by a factor of 5–10. A model is presented which describes the uptake of ammonia by ice considering the chemical processes occurring in the ice surface layer and simultaneous diffusion of ammonia into bulk ice. Even the increased uptake of ammonia by growing ice is rather small compared to the uptake by water droplets; thus, the major process for scavenging of ammonia from the atmosphere via the ice phase might not be the direct uptake by ice crystals but the riming involving super-cooled droplets containing ammonia.     

Trace element partitioning between apatite and silicate melts

We present new experimental apatite/melt trace element partition coefficients for a large number of trace elements (Cs, Rb, Ba, La, Ce, Pr, Sm, Gd, Lu, Y, Sr, Zr, Hf, Nb, Ta, U, Pb, and Th). The experiments were conducted at pressures of 1.0 GPa and temperatures of 1250 °C. The rare earth elements (La, Ce, Pr, Sm, Gd, and Lu), Y, and Sr are compatible in apatite, whereas the larger lithophile elements (Cs, Rb, and Ba) are strongly incompatible. Other trace elements such as U, Th, and Pb have partition coefficients close to unity. In all experiments we found D_Hf > D_Zr, D_Ta ≈ D_Nb, and D_Ba > D_Rb > D_Cs. The experiments reveal a strong influence of melt composition on REE partition coefficients. With increasing polymerisation of the melt, apatite/melt partition coefficients for the rare earth elements increase for about an order of magnitude. We also present some results in fluorine-rich and water-rich systems, respectively, but no significant influence of either H₂O or F on the partitioning was found. Furthermore, we also present experimentally determined partition coefficients in close-to natural compositions which should be directly applicable to magmatic processes.