Cluster–subcluster mergers and the formation of narrow-angle tailed radio sources

We examine the ROSAT PSPC X-ray properties of a sample of 15 Abell clusters containing 23 narrow-angle tailed (NAT) radio galaxies. We find that clusters with NATs show a significantly higher level of substructure than a similar sample of radio-quiet clusters, indicating that NAT radio sources are preferentially located in dynamically complex systems. Also, the velocity distribution of the NAT galaxies is similar to that of other cluster members; these velocities are inadequate for producing the ram pressure necessary to bend the radio jets. We therefore propose a new model for NAT formation, in which NATs are associated with dynamically complex clusters undergoing merger events. The U -shaped NAT morphology is produced in part by the merger-induced bulk motion of the ICM bending the jets.     

X-ray observations of distant Abell clusters

We present results from a ROSAT HRI study of 11 distant ( z  ∼ 0.2–0.3) Abell clusters. We have performed a morphological analysis to search for and quantify substructure in the clusters. About 70 per cent of the sample shows significant evidence of substructure in the form of centroid shift or obvious X-ray clumps. We examine the clusters for the presence of cooling flows, and determine the physical properties of the ICM by deprojecting the HRI data. Nine of the clusters have central cooling times less than the age of the system, in agreement with fractions determined from nearby, X-ray-bright samples. Additional PSPC results are presented for four clusters in the sample, and ASCA results for six clusters. The temperatures and metallicities for these distant clusters appear to be consistent with nearby clusters of similar richness.     

Rb-Sr dating of the Lackner Lake Complex,northern Ontario,Canada

The Lackner Lake Complex of northern Ontario consists of nepheline syenite and ijolite with associated bodies of apatite—magnetite rock and carbonatite. A whole-rock Rb-Sr isochron indicates that these rocks crystallized 1078 ± 7 Ma ago ($\text{λ}{}^{87}\text{Rb = 1.39·10}{}^{\mathrm{?11}}\text{a}{}^{\mathrm{?1}}$) and had an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.070282 ± 0.00011. This date is slightly lower than a K-Ar date of 1090 Ma for biotite reported previously, but is in agreement with K-Ar dates of several nearby syenite-carbonatite complexes.     

The effects and characteristics of atmospheric dust during martian global dust storm 2001A

We present retrieved trends in dust optical depth, dust effective radius and surface temperature from our analysis of Mars Global Surveyor Thermal Emission Spectrometer daytime data from global dust storm 2001A, and describe their significance for the martian dust cycle. The dust optical depth becomes correlated with surface pressure during southern spring and summer in years both with and without a global dust storm, indicating that global dust mixing processes are important at those seasons. The correlation is low at other times of the year. We found that the observed decay of optical depths at the later stages of the dust storm match, to first-order, theoretical values of clearing from Stokes–Cunningham fallout of the dust. Zonally averaged effective radius is constant within standard deviation of results (between 1.2 and 2.0 μm, with a global mean for all seasons of 1.7 μm), at all latitudes and seasons except at southern latitudes of 35° and higher around equinoxes in both martian years, where it is larger than average (2–3 μm). The emergence and disappearance of these larger particles correlates with observations of polar cap edge storms at those latitudes. Northern latitude observations under similar conditions did not yield a similar trend of larger average effective radii during the equinoxes. We also report on a linear correlation between daytime surface temperature drop and rise in optical depth during the global dust storm. Global dust storm 2001A produced a significant optical depth and surface temperature change.     

Retrieval algorithm for atmospheric dust properties from Mars Global Surveyor Thermal Emission Spectrometer data during global dust storm 2001A

We present a new parameter retrieval algorithm for Mars Global Surveyor Thermal Emission Spectrometer data. The algorithm uses Newtonian first-order sensitivity functions of the infrared spectrum in response to variations in physical parameters to fit a model spectrum to the data at 499, 1099, and 1301 cm⁻¹. The algorithm iteratively fits the model spectrum to data to simultaneously retrieve dust extinction optical depth, effective radius, and surface temperature. There are several sources of uncertainty in the results. The assumed dust vertical distribution can introduce errors in retrieved optical depth of a few tens of percent. The assumed dust optical constants can introduce errors in both optical depth and effective radius, although the systematic nature of these errors will not affect retrieval of trends in these parameters. The algorithm does not include the spectral signature of water ice, and hence data needs to be filtered against this parameter before the algorithm is applied. The algorithm also needs sufficient dust spectral signature, and hence surface-to-atmosphere temperature contrast, to successfully retrieve the parameters. After the application of data filters the algorithm is both relatively accurate and very fast, successfully retrieving parameters, as well as meaningful parameter variability and trends from tens of thousands of individual spectra on a global scale (Elteto, A., Toon, O.B. [2010]. Icarus, this issue). Our results for optical depth compare well with TES archive values when corrected by the single scattering albedo. Our results are on average 1–4 K higher in surface temperatures from the TES archive values, with greater differences at higher optical depths. Our retrieval of dust effective radii compare well with the retrievals of Wolff and Clancy (Wolff, M.J., Clancy, R.T. [2003]. J. Geophys. Res. 108 (E9), 5097) for the corresponding data selections from the same orbits.     

From the Sun to the Earth: The 13 May 2005 Coronal Mass Ejection

We report the results of a multi-instrument, multi-technique, coordinated study of the solar eruptive event of 13 May 2005. We discuss the resultant Earth-directed (halo) coronal mass ejection (CME), and the effects on the terrestrial space environment and upper Earth atmosphere. The interplanetary CME (ICME) impacted the Earth’s magnetosphere and caused the most-intense geomagnetic storm of 2005 with a Disturbed Storm Time (Dst) index reaching ?263 nT at its peak. The terrestrial environment responded to the storm on a global scale. We have combined observations and measurements from coronal and interplanetary remote-sensing instruments, interplanetary and near-Earth in-situ measurements, remote-sensing observations and in-situ measurements of the terrestrial magnetosphere and ionosphere, along with coronal and heliospheric modelling. These analyses are used to trace the origin, development, propagation, terrestrial impact, and subsequent consequences of this event to obtain the most comprehensive view of a geo-effective solar eruption to date. This particular event is also part of a NASA-sponsored Living With a Star (LWS) study and an on-going US NSF-sponsored Solar, Heliospheric, and INterplanetary Environment (SHINE) community investigation.     

Oxygen and carbon isotope ratios in the martian atmosphere

Oxygen and carbon isotope ratios in the martian CO₂ are key values to study evolution of volatiles on Mars. The major problems in spectroscopic determinations of these ratios on Mars are uncertainties associated with: (1) equivalent widths of the observed absorption lines, (2) line strengths in spectroscopic databases, and (3) thermal structure of the martian atmosphere during the observation. We have made special efforts to reduce all these uncertainties. We observed Mars using the Fourier Transform Spectrometer at the Canada–France–Hawaii Telescope. While the oxygen and carbon isotope ratios on Mars were byproducts in the previous observations, our observation was specifically aimed at these isotope ratios. We covered a range of 6022 to 6308 cm⁻¹ with the highest resolving power of ν/δν=3.5×10⁵ and a signal-to-noise ratio of 180 in the middle of the spectrum. The chosen spectral range involves 475 lines of the main isotope, 184 lines of ¹³CO₂, 181 lines of CO¹⁸O, and 119 lines of CO¹⁷O. (Lines with strengths exceeding 10⁻²⁷ cm at 218 K are considered here.) Due to the high spectral resolution, most of the lines are not blended. Uncertainties of retrieved isotope abundances are in inverse proportion to resolving power, signal-to-noise ratio, and square root of the number of lines. Laboratory studies of the CO₂ isotope spectra in the range of our observation achieved an accuracy of 1% in the line strengths. Detailed observations of temperature profiles using MGS/TES and data on temperature variations with local time from two GCMs are used to simulate each absorption line at various heights in each part of the instrument field of view and then sum up the results. Thermal radiation of Mars' surface and atmosphere is negligible in the chosen spectral range, and this reduces errors associated with uncertainties in the thermal structure on Mars. Using a combination of all these factors, the highest accuracy has been achieved in measuring the CO₂ isotope ratios: ¹³C/¹²C = 0.978 ± 0.020 and ¹⁸O/¹⁶O = 1.018 ± 0.018 times the terrestrial standards. Heavy isotopes in the atmosphere are enriched by nonthermal escape and sputtering, and depleted by fractionation with solid-phase reservoirs. The retrieved ratios show that isotope fractionation between CO₂ and oxygen and carbon reservoirs in the solid phase is almost balanced by nonthermal escape and sputtering of O and C from Mars.     

Reactions of aqueous iron-DFOB (desferrioxamine B) complexes with flavin mononucleotide in the absence of strong iron(II) chelators

The mechanisms controlling microbial uptake of Fe^III-siderophore complexes and subsequent release of the metal for cellular use have been extensively studied in recent years. Reduction of the Fe^III center is believed to be necessary to labilize the coordinated Fe and facilitate exchange with cellular ligands. Previous studies report reduction of Fe^III-DFOB by various reducing agents in solutions containing Fe^II-chelating colorimetric agents for monitoring reaction progress, but the importance of these findings is unclear because the colorimetric agents themselves stabilize and enhance the reactions being monitored. This study examines the reduction of Fe^III complexes with DFOB (desferrioxamine B), a trihydroxamate siderophore, by the fully reduced hydroquinone form of flavin mononucleotide (FMN_HQ) in the absence of strong Fe^II-chelating agents, and Fe redox cycling in solutions containing DFOB and oxidized and reduced FMN species. Experimental results demonstrate that the rate and extent of Fe^III-DFOB reduction is strongly dependent on pH and FMN_HQ concentration. At pH ? 5, incomplete Fe^III reduction is observed due to two processes that re-oxidize Fe^II, namely, the autodecomposition of Fe^II-DFOB complexes (Fe^II oxidation is coupled with reduction of a protonated hydroxamate moiety) and reaction of Fe^II-DFOB complexes with the fully oxidized flavin mononucleotide product (FMN_OX). Chemical speciation-dependent kinetic models for the forward reduction process and both reverse Fe^II oxidation processes are developed, and coupling kinetic models for all three Fe redox processes leads to successful predictions of steady-state Fe^II concentrations observed over a range of pH conditions in the presence of excess FMN_HQ and FMN_OX. The observed redox reactions are also in agreement with thermodynamic constraints imposed by the combination of Fe^III/Fe^II and FMN_OX/FMN_HQ redox couples. Quantitative comparison between kinetic trends and changing Fe speciation reveals that FMN species react predominantly with diprotonated Fe^III-DFOB and Fe^II-DFOB complexes, where protonation of one hydroxamate group opens up two Fe coordination positions. This finding suggests that ternary complex formation (FMN-Fe-DFOB) facilitates inner-sphere electron transfer reactions between the flavin and Fe center.     

A comparison of the atmospheres of Jupiter and Saturn: deep atmospheric composition, cloud structure, vertical mixing, and origin.

We present our current understanding of the composition, vertical mixing, cloud structure and the origin of the atmospheres of Jupiter and Saturn. Available observations point to a much more vigorous vertical mixing in Saturn's middle-upper atmosphere than in Jupiter's. The nearly cloud-free nature of the Galileo probe entry site, a 5-micron hotspot, is consistent with the depletion of condensable volatiles to great depths, which is attributed to local meteorology. Somewhat similar depletion of water may be present in the 5-micron bright regions of Saturn also. The supersolar abundances of heavy elements, particularly C and S in Jupiter's atmosphere and C in Saturn's, as well as the progressive increase of C from Jupiter to Saturn and beyond, tend to support the icy planetesimal model of the formation of the giant planets and their atmospheres. However, much work remains to be done, especially in the area of laboratory studies, including identification of possible new microwave absorbers, and modelling, in order to resolve the controversy surrounding the large discrepancy between Jupiter's global ammonia abundance, hence the nitrogen elemental ratio, derived from the earth-based microwave observations and that inferred from the analysis of the Galileo probe-orbiter radio attenuation data for the hotspot. We look forward to the observations from Cassini-Huygens spacecraft which are expected to result not only in a rich harvest of information for Saturn, but a better understanding of the formation of the giant planets and their atmospheres when these data are combined with those that exist for Jupiter.