Cassini imaging of Saturn's rings: II. A wavelet technique for analysis of density waves and other radial structure in the rings

We describe a powerful signal processing method, the continuous wavelet transform, and use it to analyze radial structure in Cassini ISS images of Saturn's rings. Wavelet analysis locally separates signal components in frequency space, causing many structures to become evident that are difficult to observe with the naked eye. Density waves, generated at resonances with saturnian satellites orbiting outside (or within) the rings, are particularly amenable to such analysis. We identify a number of previously unobserved weak waves, and demonstrate the wavelet transform's ability to isolate multiple waves superimposed on top of one another. We also present two wave-like structures that we are unable to conclusively identify. In a multi-step semi-automated process, we recover four parameters from clearly observed weak spiral density waves: the local ring surface density, the local ring viscosity, the precise resonance location (useful for pointing images, and potentially for refining saturnian astrometry), and the wave amplitude (potentially providing new constraints upon the masses of the perturbing moons). Our derived surface densities have less scatter than previous measurements that were derived from stronger non-linear waves, and suggest a gentle linear increase in surface density from the inner to the mid-A Ring. We show that ring viscosity consistently increases from the Cassini Division outward to the Encke Gap. Meaningful upper limits on ring thickness can be placed on the Cassini Division (3.0 m at r∼118,800 km, 4.5 m at r∼120,700 km) and the inner A Ring (10-15 m for r<127,000 km).     

Towards a more habitable Mars — or — the coming martian spring

Two schemes are presented in which matter is moved closer to Mars so as to increase the equinoctal precession period of Mars. In such a way the Martian springs, during which Mars is habitable in the long winter model of Sagan (1971), could be extended and, in fact, prolonged indefinitely. The schemes involve using solar energy to move the satellite Phobos and/or material from the asteroid belt. Difficulties exist with the proposals but they are presented to stimulate discussion.     

Mercury: Internal structure and thermal evolution

Astronomical observations and cosmochemical calculations suggest that the planet Mercury may be composed of materials which condensed at relatively high temperatures in the primitive solar nebula and may have a basaltic crust similar to parts of the moon. These findings, plus the long standing inference that Mercury is much richer in metallic iron than the other terrestrial planets, provide important constraints which we apply to models of the thermal evolution and density structure of the planet. The thermal history calculations include explicitly the differing thermal properties of iron and silicates and account for core segregation, melting and differentiation of heat sources, and simulated convection during melting. If the U and Th abundances of Mercury are taken from the cosmochemical model of Lewis, then the planet would have fully differentiated a metal core from the silicate mantle for all likely initial temperature distributions and heat transfer properties. Density distributions for the planet are calculated from the mean density and estimates of the present-day temperature. For the fully differentiated model, the moment of inertia C/MR² is 0.325 (J₂=0.302×10^?6). For models with lower heat source abundances, the planet may not yet have differentiated. The density profiles for such models give C/MR²=0.394 (J₂=0.487×10^?6). These results should be useful for preliminary interpretation of the Mariner 10 measurements of Mercury's gravitational field.     

Solubility of plutonium(VI) carbonate in saline solutions

Among the plutonium oxidation states found to form in the environment, mobile plutonium(VI) can exist under oxidizing conditions and in waters with high chloride content due to radiolysis effects. We are investigating the solubility and speciation of plutonium(VI) carbonate under conditions relevant to natural waters and brines such as those found near some geologic radioactive waste repositories. The solid Pu(VI) phase PuO₂CO₃(s) was prepared and its solubility was measured in NaCl and NaClO₄ solutions in a CO₂ atmosphere as a function of pH and ionic strength (0.1-5.6 m). The concentration of soluble plutonium in solution was calculated from spectroscopic data and liquid scintillation counting. Spectroscopic measurements also revealed the plutonium oxidation state. The apparent solubility product of PuO₂CO₃(s) was determined at selected electrolyte concentrations to be, log K_s,0 = −13.95 ± 0.07 (0.1 m NaCl), log K_s,0 = −14.07 ± 0.13 (5.6 m NaCl), and log K_s,0 = −15.26 ± 0.11 (5.6 m NaClO₄). Specific ion interaction theory was used to calculate the solubility product at zero ionic strength, .     

Distribution, characterization, and geochemical controls of elements of concern in uranium mine tailings, Key Lake, Saskatchewan, Canada

The distribution of As, Mo, Ni and Se in the aqueous and solid phases of U mine tailings in the Deilmann Tailings Management Facility (DTMF), located at the Key Lake mine in northern Saskatchewan, Canada, was defined using as-discharged tailings samples collected monthly starting in 1996 and core samples collected from the DTMF from 3 locations on 3 occasions between 2004 and 2009. These data indicated that the DTMF can be divided into two geochemical zones; tailings generated from the Deilmann ore body between 1996 and 2000 and tailings from the McArthur River ore body, mined after July 2000. The Deilmann tailings solids are generally characterized by greater elemental concentrations than those in the McArthur River tailings, particularly for As, Co and Ni. These elevated concentrations are attributed to the abundance of Ni–Co–As–S minerals in this ore. The mean aqueous concentrations of As, Mo, Ni, and Se are 3.7, 23.2, 0.14, and 0.02 mg L⁻¹, respectively, in the Deilmann porewaters and 0.20, 4.16, 0.06, and 0.03 mg L⁻¹, respectively, in the McArthur River porewaters. Similarly, the mean As, Mo, Ni, and Se solid phase concentrations are 5.89 × 10³, 69.9, 3.20 × 10³, and 17.4 μg g⁻¹, respectively, for the Deilmann tailings and 440, 13.6, 551, and 3.03 μg g⁻¹ in the McArthur River tailings. Statistically, pH remained unchanged from the time of discharge while Eh values have remained oxic with no significant change between the two tailings types over 15 a of residence time. Results from sequential extractions, thermodynamic modeling, and results of complimentary research indicated that ferrihydrite solubility is the dominant control on aqueous As concentrations and also plays a role in controlling dissolved Mo, Ni and Se.     

Silurian and Devonian systems

The Ediacara mineral field is situated 30 km W of Beltana on the western margins of the Flinders Ranges, South Australia, and consists of silver‐lead and copper deposits in lower Cambrian carbonate rocks that contain anomalous base‐metal contents throughout the Adelaide Geosyncline. The lower Cambrian rocks, which consist of the basal Parachilna Formation and overlying Ajax Limestone, rest disconformably on the Precambrian, and at Ediacara occupy a shallow N‐S elongate syncline near the hinge zone of the Adelaide Geosyncline. The main primary ore minerals of the silver‐lead mineralization are galena and pyrite, with very minor chalcopyrite and sphalerite, and rare tetrahedrite and pearceite. The gangue consists mainly of silica (both chalcedony and quartz), with minor dolomite and rare barite. The mineralization is stratabound and occurs in conformable zones, the lowest of which commences about 30–50 m above the base of the Cambrian sequence. The host to the silver‐lead mineralization, the Ajax Limestone, can be subdivided into three units which represent a set of lithologies, structures and organic traces indicative of a shallow near‐shore carbonate environment. The silver‐lead mineralization is mainly present in sandy and laminated dolomites which were deposited in an environment ranging from sub‐tidal to bar and channel and tidal flat, respectively. Four types of mineralization have been recognized; disseminated sulphides of syngenetic and/or diagenetic origin and epigenetic concentrations along stylolites, in veins and as breccia fillings. Post‐depositional solution activity has affected a large proportion of the carbonate sequence. The effects of this activity range from stylolites through stylobreccias to solution collapse breccias. The epigenetic concentrations of mineralizations have apparently been formed by the remobilization of the disseminated sulphides during solution activity. The ore and gangue minerals of the epigenetic mineralization display both euhedral forms and distinct colloform banding, and framboidal textures have also been observed in both pyrite and galena. There is evidence of repeated episodic precipitation and no simple paragenetic sequence can be recognized. Fluid inclusions in silica and dolomite associated with the epigenetic mineralization have homogenization temperatures of 159 to 199°C and freezing temperatures that indicate the fluids to be saline brines containing NaCl with CaCl₂ and/or MgCl₂. Sulphur isotope analyses show a range of 8³⁴S values from ‐12.5 to +8.6 per mil, with no evidence of significant differences between the four types of mineralization. The data suggest deposition of the disseminated sulphides as a result of biological reduction of seawater sulphate in a system partially open with respect to sulphate supply. Subsequent remobilization of sulphides apparently involved little or no sulphur isotope fractionation. The Ediacara silver‐lead deposits have many features in common with Mississippi Valley‐type lead‐zinc deposits and appear to have similarities in terms of genesis, in that the epigenetic mineralization has been formed as a result of post‐depositional solution activity during diagenesis in a sedimentary basin. The scale of transport of the metals deposited as the epigenetic mineralization at Ediacara appears, however, to have been very much less than that of the metals in other Mississippi Valley‐type deposits.     

An experimental study of a minette from the Milk River area, southern Alberta, Canada

Buhlmann et al. (Can J Earth Sci 37: 1629–1650, 2000) studied the minettes and xenoliths from the Milk River area of southern Alberta, Canada. Based on previous work, they hypothesized that the minettes were derived from a source containing phlogopite?+?clinopyroxene?±?olivine, at pressures ≥1.7?GPa. To test this hypothesis, liquidus experiments were performed on a primitive minette between 1.33 and 2.21?GPa and between 1,300 and 1,400?°C to constrain the mineralogy of its source region. We found a multiple saturation point along the liquidus at 1.77 GPa and 1,350?°C, where the liquid coexists with orthopyroxene and olivine. Neither phlogopite nor clinopyroxene were found to be liquidus phases, which is inconsistent with Buhlmann et al.’s hypothesis. We suggest that our minette is not primary, but had re-equilibrated with harzburgitic mantle subsequent to formation. In such a scenario, partial melting of a veined source containing mica and clinopyroxene occurred at or near the base of the Wyoming craton (~200?km). Minimal heating or the introduction of hydrous fluids into the source would be required to induce partial melting. Rapid ascent rates, coupled with slow cooling rates, of the “primary minette magma” would preserve the high temperature observed in our experiments. At ~58?km, our “primary minette magma” likely stalled and re-equilibrated with the harzburgite surroundings.     

Investigation of acidic dissolution of mixed clays between pH 1.0 and −3.0 using Si and Al X-ray absorption near edge structure

Although widely investigated in relation to acid mine drainage systems at pH > 1.0, we know little about the impact of sulfuric acid (H₂SO₄) on the geochemistry and mineralogy of clays at pH < 1.0 (including negative pH values). Thus, laboratory batch experiments were conducted on three mixed clay samples with different mass ratios of phyllosilicates (smectite, illite, and kaolinite) to investigate the impact of H₂SO₄ from pH 1.0 to −3.0 for exposure periods of 14, 90, 180, and 365 days. Si and Al K- and L_2,3-edge X-ray absorption near edge structure (XANES) spectroscopy were employed on these samples to determine the chemical and structural changes that occur during acidic dissolution of phyllosilicates that cannot be distinguished using X-ray diffraction analyses. A series of silicate, phyllosilicate, and Al-bearing standard compounds were also studied to provide an explanation for the observed changes in the clay samples. The Si XANES results indicated the preferential dissolution of the phyllosilicates (pH ? 1.0, t ? 14 d), the persistence of quartz even at pH ? −3.0 and t ? 365 d, and the formation of an amorphous silica-like phase that was confined to the surface layer of the altered clay samples at pH ? 0.0 and t ? 90 d). Al XANES results demonstrated dissolution of Al-octahedral layers (pH ? 1.0, t ? 14 d), the persistence of four-fold relative to six-fold coordinated Al, and the precipitation of an Al-SO₄-rich phase (pH ? −1.0, t ? 90 d). An existing conceptual model of phyllosilicate dissolution under extremely acidic conditions was modified to include the results of this study.     

Graphical methods of river profile analysis to unravel drainage area change,uplift and erodibility contrasts in the Central Range of Taiwan

To reveal river channel steepness patterns and variance in settings with significant variation in rock uplift rate, rock erodibility and moving water divides, we present a series of graphical methods to interpret channel profiles. To complement Cartesian χ plots, longitudinal profiles and mapping methods, we introduce a new method based on a radial coordinate system. We map each basin onto polar coordinates in which the radial dimension is χ and the azimuthal coordinate, ?, is calculated with an increment (Δ?) scaled to the distance to neighboring channel heads. The elevation is contoured on this mapping. Average channel steepness is estimated by fitting a conical surface to the elevation. The graph simplifies the comparison of χ and elevation between channels that share a divide, and helps identify spatial changes in drainage area and patterns of erodibility. We apply this approach to derive the uplift pattern in the eastern and southern Central Range of Taiwan, where the high tectonic convergence and uplift rates combined with sub‐tropical climate and frequent typhoons results in high exhumation rate, and well‐developed, detachment‐limited river networks. Additionally, the tectonic activity leads to drainage basin reorganization. We identify examples of divide migration, discrete river capture as well as anomalous steepness that we attribute to local variability in rock erodibility. Estimated basin‐average steepness values show the highest and a near constant value from Hsinwulu basin to Liwu basin in the center of the Island. To the north and south of this region, the values gradually decrease. These estimates show good correlation with the topography of the Central Range and erosion rates derived from in situ ¹⁰Be concentrations in river‐borne quartz. We conclude that the basin steepness reflects systematic differences in rock uplift rate and erosion rate. Copyright © 2016 John Wiley & Sons, Ltd.