On the perturbation of the anomalistic period of a highly eccentric orbit satellite due to the zonal harmonics

In this note a simple formula is given for the perturbation of the anomalistic period of a highly eccentric orbit due to the zonal harmonics. This perturbation depends essentially only on the semi-major axisa, the eccentricitye (or pericentre radius r =a(1-e)) and the latitude of the pericentre.     

Electrochemistry of reduced sulfur species in natural waters—I. The H2S-H2O system

Careful measurements of rest potentials of platinum electrodes (Eh) in the H₂S-H₂O system were made together with measurements of the pH and the potentials of Ag-Ag₂S electrodes (E_s^2?). The potentials of the platinum electrode are characteristic of H₂S chemisorption followed by H₂S discharge on the platinum. The relations between Eh, E_s^2? and pH are characteristic of the H₂S-H₂O system and of the hydrogen sulfide concentration. Thus these parameters can be employed to distinguish H₂S-H₂O systems from H₂S-S₈-H₂O systems. Field measurements on hot sulfurous springs are in agreement with laboratory data.     

A time evolution study of limb spicule spectra

Time sequences of simultaneous spectra of limb spicules, obtained using the Sacramento Peak Observatory's tower telescope and echelle spectrograph are analyzed. Intensity determinations of H and K, H, 8498 and 8542 of calcium are tabulated for three observing heights. Electron densities averaged over the entire visible lifetimes of spicules are -6 × 10¹⁰ cm^–3 at observing heights of 6000km, while maximum and minimum values were -1.1 × 10¹¹ cm^–3 at 6000km and - 2 × 10¹⁰ cm^–3 at 10000km. Electron temperatures range between 12 000 K and 16 000 K. Profile halfwidths indicate turbulent velocities of 12 to 22 km s^–1, and spectral tilts are interpreted as caused by differential velocity fields of -3 km s^–1 per 1000 km. No large scale spicule expansions or contractions are observed, although possible expulsions or accretions of material are observed. Spicules may be wider in the calcium K and H lines than in H.Now at School of Science and Engineering, The University of Alabama in Huntsville, Huntsville, Alabama.     

Modelling weathering processes at the catchment scale: The WITCH numerical model

A numerical model of chemical weathering in soil horizons and underlying bedrock (WITCH) has been coupled to a numerical model of water and carbon cycles in forest ecosystems (ASPECTS) to simulate the concentration of major species within the soil horizons and the stream of the Strengbach granitic watershed, located in the Vosges Mountains (France). For the first time, simulations of solute concentrations in soil layers and in the catchment river have been performed on a seasonal basis. The model is able to reproduce the concentrations of most major species within the soil horizons, as well as catching the first-order seasonal fluctuations of aqueous calcium, magnesium and silica concentrations. However, the WITCH model underestimates concentrations of Mg²⁺ and silica at the spring of the catchment stream, and significantly underestimates Ca²⁺ concentration. The deficit in calculated calcium can be compensated for by dissolution of trace apatite disseminated in the bedrock. However, the resulting increased Ca²⁺ release yields important smectite precipitation in the deepest model layer (in contact with the bedrock) and subsequent removal of large amount of silica and magnesium from solution. In contrast, the model accurately accounts for the concentrations of major species (Ca, Mg and silica) measured in the catchment stream when precipitation of clay minerals is not allowed. The model underestimation of Mg²⁺ and H₄SiO₄ concentrations when precipitation of well crystallized smectites is allowed strongly suggests that precipitation of well crystallized clay minerals is overestimated and that more soluble poorly crystallized and amorphous materials may be forming. In agreement with observations on other watersheds draining granitic rocks, this study indicates that highly soluble trace calcic phases control the aqueous calcium budget in the Strengbach watershed.     

Preservation/exhumation of ultrahigh-pressure subduction complexes

Ultrahigh-pressure (UHP) metamorphic terranes reflect subduction of continental crust to depths of 90–140 km in Phanerozoic contractional orogens. Rocks are intensely overprinted by lower pressure mineral assemblages; traces of relict UHP phases are preserved only under kinetically inhibiting circumstances. Most UHP complexes present in the upper crust are thin, imbricate sheets consisting chiefly of felsic units ± serpentinites; dense mafic and peridotitic rocks make up less than  10% of each exhumed subduction complex. Roundtrip prograde–retrograde P–T paths are completed in 10–20 Myr, and rates of ascent to mid-crustal levels approximate descent velocities. Late-stage domical uplifts typify many UHP complexes.

Sialic crust may be deeply subducted, reflecting profound underflow of an oceanic plate prior to collisional suturing. Exhumation involves decompression through the P–T stability fields of lower pressure metamorphic facies. Scattered UHP relics are retained in strong, refractory, watertight host minerals (e.g., zircon, pyroxene, garnet) typified by low rates of intracrystalline diffusion. Isolation of such inclusions from the recrystallizing rock matrix impedes back reaction. Thin-aspect ratio, ductile-deformed nappes are formed in the subduction zone; heat is conducted away from UHP complexes as they rise along the subduction channel. The low aggregate density of continental crust is much less than that of the mantle it displaces during underflow; its rapid ascent to mid-crustal levels is driven by buoyancy. Return to shallow levels does not require removal of the overlying mantle wedge. Late-stage underplating, structural contraction, tectonic aneurysms and/or plate shallowing convey mid-crustal UHP décollements surfaceward in domical uplifts where they are exposed by erosion. Unless these situations are mutually satisfied, UHP complexes are completely transformed to low-pressure assemblages, obliterating all evidence of profound subduction.     

Deformability characteristics of brazilian laterites

This paper summarizes the resilient and permanent deformation characteristics of laterite gravels, determined by cyclic loading in triaxial tests of compacted specimens. A study of laterite pavements was carried out on eight paved road sections in the state of Mato Grosso. Also reported is the influence of fine sand admixture, specimen size and soaking in two laterite samples from Roraima and Rondônia in the North of Brazil. The experimental relationships of resilient moduli against applied stresses are interpreted empirically for models what may be incorporated in a structural analysis of full depth of laterite pavement.     

Behaviour of a rupture of the 21 June 2000 earthquake in South Iceland as revealed in an asphalted car park

A major earthquake (M=6.6) occurred on 21 June 2000, in South Iceland. This paper presents an unusual example of left-lateral strike-slip displacement recorded in a newly asphalted car park surface through a mechanically consistent pattern of open fissures and pressure ridges resulting from simple shear and rotation. Measurement of these features allows accurate reconstruction of the local deformation. The behaviour of the asphalt layer resembles that of analogue physical models, especially in terms of rotations induced by shear deformation. It is finally shown that through a wide range of scales some basic patterns associating rotation and opposite senses of strike-slip exist in the South Iceland Seismic Zone.     

An X-ray absorption fine structure and nuclear magnetic resonance spectroscopy study of gallium-silica complexes in aqueous solution

The influence of aqueous silica on gallium(III) hydrolysis in dilute (2 × 10⁻⁴ ≤ m_Ga ≤ 5 × 10⁻³) and moderately concentrated (0.02 ≤ m_Ga ≤ 0.3) aqueous solutions was studied at ambient temperature, using high resolution X-ray absorption fine structure (XAFS) and nuclear magnetic resonance (NMR) spectroscopies, respectively. Results show that, in Si-free acidic solutions (pH < 3), Ga is hexa-coordinated with oxygens of H₂O molecules and/or OH groups in the first coordination sphere of the metal. With increasing pH, these hydroxyl groups are progressively replaced by bridging oxygens (-O-), and polymerized Ga-hydroxide complexes form via Ga-O-Ga chemical bonds. In the 2.5-3.5 pH range, both XAFS and NMR spectra are consistent with the dominant presence of the Ga₁₃ Keggin polycation, which has the same local structure as A1₁₃. Under basic pH (pH > 8), Ga exhibits a tetrahedral coordination, corresponding to Ga(OH)₄⁻ species, in agreement with previous NMR and potentiometric studies. Major changes in Ga hydrolysis have been detected in the presence of aqueous silica. Ga is tetra-coordinated, both in basic and acid (i.e., at pH > 2.7) Si-bearing solutions (0.01 ≤ m_Si ≤ 0.2), and forms stable gallium-silicate complexes. In these species, Ga binds via bridging oxygen to 2 ± 1 silicons, with an average Ga-Si distance of 3.16 ± 0.05 Å, and to 2 ± 1 silicons, with an average Ga-Si distance of 3.39 ± 0.03 Å. These two sets of Ga-Si distances imply the formation of two types of Ga-silicate aqueous complex, cyclic Ga-Si_2-3 species (formed by the substitution of Si in its tri-, tetra- or hexa-cyclic polymers by Ga atoms), and chainlike GaSi_2-4 species (similar to those found for A1), respectively. The increase in the number of Si neighbors (a measure of the complex concentration and stability), in alkaline media, with increasing SiO₂(aq) content and decreasing pH is similar to that for A1-Si complexes found in neutral to basic solutions. At very acid pH and moderate silica concentrations, the presence of another type of Ga-Si complex, in which Ga remains hexa-coordinated and binds to the silicon tetrahedra via the GaO₆ octahedron corners, has also been detected. These species are similar to those found for Al³⁺ in acid solutions. Thus, as for aluminum, silicic acid greatly hampers Ga hydrolysis and enhances Ga mobility in natural waters via the formation of gallium-silicate complexes.