Coherence analysis of granular intensity

A high resolution spectrogram of the Mg b₂ line from the quiet Sun disc centre is subjected to a coherence analysis. We find that the coherence between intensity fluctuations in the continuum and the wings of the line breaks down at a distance = 0.35 Å from line centre. From this and the r.m.s. intensity contrast as a function of we are led to the following simple model of temperature fluctuation T in the solar photosphere: A lower part (below 50 km, or ₅₀₀₀ > 0.25) with strongly inward increasing T and an upper part (above 50 km) with constant T = 75 K. The two parts are supposed to fluctuate incoherently.Mitteilungen aus dem Kiepenheuer Institut Nr. 166.     

Organized bacterial assemblies in manganese nodules: evidence for a role of S-layers in metal deposition

Polymetallic/ferro-manganese nodules (Mn-nodules) reach sizes of up to 10 cm in diameter and are abundantly found on the seabed. To date, the origin of Mn-nodules remains unclear, and both abiogenic and biogenic origins have been proposed. In search of evidence for a contribution of microbial processes to the formation of Mn-nodules, we analyzed those spherical nodules which contain a concentrically banded texture in their interior. The Mn-nodules were collected at a depth of 5,152 m from the Clarion-Clipperton Zone. Our high-resolution scanning electron microscopy analyses reveal first published evidence that endolithic microorganisms exist and are arranged in a highly organized manner on plane mineral surfaces within the nodules. These microorganisms are adorned on their surfaces with S-layers, which are indicative for bacteria. Moreover, the data suggest that these S-layers are the crystallization seeds for the mineralization process. We conclude that the mineral material of the Mn-nodule has a biogenic origin, and hope that these data will contribute to the development of biotechnological approaches to concentrate metals from seawater using bacteria in bioreactors.     

Maximizing Net Extraction Using an Injection‐Extraction Well Pair in a Coastal Aquifer

In this study, we examine the maximum net extraction rate from the novel arrangement of an injection‐extraction well pair in a coastal aquifer, where fresh groundwater is reinjected through the injection well located between the interface toe and extraction well. Complex potential theory is employed to derive a new analytical solution for the maximum net extraction rate and corresponding stagnation‐point locations and recirculation ratio, assuming steady‐state, sharp‐interface conditions. The injection‐extraction well‐pair system outperforms a traditional single extraction well in terms of net extraction rate for a broad range of well placement and pumping rates, which is up to 50% higher for an aquifer with a thickness of 20 m, hydraulic conductivity of 10 m/d, and fresh water influx of 0.24 m²/d. Sensitivity analyses show that for a given fresh water discharge from an inland aquifer, a larger maximum net extraction is expected in cases with a smaller hydraulic conductivity or a smaller aquifer thickness, notwithstanding physical limits to drawdown at the pumping well that are not considered here. For an extraction well with a fixed location, the optimal net extraction rate linearly increases with the distance between the injection well and the sea, and the corresponding injection rate and recirculation ratio also increase. The analytical analysis in this study provides initial guidance for the design of well‐pair systems in coastal aquifers, and is therefore an extension beyond previous applications of analytical solutions of coastal pumping that apply only to extraction or injection wells.     

Mutual Potential of Homogeneous Polyhedra

The mutual gravitational potential between a pair of homogeneous polyhedra is expressed using an infinite series. The nested volume integrals are evaluated analytically and result in simple tensor expressions containing no special functions. However, complexity increases as O(6 ⁿ ), where n is the term degree. An alternate formulation due to Liebenthal is also presented.     

<Superscript>57</Superscript>Fe Mössbauer spectroscopy,X-ray single-crystal diffractometry,and electronic structure calculations on natural alexandrite

Natural alexandrite Al₂BeO₄:Cr from Malyshevo near Terem Tschanka, Sverdlovsk, Ural, Russia, has been characterized by ⁵⁷Fe Mössbauer spectroscopy, electron microprobe, X-ray single-crystal diffractometry and by electronic structure calculations in order to determine oxidation state and location of iron. The sample contains 0.3 wt% of total iron oxide. The ⁵⁷Fe Mössbauer spectrum can be resolved into three doublets. Two of them with hyperfine parameters typical for octahedrally coordinated high-spin Fe³⁺ and Fe²⁺, respectively, are assigned to iron substituting for Al in the octahedral M2-site. The third doublet is attributed to Fe³⁺ in hematite. Electronic structure calculations in the local spin density approximation are in reasonable agreement with experimental data provided that expansion and/or distortion of the coordination octahedra are presumed upon iron substitution. The calculated hyperfine parameters of Fe³⁺ are almost identical for the M1 and M2 positions, but the calculated ligand-field splitting is by far too large for high-spin Fe³⁺ on M1.     

Volatile emissions and gas geochemistry of Hot Spring Basin,Yellowstone National Park,USA

We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640 ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H₂, and mildly enriched in CH₄ and H₂S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water–rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or ^40?Ar/^4?He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300 °C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO₂ flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO₂ fluxes across all the thermal/altered area suggests that 410 ± 140 t d^− 1 CO₂ are emitted at HSB (vent emissions not included). Diffuse fluxes of H₂S were measured in Yellowstone for the first time and likely exceed 2.4 t d^− 1 at HSB. Comparing estimates of the total estimated diffuse H₂S emission to the amount of sulfur as SO₄²⁻ in streams indicates ~ 50% of the original H₂S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140–370 MW using CO₂ as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1–3% for CO₂, 2–8% for heat) of that estimated for the entire Yellowstone system.     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Applications of the random model of drainage basin composition

The random model of drainage basin composition is founded on the assumptions that (a) natural channels are topologically random in the absence of geological controls and (b) for channel networks developed in similar environments, the exterior and interior link lengths are independent random variables with a common distribution for each type. The effectiveness of this model in estimating the values of geomorphic variables and in explaining and predicting geomorphic relationships is illustrated by several examples. The data required for these examples were obtained from map studies of 30 channel networks, comprising a total of about 8700 links, in eastern Kentucky. A common factor in the success of all three applications of the model is the way in which the planimetric features of drainage basins are determined by their underlying topologic structure.     

Functioning of intertidal flats inferred from temporal and spatial dynamics of O<Subscript>2</Subscript>, H<Subscript>2</Subscript>S and pH in their surface sediment

In this article, we describe the dynamics of pH, O₂ and H₂S in the top 5–10 cm of an intertidal flat consisting of permeable sand. These dynamics were measured at the low water line and higher up the flat and during several seasons. Together with pore water nutrient data, the dynamics confirm that two types of transport act as driving forces for the cycling of elements (Billerbeck et al. 2006b): Fast surface dynamics of pore water chemistry occur only during inundation. Thus, they must be driven by hydraulics (tidal and wave action) and are highly dependent on weather conditions. This was demonstrated clearly by quick variation in oxygen penetration depth: Seeps are active at low tide only, indicating that the pore water flow in them is driven by a pressure head developing at low tide. The seeps are fed by slow transport of pore water over long distances in the deeper sediment. In the seeps, high concentrations of degradation products such as nutrients and sulphide were found, showing them to be the outlets of deep-seated degradation processes. The degradation products appear toxic for bioturbating/bioirrigating organisms, as a consequence of which, these were absent in the wider seep areas. These two mechanisms driving advection determine oxygen dynamics in these flats, whereas bioirrigation plays a minor role. The deep circulation causes a characteristic distribution of strongly reduced pore water near the low water line and rather more oxidised sediments in the centre of the flats. The two combined transport phenomena determine the fluxes of solutes and gases from the sediment to the surface water and in this way create specific niches for various types of microorganisms.