Distribution and morphology of sinkholes triggered by flooding following Tropical Storm Alberto at Albany, Georgia, USA

Flooding of the Flint River in July 1994 triggered the collapse of at least 312 sinkholes in the karstic Dougherty Plain at Albany, Georgia. We examined the distribution and morphology of these new sinkholes to evaluate the mode of formation, to characterize early stages of the evolution of sinkhole form, and to estimate the lowering of the surface associated with the development of new sinkholes.Eighty-eight percent of sinkholes occur inside the limits of flooding, especially in areas of sandy overburden, and they often follow joint-controlled linear trends. Sinkhole dimensions are log-normally distributed with median values of circumference = 5.7 m, length = 1.8 m, width = 1.6 m, and depth = 0.7 m; asymmetry (L:W) = 1.2. Cross-sectional forms range from narrow cylinders to large bowls, with many sinkholes having undercut sides.Flooding triggered the formation of sinkholes by saturating and liquefying overburden, which caused soil arches to collapse and flow into cavities in bedrock. The prevalence of sinkholes near the periphery of flooding suggests that drainage and loss of buoyant support as flood waters subsided may also have contributed to failure. A volume ratio index is used to quantify the three dimensional geometric form of sinkholes. Initially, small cylindrical shafts open over a bedrock joint, followed by progressive slumping that leads to widening and increases in volume to a final bowl form. Estimates of the aggregate volume of overburden transported underground in flooded areas range from 7,990 to 11,130 m3. Averaged over flooded areas, this accounts for 0.26 to 0.37 mm/km² lowering of the surface. Based on a 500 year recurrence interval for the flood event, values for lowering of the surface range from 0.52 to 0.74 mm per 1,000 years. These values are an order of magnitude less than estimates of carbonate dissolution and suggest that transport of overburden underground is limited by triggering events.     

Experimental determination of the solubility of Au in silicate melts

Summary We report here new data on the solubility of Au in silicate melts of anorthite-diopside eutectic composition at a wide range of oxygen fugacities, from pure oxygen to 10^–8 atm, and at a temperature range of 1300 °C to 1480 °C. Because experiments were done with metal loops at temperatures above the Au-melting temperature, PdAu-metal-alloys had to be used. Pd-solubility data derived from the same set of experiments agree with earlier data obtained from experiments with pure Pd-metal (Borisov et al., 1994a). The results of the present experiments show that Pd-solubilities are by a factor of 2 to 6 higher than Au-solubilities. Both, Au and Pd solubilities decrease with decreasing oxygen fugacity. At oxygen fugacities below the iron-wiistite buffer (IW) Au solubility increases with decreasing fO₂ probably reflecting formation of Au-silicides at such reducing conditions. Compared to Pd, Au has higher activity coefficients in Fe-metal and lower solubility in silicate melts. This leads to similar metal-silicate partition coefficients for both elements. At a temperature of 1350 °C and an oxygen fugacity corresponding to IW-2 D^Au (met/sil) is about 2.5 · 10⁷ and D^Pd (met/sil) about 1.6 · 10⁷. Thus similar behavior is expected during metal separation in planetary bodies including core formation in the Earth. The metal/silicate partition coefficient of Ir is, however, by several orders of magnitudes higher (Borisov and Palme, 1995a). Equilibration with chondritic metal will therefore lead to grossly non-chondritic Pd/Ir or Au/Ir ratios in coexisting silicate phases. Chondritic ratios are thus indicative of the presence of unfractionated meteoritic components. Samples from the upper mantle of the Earth, for example, reflect the admixture of a late unfractionated (chondritic) veneer (e.g.,Kimura et al., 1974;Jagoutz et al., 1979).Solubilities of Pd and Au in silicate melts are much higher than the contents in terrestrial basalts implying that the abundances of these two elements are not buffered by residual PGE- and Au-containing alloys. The most likely process for fractionating PGEs in terrestrial magmas are mineral-melt (e.g., olivine/melt) equilibria.

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Experimentelle Bestimmung der Löslichkeit von Au in Silikatschmelzen

Zusammenfassung In der vorliegenden Arbeit wird über die Ergebnisse der Bestimmung der Löslichkeit von Au in Silikatschmelzen mit der Zusammensetzung des Anorthit-Diopsid Eutektikums berichtet. Die Versuche wurden mittels Metallschlaufe über einen weiten Sauerstoffpartialdruckbereich, von reinem Sauerstoff bis zu 10^–8 atm und in einem Temperaturbereich von 1300 °C bis 1480 °C, durchgeführt. Da diese Temperaturen jedoch den Au-Schmelzpunkt überschreiten, wurde mit AuPd-Legierungen gearbeitet. Die Ergebnisse der dadurch zusätzlich erhaltenen Pd-Versuche stimmen mit früher bestimmten, mit reinen Pd-Schlaufen durchgeführten Pd-Löslichkkeiten überein (Borisov et al., 1994a). Die auf reine Metalle zurückgerechneten Löslichkeiten von Pd sind um einen Faktor 2 bis 6 mal höher als die entsprechenden Au-Löslichkeiten. Die Löslichkeiten beider Metalle nehmen mit abnehmendem Sauerstoffpartialdruck ab. Unter noch stärker reduzierenden Bedingungen (Eisen-Wüstit Gleichgewicht) nimmt die Löslichkeit von Au jedoch zu. Dies könnte auf die Bildung von Au-Siliziden zurückzuführen sein.Im Vergleich zu Pd sind die Aktivitätskoeffizienten von Au in metallischem Eisen höher, die Löslichkeiten in Silikatschmelzen jedoch niedriger. Das führt zu ähnlichen Metall/Silikat Verteilungskoeffizienten von Au und Pd. Bei einer Temperatur von 1350 °C und einer Sauerstoffugazität von IW-2 ergeben sich für D^Au (met/sil) 2.5 · 10⁷ und für D^Pd (met/sil) 1.6* 10⁷. Der Metall/Silikat-Verteilungskoeffizient von Ir ist jedoch unter den gleichen Bedingungen um mehrere Größenordnungen höher (Borisov andPalme, 1995a). Ein chondritisches Pd/Ir- oder Au/Ir-Verhältnis kann also auf die Anwesenheit einer unfraktionierten chondritischen Komponente zurückgeführt werden. Dies gilt beispielsweise für Proben aus dem oberen Erdmantel. Hier handelt es sich vermutlich um Zumischung einer späten chondritischen Akkretionskomponente, die sich nicht mehr mit einer metallischen Phase (Kern) ins Gleichgewicht gesetzt hat (z.B.Kimura et al., 1974,Jagoutz et al., 1979).Die Löslichkeiten von Pd und Au in Silikatschmelzen sind wesentlich höher als ihre Gehalte in basaltischen und komatiitischen Laven. Dies bedeutet, daß Au und Pd in Schmelzen aus dem Erdmantel nicht durch residuale Au- und/oder Pd-haltige Metall phasen bestimmt sind. Gleichgewichte zwischen Schmelze und Mineralen (z.B. Olivin) sind die wahrscheinlichsten Fraktionierungsmechanismen für Platingruppenelemente in terrestrischen Magmen.

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Geostatistical regionalization of glacial aquitard thickness in northwestern Germany, based on fuzzy kriging

In many instances hydrogeological parameters obtained by conventional methods for selected localities within an aquifer or an aquitard are not sufficient for adequate regionalization at the scale of the entire layer. Here, we demonstrate an application of the fuzzy kriging method in regionalization of hydrogeological data, in which the set of conventional, crisp values is supplemented by imprecise information subjectively estimated by an expert. It is believed that such an approach eventually may reflect the real-world conditions more closely than a traditional crisp-value approach, because the former does not impose exactness artificially on phenomena which are diffuse by their nature. Spatial interpolation was done for the thickness of one of the major aquitards (till and glaciolacustrine clay) in northwestern Germany. The dataset consists of 329 crisp values from boreholes supplemented by 172 imprecise values defined as fuzzy numbers. It is demonstrated that the reliability of regionalization was higher, compared to regionalization performed with the crisp dataset only. Fuzzy kriging was performed with FUZZEKS (Fuzzy Evaluation and Kriging System) developed at the Ecosystem Research Center at the University of Kiel.     

Primary minerals of Zn-Pb mining and metallurgical dumps and their environmental behavior at Plombières,Belgium

The primary phases and minerals of the Plombières dumps include typical smelting furnace products such as metallic Fe, Pb, Cu, Zn, Fe-Zn alloys, carbides, phosphides, sulfides of Fe, Zn, Pb, Cu, Mn (alabandite), and FeAs. Spinels, mainly of Fe and Al, are common constituents of the primary assemblage; substitution by Zn, V, Cr, Ti, Mg, and Ca occurs. Primary phases also include the most common Zn-rich fayalite, Zn-rich Ca-Fe silicates, melilite, corundum, and apatite. Most of the Zn is incorporated in iron silicates, ZnO and ZnS. Lead occurs mainly as PbS, metallic lead, and is also present in coal residues. Cadmium is found mainly in metallic zinc and its alloys and in ZnO. The dumps also contain mining wastes composed of pyrite, melnikovite, and iron oxides produced by natural weathering of Zn-Pb ores. Melnikovite and iron oxides are rich in As, Pb, and Zn and possess an increased content of Tl. Leaching tests carried out on the surfaces of polished sections indicate that acid rain (solutions I and II) will mobilize mainly Zn and Cd and, to a much smaller extent, Pb and Sb. Leaching of metals by sulfate-chloride fluids present in the pore network of dumps (solutions III, IV, and V) depends on the pH, which in the dumps is controlled by the proportion of carbonates to sulfides. The more acid fluids leach both sulfides and silicates.     

Surface chemical analysis in coal preparation research: complementary information from XPS and ToF-SIMS

The application of X-ray photoelectron spectroscopy (XPS) to coal surface characterisation for preparation research is described. Progress towards the acquisition of complementary surface chemical information by time-of-flight secondary ion mass spectrometry (ToF-SIMS) is also discussed. Surface-based beneficiation techniques such as flotation are assuming greater importance as the proportion of fines in raw coal increases due to the proliferation of high capacity mining methods. A necessary condition for the floatability of a coal particle is adequate hydrophobicity, and the degree of hydrophobicity of the flotation concentrate is one factor influencing the ease with which its dewatering can be affected. The hydrophobicity of a coal is very difficult to measure directly because of microporosity, and it is often necessary to deduce the degree of hydrophobicity from a knowledge of the surface chemistry. XPS is able to provide sufficient analytical data to allow relative levels of hydrophobicity to be estimated. In principle, ToF-SIMS should be able to supply additional information enabling refinement of such estimates; however, there are insufficient data at present to allow the ionic fragments detected to be related to specific functional groups at the coal surface.     

Palaeomagnetic study of Archaean Banded Hematite Jasper Rocks from the Singhbhum-Orissa Craton, India

The Banded Hematite Jasper Formation within the Iron Ore Supergroup of the Singhbhum Craton in eastern India comprises fine alternating layers of jasper and specularite. It was deposited at 3000 Ma and deformed by a mobile episode at 2700 Ma. Hematite pigment (<1 μm) mixed with cryptocrystalline silica and specularite (> 10 μm) is chiefly responsible for red to brown rhythmic bands in the hematite jasper facies although thermomagnetic study also shows that minor amounts (1–2%) of magnetite are present. Palaeomagnetic study identifies a dual polarity remanence resident in hematite (D/I = 283/60°, α₉₅ = 12°) which predates deformation. Studies of the fabric of magnetic susceptibility and rock magnetic results suggest a diagenetic origin for this magnetisation with the hematite formed from oxidation of primary magnetite. The palaeopole (32°E, 24°N, dp/dm = 14/18°) records the earliest post-metamorphic magnetisation event in the Orissa Craton. A minimum apparent polar wander motion of the Orissa-Singhbhum craton of through 80° is identified during Late Archaean times (2900-2600 Ma).     

Time-dependent behaviour of deep clays

The time-dependent behaviour of deep saturated clays is related both to the effects of hydraulic diffusion and of viscosity. In this paper, we present first, by means of an experimental approach, the main features of the mechanical properties of deep clays. Then, we study the effects of these specific behaviours on the time-dependent behaviour of underground structures. We present theoretical and numerical investigations of the effects of pore pressure diffusion resulting from a tunnel excavation in a poroplastic or poroviscoplastic medium. Finite-element calculations show that the time-dependent convergence of the tunnel wall is non negligible. Then, we focus on the behaviour of a cylindrical thermal source buried in a deep clay.

Coupling effects between thermal, hydraulic and mechanical behaviours are very important in soft and low permeable deep clays (saturated compressible clays with high porosity). We show in particular that the displacements and the stresses are very sensitive to the constitutive model. Irreversible behaviour may be traduced by appearance of residual stresses within the rockmass.