The solubility of aragonite in seawater at 25.0°C and 32.62‰ salinity

The apparent solubility product of aragonite in 32‰ seawater at 25.0°C is reported as K′_sp = (0.869±0.049) × 10^?6(mol²kgseawater^?2) thus confirming the value of R.A. Berner, 1976 (Am. J. Sci., 276: 713–730). The apparent solubility product ratio for aragonite and calcite is reported as $\text{K′}{}_{\mathrm{aragonite}}\text{K′}{}_{\mathrm{calcite}}\text{= 2.05}$ The deviation of this value from the thermodynamic ratio is atttributed to the formation of a stable low Mg-calcite coating on pure calcite in seawater measurements of solubility.     

Decision support for conceptual performance‐based design

Performance assessment implies that the structural, non‐structural, and content systems are given and that decision variables, DVs, (e.g. expected annual loss, mean annual frequency of collapse) are computed and compared to specified performance targets. Performance‐based design (PBD) is different by virtue of the fact that the building and its components and systems first have to be created. Good designs are based on concepts that incorporate performance targets up front in the conceptual design process, so that subsequent performance assessment becomes more of a verification process of an efficient design rather than a design improvement process that may require radical changes of the initial design concept. In short, the design approach could consist of (a) specifying performance targets (e.g. tolerable probability of collapse, acceptable dollar losses) and associated seismic hazards, and (b) deriving engineering parameters for system selection, or perhaps better, using the relatively simple design decision support tools discussed in this paper. Copyright © 2005 John Wiley & Sons, Ltd.     

Ordovician K-bentonites in the upper-plate active margin of Western Gondwana, (Famatina Ranges): Stratigraphic and palaeogeographic significance

Numerous, thin-bedded, tabular pale-yellowish clay bands are interlayered with black shales in a biostratigraphically constrained Early Ordovician volcano-sedimentary succession at Famatina, western Argentina. This region was part of a fairly continuous upper-plate, convergent volcanic chain that fringed western Gondwana. Mineralogy on both clay and non-clay fractions, whole rock chemistry and field observations on these distinctive event-beds indicate that they originated as relatively coarse fallout tephras, altered first into bentonites and later, through burial metamorphism, into K-bentonites (metabentonites). These tephras were deposited as single crystals and glassy dust or pumiceous fragments in a restricted subtidal environment. The region of Famatina has previously been inferred as the source of abundant distal K-bentonites recorded in the adjacent lower-plate allochthonous Precordillera terrane. However, these K-bentonites within the proximal arc site were unknown and rather unexpected since they are generally better preserved like distal deposits, associated either with central vent plinian–ultraplinian eruptions or with accompanying co-ignimbrite ash clouds. Their chemistry and comparison with those K-bentonites in the Precordillera allow tracing an evolution from volcanic arcs into continental crust. K-bentonites described in this paper are much older than those recorded in the adjacent Precordillera terrane and seem to be associated with a first eruptive period along western Gondwana that has no counterpart in the Argentine Precordillera, suggesting a significant longitudinal separation between these two regions by the Early Ordovician.     

Geologic and tectonic setting of Deseado Massif epithermal deposits, Argentina, based on El Dorado-Monserrat

Middle–Late Jurassic bimodal volcanism, typical of a retroarc setting, developed during widespread extensional tectonism within the Deseado Massif, southern Argentina. This geologic environment led to the formation of numerous low-sulfidation epithermal deposits that are spatially and temporally related to the volcanic activity. The lack of significant high-sulfidation epithermal deposits may be because the tectonic and volcanic settings do not favor the formation of these types of deposits. El Dorado-Monserrat is a low-sulfidation epithermal prospect located near the southern boundary of the Deseado Massif. Mineralization is genetically linked to the Late Jurassic Chon Aike Formation and hosted by volcanic rocks of the middle Late Jurassic Bajo Pobre Formation. Two different mineralization areas have been identified. The Monserrat area is the most important, with veins hosted in a north-striking, left-lateral shear zone. The average thickness is 0.85 m, and the average metal content is 6.2 ppm gold and 153 ppm silver. The El Dorado area has discontinuous echelon veins within a right-lateral shear zone with low gold and silver grades. Hydrothermal alteration of the host rocks includes an inner zone of quartz-adularia and illite alteration and an outer zone of propylitic alteration. The main gangue mineral is quartz, which formed in successive pulses, plus adularia, pyrite, hematite, magnetite, and barite. Precious metals occur as zoned electrum. Ore mineral precipitation took place between 200 and 280 °C from low salinity fluids due to boiling.     

The Río Tinto Basin, Spain: Mineralogy, sedimentary geobiology, and implications for interpretation of outcrop rocks at Meridiani Planum, Mars

Exploration by the NASA rover Opportunity has revealed sulfate- and hematite-rich sedimentary rocks exposed in craters and other surface features of Meridiani Planum, Mars. Modern, Holocene, and Plio-Pleistocene deposits of the Río Tinto, southwestern Spain, provide at least a partial environmental analog to Meridiani Planum rocks, facilitating our understanding of Meridiani mineral precipitation and diagenesis, while informing considerations of martian astrobiology. Oxidation, thought to be biologically mediated, of pyritic ore bodies by groundwaters in the source area of the Río Tinto generates headwaters enriched in sulfuric acid and ferric iron. Seasonal evaporation of river water drives precipitation of hydronium jarosite and schwertmannite, while (Mg,Al,Fe³⁺)-copiapite, coquimbite, gypsum, and other sulfate minerals precipitate nearby as efflorescences where locally variable source waters are brought to the surface by capillary action. During the wet season, hydrolysis of sulfate salts results in the precipitation of nanophase goethite. Holocene and Plio-Pleistocene terraces show increasing goethite crystallinity and then replacement of goethite with hematite through time. Hematite in Meridiani spherules also formed during diagenesis, although whether these replaced precursor goethite or precipitated directly from groundwaters is not known. The retention of jarosite and other soluble sulfate salts suggests that water limited the diagenesis of Meridiani rocks.Diverse prokaryotic and eukaryotic microorganisms inhabit acidic and seasonally dry Río Tinto environments. Organic matter does not persist in Río Tinto sediments, but biosignatures imparted to sedimentary rocks as macroscopic textures of coated microbial streamers, surface blisters formed by biogenic gas, and microfossils preserved as casts and molds in iron oxides help to shape strategies for astrobiological investigation of Meridiani outcrops.     

The solubility of calcite — probably containing magnesium — in seawater

The apparent solubility product of calcite was measured by saturometry as a function of temperature and salinity. Simplified equations for the carbonic-acid dissociation constants of Mehrbach et al., 1973 (Limnol. Oceanogr., 18: 897–907) have been derived from their experimental data and used to calculate apparent solubility product, K′_sp, K′_sp at 25°C and 35‰ salinity, was found to be K′_sp = 4.70 × 10^?7(mol²kgseawater^?2) An equation was fitted to the experimental data, resulting in pK′_sp = 6.5795 ? 3.7159 × 10⁵(TS) + 0.91056(T/S) ? 22.110(1.0/S)The mean activity coefficients, $\text{γ±}\text{CaCO}{}_3$, were calculated at various temperatures and salinities, using the thermodynamic solubility product of Jacobson and Langmuir, 1974 (Geochim. Cosmochim. Acta, 38: 301–318) and the apparent solubility products quoted in their paper. The change in K′_sp at each salinity, as a function of temperature, was used to calculate the apparent enthalpy of dissociation for calcite, ΔH′, and the extrapolated value of ΔH⁰ was in good agreement with that of Jacobson and Langmuir. Finally, this work was used to calculate saturation profiles for oceanic stations and as a basis for comment of the accuracy of in-situ saturometry, as well as the applicability of in-situ K′_sp pressure corrections.