Two-dimensional dynamic analysis of concrete gravity and embankment dams including hydrodynamic effects

An analysis procedure in the frequency domain is developed for determining the earthquake response of two-dimensional concrete gravity and embankment dams including hydrodynamic effects; responses of the elastic dams and compressible water are assumed linear. The dam and fluid domain are treated as substructures and modelled with finite elements. The only geometric restriction is that an infinite fluid domain must maintain a constant depth beyond some point in the upstream direction. For such an infinite uniform region, a finite element discretization over the depth is combined with a continuum representation in the upstream direction. The fluid domain model approximately accounts for interaction between the fluid and underlying foundation medium through a damping boundary condition applied along the reservoir bottom, while the dam foundation is assumed rigid. Several examples are presented to demonstrate the accuracy of the fluid domain model and to illustrate dam responses obtained from the analysis procedure.     

Gypsum as a precursor to pyrrhotite in metamorphic rocks

During low-grade regional metamorphism, pyrrhotite can form from gypsum by the reaction: CaSO₄·2H₂O+Fe _sol. ²⁺ +2C_org.FeS+Ca _sol. ²⁺ +2H₂O+2CO₂. This reaction takes place in the anchizone, below 350°C and might be initiated by the thermal dehydration of gypsum (200°C) and aided by the generation of gaseous hydrocarbons. Evidence for the reaction is the occurrence in dolomitic layers in the Ballachulish Slate, East Larroch quarry, Argyll of lath and swallow-tail shaped quartz+dolomite+pyrrhotite pseudomorphs after gypsum. Quartz+pyrrhotite bodies in slate represent replaced and deformed (mainly flattened) crystals, concretions and possible veinlets of gypsum. Pyrite porphyroblast growth, after the peak of metamorphism and under relatively high fS₂ conditions, failed to destroy some early pyrrhotite because it is encapsulated in quartz. Pyrite-silicate reactions and hydrothermal exhalations have been suggested previously to account for pyrrhotite-enriched horizons in regionally metamorphosed rocks. Replacement of gypsum by pyrrhotite is an additional explanation for pyrrhotite-enriched horizons, especially in dolomitic and graphitic lithologies.     

Constraints on crustal hydration below the Colorado plateau from Vp measurements on crustal xenoliths

Seismic velocities have been measured as a function of confining pressure to 8 kbar for crustal xenoliths from the Moses Rock Dike and Mule Ear Diatreme, two kimberlite pipes on the Colorado Plateau. Rock types measured include rhyolite, granite, diorite, metasedimentary schists and gneisses, mafic amphibolites and granulites. Many of our samples have been hydrothermally altered to greenschist facies mineral assemblages during transport to the earth's surface. The velocity of compressional waves measured on altered amphibolites and granulites are too low by 0.1–0.3 km/s for such rock types to be characteristic of deep crustal levels. A direct correlation exists between progressive alteration and the presence of microcracks extending into the xenoliths from the kimberlitic host rock. Velocities of pristine samples are compatible with existing velocity profiles for the Colorado Plateau and we conclude that the crust at depths greater than 15 km has probably not undergone a greenschist facies metamorphic event. The xenolith suite reflects a crustal profile similar to that exposed in the Ivrea-Verbano and Strona-Ceneri zones in northern Italy.     

Sorted stripes orientated by wind action: Some observations from sub-antarctic marion island

Sorted stripes found on the volcanic scoria and glacial deposits of sub-Antarctic Marion Island indicate a distinct preferred orientation. Despite uniformity of slope and material, the stripes are predominantly aligned parallel to the wind. It is suggested that melting of needle ice by the early morning sun is of only limited importance in the sub-Antarctic owing to the almost continual overcast conditions. The effect of the wind is so great that in exposed situations stripes are formed on horizontal surfaces.     

Analysis of fluoride, chloride, nitrate and sulphate in natural waters using ion chromatography

The analysis of anion components of thirty natural water samples using an ion-chromatographic method were compared to analyses for F, Cl, NO₃ and SO₄ obtained by presently used techniques. Of these thirty samples, five were replicates. Precision estimates were also calculated from synthetic solution replicates. In addition, a comparison of results obtained through separator columns of two different lengths (250 mm and 500 mm) was completed. An inter-anion interference test indicated that, at pH 6, analysis of low concentrations of any one of the four anions studied was not affected by large concentrations of the other three anions. Reported detection limits for the ion-chromatographic technique are one to two orders of magnitude below routine methods. Replicate sample analysis indicated that a relative standard deviation below 1 percent was possible for F, Cl, NO₃ and SO₄.     

The geochemistry of El Misti volcano,Peru fumaroles

El Misti is a 5822 m strato volcano in southern Peru. The mineralogy of the fumaroles is essentially sulfur, anhydrite, gypsum and ralstonite which are precipitated by acid vapors at 100°C–125°C. There are 2 to 6 parts per thousand chloride concentrations and several parts per million sodium, potassium, magnesium, calcium, iron and zinc concentrations in the condensed vapors. Elemental ratios indicate near complete leaching of the wall rock by the vapors. Arsenic and selenium are contaminants of the sulfur but are absent from the other minerals. Both the gypsum and anhydrite contain strontium and lead and show no tendency to fractionate these metals. The anhydrite alone contains significant thallium and bismuth. Bromine, strontium, thallium and lead are present in the ralstonite. The average δ D and δ O¹⁸ ratios from the fumarolic condensates are ?31.4 ‰ and +4.8 ‰ respectively. A marine contaminated heavy water source at depth is indicated as the parent water for the vapors.